---
OA_place: publisher
_id: '11626'
abstract:
- lang: eng
  text: Plant growth and development is well known to be both, flexible and dynamic.
    The high capacity for post-embryonic organ formation and tissue regeneration requires
    tightly regulated intercellular communication and coordinated tissue polarization.
    One of the most important drivers for patterning and polarity in plant development
    is the phytohormone auxin. Auxin has the unique characteristic to establish polarized
    channels for its own active directional cell to cell transport. This fascinating
    phenomenon is called auxin canalization. Those auxin transport channels are characterized
    by the expression and polar, subcellular localization of PIN auxin efflux carriers.
    PIN proteins have the ability to dynamically change their localization and auxin
    itself can affect this by interfering with trafficking. Most of the underlying
    molecular mechanisms of canalization still remain enigmatic. What is known so
    far is that canonical auxin signaling is indispensable but also other non-canonical
    signaling components are thought to play a role. In order to shed light into the
    mysteries auf auxin canalization this study revisits the branches of auxin signaling
    in detail. Further a new auxin analogue, PISA, is developed which triggers auxin-like
    responses but does not directly activate canonical transcriptional auxin signaling.
    We revisit the direct auxin effect on PIN trafficking where we found that, contradictory
    to previous observations, auxin is very specifically promoting endocytosis of
    PIN2 but has no overall effect on endocytosis. Further, we evaluate which cellular
    processes related to PIN subcellular dynamics are involved in the establishment
    of auxin conducting channels and the formation of vascular tissue. We are re-evaluating
    the function of AUXIN BINDING PROTEIN 1 (ABP1) and provide a comprehensive picture
    about its developmental phneotypes and involvement in auxin signaling and canalization.
    Lastly, we are focusing on the crosstalk between the hormone strigolactone (SL)
    and auxin and found that SL is interfering with essentially all processes involved
    in auxin canalization in a non-transcriptional manner. Lastly we identify a new
    way of SL perception and signaling which is emanating from mitochondria, is independent
    of canonical SL signaling and is modulating primary root growth.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Michelle C
  full_name: Gallei, Michelle C
  id: 35A03822-F248-11E8-B48F-1D18A9856A87
  last_name: Gallei
  orcid: 0000-0003-1286-7368
citation:
  ama: Gallei MC. Auxin and strigolactone non-canonical signaling regulating development
    in Arabidopsis thaliana. 2022. doi:<a href="https://doi.org/10.15479/at:ista:11626">10.15479/at:ista:11626</a>
  apa: Gallei, M. C. (2022). <i>Auxin and strigolactone non-canonical signaling regulating
    development in Arabidopsis thaliana</i>. Institute of Science and Technology Austria.
    <a href="https://doi.org/10.15479/at:ista:11626">https://doi.org/10.15479/at:ista:11626</a>
  chicago: Gallei, Michelle C. “Auxin and Strigolactone Non-Canonical Signaling Regulating
    Development in Arabidopsis Thaliana.” Institute of Science and Technology Austria,
    2022. <a href="https://doi.org/10.15479/at:ista:11626">https://doi.org/10.15479/at:ista:11626</a>.
  ieee: M. C. Gallei, “Auxin and strigolactone non-canonical signaling regulating
    development in Arabidopsis thaliana,” Institute of Science and Technology Austria,
    2022.
  ista: Gallei MC. 2022. Auxin and strigolactone non-canonical signaling regulating
    development in Arabidopsis thaliana. Institute of Science and Technology Austria.
  mla: Gallei, Michelle C. <i>Auxin and Strigolactone Non-Canonical Signaling Regulating
    Development in Arabidopsis Thaliana</i>. Institute of Science and Technology Austria,
    2022, doi:<a href="https://doi.org/10.15479/at:ista:11626">10.15479/at:ista:11626</a>.
  short: M.C. Gallei, Auxin and Strigolactone Non-Canonical Signaling Regulating Development
    in Arabidopsis Thaliana, Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-07-20T11:21:53Z
date_published: 2022-07-20T00:00:00Z
date_updated: 2026-04-07T14:18:58Z
day: '20'
ddc:
- '575'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JiFr
doi: 10.15479/at:ista:11626
ec_funded: 1
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  description: This is the print version of the thesis including the full appendix
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file_date_updated: 2022-07-25T11:48:45Z
has_accepted_license: '1'
language:
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month: '07'
oa: 1
oa_version: Published Version
page: '248'
project:
- _id: 261099A6-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '742985'
  name: Tracing Evolution of Auxin Transport and Polarity in Plants
publication_identifier:
  isbn:
  - 978-3-99078-019-0
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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status: public
supervisor:
- first_name: Jiří
  full_name: Friml, Jiří
  id: 4159519E-F248-11E8-B48F-1D18A9856A87
  last_name: Friml
  orcid: 0000-0002-8302-7596
- first_name: Eva
  full_name: Benková, Eva
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
- first_name: Eilon
  full_name: Shani, Eilon
  last_name: Shani
title: Auxin and strigolactone non-canonical signaling regulating development in Arabidopsis
  thaliana
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '10799'
abstract:
- lang: eng
  text: "Because of the increasing popularity of machine learning methods, it is becoming
    important to understand the impact of learned components on automated decision-making
    systems and to guarantee that their consequences are beneficial to society. In
    other words, it is necessary to ensure that machine learning is sufficiently trustworthy
    to be used in real-world applications. This thesis studies two properties of machine
    learning models that are highly desirable for the\r\nsake of reliability: robustness
    and fairness. In the first part of the thesis we study the robustness of learning
    algorithms to training data corruption. Previous work has shown that machine learning
    models are vulnerable to a range\r\nof training set issues, varying from label
    noise through systematic biases to worst-case data manipulations. This is an especially
    relevant problem from a present perspective, since modern machine learning methods
    are particularly data hungry and therefore practitioners often have to rely on
    data collected from various external sources, e.g. from the Internet, from app
    users or via crowdsourcing. Naturally, such sources vary greatly in the quality
    and reliability of the\r\ndata they provide. With these considerations in mind,
    we study the problem of designing machine learning algorithms that are robust
    to corruptions in data coming from multiple sources. We show that, in contrast
    to the case of a single dataset with outliers, successful learning within this
    model is possible both theoretically and practically, even under worst-case data
    corruptions. The second part of this thesis deals with fairness-aware machine
    learning. There are multiple areas where machine learning models have shown promising
    results, but where careful considerations are required, in order to avoid discrimanative
    decisions taken by such learned components. Ensuring fairness can be particularly
    challenging, because real-world training datasets are expected to contain various
    forms of historical bias that may affect the learning process. In this thesis
    we show that data corruption can indeed render the problem of achieving fairness
    impossible, by tightly characterizing the theoretical limits of fair learning
    under worst-case data manipulations. However, assuming access to clean data, we
    also show how fairness-aware learning can be made practical in contexts beyond
    binary classification, in particular in the challenging learning to rank setting."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Nikola H
  full_name: Konstantinov, Nikola H
  id: 4B9D76E4-F248-11E8-B48F-1D18A9856A87
  last_name: Konstantinov
  orcid: 0009-0009-5204-7621
citation:
  ama: Konstantinov NH. Robustness and fairness in machine learning. 2022. doi:<a
    href="https://doi.org/10.15479/at:ista:10799">10.15479/at:ista:10799</a>
  apa: Konstantinov, N. H. (2022). <i>Robustness and fairness in machine learning</i>.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:10799">https://doi.org/10.15479/at:ista:10799</a>
  chicago: Konstantinov, Nikola H. “Robustness and Fairness in Machine Learning.”
    Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:10799">https://doi.org/10.15479/at:ista:10799</a>.
  ieee: N. H. Konstantinov, “Robustness and fairness in machine learning,” Institute
    of Science and Technology Austria, 2022.
  ista: Konstantinov NH. 2022. Robustness and fairness in machine learning. Institute
    of Science and Technology Austria.
  mla: Konstantinov, Nikola H. <i>Robustness and Fairness in Machine Learning</i>.
    Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:10799">10.15479/at:ista:10799</a>.
  short: N.H. Konstantinov, Robustness and Fairness in Machine Learning, Institute
    of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-02-28T13:03:49Z
date_published: 2022-03-08T00:00:00Z
date_updated: 2026-04-07T14:19:48Z
day: '08'
ddc:
- '000'
degree_awarded: PhD
department:
- _id: GradSch
- _id: ChLa
doi: 10.15479/at:ista:10799
ec_funded: 1
file:
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keyword:
- robustness
- fairness
- machine learning
- PAC learning
- adversarial learning
language:
- iso: eng
month: '03'
oa: 1
oa_version: Published Version
page: '176'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  isbn:
  - 978-3-99078-015-2
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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    relation: part_of_dissertation
    status: public
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    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Christoph
  full_name: Lampert, Christoph
  id: 40C20FD2-F248-11E8-B48F-1D18A9856A87
  last_name: Lampert
  orcid: 0000-0001-8622-7887
title: Robustness and fairness in machine learning
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '10759'
abstract:
- lang: eng
  text: In this Thesis, I study composite quantum impurities with variational techniques,
    both inspired by machine learning as well as fully analytic. I supplement this
    with exploration of other applications of machine learning, in particular artificial
    neural networks, in many-body physics. In Chapters 3 and 4, I study quasiparticle
    systems with variational approach. I derive a Hamiltonian describing the angulon
    quasiparticle in the presence of a magnetic field. I apply analytic variational
    treatment to this Hamiltonian. Then, I introduce a variational approach for non-additive
    systems, based on artificial neural networks. I exemplify this approach on the
    example of the polaron quasiparticle (Fröhlich Hamiltonian). In Chapter 5, I continue
    using artificial neural networks, albeit in a different setting. I apply artificial
    neural networks to detect phases from snapshots of two types physical systems.
    Namely, I study Monte Carlo snapshots of multilayer classical spin models as well
    as molecular dynamics maps of colloidal systems. The main type of networks that
    I use here are convolutional neural networks, known for their applicability to
    image data.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Wojciech
  full_name: Rzadkowski, Wojciech
  id: 48C55298-F248-11E8-B48F-1D18A9856A87
  last_name: Rzadkowski
  orcid: 0000-0002-1106-4419
citation:
  ama: Rzadkowski W. Analytic and machine learning approaches to composite quantum
    impurities. 2022. doi:<a href="https://doi.org/10.15479/at:ista:10759">10.15479/at:ista:10759</a>
  apa: Rzadkowski, W. (2022). <i>Analytic and machine learning approaches to composite
    quantum impurities</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:10759">https://doi.org/10.15479/at:ista:10759</a>
  chicago: Rzadkowski, Wojciech. “Analytic and Machine Learning Approaches to Composite
    Quantum Impurities.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:10759">https://doi.org/10.15479/at:ista:10759</a>.
  ieee: W. Rzadkowski, “Analytic and machine learning approaches to composite quantum
    impurities,” Institute of Science and Technology Austria, 2022.
  ista: Rzadkowski W. 2022. Analytic and machine learning approaches to composite
    quantum impurities. Institute of Science and Technology Austria.
  mla: Rzadkowski, Wojciech. <i>Analytic and Machine Learning Approaches to Composite
    Quantum Impurities</i>. Institute of Science and Technology Austria, 2022, doi:<a
    href="https://doi.org/10.15479/at:ista:10759">10.15479/at:ista:10759</a>.
  short: W. Rzadkowski, Analytic and Machine Learning Approaches to Composite Quantum
    Impurities, Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-02-16T13:27:37Z
date_published: 2022-02-21T00:00:00Z
date_updated: 2026-04-07T14:20:12Z
day: '21'
ddc:
- '530'
degree_awarded: PhD
department:
- _id: GradSch
- _id: MiLe
doi: 10.15479/at:ista:10759
ec_funded: 1
file:
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has_accepted_license: '1'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
page: '120'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
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    relation: part_of_dissertation
    status: public
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    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Mikhail
  full_name: Lemeshko, Mikhail
  id: 37CB05FA-F248-11E8-B48F-1D18A9856A87
  last_name: Lemeshko
  orcid: 0000-0002-6990-7802
title: Analytic and machine learning approaches to composite quantum impurities
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '12390'
abstract:
- lang: eng
  text: "The scope of this thesis is to study quantum systems exhibiting a continuous
    symmetry that\r\nis broken on the level of the corresponding effective theory.
