@article{9759,
  author       = {Bartlett, Michael John and Arslan, Feyza N and Bankston, Adriana and Sarabipour, Sarvenaz},
  issn         = {1553-7358},
  journal      = {PLoS Computational Biology},
  number       = {7},
  publisher    = {Public Library of Science},
  title        = {{Ten simple rules to improve academic work- life balance}},
  doi          = {10.1371/journal.pcbi.1009124},
  volume       = {17},
  year         = {2021},
}

@article{9769,
  abstract     = {A few years ago, flow equations were introduced as a technique for calculating the ground-state energies of cold Bose gases with and without impurities. In this paper, we extend this approach to compute observables other than the energy. As an example, we calculate the densities, and phase fluctuations of one-dimensional Bose gases with one and two impurities. For a single mobile impurity, we use flow equations to validate the mean-field results obtained upon the Lee-Low-Pines transformation. We show that the mean-field approximation is accurate for all values of the boson-impurity interaction strength as long as the phase coherence length is much larger than the healing length of the condensate. For two static impurities, we calculate impurity-impurity interactions induced by the Bose gas. We find that leading order perturbation theory fails when boson-impurity interactions are stronger than boson-boson interactions. The mean-field approximation reproduces the flow equation results for all values of the boson-impurity interaction strength as long as boson-boson interactions are weak.},
  author       = {Brauneis, Fabian and Hammer, Hans-Werner and Lemeshko, Mikhail and Volosniev, Artem},
  issn         = {2542-4653},
  journal      = {SciPost Physics},
  number       = {1},
  publisher    = {SciPost Foundation},
  title        = {{Impurities in a one-dimensional Bose gas: The flow equation approach}},
  doi          = {10.21468/scipostphys.11.1.008},
  volume       = {11},
  year         = {2021},
}

@article{9770,
  abstract     = {We study an effective one-dimensional quantum model that includes friction and spin-orbit coupling (SOC), and show that the model exhibits spin polarization when both terms are finite. Most important, strong spin polarization can be observed even for moderate SOC, provided that the friction is strong. Our findings might help to explain the pronounced effect of chirality on spin distribution and transport in chiral molecules. In particular, our model implies static magnetic properties of a chiral molecule, which lead to Shiba-like states when a molecule is placed on a superconductor, in accordance with recent experimental data.},
  author       = {Volosniev, Artem and Alpern, Hen and Paltiel, Yossi and Millo, Oded and Lemeshko, Mikhail and Ghazaryan, Areg},
  issn         = {2469-9969},
  journal      = {Physical Review B},
  number       = {2},
  publisher    = {American Physical Society},
  title        = {{Interplay between friction and spin-orbit coupling as a source of spin polarization}},
  doi          = {10.1103/physrevb.104.024430},
  volume       = {104},
  year         = {2021},
}

@article{9778,
  abstract     = {The hippocampal mossy fiber synapse is a key synapse of the trisynaptic circuit. Post-tetanic potentiation (PTP) is the most powerful form of plasticity at this synaptic connection. It is widely believed that mossy fiber PTP is an entirely presynaptic phenomenon, implying that PTP induction is input-specific, and requires neither activity of multiple inputs nor stimulation of postsynaptic neurons. To directly test cooperativity and associativity, we made paired recordings between single mossy fiber terminals and postsynaptic CA3 pyramidal neurons in rat brain slices. By stimulating non-overlapping mossy fiber inputs converging onto single CA3 neurons, we confirm that PTP is input-specific and non-cooperative. Unexpectedly, mossy fiber PTP exhibits anti-associative induction properties. EPSCs show only minimal PTP after combined pre- and postsynaptic high-frequency stimulation with intact postsynaptic Ca2+ signaling, but marked PTP in the absence of postsynaptic spiking and after suppression of postsynaptic Ca2+ signaling (10 mM EGTA). PTP is largely recovered by inhibitors of voltage-gated R- and L-type Ca2+ channels, group II mGluRs, and vacuolar-type H+-ATPase, suggesting the involvement of retrograde vesicular glutamate signaling. Transsynaptic regulation of PTP extends the repertoire of synaptic computations, implementing a brake on mossy fiber detonation and a “smart teacher” function of hippocampal mossy fiber synapses.},
  author       = {Vandael, David H and Okamoto, Yuji and Jonas, Peter M},
  issn         = {2041-1723},
  journal      = {Nature Communications},
  keywords     = {general physics and astronomy, general biochemistry, genetics and molecular biology, general chemistry},
  number       = {1},
  publisher    = {Springer},
  title        = {{Transsynaptic modulation of presynaptic short-term plasticity in hippocampal mossy fiber synapses}},
  doi          = {10.1038/s41467-021-23153-5},
  volume       = {12},
  year         = {2021},
}

