@inproceedings{20054,
  author       = {Horta, Sharona},
  booktitle    = {Proceedings of the MATSUS Spring 2025 Conference},
  location     = {Sevilla, Spain},
  publisher    = {Fundació de la comunitat valenciana SCITO},
  title        = {{Solid state diffusion in metal-semiconductors core-shell nanoparticle}},
  doi          = {10.29363/nanoge.matsusspring.2025.220},
  year         = {2025},
}

@inproceedings{20055,
  abstract     = {Supercrystals represent three-dimensional orderings of colloidal nanocrystals (NCs), showcasing collective properties in photonics, phononics, and electronics applications.1,2 Recent studies have shown that such assemblies are directly produced during nanocrystal reactions.3–6 However, a fundamental understanding of in situ formed supercrystals that withstand typical NC purification processes remains underexplored, which is important for further use. Herein, we report the reaction precursor-mediated formation of stable PbTe supercrystals. Rationalizing the formation of these assemblies through small-angle x-ray scattering (SAXS) measurements, we unveil their formation mechanism. Our findings reveal that the supercrystal formation occurs in the presence of an excess of lead oleates in the crude solution. It should be noted that the formed supercrystals can be stabilized under specific conditions determined by the lead oleate cluster concentration, content of trioctylphosphine telluride (TOP-Te), NC size and the need of an annealing step at mild conditions. Furthermore, this approach allows for the continuous growth of a secondary phase within the supercrystal; for example in the case of PbTe supercrystals, a PbS shell can be grown on each PbTe NC constituent, resulting in core-shell PbTe-PbS supercrystals. Our work elucidates that reaction precursors play an important role in in situ SC formation and stabilization, implying the possibility of applying this knowledge to other NC reactions.},
  author       = {Lee, Seungho and Balazs, Daniel and Horta, Sharona and Rayaroth Puthiyaveettil, Aiswarya and Ibáñez, Maria},
  booktitle    = {Proceedings of the MATSUS Spring 2025 Conference},
  location     = {Sevilla, Spain},
  publisher    = {Fundació de la comunitat valenciana SCITO},
  title        = {{Reaction precursor-mediated formation of stable supercrystals in colloidal nanocrystal synthesis: PbTe case}},
  doi          = {10.29363/nanoge.matsusspring.2025.173},
  year         = {2025},
}

@article{20056,
  abstract     = {Theoretical studies have shown that stochasticity can affect the dynamics of ecosystems in counterintuitive ways. However, without knowing the equations governing the dynamics of populations or ecosystems, it is difficult to ascertain the role of stochasticity in real datasets. Therefore, the inverse problem of inferring the governing stochastic equations from datasets is important. Here, we present an equation discovery methodology that takes time series data of state variables as input and outputs a stochastic differential equation. We achieve this by combining traditional approaches from stochastic calculus with the equation discovery techniques. We demonstrate the generality of the method via several applications. First, we deliberately choose various stochastic models with fundamentally different governing equations, yet they produce nearly identical steady-state distributions. We show that we can recover the correct underlying equations, and thus infer the structure of their stability, accurately from the analysis of time series data alone. We demonstrate our method on two real-world datasets—fish schooling and single-cell migration—that have vastly different spatiotemporal scales and dynamics. We illustrate various limitations and potential pitfalls of the method and how to overcome them via diagnostic measures. Finally, we provide our open-source code via a package named PyDaDDy (Python Library for Data-Driven Dynamics).},
  author       = {Nabeel, Arshed and Karichannavar, Ashwin and Palathingal, Shuaib and Jhawar, Jitesh and Brückner, David and Raj M, Danny and Guttal, Vishwesha},
  issn         = {1537-5323},
  journal      = {The American Naturalist},
  number       = {4},
  pages        = {E100--E117},
  publisher    = {University of Chicago Press},
  title        = {{Discovering stochastic dynamical equations from ecological time series data}},
  doi          = {10.1086/734083},
  volume       = {205},
  year         = {2025},
}

