@article{7550,
  abstract     = {We consider an optimal control problem for an abstract nonlinear dissipative evolution equation. The differential constraint is penalized by augmenting the target functional by a nonnegative global-in-time functional which is null-minimized in the evolution equation is satisfied. Different variational settings are presented, leading to the convergence of the penalization method for gradient flows, noncyclic and semimonotone flows, doubly nonlinear evolutions, and GENERIC systems. },
  author       = {Portinale, Lorenzo and Stefanelli, Ulisse},
  issn         = {1343-4373},
  journal      = {Advances in Mathematical Sciences and Applications},
  number       = {2},
  pages        = {425--447},
  publisher    = {Gakko Tosho},
  title        = {{Penalization via global functionals of optimal-control problems for dissipative evolution}},
  volume       = {28},
  year         = {2019},
}

@unpublished{7552,
  abstract     = {There is increasing evidence that protein binding to specific sites along DNA can activate the reading out of genetic information without coming into direct physical contact with the gene. There also is evidence that these distant but interacting sites are embedded in a liquid droplet of proteins which condenses out of the surrounding solution. We argue that droplet-mediated interactions can account for crucial features of gene regulation only if the droplet is poised at a non-generic point in its phase diagram. We explore a minimal model that embodies this idea, show that this model has a natural mechanism for self-tuning, and suggest direct experimental tests. },
  author       = {Bialek, William and Gregor, Thomas and Tkačik, Gašper},
  booktitle    = {arXiv},
  publisher    = {ArXiv},
  title        = {{Action at a distance in transcriptional regulation}},
  doi          = {10.48550/arXiv.1912.08579},
  year         = {2019},
}

@inproceedings{7576,
  abstract     = {We present the results of a friendly competition for formal verification of continuous and hybrid systems with nonlinear continuous dynamics. The friendly competition took place as part of the workshop Applied Verification for Continuous and Hybrid Systems (ARCH) in 2019. In this year, 6 tools Ariadne, CORA, DynIbex, Flow*, Isabelle/HOL, and JuliaReach (in alphabetic order) participated. They are applied to solve reachability analysis problems on four benchmark problems, one of them with hybrid dynamics. We do not rank the tools based on the results, but show the current status and discover the potential advantages of different tools.},
  author       = {Immler, Fabian and Althoff, Matthias and Benet, Luis and Chapoutot, Alexandre and Chen, Xin and Forets, Marcelo and Geretti, Luca and Kochdumper, Niklas and Sanders, David P. and Schilling, Christian},
  booktitle    = {EPiC Series in Computing},
  issn         = {2398-7340},
  location     = {Montreal, Canada},
  pages        = {41--61},
  publisher    = {EasyChair},
  title        = {{ARCH-COMP19 Category Report: Continuous and hybrid systems with nonlinear dynamics}},
  doi          = {10.29007/m75b},
  volume       = {61},
  year         = {2019},
}

@inproceedings{7606,
  abstract     = {We derive a tight lower bound on equivocation (conditional entropy), or equivalently a tight upper bound on mutual information between a signal variable and channel outputs. The bound is in terms of the joint distribution of the signals and maximum a posteriori decodes (most probable signals given channel output). As part of our derivation, we describe the key properties of the distribution of signals, channel outputs and decodes, that minimizes equivocation and maximizes mutual information. This work addresses a problem in data analysis, where mutual information between signals and decodes is sometimes used to lower bound the mutual information between signals and channel outputs. Our result provides a corresponding upper bound.},
  author       = {Hledik, Michal and Sokolowski, Thomas R and Tkačik, Gašper},
  booktitle    = {IEEE Information Theory Workshop, ITW 2019},
  isbn         = {9781538669006},
  location     = {Visby, Sweden},
  publisher    = {IEEE},
  title        = {{A tight upper bound on mutual information}},
  doi          = {10.1109/ITW44776.2019.8989292},
  year         = {2019},
}