@article{9793,
  abstract     = {Astrocytes extensively infiltrate the neuropil to regulate critical aspects of synaptic development and function. This process is regulated by transcellular interactions between astrocytes and neurons via cell adhesion molecules. How astrocytes coordinate developmental processes among one another to parse out the synaptic neuropil and form non-overlapping territories is unknown. Here we identify a molecular mechanism regulating astrocyte-astrocyte interactions during development to coordinate astrocyte morphogenesis and gap junction coupling. We show that hepaCAM, a disease-linked, astrocyte-enriched cell adhesion molecule, regulates astrocyte competition for territory and morphological complexity in the developing mouse cortex. Furthermore, conditional deletion of Hepacam from developing astrocytes significantly impairs gap junction coupling between astrocytes and disrupts the balance between synaptic excitation and inhibition. Mutations in HEPACAM cause megalencephalic leukoencephalopathy with subcortical cysts in humans. Therefore, our findings suggest that disruption of astrocyte self-organization mechanisms could be an underlying cause of neural pathology.},
  author       = {Baldwin, Katherine T. and Tan, Christabel X. and Strader, Samuel T. and Jiang, Changyu and Savage, Justin T. and Elorza-Vidal, Xabier and Contreras, Ximena and Rülicke, Thomas and Hippenmeyer, Simon and Estévez, Raúl and Ji, Ru-Rong and Eroglu, Cagla},
  issn         = {1097-4199},
  journal      = {Neuron},
  number       = {15},
  pages        = {2427--2442.e10},
  publisher    = {Elsevier},
  title        = {{HepaCAM controls astrocyte self-organization and coupling}},
  doi          = {10.1016/j.neuron.2021.05.025},
  volume       = {109},
  year         = {2021},
}

@article{9815,
  abstract     = {The quantum bits (qubits) on which superconducting quantum computers are based have energy scales corresponding to photons with GHz frequencies. The energy of photons in the gigahertz domain is too low to allow transmission through the noisy room-temperature environment, where the signal would be lost in thermal noise. Optical photons, on the other hand, have much higher energies, and signals can be detected using highly efficient single-photon detectors. Transduction from microwave to optical frequencies is therefore a potential enabling technology for quantum devices. However, in such a device the optical pump can be a source of thermal noise and thus degrade the fidelity; the similarity of input microwave state to the output optical state. In order to investigate the magnitude of this effect we model the sub-Kelvin thermal behavior of an electro-optic transducer based on a lithium niobate whispering gallery mode resonator. We find that there is an optimum power level for a continuous pump, whilst pulsed operation of the pump increases the fidelity of the conversion.},
  author       = {Mobassem, Sonia and Lambert, Nicholas J. and Rueda Sanchez, Alfredo R and Fink, Johannes M and Leuchs, Gerd and Schwefel, Harald G.L.},
  issn         = {2058-9565},
  journal      = {Quantum Science and Technology},
  number       = {4},
  publisher    = {IOP Publishing},
  title        = {{Thermal noise in electro-optic devices at cryogenic temperatures}},
  doi          = {10.1088/2058-9565/ac0f36},
  volume       = {6},
  year         = {2021},
}

