@article{6952,
  abstract     = {We present a unified framework tackling two problems: class-specific 3D reconstruction from a single image, and generation of new 3D shape samples. These tasks have received considerable attention recently; however, most existing approaches rely on 3D supervision, annotation of 2D images with keypoints or poses, and/or training with multiple views of each object instance. Our framework is very general: it can be trained in similar settings to existing approaches, while also supporting weaker supervision. Importantly, it can be trained purely from 2D images, without pose annotations, and with only a single view per instance. We employ meshes as an output representation, instead of voxels used in most prior work. This allows us to reason over lighting parameters and exploit shading information during training, which previous 2D-supervised methods cannot. Thus, our method can learn to generate and reconstruct concave object classes. We evaluate our approach in various settings, showing that: (i) it learns to disentangle shape from pose and lighting; (ii) using shading in the loss improves performance compared to just silhouettes; (iii) when using a standard single white light, our model outperforms state-of-the-art 2D-supervised methods, both with and without pose supervision, thanks to exploiting shading cues; (iv) performance improves further when using multiple coloured lights, even approaching that of state-of-the-art 3D-supervised methods; (v) shapes produced by our model capture smooth surfaces and fine details better than voxel-based approaches; and (vi) our approach supports concave classes such as bathtubs and sofas, which methods based on silhouettes cannot learn.},
  author       = {Henderson, Paul M and Ferrari, Vittorio},
  issn         = {1573-1405},
  journal      = {International Journal of Computer Vision},
  pages        = {835--854},
  publisher    = {Springer Nature},
  title        = {{Learning single-image 3D reconstruction by generative modelling of shape, pose and shading}},
  doi          = {10.1007/s11263-019-01219-8},
  volume       = {128},
  year         = {2020},
}

@article{6976,
  abstract     = {Origami is rapidly transforming the design of robots1,2, deployable structures3,4,5,6 and metamaterials7,8,9,10,11,12,13,14. However, as foldability requires a large number of complex compatibility conditions that are difficult to satisfy, the design of crease patterns is limited to heuristics and computer optimization. Here we introduce a systematic strategy that enables intuitive and effective design of complex crease patterns that are guaranteed to fold. First, we exploit symmetries to construct 140 distinct foldable motifs, and represent these as jigsaw puzzle pieces. We then show that when these pieces are fitted together they encode foldable crease patterns. This maps origami design to solving combinatorial problems, which allows us to systematically create, count and classify a vast number of crease patterns. We show that all of these crease patterns are pluripotent—capable of folding into multiple shapes—and solve exactly for the number of possible shapes for each pattern. Finally, we employ our framework to rationally design a crease pattern that folds into two independently defined target shapes, and fabricate such pluripotent origami. Our results provide physicists, mathematicians and engineers with a powerful new design strategy.},
  author       = {Dieleman, Peter and Vasmel, Niek and Waitukaitis, Scott R and van Hecke, Martin},
  issn         = {1745-2481},
  journal      = {Nature Physics},
  number       = {1},
  pages        = {63–68},
  publisher    = {Springer Nature},
  title        = {{Jigsaw puzzle design of pluripotent origami}},
  doi          = {10.1038/s41567-019-0677-3},
  volume       = {16},
  year         = {2020},
}

@article{6997,
  author       = {Zhang, Yuzhou and Friml, Jiří},
  issn         = {1469-8137},
  journal      = {New Phytologist},
  number       = {3},
  pages        = {1049--1052},
  publisher    = {Wiley},
  title        = {{Auxin guides roots to avoid obstacles during gravitropic growth}},
  doi          = {10.1111/nph.16203},
  volume       = {225},
  year         = {2020},
}