@article{20077,
  abstract     = {Hyaluronic acid (HA) is a key extracellular matrix component of vertebrates, where it mediates cell adhesion, immune regulation, and tissue remodeling through its interaction with specific receptors. Although HA has been detected in a few invertebrate species, the lack of fundamental components of the molecular HA pathway poses relevant objections about its functional role in these species. Mining genomic and transcriptomic data, we considered the conservation of the gene locus encoding for the extracellular link protein (XLINK) in marine mussels as well as its expression patterns. Structural and phylogenetic analyses were undertaken to evaluate possible similarities with vertebrate orthologs and to infer the origin of this gene in invertebrates. Biochemical analysis was used to quantify HA in tissues of Mytilus galloprovincialis. As a result, we confirm that the mussel can produce HA (up to 1.02 ng/mg in mantle) and that its genome encodes two XLINK gene loci. These loci are conserved in Mytilidae species and show a complex evolutionary path. Mussel XLINK genes appeared to be expressed during developmental stages in three mussel species, ranking in the top 100 expressed genes in M. trossulus at 17 h post-fertilization. In conclusion, the presence of HA and an active gene with the potential to bind HA suggests that mussels have the potential to synthesize and use HA and are among the few invertebrates encoding this gene.},
  author       = {Rosani, Umberto and Altan, Nehir and Venier, Paola and Bortoletto, Enrico and Volpi, Nicola and Bernecky, Carrie A},
  issn         = {2079-7737},
  journal      = {Biology},
  number       = {8},
  publisher    = {MDPI},
  title        = {{Ancestral origin and functional expression of a hyaluronic acid pathway complement in mussels}},
  doi          = {10.3390/biology14080930},
  volume       = {14},
  year         = {2025},
}

@article{20078,
  abstract     = {Let A be an abelian variety defined over a number field K, E/K be an elliptic curve, and ϕ : A → Em be an isogeny defined over K. Let P ∈ A(K) be such that ϕ(P)=(Q1,..., Qm) with RankZ(⟨Q1,...,Qm⟩)=1. We will study a divisibility sequence related to the point P and show its relation with elliptic divisibility sequences.},
  author       = {Barańczuk, Stefan and Naskręcki, Bartosz and Verzobio, Matteo},
  issn         = {0022-314X},
  journal      = {Journal of Number Theory},
  pages        = {170--183},
  publisher    = {Elsevier},
  title        = {{Divisibility sequences related to abelian varieties isogenous to a power of an elliptic curve}},
  doi          = {10.1016/j.jnt.2025.06.001},
  volume       = {279},
  year         = {2025},
}

@article{20079,
  abstract     = {Research question: Is LINC01638 involved in regulation of epithelial-to-mesenchymal transition (EMT) in endometriosis?
Design: A prospective patient cohort study was combined with functional experiments in the 12Z endometriosis epithelial cell line to investigate the role of LINC01638 in endometriosis. Eutopic endometrial samples were collected by curettage, and ectopic endometrial lesion samples were collected by laparoscopic surgery from 24 control patients and 41 patients with endometriosis. The phenotype of 12Z cells was assessed following LINC01638 knockdown using siRNA, performing proliferation, adhesion, migration and invasion assays, as well as assessing apoptosis and cell cycle changes with flow cytometry assays. In order to assess the relationship between LINC01638 and histone deacetylase class 1 enzyme (HDAC1), LINC01638 knockdown was combined with HDAC inhibition with the specific HDAC inhibitor romidepsin.
Results: LINC01638 was up-regulated in the epithelial layer of endometriotic lesions, and LINC01638 knockdown in 12Z cells led to reduced proliferation, adhesion, migration and invasion. The reduction in proliferation was associated with increased p21 and p27 expression, and G1 phase arrest. Further analysis of LINC01638 control and knockdown cells revealed that a number of transcription factors associated with EMT are down-regulated in knockdown cells, along with the cytoskeleton regulatory gene RHOB, while HDAC1 was up-regulated. Chromatin immunoprecipitation analysis and HDAC1 inhibitory treatment combined with LINC01638 knockdown indicated that LINC01638 regulates RHOB expression via HDAC1-mediated promoter deacetylation. RHOB is up-regulated in the epithelial layer of endometriotic lesions compared with eutopic endometrium, supporting a role in the disease.
Conclusions: LINC01638 is an epigenetic regulator of the pathogenesis of endometriosis, promoting proliferation and EMT of endometriotic lesions.},
  author       = {Yotova, Iveta and Proestling, Katharina and Pauler, Florian and Rainer, Lisa and Kaup, Leonie and Heine, Jana and Sandrieser, Lejla and Wenzl, René and Hudson, Quanah J.},
  issn         = {1472-6491},
  journal      = {Reproductive Biomedicine Online},
  number       = {3},
  publisher    = {Elsevier},
  title        = {{LINC01638 promotes epithelial-to-mesenchymal transition in endometriosis epithelial cells by up-regulating RHOB via HDAC1 suppression}},
  doi          = {10.1016/j.rbmo.2025.104942},
  volume       = {51},
  year         = {2025},
}