@article{9816,
  abstract     = {Aims: Mass antigen testing programs have been challenged because of an alleged insufficient specificity, leading to a large number of false positives. The objective of this study is to derive a lower bound of the specificity of the SD Biosensor Standard Q Ag-Test in large scale practical use.
Methods: Based on county data from the nationwide tests for SARS-CoV-2 in Slovakia between 31.10.–1.11. 2020 we calculate a lower confidence bound for the specificity. As positive test results were not systematically verified by PCR tests, we base the lower bound on a worst case assumption, assuming all positives to be false positives.
Results: 3,625,332 persons from 79 counties were tested. The lowest positivity rate was observed in the county of Rožňava where 100 out of 34307 (0.29%) tests were positive. This implies a test specificity of at least 99.6% (97.5% one-sided lower confidence bound, adjusted for multiplicity).
Conclusion: The obtained lower bound suggests a higher specificity compared to earlier studies in spite of the underlying worst case assumption and the application in a mass testing setting. The actual specificity is expected to exceed 99.6% if the prevalence in the respective regions was non-negligible at the time of testing. To our knowledge, this estimate constitutes the first bound obtained from large scale practical use of an antigen test.},
  author       = {Hledik, Michal and Polechova, Jitka and Beiglböck, Mathias and Herdina, Anna Nele and Strassl, Robert and Posch, Martin},
  issn         = {1932-6203},
  journal      = {PLoS ONE},
  number       = {7},
  publisher    = {Public Library of Science},
  title        = {{Analysis of the specificity of a COVID-19 antigen test in the Slovak mass testing program}},
  doi          = {10.1371/journal.pone.0255267},
  volume       = {16},
  year         = {2021},
}

@article{6965,
  abstract     = {The central object of investigation of this paper is the Hirzebruch class, a deformation of the Todd class, given by Hirzebruch (for smooth varieties). The generalization for singular varieties is due to Brasselet–Schürmann–Yokura. Following the work of Weber, we investigate its equivariant version for (possibly singular) toric varieties. The local decomposition of the Hirzebruch class to the fixed points of the torus action and a formula for the local class in terms of the defining fan are recalled. After this review part, we prove the positivity of local Hirzebruch classes for all toric varieties, thus proving false the alleged counterexample given by Weber.},
  author       = {Rychlewicz, Kamil P},
  issn         = {1469-2120},
  journal      = {Bulletin of the London Mathematical Society},
  number       = {2},
  pages        = {560--574},
  publisher    = {Wiley},
  title        = {{The positivity of local equivariant Hirzebruch class for toric varieties}},
  doi          = {10.1112/blms.12442},
  volume       = {53},
  year         = {2021},
}

@article{6995,
  abstract     = {Human brain organoids represent a powerful tool for the study of human neurological diseases particularly those that impact brain growth and structure. However, many neurological diseases lack obvious anatomical abnormalities, yet significantly impact neural network functions, raising the question of whether organoids possess sufficient neural network architecture and complexity to model these conditions. Here, we explore the network level functions of brain organoids using calcium sensor imaging and extracellular recording approaches that together reveal the existence of complex oscillatory network behaviors reminiscent of intact brain preparations. We further demonstrate strikingly abnormal epileptiform network activity in organoids derived from a Rett Syndrome patient despite only modest anatomical differences from isogenically matched controls, and rescue with an unconventional neuromodulatory drug Pifithrin-α. Together, these findings provide an essential foundation for the utilization of human brain organoids to study intact and disordered human brain network formation and illustrate their utility in therapeutic discovery.},
  author       = {Samarasinghe, Ranmal A. and Miranda, Osvaldo and Buth, Jessie E. and Mitchell, Simon and Ferando, Isabella and Watanabe, Momoko and Kurdian, Arinnae and Golshani, Peyman and Plath, Kathrin and Lowry, William E. and Parent, Jack M. and Mody, Istvan and Novitch, Bennett G.},
  issn         = {1546-1726},
  journal      = {Nature Neuroscience},
  pages        = {32},
  publisher    = {Springer Nature},
  title        = {{Identification of neural oscillations and epileptiform changes in human brain organoids}},
  doi          = {10.1038/s41593-021-00906-5},
  volume       = {24},
  year         = {2021},
}

