@article{9960,
  abstract     = {The control of many-body quantum dynamics in complex systems is a key challenge in the quest to reliably produce and manipulate large-scale quantum entangled states. Recently, quench experiments in Rydberg atom arrays [Bluvstein et al. Science 371, 1355 (2021)] demonstrated that coherent revivals associated with quantum many-body scars can be stabilized by periodic driving, generating stable subharmonic responses over a wide parameter regime. We analyze a simple, related model where these phenomena originate from spatiotemporal ordering in an effective Floquet unitary, corresponding to discrete time-crystalline behavior in a prethermal regime. Unlike conventional discrete time crystals, the subharmonic response exists only for Néel-like initial states, associated with quantum scars. We predict robustness to perturbations and identify emergent timescales that could be observed in future experiments. Our results suggest a route to controlling entanglement in interacting quantum systems by combining periodic driving with many-body scars.},
  author       = {Maskara, N. and Michailidis, Alexios and Ho, W. W. and Bluvstein, D. and Choi, S. and Lukin, M. D. and Serbyn, Maksym},
  issn         = {1079-7114},
  journal      = {Physical Review Letters},
  number       = {9},
  publisher    = {American Physical Society},
  title        = {{Discrete time-crystalline order enabled by quantum many-body scars: Entanglement steering via periodic driving}},
  doi          = {10.1103/PhysRevLett.127.090602},
  volume       = {127},
  year         = {2021},
}

@article{9961,
  abstract     = {The notion of Thouless energy plays a central role in the theory of Anderson localization. We investigate and compare the scaling of Thouless energy across the many-body localization (MBL) transition in a Floquet model. We use a combination of methods that are reliable on the ergodic side of the transition (e.g., spectral form factor) and methods that work on the MBL side (e.g., typical matrix elements of local operators) to obtain a complete picture of the Thouless energy behavior across the transition. On the ergodic side, Thouless energy decreases slowly with the system size, while at the transition it becomes comparable to the level spacing. Different probes yield consistent estimates of Thouless energy in their overlapping regime of applicability, giving the location of the transition point nearly free of finite-size drift. This work establishes a connection between different definitions of Thouless energy in a many-body setting and yields insights into the MBL transition in Floquet systems.},
  author       = {Sonner, Michael and Serbyn, Maksym and Papić, Zlatko and Abanin, Dmitry A.},
  issn         = {2469-9969},
  journal      = {Physical Review B},
  number       = {8},
  publisher    = {American Physical Society},
  title        = {{Thouless energy across the many-body localization transition in Floquet systems}},
  doi          = {10.1103/PhysRevB.104.L081112},
  volume       = {104},
  year         = {2021},
}

@article{9973,
  abstract     = {In this article we introduce a complete gradient estimate for symmetric quantum Markov semigroups on von Neumann algebras equipped with a normal faithful tracial state, which implies semi-convexity of the entropy with respect to the recently introduced noncommutative 2-Wasserstein distance. We show that this complete gradient estimate is stable under tensor products and free products and establish its validity for a number of examples. As an application we prove a complete modified logarithmic Sobolev inequality with optimal constant for Poisson-type semigroups on free group factors.},
  author       = {Wirth, Melchior and Zhang, Haonan},
  issn         = {1432-0916},
  journal      = {Communications in Mathematical Physics},
  keywords     = {Mathematical Physics, Statistical and Nonlinear Physics},
  pages        = {761–791},
  publisher    = {Springer Nature},
  title        = {{Complete gradient estimates of quantum Markov semigroups}},
  doi          = {10.1007/s00220-021-04199-4},
  volume       = {387},
  year         = {2021},
}