    In particular we are going to\r\ninvestigate translation-invariant Bose gases
    in the mean field limit, effectively described by\r\nthe Hartree functional, and
    the Fröhlich Polaron in the regime of strong coupling, effectively\r\ndescribed
    by the Pekar functional. The latter is a model describing the interaction between
    a\r\ncharged particle and the optical modes of a polar crystal. Regarding the
    former, we assume in\r\naddition that the particles in the gas are unconfined,
    and typically we will consider particles\r\nthat are subject to an attractive
    interaction. In both cases the ground state energy of the\r\nHamiltonian is not
    a proper eigenvalue due to the underlying translation-invariance, while on\r\nthe
    contrary there exists a whole invariant orbit of minimizers for the corresponding
    effective\r\nfunctionals. Both, the absence of proper eigenstates and the broken
    symmetry of the effective\r\ntheory, make the study significantly more involved
    and it is the content of this thesis to\r\ndevelop a frameworks which allows for
    a systematic way to circumvent these issues.\r\nIt is a well-established result
    that the ground state energy of Bose gases in the mean field limit,\r\nas well
    as the ground state energy of the Fröhlich Polaron in the regime of strong coupling,
    is\r\nto leading order given by the minimal energy of the corresponding effective
    theory. As part\r\nof this thesis we identify the sub-leading term in the expansion
    of the ground state energy,\r\nwhich can be interpreted as the quantum correction
    to the classical energy, since the effective\r\ntheories under consideration can
    be seen as classical counterparts.\r\nWe are further going to establish an asymptotic
    expression for the energy-momentum relation\r\nof the Fröhlich Polaron in the
    strong coupling limit. In the regime of suitably small momenta,\r\nthis asymptotic
    expression agrees with the energy-momentum relation of a free particle having\r\nan
    effectively increased mass, and we find that this effectively increased mass agrees
    with the\r\nconjectured value in the physics literature.\r\nIn addition we will
    discuss two unrelated papers written by the author during his stay at ISTA\r\nin
    the appendix. The first one concerns the realization of anyons, which are quasi-particles\r\nacquiring
    a non-trivial phase under the exchange of two particles, as molecular impurities.\r\nThe
    second one provides a classification of those vector fields defined on a given
    manifold\r\nthat can be written as the gradient of a given functional with respect
    to a suitable metric,\r\nprovided that some mild smoothness assumptions hold.
    This classification is subsequently\r\nused to identify those quantum Markov semigroups
    that can be written as a gradient flow of\r\nthe relative entropy.\r\n"
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Morris
  full_name: Brooks, Morris
  id: B7ECF9FC-AA38-11E9-AC9A-0930E6697425
  last_name: Brooks
  orcid: 0000-0002-6249-0928
citation:
  ama: Brooks M. Translation-invariant quantum systems with effectively broken symmetry.
    2022. doi:<a href="https://doi.org/10.15479/at:ista:12390">10.15479/at:ista:12390</a>
  apa: Brooks, M. (2022). <i>Translation-invariant quantum systems with effectively
    broken symmetry</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:12390">https://doi.org/10.15479/at:ista:12390</a>
  chicago: Brooks, Morris. “Translation-Invariant Quantum Systems with Effectively
    Broken Symmetry.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:12390">https://doi.org/10.15479/at:ista:12390</a>.
  ieee: M. Brooks, “Translation-invariant quantum systems with effectively broken
    symmetry,” Institute of Science and Technology Austria, 2022.
  ista: Brooks M. 2022. Translation-invariant quantum systems with effectively broken
    symmetry. Institute of Science and Technology Austria.
  mla: Brooks, Morris. <i>Translation-Invariant Quantum Systems with Effectively Broken
    Symmetry</i>. Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:12390">10.15479/at:ista:12390</a>.
  short: M. Brooks, Translation-Invariant Quantum Systems with Effectively Broken
    Symmetry, Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2023-01-26T10:00:42Z
date_published: 2022-12-15T00:00:00Z
date_updated: 2026-04-16T08:20:52Z
day: '15'
ddc:
- '500'
degree_awarded: PhD
department:
- _id: GradSch
- _id: RoSe
doi: 10.15479/at:ista:12390
ec_funded: 1
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has_accepted_license: '1'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-sa/4.0/
month: '12'
oa: 1
oa_version: Published Version
page: '196'
project:
- _id: 25C6DC12-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '694227'
  name: Analysis of quantum many-body systems
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '9005'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
title: Translation-invariant quantum systems with effectively broken symmetry
tmp:
  image: /images/cc_by_nc_sa.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-sa/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC
    BY-NC-SA 4.0)
  short: CC BY-NC-SA (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '12358'
abstract:
- lang: eng
  text: "The complex yarn structure of knitted and woven fabrics gives rise to both
    a mechanical and\r\nvisual complexity. The small-scale interactions of yarns colliding
    with and pulling on each\r\nother result in drastically different large-scale
    stretching and bending behavior, introducing\r\nanisotropy, curling, and more.
    While simulating cloth as individual yarns can reproduce this\r\ncomplexity and
    match the quality of real fabric, it may be too computationally expensive for\r\nlarge
    fabrics. On the other hand, continuum-based approaches do not need to discretize
    the\r\ncloth at a stitch-level, but it is non-trivial to find a material model
    that would replicate the\r\nlarge-scale behavior of yarn fabrics, and they discard
    the intricate visual detail. In this thesis,\r\nwe discuss three methods to try
    and bridge the gap between small-scale and large-scale yarn\r\nmechanics using
    numerical homogenization: fitting a continuum model to periodic yarn simulations,
    adding mechanics-aware yarn detail onto thin-shell simulations, and quantitatively\r\nfitting
    yarn parameters to physical measurements of real fabric.\r\nTo start, we present
    a method for animating yarn-level cloth effects using a thin-shell solver.\r\nWe
    first use a large number of periodic yarn-level simulations to build a model of
    the potential\r\nenergy density of the cloth, and then use it to compute forces
    in a thin-shell simulator. The\r\nresulting simulations faithfully reproduce expected
    effects like the stiffening of woven fabrics\r\nand the highly deformable nature
    and anisotropy of knitted fabrics at a fraction of the cost of\r\nfull yarn-level
    simulation.\r\nWhile our thin-shell simulations are able to capture large-scale
    yarn mechanics, they lack\r\nthe rich visual detail of yarn-level simulations.
    Therefore, we propose a method to animate\r\nyarn-level cloth geometry on top
    of an underlying deforming mesh in a mechanics-aware\r\nfashion in real time.
    Using triangle strains to interpolate precomputed yarn geometry, we are\r\nable
    to reproduce effects such as knit loops tightening under stretching at negligible
    cost.\r\nFinally, we introduce a methodology for inverse-modeling of yarn-level
    mechanics of cloth,\r\nbased on the mechanical response of fabrics in the real
    world. We compile a database from\r\nphysical tests of several knitted fabrics
    used in the textile industry spanning diverse physical\r\nproperties like stiffness,
    nonlinearity, and anisotropy. We then develop a system for approximating these
    mechanical responses with yarn-level cloth simulation, using homogenized\r\nshell
    models to speed up computation and adding some small-but-necessary extensions
    to\r\nyarn-level models used in computer graphics.\r\n"
acknowledged_ssus:
- _id: SSU
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Georg
  full_name: Sperl, Georg
  id: 4DD40360-F248-11E8-B48F-1D18A9856A87
  last_name: Sperl
citation:
  ama: 'Sperl G. Homogenizing yarn simulations: Large-scale mechanics, small-scale
    detail, and quantitative fitting. 2022. doi:<a href="https://doi.org/10.15479/at:ista:12103">10.15479/at:ista:12103</a>'
  apa: 'Sperl, G. (2022). <i>Homogenizing yarn simulations: Large-scale mechanics,
    small-scale detail, and quantitative fitting</i>. Institute of Science and Technology
    Austria. <a href="https://doi.org/10.15479/at:ista:12103">https://doi.org/10.15479/at:ista:12103</a>'
  chicago: 'Sperl, Georg. “Homogenizing Yarn Simulations: Large-Scale Mechanics, Small-Scale
    Detail, and Quantitative Fitting.” Institute of Science and Technology Austria,
    2022. <a href="https://doi.org/10.15479/at:ista:12103">https://doi.org/10.15479/at:ista:12103</a>.'
  ieee: 'G. Sperl, “Homogenizing yarn simulations: Large-scale mechanics, small-scale
    detail, and quantitative fitting,” Institute of Science and Technology Austria,
    2022.'
  ista: 'Sperl G. 2022. Homogenizing yarn simulations: Large-scale mechanics, small-scale
    detail, and quantitative fitting. Institute of Science and Technology Austria.'
  mla: 'Sperl, Georg. <i>Homogenizing Yarn Simulations: Large-Scale Mechanics, Small-Scale
    Detail, and Quantitative Fitting</i>. Institute of Science and Technology Austria,
    2022, doi:<a href="https://doi.org/10.15479/at:ista:12103">10.15479/at:ista:12103</a>.'
  short: 'G. Sperl, Homogenizing Yarn Simulations: Large-Scale Mechanics, Small-Scale
    Detail, and Quantitative Fitting, Institute of Science and Technology Austria,
    2022.'
corr_author: '1'
date_created: 2023-01-24T10:49:46Z
date_published: 2022-09-22T00:00:00Z
date_updated: 2026-04-16T08:31:54Z
day: '22'
ddc:
- '000'
- '620'
degree_awarded: PhD
department:
- _id: GradSch
- _id: ChWo
doi: 10.15479/at:ista:12103
ec_funded: 1
file:
- access_level: open_access
  checksum: 083722acbb8115e52e3b0fdec6226769
  content_type: application/pdf
  creator: cchlebak
  date_created: 2023-01-25T12:04:41Z
  date_updated: 2023-02-02T09:29:57Z
  description: 'This is the main PDF file of the thesis. File size: 105 MB'
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  file_size: 104497530
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  creator: cchlebak
  date_created: 2023-02-02T09:33:37Z
  date_updated: 2023-02-02T09:33:37Z
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  date_updated: 2023-02-02T09:39:25Z
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file_date_updated: 2023-02-02T09:39:25Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '138'
project:
- _id: 2533E772-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '638176'
  name: 'Big Splash: Efficient Simulation of Natural Phenomena at Extremely Large
    Scales'
publication_identifier:
  isbn:
  - 978-3-99078-020-6
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '11736'
    relation: part_of_dissertation
    status: public
  - id: '9818'
    relation: part_of_dissertation
    status: public
  - id: '8385'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Christopher J
  full_name: Wojtan, Christopher J
  id: 3C61F1D2-F248-11E8-B48F-1D18A9856A87
  last_name: Wojtan
  orcid: 0000-0001-6646-5546
title: 'Homogenizing yarn simulations: Large-scale mechanics, small-scale detail,
  and quantitative fitting'
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '11196'
abstract:
- lang: eng
  text: "One of the fundamental questions in Neuroscience is how the structure of
    synapses and their physiological properties are related. While synaptic transmission
    remains a dynamic process, electron microscopy provides images with comparably
    low temporal resolution (Studer et al., 2014). The current work overcomes this
    challenge and describes an improved “Flash and Freeze” technique (Watanabe et
    al., 2013a; Watanabe et al., 2013b) to study synaptic transmission at the hippocampal
    mossy fiber-CA3 pyramidal neuron synapses, using mouse acute brain slices and
    organotypic slices culture. The improved method allowed for selective stimulation
    of presynaptic mossy fiber boutons and the observation of synaptic vesicle pool
    dynamics at the active zones. Our results uncovered several intriguing morphological
    features of mossy fiber boutons. First, the docked vesicle pool was largely depleted
    (more than 70%) after stimulation, implying that the docked synaptic vesicles
    pool and readily releasable pool are vastly overlapping in mossy fiber boutons.
    Second, the synaptic vesicles are skewed towards larger diameters, displaying
    a wide range of sizes. An increase in the mean diameter of synaptic vesicles,
    after single and repetitive stimulation, suggests that smaller vesicles have a
    higher release probability. Third, we observed putative endocytotic structures
    after moderate light stimulation, matching the timing of previously described
    ultrafast endocytosis (Watanabe et al., 2013a; Delvendahl et al., 2016). \r\n\tIn
    addition, synaptic transmission depends on a sophisticated system of protein machinery
    and calcium channels (Südhof, 2013b), which amplifies the challenge in studying
    synaptic communication as these interactions can be potentially modified during
    synaptic plasticity. And although recent study elucidated the potential correlation
    between physiological and morphological properties of synapses during synaptic
    plasticity (Vandael et al., 2020), the molecular underpinning of it remains unknown.
    Thus, the presented work tries to overcome this challenge and aims to pinpoint
    changes in the molecular architecture at hippocampal mossy fiber bouton synapses
    during short- and long-term potentiation (STP and LTP), we combined chemical potentiation,
    with the application of a cyclic adenosine monophosphate agonist (i.e. forskolin)
    and freeze-fracture replica immunolabelling. This method allowed the localization
    of membrane-bound proteins with nanometer precision within the active zone, in
    particular, P/Q-type calcium channels and synaptic vesicle priming proteins Munc13-1/2.
