[{"page":"89","file":[{"date_created":"2024-03-01T08:56:06Z","checksum":"55c876b73d49db15228a7f571592ec77","creator":"cchlebak","content_type":"application/pdf","file_size":10416761,"title":"Combined Version of original Thesis and Addendum","file_id":"15044","access_level":"open_access","date_updated":"2024-10-29T23:31:04Z","embargo_to":"open_access","file_name":"Print_Version_Franschitz_Anna_Thesis.pdf","relation":"main_file"},{"checksum":"27220243d5d51c3b0d7d61c0879d7a0c","creator":"afransch","date_created":"2023-08-08T18:01:28Z","content_type":"application/pdf","file_size":10797612,"embargo":"2024-08-08","date_updated":"2024-08-09T22:30:03Z","file_id":"13986","access_level":"open_access","file_name":"Thesis_AnnaFranschitz_202308.pdf","relation":"main_file"},{"content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document","file_size":2619085,"date_created":"2023-08-08T18:02:25Z","creator":"afransch","checksum":"40abf7ccca14a3893f72dc7fb88585d6","embargo_to":"open_access","relation":"source_file","file_name":"Thesis_AnnaFranschitz_202308.docx","access_level":"closed","file_id":"13987","date_updated":"2024-08-09T22:30:03Z"},{"file_size":85956,"content_type":"application/pdf","checksum":"8b991ecc2d59d045cc3cf0d676785ec7","creator":"cchlebak","date_created":"2024-03-01T08:37:15Z","file_name":"Addendum_AnnaFranschitz202402.pdf","relation":"main_file","date_updated":"2024-10-29T23:31:04Z","description":"Minor modifications and clarifications - Feb 2024","embargo":"2024-08-08","title":"Addendum","file_id":"15042","access_level":"open_access"},{"file_id":"15043","title":"Addendum - source file","access_level":"closed","date_updated":"2024-08-09T22:30:03Z","embargo_to":"open_access","file_name":"Addendum_AnnaFranschitz202402.docx","relation":"source_file","date_created":"2024-03-01T08:39:20Z","checksum":"66745aa01f960f17472c024875c049ed","creator":"cchlebak","file_size":11818,"content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document"}],"author":[{"last_name":"Franschitz","full_name":"Franschitz, Anna","id":"480826C8-F248-11E8-B48F-1D18A9856A87","first_name":"Anna"}],"date_created":"2023-08-08T15:33:29Z","department":[{"_id":"GradSch"},{"_id":"SyCr"}],"language":[{"iso":"eng"}],"month":"08","supervisor":[{"first_name":"Sylvia","id":"2F64EC8C-F248-11E8-B48F-1D18A9856A87","full_name":"Cremer, Sylvia","last_name":"Cremer","orcid":"0000-0002-2193-3868"}],"alternative_title":["ISTA Thesis"],"publication_identifier":{"issn":["2663-337X"],"isbn":["978-3-99078-034-3"]},"year":"2023","ddc":["570","577"],"corr_author":"1","type":"dissertation","abstract":[{"text":"Social insects fight disease using their individual immune systems and the cooperative\r\nsanitary behaviors of colony members. These social defenses are well explored against\r\nexternally-infecting pathogens, but little is known about defense strategies against\r\ninternally-infecting pathogens, such as viruses. Viruses are ubiquitous and in the last decades\r\nit has become evident that also many ant species harbor viruses. We present one of the first\r\nstudies addressing transmission dynamics and collective disease defenses against viruses in\r\nants on a mechanistic level. I successfully established an experimental ant host – viral\r\npathogen system as a model for the defense strategies used by social insects against internal\r\npathogen infections, as outlined in the third chapter. In particular, we studied how garden ants\r\n(Lasius neglectus) defend themselves and their colonies against the generalist insect virus\r\nCrPV (cricket paralysis virus). We chose microinjections of virus directly into the ants’\r\nhemolymph because it allowed us to use a defined exposure dose. Here we show that this is a\r\ngood model system, as the virus is replicating and thus infecting the host. The ants mount a\r\nclear individual immune response against the viral infection, which is characterized by a\r\nspecific siRNA pattern, namely siRNAs mapping against the viral genome with a peak of 21\r\nand 22 bp long fragments. The onset of this immune response is consistent with the timeline\r\nof viral replication that starts already within two days post injection. The disease manifests in\r\ndecreased survival over a course of two to three weeks.\r\nRegarding group living, we find that infected ants show a strong individual immune response,\r\nbut that their course of disease is little affected by nestmate presence, as described in chapter\r\nfour. Hence, we do not find social immunity in the context of viral infections in ants.\r\nNestmates, however, can contract the virus. Using Drosophila S2R+ cells in culture, we\r\nshowed that 94 % of the nestmates contract active virus within four days of social contact to\r\nan infected individual. Virus is transmitted in low doses, thus not causing disease\r\ntransmission within the colony. While virus can be transmitted during short direct contacts,\r\nwe also assume transmission from deceased ants and show that the nestmates’ immune\r\nsystem gets activated after contracting a low viral dose. We find considerable potential for\r\nindirect transmission via the nest space. Virus is shed to the nest, where it stays viable for one\r\nweek and is also picked up by other ants. Apart from that, we want to underline the potential\r\nof ant poison as antiviral agent. We determined that ant poison successfully inactivates CrPV\r\nin vitro. However, we found no evidence for effective poison use to sanitize the nest space.\r\nOn the other hand, local application of ant poison by oral poison uptake, which is part of the\r\nants prophylactic behavioral repertoire, probably contributes to keeping the gut of each\r\nindividual sanitized. We hypothesize that oral poison uptake might be the reason why we did\r\nnot find viable virus in the trophallactic fluid.\r\nThe fifth chapter encompasses preliminary data on potential social immunization. However,\r\nour experiments do not confirm an actual survival benefit for the nestmates upon pathogen\r\nchallenge under the given experimental settings. Nevertheless, we do not want to rule out the\r\npossibility for nestmate immunization, but rather emphasize that considering different\r\nexperimental timelines and viral doses would provide a multitude of options for follow-up\r\nexperiments.\r\nIn conclusion, we find that prophylactic individual behaviors, such as oral poison uptake,\r\nmight play a role in preventing viral disease transmission. Compared to colony defense\r\nagainst external pathogens, internal pathogen infections require a stronger component of\r\nindividual physiological immunity than behavioral social immunity, yet could still lead to\r\ncollective protection.","lang":"eng"}],"oa":1,"date_updated":"2026-04-07T13:51:29Z","doi":"10.15479/at:ista:13984","article_processing_charge":"No","date_published":"2023-08-08T00:00:00Z","citation":{"ama":"Franschitz A. Individual and social immunity against viral infections in ants. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:13984\">10.15479/at:ista:13984</a>","apa":"Franschitz, A. (2023). <i>Individual and social immunity against viral infections in ants</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:13984\">https://doi.org/10.15479/at:ista:13984</a>","short":"A. Franschitz, Individual and Social Immunity against Viral Infections in Ants, Institute of Science and Technology Austria, 2023.","mla":"Franschitz, Anna. <i>Individual and Social Immunity against Viral Infections in Ants</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:13984\">10.15479/at:ista:13984</a>.","ieee":"A. Franschitz, “Individual and social immunity against viral infections in ants,” Institute of Science and Technology Austria, 2023.","chicago":"Franschitz, Anna. “Individual and Social Immunity against Viral Infections in Ants.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:13984\">https://doi.org/10.15479/at:ista:13984</a>.","ista":"Franschitz A. 2023. Individual and social immunity against viral infections in ants. Institute of Science and Technology Austria."},"_id":"13984","oa_version":"Published Version","file_date_updated":"2024-10-29T23:31:04Z","OA_place":"publisher","title":"Individual and social immunity against viral infections in ants","degree_awarded":"PhD","acknowledged_ssus":[{"_id":"LifeSc"}],"publication_status":"published","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","day":"08","publisher":"Institute of Science and Technology Austria","has_accepted_license":"1","status":"public"},{"oa":1,"date_updated":"2026-04-07T13:52:57Z","doi":"10.15479/at:ista:12964","article_processing_charge":"No","date_published":"2023-05-17T00:00:00Z","ddc":["530"],"corr_author":"1","type":"dissertation","abstract":[{"text":"Pattern formation is of great importance for its contribution across different biological behaviours. During developmental processes for example, patterns of chemical gradients are\r\nestablished to determine cell fate and complex tissue patterns emerge to define structures such\r\nas limbs and vascular networks. Patterns are also seen in collectively migrating groups, for\r\ninstance traveling waves of density emerging in moving animal flocks as well as collectively migrating cells and tissues. To what extent these biological patterns arise spontaneously through\r\nthe local interaction of individual constituents or are dictated by higher level instructions is\r\nstill an open question however there is evidence for the involvement of both types of process.\r\nWhere patterns arise spontaneously there is a long standing interest in how far the interplay\r\nof mechanics, e.g. force generation and deformation, and chemistry, e.g. gene regulation\r\nand signaling, contributes to the behaviour. This is because many systems are able to both\r\nchemically regulate mechanical force production and chemically sense mechanical deformation,\r\nforming mechano-chemical feedback loops which can potentially become unstable towards\r\nspatio and/or temporal patterning.\r\nWe work with experimental collaborators to investigate the possibility that this type of\r\ninteraction drives pattern formation in biological systems at different scales. We focus first on\r\ntissue-level ERK-density waves observed during the wound healing response across different\r\nsystems where many previous studies have proposed that patterns depend on polarized cell\r\nmigration and arise from a mechanical flocking-like mechanism. By combining theory with\r\nmechanical and optogenetic perturbation experiments on in vitro monolayers we instead find\r\nevidence for mechanochemical pattern formation involving only scalar bilateral feedbacks\r\nbetween ERK signaling and cell contraction. We perform further modeling and experiment\r\nto study how this instability couples with polar cell migration in order to produce a robust\r\nand efficient wound healing response. In a following chapter we implement ERK-density\r\ncoupling and cell migration in a 2D active vertex model to investigate the interaction of\r\nERK-density patterning with different tissue rheologies and find that the spatio-temporal\r\ndynamics are able to both locally and globally fluidize a tissue across the solid-fluid glass\r\ntransition. In a last chapter we move towards lower spatial scales in the context of subcellular\r\npatterning of the cell cytoskeleton where we investigate the transition between phases of\r\nspatially homogeneous temporal oscillations and chaotic spatio-temporal patterning in the\r\ndynamics of myosin and ROCK activities (a motor component of the actomyosin cytoskeleton\r\nand its activator). Experimental evidence supports an intrinsic chemical oscillator which we\r\nencode in a reaction model and couple to a contractile active gel description of the cell cortex.\r\nThe model exhibits phases of chemical oscillations and contractile spatial patterning which\r\nreproduce many features of the dynamics seen in Drosophila oocyte epithelia in vivo. However,\r\nadditional pharmacological perturbations to inhibit myosin contractility leaves the role of\r\ncontractile instability unclear. We discuss alternative hypotheses and investigate the possibility\r\nof reaction-diffusion instability.","lang":"eng"}],"ec_funded":1,"alternative_title":["ISTA Thesis"],"publication_identifier":{"issn":["2663-337X"],"isbn":["978-3-99078-032-9"]},"year":"2023","page":"146","file":[{"file_size":40414730,"content_type":"application/pdf","date_created":"2023-05-17T13:39:54Z","creator":"dboocock","checksum":"d51240675fc6dc0e3f5dc0c902695d3a","relation":"main_file","file_name":"thesis_boocock.pdf","access_level":"open_access","file_id":"12988","embargo":"2024-05-17","date_updated":"2024-05-18T22:30:03Z"},{"content_type":"application/zip","file_size":34338567,"date_created":"2023-05-17T13:39:53Z","creator":"dboocock","checksum":"581a2313ffeb40fe77e8a122a25a7795","embargo_to":"open_access","relation":"source_file","file_name":"thesis_boocock.zip","access_level":"closed","file_id":"12989","date_updated":"2024-05-18T22:30:03Z"}],"author":[{"id":"453AF628-F248-11E8-B48F-1D18A9856A87","first_name":"Daniel R","orcid":"0000-0002-1585-2631","last_name":"Boocock","full_name":"Boocock, Daniel R"}],"language":[{"iso":"eng"}],"department":[{"_id":"GradSch"},{"_id":"EdHa"}],"date_created":"2023-05-15T14:52:36Z","supervisor":[{"orcid":"0000-0001-6005-1561","last_name":"Hannezo","full_name":"Hannezo, Edouard B","id":"3A9DB764-F248-11E8-B48F-1D18A9856A87","first_name":"Edouard B"}],"month":"05","publisher":"Institute of Science and Technology Austria","has_accepted_license":"1","status":"public","tmp":{"image":"/images/cc_by_nc_sa.png","name":"Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode","short":"CC BY-NC-SA (4.0)"},"publication_status":"published","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","day":"17","file_date_updated":"2024-05-18T22:30:03Z","OA_place":"publisher","title":"Mechanochemical pattern formation across biological scales","degree_awarded":"PhD","citation":{"ista":"Boocock DR. 2023. Mechanochemical pattern formation across biological scales. Institute of Science and Technology Austria.","ieee":"D. R. Boocock, “Mechanochemical pattern formation across biological scales,” Institute of Science and Technology Austria, 2023.","chicago":"Boocock, Daniel R. “Mechanochemical Pattern Formation across Biological Scales.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:12964\">https://doi.org/10.15479/at:ista:12964</a>.","mla":"Boocock, Daniel R. <i>Mechanochemical Pattern Formation across Biological Scales</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:12964\">10.15479/at:ista:12964</a>.","short":"D.R. Boocock, Mechanochemical Pattern Formation across Biological Scales, Institute of Science and Technology Austria, 2023.","apa":"Boocock, D. R. (2023). <i>Mechanochemical pattern formation across biological scales</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:12964\">https://doi.org/10.15479/at:ista:12964</a>","ama":"Boocock DR. Mechanochemical pattern formation across biological scales. