@article{725,
  abstract     = {Individual computations and social interactions underlying collective behavior in groups of animals are of great ethological, behavioral, and theoretical interest. While complex individual behaviors have successfully been parsed into small dictionaries of stereotyped behavioral modes, studies of collective behavior largely ignored these findings; instead, their focus was on inferring single, mode-independent social interaction rules that reproduced macroscopic and often qualitative features of group behavior. Here, we bring these two approaches together to predict individual swimming patterns of adult zebrafish in a group. We show that fish alternate between an “active” mode, in which they are sensitive to the swimming patterns of conspecifics, and a “passive” mode, where they ignore them. Using a model that accounts for these two modes explicitly, we predict behaviors of individual fish with high accuracy, outperforming previous approaches that assumed a single continuous computation by individuals and simple metric or topological weighing of neighbors’ behavior. At the group level, switching between active and passive modes is uncorrelated among fish, but correlated directional swimming behavior still emerges. Our quantitative approach for studying complex, multi-modal individual behavior jointly with emergent group behavior is readily extensible to additional behavioral modes and their neural correlates as well as to other species.},
  author       = {Harpaz, Roy and Tkacik, Gasper and Schneidman, Elad},
  issn         = {00278424},
  journal      = {PNAS},
  number       = {38},
  pages        = {10149 -- 10154},
  publisher    = {National Academy of Sciences},
  title        = {{Discrete modes of social information processing predict individual behavior of fish in a group}},
  doi          = {10.1073/pnas.1703817114},
  volume       = {114},
  year         = {2017},
}

@article{726,
  abstract     = {The morphogenesis of branched organs remains a subject of abiding interest. Although much is known about the underlying signaling pathways, it remains unclear how macroscopic features of branched organs, including their size, network topology, and spatial patterning, are encoded. Here, we show that, in mouse mammary gland, kidney, and human prostate, these features can be explained quantitatively within a single unifying framework of branching and annihilating random walks. Based on quantitative analyses of large-scale organ reconstructions and proliferation kinetics measurements, we propose that morphogenesis follows from the proliferative activity of equipotent tips that stochastically branch and randomly explore their environment but compete neutrally for space, becoming proliferatively inactive when in proximity with neighboring ducts. These results show that complex branched epithelial structures develop as a self-organized process, reliant upon a strikingly simple but generic rule, without recourse to a rigid and deterministic sequence of genetically programmed events.},
  author       = {Hannezo, Edouard B and Scheele, Colinda and Moad, Mohammad and Drogo, Nicholas and Heer, Rakesh and Sampogna, Rosemary and Van Rheenen, Jacco and Simons, Benjamin},
  issn         = {00928674},
  journal      = {Cell},
  number       = {1},
  pages        = {242 -- 255},
  publisher    = {Cell Press},
  title        = {{A unifying theory of branching morphogenesis}},
  doi          = {10.1016/j.cell.2017.08.026},
  volume       = {171},
  year         = {2017},
}

@article{727,
  abstract     = {Actin filaments polymerizing against membranes power endocytosis, vesicular traffic, and cell motility. In vitro reconstitution studies suggest that the structure and the dynamics of actin networks respond to mechanical forces. We demonstrate that lamellipodial actin of migrating cells responds to mechanical load when membrane tension is modulated. In a steady state, migrating cell filaments assume the canonical dendritic geometry, defined by Arp2/3-generated 70° branch points. Increased tension triggers a dense network with a broadened range of angles, whereas decreased tension causes a shift to a sparse configuration dominated by filaments growing perpendicularly to the plasma membrane. We show that these responses emerge from the geometry of branched actin: when load per filament decreases, elongation speed increases and perpendicular filaments gradually outcompete others because they polymerize the shortest distance to the membrane, where they are protected from capping. This network-intrinsic geometrical adaptation mechanism tunes protrusive force in response to mechanical load.},
  author       = {Mueller, Jan and Szep, Gregory and Nemethova, Maria and De Vries, Ingrid and Lieber, Arnon and Winkler, Christoph and Kruse, Karsten and Small, John and Schmeiser, Christian and Keren, Kinneret and Hauschild, Robert and Sixt, Michael K},
  issn         = {00928674},
  journal      = {Cell},
  number       = {1},
  pages        = {188 -- 200},
  publisher    = {Cell Press},
  title        = {{Load adaptation of lamellipodial actin networks}},
  doi          = {10.1016/j.cell.2017.07.051},
  volume       = {171},
  year         = {2017},
}