@unpublished{9978,
  abstract     = {Redox mediators could catalyse otherwise slow and energy-inefficient cycling of Li-S and Li-O 2 batteries by shuttling electrons/holes between the electrode and the solid insulating storage materials. For mediators to work efficiently they need to oxidize the solid with fast kinetics yet the lowest possible overpotential. Here, we found that when the redox potentials of mediators are tuned via, e.g., Li + concentration in the electrolyte, they exhibit distinct threshold potentials, where the kinetics accelerate several-fold within a range as small as 10 mV. This phenomenon is independent of types of mediators and electrolyte. The acceleration originates from the overpotentials required to activate fast Li + /e – extraction and the following chemical step at specific abundant surface facets. Efficient redox catalysis at insulating solids requires therefore carefully considering the surface conditions of the storage materials and electrolyte-dependent redox potentials, which may be tuned by salt concentrations or solvents.},
  author       = {Cao, Deqing and Shen, Xiaoxiao and Wang, Aiping and Yu, Fengjiao and Wu, Yuping and Shi, Siqi and Freunberger, Stefan Alexander and Chen, Yuhui},
  booktitle    = {Research Square},
  issn         = {2693-5015},
  keywords     = {Catalysis, Energy engineering, Materials theory and modeling},
  pages        = {21},
  publisher    = {Research Square},
  title        = {{Sharp kinetic acceleration potentials during mediated redox catalysis of insulators}},
  doi          = {10.21203/rs.3.rs-750965/v1},
  year         = {2021},
}

@unpublished{9980,
  abstract     = {Insufficient understanding of the mechanism that reversibly converts sulphur into lithium sulphide (Li2S) via soluble polysulphides (PS) hampers the realization of high performance lithium-sulphur cells. Typically Li2S formation is explained by direct electroreduction of a PS to Li2S; however, this is not consistent with the size of the insulating Li2S deposits. Here, we use in situ small and wide angle X-ray scattering (SAXS/WAXS) to track the growth and dissolution of crystalline and amorphous deposits from atomic to sub-micron scales during charge and discharge. Stochastic modelling based on the SAXS data allows quantification of the chemical phase evolution during discharge and charge. We show that Li2S deposits predominantly via disproportionation of transient, solid Li2S2 to form primary Li2S crystallites and solid Li2S4 particles. We further demonstrate that this process happens in reverse during charge. These findings show that the discharge capacity and rate capability in Li-S battery cathodes are therefore limited by mass transport through the increasingly tortuous network of Li2S / Li2S4 / carbon pores rather than electron transport through a passivating surface film.},
  author       = {Prehal, Christian and Talian, Sara Drvarič and Vizintin, Alen and Amenitsch, Heinz and Dominko, Robert and Freunberger, Stefan Alexander and Wood, Vanessa},
  booktitle    = {Research Square},
  keywords     = {Li2S, Lithium Sulphur Batteries, SAXS, WAXS},
  pages        = {21},
  title        = {{Mechanism of Li2S formation and dissolution in Lithium-Sulphur batteries}},
  doi          = {10.21203/rs.3.rs-818607/v1},
  year         = {2021},
}

@article{9981,
  abstract     = {The numerical simulation of dynamical phenomena in interacting quantum systems is a notoriously hard problem. Although a number of promising numerical methods exist, they often have limited applicability due to the growth of entanglement or the presence of the so-called sign problem. In this work, we develop an importance sampling scheme for the simulation of quantum spin dynamics, building on a recent approach mapping quantum spin systems to classical stochastic processes. The importance sampling scheme is based on identifying the classical trajectory that yields the largest contribution to a given quantum observable. An exact transformation is then carried out to preferentially sample trajectories that are close to the dominant one. We demonstrate that this approach is capable of reducing the temporal growth of fluctuations in the stochastic quantities, thus extending the range of accessible times and system sizes compared to direct sampling. We discuss advantages and limitations of the proposed approach, outlining directions
for further developments.},
  author       = {De Nicola, Stefano},
  issn         = {2666-9366},
  journal      = {SciPost Physics},
  keywords     = {General Physics and Astronomy},
  number       = {3},
  publisher    = {SciPost Foundation},
  title        = {{Importance sampling scheme for the stochastic simulation of quantum spin dynamics}},
  doi          = {10.21468/scipostphys.11.3.048},
  volume       = {11},
  year         = {2021},
}