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:12964\">10.15479/at:ista:12964</a>"},"related_material":{"record":[{"relation":"part_of_dissertation","id":"8602","status":"public"}]},"_id":"12964","oa_version":"Published Version","project":[{"name":"International IST Doctoral Program","call_identifier":"H2020","grant_number":"665385","_id":"2564DBCA-B435-11E9-9278-68D0E5697425"}]},{"type":"dissertation","corr_author":"1","ddc":["516","004","518","531"],"abstract":[{"lang":"eng","text":"Inverse design problems in fabrication-aware shape optimization are typically solved on discrete representations such as polygonal meshes. This thesis argues that there are benefits to treating these problems in the same domain as human designers, namely, the parametric one. One reason is that discretizing a parametric model usually removes the capability of making further manual changes to the design, because the human intent is captured by the shape parameters. Beyond this, knowledge about a design problem can sometimes reveal a structure that is present in a smooth representation, but is fundamentally altered by discretizing. In this case, working in the parametric domain may even simplify the optimization task. We present two lines of research that explore both of these aspects of fabrication-aware shape optimization on parametric representations.\r\n\r\nThe first project studies the design of plane elastic curves and Kirchhoff rods, which are common mathematical models for describing the deformation of thin elastic rods such as beams, ribbons, cables, and hair. Our main contribution is a characterization of all curved shapes that can be attained by bending and twisting elastic rods having a stiffness that is allowed to vary across the length. Elements like these can be manufactured using digital fabrication devices such as 3d printers and digital cutters, and have applications in free-form architecture and soft robotics.\r\n\r\nWe show that the family of curved shapes that can be produced this way admits geometric description that is concise and computationally convenient. In the case of plane curves, the geometric description is intuitive enough to allow a designer to determine whether a curved shape is physically achievable by visual inspection alone. We also present shape optimization algorithms that convert a user-defined curve in the plane or in three dimensions into the geometry of an elastic rod that will naturally deform to follow this curve when its endpoints are attached to a support structure. Implemented in an interactive software design tool, the rod geometry is generated in real time as the user edits a curve and enables fast prototyping. \r\n\r\nThe second project tackles the problem of general-purpose shape optimization on CAD models using a novel variant of the extended finite element method (XFEM). Our goal is the decoupling between the simulation mesh and the CAD model, so no geometry-dependent meshing or remeshing needs to be performed when the CAD parameters change during optimization. This is achieved by discretizing the embedding space of the CAD model, and using a new high-accuracy numerical integration method to enable XFEM on free-form elements bounded by the parametric surface patches of the model. Our simulation is differentiable from the CAD parameters to the simulation output, which enables us to use off-the-shelf gradient-based optimization procedures. The result is a method that fits seamlessly into the CAD workflow because it works on the same representation as the designer, enabling the alternation of manual editing and fabrication-aware optimization at will."}],"ec_funded":1,"doi":"10.15479/at:ista:12897","date_updated":"2025-04-15T07:16:15Z","oa":1,"date_published":"2023-05-05T00:00:00Z","article_processing_charge":"No","department":[{"_id":"GradSch"},{"_id":"BeBi"}],"language":[{"iso":"eng"}],"date_created":"2023-05-05T10:40:14Z","author":[{"last_name":"Hafner","full_name":"Hafner, Christian","id":"400429CC-F248-11E8-B48F-1D18A9856A87","first_name":"Christian"}],"file":[{"date_created":"2023-05-11T10:43:20Z","checksum":"cc2094e92fa27000b70eb4bfb76d6b5a","creator":"chafner","file_size":50714445,"content_type":"application/pdf","file_id":"12942","access_level":"open_access","embargo":"2023-12-07","date_updated":"2023-12-08T23:30:04Z","file_name":"thesis-hafner-2023may11-a2b.pdf","relation":"main_file"},{"creator":"chafner","checksum":"a6b51334be2b81672357b1549afab40c","date_created":"2023-05-11T10:43:44Z","file_size":265319,"content_type":"application/pdf","date_updated":"2023-12-08T23:30:04Z","access_level":"closed","file_id":"12943","relation":"source_file","file_name":"thesis-release-form.pdf","embargo_to":"open_access"}],"page":"180","month":"05","supervisor":[{"id":"49876194-F248-11E8-B48F-1D18A9856A87","first_name":"Bernd","last_name":"Bickel","orcid":"0000-0001-6511-9385","full_name":"Bickel, Bernd"}],"publication_identifier":{"isbn":["978-3-99078-031-2"],"issn":["2663-337X"]},"alternative_title":["ISTA Thesis"],"year":"2023","publication_status":"published","day":"05","user_id":"400429CC-F248-11E8-B48F-1D18A9856A87","status":"public","has_accepted_license":"1","publisher":"Institute of Science and Technology Austria","related_material":{"record":[{"status":"public","id":"9817","relation":"part_of_dissertation"},{"id":"13188","status":"public","relation":"dissertation_contains"},{"relation":"part_of_dissertation","status":"public","id":"7117"}]},"citation":{"ieee":"C. Hafner, “Inverse shape design with parametric representations: Kirchhoff Rods and parametric surface models,” Institute of Science and Technology Austria, 2023.","ista":"Hafner C. 2023. Inverse shape design with parametric representations: Kirchhoff Rods and parametric surface models. Institute of Science and Technology Austria.","chicago":"Hafner, Christian. “Inverse Shape Design with Parametric Representations: Kirchhoff Rods and Parametric Surface Models.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:12897\">https://doi.org/10.15479/at:ista:12897</a>.","mla":"Hafner, Christian. <i>Inverse Shape Design with Parametric Representations: Kirchhoff Rods and Parametric Surface Models</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:12897\">10.15479/at:ista:12897</a>.","short":"C. Hafner, Inverse Shape Design with Parametric Representations: Kirchhoff Rods and Parametric Surface Models, Institute of Science and Technology Austria, 2023.","apa":"Hafner, C. (2023). <i>Inverse shape design with parametric representations: Kirchhoff Rods and parametric surface models</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:12897\">https://doi.org/10.15479/at:ista:12897</a>","ama":"Hafner C. Inverse shape design with parametric representations: Kirchhoff Rods and parametric surface models. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:12897\">10.15479/at:ista:12897</a>"},"project":[{"call_identifier":"H2020","_id":"24F9549A-B435-11E9-9278-68D0E5697425","grant_number":"715767","name":"MATERIALIZABLE: Intelligent fabrication-oriented Computational Design and Modeling"}],"_id":"12897","oa_version":"Published Version","title":"Inverse shape design with parametric representations: Kirchhoff Rods and parametric surface models","file_date_updated":"2023-12-08T23:30:04Z","acknowledged_ssus":[{"_id":"M-Shop"}],"degree_awarded":"PhD"},{"file_date_updated":"2024-04-08T22:30:03Z","OA_place":"publisher","title":"Plasticity in the cerebellum: What molecular mechanisms are behind physiological learning","degree_awarded":"PhD","acknowledged_ssus":[{"_id":"EM-Fac"},{"_id":"Bio"},{"_id":"PreCl"}],"citation":{"chicago":"Alcarva, Catarina. “Plasticity in the Cerebellum: What Molecular Mechanisms Are behind Physiological Learning.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:12809\">https://doi.org/10.15479/at:ista:12809</a>.","ista":"Alcarva C. 2023. Plasticity in the cerebellum: What molecular mechanisms are behind physiological learning. Institute of Science and Technology Austria.","ieee":"C. Alcarva, “Plasticity in the cerebellum: What molecular mechanisms are behind physiological learning,” Institute of Science and Technology Austria, 2023.","mla":"Alcarva, Catarina. <i>Plasticity in the Cerebellum: What Molecular Mechanisms Are behind Physiological Learning</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:12809\">10.15479/at:ista:12809</a>.","short":"C. Alcarva, Plasticity in the Cerebellum: What Molecular Mechanisms Are behind Physiological Learning, Institute of Science and Technology Austria, 2023.","apa":"Alcarva, C. (2023). <i>Plasticity in the cerebellum: What molecular mechanisms are behind physiological learning</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:12809\">https://doi.org/10.15479/at:ista:12809</a>","ama":"Alcarva C. Plasticity in the cerebellum: What molecular mechanisms are behind physiological learning. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:12809\">10.15479/at:ista:12809</a>"},"oa_version":"Published Version","_id":"12809","project":[{"name":"Plasticity in the cerebellum: Which molecular mechanisms are behind physiological learning?","_id":"267DFB90-B435-11E9-9278-68D0E5697425"}],"publisher":"Institute of Science and Technology Austria","status":"public","has_accepted_license":"1","publication_status":"published","day":"06","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","alternative_title":["ISTA Thesis"],"publication_identifier":{"issn":["2663-337X"]},"year":"2023","page":"115","file":[{"content_type":"application/pdf","file_size":9881969,"creator":"cchlebak","checksum":"35b5997d2b0acb461f9d33d073da0df5","date_created":"2023-04-07T06:16:06Z","relation":"main_file","file_name":"Thesis_CatarinaAlcarva_final pdfA.pdf","date_updated":"2024-04-08T22:30:03Z","embargo":"2024-04-07","access_level":"open_access","file_id":"12814"},{"file_name":"Thesis_CatarinaAlcarva_final_for printing.pdf","relation":"source_file","embargo_to":"open_access","date_updated":"2024-04-08T22:30:03Z","file_id":"12815","access_level":"closed","file_size":44201583,"content_type":"application/pdf","checksum":"81198f63c294890f6d58e8b29782efdc","creator":"cchlebak","date_created":"2023-04-07T06:17:11Z"},{"embargo_to":"open_access","relation":"source_file","file_name":"Thesis_CatarinaAlcarva_final.docx","access_level":"closed","file_id":"12816","date_updated":"2024-04-08T22:30:03Z","file_size":84731244,"content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document","date_created":"2023-04-07T06:18:05Z","creator":"cchlebak","checksum":"0317bf7f457bb585f99d453ffa69eb53"}],"author":[{"id":"3A96634C-F248-11E8-B48F-1D18A9856A87","first_name":"Catarina","last_name":"Alcarva","full_name":"Alcarva, Catarina"}],"department":[{"_id":"GradSch"},{"_id":"RySh"}],"date_created":"2023-04-06T07:54:09Z","language":[{"iso":"eng"}],"month":"04","supervisor":[{"id":"499F3ABC-F248-11E8-B48F-1D18A9856A87","first_name":"Ryuichi","orcid":"0000-0001-8761-9444","last_name":"Shigemoto","full_name":"Shigemoto, Ryuichi"}],"oa":1,"date_updated":"2026-04-07T13:53:28Z","doi":"10.15479/at:ista:12809","article_processing_charge":"No","date_published":"2023-04-06T00:00:00Z","ddc":["570"],"corr_author":"1","type":"dissertation","abstract":[{"text":"Understanding the mechanisms of learning and memory formation has always been one of\r\nthe main goals in neuroscience. Already Pavlov (1927) in his early days has used his classic\r\nconditioning experiments to study the neural mechanisms governing behavioral adaptation.\r\nWhat was not known back then was that the part of the brain that is largely responsible for\r\nthis type of associative learning is the cerebellum.\r\nSince then, plenty of theories on cerebellar learning have emerged. Despite their differences,\r\none thing they all have in common is that learning relies on synaptic and intrinsic plasticity.\r\nThe goal of my PhD project was to unravel the molecular mechanisms underlying synaptic\r\nplasticity in two synapses that have been shown to be implicated in motor learning, in an\r\neffort to understand how learning and memory formation are processed in the cerebellum.\r\nOne of the earliest and most well-known cerebellar theories postulates that motor learning\r\nlargely depends on long-term depression at the parallel fiber-Purkinje cell (PC-PC) synapse.\r\nHowever, the discovery of other types of plasticity in the cerebellar circuitry, like long-term\r\npotentiation (LTP) at the PC-PC synapse, potentiation of molecular layer interneurons (MLIs),\r\nand plasticity transfer from the cortex to the cerebellar/ vestibular nuclei has increased the\r\npopularity of the idea that multiple sites of plasticity might be involved in learning.\r\nStill a lot remains unknown about the molecular mechanisms responsible for these types of\r\nplasticity and whether they occur during physiological learning.\r\nIn the first part of this thesis we have analyzed the variation and nanodistribution of voltagegated calcium channels (VGCCs) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid\r\ntype glutamate receptors (AMPARs) on the parallel fiber-Purkinje cell synapse after vestibuloocular reflex phase reversal adaptation, a behavior that has been suggested to rely on PF-PC\r\nLTP. We have found that on the last day of adaptation there is no learning trace in form of\r\nVGCCs nor AMPARs variation at the PF-PC synapse, but instead a decrease in the number of\r\nPF-PC synapses. These data seem to support the view that learning is only stored in the\r\ncerebellar cortex in an initial learning phase, being transferred later to the vestibular nuclei.\r\nNext, we have studied the role of MLIs in motor learning using a relatively simple and well characterized behavioral paradigm – horizontal optokinetic reflex (HOKR) adaptation. We\r\nhave found behavior-induced MLI potentiation in form of release probability increase that\r\ncould be explained by the increase of VGCCs at the presynaptic side. Our results strengthen\r\nthe idea of distributed cerebellar plasticity contributing to learning and provide a novel\r\nmechanism for release probability increase. ","lang":"eng"}]},{"ec_funded":1,"abstract":[{"text":"Cell division in Escherichia coli is performed by the divisome, a multi-protein complex composed of more than 30 proteins. The divisome spans from the cytoplasm through the inner membrane to the cell wall and the outer membrane. Divisome assembly is initiated by a cytoskeletal structure, the so-called Z-ring, which localizes at the center of the E. coli cell and determines the position of the future cell septum. The Z-ring is composed of the highly conserved bacterial tubulin homologue FtsZ, which forms treadmilling filaments. These filaments are recruited to the inner membrane by FtsA, a highly conserved bacterial actin homologue. FtsA interacts with other proteins in the periplasm and thus connects the cytoplasmic and periplasmic components of the divisome. \r\nA previous model postulated that FtsA regulates maturation of the divisome by switching from an oligomeric, inactive state to a monomeric and active state. This model was based mostly on in vivo studies, as a biochemical characterization of FtsA has been hampered by difficulties in purifying the protein. Here, we studied FtsA using an in vitro reconstitution approach and aimed to answer two questions: (i) How are dynamics from cytoplasmic, treadmilling FtsZ filaments coupled to proteins acting in the periplasmic space and (ii) How does FtsA regulate the maturation of the divisome?