    First, we found that the number of clusters of Munc13-1 in the mossy fiber bouton
    active zone increased significantly during STP, but decreased to lower than the
    control value during LTP. Secondly, although the distance between the calcium
    channels and Munc13-1s did not change after induction of STP, it shortened during
    the LTP phase. Additionally, forskolin did not affect Munc13-2 distribution during
    STP and LTP. These results indicate the existence of two distinct mechanisms that
    govern STP and LTP at mossy fiber bouton synapses: an increase in the readily
    realizable pool in the case of STP and a potential increase in release probability
    during LTP. “Flash and freeze” and functional electron microscopy, are versatile
    methods that can be successfully applied to intact brain circuits to study synaptic
    transmission even at the molecular level.\r\n"
acknowledged_ssus:
- _id: EM-Fac
- _id: PreCl
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Olena
  full_name: Kim, Olena
  id: 3F8ABDDA-F248-11E8-B48F-1D18A9856A87
  last_name: Kim
  orcid: 0000-0003-2344-1039
citation:
  ama: Kim O. Nanoarchitecture of hippocampal mossy fiber-CA3 pyramidal neuron synapses.
    2022. doi:<a href="https://doi.org/10.15479/at:ista:11196">10.15479/at:ista:11196</a>
  apa: Kim, O. (2022). <i>Nanoarchitecture of hippocampal mossy fiber-CA3 pyramidal
    neuron synapses</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:11196">https://doi.org/10.15479/at:ista:11196</a>
  chicago: Kim, Olena. “Nanoarchitecture of Hippocampal Mossy Fiber-CA3 Pyramidal
    Neuron Synapses.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11196">https://doi.org/10.15479/at:ista:11196</a>.
  ieee: O. Kim, “Nanoarchitecture of hippocampal mossy fiber-CA3 pyramidal neuron
    synapses,” Institute of Science and Technology Austria, 2022.
  ista: Kim O. 2022. Nanoarchitecture of hippocampal mossy fiber-CA3 pyramidal neuron
    synapses. Institute of Science and Technology Austria.
  mla: Kim, Olena. <i>Nanoarchitecture of Hippocampal Mossy Fiber-CA3 Pyramidal Neuron
    Synapses</i>. Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11196">10.15479/at:ista:11196</a>.
  short: O. Kim, Nanoarchitecture of Hippocampal Mossy Fiber-CA3 Pyramidal Neuron
    Synapses, Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-04-20T09:47:12Z
date_published: 2022-04-20T00:00:00Z
date_updated: 2026-04-07T14:22:20Z
day: '20'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: PeJo
- _id: GradSch
doi: 10.15479/at:ista:11196
ec_funded: 1
file:
- access_level: open_access
  checksum: 1616a8bf6f13a57c892dac873dcd0936
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  creator: okim
  date_created: 2022-04-20T14:21:56Z
  date_updated: 2023-04-20T22:30:03Z
  embargo: 2023-04-19
  file_id: '11220'
  file_name: Olena_KIM_thesis_final.pdf
  file_size: 21273537
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  creator: okim
  date_created: 2022-04-20T14:22:56Z
  date_updated: 2023-04-20T22:30:03Z
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  file_id: '11221'
  file_name: KIM_thesis_final.zip
  file_size: 59248569
  relation: source_file
file_date_updated: 2023-04-20T22:30:03Z
has_accepted_license: '1'
language:
- iso: eng
license: https://creativecommons.org/licenses/by-nc-nd/4.0/
month: '04'
oa: 1
oa_version: Published Version
page: '132'
project:
- _id: 25BAF7B2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '708497'
  name: Presynaptic calcium channels distribution and impact on coupling at the hippocampal
    mossy fiber synapse
- _id: 25B7EB9E-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '692692'
  name: Biophysics and circuit function of a giant cortical glutamatergic synapse
- _id: 25C3DBB6-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W01205
  name: Zellkommunikation in Gesundheit und Krankheit
- _id: 25C5A090-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z00312
  name: Synaptic communication in neuronal microcircuits
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '7473'
    relation: part_of_dissertation
    status: public
  - id: '11222'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
title: Nanoarchitecture of hippocampal mossy fiber-CA3 pyramidal neuron synapses
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '10727'
abstract:
- lang: eng
  text: "Social insects are a common model to study disease dynamics in social animals.
    Even though pathogens should thrive in social insect colonies as the hosts engage
    in frequent social interactions, are closely related and live in a pathogen-rich
    environment, disease outbreaks are rare. This is because social insects have evolved
    mechanisms to keep pathogens at bay – and fight disease as a collective. Social
    insect colonies are often viewed as “superorganisms” with division of labor between
    reproductive “germ-like” queens and males and “somatic” workers, which together
    form an interdependent reproductive unit that parallels a multicellular body.
    Superorganisms possess a “social immune system” that comprises of collective disease
    defenses performed by the workers - summarized as “social immunity”. In social
    groups immunization (reduced susceptibility to a parasite upon secondary exposure
    to the same parasite) can e.g. be triggered by social interactions (“social immunization”).
    Social immunization can be caused by (i) asymptomatic low-level infections that
    are acquired during caregiving to a contagious individual that can give an immune
    boost, which can induce protection upon later encounter with the same pathogen
    (active immunization) or (ii) by transfer of immune effectors between individuals
    (passive immunization).\r\nIn the second chapter, I built up on a study that I
    co-authored that found that low-level infections can not only be protective, but
    also be costly and make the host more susceptible to detrimental superinfections
    after contact to a very dissimilar pathogen. I here now tested different degrees
    of phylogenetically-distant fungal strains of M. brunneum and M. robertsii in
    L. neglectus and can describe the occurrence of cross-protection of social immunization
    if the first and second pathogen are from the same level. Interestingly, low-level
    infections only provided protection when the first strain was less virulent than
    the second strain and elicited higher immune gene expression.\r\nIn the third
    and fourth chapters, I expanded on the role of social immunity in sexual selection,
    a so far unstudied field. I used the fungus Metarhizium robertsii and the ant
    Cardiocondyla obscurior as a model, as in this species mating occurs in the presence
    of workers and can be studied under laboratory conditions. Before males mate with
    virgin queens in the nest they engage in fierce combat over the access to their
    mating partners.\r\nFirst, I focused on male-male competition in the third chapter
    and found that fighting with a contagious male is costly as it can lead to contamination
    of the rival, but that workers can decrease the risk of disease contraction by
    performing sanitary care.\r\nIn the fourth chapter, I studied the effect of fungal
    infection on survival and mating success of sexuals (freshly emerged queens and
    males) and found that worker-performed sanitary care can buffer the negative effect
    that a pathogenic contagion would have on sexuals by spore removal from the exposed
    individuals. When social immunity was prevented and queens could contract spores
    from their mating partner, very low dosages led to negative consequences: their
    lifespan was reduced and they produced fewer offspring with poor immunocompetence
    compared to healthy queens. Interestingly, cohabitation with a late-stage infected
    male where no spore transfer was possible had a positive effect on offspring immunity
    – male offspring of mothers that apparently perceived an infected partner in their
    vicinity reacted more sensitively to fungal challenge than male offspring without
    paternal pathogen history."
acknowledged_ssus:
- _id: LifeSc
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Sina
  full_name: Metzler, Sina
  id: 48204546-F248-11E8-B48F-1D18A9856A87
  last_name: Metzler
  orcid: 0000-0002-9547-2494
citation:
  ama: Metzler S. Pathogen-mediated sexual selection and immunization in ant colonies.
    2022. doi:<a href="https://doi.org/10.15479/AT:ISTA:10727">10.15479/AT:ISTA:10727</a>
  apa: Metzler, S. (2022). <i>Pathogen-mediated sexual selection and immunization
    in ant colonies</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:10727">https://doi.org/10.15479/AT:ISTA:10727</a>
  chicago: Metzler, Sina. “Pathogen-Mediated Sexual Selection and Immunization in
    Ant Colonies.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/AT:ISTA:10727">https://doi.org/10.15479/AT:ISTA:10727</a>.
  ieee: S. Metzler, “Pathogen-mediated sexual selection and immunization in ant colonies,”
    Institute of Science and Technology Austria, 2022.
  ista: Metzler S. 2022. Pathogen-mediated sexual selection and immunization in ant
    colonies. Institute of Science and Technology Austria.
  mla: Metzler, Sina. <i>Pathogen-Mediated Sexual Selection and Immunization in Ant
    Colonies</i>. Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/AT:ISTA:10727">10.15479/AT:ISTA:10727</a>.
  short: S. Metzler, Pathogen-Mediated Sexual Selection and Immunization in Ant Colonies,
    Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-02-04T15:45:12Z
date_published: 2022-02-07T00:00:00Z
date_updated: 2026-04-07T14:30:18Z
day: '07'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: SyCr
doi: 10.15479/AT:ISTA:10727
ec_funded: 1
file:
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  creator: smetzler
  date_created: 2022-02-04T15:36:12Z
  date_updated: 2023-02-03T23:30:03Z
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  file_size: 6757886
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  creator: smetzler
  date_created: 2022-02-04T15:36:43Z
  date_updated: 2023-02-03T23:30:03Z
  embargo: 2023-02-02
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file_date_updated: 2023-02-04T23:30:03Z
has_accepted_license: '1'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
project:
- _id: 2649B4DE-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '771402'
  name: Epidemics in ant societies on a chip
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Sylvia
  full_name: Cremer, Sylvia
  id: 2F64EC8C-F248-11E8-B48F-1D18A9856A87
  last_name: Cremer
  orcid: 0000-0002-2193-3868
title: Pathogen-mediated sexual selection and immunization in ant colonies
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '11879'
abstract:
- lang: eng
  text: "As the overall global mean surface temperature is increasing due to climate
    change, plant\r\nadaptation to those stressful conditions is of utmost importance
    for their survival. Plants are\r\nsessile organisms, thus to compensate for their
    lack of mobility, they evolved a variety of\r\nmechanisms enabling them to flexibly
    adjust their physiological, growth and developmental\r\nprocesses to fluctuating
    temperatures and to survive in harsh environments. While these unique\r\nadaptation
    abilities provide an important evolutionary advantage, overall modulation of plant\r\ngrowth
    and developmental program due to non-optimal temperature negatively affects biomass\r\nproduction,
    crop productivity or sensitivity to pathogens. Thus, understanding molecular\r\nprocesses
    underlying plant adaptation to increased temperature can provide important\r\nresources
    for breeding strategies to ensure sufficient agricultural food production.\r\nAn
    increase in ambient temperature by a few degrees leads to profound changes in
    organ growth\r\nincluding enhanced hypocotyl elongation, expansion of petioles,
    hyponastic growth of leaves and\r\ncotyledons, collectively named thermomorphogenesis
    (Casal & Balasubramanian, 2019). Auxin,\r\none of the best-studied growth hormones,
    plays an essential role in this process by direct\r\nactivation of transcriptional
    and non-transcriptional processes resulting in elongation growth\r\n(Majda & Robert,
    2018).To modulate hypocotyl growth in response to high ambient temperature\r\n(hAT),
    auxin needs to be redistributed accordingly. PINs, auxin efflux transporters,
    are key\r\ncomponents of the polar auxin transport (PAT) machinery, which controls
    the amount and\r\ndirection of auxin translocated in the plant tissues and organs(Adamowski
    & Friml, 2015). Hence,\r\nPIN-mediated transport is tightly linked with thermo-morphogenesis,
    and interference with PAT\r\nthrough either chemical or genetic means dramatically
    affecting the adaptive responses to hAT.\r\nIntriguingly, despite the key role
    of PIN mediated transport in growth response to hAT, whether\r\nand how PINs at
    the level of expression adapt to fluctuation in temperature is scarcely\r\nunderstood.\r\nWith
    genetic, molecular and advanced bio-imaging approaches, we demonstrate the role
    of PIN\r\nauxin transporters in the regulation of hypocotyl growth in response
    to hAT. We show that via\r\nadjustment of PIN3, PIN4 and PIN7 expression in cotyledons
    and hypocotyls, auxin distribution is modulated thereby determining elongation
    pattern of epidermal cells at hAT. Furthermore, we\r\nidentified three Zinc-Finger
    (ZF) transcription factors as novel molecular components of the\r\nthermo-regulatory
    network, which through negative regulation of PIN transcription adjust the\r\ntransport
    of auxin at hAT. Our results suggest that the ZF-PIN module might be a part of
    the\r\nnegative feedback loop attenuating the activity of the thermo-sensing pathway
    to restrain\r\nexaggerated growth and developmental responses to hAT."
acknowledged_ssus:
- _id: Bio
- _id: LifeSc
- _id: SSU
acknowledgement: I would like to acknowledge ISTA and all the people from the Scientific
  Service Units and at ISTA, in particular Dorota Jaworska for excellent technical
  and scientific support as well as ÖAW for funding my research for over 3 years (DOC
  ÖAW Fellowship PR1022OEAW02).