@article{20080,
  abstract     = {Introduction: Acid-growth theory has been postulated in the 70s to explain the rapid elongation of plant cells in response to the hormone auxin. More recently, it has been demonstrated that activation of the proton ATPs pump (H+-ATPs) promoting acidification of the apoplast is the principal mechanism by which auxin and other hormones such as brassinosteroids (BR) induce cell elongation. Despite these advances, the impact of this acidification on the mechanical properties of the cell wall remained largely unexplored.

Methods: Here, we use elongation assays of Arabidopsis thaliana hypocotyls and Atomic Force Microscopy (AFM) to correlate hormone-induced tissue elongation and local changes in cell wall mechanical properties. Furthermore, employing transgenic lines over-expressing Pectin Methyl Esterase (PME), along with calcium chelators, we investigate the effect of pectin modification in hormone-driven cell elongation.

Results: We demonstrate that acidification of apoplast is necessary and sufficient to induce cell elongation through promoting cell wall softening. Moreover, we show that enhanced PME activity can induce both cell wall softening or stiffening in extracellular calcium dependent-manner and that tight control of PME activity is required for proper hypocotyl elongation.

Discussion: Our results confirm a dual role of PME in plant cell elongation. However, further investigation is needed to assess the status of pectin following short- or long-term PME treatments in order to determine if pectin methyl-esterification might promote its degradation as well as the role of PME inhibitors upon PME induction.},
  author       = {Gallemi, Marçal and Montesinos López, Juan C and Zarevski, Nikola and Pribyl, Jan and Skládal, Petr and Hannezo, Edouard B and Benková, Eva},
  issn         = {1664-462X},
  journal      = {Frontiers in Plant Science},
  publisher    = {Frontiers Media},
  title        = {{Dual role of pectin methyl esterase activity in the regulation of plant cell wall biophysical properties}},
  doi          = {10.3389/fpls.2025.1612366},
  volume       = {16},
  year         = {2025},
}

@article{20081,
  abstract     = {Information measures can be constructed from Rényi divergences much like mutual information from Kullback-Leibler divergence. One such information measure is known as Sibson α-mutual information and has received renewed attention recently in several contexts: concentration of measure under dependence, statistical learning, hypothesis testing, and estimation theory. In this paper, we survey and extend the state of the art. In particular, we introduce variational representations for Sibson α-mutual information and employ them in each described context to derive novel results. Namely, we produce generalized Transportation-Cost inequalities and Fano-type inequalities. We also present an overview of known applications, spanning from learning theory and Bayesian risk to universal prediction.},
  author       = {Esposito, Amedeo Roberto and Gastpar, Michael and Issa, Ibrahim},
  issn         = {1557-9654},
  journal      = {IEEE Transactions on Information Theory},
  publisher    = {IEEE},
  title        = {{Sibson α-mutual information and its variational representations}},
  doi          = {10.1109/TIT.2025.3587340},
  year         = {2025},
}