\r\nWe found that the cytoplasmic peptides of the transmembrane proteins FtsN and FtsQ interact directly with FtsA and can follow the spatiotemporal signal of FtsA/Z filaments. When we investigated the underlying mechanism by imaging single molecules of FtsNcyto, we found the peptide to interact transiently with FtsA. An in depth analysis of the single molecule trajectories helped to postulate a model where PG synthases follow the dynamics of FtsZ by a diffusion and capture mechanism. \r\nFollowing up on these findings we were interested in how the self-interaction of FtsA changes when it encounters FtsNcyto and if we can confirm the proposed oligomer-monomer switch. For this, we compared the behavior of the previously identified, hyperactive mutant FtsA R286W with wildtype FtsA. The mutant outperforms WT in mirroring and transmitting the spatiotemporal signal of treadmilling FtsZ filaments. Surprisingly however, we found that this was not due to a difference in the self-interaction strength of the two variants, but a difference in their membrane residence time. Furthermore, in contrast to our expectations, upon binding of FtsNcyto the measured self-interaction of FtsA actually increased. \r\nWe propose that FtsNcyto induces a rearrangement of the oligomeric architecture of FtsA. In further consequence this change leads to more persistent FtsZ filaments which results in a defined signalling zone, allowing formation of the mature divisome. The observed difference between FtsA WT and R286W is due to the vastly different membrane turnover of the proteins. R286W cycles 5-10x faster compared to WT which allows to sample FtsZ filaments at faster frequencies. These findings can explain the observed differences in toxicity for overexpression of FtsA WT and R286W and help to understand how FtsA regulates divisome maturation.","lang":"eng"}],"type":"dissertation","ddc":["572"],"corr_author":"1","article_processing_charge":"No","date_published":"2023-09-25T00:00:00Z","doi":"10.15479/at:ista:14280","oa":1,"date_updated":"2026-04-07T14:06:05Z","month":"09","supervisor":[{"first_name":"Martin","id":"462D4284-F248-11E8-B48F-1D18A9856A87","full_name":"Loose, Martin","last_name":"Loose","orcid":"0000-0001-7309-9724"}],"keyword":["Cell Division","Reconstitution","FtsZ","FtsA","Divisome","E.coli"],"author":[{"orcid":"0000-0001-9198-2182 ","last_name":"Radler","full_name":"Radler, Philipp","id":"40136C2A-F248-11E8-B48F-1D18A9856A87","first_name":"Philipp"}],"department":[{"_id":"GradSch"},{"_id":"MaLo"}],"date_created":"2023-09-06T10:58:25Z","language":[{"iso":"eng"}],"page":"156","file":[{"file_size":114932847,"content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document","date_created":"2023-10-04T10:11:53Z","checksum":"87eef11fbc5c7df0826f12a3a629b444","creator":"pradler","embargo_to":"open_access","file_name":"PhD Thesis_Philipp Radler_20231004.docx","relation":"source_file","file_id":"14390","access_level":"closed","date_updated":"2024-10-05T22:30:03Z"},{"file_name":"PhD Thesis_Philipp Radler_20231004.pdf","relation":"main_file","embargo":"2024-10-04","date_updated":"2024-10-05T22:30:03Z","file_id":"14391","access_level":"open_access","content_type":"application/pdf","file_size":37838778,"checksum":"3253e099b7126469d941fd9419d68b4f","creator":"pradler","date_created":"2023-10-04T10:11:21Z"}],"year":"2023","alternative_title":["ISTA Thesis"],"publication_identifier":{"issn":["2663-337X"],"isbn":["978-3-99078-033-6"]},"day":"25","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","publication_status":"published","tmp":{"short":"CC BY (4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","image":"/images/cc_by.png"},"has_accepted_license":"1","status":"public","publisher":"Institute of Science and Technology Austria","project":[{"_id":"2595697A-B435-11E9-9278-68D0E5697425","grant_number":"679239","call_identifier":"H2020","name":"Self-Organization of the Bacterial Cell"},{"name":"In vitro reconstitution of bacterial cell division","grant_number":"P34607","_id":"fc38323b-9c52-11eb-aca3-ff8afb4a011d"},{"name":"Synthesis of bacterial cell wall","grant_number":"ALTF 2015-1163","_id":"2596EAB6-B435-11E9-9278-68D0E5697425"},{"name":"Reconstitution of bacterial cell wall synthesis","grant_number":"LT000824/2016","_id":"259B655A-B435-11E9-9278-68D0E5697425"}],"_id":"14280","oa_version":"Published Version","citation":{"mla":"Radler, Philipp. <i>Spatiotemporal Signaling during Assembly of the Bacterial Divisome</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:14280\">10.15479/at:ista:14280</a>.","short":"P. Radler, Spatiotemporal Signaling during Assembly of the Bacterial Divisome, Institute of Science and Technology Austria, 2023.","ista":"Radler P. 2023. Spatiotemporal signaling during assembly of the bacterial divisome. Institute of Science and Technology Austria.","chicago":"Radler, Philipp. “Spatiotemporal Signaling during Assembly of the Bacterial Divisome.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:14280\">https://doi.org/10.15479/at:ista:14280</a>.","ieee":"P. Radler, “Spatiotemporal signaling during assembly of the bacterial divisome,” Institute of Science and Technology Austria, 2023.","ama":"Radler P. Spatiotemporal signaling during assembly of the bacterial divisome. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:14280\">10.15479/at:ista:14280</a>","apa":"Radler, P. (2023). <i>Spatiotemporal signaling during assembly of the bacterial divisome</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:14280\">https://doi.org/10.15479/at:ista:14280</a>"},"related_material":{"record":[{"id":"10934","status":"public","relation":"research_data"},{"status":"public","id":"11373","relation":"part_of_dissertation"},{"relation":"part_of_dissertation","id":"7387","status":"public"}]},"acknowledged_ssus":[{"_id":"Bio"},{"_id":"LifeSc"}],"degree_awarded":"PhD","title":"Spatiotemporal signaling during assembly of the bacterial divisome","file_date_updated":"2024-10-05T22:30:03Z","OA_place":"publisher"},{"date_published":"2023-03-23T00:00:00Z","article_processing_charge":"No","date_updated":"2026-04-07T14:10:40Z","oa":1,"doi":"10.15479/at:ista:12781","ec_funded":1,"abstract":[{"lang":"eng","text":"Most energy in humans is produced in form of ATP by the mitochondrial respiratory chain consisting of several protein assemblies embedded into lipid membrane (complexes I-V). Complex I is the first and the largest enzyme of the respiratory chain which is essential for energy production. It couples the transfer of two electrons from NADH to ubiquinone with proton translocation across bacterial or inner mitochondrial membrane. The coupling mechanism between electron transfer and proton translocation is one of the biggest enigma in bioenergetics and structural biology. Even though the enzyme has been studied for decades, only recent technological advances in cryo-EM allowed its extensive structural investigation. \r\n\r\nComplex I from E.coli appears to be of special importance because it is a perfect model system with a rich mutant library, however the structure of the entire complex was unknown. In this thesis I have resolved structures of the minimal complex I version from E. coli in different states including reduced, inhibited, under reaction turnover and several others. Extensive structural analyses of these structures and comparison to structures from other species allowed to derive general features of conformational dynamics and propose a universal coupling mechanism. The mechanism is straightforward, robust and consistent with decades of experimental data available for complex I from different species. \r\n\r\nCyanobacterial NDH (cyanobacterial complex I) is a part of broad complex I superfamily and was studied as well in this thesis. It plays an important role in cyclic electron transfer (CET), during which electrons are cycled within PSI through ferredoxin and plastoquinone to generate proton gradient without NADPH production. Here, I solved structure of NDH and revealed additional state, which was not observed before. The novel “resting” state allowed to propose the mechanism of CET regulation. Moreover, conformational dynamics of NDH resembles one in complex I which suggest more broad universality of the proposed coupling mechanism.\r\n\r\nIn summary, results presented here helped to interpret decades of experimental data for complex I and contributed to fundamental mechanistic understanding of protein function.\r\n"}],"corr_author":"1","ddc":["570","572"],"type":"dissertation","year":"2023","publication_identifier":{"isbn":["978-3-99078-029-9"],"issn":["2663-337X"]},"alternative_title":["ISTA Thesis"],"supervisor":[{"first_name":"Leonid A","id":"338D39FE-F248-11E8-B48F-1D18A9856A87","full_name":"Sazanov, Leonid A","last_name":"Sazanov","orcid":"0000-0002-0977-7989"}],"month":"03","file":[{"file_id":"12852","access_level":"open_access","embargo":"2024-04-20","date_updated":"2024-04-22T22:30:06Z","file_name":"VladyslavKravchuk_PhD_Thesis_PostSub_Final_1.pdf","relation":"main_file","date_created":"2023-04-19T14:33:41Z","checksum":"5ebb6345cb4119f93460c81310265a6d","creator":"vkravchu","file_size":6071553,"content_type":"application/pdf"},{"date_created":"2023-04-19T14:33:52Z","creator":"vkravchu","checksum":"c12055c48411d030d2afa51de2166221","content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document","file_size":19468766,"access_level":"open_access","file_id":"12853","embargo":"2024-04-20","date_updated":"2024-04-22T22:30:06Z","relation":"source_file","file_name":"VladyslavKravchuk_PhD_Thesis_PostSub_Final.docx"}],"page":"127","language":[{"iso":"eng"}],"date_created":"2023-03-31T12:24:42Z","department":[{"_id":"GradSch"},{"_id":"LeSa"}],"author":[{"orcid":"0000-0001-9523-9089","last_name":"Kravchuk","full_name":"Kravchuk, Vladyslav","id":"4D62F2A6-F248-11E8-B48F-1D18A9856A87","first_name":"Vladyslav"}],"publisher":"Institute of Science and Technology Austria","status":"public","has_accepted_license":"1","day":"23","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","publication_status":"published","degree_awarded":"PhD","acknowledged_ssus":[{"_id":"EM-Fac"}],"OA_place":"publisher","file_date_updated":"2024-04-22T22:30:06Z","title":"Structural and mechanistic study of bacterial complex I and its cyanobacterial ortholog","oa_version":"Published Version","_id":"12781","project":[{"name":"Structural characterization of E. coli complex I: an important mechanistic model","grant_number":"25541","_id":"238A0A5A-32DE-11EA-91FC-C7463DDC885E"},{"_id":"627abdeb-2b32-11ec-9570-ec31a97243d3","grant_number":"101020697","call_identifier":"H2020","name":"Structure and mechanism of respiratory chain molecular machines"}],"related_material":{"record":[{"relation":"part_of_dissertation","status":"public","id":"12138"}]},"citation":{"short":"V. Kravchuk, Structural and Mechanistic Study of Bacterial Complex I and Its Cyanobacterial Ortholog, Institute of Science and Technology Austria, 2023.","mla":"Kravchuk, Vladyslav. <i>Structural and Mechanistic Study of Bacterial Complex I and Its Cyanobacterial Ortholog</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:12781\">10.15479/at:ista:12781</a>.","ieee":"V. Kravchuk, “Structural and mechanistic study of bacterial complex I and its cyanobacterial ortholog,” Institute of Science and Technology Austria, 2023.","ista":"Kravchuk V. 2023. Structural and mechanistic study of bacterial complex I and its cyanobacterial ortholog. Institute of Science and Technology Austria.","chicago":"Kravchuk, Vladyslav. “Structural and Mechanistic Study of Bacterial Complex I and Its Cyanobacterial Ortholog.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:12781\">https://doi.org/10.15479/at:ista:12781</a>.","ama":"Kravchuk V. Structural and mechanistic study of bacterial complex I and its cyanobacterial ortholog. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:12781\">10.15479/at:ista:12781</a>","apa":"Kravchuk, V. (2023). <i>Structural and mechanistic study of bacterial complex I and its cyanobacterial ortholog</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:12781\">https://doi.org/10.15479/at:ista:12781</a>"}},{"page":"190","file":[{"file_name":"Thesis_Schauer_final.pdf","relation":"main_file","file_id":"12907","access_level":"open_access","date_updated":"2024-05-06T22:30:03Z","embargo":"2024-05-05","file_size":31434230,"content_type":"application/pdf","date_created":"2023-05-05T13:01:14Z","checksum":"59b0303dc483f40a96a610a90aab7ee9","creator":"aschauer"},{"date_created":"2023-05-05T13:04:15Z","checksum":"25f54e12479b6adaabd129a20568e6c1","creator":"aschauer","file_size":43809109,"content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document","file_id":"12908","access_level":"closed","date_updated":"2024-05-06T22:30:03Z","embargo_to":"open_access","file_name":"Thesis_Schauer_final.docx","relation":"source_file"}],"author":[{"id":"30A536BA-F248-11E8-B48F-1D18A9856A87","first_name":"Alexandra","orcid":"0000-0001-7659-9142","last_name":"Schauer","full_name":"Schauer, Alexandra"}],"date_created":"2023-05-05T08:48:20Z","department":[{"_id":"GradSch"},{"_id":"CaHe"}],"language":[{"iso":"eng"}],"supervisor":[{"id":"39427864-F248-11E8-B48F-1D18A9856A87","first_name":"Carl-Philipp J","orcid":"0000-0002-0912-4566","last_name":"Heisenberg","full_name":"Heisenberg, Carl-Philipp J"}],"month":"05","alternative_title":["ISTA Thesis"],"publication_identifier":{"issn":["2663-337X"]},"year":"2023","ddc":["570"],"corr_author":"1","type":"dissertation","ec_funded":1,"abstract":[{"text":"The tight spatiotemporal coordination of signaling activity determining embryo\r\npatterning and the physical processes driving embryo morphogenesis renders\r\nembryonic development robust, such that key developmental processes can unfold\r\nrelatively normally even outside of the full embryonic context. For instance, embryonic\r\nstem cell cultures can recapitulate the hallmarks of gastrulation, i.e. break symmetry\r\nleading to germ layer formation and morphogenesis, in a very reduced environment.\r\nThis leads to questions on specific contributions of embryo-specific features, such as\r\nthe presence of extraembryonic tissues, which are inherently involved in gastrulation\r\nin the full embryonic context. To address this, we established zebrafish embryonic\r\nexplants without the extraembryonic yolk cell, an important player as a signaling\r\nsource and for morphogenesis during gastrulation, as a model of ex vivo development.\r\nWe found that dorsal-marginal determinants are required and sufficient in these\r\nexplants to form and pattern all three germ layers. However, formation of tissues,\r\nwhich require the highest Nodal-signaling levels, is variable, demonstrating a\r\ncontribution of extraembryonic tissues for reaching peak Nodal signaling levels.\r\nBlastoderm explants also undergo gastrulation-like axis elongation. We found that this\r\nelongation movement shows hallmarks of oriented mesendoderm cell intercalations\r\ntypically associated with dorsal tissues in the intact embryo. These are disrupted by\r\nuniform upregulation of BMP signaling activity and concomitant explant ventralization,\r\nsuggesting that tight spatial control of BMP signaling is a prerequisite for explant\r\nmorphogenesis. This control is achieved by Nodal signaling, which is critical for\r\neffectively downregulating BMP signaling in the mesendoderm, highlighting that Nodal\r\nsignaling is not only directly required for mesendoderm cell fate specification and\r\nmorphogenesis, but also by maintaining low levels of BMP signaling at the dorsal side.