@article{728,
  abstract     = {During animal development, cell-fate-specific changes in gene expression can modify the material properties of a tissue and drive tissue morphogenesis. While mechanistic insights into the genetic control of tissue-shaping events are beginning to emerge, how tissue morphogenesis and mechanics can reciprocally impact cell-fate specification remains relatively unexplored. Here we review recent findings reporting how multicellular morphogenetic events and their underlying mechanical forces can feed back into gene regulatory pathways to specify cell fate. We further discuss emerging techniques that allow for the direct measurement and manipulation of mechanical signals in vivo, offering unprecedented access to study mechanotransduction during development. Examination of the mechanical control of cell fate during tissue morphogenesis will pave the way to an integrated understanding of the design principles that underlie robust tissue patterning in embryonic development.},
  author       = {Chan, Chii and Heisenberg, Carl-Philipp J and Hiiragi, Takashi},
  issn         = {09609822},
  journal      = {Current Biology},
  number       = {18},
  pages        = {R1024 -- R1035},
  publisher    = {Cell Press},
  title        = {{Coordination of morphogenesis and cell fate specification in development}},
  doi          = {10.1016/j.cub.2017.07.010},
  volume       = {27},
  year         = {2017},
}

@article{7288,
  abstract     = {Nowadays commercial supercapacitors are based on purely capacitive storage at the porous carbons that are used for the electrodes. However, the limits that capacitive storage imposes on energy density calls to investigate new materials to improve the capacitance of the device. This new type of electrodes (e.g., RuO2, MnO2…) involves pseudo-capacitive faradaic redox processes with the solid material. Ion exchange with solid materials is, however, much slower than the adsorption process in capacitive storage and inevitably leads to significant loss of power. Faradaic process in the liquid state, in contrast can be similarly fast as capacitive processes due to the fast ion transport. Designing new devices with liquid like dynamics and improved specific capacitance is challenging. We present a new approach to increase the specific capacitance using biredox ionic liquids, where redox moieties are tethered to the electrolyte ions, allowing high redox concentrations and significant pseudo-capacitive storage in the liquid state. Anions and cations are functionalized with anthraquinone (AQ) and 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO) moieties, respectively. Glassy carbon, carbon-onion, and commercial activated carbon electrodes that exhibit different double layer structures and thus different diffusion dynamics were used to simultaneously study the electrochemical response of biredox ionic liquids at the positive and negative electrode.},
  author       = {Bodin, C. and Mourad, E. and Zigah, D. and Le Vot, S. and Freunberger, Stefan Alexander and Favier, F. and Fontaine, O.},
  issn         = {1359-6640},
  journal      = {Faraday Discussions},
  pages        = {393--404},
  publisher    = {Royal Society of Chemistry},
  title        = {{Biredox ionic liquids: New opportunities toward high performance supercapacitors}},
  doi          = {10.1039/c7fd00174f},
  volume       = {206},
  year         = {2017},
}

@article{7289,
  abstract     = {Aprotic sodium–O2 batteries require the reversible formation/dissolution of sodium superoxide (NaO2) on cycling. Poor cycle life has been associated with parasitic chemistry caused by the reactivity of electrolyte and electrode with NaO2, a strong nucleophile and base. Its reactivity can, however, not consistently explain the side reactions and irreversibility. Herein we show that singlet oxygen (1O2) forms at all stages of cycling and that it is a main driver for parasitic chemistry. It was detected in‐ and ex‐situ via a 1O2 trap that selectively and rapidly forms a stable adduct with 1O2. The 1O2 formation mechanism involves proton‐mediated superoxide disproportionation on discharge, rest, and charge below ca. 3.3 V, and direct electrochemical 1O2 evolution above ca. 3.3 V. Trace water, which is needed for high capacities also drives parasitic chemistry. Controlling the highly reactive singlet oxygen is thus crucial for achieving highly reversible cell operation.},
  author       = {Schafzahl, Lukas and Mahne, Nika and Schafzahl, Bettina and Wilkening, Martin and Slugovc, Christian and Borisov, Sergey M. and Freunberger, Stefan Alexander},
  issn         = {1433-7851},
  journal      = {Angewandte Chemie International Edition},
  number       = {49},
  pages        = {15728--15732},
  publisher    = {Wiley},
  title        = {{Singlet oxygen during cycling of the aprotic sodium-O2 battery}},
  doi          = {10.1002/anie.201709351},
  volume       = {56},
  year         = {2017},
}