@article{7463,
  abstract     = {Resting-state brain activity is characterized by the presence of neuronal avalanches showing absence of characteristic size. Such evidence has been interpreted in the context of criticality and associated with the normal functioning of the brain. A distinctive attribute of systems at criticality is the presence of long-range correlations. Thus, to verify the hypothesis that the brain operates close to a critical point and consequently assess deviations from criticality for diagnostic purposes, it is of primary importance to robustly and reliably characterize correlations in resting-state brain activity. Recent works focused on the analysis of narrow-band electroencephalography (EEG) and magnetoencephalography (MEG) signal amplitude envelope, showing evidence of long-range temporal correlations (LRTC) in neural oscillations. However, brain activity is a broadband phenomenon, and a significant piece of information useful to precisely discriminate between normal (critical) and pathological behavior (non-critical), may be encoded in the broadband spatio-temporal cortical dynamics. Here we propose to characterize the temporal correlations in the broadband brain activity through the lens of neuronal avalanches. To this end, we consider resting-state EEG and long-term MEG recordings, extract the corresponding neuronal avalanche sequences, and study their temporal correlations. We demonstrate that the broadband resting-state brain activity consistently exhibits long-range power-law correlations in both EEG and MEG recordings, with similar values of the scaling exponents. Importantly, although we observe that the avalanche size distribution depends on scale parameters, scaling exponents characterizing long-range correlations are quite robust. In particular, they are independent of the temporal binning (scale of analysis), indicating that our analysis captures intrinsic characteristics of the underlying dynamics. Because neuronal avalanches constitute a fundamental feature of neural systems with universal characteristics, the proposed approach may serve as a general, systems- and experiment-independent procedure to infer the existence of underlying long-range correlations in extended neural systems, and identify pathological behaviors in the complex spatio-temporal interplay of cortical rhythms.},
  author       = {Lombardi, Fabrizio and Shriki, Oren and Herrmann, Hans J and de Arcangelis, Lucilla},
  issn         = {1872-8286},
  journal      = {Neurocomputing},
  pages        = {657--666},
  publisher    = {Elsevier},
  title        = {{Long-range temporal correlations in the broadband resting state activity of the human brain revealed by neuronal avalanches}},
  doi          = {10.1016/j.neucom.2020.05.126},
  volume       = {461},
  year         = {2021},
}

@article{7551,
  abstract     = {Novelty facilitates formation of memories. The detection of novelty and storage of contextual memories are both mediated by the hippocampus, yet the mechanisms that link these two functions remain to be defined. Dentate granule cells (GCs) of the dorsal hippocampus fire upon novelty exposure forming engrams of contextual memory. However, their key excitatory inputs from the entorhinal cortex are not responsive to novelty and are insufficient to make dorsal GCs fire reliably. Here we uncover a powerful glutamatergic pathway to dorsal GCs from ventral hippocampal mossy cells (MCs) that relays novelty, and is necessary and sufficient for driving dorsal GCs activation. Furthermore, manipulation of ventral MCs activity bidirectionally regulates novelty-induced contextual memory acquisition. Our results show that ventral MCs activity controls memory formation through an intra-hippocampal interaction mechanism gated by novelty.},
  author       = {Fredes Tolorza, Felipe A and Silva Sifuentes, Maria A and Koppensteiner, Peter and Kobayashi, Kenta and Jösch, Maximilian A and Shigemoto, Ryuichi},
  journal      = {Current Biology},
  number       = {1},
  pages        = {P25--38.E5},
  publisher    = {Elsevier},
  title        = {{Ventro-dorsal hippocampal pathway gates novelty-induced contextual memory formation}},
  doi          = {10.1016/j.cub.2020.09.074},
  volume       = {31},
  year         = {2021},
}