@inproceedings{7639,
  abstract     = {Deep neural networks (DNNs) have become increasingly important due to their excellent empirical performance on a wide range of problems. However, regularization is generally achieved by indirect means, largely due to the complex set of functions defined by a network and the difficulty in measuring function complexity. There exists no method in the literature for additive regularization based on a norm of the function, as is classically considered in statistical learning theory. In this work, we study the tractability of function norms for deep neural networks with ReLU activations. We provide, to the best of our knowledge, the first proof in the literature of the NP-hardness of computing function norms of DNNs of 3 or more layers. We also highlight a fundamental difference between shallow and deep networks. In the light on these results, we propose a new regularization strategy based on approximate function norms, and show its efficiency on a segmentation task with a DNN.},
  author       = {Rannen-Triki, Amal and Berman, Maxim and Kolmogorov, Vladimir and Blaschko, Matthew B.},
  booktitle    = {Proceedings of the 2019 International Conference on Computer Vision Workshop},
  isbn         = {9781728150239},
  location     = {Seoul, South Korea},
  publisher    = {IEEE},
  title        = {{Function norms for neural networks}},
  doi          = {10.1109/ICCVW.2019.00097},
  year         = {2019},
}

@inproceedings{7640,
  abstract     = {We propose a new model for detecting visual relationships, such as "person riding motorcycle" or "bottle on table". This task is an important step towards comprehensive structured mage understanding, going beyond detecting individual objects. Our main novelty is a Box Attention mechanism that allows to model pairwise interactions between objects using standard object detection pipelines. The resulting model is conceptually clean, expressive and relies on well-justified training and prediction procedures. Moreover, unlike previously proposed approaches, our model does not introduce any additional complex components or hyperparameters on top of those already required by the underlying detection model. We conduct an experimental evaluation on two datasets, V-COCO and Open Images, demonstrating strong quantitative and qualitative results.},
  author       = {Kolesnikov, Alexander and Kuznetsova, Alina and Lampert, Christoph and Ferrari, Vittorio},
  booktitle    = {Proceedings of the 2019 International Conference on Computer Vision Workshop},
  isbn         = {9781728150239},
  location     = {Seoul, South Korea},
  publisher    = {IEEE},
  title        = {{Detecting visual relationships using box attention}},
  doi          = {10.1109/ICCVW.2019.00217},
  year         = {2019},
}

@unpublished{7950,
  abstract     = {The input to the token swapping problem is a graph with vertices v1, v2, . . . , vn, and n tokens with labels 1,2, . . . , n, one on each vertex.  The goal is to get token i to vertex vi for all i= 1, . . . , n using a minimum number of swaps, where a swap exchanges the tokens on the endpoints of an edge.Token swapping on a tree, also known as “sorting with a transposition tree,” is not known to be in P nor NP-complete.  We present some partial results:
1.  An optimum swap sequence may need to perform a swap on a leaf vertex that has the correct token (a “happy leaf”), disproving a conjecture of Vaughan.
2.  Any algorithm that fixes happy leaves—as all known approximation algorithms for the problem do—has approximation factor at least 4/3.  Furthermore, the two best-known 2-approximation algorithms have approximation factor exactly 2.
3.  A generalized problem—weighted coloured token swapping—is NP-complete on trees, but solvable in polynomial time on paths and stars.  In this version, tokens and  vertices  have  colours,  and  colours  have  weights.   The  goal  is  to  get  every token to a vertex of the same colour, and the cost of a swap is the sum of the weights of the two tokens involved.},
  author       = {Biniaz, Ahmad and Jain, Kshitij and Lubiw, Anna and Masárová, Zuzana and Miltzow, Tillmann and Mondal, Debajyoti and Naredla, Anurag Murty and Tkadlec, Josef and Turcotte, Alexi},
  booktitle    = {arXiv},
  title        = {{Token swapping on trees}},
  doi          = {10.48550/arXiv.1903.06981},
  year         = {2019},
}