\r\nCollectively, we provide insights into the capacity and organization of signaling and\r\nmorphogenetic domains to recapitulate features of zebrafish gastrulation outside of\r\nthe full embryonic context.","lang":"eng"}],"oa":1,"date_updated":"2025-06-12T06:56:58Z","doi":"10.15479/at:ista:12891","article_processing_charge":"No","date_published":"2023-05-05T00:00:00Z","citation":{"ista":"Schauer A. 2023. Mesendoderm formation in zebrafish gastrulation: The role of extraembryonic tissues. Institute of Science and Technology Austria.","ieee":"A. Schauer, “Mesendoderm formation in zebrafish gastrulation: The role of extraembryonic tissues,” Institute of Science and Technology Austria, 2023.","chicago":"Schauer, Alexandra. “Mesendoderm Formation in Zebrafish Gastrulation: The Role of Extraembryonic Tissues.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:12891\">https://doi.org/10.15479/at:ista:12891</a>.","mla":"Schauer, Alexandra. <i>Mesendoderm Formation in Zebrafish Gastrulation: The Role of Extraembryonic Tissues</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:12891\">10.15479/at:ista:12891</a>.","short":"A. Schauer, Mesendoderm Formation in Zebrafish Gastrulation: The Role of Extraembryonic Tissues, Institute of Science and Technology Austria, 2023.","apa":"Schauer, A. (2023). <i>Mesendoderm formation in zebrafish gastrulation: The role of extraembryonic tissues</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:12891\">https://doi.org/10.15479/at:ista:12891</a>","ama":"Schauer A. Mesendoderm formation in zebrafish gastrulation: The role of extraembryonic tissues. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:12891\">10.15479/at:ista:12891</a>"},"related_material":{"record":[{"status":"public","id":"7888","relation":"part_of_dissertation"},{"relation":"part_of_dissertation","id":"8966","status":"public"}]},"_id":"12891","oa_version":"Published Version","project":[{"_id":"260F1432-B435-11E9-9278-68D0E5697425","grant_number":"742573","call_identifier":"H2020","name":"Interaction and feedback between cell mechanics and fate specification in vertebrate gastrulation"},{"name":"Mesendoderm specification in zebrafish: The role of extraembryonic tissues","_id":"26B1E39C-B435-11E9-9278-68D0E5697425","grant_number":"25239"}],"file_date_updated":"2024-05-06T22:30:03Z","title":"Mesendoderm formation in zebrafish gastrulation: The role of extraembryonic tissues","degree_awarded":"PhD","acknowledged_ssus":[{"_id":"Bio"},{"_id":"LifeSc"}],"publication_status":"published","day":"05","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publisher":"Institute of Science and Technology Austria","status":"public","has_accepted_license":"1"},{"day":"08","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","publication_status":"published","tmp":{"image":"/images/cc_by_nc_sa.png","name":"Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode","short":"CC BY-NC-SA (4.0)"},"publisher":"Institute of Science and Technology Austria","has_accepted_license":"1","status":"public","oa_version":"Published Version","_id":"12531","citation":{"ama":"Kirillova K. Panoramic functional gradients across the mouse retina. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:12531\">10.15479/at:ista:12531</a>","apa":"Kirillova, K. (2023). <i>Panoramic functional gradients across the mouse retina</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:12531\">https://doi.org/10.15479/at:ista:12531</a>","short":"K. Kirillova, Panoramic Functional Gradients across the Mouse Retina, Institute of Science and Technology Austria, 2023.","mla":"Kirillova, Kseniia. <i>Panoramic Functional Gradients across the Mouse Retina</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:12531\">10.15479/at:ista:12531</a>.","chicago":"Kirillova, Kseniia. “Panoramic Functional Gradients across the Mouse Retina.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:12531\">https://doi.org/10.15479/at:ista:12531</a>.","ieee":"K. Kirillova, “Panoramic functional gradients across the mouse retina,” Institute of Science and Technology Austria, 2023.","ista":"Kirillova K. 2023. Panoramic functional gradients across the mouse retina. Institute of Science and Technology Austria."},"degree_awarded":"MS","file_date_updated":"2024-02-09T23:30:03Z","OA_place":"publisher","title":"Panoramic functional gradients across the mouse retina","abstract":[{"text":"All visual experiences of the vertebrates begin with light being converted into electrical signals\r\nby the eye retina. Retinal ganglion cells (RGCs) are the neurons of the innermost layer of the\r\nmammal retina, and they transmit visual information to the rest of the brain.\r\nIt has been shown that RGCs vary in their morphology and genetic profiles, moreover they can\r\nbe unambiguously grouped into subtypes that share the same morphological and/or molecular\r\nproperties. However, in terms of RGCs function, it remains unclear how many distinct types\r\nthere are and what response properties their typology relies on. Even given the recent studies\r\nthat successfully classified RGCs in a patch of the retina [1] and in scotopic conditions [2], the\r\nquestion remains whether the found subtypes persist across the entire retina.\r\nIn this work, using a novel imaging method, we show that, when sampled from a large portion\r\nof the retina, RGCs can not be clearly divided into functional subtypes. We found that in\r\nphotopic conditions, which implies more prominent natural scene statistic differences across\r\nthe visual field, response properties can be exhibited by cells differently depending on their\r\nlocation in the retina, which leads to formation of a gradient of features rather than distinct\r\nclasses.\r\nThis finding suggests that RGCs follow a global organization across the visual field of the\r\nanimal, adapting each RGC subtype to the requirements imposed by the natural scene statistics.","lang":"eng"}],"ddc":["570"],"corr_author":"1","type":"dissertation","article_processing_charge":"No","date_published":"2023-02-08T00:00:00Z","oa":1,"date_updated":"2026-04-07T14:06:26Z","doi":"10.15479/at:ista:12531","supervisor":[{"last_name":"Jösch","orcid":"0000-0002-3937-1330","full_name":"Jösch, Maximilian A","id":"2BD278E6-F248-11E8-B48F-1D18A9856A87","first_name":"Maximilian A"}],"month":"02","page":"46","file":[{"file_size":8369317,"content_type":"application/pdf","date_created":"2023-02-09T08:03:32Z","checksum":"57d8da3a6c749eb1556b7435fe266a5f","creator":"cchlebak","file_name":"Thesis_Kseniia___ISTA__istaustriathesis_PDF-A.pdf","relation":"main_file","file_id":"12532","access_level":"open_access","date_updated":"2024-02-09T23:30:03Z","embargo":"2024-02-08"},{"creator":"cchlebak","checksum":"87fb44318e4f9eb9da2ad9ad6ca8e76f","date_created":"2023-02-10T09:32:06Z","file_size":11204408,"content_type":"application/x-zip-compressed","date_updated":"2024-02-09T23:30:03Z","access_level":"closed","file_id":"12535","relation":"source_file","file_name":"Thesis Kseniia - ISTA [istaustriathesis]-FINAL.zip","embargo_to":"open_access"}],"author":[{"id":"8e3f931e-dc85-11ea-9058-e7b957bf23f0","first_name":"Kseniia","last_name":"Kirillova","full_name":"Kirillova, Kseniia"}],"date_created":"2023-02-09T07:45:05Z","language":[{"iso":"eng"}],"department":[{"_id":"GradSch"},{"_id":"MaJö"}],"year":"2023","alternative_title":["ISTA Master's Thesis"],"publication_identifier":{"issn":["2791-4585"]}},{"abstract":[{"lang":"eng","text":"The evolutionary processes that brought about today’s plethora of living species and the many billions more ancient ones all underlie biology. Evolutionary pathways are neither directed nor deterministic, but rather an interplay between selection, migration, mutation, genetic drift and other environmental factors. Hybrid zones, as natural crossing experiments, offer a great opportunity to use cline analysis to deduce different evolutionary processes - for example, selection strength. Theoretical cline models, largely assuming uniform distribution of individuals, often lack the capability of incorporating population structure. Since in reality organisms mostly live in patchy distributions and their dispersal is hardly ever Gaussian, it is necessary to unravel the effect of these different elements of population structure on cline parameters and shape. In this thesis, I develop a simulation inspired by the A. majus hybrid zone of a single selected locus under frequency dependent selection. This simulation enables us to untangle the effects of different elements of population structure as for example a low-density center and long-range dispersal. This thesis is therefore a first step towards theoretically untangling the effects of different elements of population structure on cline parameters and shape. "}],"corr_author":"1","ddc":["576"],"type":"dissertation","date_published":"2023-04-05T00:00:00Z","article_processing_charge":"No","date_updated":"2026-04-07T14:01:51Z","oa":1,"doi":"10.15479/at:ista:12800","supervisor":[{"id":"4880FE40-F248-11E8-B48F-1D18A9856A87","first_name":"Nicholas H","orcid":"0000-0002-8548-5240","last_name":"Barton","full_name":"Barton, Nicholas H"}],"month":"04","file":[{"file_size":52795,"content_type":"application/vnd.openxmlformats-officedocument.spreadsheetml.sheet","creator":"mjulseth","checksum":"b76cf6d69f2093d8248f6a3f9d4654a4","date_created":"2023-04-06T06:09:40Z","relation":"supplementary_material","file_name":"Dispersaldata.xlsx","embargo_to":"open_access","date_updated":"2023-06-02T22:30:04Z","access_level":"closed","file_id":"12805"},{"file_name":"2023_MSc_ThesisMaraJulseth_Notebook.nb","relation":"supplementary_material","embargo":"2023-06-01","date_updated":"2023-06-02T22:30:04Z","file_id":"12806","access_level":"open_access","content_type":"application/vnd.wolfram.nb","file_size":787239,"checksum":"5a13b6d204371572e249f03795bc0d04","creator":"mjulseth","date_created":"2023-04-06T06:11:27Z"},{"date_created":"2023-04-06T08:26:12Z","checksum":"c3ec842839ed1e66bf2618ae33047df8","creator":"mjulseth","content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document","file_size":1061763,"file_id":"12812","access_level":"closed","date_updated":"2023-06-02T22:30:04Z","embargo_to":"open_access","file_name":"ThesisMaraJulseth_04_23.docx","relation":"source_file"},{"date_created":"2023-04-06T08:26:37Z","checksum":"3132cc998fbe3ae2a3a83c2a69367f37","creator":"mjulseth","content_type":"application/pdf","file_size":1741364,"file_id":"12813","access_level":"open_access","embargo":"2023-06-01","date_updated":"2023-06-02T22:30:04Z","file_name":"ThesisMaraJulseth_04_23.pdf","relation":"main_file"}],"page":"21","language":[{"iso":"eng"}],"department":[{"_id":"GradSch"},{"_id":"NiBa"}],"date_created":"2023-04-04T18:57:11Z","author":[{"first_name":"Mara","id":"1cf464b2-dc7d-11ea-9b2f-f9b1aa9417d1","full_name":"Julseth, Mara","last_name":"Julseth"}],"year":"2023","publication_identifier":{"issn":["2791-4585"]},"alternative_title":["ISTA Master's Thesis"],"user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","day":"05","publication_status":"published","publisher":"Institute of Science and Technology Austria","status":"public","has_accepted_license":"1","oa_version":"Published Version","_id":"12800","citation":{"ama":"Julseth M. The effect of local population structure on genetic variation at selected loci in the A. majus hybrid zone. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:12800\">10.15479/at:ista:12800</a>","apa":"Julseth, M. (2023). <i>The effect of local population structure on genetic variation at selected loci in the A. majus hybrid zone</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:12800\">https://doi.org/10.15479/at:ista:12800</a>","short":"M. Julseth, The Effect of Local Population Structure on Genetic Variation at Selected Loci in the A. Majus Hybrid Zone, Institute of Science and Technology Austria, 2023.","mla":"Julseth, Mara. <i>The Effect of Local Population Structure on Genetic Variation at Selected Loci in the A. Majus Hybrid Zone</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:12800\">10.15479/at:ista:12800</a>.","ista":"Julseth M. 2023. The effect of local population structure on genetic variation at selected loci in the A. majus hybrid zone. Institute of Science and Technology Austria.","chicago":"Julseth, Mara. “The Effect of Local Population Structure on Genetic Variation at Selected Loci in the A. Majus Hybrid Zone.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:12800\">https://doi.org/10.15479/at:ista:12800</a>.","ieee":"M. Julseth, “The effect of local population structure on genetic variation at selected loci in the A. majus hybrid zone,” Institute of Science and Technology Austria, 2023."},"degree_awarded":"MS","OA_place":"publisher","file_date_updated":"2023-06-02T22:30:04Z","title":"The effect of local population structure on genetic variation at selected loci in the A. majus hybrid zone"},{"year":"2023","alternative_title":["ISTA Thesis"],"publication_identifier":{"isbn":["978-3-99078-038-1"],"issn":["2663-337X"]},"month":"12","supervisor":[{"full_name":"Sixt, Michael K","orcid":"0000-0002-6620-9179","last_name":"Sixt","first_name":"Michael K","id":"41E9FBEA-F248-11E8-B48F-1D18A9856A87"}],"page":"226","file":[{"file_size":51585778,"content_type":"application/pdf","date_created":"2023-12-20T09:35:34Z","checksum":"457927165d5d556305d3086f6b83e5c7","creator":"jstopp","file_name":"Thesis.pdf","relation":"main_file","file_id":"14699","access_level":"open_access","embargo":"2024-12-20","date_updated":"2024-12-20T23:30:04Z"},{"file_name":"Thesis.docx","relation":"source_file","embargo_to":"open_access","date_updated":"2024-12-20T23:30:04Z","file_id":"14700","access_level":"closed","file_size":69625950,"content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document","checksum":"e8d26449ac461f5e8478a62c9507506f","creator":"jstopp","date_created":"2023-12-20T09:35:35Z"}],"author":[{"id":"489E3F00-F248-11E8-B48F-1D18A9856A87","first_name":"Julian A","last_name":"Stopp","full_name":"Stopp, Julian A"}],"language":[{"iso":"eng"}],"department":[{"_id":"GradSch"},{"_id":"MiSi"}],"date_created":"2023-12-18T19:14:28Z","article_processing_charge":"No","date_published":"2023-12-20T00:00:00Z","oa":1,"date_updated":"2026-06-18T17:34:48Z","doi":"10.15479/at:ista:14697","abstract":[{"text":"During my Ph.D. research, I managed a series of projects, each focused on the\r\nmechanisms underlying cell migration. My work involved an in-depth examination of\r\nthe complex strategies employed by neutrophils, with a specific focus on their ability to\r\nsynchronize spatial-temporal cues and optimize their gradient perception. However, it\r\nis essential to acknowledge that not all projects yielded successful results, as some\r\nideas were discontinued and are archived for future reference within this thesis.\r\nMy main project investigated how neutrophils decode spatial cues for precise navigation. Human neutrophils showcased distinct movement patterns based on source\r\ntype – linear or point-like. By combining single-cell tracking in 3D environments with\r\nproxy dyes, this project linked cell behaviors to gradient changes, revealing a stronger\r\nresponse to semi-exponential gradients from point sources. In addition, neutrophils\r\nexhibited oscillating migration speeds, using speed minima to adjust trajectories toward sources. Experiencing continuous concentration changes, they accelerated over\r\ntime and employed a \"Run and Fumble\" strategy, alternating between consistent runs\r\nand strategic \"tumbles\" for efficient navigation.