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Institution

United States Department of Energy

GovernmentWashington D.C., District of Columbia, United States
About: United States Department of Energy is a government organization based out in Washington D.C., District of Columbia, United States. It is known for research contribution in the topics: Catalysis & Coal. The organization has 13656 authors who have published 14177 publications receiving 556962 citations. The organization is also known as: DOE & Department of Energy.
Topics: Catalysis, Coal, Combustion, Adsorption, Hydrogen


Papers
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Journal ArticleDOI
TL;DR: In numerical experiments carried out on a turbulent compressible-flow problem with over one million unknowns, it is shown that increasing the time step to an intermediate value decreases both the error and the simulation time of the LSPG reduced-order model by an order of magnitude.

225 citations

Journal ArticleDOI
25 Oct 2013-Science
TL;DR: The results support that variation in the sequence or copy number of craniofacial enhancers may contribute to the spectrum of facial variation the authors find in human populations.
Abstract: The shape of the human face and skull is largely genetically determined. However, the genomic basis of craniofacial morphology is incompletely understood and hypothesized to involve protein-coding genes, as well as gene regulatory sequences. We used a combination of epigenomic profiling, in vivo characterization of candidate enhancer sequences in transgenic mice, and targeted deletion experiments to examine the role of distant-acting enhancers in craniofacial development. We identified complex regulatory landscapes consisting of enhancers that drive spatially complex developmental expression patterns. Analysis of mouse lines in which individual craniofacial enhancers had been deleted revealed significant alterations of craniofacial shape, demonstrating the functional importance of enhancers in defining face and skull morphology. These results demonstrate that enhancers are involved in craniofacial development and suggest that enhancer sequence variation contributes to the diversity of human facial morphology.

225 citations

Journal ArticleDOI
TL;DR: To assess the progression of the infant microbiota toward an adult-like state and to evaluate the contribution of maternal GIT bacteria to the infant gut, this work compares the infant’s microbiota with that of the mother at 1 and 11 months after delivery.
Abstract: Colonization of the gastrointestinal tract (GIT) of human infants with a suitable microbial community is essential for numerous aspects of health, but the progression of events by which this microbiota becomes established is poorly understood Here, we investigate two previously unexplored areas of microbiota development in infants: the deployment of functional capabilities at the community level and the population genetics of its most abundant genera To assess the progression of the infant microbiota toward an adult-like state and to evaluate the contribution of maternal GIT bacteria to the infant gut, we compare the infant’s microbiota with that of the mother at 1 and 11 months after delivery These comparisons reveal that the infant’s microbiota rapidly acquires and maintains the range of gene functions present in the mother, without replicating the phylogenetic composition of her microbiota Microdiversity analyses for Bacteroides and Bifidobacterium, two of the main microbiota constituents, reveal that by 11 months, the phylotypes detected in the infant are distinct from those in the mother, although the maternal Bacteroides phylotypes were transiently present at 1 month of age The configuration of genetic variants within these genera reveals populations far from equilibrium and likely to be undergoing rapid growth, consistent with recent population turnovers Such compositional turnovers and the associated loss of maternal phylotypes should limit the potential for long-term coadaptation between specific bacterial and host genotypes

225 citations

Journal ArticleDOI
TL;DR: In this article, a simple theoretical model is proposed for the reversible magnetization of type-II superconductors as a function of the applied field H for the entire field region between H and the principal axis.
Abstract: A simple theoretical model is proposed for the reversible magnetization of type-II superconductors as a function of the applied field H for the entire field region between ${\mathit{H}}_{\mathit{c}1}$ and ${\mathit{H}}_{\mathit{c}2}$. For H\ensuremath{\simeq}${\mathit{H}}_{\mathit{c}1}$, the theory reduces to a variational model, from which ${\mathit{H}}_{\mathit{c}1}$ can be accurately computed in the Ginzburg-Landau regime. In calculating the free energy, we include, in addition to the supercurrent kinetic energy and the magnetic-field energy, the kinetic-energy and the condensation-energy terms arising from suppression of the order parameter in the vortex core. The model is further extended to include anisotropy by introducing an effective-mass tensor for the case when H is parallel to one of the principal axes. The theory is compared to reversible-magnetization data on a ${\mathrm{YBa}}_{2}$${\mathrm{Cu}}_{3}$${\mathrm{O}}_{7}$ single crystal. The method permits an accurate determination of ${\mathit{H}}_{\mathit{c}2}$ versus temperature from measurements of the magnetization versus temperature at fixed magnetic field and explains why the measurements have different slopes in different fields, contrary to what might have been expected from the linear Abrikosov formula near ${\mathit{H}}_{\mathit{c}2}$. The deduced ${\mathit{dH}}_{\mathit{c}2}$/dT is (-1.65\ifmmode\pm\else\textpm\fi{}0.23) T/K for H parallel to the c axis near ${\mathit{T}}_{\mathit{c}}$, implying ${\ensuremath{\xi}}_{\mathit{a}\mathit{b}}$(0)=(17\ifmmode\pm\else\textpm\fi{}1) \AA{}.

224 citations

Journal ArticleDOI
11 Mar 2016-Science
TL;DR: A systems-level approach that integrates transcriptomic sequencing, proteomics, phenotype, and biochemical studies of relatively unexplored basal fungi is developed and identified several promising sequence-divergent enzyme candidates for lignocellulosic bioprocessing.
Abstract: The fungal kingdom is the source of almost all industrial enzymes in use for lignocellulose bioprocessing. We developed a systems-level approach that integrates transcriptomic sequencing, proteomics, phenotype, and biochemical studies of relatively unexplored basal fungi. Anaerobic gut fungi isolated from herbivores produce a large array of biomass-degrading enzymes that synergistically degrade crude, untreated plant biomass and are competitive with optimized commercial preparations from Aspergillus and Trichoderma. Compared to these model platforms, gut fungal enzymes are unbiased in substrate preference due to a wealth of xylan-degrading enzymes. These enzymes are universally catabolite-repressed and are further regulated by a rich landscape of noncoding regulatory RNAs. Additionally, we identified several promising sequence-divergent enzyme candidates for lignocellulosic bioprocessing.

223 citations


Authors

Showing all 13660 results

NameH-indexPapersCitations
Martin White1962038232387
Paul G. Richardson1831533155912
Jie Zhang1784857221720
Krzysztof Matyjaszewski1691431128585
Yang Gao1682047146301
David Eisenberg156697112460
Marvin Johnson1491827119520
Carlos Escobar148118495346
Joshua A. Frieman144609109562
Paul Jackson141137293464
Greg Landsberg1411709109814
J. Conway1401692105213
Pushpalatha C Bhat1391587105044
Julian Borrill139387102906
Cecilia Elena Gerber1381727106984
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20233
202223
2021633
2020601
2019654
2018598