@article{8,
  abstract     = {Despite their different origins, Drosophila glia and hemocytes are related cell populations that provide an immune function. Drosophila hemocytes patrol the body cavity and act as macrophages outside the nervous system whereas glia originate from the neuroepithelium and provide the scavenger population of the nervous system. Drosophila glia are hence the functional orthologs of vertebrate microglia, even though the latter are cells of immune origin that subsequently move into the brain during development. Interestingly, the Drosophila immune cells within (glia) and outside the nervous system (hemocytes) require the same transcription factor Glide/Gcm for their development. This raises the issue of how do glia specifically differentiate in the nervous system and hemocytes in the procephalic mesoderm. The Repo homeodomain transcription factor and pan-glial direct target of Glide/Gcm is known to ensure glial terminal differentiation. Here we show that Repo also takes center stage in the process that discriminates between glia and hemocytes. First, Repo expression is repressed in the hemocyte anlagen by mesoderm-specific factors. Second, Repo ectopic activation in the procephalic mesoderm is sufficient to repress the expression of hemocyte-specific genes. Third, the lack of Repo triggers the expression of hemocyte markers in glia. Thus, a complex network of tissue-specific cues biases the potential of Glide/Gcm. These data allow us to revise the concept of fate determinants and help us understand the bases of cell specification. Both sexes were analyzed.SIGNIFICANCE STATEMENTDistinct cell types often require the same pioneer transcription factor, raising the issue of how does one factor trigger different fates. In Drosophila, glia and hemocytes provide a scavenger activity within and outside the nervous system, respectively. While they both require the Glide/Gcm transcription factor, glia originate from the ectoderm, hemocytes from the mesoderm. Here we show that tissue-specific factors inhibit the gliogenic potential of Glide/Gcm in the mesoderm by repressing the expression of the homeodomain protein Repo, a major glial-specific target of Glide/Gcm. Repo expression in turn inhibits the expression of hemocyte-specific genes in the nervous system. These cell-specific networks secure the establishment of the glial fate only in the nervous system and allow cell diversification.},
  author       = {Trébuchet, Guillaume and Cattenoz, Pierre B and Zsámboki, János and Mazaud, David and Siekhaus, Daria E and Fanto, Manolis and Giangrande, Angela},
  journal      = {Journal of Neuroscience},
  number       = {2},
  pages        = {238--255},
  publisher    = {Society for Neuroscience},
  title        = {{The Repo homeodomain transcription factor suppresses hematopoiesis in Drosophila and preserves the glial fate}},
  doi          = {10.1523/JNEUROSCI.1059-18.2018},
  volume       = {39},
  year         = {2019},
}

@article{80,
  abstract     = {We consider an interacting, dilute Bose gas trapped in a harmonic potential at a positive temperature. The system is analyzed in a combination of a thermodynamic and a Gross–Pitaevskii (GP) limit where the trap frequency ω, the temperature T, and the particle number N are related by N∼ (T/ ω) 3→ ∞ while the scattering length is so small that the interaction energy per particle around the center of the trap is of the same order of magnitude as the spectral gap in the trap. We prove that the difference between the canonical free energy of the interacting gas and the one of the noninteracting system can be obtained by minimizing the GP energy functional. We also prove Bose–Einstein condensation in the following sense: The one-particle density matrix of any approximate minimizer of the canonical free energy functional is to leading order given by that of the noninteracting gas but with the free condensate wavefunction replaced by the GP minimizer.},
  author       = {Deuchert, Andreas and Seiringer, Robert and Yngvason, Jakob},
  journal      = {Communications in Mathematical Physics},
  number       = {2},
  pages        = {723--776},
  publisher    = {Springer},
  title        = {{Bose–Einstein condensation in a dilute, trapped gas at positive temperature}},
  doi          = {10.1007/s00220-018-3239-0},
  volume       = {368},
  year         = {2019},
}

@inproceedings{8175,
  abstract     = {We study edge asymptotics of poissonized Plancherel-type measures on skew Young diagrams (integer partitions). These measures can be seen as generalizations of those studied by Baik--Deift--Johansson and Baik--Rains in resolving Ulam's problem on longest increasing subsequences of random permutations and the last passage percolation (corner growth) discrete versions thereof. Moreover they interpolate between said measures and the uniform measure on partitions. In the new KPZ-like 1/3 exponent edge scaling limit with logarithmic corrections, we find new probability distributions generalizing the classical Tracy--Widom GUE, GOE and GSE distributions from the theory of random matrices.},
  author       = {Betea, Dan and Bouttier, Jérémie and Nejjar, Peter and Vuletíc, Mirjana},
  booktitle    = {Proceedings on the 31st International Conference on Formal Power Series and Algebraic Combinatorics},
  location     = {Ljubljana, Slovenia},
  publisher    = {Formal Power Series and Algebraic Combinatorics},
  title        = {{New edge asymptotics of skew Young diagrams via free boundaries}},
  year         = {2019},
}