@article{9985,
  abstract     = {AMPA receptor (AMPAR) abundance and positioning at excitatory synapses regulates the strength of transmission. Changes in AMPAR localisation can enact synaptic plasticity, allowing long-term information storage, and is therefore tightly controlled. Multiple mechanisms regulating AMPAR synaptic anchoring have been described, but with limited coherence or comparison between reports, our understanding of this process is unclear. Here, combining synaptic recordings from mouse hippocampal slices and super-resolution imaging in dissociated cultures, we compare the contributions of three AMPAR interaction domains controlling transmission at hippocampal CA1 synapses. We show that the AMPAR C-termini play only a modulatory role, whereas the extracellular N-terminal domain (NTD) and PDZ interactions of the auxiliary subunit TARP γ8 are both crucial, and each is sufficient to maintain transmission. Our data support a model in which γ8 accumulates AMPARs at the postsynaptic density, where the NTD further tunes their positioning. This interplay between cytosolic (TARP γ8) and synaptic cleft (NTD) interactions provides versatility to regulate synaptic transmission and plasticity.},
  author       = {Watson, Jake and Pinggera, Alexandra and Ho, Hinze and Greger, Ingo H.},
  issn         = {2041-1723},
  journal      = {Nature Communications},
  number       = {1},
  publisher    = {Nature Publishing Group},
  title        = {{AMPA receptor anchoring at CA1 synapses is determined by N-terminal domain and TARP γ8 interactions}},
  doi          = {10.1038/s41467-021-25281-4},
  volume       = {12},
  year         = {2021},
}

@article{9986,
  abstract     = {Size control is a fundamental question in biology, showing incremental complexity in plants, whose cells possess a rigid cell wall. The phytohormone auxin is a vital growth regulator with central importance for differential growth control. Our results indicate that auxin-reliant growth programs affect the molecular complexity of xyloglucans, the major type of cell wall hemicellulose in eudicots. Auxin-dependent induction and repression of growth coincide with reduced and enhanced molecular complexity of xyloglucans, respectively. In agreement with a proposed function in growth control, genetic interference with xyloglucan side decorations distinctly modulates auxin-dependent differential growth rates. Our work proposes that auxin-dependent growth programs have a spatially defined effect on xyloglucan’s molecular structure, which in turn affects cell wall mechanics and specifies differential, gravitropic hypocotyl growth.},
  author       = {Velasquez, Silvia Melina and Guo, Xiaoyuan and Gallemi, Marçal and Aryal, Bibek and Venhuizen, Peter and Barbez, Elke and Dünser, Kai Alexander and Darino, Martin and Pӗnčík, Aleš and Novák, Ondřej and Kalyna, Maria and Mouille, Gregory and Benková, Eva and Bhalerao, Rishikesh P. and Mravec, Jozef and Kleine-Vehn, Jürgen},
  issn         = {1422-0067},
  journal      = {International Journal of Molecular Sciences},
  keywords     = {auxin, growth, cell wall, xyloglucans, hypocotyls, gravitropism},
  number       = {17},
  publisher    = {MDPI},
  title        = {{Xyloglucan remodeling defines auxin-dependent differential tissue expansion in plants}},
  doi          = {10.3390/ijms22179222},
  volume       = {22},
  year         = {2021},
}

@article{9998,
  abstract     = {We define quantum equivariant K-theory of Nakajima quiver varieties. We discuss type A in detail as well as its connections with quantum XXZ spin chains and trigonometric Ruijsenaars-Schneider models. Finally we study a limit which produces a K-theoretic version of results of Givental and Kim, connecting quantum geometry of flag varieties and Toda lattice.},
  author       = {Koroteev, Peter and Pushkar, Petr and Smirnov, Andrey V. and Zeitlin, Anton M.},
  issn         = {1420-9020},
  journal      = {Selecta Mathematica},
  number       = {5},
  publisher    = {Springer Nature},
  title        = {{Quantum K-theory of quiver varieties and many-body systems}},
  doi          = {10.1007/s00029-021-00698-3},
  volume       = {27},
  year         = {2021},
}