@article{7004,
  abstract     = {We define an action of the (double of) Cohomological Hall algebra of Kontsevich and Soibelman on the cohomology of the moduli space of spiked instantons of Nekrasov. We identify this action with the one of the affine Yangian of gl(1). Based on that we derive the vertex algebra at the corner Wr1,r2,r3 of Gaiotto and Rapčák. We conjecture that our approach works for a big class of Calabi–Yau categories, including those associated with toric Calabi–Yau 3-folds.},
  author       = {Rapcak, Miroslav and Soibelman, Yan and Yang, Yaping and Zhao, Gufang},
  issn         = {1432-0916},
  journal      = {Communications in Mathematical Physics},
  pages        = {1803--1873},
  publisher    = {Springer Nature},
  title        = {{Cohomological Hall algebras, vertex algebras and instantons}},
  doi          = {10.1007/s00220-019-03575-5},
  volume       = {376},
  year         = {2020},
}

@article{7033,
  abstract     = {Removal of the Bax gene from mice completely protects the somas of retinal ganglion cells (RGCs) from apoptosis following optic nerve injury. This makes BAX a promising therapeutic target to prevent neurodegeneration. In this study, Bax+/− mice were used to test the hypothesis that lowering the quantity of BAX in RGCs would delay apoptosis following optic nerve injury. RGCs were damaged by performing optic nerve crush (ONC) and then immunostaining for phospho-cJUN, and quantitative PCR were used to monitor the status of the BAX activation mechanism in the months following injury. The apoptotic susceptibility of injured cells was directly tested by virally introducing GFP-BAX into Bax−/− RGCs after injury. The competency of quiescent RGCs to reactivate their BAX activation mechanism was tested by intravitreal injection of the JNK pathway agonist, anisomycin. Twenty-four weeks after ONC, Bax+/− mice had significantly less cell loss in their RGC layer than Bax+/+ mice 3 weeks after ONC. Bax+/− and Bax+/+ RGCs exhibited similar patterns of nuclear phospho-cJUN accumulation immediately after ONC, which persisted in Bax+/− RGCs for up to 7 weeks before abating. The transcriptional activation of BAX-activating genes was similar in Bax+/− and Bax+/+ RGCs following ONC. Intriguingly, cells deactivated their BAX activation mechanism between 7 and 12 weeks after crush. Introduction of GFP-BAX into Bax−/− cells at 4 weeks after ONC showed that these cells had a nearly normal capacity to activate this protein, but this capacity was lost 8 weeks after crush. Collectively, these data suggest that 8–12 weeks after crush, damaged cells no longer displayed increased susceptibility to BAX activation relative to their naïve counterparts. In this same timeframe, retinal glial activation and the signaling of the pro-apoptotic JNK pathway also abated. Quiescent RGCs did not show a timely reactivation of their JNK pathway following intravitreal injection with anisomycin. These findings demonstrate that lowering the quantity of BAX in RGCs is neuroprotective after acute injury. Damaged RGCs enter a quiescent state months after injury and are no longer responsive to an apoptotic stimulus. Quiescent RGCs will require rejuvenation to reacquire functionality.},
  author       = {Donahue, RJ and Maes, Margaret E and Grosser, JA and Nickells, RW},
  issn         = {1559-1182},
  journal      = {Molecular Neurobiology},
  number       = {2},
  pages        = {1070–1084},
  publisher    = {Springer Nature},
  title        = {{BAX-depleted retinal ganglion cells survive and become quiescent following optic nerve damage}},
  doi          = {10.1007/s12035-019-01783-7},
  volume       = {57},
  year         = {2020},
}

@article{7084,
  abstract     = {The unusual correlated state that emerges in URu2Si2 below THO = 17.5 K is known as “hidden order” because even basic characteristics of the order parameter, such as its dimensionality (whether it has one component or two), are “hidden.” We use resonant ultrasound spectroscopy to measure the symmetry-resolved elastic anomalies across THO. We observe no anomalies in the shear elastic moduli, providing strong thermodynamic evidence for a one-component order parameter. We develop a machine learning framework that reaches this conclusion directly from the raw data, even in a crystal that is too small for traditional resonant ultrasound. Our result rules out a broad class of theories of hidden order based on two-component order parameters, and constrains the nature of the fluctuations from which unconventional superconductivity emerges at lower temperature. Our machine learning framework is a powerful new tool for classifying the ubiquitous competing orders in correlated electron systems.},
  author       = {Ghosh, Sayak and Matty, Michael and Baumbach, Ryan and Bauer, Eric D. and Modic, Kimberly A and Shekhter, Arkady and Mydosh, J. A. and Kim, Eun-Ah and Ramshaw, B. J.},
  journal      = {Science Advances},
  number       = {10},
  publisher    = {American Association for the Advancement of Science},
  title        = {{One-component order parameter in URu2Si2 uncovered by resonant  ultrasound spectroscopy and machine learning}},
  doi          = {10.1126/sciadv.aaz4074},
  volume       = {6},
  year         = {2020},
}