@article{20098,
  abstract     = {Climate change is causing wildfires to become more frequent and intense. While predicting burned areas using bioclimatic and anthropogenic factors is an active research area, few studies have examined what drives the economic damages of wildfires. Our study aims to fill this gap by analyzing key factors influencing global economic wildfire damages and projecting future damages under three shared socioeconomic pathways (SSPs). We apply regression analyses to identify significant predictors of economic wildfire damages at country levels and use the fitted model to project future damages under SSP126, SSP245, and SSP370. Results show that the human vulnerability index (HVI), reflecting socioeconomic conditions, is the strongest predictor of historical wildfire damages, followed by water vapor pressure deficit during the fire season and population density around forested areas. We found high population density to be associated with lower damages. These findings contrast with studies of burned areas, where climate factors are more dominant. Our model projects that by 2070, average global economic wildfire damages will be three times higher under SSP370 than SSP126. Our model also shows that following SSP126 not only reduces wildfire damages but also lessens the inequalities in damage distribution across countries. This pathway’s dual focus on equitable socioeconomic progress and climate action potentially enhances a country’s resilience that helps mitigate wildfire damages. Our analyses also indicate that strong socioeconomic development can offset wildfire damages associated with climate hazards, although this is less certain under SSP370. SSP126’s integrated approach improves both socioeconomic conditions and limits global warming, providing substantial benefits to less developed countries while still reducing damages in developed nations, despite their already low HVI scores. Our work complements existing research on burned areas and underscores the importance of sustainable development and international collaboration in reducing the economic damages of wildfires.},
  author       = {Hwong, Yi-Ling and Byers, Edward and Werning, Michaela and Quilcaille, Yann},
  issn         = {2752-5295},
  journal      = {Environmental Research: Climate},
  number       = {3},
  publisher    = {IOP Publishing},
  title        = {{Sustainable development key to limiting climate change-driven wildfire damages}},
  doi          = {10.1088/2752-5295/adec11},
  volume       = {4},
  year         = {2025},
}

@article{20099,
  abstract     = {The hippocampus, critical for learning and memory, is dogmatically described as a trisynaptic circuit where dentate gyrus granule cells (GCs), CA3 pyramidal neurons (PNs), and CA1 PNs are serially connected. However, CA3 also forms an autoassociative network, and its PNs have diverse morphologies, intrinsic properties, and GC input levels. How PN subtypes compose this recurrent network is unknown. To determine the synaptic arrangement of identified CA3 PNs, we combine multicellular patch-clamp recording and post hoc morphological analysis in mouse hippocampal slices. PNs can be divided into distinct “superficial” and “deep” subclasses, the latter including previously reported “athorny” cells. Subclasses have distinct input-output transformations and asymmetric connectivity, which is more abundant from superficial to deep PNs, splitting CA3 locally into two parallel recurrent networks. Coincident spontaneous inhibition occurs frequently within but not between subclasses, implying subclass-specific inhibitory innervation. Our results suggest two separately controlled sublayers for parallel information processing in hippocampal CA3.},
  author       = {Watson, Jake and Vargas Barroso, Victor M and Jonas, Peter M},
  issn         = {2211-1247},
  journal      = {Cell Reports},
  number       = {8},
  publisher    = {Elsevier},
  title        = {{Cell-specific wiring routes information flow through hippocampal CA3}},
  doi          = {10.1016/j.celrep.2025.116080},
  volume       = {44},
  year         = {2025},
}

@article{20100,
  abstract     = {A key step in protein structure prediction involves the detection of co-evolving pairs of residues, a signal for spatial proximity. This information is gleaned from multiple sequence alignment and underscores Alphafold’s structure prediction for almost every known protein. A simple means to create proteins beyond those found in nature, is by unnaturally fusing together two known proteins or protein parts. Here we demonstrate that structured peptides are predicted with significantly reduced accuracy when added to the terminal ends of scaffold proteins. Appending the multiple sequence alignment for the individual peptide tags to that of the scaffold protein often restores prediction accuracy. This work suggests that this windowed multiple sequence alignment approach can be a useful tool for predicting the structure of fused, chimeric proteins.},
  author       = {Vedula, Sanketh and Bronstein, Alexander and Marx, Ailie},
  issn         = {2001-0370},
  journal      = {Computational and Structural Biotechnology Journal},
  pages        = {3292--3298},
  publisher    = {Elsevier},
  title        = {{Improving prediction accuracy in chimeric proteins with windowed multiple sequence alignment}},
  doi          = {10.1016/j.csbj.2025.07.039},
  volume       = {27},
  year         = {2025},
}