@article{9822,
  abstract     = {Attachment of adhesive molecules on cell culture surfaces to restrict cell adhesion to defined areas and shapes has been vital for the progress of in vitro research. In currently existing patterning methods, a combination of pattern properties such as stability, precision, specificity, high-throughput outcome, and spatiotemporal control is highly desirable but challenging to achieve. Here, we introduce a versatile and high-throughput covalent photoimmobilization technique, comprising a light-dose-dependent patterning step and a subsequent functionalization of the pattern via click chemistry. This two-step process is feasible on arbitrary surfaces and allows for generation of sustainable patterns and gradients. The method is validated in different biological systems by patterning adhesive ligands on cell-repellent surfaces, thereby constraining the growth and migration of cells to the designated areas. We then implement a sequential photopatterning approach by adding a second switchable patterning step, allowing for spatiotemporal control over two distinct surface patterns. As a proof of concept, we reconstruct the dynamics of the tip/stalk cell switch during angiogenesis. Our results show that the spatiotemporal control provided by our “sequential photopatterning” system is essential for mimicking dynamic biological processes and that our innovative approach has great potential for further applications in cell science.},
  author       = {Zisis, Themistoklis and Schwarz, Jan and Balles, Miriam and Kretschmer, Maibritt and Nemethova, Maria and Chait, Remy P and Hauschild, Robert and Lange, Janina and Guet, Calin C and Sixt, Michael K and Zahler, Stefan},
  issn         = {1944-8252},
  journal      = {ACS Applied Materials and Interfaces},
  number       = {30},
  pages        = {35545–35560},
  publisher    = {American Chemical Society},
  title        = {{Sequential and switchable patterning for studying cellular processes under spatiotemporal control}},
  doi          = {10.1021/acsami.1c09850},
  volume       = {13},
  year         = {2021},
}

@article{9827,
  abstract     = {The Nearest neighbour search (NNS) is a fundamental problem in many application domains dealing with multidimensional data. In a concurrent setting, where dynamic modifications are allowed, a linearizable implementation of the NNS is highly desirable.This paper introduces the LockFree-kD-tree (LFkD-tree ): a lock-free concurrent kD-tree, which implements an abstract data type (ADT) that provides the operations Add, Remove, Contains, and NNS. Our implementation is linearizable. The operations in the LFkD-tree use single-word read and compare-and-swap (Image 1 ) atomic primitives, which are readily supported on available multi-core processors. We experimentally evaluate the LFkD-tree using several benchmarks comprising real-world and synthetic datasets. The experiments show that the presented design is scalable and achieves significant speed-up compared to the implementations of an existing sequential kD-tree and a recently proposed multidimensional indexing structure, PH-tree.},
  author       = {Chatterjee, Bapi and Walulya, Ivan and Tsigas, Philippas},
  issn         = {0304-3975},
  journal      = {Theoretical Computer Science},
  keywords     = {Concurrent data structure, kD-tree, Nearest neighbor search, Similarity search, Lock-free, Linearizability},
  pages        = {27--48},
  publisher    = {Elsevier},
  title        = {{Concurrent linearizable nearest neighbour search in LockFree-kD-tree}},
  doi          = {10.1016/j.tcs.2021.06.041},
  volume       = {886},
  year         = {2021},
}