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Christina
  full_name: Artner, Christina
  id: 45DF286A-F248-11E8-B48F-1D18A9856A87
  last_name: Artner
citation:
  ama: Artner C. Modulation of auxin transport via ZF proteins adjust plant response
    to high ambient temperature. 2022. doi:<a href="https://doi.org/10.15479/at:ista:11879">10.15479/at:ista:11879</a>
  apa: Artner, C. (2022). <i>Modulation of auxin transport via ZF proteins adjust
    plant response to high ambient temperature</i>. Institute of Science and Technology
    Austria. <a href="https://doi.org/10.15479/at:ista:11879">https://doi.org/10.15479/at:ista:11879</a>
  chicago: Artner, Christina. “Modulation of Auxin Transport via ZF Proteins Adjust
    Plant Response to High Ambient Temperature.” Institute of Science and Technology
    Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11879">https://doi.org/10.15479/at:ista:11879</a>.
  ieee: C. Artner, “Modulation of auxin transport via ZF proteins adjust plant response
    to high ambient temperature,” Institute of Science and Technology Austria, 2022.
  ista: Artner C. 2022. Modulation of auxin transport via ZF proteins adjust plant
    response to high ambient temperature. Institute of Science and Technology Austria.
  mla: Artner, Christina. <i>Modulation of Auxin Transport via ZF Proteins Adjust
    Plant Response to High Ambient Temperature</i>. Institute of Science and Technology
    Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11879">10.15479/at:ista:11879</a>.
  short: C. Artner, Modulation of Auxin Transport via ZF Proteins Adjust Plant Response
    to High Ambient Temperature, Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-08-17T07:58:53Z
date_published: 2022-08-17T00:00:00Z
date_updated: 2026-04-07T14:30:39Z
day: '17'
ddc:
- '580'
degree_awarded: PhD
department:
- _id: GradSch
- _id: EvBe
doi: 10.15479/at:ista:11879
file:
- access_level: open_access
  checksum: a2c2fdc28002538840490bfa6a08b2cb
  content_type: application/pdf
  creator: cartner
  date_created: 2022-08-17T12:08:49Z
  date_updated: 2023-09-09T22:30:03Z
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  content_type: application/octet-stream
  creator: cartner
  date_created: 2022-08-17T12:08:59Z
  date_updated: 2023-09-09T22:30:03Z
  embargo_to: open_access
  file_id: '11908'
  file_name: ChristinaArtner_PhD_Thesis_2022.7z
  file_size: 19097730
  relation: source_file
file_date_updated: 2023-09-09T22:30:03Z
has_accepted_license: '1'
keyword:
- high ambient temperature
- auxin
- PINs
- Zinc-Finger proteins
- thermomorphogenesis
- stress
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: '128'
project:
- _id: 2685A872-B435-11E9-9278-68D0E5697425
  name: Hormonal regulation of plant adaptive responses to environmental signals
publication_identifier:
  isbn:
  - 978-3-99078-022-0
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Eva
  full_name: Benková, Eva
  id: 38F4F166-F248-11E8-B48F-1D18A9856A87
  last_name: Benková
  orcid: 0000-0002-8510-9739
title: Modulation of auxin transport via ZF proteins adjust plant response to high
  ambient temperature
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '12364'
abstract:
- lang: eng
  text: "Autism spectrum disorders (ASDs) are a group of neurodevelopmental disorders
    character\x02ized by behavioral symptoms such as problems in social communication
    and interaction, as\r\nwell as repetitive, restricted behaviors and interests.
    These disorders show a high degree\r\nof heritability and hundreds of risk genes
    have been identifed using high throughput\r\nsequencing technologies. This genetic
    heterogeneity has hampered eforts in understanding\r\nthe pathogenesis of ASD
    but at the same time given rise to the concept of convergent\r\nmechanisms. Previous
    studies have identifed that risk genes for ASD broadly converge\r\nonto specifc
    functional categories with transcriptional regulation being one of the biggest\r\ngroups.
    In this thesis, I focus on this subgroup of genes and investigate the gene regulatory\r\nconsequences
    of some of them in the context of neurodevelopment.\r\nFirst, we showed that mutations
    in the ASD and intellectual disability risk gene Setd5 lead\r\nto perturbations
    of gene regulatory programs in early cell fate specifcation. In addition,\r\nadult
    animals display abnormal learning behavior which is mirrored at the transcriptional\r\nlevel
    by altered activity dependent regulation of postsynaptic gene expression. Lastly,\r\nwe
    link the regulatory function of Setd5 to its interaction with the Paf1 and the
    NCoR\r\ncomplex.\r\nSecond, by modeling the heterozygous loss of the top ASD gene
    CHD8 in human cerebral\r\norganoids we demonstrate profound changes in the developmental
    trajectories of both\r\ninhibitory and excitatory neurons using single cell RNA-sequencing.
    While the former\r\nwere generated earlier in CHD8+/- organoids, the generation
    of the latter was shifted to\r\nlater times in favor of a prolonged progenitor
    expansion phase and ultimately increased\r\norganoid size.\r\nFinally, by modeling
    heterozygous mutations for four ASD associated chromatin modifers,\r\nASH1L, KDM6B,
    KMT5B, and SETD5 in human cortical spheroids we show evidence of\r\nregulatory
    convergence across three of those genes. We observe a shift from dorsal cortical\r\nexcitatory
    neuron fates towards partially ventralized cell types resembling cells from the\r\nlateral
    ganglionic eminence. As this project is still ongoing at the time of writing,
    future\r\nexperiments will aim at elucidating the regulatory mechanisms underlying
    this shift with\r\nthe aim of linking these three ASD risk genes through biological
    convergence."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Christoph
  full_name: Dotter, Christoph
  id: 4C66542E-F248-11E8-B48F-1D18A9856A87
  last_name: Dotter
  orcid: 0000-0002-9033-9096
citation:
  ama: Dotter C. Transcriptional consequences of mutations in genes associated with
    Autism Spectrum Disorder. 2022. doi:<a href="https://doi.org/10.15479/at:ista:12094">10.15479/at:ista:12094</a>
  apa: Dotter, C. (2022). <i>Transcriptional consequences of mutations in genes associated
    with Autism Spectrum Disorder</i>. Institute of Science and Technology Austria.
    <a href="https://doi.org/10.15479/at:ista:12094">https://doi.org/10.15479/at:ista:12094</a>
  chicago: Dotter, Christoph. “Transcriptional Consequences of Mutations in Genes
    Associated with Autism Spectrum Disorder.” Institute of Science and Technology
    Austria, 2022. <a href="https://doi.org/10.15479/at:ista:12094">https://doi.org/10.15479/at:ista:12094</a>.
  ieee: C. Dotter, “Transcriptional consequences of mutations in genes associated
    with Autism Spectrum Disorder,” Institute of Science and Technology Austria, 2022.
  ista: Dotter C. 2022. Transcriptional consequences of mutations in genes associated
    with Autism Spectrum Disorder. Institute of Science and Technology Austria.
  mla: Dotter, Christoph. <i>Transcriptional Consequences of Mutations in Genes Associated
    with Autism Spectrum Disorder</i>. Institute of Science and Technology Austria,
    2022, doi:<a href="https://doi.org/10.15479/at:ista:12094">10.15479/at:ista:12094</a>.
  short: C. Dotter, Transcriptional Consequences of Mutations in Genes Associated
    with Autism Spectrum Disorder, Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2023-01-24T13:09:57Z
date_published: 2022-09-19T00:00:00Z
date_updated: 2026-04-07T14:30:57Z
day: '19'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: GaNo
doi: 10.15479/at:ista:12094
ec_funded: 1
file:
- access_level: open_access
  checksum: 896f4cac9adb6d3f26a6605772f4e1a3
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  creator: cchlebak
  date_created: 2023-01-24T13:15:45Z
  date_updated: 2023-09-20T22:30:03Z
  embargo: 2023-09-19
  file_id: '12365'
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  file_size: 20457465
  relation: main_file
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  creator: cchlebak
  date_created: 2023-02-02T09:15:35Z
  date_updated: 2023-09-20T22:30:03Z
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  file_id: '12482'
  file_name: latex_source_CDotter_Thesis_2022.zip
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  relation: source_file
file_date_updated: 2023-09-20T22:30:03Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '152'
project:
- _id: 254BA948-B435-11E9-9278-68D0E5697425
  grant_number: '401299'
  name: Probing development and reversibility of autism spectrum disorders
- _id: 9B91375C-BA93-11EA-9121-9846C619BF3A
  grant_number: '707964'
  name: Critical windows and reversibility of ASD associated with mutations in chromatin
    remodelers
- _id: 25444568-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '715508'
  name: Probing the Reversibility of Autism Spectrum Disorders by Employing in vivo
    and in vitro Models
- _id: 2690FEAC-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: I04205
  name: Identification of converging Molecular Pathways Across Chromatinopathies as
    Targets for Therapy
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '11160'
    relation: part_of_dissertation
    status: public
  - id: '3'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Gaia
  full_name: Novarino, Gaia
  id: 3E57A680-F248-11E8-B48F-1D18A9856A87
  last_name: Novarino
  orcid: 0000-0002-7673-7178
title: Transcriptional consequences of mutations in genes associated with Autism Spectrum
  Disorder
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '11393'
abstract:
- lang: eng
  text: "AMPA receptors (AMPARs) mediate fast excitatory neurotransmission and their
    role is\r\nimplicated in complex processes such as learning and memory and various
    neurological\r\ndiseases. These receptors are composed of different subunits and
    the subunit composition can\r\naffect channel properties, receptor trafficking
    and interaction with other associated proteins.\r\nUsing the high sensitivity
    SDS-digested freeze-fracture replica labeling (SDS-FRL) for\r\nelectron microscopy
    I investigated the number, density, and localization of AMPAR subunits,\r\nGluA1,
    GluA2, GluA3, and GluA1-3 (panAMPA) in pyramidal cells in the CA1 area of mouse\r\nhippocampus.
    I have found that the immunogold labeling for all of these subunits in the\r\npostsynaptic
    sites was highest in stratum radiatum and lowest in stratum lacunosummoleculare.
    The labeling density for the all subunits in the extrasynaptic sites showed a
    gradual\r\nincrease from the pyramidal cell soma towards the distal part of stratum
    radiatum. The densities\r\nof extrasynaptic GluA1, GluA2 and panAMPA labeling
    reached 10-15% of synaptic densities,\r\nwhile the ratio of extrasynaptic labeling
    for GluA3 was significantly lower compared than those\r\nfor other subunits. The
    labeling patterns for GluA1, GluA2 and GluA1-3 are similar and their\r\ndensities
    were higher in the periphery than center of synapses. In contrast, the GluA3-\r\ncontaining
    receptors were more centrally localized compared to the GluA1- and GluA2-\r\ncontaining
    receptors.\r\nThe hippocampus plays a central role in learning and memory. Contextual
    learning has been\r\nshown to require the delivery of AMPA receptors to CA1 synapses
    in the dorsal hippocampus.\r\nHowever, proximodistal heterogeneity of this plasticity
    and particular contribution of different\r\nAMPA receptor subunits are not fully
    understood. By combining inhibitory avoidance task, a\r\nhippocampus-dependent
    contextual fear-learning paradigm, with SDS-FRL, I have revealed an\r\nincrease
    in synaptic density specific to GluA1-containing AMPA receptors in the CA1 area.\r\nThe
    intrasynaptic distribution of GluA1 also changed from the periphery to center-preferred\r\npattern.