@article{20101,
  abstract     = {Evading imminent threat from predators is critical for animal survival. Effective defensive strategies can vary, even between closely related species. However, the neural basis of such species-specific behaviours remains poorly understood1,2,3,4. Here we find that two sister species of deer mice (genus Peromyscus)5 show different responses to the same looming stimulus: Peromyscus maniculatus, which occupies densely vegetated habitats, predominantly escapes, whereas the open field specialist, Peromyscus polionotus, briefly freezes. This difference arises from species-specific escape thresholds, is largely context-independent, and can be triggered by both visual and auditory threat stimuli. Using immunohistochemistry and electrophysiological recordings, we find that although visual threat activates the superior colliculus in both species, the role of the dorsal periaqueductal grey (dPAG) in driving behaviour differs. Whereas dPAG activity scales with running speed in P. maniculatus, neural activity in the dPAG of P. polionotus correlates poorly with movement, including during visually triggered escape. Moreover, optogenetic activation of dPAG neurons elicits acceleration in P. maniculatus but not in P. polionotus, and their chemogenetic inhibition during a looming stimulus delays escape onset in P. maniculatus to match that of P. polionotus. Together, we trace species-specific escape thresholds to a central circuit node, downstream of peripheral sensory neurons, localizing an ecologically relevant behavioural difference to a specific region of the mammalian brain.},
  author       = {Baier, Felix and Reinhard, Katja and Nuttin, Bram and Sans-Dublanc, Arnau and Liu, Chen and Tong, Victoria and Murmann, Julie Stefanie and Wierda, Keimpe and Farrow, Karl and Hoekstra, Hopi E.},
  issn         = {1476-4687},
  journal      = {Nature},
  pages        = {439--447},
  publisher    = {Springer Nature},
  title        = {{The neural basis of species-specific defensive behaviour in Peromyscus mice}},
  doi          = {10.1038/s41586-025-09241-2},
  volume       = {645},
  year         = {2025},
}

@article{20102,
  abstract     = {Speciation is rarely observable directly. A way forward is to compare pairs of ecotypes that evolved in parallel in similar contexts but have reached different degrees of reproductive isolation. Such comparisons are possible in the marine snail Littorina saxatilis by contrasting barriers to gene flow between parallel ecotypes in Spain and Sweden. In both countries, divergent ecotypes have evolved to withstand either crab predation or wave action. Here, we explore transects spanning contact zones between the Crab and the Wave ecotypes using low-coverage whole-genome sequencing, morphological and behavioural traits. Despite parallel phenotypic divergence, distinct patterns of differentiation between the ecotypes emerged: a continuous cline in Sweden indicating a weak barrier to gene flow, but two highly genetically and phenotypically divergent, and partly spatially overlapping clusters in Spain suggesting a much stronger barrier to gene flow. The absence of Spanish early-generation hybrids supported strong isolation, but a low level of gene flow is evident from molecular data. In both countries, highly differentiated loci were located in both shared and country-specific chromosomal inversions but were also present in collinear regions. Despite being considered the same species and showing similar levels of phenotypic divergence, the Spanish ecotypes are much closer to full reproductive isolation than the Swedish ones. Barriers to gene flow of very different strengths between ecotypes within the same species might be explained by dissimilarities in the spatial arrangement of habitats, the selection gradients or the ages of the systems.},
  author       = {Raffini, Francesca and De Jode, Aurélien and Johannesson, Kerstin and Faria, Rui and Zagrodzka, Zuzanna B. and Westram, Anja M and Galindo, Juan and Rolán-Alvarez, Emilio and Butlin, Roger K.},
  issn         = {1365-294X},
  journal      = {Molecular Ecology},
  number       = {21},
  publisher    = {Wiley},
  title        = {{Phenotypic divergence and genomic architecture between parallel ecotypes at two different points on the speciation continuum in a marine snail}},
  doi          = {10.1111/mec.70025},
  volume       = {34},
  year         = {2025},
}