@article{71,
  abstract     = {We consider dynamical transport metrics for probability measures on discretisations of a bounded convex domain in ℝd. These metrics are natural discrete counterparts to the Kantorovich metric 𝕎2, defined using a Benamou-Brenier type formula. Under mild assumptions we prove an asymptotic upper bound for the discrete transport metric Wt in terms of 𝕎2, as the size of the mesh T tends to 0. However, we show that the corresponding lower bound may fail in general, even on certain one-dimensional and symmetric two-dimensional meshes. In addition, we show that the asymptotic lower bound holds under an isotropy assumption on the mesh, which turns out to be essentially necessary. This assumption is satisfied, e.g., for tilings by convex regular polygons, and it implies Gromov-Hausdorff convergence of the transport metric.},
  author       = {Gladbach, Peter and Kopfer, Eva and Maas, Jan},
  issn         = {1095-7154},
  journal      = {SIAM Journal on Mathematical Analysis},
  number       = {3},
  pages        = {2759--2802},
  publisher    = {Society for Industrial and Applied Mathematics},
  title        = {{Scaling limits of discrete optimal transport}},
  doi          = {10.1137/19M1243440},
  volume       = {52},
  year         = {2020},
}

@article{7142,
  abstract     = {The phytohormone auxin acts as an amazingly versatile coordinator of plant growth and development. With its morphogen-like properties, auxin controls sites and timing of differentiation and/or growth responses both, in quantitative and qualitative terms. Specificity in the auxin response depends largely on distinct modes of signal transmission, by which individual cells perceive and convert auxin signals into a remarkable diversity of responses. The best understood, or so-called canonical mechanism of auxin perception ultimately results in variable adjustments of the cellular transcriptome, via a short, nuclear signal transduction pathway. Additional findings that accumulated over decades implied that an additional, presumably, cell surface-based auxin perception mechanism mediates very rapid cellular responses and decisively contributes to the cell's overall hormonal response. Recent investigations into both, nuclear and cell surface auxin signalling challenged this assumed partition of roles for different auxin signalling pathways and revealed an unexpected complexity in transcriptional and non-transcriptional cellular responses mediated by auxin.},
  author       = {Gallei, Michelle C and Luschnig, Christian and Friml, Jiří},
  issn         = {1879-0356},
  journal      = {Current Opinion in Plant Biology},
  number       = {2},
  pages        = {43--49},
  publisher    = {Elsevier},
  title        = {{Auxin signalling in growth: Schrödinger's cat out of the bag}},
  doi          = {10.1016/j.pbi.2019.10.003},
  volume       = {53},
  year         = {2020},
}