    Furthermore, this synaptic plasticity was evident selectively in stratum radiatum
    but\r\nnot stratum oriens, and in the CA1 subregion proximal but not distal to
    CA2. These findings\r\nfurther contribute to our understanding of how specific
    hippocampal subregions and AMPA\r\nreceptor subunits are involved in physiological
    learning.\r\nAlthough the immunolabeling results above shed light on subunit-specific
    plasticity in\r\nAMPAR distribution, no tools to visualize and study the subunit
    composition at the single\r\nchannel level in situ have been available. Electron
    microscopy with conventional immunogold\r\nlabeling approaches has limitations
    in the single channel analysis because of the large size of\r\nantibodies and
    steric hindrance hampering multiple subunit labeling of single channels. I\r\nmanaged
    to develop a new chemical labeling system using a short peptide tag and small\r\nsynthetic
    probes, which form specific covalent bond with a cysteine residue in the tag fused
    to\r\nproteins of interest (reactive tag system). I additionally made substantial
    progress into adapting\r\nthis system for AMPA receptor subunits."
acknowledged_ssus:
- _id: EM-Fac
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Marijo
  full_name: Jevtic, Marijo
  id: 4BE3BC94-F248-11E8-B48F-1D18A9856A87
  last_name: Jevtic
citation:
  ama: Jevtic M. Contextual fear learning induced changes in AMPA receptor subtypes
    along the proximodistal axis in dorsal hippocampus. 2022. doi:<a href="https://doi.org/10.15479/at:ista:11393">10.15479/at:ista:11393</a>
  apa: Jevtic, M. (2022). <i>Contextual fear learning induced changes in AMPA receptor
    subtypes along the proximodistal axis in dorsal hippocampus</i>. Institute of
    Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:11393">https://doi.org/10.15479/at:ista:11393</a>
  chicago: Jevtic, Marijo. “Contextual Fear Learning Induced Changes in AMPA Receptor
    Subtypes along the Proximodistal Axis in Dorsal Hippocampus.” Institute of Science
    and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11393">https://doi.org/10.15479/at:ista:11393</a>.
  ieee: M. Jevtic, “Contextual fear learning induced changes in AMPA receptor subtypes
    along the proximodistal axis in dorsal hippocampus,” Institute of Science and
    Technology Austria, 2022.
  ista: Jevtic M. 2022. Contextual fear learning induced changes in AMPA receptor
    subtypes along the proximodistal axis in dorsal hippocampus. Institute of Science
    and Technology Austria.
  mla: Jevtic, Marijo. <i>Contextual Fear Learning Induced Changes in AMPA Receptor
    Subtypes along the Proximodistal Axis in Dorsal Hippocampus</i>. Institute of
    Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11393">10.15479/at:ista:11393</a>.
  short: M. Jevtic, Contextual Fear Learning Induced Changes in AMPA Receptor Subtypes
    along the Proximodistal Axis in Dorsal Hippocampus, Institute of Science and Technology
    Austria, 2022.
corr_author: '1'
date_created: 2022-05-17T08:57:41Z
date_published: 2022-05-16T00:00:00Z
date_updated: 2026-04-07T14:31:19Z
day: '16'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: RySh
doi: 10.15479/at:ista:11393
file:
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  creator: cchlebak
  date_created: 2022-05-17T09:08:06Z
  date_updated: 2023-05-17T22:30:03Z
  embargo_to: open_access
  file_id: '11395'
  file_name: MJ thesis.docx
  file_size: 56427603
  relation: source_file
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  checksum: c1dd20a1aece521b3500607b00e463d6
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  creator: cchlebak
  date_created: 2022-05-17T12:09:25Z
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file_date_updated: 2023-05-17T22:30:03Z
has_accepted_license: '1'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
page: '108'
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '7391'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
title: Contextual fear learning induced changes in AMPA receptor subtypes along the
  proximodistal axis in dorsal hippocampus
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '12366'
abstract:
- lang: eng
  text: "Recent substantial advances in the feld of superconducting circuits have
    shown its\r\npotential as a leading platform for future quantum computing. In
    contrast to classical\r\ncomputers based on bits that are represented by a single
    binary value, 0 or 1, quantum\r\nbits (or qubits) can be in a superposition of
    both. Thus, quantum computers can store\r\nand handle more information at the
    same time and a quantum advantage has already\r\nbeen demonstrated for two types
    of computational tasks. Rapid progress in academic\r\nand industry labs accelerates
    the development of superconducting processors which may\r\nsoon fnd applications
    in complex computations, chemical simulations, cryptography, and\r\noptimization.
    Now that these machines are scaled up to tackle such problems the questions\r\nof
    qubit interconnects and networks becomes very relevant. How to route signals on-chip\r\nbetween
    diferent processor components? What is the most efcient way to entangle\r\nqubits?
    And how to then send and process entangled signals between distant cryostats\r\nhosting
    superconducting processors?\r\nIn this thesis, we are looking for solutions to
    these problems by studying the collective\r\nbehavior of superconducting qubit
    ensembles. We frst demonstrate on-demand tunable\r\ndirectional scattering of
    microwave photons from a pair of qubits in a waveguide. Such a\r\ndevice can route
    microwave photons on-chip with a high diode efciency. Then we focus\r\non studying
    ultra-strong coupling regimes between light (microwave photons) and matter\r\n(superconducting
    qubits), a regime that could be promising for extremely fast multi-qubit\r\nentanglement
    generation. Finally, we show coherent pulse storage and periodic revivals\r\nin
    a fve qubit ensemble strongly coupled to a resonator. Such a reconfgurable storage\r\ndevice
    could be used as part of a quantum repeater that is needed for longer-distance\r\nquantum
    communication.\r\nThe achieved high degree of control over multi-qubit ensembles
    highlights not only the\r\nbeautiful physics of circuit quantum electrodynamics,
    it also represents the frst step\r\ntoward new quantum simulation and communication
    methods, and certain techniques\r\nmay also fnd applications in future superconducting
    quantum computing hardware.\r\n"
acknowledged_ssus:
- _id: NanoFab
- _id: M-Shop
- _id: EM-Fac
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Elena
  full_name: Redchenko, Elena
  id: 2C21D6E8-F248-11E8-B48F-1D18A9856A87
  last_name: Redchenko
citation:
  ama: Redchenko E. Controllable states of superconducting Qubit ensembles. 2022.
    doi:<a href="https://doi.org/10.15479/at:ista:12132">10.15479/at:ista:12132</a>
  apa: Redchenko, E. (2022). <i>Controllable states of superconducting Qubit ensembles</i>.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:12132">https://doi.org/10.15479/at:ista:12132</a>
  chicago: Redchenko, Elena. “Controllable States of Superconducting Qubit Ensembles.”
    Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:12132">https://doi.org/10.15479/at:ista:12132</a>.
  ieee: E. Redchenko, “Controllable states of superconducting Qubit ensembles,” Institute
    of Science and Technology Austria, 2022.
  ista: Redchenko E. 2022. Controllable states of superconducting Qubit ensembles.
    Institute of Science and Technology Austria.
  mla: Redchenko, Elena. <i>Controllable States of Superconducting Qubit Ensembles</i>.
    Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:12132">10.15479/at:ista:12132</a>.
  short: E. Redchenko, Controllable States of Superconducting Qubit Ensembles, Institute
    of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2023-01-25T09:17:02Z
date_published: 2022-09-26T00:00:00Z
date_updated: 2026-04-07T14:22:39Z
day: '26'
ddc:
- '530'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JoFi
doi: 10.15479/at:ista:12132
ec_funded: 1
file:
- access_level: open_access
  checksum: 39eabb1e006b41335f17f3b29af09648
  content_type: application/pdf
  creator: cchlebak
  date_created: 2023-01-25T09:41:49Z
  date_updated: 2023-01-26T23:30:44Z
  embargo: 2022-12-28
  file_id: '12367'
  file_name: Final_Thesis_ES_Redchenko.pdf
  file_size: 56076868
  relation: main_file
file_date_updated: 2023-01-26T23:30:44Z
has_accepted_license: '1'
language:
- iso: eng
month: '09'
oa: 1
oa_version: Published Version
page: '168'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
- _id: 26336814-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '758053'
  name: A Fiber Optic Transceiver for Superconducting Qubits
- _id: 237CBA6C-32DE-11EA-91FC-C7463DDC885E
  call_identifier: H2020
  grant_number: '862644'
  name: Quantum readout techniques and technologies
publication_identifier:
  isbn:
  - 978-3-99078-024-4
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: Johannes M
  full_name: Fink, Johannes M
  id: 4B591CBA-F248-11E8-B48F-1D18A9856A87
  last_name: Fink
  orcid: 0000-0001-8112-028X
title: Controllable states of superconducting Qubit ensembles
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '11932'
abstract:
- lang: eng
  text: "The ability to form and retrieve memories is central to survival. In mammals,
    the hippocampus\r\nis a brain region essential to the acquisition and consolidation
    of new memories. It is also\r\ninvolved in keeping track of one’s position in
    space and aids navigation. Although this\r\nspace-memory has been a source of
    contradiction, evidence supports the view that the role of\r\nthe hippocampus
    in navigation is memory, thanks to the formation of cognitive maps. First\r\nintroduced
    by Tolman in 1948, cognitive maps are generally used to organize experiences in\r\nmemory;
    however, the detailed mechanisms by which these maps are formed and stored are
    not\r\nyet agreed upon. Some influential theories describe this process as involving
    three fundamental\r\nsteps: initial encoding by the hippocampus, interactions
    between the hippocampus and other\r\ncortical areas, and long-term extra-hippocampal
    consolidation. In this thesis, I will show how\r\nthe investigation of cognitive
    maps of space helped to shed light on each of these three memory\r\nprocesses.\r\nThe
    first study included in this thesis deals with the initial encoding of spatial
    memories in\r\nthe hippocampus. Much is known about encoding at the level of single
    cells, but less about\r\ntheir co-activity or joint contribution to the encoding
    of novel spatial information. I will\r\ndescribe the structure of an interaction
    network that allows for efficient encoding of noisy\r\nspatial information during
    the first exploration of a novel environment.\r\nThe second study describes the
    interactions between the hippocampus and the prefrontal\r\ncortex (PFC), two areas
    directly and indirectly connected. It is known that the PFC, in concert\r\nwith
    the hippocampus, is involved in various processes, including memory storage and
    spatial\r\nnavigation. Nonetheless, the detailed mechanisms by which PFC receives
    information from the\r\nhippocampus are not clear. I will show how a transient
    improvement in theta phase locking of\r\nPFC cells enables interactions of cell
    pairs across the two regions.\r\nThe third study describes the learning of behaviorally-relevant
    spatial locations in the hippocampus and the medial entorhinal cortex. I will
    show how the accumulation of firing around\r\ngoal locations, a correlate of learning,
    can shed light on the transition from short- to long-term\r\nspatial memories
    and the speed of consolidation in different brain areas.\r\nThe studies included
    in this thesis represent the main scientific contributions of my Ph.D. They\r\ninvolve
    statistical analyses and models of neural responses of cells in different brain
    areas of\r\nrats executing spatial tasks. I will conclude the thesis by discussing
    the impact of the findings\r\non principles of memory formation and retention,
    including the mechanisms, the speed, and\r\nthe duration of these processes."
acknowledgement: I acknowledge the support from the European Union’s Horizon 2020
  research and innovation program under the Marie Skłodowska-Curie Grant Agreement
  No. 665385.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Michele
  full_name: Nardin, Michele
  id: 30BD0376-F248-11E8-B48F-1D18A9856A87
  last_name: Nardin
  orcid: 0000-0001-8849-6570
citation:
  ama: Nardin M. On the encoding, transfer, and consolidation of spatial memories.
    2022. doi:<a href="https://doi.org/10.15479/at:ista:11932">10.15479/at:ista:11932</a>
  apa: Nardin, M. (2022). <i>On the encoding, transfer, and consolidation of spatial
    memories</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:11932">https://doi.org/10.15479/at:ista:11932</a>
  chicago: Nardin, Michele. “On the Encoding, Transfer, and Consolidation of Spatial
    Memories.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11932">https://doi.org/10.15479/at:ista:11932</a>.
  ieee: M. Nardin, “On the encoding, transfer, and consolidation of spatial memories,”
    Institute of Science and Technology Austria, 2022.
  ista: Nardin M. 2022. On the encoding, transfer, and consolidation of spatial memories.
