798 research outputs found

    Bose-glass to Superfluid transition in the three-dimensional Bose-Hubbard Model

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    We present a Monte Carlo study of the Bose-glass to superfluid transition in the three-dimensional Bose-Hubbard model. Simulations are performed on the classical (3 + 1) dimensional link-current representation using the geometrical worm algorithm. Finite-size scaling analysis (on lattices as large as 16x16x16x512 sites) of the superfluid stiffness and the compressibility is consistent with a value of the dynamical critical exponent z = 3, in agreement with existing scaling and renormalization group arguments that z = d. We find also a value of Ī½=0.70(12)\nu = 0.70(12) for the correlation length exponent, satisfying the relation Ī½>=2/d\nu >= 2/d. However, a detailed study of the correlation functions, C(r, tau), at the quantum critical point are not consistent with this value of z. We speculate that this discrepancy could be due to the fact that the correlation functions have not reached their true asymptotic behavior because of the relatively small spatial extent of the lattices used in the present study.Comment: 9 pages, 8 figures, submitted to PR

    Kwame Dawes. Natural Mysticism: Towards a New Reggae Aesthetic.

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    Progranulin regulates neurogenesis in the developing vertebrate retina

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    We evaluated the expression and function of the microgliaā€specific growth factor, Progranulinā€a (Pgrnā€a) during developmental neurogenesis in the embryonic retina of zebrafish. At 24 hpf pgrnā€a is expressed throughout the forebrain, but by 48 hpf pgrnā€a is exclusively expressed by microglia and/or microglial precursors within the brain and retina. Knockdown of Pgrnā€a does not alter the onset of neurogenic programs or increase cell death, however, in its absence, neurogenesis is significantly delayedā€”retinal progenitors fail to exit the cell cycle at the appropriate developmental time and postmitotic cells do not acquire markers of terminal differentiation, and microglial precursors do not colonize the retina. Given the link between Progranulin and cell cycle regulation in peripheral tissues and transformed cells, we analyzed cell cycle kinetics among retinal progenitors following Pgrnā€a knockdown. Depleting Pgrnā€a results in a significant lengthening of the cell cycle. These data suggest that Pgrnā€a plays a dual role during nervous system development by governing the rate at which progenitors progress through the cell cycle and attracting microglial progenitors into the embryonic brain and retina. Collectively, these data show that Pgrnā€a governs neurogenesis by regulating cell cycle kinetics and the transition from proliferation to cell cycle exit and differentiation. Ā© 2017 The Authors. Developmental Neurobiology Published by Wiley Periodicals, Inc. Develop Neurobiol 77: 1114ā€“1129, 2017Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/138360/1/dneu22499.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/138360/2/dneu22499_am.pd

    Dynamic expression of the basic helix-loop-helix transcription factor neuroD in the rod and cone photoreceptor lineages in the retina of the embryonic and larval zebrafish

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    NeuroD is a basic helix-loop-helix (bHLH) transcription factor critical for determining neuronal cell fate and regulating withdrawal from the cell cycle. We showed previously that, in goldfish, neuroD is expressed in the rod photoreceptor lineage, and we inferred that neuroD is also expressed in a subset of amacrine cells and nascent cone photoreceptors. Here we extended that study by examining the temporal and spatial expression pattern of neuroD in the embryonic and larval zebrafish and by identifying the cell types that express this gene. NeuroD expression in the developing zebrafish retina is dynamic, spanning early retinogenesis and the maturation of cone photoreceptors. In early retinogenesis neuroD expression expands from a small patch in the ventronasal retina, through the remaining retinal neuroepithelium. As retinogenesis progresses, neuroD expression becomes restricted to amacrine cells, immature cones, and cells of rod and cone lineages. This expression achieves an adult pattern by 96 hours postfertilization (hpf), whereupon the temporal pattern of neuroD expression in central retina is spatially recapitulated at the germinative margin. The cellular pattern of expression suggests that neuroD regulates aspects of rod and cone genesis, but through separate cellular lineages. Furthermore, neuroD is coexpressed with the cone-rod-homeobox transcription factor (Crx) in putative cone progenitors and nascent cone photoreceptors, suggesting that, in the zebrafish retina, as in other vertebrate retinas, similar genetic cascades regulate photoreceptor genesis and maturation. J. Comp. Neurol. 501:1ā€“12, 2007. Ā© 2007 Wiley-Liss, Inc.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/55874/1/21150_ftp.pd

    A Framework for Deliberation Dialogues

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    Everythingā€™s Gone Green: The Environment of BPā€™s Narrative

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