@article{9999,
  abstract     = {The developmental strategies used by progenitor cells to endure a safe journey from their induction place towards the site of terminal differentiation are still poorly understood. Here we uncovered a progenitor cell allocation mechanism that stems from an incomplete process of epithelial delamination that allows progenitors to coordinate their movement with adjacent extra-embryonic tissues. Progenitors of the zebrafish laterality organ originate from the surface epithelial enveloping layer by an apical constriction process of cell delamination. During this process, progenitors retain long-term apical contacts that enable the epithelial layer to pull a subset of progenitors along their way towards the vegetal pole. The remaining delaminated progenitors follow apically-attached progenitors’ movement by a co-attraction mechanism, avoiding sequestration by the adjacent endoderm, ensuring their fate and collective allocation at the differentiation site. Thus, we reveal that incomplete delamination serves as a cellular platform for coordinated tissue movements during development. Impact Statement: Incomplete delamination serves as a cellular platform for coordinated tissue movements during development, guiding newly formed progenitor cell groups to the differentiation site.},
  author       = {Pulgar, Eduardo and Schwayer, Cornelia and Guerrero, Néstor and López, Loreto and Márquez, Susana and Härtel, Steffen and Soto, Rodrigo and Heisenberg, Carl Philipp and Concha, Miguel L.},
  issn         = {2050-084X},
  journal      = {eLife},
  keywords     = {cell delamination, apical constriction, dragging, mechanical forces, collective 18 locomotion, dorsal forerunner cells, zebrafish},
  publisher    = {eLife Sciences Publications},
  title        = {{Apical contacts stemming from incomplete delamination guide progenitor cell allocation through a dragging mechanism}},
  doi          = {10.7554/eLife.66483},
  volume       = {10},
  year         = {2021},
}

@article{12187,
  abstract     = {Genomes of germ cells present an existential vulnerability to organisms because germ cell mutations will propagate to future generations. Transposable elements are one source of such mutations. In the small flowering plant Arabidopsis, Long et al. found that genome methylation in the male germline is directed by small interfering RNAs (siRNAs) imperfectly transcribed from transposons (see the Perspective by Mosher). These germline siRNAs silence germline transposons and establish inherited methylation patterns in sperm, thus maintaining the integrity of the plant genome across generations.},
  author       = {Long, Jincheng and Walker, James and She, Wenjing and Aldridge, Billy and Gao, Hongbo and Deans, Samuel and Vickers, Martin and Feng, Xiaoqi},
  issn         = {1095-9203},
  journal      = {Science},
  keywords     = {Multidisciplinary},
  number       = {6550},
  publisher    = {American Association for the Advancement of Science},
  title        = {{Nurse cell-derived small RNAs define paternal epigenetic inheritance in Arabidopsis}},
  doi          = {10.1126/science.abh0556},
  volume       = {373},
  year         = {2021},
}

@article{8546,
  abstract     = {Brain neurons arise from relatively few progenitors generating an enormous diversity of neuronal types. Nonetheless, a cardinal feature of mammalian brain neurogenesis is thought to be that excitatory and inhibitory neurons derive from separate, spatially segregated progenitors. Whether bi-potential progenitors with an intrinsic capacity to generate both lineages exist and how such a fate decision may be regulated are unknown. Using cerebellar development as a model, we discover that individual progenitors can give rise to both inhibitory and excitatory lineages. Gradations of Notch activity determine the fates of the progenitors and their daughters. Daughters with the highest levels of Notch activity retain the progenitor fate, while intermediate levels of Notch activity generate inhibitory neurons, and daughters with very low levels of Notch signaling adopt the excitatory fate. Therefore, Notch-mediated binary cell fate choice is a mechanism for regulating the ratio of excitatory to inhibitory neurons from common progenitors.},
  author       = {Zhang, Tingting and Liu, Tengyuan and Mora, Natalia and Guegan, Justine and Bertrand, Mathilde and Contreras, Ximena and Hansen, Andi H and Streicher, Carmen and Anderle, Marica and Danda, Natasha and Tiberi, Luca and Hippenmeyer, Simon and Hassan, Bassem A.},
  issn         = { 2211-1247},
  journal      = {Cell Reports},
  number       = {10},
  publisher    = {Elsevier},
  title        = {{Generation of excitatory and inhibitory neurons from common progenitors via Notch signaling in the cerebellum}},
  doi          = {10.1016/j.celrep.2021.109208},
  volume       = {35},
  year         = {2021},
}