    Institute of Science and Technology Austria.
  mla: Nardin, Michele. <i>On the Encoding, Transfer, and Consolidation of Spatial
    Memories</i>. Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11932">10.15479/at:ista:11932</a>.
  short: M. Nardin, On the Encoding, Transfer, and Consolidation of Spatial Memories,
    Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2022-08-19T08:52:30Z
date_published: 2022-08-19T00:00:00Z
date_updated: 2026-04-07T14:22:58Z
day: '19'
ddc:
- '573'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JoCs
doi: 10.15479/at:ista:11932
ec_funded: 1
file:
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  date_updated: 2023-06-20T22:30:04Z
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file_date_updated: 2023-06-20T22:30:04Z
has_accepted_license: '1'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
page: '136'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '6194'
    relation: part_of_dissertation
    status: public
  - id: '10077'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Jozsef L
  full_name: Csicsvari, Jozsef L
  id: 3FA14672-F248-11E8-B48F-1D18A9856A87
  last_name: Csicsvari
  orcid: 0000-0002-5193-4036
title: On the encoding, transfer, and consolidation of spatial memories
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '11193'
abstract:
- lang: eng
  text: "The infiltration of immune cells into tissues underlies the establishment
    of tissue-resident\r\nmacrophages and responses to infections and tumors. However,
    the mechanisms immune\r\ncells utilize to collectively migrate through tissue
    barriers in vivo are not yet well understood.\r\nIn this thesis, I describe two
    mechanisms that Drosophila immune cells (hemocytes) use to\r\novercome the tissue
    barrier of the germband in the embryo. One strategy is the strengthening\r\nof
    the actin cortex through developmentally controlled transcriptional regulation
    induced by\r\nthe Drosophila proto-oncogene family member Dfos, which I show in
    Chapter 2. Dfos induces\r\nexpression of the tetraspanin TM4SF and the filamin
    Cher leading to higher levels of the\r\nactivated formin Dia at the cortex and
    increased cortical F-actin. This enhanced cortical\r\nstrength allows hemocytes
    to overcome the physical resistance of the surrounding tissue and\r\ntranslocate
    their nucleus to move forward. This mechanism affects the speed of migration\r\nwhen
    hemocytes face a confined environment in vivo.\r\nAnother aspect of the invasion
    process is the initial step of the leading hemocytes entering\r\nthe tissue, which
    potentially guides the follower cells. In Chapter 3, I describe a novel\r\nsubpopulation
    of hemocytes activated by BMP signaling prior to tissue invasion that leads\r\npenetration
    into the germband. Hemocytes that are deficient in BMP signaling activation\r\nshow
    impaired persistence at the tissue entry, while their migration speed remains\r\nunaffected.\r\nThis
    suggests that there might be different mechanisms controlling immune cell migration\r\nwithin
    the confined environment in vivo, one of these being the general ability to overcome\r\nthe
    resistance of the surrounding tissue and another affecting the order of hemocytes
    that\r\ncollectively invade the tissue in a stream of individual cells.\r\nTogether,
    my findings provide deeper insights into transcriptional changes in immune\r\ncells
    that enable efficient tissue invasion and pave the way for future studies investigating
    the\r\nearly colonization of tissues by macrophages in higher organisms. Moreover,
    they extend the\r\ncurrent view of Drosophila immune cell heterogeneity and point
    toward a potentially\r\nconserved role for canonical BMP signaling in specifying
    immune cells that lead the migration\r\nof tissue resident macrophages during
    embryogenesis."
acknowledged_ssus:
- _id: LifeSc
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Stephanie
  full_name: Wachner, Stephanie
  id: 2A95E7B0-F248-11E8-B48F-1D18A9856A87
  last_name: Wachner
citation:
  ama: Wachner S. Transcriptional regulation by Dfos and BMP-signaling support tissue
    invasion of Drosophila immune cells. 2022. doi:<a href="https://doi.org/10.15479/at:ista:11193">10.15479/at:ista:11193</a>
  apa: Wachner, S. (2022). <i>Transcriptional regulation by Dfos and BMP-signaling
    support tissue invasion of Drosophila immune cells</i>. Institute of Science and
    Technology Austria. <a href="https://doi.org/10.15479/at:ista:11193">https://doi.org/10.15479/at:ista:11193</a>
  chicago: Wachner, Stephanie. “Transcriptional Regulation by Dfos and BMP-Signaling
    Support Tissue Invasion of Drosophila Immune Cells.” Institute of Science and
    Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:11193">https://doi.org/10.15479/at:ista:11193</a>.
  ieee: S. Wachner, “Transcriptional regulation by Dfos and BMP-signaling support
    tissue invasion of Drosophila immune cells,” Institute of Science and Technology
    Austria, 2022.
  ista: Wachner S. 2022. Transcriptional regulation by Dfos and BMP-signaling support
    tissue invasion of Drosophila immune cells. Institute of Science and Technology
    Austria.
  mla: Wachner, Stephanie. <i>Transcriptional Regulation by Dfos and BMP-Signaling
    Support Tissue Invasion of Drosophila Immune Cells</i>. Institute of Science and
    Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:11193">10.15479/at:ista:11193</a>.
  short: S. Wachner, Transcriptional Regulation by Dfos and BMP-Signaling Support
    Tissue Invasion of Drosophila Immune Cells, Institute of Science and Technology
    Austria, 2022.
corr_author: '1'
date_created: 2022-04-20T08:59:07Z
date_published: 2022-04-20T00:00:00Z
date_updated: 2026-04-07T14:24:19Z
day: '20'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: DaSi
doi: 10.15479/at:ista:11193
file:
- access_level: open_access
  checksum: 999ab16884c4522486136ebc5ae8dbff
  content_type: application/pdf
  creator: cchlebak
  date_created: 2022-04-20T09:03:57Z
  date_updated: 2023-04-21T22:30:03Z
  embargo: 2023-04-20
  file_id: '11195'
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  file_size: 8820951
  relation: main_file
- access_level: closed
  checksum: fd92b1e38d53bdf8b458213882d41383
  content_type: application/x-zip-compressed
  creator: cchlebak
  date_created: 2022-04-22T12:41:00Z
  date_updated: 2023-04-21T22:30:03Z
  embargo_to: open_access
  file_id: '11329'
  file_name: Thesis_Stephanie_Wachner_20200414.zip
  file_size: 65864612
  relation: source_file
file_date_updated: 2023-04-21T22:30:03Z
has_accepted_license: '1'
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '04'
oa: 1
oa_version: Published Version
page: '170'
project:
- _id: 26199CA4-B435-11E9-9278-68D0E5697425
  grant_number: '24800'
  name: Implications of a TGFÎ²/Dpp-activated subpopulation for Drosophila macrophage
    migration
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '10614'
    relation: part_of_dissertation
    status: public
  - id: '544'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Daria E
  full_name: Siekhaus, Daria E
  id: 3D224B9E-F248-11E8-B48F-1D18A9856A87
  last_name: Siekhaus
  orcid: 0000-0001-8323-8353
title: Transcriptional regulation by Dfos and BMP-signaling support tissue invasion
  of Drosophila immune cells
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '12378'
abstract:
- lang: eng
  text: "Environmental cues influence the highly dynamic morphology of microglia.
    Strategies to \r\ncharacterize these changes usually involve user-selected morphometric
    features, which \r\npreclude the identification of a spectrum of context-dependent
    morphological phenotypes. \r\nHere, we develop MorphOMICs, a topological data
    analysis approach, which enables semi\x02automatic mapping of microglial morphology
    into an atlas of cue-dependent phenotypes,\r\novercomes feature-selection bias
    and minimizes biological variability. \r\nFirst, with MorphOMICs we derive the
    morphological spectrum of microglia across seven \r\nbrain regions during postnatal
    development and in two distinct Alzheimer’s disease \r\ndegeneration mouse models.
    We uncover region-specific and sexually dimorphic\r\nmorphological trajectories,
    with females showing an earlier morphological shift than males in \r\nthe degenerating
    brain. Overall, we demonstrate that both long primary- and short terminal \r\nprocesses
    provide distinct insights to morphological phenotypes. Moreover, using machine
    \r\nlearning to map novel condition on the spectrum, we observe that microglia
    morphologies \r\nreflect a dose-dependent adaptation upon ketamine anesthesia
    and do not recover to control \r\nmorphologies.\r\nNext, we took advantage of
    MorphOMICs to build a high-resolution and layer-specific map of \r\nmicroglial
    morphological spectrum in the retina, covering postnatal development and rd10
    \r\ndegeneration. Here, following photoreceptor death, microglia assume an early
    development\x02like morphology. Finally, we map microglial morphology following
    optic nerve crush on the \r\nretinal spectrum and observe a layer- and sex-dependent
    response. \r\nOverall, MorphOMICs opens a new perspective to analyze microglial
    morphology across \r\nmultiple conditions, and provides a novel tool to characterize
    microglial morphology beyond \r\nthe traditionally dichotomized view of microglia."
acknowledged_ssus:
- _id: PreCl
- _id: Bio
- _id: ScienComp
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Gloria
  full_name: Colombo, Gloria
  id: 3483CF6C-F248-11E8-B48F-1D18A9856A87
  last_name: Colombo
  orcid: 0000-0001-9434-8902
citation:
  ama: Colombo G. MorphOMICs, a tool for mapping microglial morphology, reveals brain
    region- and sex-dependent phenotypes. 2022. doi:<a href="https://doi.org/10.15479/at:ista:12378">10.15479/at:ista:12378</a>
  apa: Colombo, G. (2022). <i>MorphOMICs, a tool for mapping microglial morphology,
    reveals brain region- and sex-dependent phenotypes</i>. Institute of Science and
    Technology Austria. <a href="https://doi.org/10.15479/at:ista:12378">https://doi.org/10.15479/at:ista:12378</a>
  chicago: Colombo, Gloria. “MorphOMICs, a Tool for Mapping Microglial Morphology,
    Reveals Brain Region- and Sex-Dependent Phenotypes.” Institute of Science and
    Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:12378">https://doi.org/10.15479/at:ista:12378</a>.
  ieee: G. Colombo, “MorphOMICs, a tool for mapping microglial morphology, reveals
    brain region- and sex-dependent phenotypes,” Institute of Science and Technology
    Austria, 2022.
  ista: Colombo G. 2022. MorphOMICs, a tool for mapping microglial morphology, reveals
    brain region- and sex-dependent phenotypes. Institute of Science and Technology
    Austria.
  mla: Colombo, Gloria. <i>MorphOMICs, a Tool for Mapping Microglial Morphology, Reveals
    Brain Region- and Sex-Dependent Phenotypes</i>. Institute of Science and Technology
    Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:12378">10.15479/at:ista:12378</a>.
  short: G. Colombo, MorphOMICs, a Tool for Mapping Microglial Morphology, Reveals
    Brain Region- and Sex-Dependent Phenotypes, Institute of Science and Technology
    Austria, 2022.
corr_author: '1'
date_created: 2023-01-25T14:27:43Z
date_published: 2022-11-11T00:00:00Z
date_updated: 2026-04-07T14:29:41Z
day: '11'
ddc:
- '570'
degree_awarded: PhD
department:
- _id: GradSch
- _id: SaSi
doi: 10.15479/at:ista:12378
ec_funded: 1
file:
- access_level: closed
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  content_type: application/vnd.openxmlformats-officedocument.wordprocessingml.document
  creator: cchlebak
  date_created: 2023-01-25T14:31:32Z
  date_updated: 2023-04-12T22:30:03Z
  embargo_to: open_access
  file_id: '12379'
  file_name: Gloria_Colombo_Thesis.docx
  file_size: 23890382
  relation: source_file
- access_level: open_access
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  creator: cchlebak
  date_created: 2023-01-25T14:31:36Z
  date_updated: 2023-04-12T22:30:03Z
  embargo: 2023-04-11
  file_id: '12380'
  file_name: Gloria_Colombo_Thesis.pdf
  file_size: 13802421
  relation: main_file
file_date_updated: 2023-04-12T22:30:03Z
has_accepted_license: '1'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
page: '142'
project:
- _id: 2564DBCA-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
  record:
  - id: '12244'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Sandra
  full_name: Siegert, Sandra
  id: 36ACD32E-F248-11E8-B48F-1D18A9856A87
  last_name: Siegert
  orcid: 0000-0001-8635-0877
title: MorphOMICs, a tool for mapping microglial morphology, reveals brain region-
  and sex-dependent phenotypes
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '12401'
abstract:
- lang: eng
  text: "Detachment of the cancer cells from the bulk of the tumor is the first step
    of metastasis, which\r\nis the primary cause of cancer related deaths. It is unclear,
    which factors contribute to this step.\r\nRecent studies indicate a crucial role
    of the tumor microenvironment in malignant\r\ntransformation and metastasis. Studying
    cancer cell invasion and detachments quantitatively in\r\nthe context of its physiological
    microenvironment is technically challenging. Especially, precise\r\ncontrol of
    microenvironmental properties in vivo is currently not possible. Here, I studied
    the\r\nrole of microenvironment geometry in the invasion and detachment of cancer
    cells from the\r\nbulk with a simplistic and reductionist approach. In this approach,
    I engineered microfluidic\r\ndevices to mimic a pseudo 3D extracellular matrix
    environment, where I was able to\r\nquantitatively tune the geometrical configuration
    of the microenvironment and follow tumor\r\ncells with fluorescence live imaging.
    To aid quantitative analysis I developed a widely applicable\r\nsoftware application
    to automatically analyze and visualize particle tracking data.\r\nQuantitative
    analysis of tumor cell invasion in isotropic and anisotropic microenvironments\r\nshowed
    that heterogeneity in the microenvironment promotes faster invasion and more\r\nfrequent
    detachment of cells. These observations correlated with overall higher speed of
    cells at\r\nthe edge of the bulk of the cells. In heterogeneous microenvironments
    cells preferentially\r\npassed through larger pores, thus invading areas of least
    resistance and generating finger-like\r\ninvasive structures. The detachments
    occurred mostly at the tips of these structures.\r\nTo investigate the potential
    mechanism, we established a two dimensional model to simulate\r\nactive Brownian
    particles representing the cell nuclei dynamics. These simulations backed our
    in\r\nvitro observations without the need of precise fitting the simulation parameters.
    Our model\r\nsuggests the importance of the pore heterogeneity in the direction
    perpendicular to the\r\norientation of bias field (lateral heterogeneity), which
    causes the interface roughening."