@article{7148,
  abstract     = {In the cerebellum, GluD2 is exclusively expressed in Purkinje cells, where it regulates synapse formation and regeneration, synaptic plasticity, and motor learning. Delayed cognitive development in humans with GluD2 gene mutations suggests extracerebellar functions of GluD2. However, extracerebellar expression of GluD2 and its relationship with that of GluD1 are poorly understood. GluD2 mRNA and protein were widely detected, with relatively high levels observed in the olfactory glomerular layer, medial prefrontal cortex, cingulate cortex, retrosplenial granular cortex, olfactory tubercle, subiculum, striatum, lateral septum, anterodorsal thalamic nucleus, and arcuate hypothalamic nucleus. These regions were also enriched for GluD1, and many individual neurons coexpressed the two GluDs. In the retrosplenial granular cortex, GluD1 and GluD2 were selectively expressed at PSD‐95‐expressing glutamatergic synapses, and their coexpression on the same synapses was shown by SDS‐digested freeze‐fracture replica labeling. Biochemically, GluD1 and GluD2 formed coimmunoprecipitable complex formation in HEK293T cells and in the cerebral cortex and hippocampus. We further estimated the relative protein amount by quantitative immunoblotting using GluA2/GluD2 and GluA2/GluD1 chimeric proteins as standards for titration of GluD1 and GluD2 antibodies. Intriguingly, the relative amount of GluD2 was almost comparable to that of GluD1 in the postsynaptic density fraction prepared from the cerebral cortex and hippocampus. In contrast, GluD2 was overwhelmingly predominant in the cerebellum. Thus, we have determined the relative extracerebellar expression of GluD1 and GluD2 at regional, neuronal, and synaptic levels. These data provide a molecular–anatomical basis for possible competitive and cooperative interactions of GluD family members at synapses in various brain regions.},
  author       = {Nakamoto, Chihiro and Konno, Kohtarou and Miyazaki, Taisuke and Nakatsukasa, Ena and Natsume, Rie and Abe, Manabu and Kawamura, Meiko and Fukazawa, Yugo and Shigemoto, Ryuichi and Yamasaki, Miwako and Sakimura, Kenji and Watanabe, Masahiko},
  issn         = {1096-9861},
  journal      = {Journal of Comparative Neurology},
  number       = {6},
  pages        = {1003--1027},
  publisher    = {Wiley},
  title        = {{Expression mapping, quantification, and complex formation of GluD1 and GluD2 glutamate receptors in adult mouse brain}},
  doi          = {10.1002/cne.24792},
  volume       = {528},
  year         = {2020},
}

@article{7149,
  abstract     = {In recent years, many genes have been associated with chromatinopathies classified as “Cornelia de Lange Syndrome‐like.” It is known that the phenotype of these patients becomes less recognizable, overlapping to features characteristic of other syndromes caused by genetic variants affecting different regulators of chromatin structure and function. Therefore, Cornelia de Lange syndrome diagnosis might be arduous due to the seldom discordance between unexpected molecular diagnosis and clinical evaluation. Here, we review the molecular features of Cornelia de Lange syndrome, supporting the hypothesis that “CdLS‐like syndromes” are part of a larger “rare disease family” sharing multiple clinical features and common disrupted molecular pathways.},
  author       = {Avagliano, Laura and Parenti, Ilaria and Grazioli, Paolo and Di Fede, Elisabetta and Parodi, Chiara and Mariani, Milena and Kaiser, Frank J. and Selicorni, Angelo and Gervasini, Cristina and Massa, Valentina},
  issn         = {1399-0004},
  journal      = {Clinical Genetics},
  number       = {1},
  pages        = {3--11},
  publisher    = {Wiley},
  title        = {{Chromatinopathies: A focus on Cornelia de Lange syndrome}},
  doi          = {10.1111/cge.13674},
  volume       = {97},
  year         = {2020},
}