@unpublished{8182,
  abstract     = {Suppose that $n\neq p^k$ and $n\neq 2p^k$ for all $k$ and all primes $p$. We prove that for any Hausdorff compactum $X$ with a free action of the symmetric group $\mathfrak S_n$ there exists an $\mathfrak S_n$-equivariant map $X \to
{\mathbb R}^n$ whose image avoids the diagonal $\{(x,x\dots,x)\in {\mathbb R}^n|x\in {\mathbb R}\}$.
  Previously, the special cases of this statement for certain $X$ were usually proved using the equivartiant obstruction theory. Such calculations are difficult and may become infeasible past the first (primary) obstruction. We
take a different approach which allows us to prove the vanishing of all obstructions simultaneously. The essential step in the proof is classifying the possible degrees of $\mathfrak S_n$-equivariant maps from the boundary
$\partial\Delta^{n-1}$ of $(n-1)$-simplex to itself.  Existence of equivariant maps between spaces is important for many questions arising from discrete mathematics and geometry, such as Kneser's conjecture, the Square Peg conjecture, the Splitting Necklace problem, and the Topological Tverberg conjecture, etc. We demonstrate the utility of our result  applying it to one such question, a specific instance of envy-free division problem.},
  author       = {Avvakumov, Sergey and Kudrya, Sergey},
  booktitle    = {arXiv},
  title        = {{Vanishing of all equivariant obstructions and the mapping degree}},
  doi          = {10.48550/arXiv.1910.12628},
  year         = {2019},
}

@unpublished{8184,
  abstract     = {Denote by ∆N the N-dimensional simplex. A map f : ∆N → Rd is an almost r-embedding if fσ1∩. . .∩fσr = ∅ whenever σ1, . . . , σr are pairwise disjoint faces. A counterexample to the topological Tverberg conjecture asserts that if r is not a prime power and d ≥ 2r + 1, then there is an almost r-embedding ∆(d+1)(r−1) → Rd. This was improved by Blagojevi´c–Frick–Ziegler using a simple construction of higher-dimensional counterexamples by taking k-fold join power of lower-dimensional ones. We improve this further (for d large compared to r): If r is not a prime power and N := (d+ 1)r−r l
d + 2 r + 1 m−2, then there is an almost r-embedding ∆N → Rd. For the r-fold van Kampen–Flores conjecture we also produce counterexamples which are stronger than previously known. Our proof is based on generalizations of the Mabillard–Wagner theorem on construction of almost r-embeddings from equivariant maps, and of the Ozaydin theorem on existence of equivariant maps. },
  author       = {Avvakumov, Sergey and Karasev, R. and Skopenkov, A.},
  booktitle    = {arXiv},
  title        = {{Stronger counterexamples to the topological Tverberg conjecture}},
  doi          = {10.48550/arXiv.1908.08731},
  year         = {2019},
}

@unpublished{8185,
  abstract     = {In this paper we study envy-free division problems. The classical approach to some of such problems, used by David Gale, reduces to considering continuous maps of a simplex to itself and finding sufficient conditions when this map hits the center of the simplex. The mere continuity is not sufficient for such a conclusion, the usual assumption (for example, in the Knaster--Kuratowski--Mazurkiewicz and the Gale theorem) is a certain boundary condition.
  We follow Erel Segal-Halevi, Fr\'ed\'eric Meunier, and Shira Zerbib, and replace the boundary condition by another assumption, which has the economic meaning of possibility for a player to prefer an empty part in the segment
partition problem. We solve the problem positively when $n$, the number of players that divide the segment, is a prime power, and we provide counterexamples for every $n$ which is not a prime power. We also provide counterexamples relevant to a wider class of fair or envy-free partition problems when $n$ is odd and not a prime power.},
  author       = {Avvakumov, Sergey and Karasev, Roman},
  booktitle    = {arXiv},
  title        = {{Envy-free division using mapping degree}},
  doi          = {10.48550/arXiv.1907.11183},
  year         = {2019},
}