@article{729,
  abstract     = {The cellular mechanisms allowing tissues to efficiently regenerate are not fully understood. In this issue of Developmental Cell, Cao et al. (2017)) discover that during zebrafish heart regeneration, epicardial cells at the leading edge of regenerating tissue undergo endoreplication, possibly due to increased tissue tension, thereby boosting their regenerative capacity.},
  author       = {Spiro, Zoltan P and Heisenberg, Carl-Philipp J},
  issn         = {15345807},
  journal      = {Developmental Cell},
  number       = {6},
  pages        = {559 -- 560},
  publisher    = {Cell Press},
  title        = {{Regeneration tensed up polyploidy takes the lead}},
  doi          = {10.1016/j.devcel.2017.09.008},
  volume       = {42},
  year         = {2017},
}

@article{7290,
  abstract     = {We report a family of Pt and Pd benzoporphyrin dyes with versatile photophysical properties and easy access from cheap and abundant chemicals. Attaching 4 or 8 alkylsulfone groups onto a meso-tetraphenyltetrabenzoporphyrin (TPTBP) macrocylcle renders the dyes highly soluble in organic solvents, photostable, and electron-deficient with the redox potential raised up to 0.65 V versus the parent porphyrin. The new dyes intensively absorb in the blue (Soret band, 440–480 nm) and in the red (Q-band, 620–650 nm) parts of the electromagnetic spectrum and show bright phosphorescence at room-temperature in the NIR with quantum yields up to 30% in solution. The small singlet–triplet energy gap yields unusually efficient thermally activated delayed fluorescence (TADF) at elevated temperatures in solution and in polymeric matrices with quantum yields as high as 27% at 120 °C, which is remarkable for benzoporphyrins. Apart from oxygen sensing, these properties enable unprecedented simultaneous, self-referenced oxygen and temperature sensing with a single indicator dye: whereas oxygen can be determined either via the decay time of phosphorescence or TADF, the temperature is accessed via the ratio of the two emissions. Moreover, the dyes are efficient sensitizers for triplet–triplet annihilation (TTA)-based upconversion making possible longer sensitization wavelength than the conventional benzoporphyrin complexes. The Pt-octa-sulfone dye also features interesting semireversible transformation in basic media, which generates new NIR absorbing species.},
  author       = {Zach, Peter W. and Freunberger, Stefan Alexander and Klimant, Ingo and Borisov, Sergey M.},
  issn         = {1944-8252},
  journal      = {ACS Applied Materials & Interfaces},
  number       = {43},
  pages        = {38008--38023},
  publisher    = {ACS},
  title        = {{Electron-deficient near-infrared Pt(II) and Pd(II) benzoporphyrins with dual phosphorescence and unusually efficient thermally activated delayed fluorescence: First demonstration of simultaneous oxygen and temperature sensing with a single emitter}},
  doi          = {10.1021/acsami.7b10669},
  volume       = {9},
  year         = {2017},
}

@article{7291,
  abstract     = {Na battery chemistries show poor passivation behavior of low voltage Na storage compounds and Na metal with organic carbonate‐based electrolytes adopted from Li‐ion batteries. Therefore, a suitable electrolyte remains a major challenge for establishing Na batteries. Here we report highly concentrated sodium bis(fluorosulfonyl)imide (NaFSI) in dimethoxyethane (DME) electrolytes and investigate them for Na metal and hard carbon anodes and intercalation cathodes. For a DME/NaFSI ratio of 2, a stable passivation of anode materials was found owing to the formation of a stable solid electrolyte interface, which was characterized spectroscopically. This permitted non‐dentritic Na metal cycling with approximately 98 % coulombic efficiency as shown for up to 300 cycles. The NaFSI/DME electrolyte may enable Na‐metal anodes and allows for more reliable assessment of electrode materials in Na‐ion half‐cells, as is demonstrated by comparing half‐cell cycling of hard carbon anodes and Na3V2(PO4)3 cathodes with a widely used carbonate and the NaFSI/DME electrolyte.},
  author       = {Schafzahl, Lukas and Hanzu, Ilie and Wilkening, Martin and Freunberger, Stefan Alexander},
  issn         = {1864-5631},
  journal      = {ChemSusChem},
  number       = {2},
  pages        = {401--408},
  publisher    = {Wiley},
  title        = {{An electrolyte for reversible cycling of sodium metal and intercalation compounds}},
  doi          = {10.1002/cssc.201601222},
  volume       = {10},
  year         = {2017},
}