\r\nThe project extended to the possibility of cells amplifying perceived gradients by\r\nenclosing their immediate surroundings, pushing attractants forward for enrichment\r\nwhile depleting it at the cell rear. Microfluidic devices were employed, and various experimental parameters configurations were optimized. Although significant differences\r\nin migratory efficacy were detected across pore sizes and device heights, quantifying\r\ngradient manipulation effects proved challenging.\r\nThe \"Laser-Assisted Protein Adsorption by Photobleaching\" (LAPAP) project was\r\npromising, as it allowed the printing of gradients. Initially successful with dendritic cells,\r\nwe aimed to adapt it for neutrophils. Through extensive experimentation with multiple\r\nparameters, we attempted to trigger responses from neutrophils. Despite these efforts\r\nand collaboration, the project failed due to practical challenges and limitations.\r\nFacing a lack of neutrophil-like cells at IST, we initially established the SCF-HoxB8\r\nprimary murine cell line. Despite their existence, their migratory behavior was largely\r\nunexplored due to potential limitations. Through differentiation protocol refinements we\r\nenhanced their migratory capabilities, though their capacity still lagged behind human\r\nneutrophils. Despite this, the improved migration potential of these cells pointed toward\r\ntheir utility for in vitro murine neutrophil migration studies.","lang":"eng"}],"ec_funded":1,"ddc":["570"],"corr_author":"1","type":"dissertation","degree_awarded":"PhD","acknowledged_ssus":[{"_id":"LifeSc"},{"_id":"Bio"}],"file_date_updated":"2024-12-20T23:30:04Z","OA_place":"publisher","title":"Neutrophils on the hunt : Migratory strategies employed by neutrophils to fulfill their effector function","_id":"14697","oa_version":"Published Version","project":[{"name":"International IST Doctoral Program","grant_number":"665385","_id":"2564DBCA-B435-11E9-9278-68D0E5697425","call_identifier":"H2020"}],"citation":{"mla":"Stopp, Julian A. <i>Neutrophils on the Hunt : Migratory Strategies Employed by Neutrophils to Fulfill Their Effector Function</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:14697\">10.15479/at:ista:14697</a>.","short":"J.A. Stopp, Neutrophils on the Hunt : Migratory Strategies Employed by Neutrophils to Fulfill Their Effector Function, Institute of Science and Technology Austria, 2023.","chicago":"Stopp, Julian A. “Neutrophils on the Hunt : Migratory Strategies Employed by Neutrophils to Fulfill Their Effector Function.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:14697\">https://doi.org/10.15479/at:ista:14697</a>.","ista":"Stopp JA. 2023. Neutrophils on the hunt : Migratory strategies employed by neutrophils to fulfill their effector function. Institute of Science and Technology Austria.","ieee":"J. A. Stopp, “Neutrophils on the hunt : Migratory strategies employed by neutrophils to fulfill their effector function,” Institute of Science and Technology Austria, 2023.","ama":"Stopp JA. Neutrophils on the hunt : Migratory strategies employed by neutrophils to fulfill their effector function. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:14697\">10.15479/at:ista:14697</a>","apa":"Stopp, J. A. (2023). <i>Neutrophils on the hunt : Migratory strategies employed by neutrophils to fulfill their effector function</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:14697\">https://doi.org/10.15479/at:ista:14697</a>"},"related_material":{"record":[{"id":"14360","status":"public","relation":"part_of_dissertation"},{"id":"12272","status":"public","relation":"part_of_dissertation"},{"relation":"part_of_dissertation","id":"6328","status":"public"},{"id":"7885","status":"public","relation":"part_of_dissertation"},{"id":"14274","status":"public","relation":"part_of_dissertation"}]},"publisher":"Institute of Science and Technology Austria","has_accepted_license":"1","status":"public","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","day":"20","publication_status":"published"},{"doi":"10.15479/at:ista:13081","oa":1,"date_updated":"2026-04-14T09:50:54Z","article_processing_charge":"No","date_published":"2023-05-23T00:00:00Z","type":"dissertation","ddc":["570"],"corr_author":"1","abstract":[{"lang":"eng","text":"During development, tissues undergo changes in size and shape to form functional organs. Distinct cellular processes such as cell division and cell rearrangements underlie tissue morphogenesis. Yet how the distinct processes are controlled and coordinated, and how they contribute to morphogenesis is poorly understood. In our study, we addressed these questions using the developing mouse neural tube. This epithelial organ transforms from a flat epithelial sheet to an epithelial tube while increasing in size and undergoing morpho-gen-mediated patterning. The extent and mechanism of neural progenitor rearrangement within the developing mouse neuroepithelium is unknown. To investigate this, we per-formed high resolution lineage tracing analysis to quantify the extent of epithelial rear-rangement at different stages of neural tube development. We quantitatively described the relationship between apical cell size with cell cycle dependent interkinetic nuclear migra-tions (IKNM) and performed high cellular resolution live imaging of the neuroepithelium to study the dynamics of junctional remodeling.  Furthermore, developed a vertex model of the neuroepithelium to investigate the quantitative contribution of cell proliferation, cell differentiation and mechanical properties to the epithelial rearrangement dynamics and validated the model predictions through functional experiments. Our analysis revealed that at early developmental stages, the apical cell area kinetics driven by IKNM induce high lev-els of cell rearrangements in a regime of high junctional tension and contractility. After E9.5, there is a sharp decline in the extent of cell rearrangements, suggesting that the epi-thelium transitions from a fluid-like to a solid-like state. We found that this transition is regulated by the growth rate of the tissue, rather than by changes in cell-cell adhesion and contractile forces. Overall, our study provides a quantitative description of the relationship between tissue growth, cell cycle dynamics, epithelia rearrangements and the emergent tissue material properties, and novel insights on how epithelial cell dynamics influences tissue morphogenesis."}],"alternative_title":["ISTA Thesis"],"publication_identifier":{"issn":["2663-337X"]},"year":"2023","author":[{"first_name":"Laura","id":"4896F754-F248-11E8-B48F-1D18A9856A87","full_name":"Bocanegra, Laura","last_name":"Bocanegra"}],"date_created":"2023-05-23T19:10:42Z","language":[{"iso":"eng"}],"department":[{"_id":"GradSch"},{"_id":"AnKi"}],"page":"93","file":[{"content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document","file_size":25615534,"creator":"lbocaneg","checksum":"74f3f89e59a0189bee53ebfad9c1b9af","date_created":"2023-05-25T06:32:12Z","relation":"source_file","file_name":"Thesis_final_LauraBocanegra.docx","embargo_to":"open_access","date_updated":"2024-06-01T22:30:04Z","access_level":"closed","file_id":"13089"},{"file_name":"TotalFinal_Thesis_LauraBocanegraArx.pdf","relation":"main_file","date_updated":"2024-06-01T22:30:04Z","embargo":"2024-05-31","file_id":"13090","access_level":"open_access","content_type":"application/pdf","file_size":12386046,"checksum":"c6cdef6323eacfb4b7a8af20f32eae97","creator":"lbocaneg","date_created":"2023-05-25T06:32:16Z"}],"month":"05","supervisor":[{"id":"3959A2A0-F248-11E8-B48F-1D18A9856A87","first_name":"Anna","orcid":"0000-0003-4509-4998","last_name":"Kicheva","full_name":"Kicheva, Anna"}],"has_accepted_license":"1","status":"public","publisher":"Institute of Science and Technology Austria","tmp":{"image":"/images/cc_by_nc_nd.png","name":"Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode","short":"CC BY-NC-ND (4.0)"},"publication_status":"published","day":"23","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","title":"Epithelial dynamics during mouse neural tube development","file_date_updated":"2024-06-01T22:30:04Z","OA_place":"publisher","acknowledged_ssus":[{"_id":"Bio"},{"_id":"LifeSc"}],"degree_awarded":"PhD","citation":{"ista":"Bocanegra L. 2023. Epithelial dynamics during mouse neural tube development. Institute of Science and Technology Austria.","chicago":"Bocanegra, Laura. “Epithelial Dynamics during Mouse Neural Tube Development.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:13081\">https://doi.org/10.15479/at:ista:13081</a>.","ieee":"L. Bocanegra, “Epithelial dynamics during mouse neural tube development,” Institute of Science and Technology Austria, 2023.","short":"L. Bocanegra, Epithelial Dynamics during Mouse Neural Tube Development, Institute of Science and Technology Austria, 2023.","mla":"Bocanegra, Laura. <i>Epithelial Dynamics during Mouse Neural Tube Development</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:13081\">10.15479/at:ista:13081</a>.","apa":"Bocanegra, L. (2023). <i>Epithelial dynamics during mouse neural tube development</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:13081\">https://doi.org/10.15479/at:ista:13081</a>","ama":"Bocanegra L. Epithelial dynamics during mouse neural tube development. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:13081\">10.15479/at:ista:13081</a>"},"related_material":{"record":[{"id":"9349","status":"public","relation":"part_of_dissertation"},{"relation":"part_of_dissertation","id":"12837","status":"public"}]},"oa_version":"Published Version","_id":"13081"},{"user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","day":"13","publication_status":"published","tmp":{"image":"/images/cc_by_nc_nd.png","name":"Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode","short":"CC BY-NC-ND (4.0)"},"has_accepted_license":"1","status":"public","publisher":"Institute of Science and Technology Austria","project":[{"_id":"267AF0E4-B435-11E9-9278-68D0E5697425","name":"The role of morphogens in the regulation of neural tube growth"}],"oa_version":"Published Version","_id":"14323","related_material":{"record":[{"relation":"part_of_dissertation","status":"public","id":"7883"}]},"citation":{"ista":"Kuzmicz-Kowalska K. 2023. Regulation of neural progenitor survival by Shh and BMP in the developing spinal cord. Institute of Science and Technology Austria.","chicago":"Kuzmicz-Kowalska, Katarzyna. “Regulation of Neural Progenitor Survival by Shh and BMP in the Developing Spinal Cord.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:14323\">https://doi.org/10.15479/at:ista:14323</a>.","ieee":"K. Kuzmicz-Kowalska, “Regulation of neural progenitor survival by Shh and BMP in the developing spinal cord,” Institute of Science and Technology Austria, 2023.","short":"K. Kuzmicz-Kowalska, Regulation of Neural Progenitor Survival by Shh and BMP in the Developing Spinal Cord, Institute of Science and Technology Austria, 2023.","mla":"Kuzmicz-Kowalska, Katarzyna. <i>Regulation of Neural Progenitor Survival by Shh and BMP in the Developing Spinal Cord</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:14323\">10.15479/at:ista:14323</a>.","apa":"Kuzmicz-Kowalska, K. (2023). <i>Regulation of neural progenitor survival by Shh and BMP in the developing spinal cord</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:14323\">https://doi.org/10.15479/at:ista:14323</a>","ama":"Kuzmicz-Kowalska K. Regulation of neural progenitor survival by Shh and BMP in the developing spinal cord. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:14323\">10.15479/at:ista:14323</a>"},"acknowledged_ssus":[{"_id":"Bio"},{"_id":"PreCl"}],"degree_awarded":"PhD","title":"Regulation of neural progenitor survival by Shh and BMP in the developing spinal cord","OA_place":"publisher","file_date_updated":"2025-03-13T23:30:05Z","abstract":[{"text":"Morphogens are signaling molecules that are known for their prominent role in pattern formation within developing tissues. In addition to patterning, morphogens also control tissue growth. However, the underlying mechanisms are poorly understood. We studied the role of morphogens in regulating tissue growth in the developing vertebrate neural tube. In this system, opposing morphogen gradients of Shh and BMP establish the dorsoventral pattern of neural progenitor domains. Perturbations in these morphogen pathways result in alterations in tissue growth and cell cycle progression, however, it has been unclear what cellular process is affected. To address this, we analysed the rates of cell proliferation and cell death in mouse mutants in which signaling is perturbed, as well as in chick neural plate explants exposed to defined concentrations of signaling activators or inhibitors. Our results indicated that the rate of cell proliferation was not altered in these assays. By contrast, both the Shh and BMP signaling pathways had profound effects on neural progenitor survival. Our results indicate that these pathways synergise to promote cell survival within neural progenitors. Consistent with this, we found that progenitors within the intermediate region of the neural tube, where the combined levels of Shh and BMP are the lowest, are most prone to cell death when signaling activity is inhibited. In addition, we found that downregulation of Shh results in increased apoptosis within the roof plate, which is the dorsal source of BMP ligand production. This revealed a cross-interaction between the Shh and BMP morphogen signaling pathways that may be relevant for understanding how gradients scale in neural tubes with different overall sizes. We further studied the mechanism acting downstream of Shh in cell survival regulation using genetic and genomic approaches. We propose that Shh transcriptionally regulates a non-canonical apoptotic pathway. Altogether, our study points to a novel role of opposing morphogen gradients in tissue size regulation and provides new insights into complex interactions between Shh and BMP signaling gradients in the neural tube.","lang":"eng"}],"type":"dissertation","corr_author":"1","ddc":["570"],"date_published":"2023-09-13T00:00:00Z","article_processing_charge":"No","doi":"10.15479/at:ista:14323","date_updated":"2026-04-14T09:50:54Z","oa":1,"supervisor":[{"full_name":"Kicheva, Anna","orcid":"0000-0003-4509-4998","last_name":"Kicheva","first_name":"Anna","id":"3959A2A0-F248-11E8-B48F-1D18A9856A87"}],"month":"09","date_created":"2023-09-13T10:07:18Z","department":[{"_id":"GradSch"},{"_id":"AnKi"}],"language":[{"iso":"eng"}],"author":[{"first_name":"Katarzyna","id":"4CED352A-F248-11E8-B48F-1D18A9856A87","full_name":"Kuzmicz-Kowalska, Katarzyna","last_name":"Kuzmicz-Kowalska"}],"file":[{"file_size":10147911,"content_type":"application/pdf","date_created":"2023-09-13T09:52:52Z","checksum":"bd83596869c814b24aeff7077d031c0e","creator":"kkuzmicz","file_name":"PhDThesis_KK_final_pdfA.pdf","relation":"main_file","file_id":"14324","access_level":"open_access","date_updated":"2025-03-13T23:30:05Z","embargo":"2025-03-13"},{"date_updated":"2025-03-13T23:30:05Z","file_id":"14325","access_level":"closed","file_name":"thesis_KK_final_corrections_092023.docx","relation":"source_file","embargo_to":"open_access","checksum":"aa2757ae4c3478041fd7e62c587d3e4d","creator":"kkuzmicz","date_created":"2023-09-13T09:53:29Z","content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document","file_size":103980668}],"page":"151","year":"2023","publication_identifier":{"issn":["2663-337X"]},"alternative_title":["ISTA