@misc{20103,
  abstract     = {Official implementation, windowed MSAs, and the predictions as reported in the manuscript titled "Improving Prediction Accuracy in Chimeric Proteins with Windowed Multiple Sequence Alignment". (2025-06-27)},
  author       = {Vedula, Sanketh and Bronstein, Alexander and Marx, Ailie},
  publisher    = {Harvard Dataverse},
  title        = {{Replication Data for: "Improving Prediction Accuracy in Chimeric Proteins with Windowed Multiple Sequence Alignment"}},
  doi          = {10.7910/DVN/DYEBVM},
  year         = {2025},
}

@misc{20107,
  abstract     = {This repository contains the data and scripts required to reproduce the results of the manuscript "Sustainable Development Key to Limiting Climate Change-Driven Wildfire Damages" submitted to the Environmental Research Climate Journal (ERCL). },
  author       = {Hwong, Yi-Ling and Byers, Edward and Werning, Michaela and Quilcaille, Yann},
  publisher    = {Zenodo},
  title        = {{Data - Sustainable Development Key to Limiting Climate Change-Driven Wildfire Damages}},
  doi          = {10.5281/ZENODO.13988679},
  year         = {2025},
}

@article{20116,
  abstract     = {Auxin regulates various aspects of plant growth and development by modulating the transcription of target genes through the degradation of auxin/indole-3-acetic acid (Aux/IAA) repressors via the 26S proteasome. Proteasome regulator 1 (PTRE1), a positive regulator of proteasome activity, has been implicated in auxin-mediated proteasome suppression; however, the mechanism by which auxin modulates PTRE1 function remains unclear. Here, we demonstrate that auxin promotes the interaction between germin-like protein 1 (GLP1) and PTRE1, facilitating PTRE1 retention at the plasma membrane. The relocation of PTRE1 results in reduced nuclear 26S proteasome activity, and thus the attenuated Aux/IAA degradation and altered Aux/IAA homeostasis, ultimately resulting in suppressed auxin-mediated transcriptional regulation. Our findings uncover a previously uncharacterized regulatory axis in auxin signaling that controls Aux/IAA protein stability, functioning alongside the TIR1- and TRANSMEMBRANE KINASE 1 (TMK1)-mediated pathways, and highlight the coordination of auxin signaling from the cell surface to the nucleus via auxin-induced PTRE1 relocation, which fine-tunes Aux/IAA protein homeostasis and auxin responses.},
  author       = {Xu, Faqing and Yu, Yongqiang and Guan, Bin and Xu, Tongda and Xu, Zhihong and Xue, Hongwei},
  issn         = {2211-1247},
  journal      = {Cell Reports},
  number       = {8},
  publisher    = {Elsevier},
  title        = {{Germin-like protein 1 interacts with proteasome regulator 1 to regulate auxin signaling by controlling Aux/IAA homeostasis}},
  doi          = {10.1016/j.celrep.2025.116056},
  volume       = {44},
  year         = {2025},
}