@article{10202,
  abstract     = {Zygotic genome activation (ZGA) initiates regionalized transcription underlying distinct cellular identities. ZGA is dependent upon dynamic chromatin architecture sculpted by conserved DNA-binding proteins. However, the direct mechanistic link between the onset of ZGA and the tissue-specific transcription remains unclear. Here, we have addressed the involvement of chromatin organizer Satb2 in orchestrating both processes during zebrafish embryogenesis. Integrative analysis of transcriptome, genome-wide occupancy and chromatin accessibility reveals contrasting molecular activities of maternally deposited and zygotically synthesized Satb2. Maternal Satb2 prevents premature transcription of zygotic genes by influencing the interplay between the pluripotency factors. By contrast, zygotic Satb2 activates transcription of the same group of genes during neural crest development and organogenesis. Thus, our comparative analysis of maternal versus zygotic function of Satb2 underscores how these antithetical activities are temporally coordinated and functionally implemented highlighting the evolutionary implications of the biphasic and bimodal regulation of landmark developmental transitions by a single determinant.},
  author       = {Pradhan, Saurabh J. and Reddy, Puli Chandramouli and Smutny, Michael and Sharma, Ankita and Sako, Keisuke and Oak, Meghana S. and Shah, Rini and Pal, Mrinmoy and Deshpande, Ojas and Dsilva, Greg and Tang, Yin and Mishra, Rakesh and Deshpande, Girish and Giraldez, Antonio J. and Sonawane, Mahendra and Heisenberg, Carl-Philipp J and Galande, Sanjeev},
  issn         = {2041-1723},
  journal      = {Nature Communications},
  number       = {1},
  publisher    = {Springer Nature},
  title        = {{Satb2 acts as a gatekeeper for major developmental transitions during early vertebrate embryogenesis}},
  doi          = {10.1038/s41467-021-26234-7},
  volume       = {12},
  year         = {2021},
}

@article{10177,
  abstract     = {Phonon polaritons (PhPs)—light coupled to lattice vibrations—with in-plane hyperbolic dispersion exhibit ray-like propagation with large wave vectors and enhanced density of optical states along certain directions on a surface. As such, they have raised a surge of interest, promising unprecedented manipulation of infrared light at the nanoscale in a planar circuitry. Here, we demonstrate focusing of in-plane hyperbolic PhPs propagating along thin slabs of α-MoO3. To that end, we developed metallic nanoantennas of convex geometries for both efficient launching and focusing of the polaritons. The foci obtained exhibit enhanced near-field confinement and absorption compared to foci produced by in-plane isotropic PhPs. Foci sizes as small as λp/4.5 = λ0/50 were achieved (λp is the polariton wavelength and λ0 is the photon wavelength). Focusing of in-plane hyperbolic polaritons introduces a first and most basic building block developing planar polariton optics using in-plane anisotropic van der Waals materials.},
  author       = {Martín-Sánchez, Javier and Duan, Jiahua and Taboada-Gutiérrez, Javier and Álvarez-Pérez, Gonzalo and Voronin, Kirill V. and Prieto Gonzalez, Ivan and Ma, Weiliang and Bao, Qiaoliang and Volkov, Valentyn S. and Hillenbrand, Rainer and Nikitin, Alexey Y. and Alonso-González, Pablo},
  issn         = {2375-2548},
  journal      = {Science Advances},
  number       = {41},
  publisher    = {American Association for the Advancement of Science},
  title        = {{Focusing of in-plane hyperbolic polaritons in van der Waals crystals with tailored infrared nanoantennas}},
  doi          = {10.1126/sciadv.abj0127},
  volume       = {7},
  year         = {2021},
}