Thesis"]},{"date_published":"2023-11-01T00:00:00Z","article_processing_charge":"Yes (in subscription journal)","date_updated":"2026-07-30T22:30:18Z","oa":1,"doi":"10.1038/s41567-023-02161-w","volume":19,"article_type":"original","quality_controlled":"1","ec_funded":1,"abstract":[{"text":"Arrays of Josephson junctions are governed by a competition between superconductivity and repulsive Coulomb interactions, and are expected to exhibit diverging low-temperature resistance when interactions exceed a critical level. Here we report a study of the transport and microwave response of Josephson arrays with interactions exceeding this level. Contrary to expectations, we observe that the array resistance drops dramatically as the temperature is decreased—reminiscent of superconducting behaviour—and then saturates at low temperature. Applying a magnetic field, we eventually observe a transition to a highly resistive regime. These observations can be understood within a theoretical picture that accounts for the effect of thermal fluctuations on the insulating phase. On the basis of the agreement between experiment and theory, we suggest that apparent superconductivity in our Josephson arrays arises from melting the zero-temperature insulator.","lang":"eng"}],"intvolume":"        19","corr_author":"1","publication":"Nature Physics","ddc":["530"],"type":"journal_article","scopus_import":"1","year":"2023","publication_identifier":{"eissn":["1745-2481"],"issn":["1745-2473"]},"keyword":["General Physics and Astronomy"],"month":"11","file":[{"content_type":"application/pdf","file_size":1977706,"success":1,"checksum":"1fc86d71bfbf836e221c1e925343adc5","creator":"dernst","date_created":"2024-01-29T11:25:38Z","file_name":"2023_NaturePhysics_Mukhopadhyay.pdf","relation":"main_file","date_updated":"2024-01-29T11:25:38Z","file_id":"14899","access_level":"open_access"}],"page":"1630-1635","department":[{"_id":"GradSch"},{"_id":"AnHi"},{"_id":"JoFi"}],"language":[{"iso":"eng"}],"date_created":"2023-08-11T07:41:17Z","author":[{"full_name":"Mukhopadhyay, Soham","last_name":"Mukhopadhyay","orcid":"0000-0001-5263-5559","first_name":"Soham","id":"FDE60288-A89D-11E9-947F-1AF6E5697425"},{"full_name":"Senior, Jorden L","last_name":"Senior","orcid":"0000-0002-0672-9295","first_name":"Jorden L","id":"5479D234-2D30-11EA-89CC-40953DDC885E"},{"last_name":"Saez Mollejo","full_name":"Saez Mollejo, Jaime","id":"e0390f72-f6e0-11ea-865d-862393336714","first_name":"Jaime"},{"first_name":"Denise","id":"4D495994-AE37-11E9-AC72-31CAE5697425","full_name":"Puglia, Denise","last_name":"Puglia","orcid":"0000-0003-1144-2763"},{"id":"2DCF8DE6-F248-11E8-B48F-1D18A9856A87","first_name":"Martin","last_name":"Zemlicka","orcid":"0009-0005-0878-3032","full_name":"Zemlicka, Martin"},{"id":"4B591CBA-F248-11E8-B48F-1D18A9856A87","first_name":"Johannes M","last_name":"Fink","orcid":"0000-0001-8112-028X","full_name":"Fink, Johannes M"},{"full_name":"Higginbotham, Andrew P","orcid":"0000-0003-2607-2363","last_name":"Higginbotham","first_name":"Andrew P","id":"4AD6785A-F248-11E8-B48F-1D18A9856A87"}],"tmp":{"short":"CC BY (4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","image":"/images/cc_by.png"},"isi":1,"external_id":{"isi":["001054563800006"]},"publisher":"Springer Nature","status":"public","has_accepted_license":"1","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","day":"01","acknowledgement":"We thank D. Haviland, J. Pekola, C. Ciuti, A. Bubis and A. Shnirman for helpful feedback on the paper. This research was supported by the Scientific Service Units of IST Austria through resources provided by the MIBA Machine Shop and the Nanofabrication Facility. Work supported by the Austrian FWF grant P33692-N (S.M., J.S. and A.P.H.), the European Union’s Horizon 2020 Research and Innovation programme under the Marie Skłodowska-Curie Grant Agreement No. 754411 (J.S.) and a NOMIS foundation research grant (J.M.F. and A.P.H.).","publication_status":"published","acknowledged_ssus":[{"_id":"M-Shop"},{"_id":"NanoFab"}],"file_date_updated":"2024-01-29T11:25:38Z","title":"Superconductivity from a melted insulator in Josephson junction arrays","_id":"14032","oa_version":"Published Version","project":[{"name":"Cavity electromechanics across a quantum phase transition","grant_number":"P33692","_id":"0aa3608a-070f-11eb-9043-e9cd8a2bd931"},{"name":"ISTplus - Postdoctoral Fellowships","grant_number":"754411","_id":"260C2330-B435-11E9-9278-68D0E5697425","call_identifier":"H2020"},{"_id":"eb9b30ac-77a9-11ec-83b8-871f581d53d2","name":"Protected states of quantum matter"}],"related_material":{"record":[{"id":"17881","status":"public","relation":"dissertation_contains"}]},"citation":{"apa":"Mukhopadhyay, S., Senior, J. L., Saez Mollejo, J., Puglia, D., Zemlicka, M., Fink, J. M., &#38; Higginbotham, A. P. (2023). Superconductivity from a melted insulator in Josephson junction arrays. <i>Nature Physics</i>. Springer Nature. <a href=\"https://doi.org/10.1038/s41567-023-02161-w\">https://doi.org/10.1038/s41567-023-02161-w</a>","ama":"Mukhopadhyay S, Senior JL, Saez Mollejo J, et al. Superconductivity from a melted insulator in Josephson junction arrays. <i>Nature Physics</i>. 2023;19:1630-1635. doi:<a href=\"https://doi.org/10.1038/s41567-023-02161-w\">10.1038/s41567-023-02161-w</a>","ista":"Mukhopadhyay S, Senior JL, Saez Mollejo J, Puglia D, Zemlicka M, Fink JM, Higginbotham AP. 2023. Superconductivity from a melted insulator in Josephson junction arrays. Nature Physics. 19, 1630–1635.","ieee":"S. Mukhopadhyay <i>et al.</i>, “Superconductivity from a melted insulator in Josephson junction arrays,” <i>Nature Physics</i>, vol. 19. Springer Nature, pp. 1630–1635, 2023.","chicago":"Mukhopadhyay, Soham, Jorden L Senior, Jaime Saez Mollejo, Denise Puglia, Martin Zemlicka, Johannes M Fink, and Andrew P Higginbotham. “Superconductivity from a Melted Insulator in Josephson Junction Arrays.” <i>Nature Physics</i>. Springer Nature, 2023. <a href=\"https://doi.org/10.1038/s41567-023-02161-w\">https://doi.org/10.1038/s41567-023-02161-w</a>.","short":"S. Mukhopadhyay, J.L. Senior, J. Saez Mollejo, D. Puglia, M. Zemlicka, J.M. Fink, A.P. Higginbotham, Nature Physics 19 (2023) 1630–1635.","mla":"Mukhopadhyay, Soham, et al. “Superconductivity from a Melted Insulator in Josephson Junction Arrays.” <i>Nature Physics</i>, vol. 19, Springer Nature, 2023, pp. 1630–35, doi:<a href=\"https://doi.org/10.1038/s41567-023-02161-w\">10.1038/s41567-023-02161-w</a>."}},{"tmp":{"image":"/images/cc_by_nc_sa.png","name":"Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode","short":"CC BY-NC-SA (4.0)"},"publisher":"Institute of Science and Technology Austria","has_accepted_license":"1","status":"public","day":"12","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","publication_status":"published","degree_awarded":"PhD","file_date_updated":"2024-10-13T22:30:04Z","OA_place":"publisher","title":"Synapseek: Meta-learning synaptic plasticity rules","oa_version":"Published Version","_id":"14422","project":[{"name":"Learning the shape of synaptic plasticity rules for neuronal architectures and function through machine learning.","call_identifier":"H2020","grant_number":"819603","_id":"0aacfa84-070f-11eb-9043-d7eb2c709234"}],"citation":{"mla":"Confavreux, Basile J. <i>Synapseek: Meta-Learning Synaptic Plasticity Rules</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:14422\">10.15479/at:ista:14422</a>.","short":"B.J. Confavreux, Synapseek: Meta-Learning Synaptic Plasticity Rules, Institute of Science and Technology Austria, 2023.","chicago":"Confavreux, Basile J. “Synapseek: Meta-Learning Synaptic Plasticity Rules.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:14422\">https://doi.org/10.15479/at:ista:14422</a>.","ieee":"B. J. Confavreux, “Synapseek: Meta-learning synaptic plasticity rules,” Institute of Science and Technology Austria, 2023.","ista":"Confavreux BJ. 2023. Synapseek: Meta-learning synaptic plasticity rules. Institute of Science and Technology Austria.","ama":"Confavreux BJ. Synapseek: Meta-learning synaptic plasticity rules. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:14422\">10.15479/at:ista:14422</a>","apa":"Confavreux, B. J. (2023). <i>Synapseek: Meta-learning synaptic plasticity rules</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:14422\">https://doi.org/10.15479/at:ista:14422</a>"},"related_material":{"record":[{"relation":"part_of_dissertation","status":"public","id":"9633"}]},"article_processing_charge":"No","date_published":"2023-10-12T00:00:00Z","oa":1,"date_updated":"2026-07-07T06:53:33Z","doi":"10.15479/at:ista:14422","abstract":[{"text":"Animals exhibit a remarkable ability to learn and remember new behaviors, skills, and associations throughout their lifetime. These capabilities are made possible thanks to a variety of\r\nchanges in the brain throughout adulthood, regrouped under the term \"plasticity\". Some cells\r\nin the brain —neurons— and specifically changes in the connections between neurons, the\r\nsynapses, were shown to be crucial for the formation, selection, and consolidation of memories\r\nfrom past experiences. These ongoing changes of synapses across time are called synaptic\r\nplasticity. Understanding how a myriad of biochemical processes operating at individual\r\nsynapses can somehow work in concert to give rise to meaningful changes in behavior is a\r\nfascinating problem and an active area of research.\r\nHowever, the experimental search for the precise plasticity mechanisms at play in the brain\r\nis daunting, as it is difficult to control and observe synapses during learning. Theoretical\r\napproaches have thus been the default method to probe the plasticity-behavior connection. Such\r\nstudies attempt to extract unifying principles across synapses and model all observed synaptic\r\nchanges using plasticity rules: equations that govern the evolution of synaptic strengths across\r\ntime in neuronal network models. These rules can use many relevant quantities to determine\r\nthe magnitude of synaptic changes, such as the precise timings of pre- and postsynaptic\r\naction potentials, the recent neuronal activity levels, the state of neighboring synapses, etc.\r\nHowever, analytical studies rely heavily on human intuition and are forced to make simplifying\r\nassumptions about plasticity rules.\r\nIn this thesis, we aim to assist and augment human intuition in this search for plasticity rules.\r\nWe explore whether a numerical approach could automatically discover the plasticity rules\r\nthat elicit desired behaviors in large networks of interconnected neurons. This approach is\r\ndubbed meta-learning synaptic plasticity: learning plasticity rules which themselves will make\r\nneuronal networks learn how to solve a desired task. We first write all the potential plasticity\r\nmechanisms to consider using a single expression with adjustable parameters. We then optimize\r\nthese plasticity parameters using evolutionary strategies or Bayesian inference on tasks known\r\nto involve synaptic plasticity, such as familiarity detection and network stabilization.\r\nWe show that these automated approaches are powerful tools, able to complement established\r\nanalytical methods. By comprehensively screening plasticity rules at all synapse types in\r\nrealistic, spiking neuronal network models, we discover entire sets of degenerate plausible\r\nplasticity rules that reliably elicit memory-related behaviors. Our approaches allow for more\r\nrobust experimental predictions, by abstracting out the idiosyncrasies of individual plasticity\r\nrules, and provide fresh insights on synaptic plasticity in spiking network models.\r\n","lang":"eng"}],"ec_funded":1,"ddc":["610"],"corr_author":"1","type":"dissertation","year":"2023","alternative_title":["ISTA Thesis"],"publication_identifier":{"issn":["2663-337X"]},"month":"10","supervisor":[{"id":"CB6FF8D2-008F-11EA-8E08-2637E6697425","first_name":"Tim P","last_name":"Vogels","orcid":"0000-0003-3295-6181","full_name":"Vogels, Tim P"}],"page":"148","file":[{"file_size":30599717,"content_type":"application/pdf","date_created":"2023-10-12T14:53:50Z","creator":"cchlebak","checksum":"7f636555eae7803323df287672fd13ed","relation":"main_file","file_name":"Confavreux_Thesis_2A.pdf","access_level":"open_access","file_id":"14424","embargo":"2024-10-12","date_updated":"2024-10-13T22:30:04Z"},{"date_created":"2023-10-18T07:38:34Z","checksum":"725e85946db92290a4583a0de9779e1b","creator":"cchlebak","file_size":68406739,"content_type":"application/x-zip-compressed","file_id":"14440","access_level":"closed","date_updated":"2024-10-13T22:30:04Z","embargo_to":"open_access","file_name":"Confavreux Thesis.zip","relation":"source_file"}],"author":[{"first_name":"Basile J","id":"C7610134-B532-11EA-BD9F-F5753DDC885E","full_name":"Confavreux, Basile J","last_name":"Confavreux"}],"language":[{"iso":"eng"}],"date_created":"2023-10-12T14:13:25Z","department":[{"_id":"GradSch"},{"_id":"TiVo"}]},{"year":"2023","publication_identifier":{"issn":["1097-6256"],"eissn":["1546-1726"]},"month":"04","author":[{"first_name":"Divyansh","id":"2A485EBE-F248-11E8-B48F-1D18A9856A87","full_name":"Gupta, Divyansh","orcid":"0000-0001-7400-6665","last_name":"Gupta"},{"first_name":"Wiktor F","id":"358A453A-F248-11E8-B48F-1D18A9856A87","full_name":"Mlynarski, Wiktor F","last_name":"Mlynarski"},{"full_name":"Sumser, Anton L","orcid":"0000-0002-4792-1881","last_name":"Sumser","first_name":"Anton L","id":"3320A096-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Olga","id":"3C0C7BC6-F248-11E8-B48F-1D18A9856A87","full_name":"Symonova, Olga","orcid":"0000-0003-2012-9947","last_name":"Symonova"},{"full_name":"Svaton, Jan","last_name":"Svaton","orcid":"0000-0002-6198-2939","first_name":"Jan","id":"f7f724c3-9d6f-11ed-9f44-e5c5f3a5bee2"},{"full_name":"Jösch, Maximilian A","last_name":"Jösch","orcid":"0000-0002-3937-1330","first_name":"Maximilian A","id":"2BD278E6-F248-11E8-B48F-1D18A9856A87"}],"date_created":"2023-01-23T14:14:19Z","language":[{"iso":"eng"}],"department":[{"_id":"GradSch"},{"_id":"MaJö"}],"page":"606-614","file":[{"checksum":"a33d91e398e548f34003170e10988368","creator":"dernst","date_created":"2023-10-04T11:40:51Z","file_size":6144866,"success":1,"content_type":"application/pdf","date_updated":"2023-10-04T11:40:51Z","file_id":"14395","access_level":"open_access","file_name":"2023_NatureNeuroscience_Gupta.pdf","relation":"main_file"}],"article_processing_charge":"Yes (in subscription journal)","date_published":"2023-04-01T00:00:00Z","doi":"10.1038/s41593-023-01280-0","volume":26,"oa":1,"date_updated":"2026-07-30T22:30:33Z","ec_funded":1,"abstract":[{"text":"Statistics of natural scenes are not uniform - their structure varies dramatically from ground to sky. It remains unknown whether these non-uniformities are reflected in the large-scale organization of the early visual system and what benefits such adaptations would confer. Here, by relying on the efficient coding hypothesis, we predict that changes in the structure of receptive fields across visual space increase the efficiency of sensory coding. We show experimentally that, in agreement with our predictions, receptive fields of retinal ganglion cells change their shape along the dorsoventral retinal axis, with a marked surround asymmetry at the visual horizon. Our work demonstrates that, according to principles of efficient coding, the panoramic structure of natural scenes is exploited by the retina across space and cell-types.","lang":"eng"}],"quality_controlled":"1","article_type":"original","type":"journal_article","scopus_import":"1","ddc":["570"],"publication":"Nature Neuroscience","intvolume":"        26","corr_author":"1","acknowledged_ssus":[{"_id":"ScienComp"},{"_id":"PreCl"},{"_id":"LifeSc"},{"_id":"Bio"}],"title":"Panoramic visual statistics shape retina-wide organization of receptive fields","file_date_updated":"2023-10-04T11:40:51Z","project":[{"_id":"2564DBCA-B435-11E9-9278-68D0E5697425","grant_number":"665385","call_identifier":"H2020","name":"International IST Doctoral Program"},{"name":"Efficient coding with biophysical realism","grant_number":"P34015","_id":"626c45b5-2b32-11ec-9570-e509828c1ba6"},{"name":"Circuits of Visual Attention","grant_number":"756502","_id":"2634E9D2-B435-11E9-9278-68D0E5697425","call_identifier":"H2020"},{"name":"Neuronal networks of salience and spatial detection in the murine superior colliculus","grant_number":"LT000256","_id":"266D407A-B435-11E9-9278-68D0E5697425"},{"name":"Connecting sensory with motor processing in the superior colliculus","_id":"264FEA02-B435-11E9-9278-68D0E5697425","grant_number":"ALTF 1098-2017"}],"oa_version":"Published Version","_id":"12349","citation":{"apa":"Gupta, D., Mlynarski, W. F., Sumser, A. L., Symonova, O., Svaton, J., &#38; Jösch, M. A. (2023). Panoramic visual statistics shape retina-wide organization of receptive fields. <i>Nature Neuroscience</i>. Springer Nature. <a href=\"https://doi.org/10.1038/s41593-023-01280-0\">https://doi.org/10.1038/s41593-023-01280-0</a>","ama":"Gupta D, Mlynarski WF, Sumser AL, Symonova O, Svaton J, Jösch MA. Panoramic visual statistics shape retina-wide organization of receptive fields. <i>Nature Neuroscience</i>. 