@article{9828,
  abstract     = {Amplitude demodulation is a classical operation used in signal processing. For a long time, its effective applications in practice have been limited to narrowband signals. In this work, we generalize amplitude demodulation to wideband signals. We pose demodulation as a recovery problem of an oversampled corrupted signal and introduce special iterative schemes belonging to the family of alternating projection algorithms to solve it. Sensibly chosen structural assumptions on the demodulation outputs allow us to reveal the high inferential accuracy of the method over a rich set of relevant signals. This new approach surpasses current state-of-the-art demodulation techniques apt to wideband signals in computational efficiency by up to many orders of magnitude with no sacrifice in quality. Such performance opens the door for applications of the amplitude demodulation procedure in new contexts. In particular, the new method makes online and large-scale offline data processing feasible, including the calculation of modulator-carrier pairs in higher dimensions and poor sampling conditions, independent of the signal bandwidth. We illustrate the utility and specifics of applications of the new method in practice by using natural speech and synthetic signals.},
  author       = {Gabrielaitis, Mantas},
  issn         = {1941-0476},
  journal      = {IEEE Transactions on Signal Processing},
  pages        = {4039 -- 4054},
  publisher    = {Institute of Electrical and Electronics Engineers},
  title        = {{Fast and accurate amplitude demodulation of wideband signals}},
  doi          = {10.1109/TSP.2021.3087899},
  volume       = {69},
  year         = {2021},
}

@article{9829,
  abstract     = {In 2020, many in-person scientific events were canceled due to the COVID-19 pandemic, creating a vacuum in networking and knowledge exchange between scientists. To fill this void in scientific communication, a group of early career nanocrystal enthusiasts launched the virtual seminar series, News in Nanocrystals, in the summer of 2020. By the end of the year, the series had attracted over 850 participants from 46 countries. In this Nano Focus, we describe the process of organizing the News in Nanocrystals seminar series; discuss its growth, emphasizing what the organizers have learned in terms of diversity and accessibility; and provide an outlook for the next steps and future opportunities. This summary and analysis of experiences and learned lessons are intended to inform the broader scientific community, especially those who are looking for avenues to continue fostering discussion and scientific engagement virtually, both during the pandemic and after.},
  author       = {Baranov, Dmitry and Šverko, Tara and Moot, Taylor and Keller, Helena R. and Klein, Megan D. and Vishnu, E. K. and Balazs, Daniel and Shulenberger, Katherine E.},
  issn         = {1936-086X},
  journal      = {ACS Nano},
  number       = {7},
  pages        = {10743–10747},
  publisher    = {American Chemical Society},
  title        = {{News in Nanocrystals seminar: Self-assembly of early career researchers toward globally accessible nanoscience}},
  doi          = {10.1021/acsnano.1c03276},
  volume       = {15},
  year         = {2021},
}

@article{9874,
  abstract     = {Myocardial regeneration is restricted to early postnatal life, when mammalian cardiomyocytes still retain the ability to proliferate. The molecular cues that induce cell cycle arrest of neonatal cardiomyocytes towards terminally differentiated adult heart muscle cells remain obscure. Here we report that the miR-106b~25 cluster is higher expressed in the early postnatal myocardium and decreases in expression towards adulthood, especially under conditions of overload, and orchestrates the transition of cardiomyocyte hyperplasia towards cell cycle arrest and hypertrophy by virtue of its targetome. In line, gene delivery of miR-106b~25 to the mouse heart provokes cardiomyocyte proliferation by targeting a network of negative cell cycle regulators including E2f5, Cdkn1c, Ccne1 and Wee1. Conversely, gene-targeted miR-106b~25 null mice display spontaneous hypertrophic remodeling and exaggerated remodeling to overload by derepression of the prohypertrophic transcription factors Hand2 and Mef2d. Taking advantage of the regulatory function of miR-106b~25 on cardiomyocyte hyperplasia and hypertrophy, viral gene delivery of miR-106b~25 provokes nearly complete regeneration of the adult myocardium after ischemic injury. Our data demonstrate that exploitation of conserved molecular programs can enhance the regenerative capacity of the injured heart.},
  author       = {Raso, Andrea and Dirkx, Ellen and Sampaio-Pinto, Vasco and el Azzouzi, Hamid and Cubero, Ryan J and Sorensen, Daniel W. and Ottaviani, Lara and Olieslagers, Servé and Huibers, Manon M. and de Weger, Roel and Siddiqi, Sailay and Moimas, Silvia and Torrini, Consuelo and Zentillin, Lorena and Braga, Luca and Nascimento, Diana S. and da Costa Martins, Paula A. and van Berlo, Jop H. and Zacchigna, Serena and Giacca, Mauro and De Windt, Leon J.},
  issn         = {2041-1723},
  journal      = {Nature Communications},
  publisher    = {Springer Nature},
  title        = {{A microRNA program regulates the balance between cardiomyocyte hyperplasia and hypertrophy and stimulates cardiac regeneration}},
  doi          = {10.1038/s41467-021-25211-4},
  volume       = {12},
  year         = {2021},
}