@article{7292,
  abstract     = {Rechargeable Li–O2 batteries have amongst the highest formal energy and could store significantly more energy than other rechargeable batteries in practice if at least a large part of their promise could be realized. Realization, however, still faces many challenges than can only be overcome by fundamental understanding of the processes taking place. Here, we review recent advances in understanding the chemistry of the Li–O2 cathode and provide a perspective on dominant research needs. We put particular emphasis on issues that are often grossly misunderstood: realistic performance metrics and their reporting as well as identifying reversibility and quantitative measures to do so. Parasitic reactions are the prime obstacle for reversible cell operation and have recently been identified to be predominantly caused by singlet oxygen and not by reduced oxygen species as thought before. We discuss the far reaching implications of this finding on electrolyte and cathode stability, electrocatalysis, and future research needs.},
  author       = {Mahne, Nika and Fontaine, Olivier and Thotiyl, Musthafa Ottakam and Wilkening, Martin and Freunberger, Stefan Alexander},
  issn         = {2041-6539},
  journal      = {Chemical Science},
  number       = {10},
  pages        = {6716--6729},
  publisher    = {RSC},
  title        = {{Mechanism and performance of lithium–oxygen batteries – a perspective}},
  doi          = {10.1039/c7sc02519j},
  volume       = {8},
  year         = {2017},
}

@article{730,
  abstract     = {Neural responses are highly structured, with population activity restricted to a small subset of the astronomical range of possible activity patterns. Characterizing these statistical regularities is important for understanding circuit computation, but challenging in practice. Here we review recent approaches based on the maximum entropy principle used for quantifying collective behavior in neural activity. We highlight recent models that capture population-level statistics of neural data, yielding insights into the organization of the neural code and its biological substrate. Furthermore, the MaxEnt framework provides a general recipe for constructing surrogate ensembles that preserve aspects of the data, but are otherwise maximally unstructured. This idea can be used to generate a hierarchy of controls against which rigorous statistical tests are possible.},
  author       = {Savin, Cristina and Tkacik, Gasper},
  issn         = {09594388},
  journal      = {Current Opinion in Neurobiology},
  pages        = {120 -- 126},
  publisher    = {Elsevier},
  title        = {{Maximum entropy models as a tool for building precise neural controls}},
  doi          = {10.1016/j.conb.2017.08.001},
  volume       = {46},
  year         = {2017},
}

@article{731,
  abstract     = {Genetic variations in the oxytocin receptor gene affect patients with ASD and ADHD differently.},
  author       = {Novarino, Gaia},
  issn         = {19466234},
  journal      = {Science Translational Medicine},
  number       = {411},
  publisher    = {American Association for the Advancement of Science},
  title        = {{The science of love in ASD and ADHD}},
  doi          = {10.1126/scitranslmed.aap8168},
  volume       = {9},
  year         = {2017},
}

@article{732,
  abstract     = {Background: Social insects form densely crowded societies in environments with high pathogen loads, but have evolved collective defences that mitigate the impact of disease. However, colony-founding queens lack this protection and suffer high rates of mortality. The impact of pathogens may be exacerbated in species where queens found colonies together, as healthy individuals may contract pathogens from infectious co-founders. Therefore, we tested whether ant queens avoid founding colonies with pathogen-exposed conspecifics and how they might limit disease transmission from infectious individuals. Results: Using Lasius Niger queens and a naturally infecting fungal pathogen Metarhizium brunneum, we observed that queens were equally likely to found colonies with another pathogen-exposed or sham-treated queen. However, when one queen died, the surviving individual performed biting, burial and removal of the corpse. These undertaking behaviours were performed prophylactically, i.e. targeted equally towards non-infected and infected corpses, as well as carried out before infected corpses became infectious. Biting and burial reduced the risk of the queens contracting and dying from disease from an infectious corpse of a dead co-foundress. Conclusions: We show that co-founding ant queens express undertaking behaviours that, in mature colonies, are performed exclusively by workers. Such infection avoidance behaviours act before the queens can contract the disease and will therefore improve the overall chance of colony founding success in ant queens.},
  author       = {Pull, Christopher and Cremer, Sylvia},
  issn         = {14712148},
  journal      = {BMC Evolutionary Biology},
  number       = {1},
  publisher    = {BioMed Central},
  title        = {{Co-founding ant queens prevent disease by performing prophylactic undertaking behaviour}},
  doi          = {10.1186/s12862-017-1062-4},
  volume       = {17},
  year         = {2017},
}