@article{7160,
  abstract     = {Nocturnal animals that rely on their visual system for foraging, mating, and navigation usually exhibit specific traits associated with living in scotopic conditions. Most nocturnal birds have several visual specializations, such as enlarged eyes and an increased orbital convergence. However, the actual role of binocular vision in nocturnal foraging is still debated. Nightjars (Aves: Caprimulgidae) are predators that actively pursue and capture flying insects in crepuscular and nocturnal environments, mainly using a conspicuous “sit-and-wait” tactic on which pursuit begins with an insect flying over the bird that sits on the ground. In this study, we describe the visual system of the band-winged nightjar (Systellura longirostris), with emphasis on anatomical features previously described as relevant for nocturnal birds. Orbit convergence, determined by 3D scanning of the skull, was 73.28°. The visual field, determined by ophthalmoscopic reflex, exhibits an area of maximum binocular overlap of 42°, and it is dorsally oriented. The eyes showed a nocturnal-like normalized corneal aperture/axial length index. Retinal ganglion cells (RGCs) were relatively scant, and distributed in an unusual oblique-band pattern, with higher concentrations in the ventrotemporal quadrant. Together, these results indicate that the band-winged nightjar exhibits a retinal specialization associated with the binocular area of their dorsal visual field, a relevant area for pursuit triggering and prey attacks. The RGC distribution observed is unusual among birds, but similar to that of some visually dependent insectivorous bats, suggesting that those features might be convergent in relation to feeding strategies.},
  author       = {Salazar, Juan Esteban and Severin, Daniel and Vega Zuniga, Tomas A and Fernández-Aburto, Pedro and Deichler, Alfonso and Sallaberry A., Michel and Mpodozis, Jorge},
  issn         = {1421-9743},
  journal      = {Brain, Behavior and Evolution},
  number       = {1-4},
  pages        = {27--36},
  publisher    = {Karger Publishers},
  title        = {{Anatomical specializations related to foraging in the visual system of a nocturnal insectivorous bird, the band-winged nightjar (Aves: Caprimulgiformes)}},
  doi          = {10.1159/000504162},
  volume       = {94},
  year         = {2020},
}

@article{7166,
  abstract     = {In the living cell, we encounter a large variety of motile processes such as organelle transport and cytoskeleton remodeling. These processes are driven by motor proteins that generate force by transducing chemical free energy into mechanical work. In many cases, the molecular motors work in teams to collectively generate larger forces. Recent optical trapping experiments on small teams of cytoskeletal motors indicated that the collectively generated force increases with the size of the motor team but that this increase depends on the motor type and on whether the motors are studied in vitro or in vivo. Here, we use the theory of stochastic processes to describe the motion of N motors in a stationary optical trap and to compute the N-dependence of the collectively generated forces. We consider six distinct motor types, two kinesins, two dyneins, and two myosins. We show that the force increases always linearly with N but with a prefactor that depends on the performance of the single motor. Surprisingly, this prefactor increases for weaker motors with a lower stall force. This counter-intuitive behavior reflects the increased probability with which stronger motors detach from the filament during strain generation. Our theoretical results are in quantitative agreement with experimental data on small teams of kinesin-1 motors.},
  author       = {Ucar, Mehmet C and Lipowsky, Reinhard},
  issn         = {1530-6992},
  journal      = {Nano Letters},
  number       = {1},
  pages        = {669--676},
  publisher    = {American Chemical Society},
  title        = {{Collective force generation by molecular motors is determined by strain-induced unbinding}},
  doi          = {10.1021/acs.nanolett.9b04445},
  volume       = {20},
  year         = {2020},
}

@phdthesis{7196,
  abstract     = {In this thesis we study certain mathematical aspects of evolution. The two primary forces that drive an evolutionary process are mutation and selection. Mutation generates new variants in a population. Selection chooses among the variants depending on the reproductive rates of individuals. Evolutionary processes are intrinsically random – a new mutation that is initially present in the population at low frequency can go extinct, even if it confers a reproductive advantage. The overall rate of evolution is largely determined by two quantities: the probability that an invading advantageous mutation spreads through the population (called fixation probability) and the time until it does so (called fixation time). Both those quantities crucially depend not only on the strength of the invading mutation but also on the population structure. In this thesis, we aim to understand how the underlying population structure affects the overall rate of evolution. Specifically, we study population structures that increase the fixation probability of advantageous mutants (called amplifiers of selection). Broadly speaking, our results are of three different types: We present various strong amplifiers, we identify regimes under which only limited amplification is feasible, and we propose population structures that provide different tradeoffs between high fixation probability and short fixation time.},
  author       = {Tkadlec, Josef},
  issn         = {2663-337X},
  pages        = {144},
  publisher    = {Institute of Science and Technology Austria},
  title        = {{A role of graphs in evolutionary processes}},
  doi          = {10.15479/AT:ISTA:7196},
  year         = {2020},
}