@article{9877,
  abstract     = {Parent-of-origin–dependent gene expression in mammals and flowering plants results from differing chromatin imprints (genomic imprinting) between maternally and paternally inherited alleles. Imprinted gene expression in the endosperm of seeds is associated with localized hypomethylation of maternally but not paternally inherited DNA, with certain small RNAs also displaying parent-of-origin–specific expression. To understand the evolution of imprinting mechanisms in Oryza sativa (rice), we analyzed imprinting divergence among four cultivars that span both japonica and indica subspecies: Nipponbare, Kitaake, 93-11, and IR64. Most imprinted genes are imprinted across cultivars and enriched for functions in chromatin and transcriptional regulation, development, and signaling. However, 4 to 11% of imprinted genes display divergent imprinting. Analyses of DNA methylation and small RNAs revealed that endosperm-specific 24-nt small RNA–producing loci show weak RNA-directed DNA methylation, frequently overlap genes, and are imprinted four times more often than genes. However, imprinting divergence most often correlated with local DNA methylation epimutations (9 of 17 assessable loci), which were largely stable within subspecies. Small insertion/deletion events and transposable element insertions accompanied 4 of the 9 locally epimutated loci and associated with imprinting divergence at another 4 of the remaining 8 loci. Correlating epigenetic and genetic variation occurred at key regulatory regions—the promoter and transcription start site of maternally biased genes, and the promoter and gene body of paternally biased genes. Our results reinforce models for the role of maternal-specific DNA hypomethylation in imprinting of both maternally and paternally biased genes, and highlight the role of transposition and epimutation in rice imprinting evolution.},
  author       = {Rodrigues, Jessica A. and Hsieh, Ping-Hung and Ruan, Deling and Nishimura, Toshiro and Sharma, Manoj K. and Sharma, Rita and Ye, XinYi and Nguyen, Nicholas D. and Nijjar, Sukhranjan and Ronald, Pamela C. and Fischer, Robert L. and Zilberman, Daniel},
  issn         = {1091-6490},
  journal      = {Proceedings of the National Academy of Sciences of the United States of America},
  number       = {29},
  publisher    = {National Academy of Sciences},
  title        = {{Divergence among rice cultivars reveals roles for transposition and epimutation in ongoing evolution of genomic imprinting}},
  doi          = {10.1073/pnas.2104445118},
  volume       = {118},
  year         = {2021},
}

@article{9891,
  abstract     = {Extending on ideas of Lewin, Lieb, and Seiringer [Phys. Rev. B 100, 035127 (2019)], we present a modified “floating crystal” trial state for jellium (also known as the classical homogeneous electron gas) with density equal to a characteristic function. This allows us to show that three definitions of the jellium energy coincide in dimensions d ≥ 2, thus extending the result of Cotar and Petrache [“Equality of the Jellium and uniform electron gas next-order asymptotic terms for Coulomb and Riesz potentials,” arXiv: 1707.07664 (2019)] and Lewin, Lieb, and Seiringer [Phys. Rev. B 100, 035127 (2019)] that the three definitions coincide in dimension d ≥ 3. We show that the jellium energy is also equivalent to a “renormalized energy” studied in a series of papers by Serfaty and others, and thus, by the work of Bétermin and Sandier [Constr. Approximation 47, 39–74 (2018)], we relate the jellium energy to the order n term in the logarithmic energy of n points on the unit 2-sphere. We improve upon known lower bounds for this renormalized energy. Additionally, we derive formulas for the jellium energy of periodic configurations.},
  author       = {Lauritsen, Asbjørn Bækgaard},
  issn         = {1089-7658},
  journal      = {Journal of Mathematical Physics},
  keywords     = {Mathematical Physics, Statistical and Nonlinear Physics},
  number       = {8},
  publisher    = {AIP Publishing},
  title        = {{Floating Wigner crystal and periodic jellium configurations}},
  doi          = {10.1063/5.0053494},
  volume       = {62},
  year         = {2021},
}