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Saren
  full_name: Tasciyan, Saren
  id: 4323B49C-F248-11E8-B48F-1D18A9856A87
  last_name: Tasciyan
  orcid: 0000-0003-1671-393X
citation:
  ama: Tasciyan S. Role of microenvironment heterogeneity in cancer cell invasion.
    2022. doi:<a href="https://doi.org/10.15479/at:ista:12401">10.15479/at:ista:12401</a>
  apa: Tasciyan, S. (2022). <i>Role of microenvironment heterogeneity in cancer cell
    invasion</i>. Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:12401">https://doi.org/10.15479/at:ista:12401</a>
  chicago: Tasciyan, Saren. “Role of Microenvironment Heterogeneity in Cancer Cell
    Invasion.” Institute of Science and Technology Austria, 2022. <a href="https://doi.org/10.15479/at:ista:12401">https://doi.org/10.15479/at:ista:12401</a>.
  ieee: S. Tasciyan, “Role of microenvironment heterogeneity in cancer cell invasion,”
    Institute of Science and Technology Austria, 2022.
  ista: Tasciyan S. 2022. Role of microenvironment heterogeneity in cancer cell invasion.
    Institute of Science and Technology Austria.
  mla: Tasciyan, Saren. <i>Role of Microenvironment Heterogeneity in Cancer Cell Invasion</i>.
    Institute of Science and Technology Austria, 2022, doi:<a href="https://doi.org/10.15479/at:ista:12401">10.15479/at:ista:12401</a>.
  short: S. Tasciyan, Role of Microenvironment Heterogeneity in Cancer Cell Invasion,
    Institute of Science and Technology Austria, 2022.
corr_author: '1'
date_created: 2023-01-26T11:55:16Z
date_published: 2022-12-22T00:00:00Z
date_updated: 2026-04-14T09:07:14Z
day: '22'
ddc:
- '610'
degree_awarded: PhD
department:
- _id: GradSch
- _id: MiSi
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supervisor:
- first_name: Michael K
  full_name: Sixt, Michael K
  id: 41E9FBEA-F248-11E8-B48F-1D18A9856A87
  last_name: Sixt
  orcid: 0000-0002-6620-9179
title: Role of microenvironment heterogeneity in cancer cell invasion
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2022'
...
---
OA_place: publisher
_id: '9022'
abstract:
- lang: eng
  text: "In the first part of the thesis we consider Hermitian random matrices. Firstly,
    we consider sample covariance matrices XX∗ with X having independent identically
    distributed (i.i.d.) centred entries. We prove a Central Limit Theorem for differences
    of linear statistics of XX∗ and its minor after removing the first column of X.
    Secondly, we consider Wigner-type matrices and prove that the eigenvalue statistics
    near cusp singularities of the limiting density of states are universal and that
    they form a Pearcey process. Since the limiting eigenvalue distribution admits
    only square root (edge) and cubic root (cusp) singularities, this concludes the
    third and last remaining case of the Wigner-Dyson-Mehta universality conjecture.
    The main technical ingredients are an optimal local law at the cusp, and the proof
    of the fast relaxation to equilibrium of the Dyson Brownian motion in the cusp
    regime.\r\nIn the second part we consider non-Hermitian matrices X with centred
    i.i.d. entries. We normalise the entries of X to have variance N −1. It is well
    known that the empirical eigenvalue density converges to the uniform distribution
    on the unit disk (circular law). In the first project, we prove universality of
    the local eigenvalue statistics close to the edge of the spectrum. This is the
    non-Hermitian analogue of the TracyWidom universality at the Hermitian edge. Technically
    we analyse the evolution of the spectral distribution of X along the Ornstein-Uhlenbeck
    flow for very long time\r\n(up to t = +∞). In the second project, we consider
    linear statistics of eigenvalues for macroscopic test functions f in the Sobolev
    space H2+ϵ and prove their convergence to the projection of the Gaussian Free
    Field on the unit disk. We prove this result for non-Hermitian matrices with real
    or complex entries. The main technical ingredients are: (i) local law for products
    of two resolvents at different spectral parameters, (ii) analysis of correlated
    Dyson Brownian motions.\r\nIn the third and final part we discuss the mathematically
    rigorous application of supersymmetric techniques (SUSY ) to give a lower tail
    estimate of the lowest singular value of X − z, with z ∈ C. More precisely, we
    use superbosonisation formula to give an integral representation of the resolvent
    of (X − z)(X − z)∗ which reduces to two and three contour integrals in the complex
    and real case, respectively. The rigorous analysis of these integrals is quite
    challenging since simple saddle point analysis cannot be applied (the main contribution
    comes from a non-trivial manifold). Our result\r\nimproves classical smoothing
    inequalities in the regime |z| ≈ 1; this result is essential to prove edge universality
    for i.i.d. non-Hermitian matrices."
acknowledgement: I gratefully acknowledge the financial support from the European
  Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie
  Grant Agreement No. 665385 and my advisor’s ERC Advanced Grant No. 338804.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Giorgio
  full_name: Cipolloni, Giorgio
  id: 42198EFA-F248-11E8-B48F-1D18A9856A87
  last_name: Cipolloni
  orcid: 0000-0002-4901-7992
citation:
  ama: Cipolloni G. Fluctuations in the spectrum of random matrices. 2021. doi:<a
    href="https://doi.org/10.15479/AT:ISTA:9022">10.15479/AT:ISTA:9022</a>
  apa: Cipolloni, G. (2021). <i>Fluctuations in the spectrum of random matrices</i>.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:9022">https://doi.org/10.15479/AT:ISTA:9022</a>
  chicago: Cipolloni, Giorgio. “Fluctuations in the Spectrum of Random Matrices.”
    Institute of Science and Technology Austria, 2021. <a href="https://doi.org/10.15479/AT:ISTA:9022">https://doi.org/10.15479/AT:ISTA:9022</a>.
  ieee: G. Cipolloni, “Fluctuations in the spectrum of random matrices,” Institute
    of Science and Technology Austria, 2021.
  ista: Cipolloni G. 2021. Fluctuations in the spectrum of random matrices. Institute
    of Science and Technology Austria.
  mla: Cipolloni, Giorgio. <i>Fluctuations in the Spectrum of Random Matrices</i>.
    Institute of Science and Technology Austria, 2021, doi:<a href="https://doi.org/10.15479/AT:ISTA:9022">10.15479/AT:ISTA:9022</a>.
  short: G. Cipolloni, Fluctuations in the Spectrum of Random Matrices, Institute
    of Science and Technology Austria, 2021.
corr_author: '1'
date_created: 2021-01-21T18:16:54Z
date_published: 2021-01-25T00:00:00Z
date_updated: 2026-04-08T06:59:33Z
day: '25'
ddc:
- '510'
degree_awarded: PhD
department:
- _id: GradSch
- _id: LaEr
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month: '01'
oa: 1
oa_version: Published Version
page: '380'
project:
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  call_identifier: H2020
  grant_number: '665385'
  name: International IST Doctoral Program
- _id: 258DCDE6-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '338804'
  name: Random matrices, universality and disordered quantum systems
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
status: public
supervisor:
- first_name: László
  full_name: Erdös, László
  id: 4DBD5372-F248-11E8-B48F-1D18A9856A87
  last_name: Erdös
  orcid: 0000-0001-5366-9603
title: Fluctuations in the spectrum of random matrices
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2021'
...
---
OA_place: publisher
_id: '10030'
abstract:
- lang: eng
  text: "This PhD thesis is primarily focused on the study of discrete transport problems,
    introduced for the first time in the seminal works of Maas [Maa11] and Mielke
    [Mie11] on finite state Markov chains and reaction-diffusion equations, respectively.
    More in detail, my research focuses on the study of transport costs on graphs,
    in particular the convergence and the stability of such problems in the discrete-to-continuum
    limit. This thesis also includes some results concerning\r\nnon-commutative optimal
    transport. The first chapter of this thesis consists of a general introduction
    to the optimal transport problems, both in the discrete, the continuous, and the
    non-commutative setting. Chapters 2 and 3 present the content of two works, obtained
    in collaboration with Peter Gladbach, Eva Kopfer, and Jan Maas, where we have
    been able to show the convergence of discrete transport costs on periodic graphs
    to suitable continuous ones, which can be described by means of a homogenisation
    result. We first focus on the particular case of quadratic costs on the real line
    and then extending the result to more general costs in arbitrary dimension. Our
    results are the first complete characterisation of limits of transport costs on
    periodic graphs in arbitrary dimension which do not rely on any additional symmetry.
    In Chapter 4 we turn our attention to one of the intriguing connection between
    evolution equations and optimal transport, represented by the theory of gradient
    flows. We show that discrete gradient flow structures associated to a finite volume
    approximation of a certain class of diffusive equations (Fokker–Planck) is stable
    in the limit of vanishing meshes, reproving the convergence of the scheme via
    the method of evolutionary Γ-convergence and exploiting a more variational point
    of view on the problem. This is based on a collaboration with Dominik Forkert
    and Jan Maas. Chapter 5 represents a change of perspective, moving away from the
    discrete world and reaching the non-commutative one. As in the discrete case,
    we discuss how classical tools coming from the commutative optimal transport can
    be translated into the setting of density matrices. In particular, in this final
    chapter we present a non-commutative version of the Schrödinger problem (or entropic
    regularised optimal transport problem) and discuss existence and characterisation
    of minimisers, a duality result, and present a non-commutative version of the
    well-known Sinkhorn algorithm to compute the above mentioned optimisers. This
    is based on a joint work with Dario Feliciangeli and Augusto Gerolin. Finally,
    Appendix A and B contain some additional material and discussions, with particular
    attention to Harnack inequalities and the regularity of flows on discrete spaces."
acknowledged_ssus:
- _id: M-Shop
- _id: NanoFab
acknowledgement: The author gratefully acknowledges support by the Austrian Science
  Fund (FWF), grants No W1245.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Lorenzo
  full_name: Portinale, Lorenzo
  id: 30AD2CBC-F248-11E8-B48F-1D18A9856A87
  last_name: Portinale
citation:
  ama: Portinale L. Discrete-to-continuum limits of transport problems and gradient
    flows in the space of measures. 2021. doi:<a href="https://doi.org/10.15479/at:ista:10030">10.15479/at:ista:10030</a>
  apa: Portinale, L. (2021). <i>Discrete-to-continuum limits of transport problems
    and gradient flows in the space of measures</i>. Institute of Science and Technology
    Austria. <a href="https://doi.org/10.15479/at:ista:10030">https://doi.org/10.15479/at:ista:10030</a>
  chicago: Portinale, Lorenzo. “Discrete-to-Continuum Limits of Transport Problems
    and Gradient Flows in the Space of Measures.” Institute of Science and Technology
    Austria, 2021. <a href="https://doi.org/10.15479/at:ista:10030">https://doi.org/10.15479/at:ista:10030</a>.
  ieee: L. Portinale, “Discrete-to-continuum limits of transport problems and gradient
    flows in the space of measures,” Institute of Science and Technology Austria,
    2021.
  ista: Portinale L. 2021. Discrete-to-continuum limits of transport problems and
    gradient flows in the space of measures. Institute of Science and Technology Austria.
  mla: Portinale, Lorenzo. <i>Discrete-to-Continuum Limits of Transport Problems and
    Gradient Flows in the Space of Measures</i>. Institute of Science and Technology
    Austria, 2021, doi:<a href="https://doi.org/10.15479/at:ista:10030">10.15479/at:ista:10030</a>.
  short: L. Portinale, Discrete-to-Continuum Limits of Transport Problems and Gradient
    Flows in the Space of Measures, Institute of Science and Technology Austria, 2021.
corr_author: '1'
date_created: 2021-09-21T09:14:15Z
date_published: 2021-09-22T00:00:00Z
date_updated: 2026-04-08T07:00:04Z
day: '22'
ddc:
- '515'
degree_awarded: PhD
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- _id: JaMa
doi: 10.15479/at:ista:10030
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month: '09'
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project:
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  call_identifier: FWF
  grant_number: W1245
  name: Dissipation and dispersion in nonlinear partial differential equations
- _id: fc31cba2-9c52-11eb-aca3-ff467d239cd2
  grant_number: F6504
  name: Taming Complexity in Partial Differential Systems
publication_identifier:
  issn:
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publisher: Institute of Science and Technology Austria
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    status: public
status: public
supervisor:
- first_name: Jan
  full_name: Maas, Jan
  id: 4C5696CE-F248-11E8-B48F-1D18A9856A87
  last_name: Maas
  orcid: 0000-0002-0845-1338
title: Discrete-to-continuum limits of transport problems and gradient flows in the
  space of measures
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  short: CC BY (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2021'
...
---
OA_place: publisher
_id: '9733'
abstract:
- lang: eng
  text: This thesis is the result of the research carried out by the author during
    his PhD at IST Austria between 2017 and 2021. It mainly focuses on the Fröhlich
    polaron model, specifically to its regime of strong coupling. This model, which
    is rigorously introduced and discussed in the introduction, has been of great
    interest in condensed matter physics and field theory for more than eighty years.