@article{7204,
  abstract     = {Plant root architecture dynamically adapts to various environmental conditions, such as salt‐containing soil. The phytohormone abscisic acid (ABA) is involved among others also in these developmental adaptations, but the underlying molecular mechanism remains elusive. Here, a novel branch of the ABA signaling pathway in Arabidopsis involving PYR/PYL/RCAR (abbreviated as PYLs) receptor‐protein phosphatase 2A (PP2A) complex that acts in parallel to the canonical PYLs‐protein phosphatase 2C (PP2C) mechanism is identified. The PYLs‐PP2A signaling modulates root gravitropism and lateral root formation through regulating phytohormone auxin transport. In optimal conditions, PYLs ABA receptor interacts with the catalytic subunits of PP2A, increasing their phosphatase activity and thus counteracting PINOID (PID) kinase‐mediated phosphorylation of PIN‐FORMED (PIN) auxin transporters. By contrast, in salt and osmotic stress conditions, ABA binds to PYLs, inhibiting the PP2A activity, which leads to increased PIN phosphorylation and consequently modulated directional auxin transport leading to adapted root architecture. This work reveals an adaptive mechanism that may flexibly adjust plant root growth to withstand saline and osmotic stresses. It occurs via the cross‐talk between the stress hormone ABA and the versatile developmental regulator auxin.},
  author       = {Li, Yang and Wang, Yaping and Tan, Shutang and Li, Zhen and Yuan, Zhi and Glanc, Matous and Domjan, David and Wang, Kai and Xuan, Wei and Guo, Yan and Gong, Zhizhong and Friml, Jiří and Zhang, Jing},
  issn         = {2198-3844},
  journal      = {Advanced Science},
  number       = {3},
  publisher    = {Wiley},
  title        = {{Root growth adaptation is mediated by PYLs ABA receptor-PP2A protein phosphatase complex}},
  doi          = {10.1002/advs.201901455},
  volume       = {7},
  year         = {2020},
}

@article{7205,
  abstract     = {Genetic incompatibilities contribute to reproductive isolation between many diverging populations, but it is still unclear to what extent they play a role if divergence happens with gene flow. In contact zones between the "Crab" and "Wave" ecotypes of the snail Littorina saxatilis, divergent selection forms strong barriers to gene flow, while the role of post‐zygotic barriers due to selection against hybrids remains unclear. High embryo abortion rates in this species could indicate the presence of such barriers. Post‐zygotic barriers might include genetic incompatibilities (e.g. Dobzhansky–Muller incompatibilities) but also maladaptation, both expected to be most pronounced in contact zones. In addition, embryo abortion might reflect physiological stress on females and embryos independent of any genetic stress. We examined all embryos of >500 females sampled outside and inside contact zones of three populations in Sweden. Females' clutch size ranged from 0 to 1,011 embryos (mean 130 ± 123), and abortion rates varied between 0% and 100% (mean 12%). We described female genotypes by using a hybrid index based on hundreds of SNPs differentiated between ecotypes with which we characterized female genotypes. We also calculated female SNP heterozygosity and inversion karyotype. Clutch size did not vary with female hybrid index, and abortion rates were only weakly related to hybrid index in two sites but not at all in a third site. No additional variation in abortion rate was explained by female SNP heterozygosity, but increased female inversion heterozygosity added slightly to increased abortion. Our results show only weak and probably biologically insignificant post‐zygotic barriers contributing to ecotype divergence, and the high and variable abortion rates were marginally, if at all, explained by hybrid index of females.},
  author       = {Johannesson, Kerstin and Zagrodzka, Zuzanna and Faria, Rui and Westram, Anja M and Butlin, Roger K.},
  issn         = {1420-9101},
  journal      = {Journal of Evolutionary Biology},
  number       = {3},
  pages        = {342--351},
  publisher    = {Wiley},
  title        = {{Is embryo abortion a post-zygotic barrier to gene flow between Littorina ecotypes?}},
  doi          = {10.1111/jeb.13570},
  volume       = {33},
  year         = {2020},
}