@article{9607,
  abstract     = {While high risk of failure is an inherent part of developing innovative therapies, it can be reduced by adherence to evidence-based rigorous research practices. Numerous analyses conducted to date have clearly identified measures that need to be taken to improve research rigor. Supported through the European Union's Innovative Medicines Initiative, the EQIPD consortium has developed a novel preclinical research quality system that can be applied in both public and private sectors and is free for anyone to use. The EQIPD Quality System was designed to be suited to boost innovation by ensuring the generation of robust and reliable preclinical data while being lean, effective and not becoming a burden that could negatively impact the freedom to explore scientific questions. EQIPD defines research quality as the extent to which research data are fit for their intended use. Fitness, in this context, is defined by the stakeholders, who are the scientists directly involved in the research, but also their funders, sponsors, publishers, research tool manufacturers and collaboration partners such as peers in a multi-site research project. The essence of the EQIPD Quality System is the set of 18 core requirements that can be addressed flexibly, according to user-specific needs and following a user-defined trajectory. The EQIPD Quality System proposes guidance on expectations for quality-related measures, defines criteria for adequate processes (i.e., performance standards) and provides examples of how such measures can be developed and implemented. However, it does not prescribe any pre-determined solutions. EQIPD has also developed tools (for optional use) to support users in implementing the system and assessment services for those research units that successfully implement the quality system and seek formal accreditation. Building upon the feedback from users and continuous improvement, a sustainable EQIPD Quality System will ultimately serve the entire community of scientists conducting non-regulated preclinical research, by helping them generate reliable data that are fit for their intended use.},
  author       = {Bespalov, Anton and Bernard, René and Gilis, Anja and Gerlach, Björn and Guillén, Javier and Castagné, Vincent and Lefevre, Isabel A. and Ducrey, Fiona and Monk, Lee and Bongiovanni, Sandrine and Altevogt, Bruce and Arroyo-Araujo, María and Bikovski, Lior and De Bruin, Natasja and Castaños-Vélez, Esmeralda and Dityatev, Alexander and Emmerich, Christoph H. and Fares, Raafat and Ferland-Beckham, Chantelle and Froger-Colléaux, Christelle and Gailus-Durner, Valerie and Hölter, Sabine M. and Hofmann, Martine Cj and Kabitzke, Patricia and Kas, Martien Jh and Kurreck, Claudia and Moser, Paul and Pietraszek, Malgorzata and Popik, Piotr and Potschka, Heidrun and Prado Montes De Oca, Ernesto and Restivo, Leonardo and Riedel, Gernot and Ritskes-Hoitinga, Merel and Samardzic, Janko and Schunn, Michael and Stöger, Claudia and Voikar, Vootele and Vollert, Jan and Wever, Kimberley E. and Wuyts, Kathleen and Macleod, Malcolm R. and Dirnagl, Ulrich and Steckler, Thomas},
  issn         = {2050-084X},
  journal      = {eLife},
  publisher    = {eLife Sciences Publications},
  title        = {{Introduction to the EQIPD quality system}},
  doi          = {10.7554/eLife.63294},
  volume       = {10},
  year         = {2021},
}