@article{9906,
  abstract     = {Endometriosis is a common gynecological disorder characterized by ectopic growth of endometrium outside the uterus and is associated with chronic pain and infertility. We investigated the role of the long intergenic noncoding RNA 01133 (LINC01133) in endometriosis, an lncRNA that has been implicated in several types of cancer. We found that LINC01133 is upregulated in ectopic endometriotic lesions. As expression appeared higher in the epithelial endometrial layer, we performed a siRNA knockdown of LINC01133 in an endometriosis epithelial cell line. Phenotypic assays indicated that LINC01133 may promote proliferation and suppress cellular migration, and affect the cytoskeleton and morphology of the cells. Gene ontology analysis of differentially expressed genes indicated that cell proliferation and migration pathways were affected in line with the observed phenotype. We validated upregulation of p21 and downregulation of Cyclin A at the protein level, which together with the quantification of the DNA content using fluorescence-activated cell sorting (FACS) analysis indicated that the observed effects on cellular proliferation may be due to changes in cell cycle. Further, we found testis-specific protein kinase 1 (TESK1) kinase upregulation corresponding with phosphorylation and inactivation of actin severing protein Cofilin, which could explain changes in the cytoskeleton and cellular migration. These results indicate that endometriosis is associated with LINC01133 upregulation, which may affect pathogenesis via the cellular proliferation and migration pathways.},
  author       = {Yotova, Iveta and Hudson, Quanah J. and Pauler, Florian and Proestling, Katharina and Haslinger, Isabella and Kuessel, Lorenz and Perricos, Alexandra and Husslein, Heinrich and Wenzl, René},
  issn         = {1422-0067},
  journal      = {International Journal of Molecular Sciences},
  number       = {16},
  publisher    = {MDPI},
  title        = {{LINC01133 inhibits invasion and promotes proliferation in an endometriosis epithelial cell line}},
  doi          = {10.3390/ijms22168385},
  volume       = {22},
  year         = {2021},
}

@article{9907,
  abstract     = {DivIVA is a protein initially identified as a spatial regulator of cell division in the model organism Bacillus subtilis, but its homologues are present in many other Gram-positive bacteria, including Clostridia species. Besides its role as topological regulator of the Min system during bacterial cell division, DivIVA is involved in chromosome segregation during sporulation, genetic competence, and cell wall synthesis. DivIVA localizes to regions of high membrane curvature, such as the cell poles and cell division site, where it recruits distinct binding partners. Previously, it was suggested that negative curvature sensing is the main mechanism by which DivIVA binds to these specific regions. Here, we show that Clostridioides difficile DivIVA binds preferably to membranes containing negatively charged phospholipids, especially cardiolipin. Strikingly, we observed that upon binding, DivIVA modifies the lipid distribution and induces changes to lipid bilayers containing cardiolipin. Our observations indicate that DivIVA might play a more complex and so far unknown active role during the formation of the cell division septal membrane. },
  author       = {Labajová, Naďa and Baranova, Natalia S. and Jurásek, Miroslav and Vácha, Robert and Loose, Martin and Barák, Imrich},
  issn         = {1422-0067},
  journal      = {International Journal of Molecular Sciences},
  number       = {15},
  publisher    = {MDPI},
  title        = {{Cardiolipin-containing lipid membranes attract the bacterial cell division protein diviva}},
  doi          = {10.3390/ijms22158350},
  volume       = {22},
  year         = {2021},
}