@article{5790,
  abstract     = {The partial representation extension problem is a recently introduced generalization of the recognition problem. A circle graph is an intersection graph of chords of a circle. We study the partial representation extension problem for circle graphs, where the input consists of a graph G and a partial representation R′ giving some predrawn chords that represent an induced subgraph of G. The question is whether one can extend R′ to a representation R of the entire graph G, that is, whether one can draw the remaining chords into a partially predrawn representation to obtain a representation of G. Our main result is an O(n3) time algorithm for partial representation extension of circle graphs, where n is the number of vertices. To show this, we describe the structure of all representations of a circle graph using split decomposition. This can be of independent interest.},
  author       = {Chaplick, Steven and Fulek, Radoslav and Klavík, Pavel},
  issn         = {0364-9024},
  journal      = {Journal of Graph Theory},
  number       = {4},
  pages        = {365--394},
  publisher    = {Wiley},
  title        = {{Extending partial representations of circle graphs}},
  doi          = {10.1002/jgt.22436},
  volume       = {91},
  year         = {2019},
}

@inbook{5793,
  abstract     = {The transcription coactivator, Yes-associated protein (YAP), which is a nuclear effector of the Hippo signaling pathway, has been shown to be a mechano-transducer. By using mutant fish and human 3D spheroids, we have recently demonstrated that YAP is also a mechano-effector. YAP functions in three-dimensional (3D) morphogenesis of organ and global body shape by controlling actomyosin-mediated tissue tension. In this chapter, we present a platform that links the findings in fish embryos with human cells. The protocols for analyzing tissue tension-mediated global body shape/organ morphogenesis in vivo and ex vivo using medaka fish embryos and in vitro using human cell spheroids represent useful tools for unraveling the molecular mechanisms by which YAP functions in regulating global body/organ morphogenesis.},
  author       = {Asaoka, Yoichi and Morita, Hitoshi and Furumoto, Hiroko and Heisenberg, Carl-Philipp J and Furutani-Seiki, Makoto},
  booktitle    = {The hippo pathway},
  editor       = {Hergovich, Alexander},
  isbn         = {978-1-4939-8909-6},
  pages        = {167--181},
  publisher    = {Springer},
  title        = {{Studying YAP-mediated 3D morphogenesis using fish embryos and human spheroids}},
  doi          = {10.1007/978-1-4939-8910-2_14},
  volume       = {1893},
  year         = {2019},
}

@article{5817,
  abstract     = {We theoretically study the shapes of lipid vesicles confined to a spherical cavity, elaborating a framework based on the so-called limiting shapes constructed from geometrically simple structural elements such as double-membrane walls and edges. Partly inspired by numerical results, the proposed non-compartmentalized and compartmentalized limiting shapes are arranged in the bilayer-couple phase diagram which is then compared to its free-vesicle counterpart. We also compute the area-difference-elasticity phase diagram of the limiting shapes and we use it to interpret shape transitions experimentally observed in vesicles confined within another vesicle. The limiting-shape framework may be generalized to theoretically investigate the structure of certain cell organelles such as the mitochondrion.},
  author       = {Kavcic, Bor and Sakashita, A. and Noguchi, H. and Ziherl, P.},
  issn         = {1744-6848},
  journal      = {Soft Matter},
  number       = {4},
  pages        = {602--614},
  publisher    = {Royal Society of Chemistry},
  title        = {{Limiting shapes of confined lipid vesicles}},
  doi          = {10.1039/c8sm01956h},
  volume       = {15},
  year         = {2019},
}

@article{5828,
  abstract     = {Hippocampus is needed for both spatial working and reference memories. Here, using a radial eight-arm maze, we examined how the combined demand on these memories influenced CA1 place cell assemblies while reference memories were partially updated. This was contrasted with control tasks requiring only working memory or the update of reference memory. Reference memory update led to the reward-directed place field shifts at newly rewarded arms and to the gradual strengthening of firing in passes between newly rewarded arms but not between those passes that included a familiar-rewarded arm. At the maze center, transient network synchronization periods preferentially replayed trajectories of the next chosen arm in reference memory tasks but the previously visited arm in the working memory task. Hence, reference memory demand was uniquely associated with a gradual, goal novelty-related reorganization of place cell assemblies and with trajectory replay that reflected the animal's decision of which arm to visit next.},
  author       = {Xu, Haibing and Baracskay, Peter and O'Neill, Joseph and Csicsvari, Jozsef L},
  issn         = {1097-4199},
  journal      = {Neuron},
  number       = {1},
  pages        = {119--132.e4},
  publisher    = {Elsevier},
  title        = {{Assembly responses of hippocampal CA1 place cells predict learned behavior in goal-directed spatial tasks on the radial eight-arm maze}},
  doi          = {10.1016/j.neuron.2018.11.015},
  volume       = {101},
  year         = {2019},
}