@article{733,
  abstract     = {Let A and B be two N by N deterministic Hermitian matrices and let U be an N by N Haar distributed unitary matrix. It is well known that the spectral distribution of the sum H = A + UBU∗ converges weakly to the free additive convolution of the spectral distributions of A and B, as N tends to infinity. We establish the optimal convergence rate in the bulk of the spectrum.},
  author       = {Bao, Zhigang and Erdös, László and Schnelli, Kevin},
  journal      = {Advances in Mathematics},
  pages        = {251 -- 291},
  publisher    = {Academic Press},
  title        = {{Convergence rate for spectral distribution of addition of random matrices}},
  doi          = {10.1016/j.aim.2017.08.028},
  volume       = {319},
  year         = {2017},
}

@article{734,
  abstract     = {Social insect societies are long-standing models for understanding social behaviour and evolution. Unlike other advanced biological societies (such as the multicellular body), the component parts of social insect societies can be easily deconstructed and manipulated. Recent methodological and theoretical innovations have exploited this trait to address an expanded range of biological questions. We illustrate the broadening range of biological insight coming from social insect biology with four examples. These new frontiers promote open-minded, interdisciplinary exploration of one of the richest and most complex of biological phenomena: sociality.},
  author       = {Kennedy, Patrick and Baron, Gemma and Qiu, Bitao and Freitak, Dalial and Helantera, Heikki and Hunt, Edmund and Manfredini, Fabio and O'Shea Wheller, Thomas and Patalano, Solenn and Pull, Christopher and Sasaki, Takao and Taylor, Daisy and Wyatt, Christopher and Sumner, Seirian},
  issn         = {01695347},
  journal      = {Trends in Ecology and Evolution},
  number       = {11},
  pages        = {861 -- 872},
  publisher    = {Cell Press},
  title        = {{Deconstructing superorganisms and societies to address big questions in biology}},
  doi          = {10.1016/j.tree.2017.08.004},
  volume       = {32},
  year         = {2017},
}

@article{735,
  abstract     = {Cell-cell contact formation constitutes an essential step in evolution, leading to the differentiation of specialized cell types. However, remarkably little is known about whether and how the interplay between contact formation and fate specification affects development. Here, we identify a positive feedback loop between cell-cell contact duration, morphogen signaling, and mesendoderm cell-fate specification during zebrafish gastrulation. We show that long-lasting cell-cell contacts enhance the competence of prechordal plate (ppl) progenitor cells to respond to Nodal signaling, required for ppl cell-fate specification. We further show that Nodal signaling promotes ppl cell-cell contact duration, generating a positive feedback loop between ppl cell-cell contact duration and cell-fate specification. Finally, by combining mathematical modeling and experimentation, we show that this feedback determines whether anterior axial mesendoderm cells become ppl or, instead, turn into endoderm. Thus, the interdependent activities of cell-cell signaling and contact formation control fate diversification within the developing embryo.},
  author       = {Barone, Vanessa and Lang, Moritz and Krens, Gabriel and Pradhan, Saurabh and Shamipour, Shayan and Sako, Keisuke and Sikora, Mateusz K and Guet, Calin C and Heisenberg, Carl-Philipp J},
  issn         = {15345807},
  journal      = {Developmental Cell},
  number       = {2},
  pages        = {198 -- 211},
  publisher    = {Cell Press},
  title        = {{An effective feedback loop between cell-cell contact duration and morphogen signaling determines cell fate}},
  doi          = {10.1016/j.devcel.2017.09.014},
  volume       = {43},
  year         = {2017},
}