@article{9038,
  abstract     = {Layered materials in which individual atomic layers are bonded by weak van der Waals forces (vdW materials) constitute one of the most prominent platforms for materials research. Particularly, polar vdW crystals, such as hexagonal boron nitride (h-BN), alpha-molybdenum trioxide (α-MoO3) or alpha-vanadium pentoxide (α-V2O5), have received significant attention in nano-optics, since they support phonon polaritons (PhPs)―light coupled to lattice vibrations― with strong electromagnetic confinement and low optical losses. Recently, correlative far- and near-field studies of α-MoO3 have been demonstrated as an effective strategy to accurately extract the permittivity of this material. Here, we use this accurately characterized and low-loss polaritonic material to sense its local dielectric environment, namely silica (SiO2), one of the most widespread substrates in nanotechnology. By studying the propagation of PhPs on α-MoO3 flakes with different thicknesses laying on SiO2 substrates via near-field microscopy (s-SNOM), we extract locally the infrared permittivity of SiO2. Our work reveals PhPs nanoimaging as a versatile method for the quantitative characterization of the local optical properties of dielectric substrates, crucial for understanding and predicting the response of nanomaterials and for the future scalability of integrated nanophotonic devices. },
  author       = {Aguilar-Merino, Patricia and Álvarez-Pérez, Gonzalo and Taboada-Gutiérrez, Javier and Duan, Jiahua and Prieto Gonzalez, Ivan and Álvarez-Prado, Luis Manuel and Nikitin, Alexey Y. and Martín-Sánchez, Javier and Alonso-González, Pablo},
  issn         = {2079-4991},
  journal      = {Nanomaterials},
  number       = {1},
  publisher    = {MDPI},
  title        = {{Extracting the infrared permittivity of SiO2 substrates locally by near-field imaging of phonon polaritons in a van der Waals crystal}},
  doi          = {10.3390/nano11010120},
  volume       = {11},
  year         = {2021},
}

@article{9601,
  abstract     = {In mammalian genomes, differentially methylated regions (DMRs) and histone marks including trimethylation of histone 3 lysine 27 (H3K27me3) at imprinted genes are asymmetrically inherited to control parentally-biased gene expression. However, neither parent-of-origin-specific transcription nor imprints have been comprehensively mapped at the blastocyst stage of preimplantation development. Here, we address this by integrating transcriptomic and epigenomic approaches in mouse preimplantation embryos. We find that seventy-one genes exhibit previously unreported parent-of-origin-specific expression in blastocysts (nBiX: novel blastocyst-imprinted expressed). Uniparental expression of nBiX genes disappears soon after implantation. Micro-whole-genome bisulfite sequencing (µWGBS) of individual uniparental blastocysts detects 859 DMRs. We further find that 16% of nBiX genes are associated with a DMR, whereas most are associated with parentally-biased H3K27me3, suggesting a role for Polycomb-mediated imprinting in blastocysts. nBiX genes are clustered: five clusters contained at least one published imprinted gene, and five clusters exclusively contained nBiX genes. These data suggest that early development undergoes a complex program of stage-specific imprinting involving different tiers of regulation.},
  author       = {Santini, Laura and Halbritter, Florian and Titz-Teixeira, Fabian and Suzuki, Toru and Asami, Maki and Ma, Xiaoyan and Ramesmayer, Julia and Lackner, Andreas and Warr, Nick and Pauler, Florian and Hippenmeyer, Simon and Laue, Ernest and Farlik, Matthias and Bock, Christoph and Beyer, Andreas and Perry, Anthony C.F. and Leeb, Martin},
  issn         = {2041-1723},
  journal      = {Nature Communications},
  number       = {1},
  publisher    = {Springer Nature},
  title        = {{Genomic imprinting in mouse blastocysts is predominantly associated with H3K27me3}},
  doi          = {10.1038/s41467-021-23510-4},
  volume       = {12},
  year         = {2021},
}

@article{9761,
  abstract     = {The important roles of mitochondrial function and dysfunction in the process of neurodegeneration are widely acknowledged. Retinal ganglion cells (RGCs) appear to be a highly vulnerable neuronal cell type in the central nervous system with respect to mitochondrial dysfunction but the actual reasons for this are still incompletely understood. These cells have a unique circumstance where unmyelinated axons must bend nearly 90° to exit the eye and then cross a translaminar pressure gradient before becoming myelinated in the optic nerve. This region, the optic nerve head, contains some of the highest density of mitochondria present in these cells. Glaucoma represents a perfect storm of events occurring at this location, with a combination of changes in the translaminar pressure gradient and reassignment of the metabolic support functions of supporting glia, which appears to apply increased metabolic stress to the RGC axons leading to a failure of axonal transport mechanisms. However, RGCs themselves are also extremely sensitive to genetic mutations, particularly in genes affecting mitochondrial dynamics and mitochondrial clearance. These mutations, which systemically affect the mitochondria in every cell, often lead to an optic neuropathy as the sole pathologic defect in affected patients. This review summarizes knowledge of mitochondrial structure and function, the known energy demands of neurons in general, and places these in the context of normal and pathological characteristics of mitochondria attributed to RGCs. },
  author       = {Muench, Nicole A. and Patel, Sonia and Maes, Margaret E and Donahue, Ryan J. and Ikeda, Akihiro and Nickells, Robert W.},
  issn         = {2073-4409},
  journal      = {Cells},
  number       = {7},
  publisher    = {MDPI},
  title        = {{The influence of mitochondrial dynamics and function on retinal ganglion cell susceptibility in optic nerve disease}},
  doi          = {10.3390/cells10071593},
  volume       = {10},
  year         = {2021},
}