@article{20143,
  abstract     = {Bacteria and archaea deploy diverse antiviral defense systems, many of which remain mechanistically uncharacterized. Here, we characterize Kiwa, a widespread two-component system composed of the transmembrane sensor KwaA and the DNA-binding effector KwaB. Cryogenic electron microscopy (cryo-EM) analysis reveals that KwaA and KwaB assemble into a large, membrane-associated supercomplex. Upon phage binding, KwaA senses infection at the membrane, leading to KwaB binding of ejected phage DNA and inhibition of replication and late transcription, without inducing host cell death. Although KwaB can bind DNA independently, its antiviral activity requires association with KwaA, suggesting spatial or conformational regulation. We show that the phage-encoded DNA-mimic protein Gam directly binds and inhibits KwaB but that co-expression with the Gam-targeted RecBCD system restores protection by Kiwa. Our findings support a model in which Kiwa coordinates membrane-associated detection of phage infection with downstream DNA binding by its effector, forming a spatially coordinated antiviral mechanism.},
  author       = {Zhang, Zhiying and Todeschini, Thomas C. and Wu, Yi and Kogay, Roman and Naji, Ameena and Cardenas Rodriguez, Joaquin and Mondi, Rupavidhya and Kaganovich, Daniel and Taylor, David W. and Bravo, Jack Peter Kelly and Teplova, Marianna and Amen, Triana and Koonin, Eugene and Patel, Dinshaw J. and Nobrega, Franklin L.},
  issn         = {1097-4172},
  journal      = {Cell},
  number       = {21},
  pages        = {5862--5877.e23},
  publisher    = {Elsevier},
  title        = {{Kiwa is a membrane-embedded defense supercomplex activated at phage attachment sites}},
  doi          = {10.1016/j.cell.2025.07.002},
  volume       = {188},
  year         = {2025},
}

@techreport{20146,
  abstract     = {This criteria catalogue and the accompanying assessment questions were developed by a working group of KEMÖ (Kooperation E-Medien Österreich, the Austrian Academic Library Consortium). They are intended to support research institutions and organisations in the evaluation of Open Science Infrastructures. The 20 criteria outlined in the catalogue provide a structured basis for making informed decisions regarding the financial support of these infrastructures.

The assessment questions are intended to be completed by Open Science Infrastructures and can be shared with them accordingly.},
  author       = {Gredler, Paul and Kaier, Christian and Danowski, Patrick and Zoyer, Michael and Rieck, Katharina and Ferus, Andreas and Rosenberger, Elisabeth and Löffler, Alexander and Hofer, Lisa and Still, Laura},
  publisher    = {Zenodo},
  title        = {{Catalogue of criteria for assessing the funding eligibility of Open Science infrastructures}},
  doi          = {10.5281/zenodo.15269364},
  year         = {2025},
}

@article{20154,
  abstract     = {In long-lived mammals, including humans, brain cell homeostasis is critical for maintaining brain function throughout life. Most neurons are generated during development and must maintain their cellular identity and plasticity to preserve brain function. Although extensive studies indicate the importance of recycling and regenerating cellular molecules to maintain cellular homeostasis, recent evidence has shown that some proteins and RNAs do not turn over for months and even years. We propose that these long-lived cellular molecules may be the basis for maintaining brain function in the long term, but also a potential convergent target of brain aging. We highlight key discoveries and challenges, and propose potential directions to unravel the mystery of brain cell longevity.},
  author       = {Hetzer, Martin W and Toda, Tomohisa},
  issn         = {1878-108X},
  journal      = {Trends in Neurosciences},
  number       = {9},
  pages        = {645--654},
  publisher    = {Elsevier},
  title        = {{Long-lived cellular molecules in the brain}},
  doi          = {10.1016/j.tins.2025.07.004},
  volume       = {48},
  year         = {2025},
}

@article{20155,
  abstract     = {We study time averages for the norm of solutions to kinetic Fokker–Planck equations associated with general Hamiltonians. We provide fully explicit and constructive decay estimates for systems subject to a confining potential, allowing fat-tail, subexponential and (super-)exponential local equilibria, which also include the classic Maxwellian case. The key step in our estimates is a modified Poincaré inequality, obtained via a Lions–Poincaré inequality and an averaging lemma.},
  author       = {Brigati, Giovanni and Stoltz, Gabriel},
  issn         = {1095-7154},
  journal      = {SIAM Journal on Mathematical Analysis},
  number       = {4},
  pages        = {3587--3622},
  publisher    = {Society for Industrial and Applied Mathematics},
  title        = {{How to construct explicit decay rates for kinetic Fokker–Planck equations?}},
  doi          = {10.1137/24M1700351},
  volume       = {57},
  year         = {2025},
}