@article{7207,
  abstract     = {The hippocampus plays key roles in learning and memory and is a main target of Alzheimer's disease (AD), which causes progressive memory impairments. Despite numerous investigations about the processes required for the normal hippocampal functions, the neurotransmitter receptors involved in the synaptic deficits by which AD disables the hippocampus are not yet characterized. By combining histoblots, western blots, immunohistochemistry and high‐resolution immunoelectron microscopic methods for GABAB receptors, this study provides a quantitative description of the expression and the subcellular localization of GABAB1 in the hippocampus in a mouse model of AD at 1, 6 and 12 months of age. Western blots and histoblots showed that the total amount of protein and the laminar expression pattern of GABAB1 were similar in APP/PS1 mice and in age‐matched wild‐type mice. In contrast, immunoelectron microscopic techniques showed that the subcellular localization of GABAB1 subunit did not change significantly in APP/PS1 mice at 1 month of age, was significantly reduced in the stratum lacunosum‐moleculare of CA1 pyramidal cells at 6 months of age and significantly reduced at the membrane surface of CA1 pyramidal cells at 12 months of age. This reduction of plasma membrane GABAB1 was paralleled by a significant increase of the subunit at the intracellular sites. We further observed a decrease of membrane‐targeted GABAB receptors in axon terminals contacting CA1 pyramidal cells. Our data demonstrate compartment‐ and age‐dependent reduction of plasma membrane‐targeted GABAB receptors in the CA1 region of the hippocampus, suggesting that this decrease might be enough to alter the GABAB‐mediated synaptic transmission taking place in AD.},
  author       = {Martín-Belmonte, Alejandro and Aguado, Carolina and Alfaro-Ruíz, Rocío and Moreno-Martínez, Ana Esther and De La Ossa, Luis and Martínez-Hernández, José and Buisson, Alain and Früh, Simon and Bettler, Bernhard and Shigemoto, Ryuichi and Fukazawa, Yugo and Luján, Rafael},
  issn         = {1750-3639},
  journal      = {Brain Pathology},
  number       = {3},
  pages        = {554--575},
  publisher    = {Wiley},
  title        = {{Reduction in the neuronal surface of post and presynaptic GABA>B< receptors in the hippocampus in a mouse model of Alzheimer's disease}},
  doi          = {10.1111/bpa.12802},
  volume       = {30},
  year         = {2020},
}

@article{7212,
  abstract     = {The fixation probability of a single mutant invading a population of residents is among the most widely-studied quantities in evolutionary dynamics. Amplifiers of natural selection are population structures that increase the fixation probability of advantageous mutants, compared to well-mixed populations. Extensive studies have shown that many amplifiers exist for the Birth-death Moran process, some of them substantially increasing the fixation probability or even guaranteeing fixation in the limit of large population size. On the other hand, no amplifiers are known for the death-Birth Moran process, and computer-assisted exhaustive searches have failed to discover amplification. In this work we resolve this disparity, by showing that any amplification under death-Birth updating is necessarily bounded and transient. Our boundedness result states that even if a population structure does amplify selection, the resulting fixation probability is close to that of the well-mixed population. Our transience result states that for any population structure there exists a threshold r⋆ such that the population structure ceases to amplify selection if the mutant fitness advantage r is larger than r⋆. Finally, we also extend the above results to δ-death-Birth updating, which is a combination of Birth-death and death-Birth updating. On the positive side, we identify population structures that maintain amplification for a wide range of values r and δ. These results demonstrate that amplification of natural selection depends on the specific mechanisms of the evolutionary process.},
  author       = {Tkadlec, Josef and Pavlogiannis, Andreas and Chatterjee, Krishnendu and Nowak, Martin A.},
  issn         = {15537358},
  journal      = {PLoS computational biology},
  publisher    = {Public Library of Science},
  title        = {{Limits on amplifiers of natural selection under death-Birth updating}},
  doi          = {10.1371/journal.pcbi.1007494},
  volume       = {16},
  year         = {2020},
}