@article{5830,
  abstract     = {CLE peptides have been implicated in various developmental processes of plants and mediate their responses to environmental stimuli. However, the biological relevance of most CLE genes remains to be functionally characterized. Here, we report that CLE9, which is expressed in stomata, acts as an essential regulator in the induction of stomatal closure. Exogenous application of CLE9 peptides or overexpression of CLE9 effectively led to stomatal closure and enhanced drought tolerance, whereas CLE9 loss-of-function mutants were sensitivity to drought stress. CLE9-induced stomatal closure was impaired in abscisic acid (ABA)-deficient mutants, indicating that ABA is required for CLE9-medaited guard cell signalling. We further deciphered that two guard cell ABA-signalling components, OST1 and SLAC1, were responsible for CLE9-induced stomatal closure. MPK3 and MPK6 were activated by the CLE9 peptide, and CLE9 peptides failed to close stomata in mpk3 and mpk6 mutants. In addition, CLE9 peptides stimulated the induction of hydrogen peroxide (H2O2) and nitric oxide (NO) synthesis associated with stomatal closure, which was abolished in the NADPH oxidase-deficient mutants or nitric reductase mutants, respectively. Collectively, our results reveal a novel ABA-dependent function of CLE9 in the regulation of stomatal apertures, thereby suggesting a potential role of CLE9 in the stress acclimatization of plants.},
  author       = {Zhang, Luosha and Shi, Xiong and Zhang, Yutao and Wang, Jiajing and Yang, Jingwei and Ishida, Takashi and Jiang, Wenqian and Han, Xiangyu and Kang, Jingke and Wang, Xuening and Pan, Lixia and Lv, Shuo and Cao, Bing and Zhang, Yonghong and Wu, Jinbin and Han, Huibin and Hu, Zhubing and Cui, Langjun and Sawa, Shinichiro and He, Junmin and Wang, Guodong},
  issn         = {0140-7791},
  journal      = {Plant Cell and Environment},
  number       = {3},
  pages        = {1033--1044},
  publisher    = {Wiley},
  title        = {{CLE9 peptide-induced stomatal closure is mediated by abscisic acid, hydrogen peroxide, and nitric oxide in arabidopsis thaliana}},
  doi          = {10.1111/pce.13475},
  volume       = {42},
  year         = {2019},
}

@article{5856,
  abstract     = {We give a bound on the ground-state energy of a system of N non-interacting fermions in a three-dimensional cubic box interacting with an impurity particle via point interactions. We show that the change in energy compared to the system in the absence of the impurity is bounded in terms of the gas density and the scattering length of the interaction, independently of N. Our bound holds as long as the ratio of the mass of the impurity to the one of the gas particles is larger than a critical value m∗ ∗≈ 0.36 , which is the same regime for which we recently showed stability of the system.},
  author       = {Moser, Thomas and Seiringer, Robert},
  issn         = {1424-0637},
  journal      = {Annales Henri Poincare},
  number       = {4},
  pages        = {1325–1365},
  publisher    = {Springer},
  title        = {{Energy contribution of a point-interacting impurity in a Fermi gas}},
  doi          = {10.1007/s00023-018-00757-0},
  volume       = {20},
  year         = {2019},
}

@article{5857,
  abstract     = {A thrackle is a graph drawn in the plane so that every pair of its edges meet exactly once: either at a common end vertex or in a proper crossing. We prove that any thrackle of n vertices has at most 1.3984n edges. Quasi-thrackles are defined similarly, except that every pair of edges that do not share a vertex are allowed to cross an odd number of times. It is also shown that the maximum number of edges of a quasi-thrackle on n vertices is [Formula presented](n−1), and that this bound is best possible for infinitely many values of n.},
  author       = {Fulek, Radoslav and Pach, János},
  issn         = {0166-218X},
  journal      = {Discrete Applied Mathematics},
  number       = {4},
  pages        = {266--231},
  publisher    = {Elsevier},
  title        = {{Thrackles: An improved upper bound}},
  doi          = {10.1016/j.dam.2018.12.025},
  volume       = {259},
  year         = {2019},
}