@article{736,
  abstract     = {The neurotransmitter receptor subtype, number, density, and distribution relative to the location of transmitter release sites are key determinants of signal transmission. AMPA-type ionotropic glutamate receptors (AMPARs) containing GluA3 and GluA4 subunits are prominently expressed in subsets of neurons capable of firing action potentials at high frequencies, such as auditory relay neurons. The auditory nerve (AN) forms glutamatergic synapses on two types of relay neurons, bushy cells (BCs) and fusiform cells (FCs) of the cochlear nucleus. AN-BC and AN-FC synapses have distinct kinetics; thus, we investigated whether the number, density, and localization of GluA3 and GluA4 subunits in these synapses are differentially organized using quantitative freeze-fracture replica immunogold labeling. We identify a positive correlation between the number of AMPARs and the size of AN-BC and AN-FC synapses. Both types of AN synapses have similar numbers of AMPARs; however, the AN-BC have a higher density of AMPARs than AN-FC synapses, because the AN-BC synapses are smaller. A higher number and density of GluA3 subunits are observed at AN-BC synapses, whereas a higher number and density of GluA4 subunits are observed at AN-FC synapses. The intrasynaptic distribution of immunogold labeling revealed that AMPAR subunits, particularly GluA3, are concentrated at the center of the AN-BC synapses. The central distribution of AMPARs is absent in GluA3-knockout mice, and gold particles are evenly distributed along the postsynaptic density. GluA4 gold labeling was homogenously distributed along both synapse types. Thus, GluA3 and GluA4 subunits are distributed at AN synapses in a target-cell-dependent manner.},
  author       = {Rubio, María and Matsui, Ko and Fukazawa, Yugo and Kamasawa, Naomi and Harada, Harumi and Itakura, Makoto and Molnár, Elek and Abe, Manabu and Sakimura, Kenji and Shigemoto, Ryuichi},
  issn         = {18632653},
  journal      = {Brain Structure and Function},
  number       = {8},
  pages        = {3375 -- 3393},
  publisher    = {Springer},
  title        = {{The number and distribution of AMPA receptor channels containing fast kinetic GluA3 and GluA4 subunits at auditory nerve synapses depend on the target cells}},
  doi          = {10.1007/s00429-017-1408-0},
  volume       = {222},
  year         = {2017},
}

@article{7360,
  abstract     = {Inflammation, which is a highly regulated host response against danger signals, may be harmful if it is excessive and deregulated. Ideally, anti-inflammatory therapy should autonomously commence as soon as possible after the onset of inflammation, should be controllable by a physician, and should not systemically block beneficial immune response in the long term. We describe a genetically encoded anti-inflammatory mammalian cell device based on a modular engineered genetic circuit comprising a sensor, an amplifier, a “thresholder” to restrict activation of a positive-feedback loop, a combination of advanced clinically used biopharmaceutical proteins, and orthogonal regulatory elements that linked modules into the functional device. This genetic circuit was autonomously activated by inflammatory signals, including endogenous cecal ligation and puncture (CLP)-induced inflammation in mice and serum from a systemic juvenile idiopathic arthritis (sIJA) patient, and could be reset externally by a chemical signal. The microencapsulated anti-inflammatory device significantly reduced the pathology in dextran sodium sulfate (DSS)-induced acute murine colitis, demonstrating a synthetic immunological approach for autonomous anti-inflammatory therapy.},
  author       = {Smole, Anže and Lainšček, Duško and Bezeljak, Urban and Horvat, Simon and Jerala, Roman},
  issn         = {1525-0016},
  journal      = {Molecular Therapy},
  number       = {1},
  pages        = {102--119},
  publisher    = {Elsevier},
  title        = {{A synthetic mammalian therapeutic gene circuit for sensing and suppressing inflammation}},
  doi          = {10.1016/j.ymthe.2016.10.005},
  volume       = {25},
  year         = {2017},
}

@article{737,
  abstract     = {We generalize Brazas’ topology on the fundamental group to the whole universal path space X˜ i.e., to the set of homotopy classes of all based paths. We develop basic properties of the new notion and provide a complete comparison of the obtained topology with the established topologies, in particular with the Lasso topology and the CO topology, i.e., the topology that is induced by the compact-open topology. It turns out that the new topology is the finest topology contained in the CO topology, for which the action of the fundamental group on the universal path space is a continuous group action.},
  author       = {Virk, Ziga and Zastrow, Andreas},
  issn         = {01668641},
  journal      = {Topology and its Applications},
  pages        = {186 -- 196},
  publisher    = {Elsevier},
  title        = {{A new topology on the universal path space}},
  doi          = {10.1016/j.topol.2017.09.015},
  volume       = {231},
  year         = {2017},
}

@article{739,
  abstract     = {We study the norm approximation to the Schrödinger dynamics of N bosons in with an interaction potential of the form . Assuming that in the initial state the particles outside of the condensate form a quasi-free state with finite kinetic energy, we show that in the large N limit, the fluctuations around the condensate can be effectively described using Bogoliubov approximation for all . The range of β is expected to be optimal for this large class of initial states.},
  author       = {Nam, Phan and Napiórkowski, Marcin M},
  issn         = {00217824},
  journal      = {Journal de Mathématiques Pures et Appliquées},
  number       = {5},
  pages        = {662 -- 688},
  publisher    = {Elsevier},
  title        = {{A note on the validity of Bogoliubov correction to mean field dynamics}},
  doi          = {10.1016/j.matpur.2017.05.013},
  volume       = {108},
  year         = {2017},
}