@inproceedings{7213,
  abstract     = {Persistent homology is a powerful tool in Topological Data Analysis (TDA) to capture the topological properties of data succinctly at different spatial resolutions. For graphical data, the shape, and structure of the neighborhood of individual data items (nodes) are an essential means of characterizing their properties. We propose the use of persistent homology methods to capture structural and topological properties of graphs and use it to address the problem of link prediction. We achieve encouraging results on nine different real-world datasets that attest to the potential of persistent homology-based methods for network analysis.},
  author       = {Bhatia, Sumit and Chatterjee, Bapi and Nathani, Deepak and Kaul, Manohar},
  booktitle    = {Complex Networks and their applications VIII},
  isbn         = {9783030366865},
  issn         = {1860-9503},
  location     = {Lisbon, Portugal},
  pages        = {27--39},
  publisher    = {Springer Nature},
  title        = {{A persistent homology perspective to the link prediction problem}},
  doi          = {10.1007/978-3-030-36687-2_3},
  volume       = {881},
  year         = {2020},
}

@article{7218,
  abstract     = {The combined resection of skull-infiltrating tumours and immediate cranioplastic reconstruction predominantly relies on freehand-moulded solutions. Techniques that enable this procedure to be performed easily in routine clinical practice would be useful. A cadaveric study was developed in which a new software tool was used to perform single-stage reconstructions with prefabricated implants after the resection of skull-infiltrating pathologies. A novel 3D visualization and interaction framework was developed to create 10 virtual craniotomies in five cadaveric specimens. Polyether ether ketone (PEEK) implants were manufactured according to the bone defects. The image-guided craniotomy was reconstructed with PEEK and compared to polymethyl methacrylate (PMMA). Navigational accuracy and surgical precision were assessed. The PEEK workflow resulted in up to 10-fold shorter reconstruction times than the standard technique. Surgical precision was reflected by the mean 1.1 ± 0.29 mm distance between the virtual and real craniotomy, with submillimetre precision in 50%. Assessment of the global offset between virtual and actual craniotomy revealed an average shift of 4.5 ± 3.6 mm. The results validated the ‘elective single-stage cranioplasty’ technique as a state-of-the-art virtual planning method and surgical workflow. This patient-tailored workflow could significantly reduce surgical times compared to the traditional, intraoperative acrylic moulding method and may be an option for the reconstruction of bone defects in the craniofacial region.},
  author       = {Dodier, Philippe and Winter, Fabian and Auzinger, Thomas and Mistelbauer, Gabriel and Frischer, Josa M. and Wang, Wei Te and Mallouhi, Ammar and Marik, Wolfgang and Wolfsberger, Stefan and Reissig, Lukas and Hammadi, Firas and Matula, Christian and Baumann, Arnulf and Bavinzski, Gerhard},
  issn         = {1399-0020},
  journal      = {International Journal of Oral and Maxillofacial Surgery},
  number       = {8},
  pages        = {P1007--1015},
  publisher    = {Elsevier},
  title        = {{Single-stage bone resection and cranioplastic reconstruction: Comparison of a novel software-derived PEEK workflow with the standard reconstructive method}},
  doi          = {10.1016/j.ijom.2019.11.011},
  volume       = {49},
  year         = {2020},
}

@article{7219,
  abstract     = {Root system architecture (RSA), governed by the phytohormone auxin, endows plants with an adaptive advantage in particular environments. Using geographically representative arabidopsis (Arabidopsis thaliana) accessions as a resource for GWA mapping, Waidmann et al. and Ogura et al. recently identified two novel components involved in modulating auxin-mediated RSA and conferring plant fitness in particular habitats.},
  author       = {Xiao, Guanghui and Zhang, Yuzhou},
  issn         = {1360-1385},
  journal      = {Trends in Plant Science},
  number       = {2},
  pages        = {P121--123},
  publisher    = {Elsevier},
  title        = {{Adaptive growth: Shaping auxin-mediated root system architecture}},
  doi          = {10.1016/j.tplants.2019.12.001},
  volume       = {25},
  year         = {2020},
}