2023;26:606-614. doi:<a href=\"https://doi.org/10.1038/s41593-023-01280-0\">10.1038/s41593-023-01280-0</a>","ieee":"D. Gupta, W. F. Mlynarski, A. L. Sumser, O. Symonova, J. Svaton, and M. A. Jösch, “Panoramic visual statistics shape retina-wide organization of receptive fields,” <i>Nature Neuroscience</i>, vol. 26. Springer Nature, pp. 606–614, 2023.","chicago":"Gupta, Divyansh, Wiktor F Mlynarski, Anton L Sumser, Olga Symonova, Jan Svaton, and Maximilian A Jösch. “Panoramic Visual Statistics Shape Retina-Wide Organization of Receptive Fields.” <i>Nature Neuroscience</i>. Springer Nature, 2023. <a href=\"https://doi.org/10.1038/s41593-023-01280-0\">https://doi.org/10.1038/s41593-023-01280-0</a>.","ista":"Gupta D, Mlynarski WF, Sumser AL, Symonova O, Svaton J, Jösch MA. 2023. Panoramic visual statistics shape retina-wide organization of receptive fields. Nature Neuroscience. 26, 606–614.","short":"D. Gupta, W.F. Mlynarski, A.L. Sumser, O. Symonova, J. Svaton, M.A. Jösch, Nature Neuroscience 26 (2023) 606–614.","mla":"Gupta, Divyansh, et al. “Panoramic Visual Statistics Shape Retina-Wide Organization of Receptive Fields.” <i>Nature Neuroscience</i>, vol. 26, Springer Nature, 2023, pp. 606–14, doi:<a href=\"https://doi.org/10.1038/s41593-023-01280-0\">10.1038/s41593-023-01280-0</a>."},"related_material":{"record":[{"relation":"research_data","status":"public","id":"12370"},{"id":"18574","status":"public","relation":"dissertation_contains"}]},"pmid":1,"external_id":{"isi":["000955258300002"],"pmid":["36959418"]},"tmp":{"short":"CC BY (4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","image":"/images/cc_by.png"},"isi":1,"status":"public","has_accepted_license":"1","publisher":"Springer Nature","acknowledgement":"We thank Hiroki Asari for sharing the dataset of naturalistic images, Anton Sumser for sharing visual stimulus code, Yoav Ben Simon for initial explorative work with the generation of AAVs, and Tomas Vega-Zuñiga for help with immunostainings. We also thank Gasper Tkacik and members of the Neuroethology group for their comments on the manuscript. This research was supported by the Scientific Service Units of IST Austria through resources provided by Scientific Computing, the Preclinical Facility, the Lab Support Facility, and the Imaging and Optics Facility. This work was supported by European Union Horizon 2020 Marie Skłodowska-Curie grant 665385 (DG), Austrian Science Fund (FWF) stand-alone grant P 34015 (WM), Human Frontiers Science Program LT000256/2018-L (AS), EMBO ALTF 1098-2017 (AS) and the European Research Council Starting Grant 756502 (MJ).","day":"01","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","publication_status":"published"},{"month":"01","author":[{"id":"2A485EBE-F248-11E8-B48F-1D18A9856A87","first_name":"Divyansh","orcid":"0000-0001-7400-6665","last_name":"Gupta","full_name":"Gupta, Divyansh"},{"last_name":"Sumser","orcid":"0000-0002-4792-1881","full_name":"Sumser, Anton L","id":"3320A096-F248-11E8-B48F-1D18A9856A87","first_name":"Anton L"},{"first_name":"Maximilian A","id":"2BD278E6-F248-11E8-B48F-1D18A9856A87","full_name":"Jösch, Maximilian 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of natural scenes are not uniform - their structure varies dramatically from ground to sky. It remains unknown whether these non-uniformities are reflected in the large-scale organization of the early visual system and what benefits such adaptations would confer. Here, by relying on the efficient coding hypothesis, we predict that changes in the structure of receptive fields across visual space increase the efficiency of sensory coding. We show experimentally that, in agreement with our predictions, receptive fields of retinal ganglion cells change their shape along the dorsoventral retinal axis, with a marked surround asymmetry at the visual horizon. Our work demonstrates that, according to principles of efficient coding, the panoramic structure of natural scenes is exploited by the retina across space and cell-types. "}],"type":"research_data","ddc":["571"],"corr_author":"1","article_processing_charge":"No","date_published":"2023-01-26T00:00:00Z","doi":"10.15479/AT:ISTA:12370","oa":1,"date_updated":"2026-07-30T22:30:34Z","project":[{"name":"International IST Doctoral Program","call_identifier":"H2020","_id":"2564DBCA-B435-11E9-9278-68D0E5697425","grant_number":"665385"},{"name":"Efficient coding with biophysical realism","_id":"626c45b5-2b32-11ec-9570-e509828c1ba6","grant_number":"P34015"},{"call_identifier":"H2020","_id":"2634E9D2-B435-11E9-9278-68D0E5697425","grant_number":"756502","name":"Circuits of Visual Attention"},{"grant_number":"LT000256","_id":"266D407A-B435-11E9-9278-68D0E5697425","name":"Neuronal networks of salience and spatial detection in the murine superior colliculus"},{"grant_number":"ALTF 1098-2017","_id":"264FEA02-B435-11E9-9278-68D0E5697425","name":"Connecting sensory with motor processing in the superior colliculus"}],"oa_version":"Published Version","_id":"12370","citation":{"ista":"Gupta D, Sumser AL, Jösch MA. 2023. Research Data for: Panoramic visual statistics shape retina-wide organization of receptive fields, Institute of Science and Technology Austria, <a href=\"https://doi.org/10.15479/AT:ISTA:12370\">10.15479/AT:ISTA:12370</a>.","chicago":"Gupta, Divyansh, Anton L Sumser, and Maximilian A Jösch. “Research Data for: Panoramic Visual Statistics Shape Retina-Wide Organization of Receptive Fields.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/AT:ISTA:12370\">https://doi.org/10.15479/AT:ISTA:12370</a>.","ieee":"D. Gupta, A. L. Sumser, and M. A. Jösch, “Research Data for: Panoramic visual statistics shape retina-wide organization of receptive fields.” Institute of Science and Technology Austria, 2023.","short":"D. Gupta, A.L. Sumser, M.A. Jösch, (2023).","mla":"Gupta, Divyansh, et al. <i>Research Data for: Panoramic Visual Statistics Shape Retina-Wide Organization of Receptive Fields</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/AT:ISTA:12370\">10.15479/AT:ISTA:12370</a>.","apa":"Gupta, D., Sumser, A. L., &#38; Jösch, M. A. (2023). Research Data for: Panoramic visual statistics shape retina-wide organization of receptive fields. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/AT:ISTA:12370\">https://doi.org/10.15479/AT:ISTA:12370</a>","ama":"Gupta D, Sumser AL, Jösch MA. Research Data for: Panoramic visual statistics shape retina-wide organization of receptive fields. 2023. doi:<a href=\"https://doi.org/10.15479/AT:ISTA:12370\">10.15479/AT:ISTA:12370</a>"},"related_material":{"record":[{"status":"public","id":"12349","relation":"used_in_publication"},{"id":"18574","status":"public","relation":"used_in_publication"}]},"acknowledged_ssus":[{"_id":"ScienComp"},{"_id":"M-Shop"},{"_id":"Bio"},{"_id":"PreCl"},{"_id":"LifeSc"}],"contributor":[{"first_name":"Olga","id":"3C0C7BC6-F248-11E8-B48F-1D18A9856A87","contributor_type":"researcher","last_name":"Symonova"},{"last_name":"Mlynarski","contributor_type":"researcher","id":"358A453A-F248-11E8-B48F-1D18A9856A87","first_name":"Wiktor F"},{"first_name":"Jan","id":"f7f724c3-9d6f-11ed-9f44-e5c5f3a5bee2","contributor_type":"researcher","last_name":"Svaton"}],"title":"Research Data for: Panoramic visual statistics shape retina-wide organization of receptive fields","file_date_updated":"2023-01-26T10:51:34Z","day":"26","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","tmp":{"image":"/images/cc_by_nc_sa.png","name":"Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)","legal_code_url":"https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode","short":"CC BY-NC-SA (4.0)"},"has_accepted_license":"1","status":"public","publisher":"Institute of Science and Technology Austria"},{"day":"24","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","publication_status":"published","status":"public","has_accepted_license":"1","publisher":"Institute of Science and Technology Austria","oa_version":"Published Version","_id":"14226","citation":{"chicago":"Stephenson, Elizabeth R. “Generalizing Medial Axes with Homology Switches.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:14226\">https://doi.org/10.15479/at:ista:14226</a>.","ieee":"E. R. Stephenson, “Generalizing medial axes with homology switches,” Institute of Science and Technology Austria, 2023.","ista":"Stephenson ER. 2023. Generalizing medial axes with homology switches. Institute of Science and Technology Austria.","short":"E.R. Stephenson, Generalizing Medial Axes with Homology Switches, Institute of Science and Technology Austria, 2023.","mla":"Stephenson, Elizabeth R. <i>Generalizing Medial Axes with Homology Switches</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:14226\">10.15479/at:ista:14226</a>.","apa":"Stephenson, E. R. (2023). <i>Generalizing medial axes with homology switches</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:14226\">https://doi.org/10.15479/at:ista:14226</a>","ama":"Stephenson ER. Generalizing medial axes with homology switches. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:14226\">10.15479/at:ista:14226</a>"},"degree_awarded":"MS","title":"Generalizing medial axes with homology switches","file_date_updated":"2024-02-26T23:30:03Z","OA_place":"publisher","abstract":[{"lang":"eng","text":"We introduce the notion of a Faustian interchange in a 1-parameter family of smooth\r\nfunctions to generalize the medial axis to critical points of index larger than 0.\r\nWe construct and implement a general purpose algorithm for approximating such\r\ngeneralized medial axes."}],"type":"dissertation","ddc":["500"],"corr_author":"1","article_processing_charge":"No","date_published":"2023-08-24T00:00:00Z","doi":"10.15479/at:ista:14226","oa":1,"date_updated":"2026-04-07T14:02:30Z","supervisor":[{"full_name":"Edelsbrunner, Herbert","orcid":"0000-0002-9823-6833","last_name":"Edelsbrunner","first_name":"Herbert","id":"3FB178DA-F248-11E8-B48F-1D18A9856A87"}],"month":"08","author":[{"id":"2D04F932-F248-11E8-B48F-1D18A9856A87","first_name":"Elizabeth R","last_name":"Stephenson","orcid":"0000-0002-6862-208X","full_name":"Stephenson, Elizabeth R"}],"date_created":"2023-08-24T13:01:18Z","department":[{"_id":"GradSch"},{"_id":"HeEd"}],"language":[{"iso":"eng"}],"page":"43","file":[{"checksum":"453caf851d75c3478c10ed09bd242a91","creator":"cchlebak","date_created":"2023-08-24T13:02:49Z","content_type":"application/x-zip-compressed","file_size":15501411,"date_updated":"2024-02-26T23:30:03Z","file_id":"14227","access_level":"closed","file_name":"documents-export-2023-08-24.zip","relation":"source_file","embargo_to":"open_access"},{"file_size":6854783,"content_type":"application/pdf","checksum":"7349d29963d6695e555e171748648d9a","creator":"cchlebak","date_created":"2023-08-24T13:03:42Z","file_name":"thesis_pdf_a.pdf","relation":"main_file","embargo":"2024-02-25","date_updated":"2024-02-26T23:30:03Z","file_id":"14228","access_level":"open_access"}],"year":"2023","alternative_title":["ISTA Master's Thesis"],"publication_identifier":{"issn":["2791-4585"]}},{"supervisor":[{"full_name":"Friml, Jiří","orcid":"0000-0002-8302-7596","last_name":"Friml","first_name":"Jiří","id":"4159519E-F248-11E8-B48F-1D18A9856A87"},{"first_name":"Martin","id":"462D4284-F248-11E8-B48F-1D18A9856A87","full_name":"Loose, Martin","orcid":"0000-0001-7309-9724","last_name":"Loose"}],"keyword":["Clathrin-Mediated Endocytosis","vesicle scission","Dynamin-Related Protein 2","SH3P2","TPLATE complex","Total internal reflection fluorescence microscopy","Arabidopsis thaliana"],"month":"11","author":[{"id":"390C1120-F248-11E8-B48F-1D18A9856A87","first_name":"Nataliia","last_name":"Gnyliukh","orcid":"0000-0002-2198-0509","full_name":"Gnyliukh, Nataliia"}],"date_created":"2023-11-10T09:10:06Z","department":[{"_id":"GradSch"},{"_id":"JiFr"},{"_id":"MaLo"}],"language":[{"iso":"eng"}],"page":"180","file":[{"embargo_to":"open_access","file_name":"Thesis_Gnyliukh_final_08_11_23.docx","relation":"source_file","file_id":"14567","access_level":"closed","date_updated":"2024-11-23T23:30:38Z","content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document","file_size":20824903,"date_created":"2023-11-20T09:18:51Z","checksum":"3d5e680bfc61f98e308c434f45cc9bd6","creator":"ngnyliuk"},{"date_updated":"2024-11-23T23:30:38Z","embargo":"2024-11-23","access_level":"open_access","file_id":"14568","relation":"main_file","file_name":"Thesis_Gnyliukh_final_20_11_23.pdf","creator":"ngnyliuk","checksum":"bfc96d47fc4e7e857dd71656097214a4","date_created":"2023-11-20T09:23:11Z","content_type":"application/pdf","file_size":24871844}],"year":"2023","alternative_title":["ISTA Thesis"],"publication_identifier":{"issn":["2663-337X"],"isbn":["978-3-99078-037-4"]},"ec_funded":1,"abstract":[{"lang":"eng","text":"Clathrin-mediated endocytosis (CME) is vital for the regulation of plant growth and\r\ndevelopment by controlling plasma membrane protein composition and cargo uptake. CME\r\nrelies on the precise recruitment control of protein regulators for vesicle maturation and\r\nrelease. During the early stages of endocytosis, an area of flat membrane is remodelled by\r\nproteins to create a spherical vesicle against intracellular forces. After the Clathrin-coated\r\nvesicle (CCV) is fully formed, scission machinery releases it from the plasma membrane,\r\nand cargo proceeds for recycling or degradation through early endosomes / Trans Golgi\r\nnetwork. Protein machineries that mediate membrane bending and vesicle release in plants\r\nare unknown. However, studies show, that plant endocytosis is actin independent, thus\r\nindicating that plants utilize a unique mechanism to mediate membrane bending against highturgor pressure compared to other model systems. First, by using biochemical and advanced\r\nlive microscopy approaches we investigate the TPLATE complex, a plant-specific\r\nendocytosis protein complex. We found that TPLATE is peripherally associated with\r\nclathrin-coated vesicles and localises at the rim of endocytosis events. Next, our study of\r\nplant Dynamin-related protein 1C (DRP1C), which was hypothesised previously to play a\r\nrole in vesicle release, shows the recruitment of the protein already at the early stages of\r\nendocytosis. Moreover, DRP1C assembles into organised ring-like structures and is able to\r\ninduce membrane deformation and tubulation, suggesting its role also in membrane bending\r\nduring early CME. Based on the data from mammalian and yeast systems, plant DynaminRelated Proteins 2 and SH3P2 protein are strong candidates to be part of the plant vesicle\r\nscission machinery; however, their precise role in plant CME has not been yet elucidated.