    It is used to describe an electron interacting with the atoms of a solid material
    (the strength of this interaction is modeled by the presence of a coupling constant
    α in the Hamiltonian of the system). The particular regime examined here, which
    is mathematically described by considering the limit α →∞, displays many interesting
    features related to the emergence of classical behavior, which allows for a simplified
    effective description of the system under analysis. The properties, the range
    of validity and a quantitative analysis of the precision of such classical approximations
    are the main object of the present work. We specify our investigation to the study
    of the ground state energy of the system, its dynamics and its effective mass.
    For each of these problems, we provide in the introduction an overview of the
    previously known results and a detailed account of the original contributions
    by the author.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Dario
  full_name: Feliciangeli, Dario
  id: 41A639AA-F248-11E8-B48F-1D18A9856A87
  last_name: Feliciangeli
  orcid: 0000-0003-0754-8530
citation:
  ama: Feliciangeli D. The polaron at strong coupling. 2021. doi:<a href="https://doi.org/10.15479/at:ista:9733">10.15479/at:ista:9733</a>
  apa: Feliciangeli, D. (2021). <i>The polaron at strong coupling</i>. Institute of
    Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:9733">https://doi.org/10.15479/at:ista:9733</a>
  chicago: Feliciangeli, Dario. “The Polaron at Strong Coupling.” Institute of Science
    and Technology Austria, 2021. <a href="https://doi.org/10.15479/at:ista:9733">https://doi.org/10.15479/at:ista:9733</a>.
  ieee: D. Feliciangeli, “The polaron at strong coupling,” Institute of Science and
    Technology Austria, 2021.
  ista: Feliciangeli D. 2021. The polaron at strong coupling. Institute of Science
    and Technology Austria.
  mla: Feliciangeli, Dario. <i>The Polaron at Strong Coupling</i>. Institute of Science
    and Technology Austria, 2021, doi:<a href="https://doi.org/10.15479/at:ista:9733">10.15479/at:ista:9733</a>.
  short: D. Feliciangeli, The Polaron at Strong Coupling, Institute of Science and
    Technology Austria, 2021.
corr_author: '1'
date_created: 2021-07-27T15:48:30Z
date_published: 2021-08-20T00:00:00Z
date_updated: 2026-04-08T06:59:50Z
day: '20'
ddc:
- '515'
- '519'
- '539'
degree_awarded: PhD
department:
- _id: GradSch
- _id: RoSe
- _id: JaMa
doi: 10.15479/at:ista:9733
ec_funded: 1
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language:
- iso: eng
license: https://creativecommons.org/licenses/by-nd/4.0/
month: '08'
oa: 1
oa_version: Published Version
page: '180'
project:
- _id: 256E75B8-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '716117'
  name: Optimal Transport and Stochastic Dynamics
- _id: 25C6DC12-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '694227'
  name: Analysis of quantum many-body systems
- _id: fc31cba2-9c52-11eb-aca3-ff467d239cd2
  grant_number: F6504
  name: Taming Complexity in Partial Differential Systems
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
related_material:
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    relation: part_of_dissertation
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    relation: part_of_dissertation
    status: public
  - id: '9791'
    relation: part_of_dissertation
    status: public
  - id: '9781'
    relation: part_of_dissertation
    status: public
  - id: '9225'
    relation: part_of_dissertation
    status: public
status: public
supervisor:
- first_name: Robert
  full_name: Seiringer, Robert
  id: 4AFD0470-F248-11E8-B48F-1D18A9856A87
  last_name: Seiringer
  orcid: 0000-0002-6781-0521
- first_name: Jan
  full_name: Maas, Jan
  id: 4C5696CE-F248-11E8-B48F-1D18A9856A87
  last_name: Maas
  orcid: 0000-0002-0845-1338
title: The polaron at strong coupling
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  name: Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0)
  short: CC BY-ND (4.0)
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2021'
...
---
OA_place: publisher
_id: '10199'
abstract:
- lang: eng
  text: The design and verification of concurrent systems remains an open challenge
    due to the non-determinism that arises from the inter-process communication. In
    particular, concurrent programs are notoriously difficult both to be written correctly
    and to be analyzed formally, as complex thread interaction has to be accounted
    for. The difficulties are further exacerbated when concurrent programs get executed
    on modern-day hardware, which contains various buffering and caching mechanisms
    for efficiency reasons. This causes further subtle non-determinism, which can
    often produce very unintuitive behavior of the concurrent programs. Model checking
    is at the forefront of tackling the verification problem, where the task is to
    decide, given as input a concurrent system and a desired property, whether the
    system satisfies the property. The inherent state-space explosion problem in model
    checking of concurrent systems causes naïve explicit methods not to scale, thus
    more inventive methods are required. One such method is stateless model checking
    (SMC), which explores in memory-efficient manner the program executions rather
    than the states of the program. State-of-the-art SMC is typically coupled with
    partial order reduction (POR) techniques, which argue that certain executions
    provably produce identical system behavior, thus limiting the amount of executions
    one needs to explore in order to cover all possible behaviors. Another method
    to tackle the state-space explosion is symbolic model checking, where the considered
    techniques operate on a succinct implicit representation of the input system rather
    than explicitly accessing the system. In this thesis we present new techniques
    for verification of concurrent systems. We present several novel POR methods for
    SMC of concurrent programs under various models of semantics, some of which account
    for write-buffering mechanisms. Additionally, we present novel algorithms for
    symbolic model checking of finite-state concurrent systems, where the desired
    property of the systems is to ensure a formally defined notion of fairness.
acknowledged_ssus:
- _id: SSU
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Viktor
  full_name: Toman, Viktor
  id: 3AF3DA7C-F248-11E8-B48F-1D18A9856A87
  last_name: Toman
  orcid: 0000-0001-9036-063X
citation:
  ama: Toman V. Improved verification techniques for concurrent systems. 2021. doi:<a
    href="https://doi.org/10.15479/at:ista:10199">10.15479/at:ista:10199</a>
  apa: Toman, V. (2021). <i>Improved verification techniques for concurrent systems</i>.
    Institute of Science and Technology Austria. <a href="https://doi.org/10.15479/at:ista:10199">https://doi.org/10.15479/at:ista:10199</a>
  chicago: Toman, Viktor. “Improved Verification Techniques for Concurrent Systems.”
    Institute of Science and Technology Austria, 2021. <a href="https://doi.org/10.15479/at:ista:10199">https://doi.org/10.15479/at:ista:10199</a>.
  ieee: V. Toman, “Improved verification techniques for concurrent systems,” Institute
    of Science and Technology Austria, 2021.
  ista: Toman V. 2021. Improved verification techniques for concurrent systems. Institute
    of Science and Technology Austria.
  mla: Toman, Viktor. <i>Improved Verification Techniques for Concurrent Systems</i>.
    Institute of Science and Technology Austria, 2021, doi:<a href="https://doi.org/10.15479/at:ista:10199">10.15479/at:ista:10199</a>.
  short: V. Toman, Improved Verification Techniques for Concurrent Systems, Institute
    of Science and Technology Austria, 2021.
corr_author: '1'
date_created: 2021-10-29T20:09:01Z
date_published: 2021-10-31T00:00:00Z
date_updated: 2026-04-08T07:00:31Z
day: '31'
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degree_awarded: PhD
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keyword:
- concurrency
- verification
- model checking
language:
- iso: eng
month: '10'
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page: '166'
project:
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  name: International IST Doctoral Program
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supervisor:
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  id: 2E5DCA20-F248-11E8-B48F-1D18A9856A87
  last_name: Chatterjee
  orcid: 0000-0002-4561-241X
title: Improved verification techniques for concurrent systems
type: dissertation
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...
---
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abstract:
- lang: eng
  text: The present thesis is concerned with the derivation of weak-strong uniqueness
    principles for curvature driven interface evolution problems not satisfying a
    comparison principle. The specific examples being treated are two-phase Navier-Stokes
    flow with surface tension, modeling the evolution of two incompressible, viscous
    and immiscible fluids separated by a sharp interface, and multiphase mean curvature
    flow, which serves as an idealized model for the motion of grain boundaries in
    an annealing polycrystalline material. Our main results - obtained in joint works
    with Julian Fischer, Tim Laux and Theresa M. Simon - state that prior to the formation
    of geometric singularities due to topology changes, the weak solution concept
    of Abels (Interfaces Free Bound. 9, 2007) to two-phase Navier-Stokes flow with
    surface tension and the weak solution concept of Laux and Otto (Calc. Var. Partial
    Differential Equations 55, 2016) to multiphase mean curvature flow (for networks
    in R^2 or double bubbles in R^3) represents the unique solution to these interface
    evolution problems within the class of classical solutions, respectively. To the
    best of the author's knowledge, for interface evolution problems not admitting
    a geometric comparison principle the derivation of a weak-strong uniqueness principle
    represented an open problem, so that the works contained in the present thesis
    constitute the first positive results in this direction. The key ingredient of
    our approach consists of the introduction of a novel concept of relative entropies
    for a class of curvature driven interface evolution problems, for which the associated
    energy contains an interfacial contribution being proportional to the surface
    area of the evolving (network of) interface(s). The interfacial part of the relative
    entropy gives sufficient control on the interface error between a weak and a classical
    solution, and its time evolution can be computed, at least in principle, for any
    energy dissipating weak solution concept. A resulting stability estimate for the
    relative entropy essentially entails the above mentioned weak-strong uniqueness
    principles. The present thesis contains a detailed introduction to our relative
    entropy approach, which in particular highlights potential applications to other
    problems in curvature driven interface evolution not treated in this thesis.
alternative_title:
- ISTA Thesis
article_processing_charge: No
author:
- first_name: Sebastian
  full_name: Hensel, Sebastian
  id: 4D23B7DA-F248-11E8-B48F-1D18A9856A87
  last_name: Hensel
  orcid: 0000-0001-7252-8072
citation:
  ama: 'Hensel S. Curvature driven interface evolution: Uniqueness properties of weak
    solution concepts. 2021. doi:<a href="https://doi.org/10.15479/at:ista:10007">10.15479/at:ista:10007</a>'
  apa: 'Hensel, S. (2021). <i>Curvature driven interface evolution: Uniqueness properties
    of weak solution concepts</i>. Institute of Science and Technology Austria. <a
    href="https://doi.org/10.15479/at:ista:10007">https://doi.org/10.15479/at:ista:10007</a>'
  chicago: 'Hensel, Sebastian. “Curvature Driven Interface Evolution: Uniqueness Properties
    of Weak Solution Concepts.” Institute of Science and Technology Austria, 2021.
    <a href="https://doi.org/10.15479/at:ista:10007">https://doi.org/10.15479/at:ista:10007</a>.'
  ieee: 'S. Hensel, “Curvature driven interface evolution: Uniqueness properties of
    weak solution concepts,” Institute of Science and Technology Austria, 2021.'
  ista: 'Hensel S. 2021. Curvature driven interface evolution: Uniqueness properties
    of weak solution concepts. Institute of Science and Technology Austria.'
  mla: 'Hensel, Sebastian. <i>Curvature Driven Interface Evolution: Uniqueness Properties
    of Weak Solution Concepts</i>. Institute of Science and Technology Austria, 2021,
    doi:<a href="https://doi.org/10.15479/at:ista:10007">10.15479/at:ista:10007</a>.'
  short: 'S. Hensel, Curvature Driven Interface Evolution: Uniqueness Properties of
    Weak Solution Concepts, Institute of Science and Technology Austria, 2021.'
corr_author: '1'
date_created: 2021-09-13T11:12:34Z
date_published: 2021-09-14T00:00:00Z
date_updated: 2026-04-08T07:01:01Z
day: '14'
ddc:
- '515'
degree_awarded: PhD
department:
- _id: GradSch
- _id: JuFi
doi: 10.15479/at:ista:10007
ec_funded: 1
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language:
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month: '09'
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page: '300'
project:
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  call_identifier: H2020
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  name: International IST Doctoral Program
- _id: 0aa76401-070f-11eb-9043-b5bb049fa26d
  call_identifier: H2020
  grant_number: '948819'
  name: Bridging Scales in Random Materials
publication_identifier:
  issn:
  - 2663-337X
publication_status: published
publisher: Institute of Science and Technology Austria
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supervisor:
- first_name: Julian L
  full_name: Fischer, Julian L
  id: 2C12A0B0-F248-11E8-B48F-1D18A9856A87
  last_name: Fischer
  orcid: 0000-0002-0479-558X
title: 'Curvature driven interface evolution: Uniqueness properties of weak solution
  concepts'
type: dissertation
user_id: ba8df636-2132-11f1-aed0-ed93e2281fdd
year: '2021'
...