@article{9254,
  abstract     = {Auxin is a key regulator of plant growth and development. Local auxin biosynthesis and intercellular transport generates regional gradients in the root that are instructive for processes such as specification of developmental zones that maintain root growth and tropic responses. Here we present a toolbox to study auxin-mediated root development that features: (i) the ability to control auxin synthesis with high spatio-temporal resolution and (ii) single-cell nucleus tracking and morphokinetic analysis infrastructure. Integration of these two features enables cutting-edge analysis of root development at single-cell resolution based on morphokinetic parameters under normal growth conditions and during cell-type-specific induction of auxin biosynthesis. We show directional auxin flow in the root and refine the contributions of key players in this process. In addition, we determine the quantitative kinetics of Arabidopsis root meristem skewing, which depends on local auxin gradients but does not require PIN2 and AUX1 auxin transporter activities. Beyond the mechanistic insights into root development, the tools developed here will enable biologists to study kinetics and morphology of various critical processes at the single cell-level in whole organisms.},
  author       = {Hu, Yangjie and Omary, Moutasem and Hu, Yun and Doron, Ohad and Hörmayer, Lukas and Chen, Qingguo and Megides, Or and Chekli, Ori and Ding, Zhaojun and Friml, Jiří and Zhao, Yunde and Tsarfaty, Ilan and Shani, Eilon},
  issn         = {2041-1723},
  journal      = {Nature Communications},
  publisher    = {Springer Nature},
  title        = {{Cell kinetics of auxin transport and activity in Arabidopsis root growth and skewing}},
  doi          = {10.1038/s41467-021-21802-3},
  volume       = {12},
  year         = {2021},
}

@article{9821,
  abstract     = {Heart rate variability (hrv) is a physiological phenomenon of the variation in the length of the time interval between consecutive heartbeats. In many cases it could be an indicator of the development of pathological states. The classical approach to the analysis of hrv includes time domain methods and frequency domain methods. However, attempts are still being made to define new and more effective hrv assessment tools. Persistent homology is a novel data analysis tool developed in the recent decades that is rooted at algebraic topology. The Topological Data Analysis (TDA) approach focuses on examining the shape of the data in terms of connectedness and holes, and has recently proved to be very effective in various fields of research. In this paper we propose the use of persistent homology to the hrv analysis. We recall selected topological descriptors used in the literature and we introduce some new topological descriptors that reflect the specificity of hrv, and we discuss their relation to the standard hrv measures. In particular, we show that this novel approach provides a collection of indices that might be at least as useful as the classical parameters in differentiating between series of beat-to-beat intervals (RR-intervals) in healthy subjects and patients suffering from a stroke episode.},
  author       = {Graff, Grzegorz and Graff, Beata and Pilarczyk, Pawel and Jablonski, Grzegorz and Gąsecki, Dariusz and Narkiewicz, Krzysztof},
  issn         = {1932-6203},
  journal      = {PLoS ONE},
  number       = {7},
  publisher    = {Public Library of Science},
  title        = {{Persistent homology as a new method of the assessment of heart rate variability}},
  doi          = {10.1371/journal.pone.0253851},
  volume       = {16},
  year         = {2021},
}