\r\nHere, we characterised DRP2s and SH3P2 roles in CME by combining high-resolution\r\nimaging of endocytic events in vivo and protein characterisation. Although DRP2s and\r\nSH3P2 arrive together during late CME and physically interact, genetic analysis using\r\n∆sh3p1,2,3 mutant and complementation with non-DRP2-interacting SH3P2 variants suggest\r\nthat SH3P2 does not directly recruit DRP2s to the site of endocytosis. Summarising our\r\nresearch, these observations provide new important insights into the mechanism of plant\r\nCME and show that, despite plants posses many homologues of mammalian and yeast CME\r\ncomponents, they do not necessarily act in the same manner. "}],"type":"dissertation","ddc":["570"],"corr_author":"1","article_processing_charge":"No","date_published":"2023-11-10T00:00:00Z","doi":"10.15479/at:ista:14510","oa":1,"date_updated":"2026-07-30T22:30:56Z","project":[{"name":"International IST Doctoral Program","_id":"2564DBCA-B435-11E9-9278-68D0E5697425","grant_number":"665385","call_identifier":"H2020"}],"_id":"14510","oa_version":"Published Version","citation":{"short":"N. Gnyliukh, Mechanism of Clathrin-Coated Vesicle  Formation during Endocytosis in Plants, Institute of Science and Technology Austria, 2023.","mla":"Gnyliukh, Nataliia. <i>Mechanism of Clathrin-Coated Vesicle  Formation during Endocytosis in Plants</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:14510\">10.15479/at:ista:14510</a>.","ieee":"N. Gnyliukh, “Mechanism of clathrin-coated vesicle  formation during endocytosis in plants,” Institute of Science and Technology Austria, 2023.","chicago":"Gnyliukh, Nataliia. “Mechanism of Clathrin-Coated Vesicle  Formation during Endocytosis in Plants.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:14510\">https://doi.org/10.15479/at:ista:14510</a>.","ista":"Gnyliukh N. 2023. Mechanism of clathrin-coated vesicle  formation during endocytosis in plants. Institute of Science and Technology Austria.","ama":"Gnyliukh N. Mechanism of clathrin-coated vesicle  formation during endocytosis in plants. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:14510\">10.15479/at:ista:14510</a>","apa":"Gnyliukh, N. (2023). <i>Mechanism of clathrin-coated vesicle  formation during endocytosis in plants</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:14510\">https://doi.org/10.15479/at:ista:14510</a>"},"related_material":{"record":[{"id":"14591","status":"public","relation":"part_of_dissertation"},{"id":"9887","status":"public","relation":"part_of_dissertation"},{"status":"public","id":"8139","relation":"part_of_dissertation"}]},"acknowledged_ssus":[{"_id":"EM-Fac"},{"_id":"Bio"},{"_id":"LifeSc"}],"degree_awarded":"PhD","title":"Mechanism of clathrin-coated vesicle  formation during endocytosis in plants","file_date_updated":"2024-11-23T23:30:38Z","OA_place":"publisher","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","day":"10","publication_status":"published","tmp":{"short":"CC BY (4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","image":"/images/cc_by.png"},"status":"public","has_accepted_license":"1","publisher":"Institute of Science and Technology Austria"},{"oa":1,"date_updated":"2026-07-06T12:50:45Z","doi":"10.15479/at:ista:12470","article_processing_charge":"No","date_published":"2023-01-09T00:00:00Z","ddc":["610"],"corr_author":"1","type":"dissertation","ec_funded":1,"abstract":[{"text":"The brain is an exceptionally sophisticated organ consisting of billions of cells and trillions of \r\nconnections that orchestrate our cognition and behavior. To decode its complex connectivity, it is \r\npivotal to disentangle its intricate architecture spanning from cm-sized circuits down to tens of \r\nnm-small synapses.\r\nTo achieve this goal, I developed CATS – Comprehensive Analysis of nervous Tissue across \r\nScales, a versatile toolbox for obtaining a holistic view of nervous tissue context with (super\u0002resolution) fluorescence microscopy. CATS combines comprehensive labeling of the extracellular\r\nspace, that is compatible with chemical fixation, with information on molecular markers, super\u0002resolved data acquisition and machine-learning based data analysis for segmentation and synapse \r\nidentification.\r\nI used CATS to analyze key features of nervous tissue connectivity, ranging from whole tissue \r\narchitecture, neuronal in- and output-fields, down to synapse morphology.\r\nFocusing on the hippocampal circuitry, I quantified synaptic transmission properties of mossy \r\nfiber boutons and analyzed the connectivity pattern of dentate gyrus granule cells with CA3 \r\npyramidal neurons. This shows that CATS is a viable tool to study hallmarks of neuronal \r\nconnectivity with light microscopy.","lang":"eng"}],"alternative_title":["ISTA Thesis"],"publication_identifier":{"issn":["2663-337X"],"isbn":["978-3-99078-026-8"]},"year":"2023","page":"201","file":[{"file_size":41771714,"content_type":"application/pdf","checksum":"1a2306e5f59f52df598e7ecfadf921ac","creator":"cchlebak","date_created":"2023-01-31T15:11:42Z","file_name":"20230109_PhD_thesis_JM_final.pdf","relation":"main_file","embargo":"2023-07-09","date_updated":"2023-07-27T22:30:54Z","file_id":"12471","access_level":"open_access"},{"date_updated":"2023-07-10T22:30:04Z","access_level":"closed","file_id":"12472","relation":"source_file","file_name":"20230109_PhD_thesis_JM_final.docx","embargo_to":"open_access","creator":"cchlebak","checksum":"0bebbdee0773443959e1f6ab8caf281f","date_created":"2023-01-31T15:11:51Z","content_type":"application/vnd.openxmlformats-officedocument.wordprocessingml.document","file_size":66983464}],"author":[{"orcid":"0000-0003-3862-1235","last_name":"Michalska","full_name":"Michalska, Julia M","id":"443DB6DE-F248-11E8-B48F-1D18A9856A87","first_name":"Julia M"}],"language":[{"iso":"eng"}],"date_created":"2023-01-31T15:10:53Z","department":[{"_id":"GradSch"},{"_id":"JoDa"}],"supervisor":[{"id":"42EFD3B6-F248-11E8-B48F-1D18A9856A87","first_name":"Johann G","last_name":"Danzl","orcid":"0000-0001-8559-3973","full_name":"Danzl, Johann G"}],"month":"01","publisher":"Institute of Science and Technology Austria","status":"public","has_accepted_license":"1","tmp":{"short":"CC BY (4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","image":"/images/cc_by.png"},"publication_status":"published","day":"09","user_id":"ba8df636-2132-11f1-aed0-ed93e2281fdd","file_date_updated":"2023-07-27T22:30:54Z","OA_place":"publisher","title":"A versatile toolbox for the comprehensive analysis of nervous tissue organization with light microscopy","degree_awarded":"PhD","acknowledged_ssus":[{"_id":"Bio"},{"_id":"LifeSc"},{"_id":"PreCl"},{"_id":"EM-Fac"},{"_id":"M-Shop"},{"_id":"ScienComp"}],"citation":{"apa":"Michalska, J. M. (2023). <i>A versatile toolbox for the comprehensive analysis of nervous tissue organization with light microscopy</i>. Institute of Science and Technology Austria. <a href=\"https://doi.org/10.15479/at:ista:12470\">https://doi.org/10.15479/at:ista:12470</a>","ama":"Michalska JM. A versatile toolbox for the comprehensive analysis of nervous tissue organization with light microscopy. 2023. doi:<a href=\"https://doi.org/10.15479/at:ista:12470\">10.15479/at:ista:12470</a>","ieee":"J. M. Michalska, “A versatile toolbox for the comprehensive analysis of nervous tissue organization with light microscopy,” Institute of Science and Technology Austria, 2023.","ista":"Michalska JM. 2023. A versatile toolbox for the comprehensive analysis of nervous tissue organization with light microscopy. Institute of Science and Technology Austria.","chicago":"Michalska, Julia M. “A Versatile Toolbox for the Comprehensive Analysis of Nervous Tissue Organization with Light Microscopy.” Institute of Science and Technology Austria, 2023. <a href=\"https://doi.org/10.15479/at:ista:12470\">https://doi.org/10.15479/at:ista:12470</a>.","short":"J.M. Michalska, A Versatile Toolbox for the Comprehensive Analysis of Nervous Tissue Organization with Light Microscopy, Institute of Science and Technology Austria, 2023.","mla":"Michalska, Julia M. <i>A Versatile Toolbox for the Comprehensive Analysis of Nervous Tissue Organization with Light Microscopy</i>. Institute of Science and Technology Austria, 2023, doi:<a href=\"https://doi.org/10.15479/at:ista:12470\">10.15479/at:ista:12470</a>."},"related_material":{"record":[{"id":"11943","status":"public","relation":"part_of_dissertation"},{"status":"public","id":"11950","relation":"part_of_dissertation"}]},"_id":"12470","oa_version":"Published Version","project":[{"name":"International IST Doctoral Program","call_identifier":"H2020","_id":"2564DBCA-B435-11E9-9278-68D0E5697425","grant_number":"665385"},{"name":"Molecular Drug Targets","call_identifier":"FWF","_id":"26AA4EF2-B435-11E9-9278-68D0E5697425","grant_number":"W1232-B24"}]},{"date_published":"2023-02-01T00:00:00Z","article_processing_charge":"Yes (via OA deal)","date_updated":"2026-07-30T22:31:09Z","oa":1,"volume":7,"doi":"10.1093/evlett/qrac004","article_type":"original","quality_controlled":"1","ec_funded":1,"abstract":[{"lang":"eng","text":"Differentiated X chromosomes are expected to have higher rates of adaptive divergence than autosomes, if new beneficial mutations are recessive (the “faster-X effect”), largely because these mutations are immediately exposed to selection in males. The evolution of X chromosomes after they stop recombining in males, but before they become hemizygous, has not been well explored theoretically. We use the diffusion approximation to infer substitution rates of beneficial and deleterious mutations under such a scenario. Our results show that selection is less efficient on diploid X loci than on autosomal and hemizygous X loci under a wide range of parameters. This “slower-X” effect is stronger for genes affecting primarily (or only) male fitness, and for sexually antagonistic genes. These unusual dynamics suggest that some of the peculiar features of X chromosomes, such as the differential accumulation of genes with sex-specific functions, may start arising earlier than previously appreciated."}],"corr_author":"1","intvolume":"         7","publication":"Evolution Letters","ddc":["570"],"type":"journal_article","scopus_import":"1","year":"2023","publication_identifier":{"issn":["2056-3744"]},"issue":"1","keyword":["Genetics","Ecology","Evolution","Behavior and Systematics"],"month":"02","file":[{"file_name":"2023_EvLetters_Mrnjavac.pdf","relation":"main_file","file_id":"14068","access_level":"open_access","date_updated":"2023-08-16T11:43:33Z","success":1,"content_type":"application/pdf","file_size":2592189,"date_created":"2023-08-16T11:43:33Z","checksum":"a240a041cb9b9b7c8ba93a4706674a3f","creator":"dernst"}],"language":[{"iso":"eng"}],"date_created":"2023-02-06T13:59:12Z","department":[{"_id":"GradSch"},{"_id":"BeVi"}],"author":[{"full_name":"Mrnjavac, Andrea","last_name":"Mrnjavac","first_name":"Andrea","id":"353FAC84-AE61-11E9-8BFC-00D3E5697425"},{"full_name":"Khudiakova, Kseniia","orcid":"0000-0002-6246-1465","last_name":"Khudiakova","first_name":"Kseniia","id":"4E6DC800-AE37-11E9-AC72-31CAE5697425"},{"first_name":"Nicholas H","id":"4880FE40-F248-11E8-B48F-1D18A9856A87","full_name":"Barton, Nicholas H","orcid":"0000-0002-8548-5240","last_name":"Barton"},{"full_name":"Vicoso, Beatriz","last_name":"Vicoso","orcid":"0000-0002-4579-8306","first_name":"Beatriz","id":"49E1C5C6-F248-11E8-B48F-1D18A9856A87"}],"tmp":{"short":"CC BY (4.0)","legal_code_url":"https://creativecommons.org/licenses/by/4.0/legalcode","name":"Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)","image":"/images/cc_by.png"},"isi":1,"external_id":{"pmid":["37065438"],"isi":["001021692200001"]},"publisher":"Oxford University Press","article_number":"qrac004","status":"public","has_accepted_license":"1","day":"01","user_id":"2DF688A6-F248-11E8-B48F-1D18A9856A87","acknowledgement":"We thank the Vicoso and Barton groups and ISTA Scientific Computing Unit. We also thank two anonymous reviewers for their valuable comments. This work was supported by the European Research Council under the European Union’s Horizon 2020 research and innovation program (grant agreements no. 715257 and no. 716117).","publication_status":"published","file_date_updated":"2023-08-16T11:43:33Z","title":"Slower-X: Reduced efficiency of selection in the early stages of X chromosome evolution","oa_version":"Published Version","_id":"12521","project":[{"call_identifier":"H2020","_id":"256E75B8-B435-11E9-9278-68D0E5697425","grant_number":"716117","name":"Optimal Transport and Stochastic Dynamics"},{"name":"Prevalence and Influence of Sexual Antagonism on Genome Evolution","call_identifier":"H2020","grant_number":"715257","_id":"250BDE62-B435-11E9-9278-68D0E5697425"}],"pmid":1,"related_material":{"record":[{"relation":"dissertation_contains","status":"public","id":"18531"}]},"citation":{"ista":"Mrnjavac A, Khudiakova K, Barton NH, Vicoso B. 2023. Slower-X: Reduced efficiency of selection in the early stages of X chromosome evolution. Evolution Letters. 7(1), qrac004.","ieee":"A. Mrnjavac, K. Khudiakova, N. H. Barton, and B. Vicoso, “Slower-X: Reduced efficiency of selection in the early stages of X chromosome evolution,” <i>Evolution Letters</i>, vol. 7, no. 1. Oxford University Press, 2023.","chicago":"Mrnjavac, Andrea, Kseniia Khudiakova, Nicholas H Barton, and Beatriz Vicoso. “Slower-X: Reduced Efficiency of Selection in the Early Stages of X Chromosome Evolution.” <i>Evolution Letters</i>. Oxford University Press, 2023. <a href=\"https://doi.org/10.1093/evlett/qrac004\">https://doi.org/10.1093/evlett/qrac004</a>.","short":"A. Mrnjavac, K. Khudiakova, N.H. Barton, B. Vicoso, Evolution Letters 7 (2023).","mla":"Mrnjavac, Andrea, et al. “Slower-X: Reduced Efficiency of Selection in the Early Stages of X Chromosome Evolution.” <i>Evolution Letters</i>, vol. 7, no. 1, qrac004, Oxford University Press, 2023, doi:<a href=\"https://doi.org/10.1093/evlett/qrac004\">10.1093/evlett/qrac004</a>.","apa":"Mrnjavac, A., Khudiakova, K., Barton, N. H., &#38; Vicoso, B. (2023). Slower-X: Reduced efficiency of selection in the early stages of X chromosome evolution. <i>Evolution Letters</i>. Oxford University Press. <a href=\"https://doi.org/10.1093/evlett/qrac004\">https://doi.org/10.1093/evlett/qrac004</a>","ama":"Mrnjavac A, Khudiakova K, Barton NH, Vicoso B. Slower-X: Reduced efficiency of selection in the early stages of X chromosome evolution. <i>Evolution Letters</i>. 2023;7(1). doi:<a href=\"https://doi.org/10.1093/evlett/qrac004\">10.1093/evlett/qrac004</a>"}}]