Institution
University of Texas at Austin
Education•Austin, Texas, United States•
About: University of Texas at Austin is a education organization based out in Austin, Texas, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 94352 authors who have published 206297 publications receiving 9070052 citations. The organization is also known as: UT-Austin & UT Austin.
Topics: Population, Poison control, Galaxy, Stars, Finite element method
Papers published on a yearly basis
Papers
More filters
••
[...]
TL;DR: The high level of collaboration on the gem5 project, combined with the previous success of the component parts and a liberal BSD-like license, make gem5 a valuable full-system simulation tool.
Abstract: The gem5 simulation infrastructure is the merger of the best aspects of the M5 [4] and GEMS [9] simulators. M5 provides a highly configurable simulation framework, multiple ISAs, and diverse CPU models. GEMS complements these features with a detailed and exible memory system, including support for multiple cache coherence protocols and interconnect models. Currently, gem5 supports most commercial ISAs (ARM, ALPHA, MIPS, Power, SPARC, and x86), including booting Linux on three of them (ARM, ALPHA, and x86).The project is the result of the combined efforts of many academic and industrial institutions, including AMD, ARM, HP, MIPS, Princeton, MIT, and the Universities of Michigan, Texas, and Wisconsin. Over the past ten years, M5 and GEMS have been used in hundreds of publications and have been downloaded tens of thousands of times. The high level of collaboration on the gem5 project, combined with the previous success of the component parts and a liberal BSD-like license, make gem5 a valuable full-system simulation tool.
4,039 citations
•
TL;DR: A novel recurrent convolutional architecture suitable for large-scale visual learning which is end-to-end trainable, and shows such models have distinct advantages over state-of-the-art models for recognition or generation which are separately defined and/or optimized.
Abstract: Models based on deep convolutional networks have dominated recent image interpretation tasks; we investigate whether models which are also recurrent, or "temporally deep", are effective for tasks involving sequences, visual and otherwise. We develop a novel recurrent convolutional architecture suitable for large-scale visual learning which is end-to-end trainable, and demonstrate the value of these models on benchmark video recognition tasks, image description and retrieval problems, and video narration challenges. In contrast to current models which assume a fixed spatio-temporal receptive field or simple temporal averaging for sequential processing, recurrent convolutional models are "doubly deep"' in that they can be compositional in spatial and temporal "layers". Such models may have advantages when target concepts are complex and/or training data are limited. Learning long-term dependencies is possible when nonlinearities are incorporated into the network state updates. Long-term RNN models are appealing in that they directly can map variable-length inputs (e.g., video frames) to variable length outputs (e.g., natural language text) and can model complex temporal dynamics; yet they can be optimized with backpropagation. Our recurrent long-term models are directly connected to modern visual convnet models and can be jointly trained to simultaneously learn temporal dynamics and convolutional perceptual representations. Our results show such models have distinct advantages over state-of-the-art models for recognition or generation which are separately defined and/or optimized.
3,935 citations
••
University of Utah1, University of Michigan2, The Royal Marsden NHS Foundation Trust3, Ohio State University4, Indiana University5, St. Jude Medical Center6, University of Queensland7, Beaumont Hospital8, BC Cancer Agency9, University of Rochester10, Harvard University11, American Society of Clinical Oncology12, National Institutes of Health13, Baylor College of Medicine14, Sungkyunkwan University15, University of the West of England16, Tohoku University17, Radboud University Nijmegen18, University of Toronto19, Saint Joseph Mercy Health System20, Mayo Clinic21, University of Washington22, Memorial Hospital of South Bend23, University of Texas at Austin24, Johns Hopkins University25
TL;DR: An international Expert Panel that conducted a systematic review and evaluation of the literature and developed recommendations for optimal IHC ER/PgR testing performance recommended that ER and PgR status be determined on all invasive breast cancers and breast cancer recurrences.
Abstract: Purpose To develop a guideline to improve the accuracy of immunohistochemical (IHC) estrogen receptor (ER) and progesterone receptor (PgR) testing in breast cancer and the utility of these receptors as predictive markers. Methods The American Society of Clinical Oncology and the College of American Pathologists convened an international Expert Panel that conducted a systematic review and evaluation of the literature in partnership with Cancer Care Ontario and developed recommendations for optimal IHC ER/PgR testing performance. Results Up to 20% of current IHC determinations of ER and PgR testing worldwide may be inaccurate (false negative or false positive). Most of the issues with testing have occurred because of variation in preanalytic variables, thresholds for positivity, and interpretation criteria. Recommendations The Panel recommends that ER and PgR status be determined on all invasive breast cancers and breast cancer recurrences. A testing algorithm that relies on accurate, reproducible assay performance is proposed. Elements to reliably reduce assay variation are specified. It is recommended that ER and PgR assays be considered positive if there are at least 1% positive tumor nuclei in the sample on testing in the presence of expected reactivity of internal (normal epithelial elements) and external controls. The absence of benefit from endocrine therapy for women with ER-negative invasive breast cancers has been confirmed in large overviews of randomized clinical trials.
3,902 citations
••
TL;DR: In this paper, a correlation between the mass Mbh of a galaxy's central black hole and the luminosity-weighted line-of-sight velocity dispersion σe within the half-light radius is described.
Abstract: We describe a correlation between the mass Mbh of a galaxy's central black hole and the luminosity-weighted line-of-sight velocity dispersion σe within the half-light radius. The result is based on a sample of 26 galaxies, including 13 galaxies with new determinations of black hole masses from Hubble Space Telescope measurements of stellar kinematics. The best-fit correlation is Mbh = 1.2(±0.2) × 108 M☉(σe/200 km s-1)3.75 (±0.3) over almost 3 orders of magnitude in Mbh; the scatter in Mbh at fixed σe is only 0.30 dex, and most of this is due to observational errors. The Mbh-σe relation is of interest not only for its strong predictive power but also because it implies that central black hole mass is constrained by and closely related to properties of the host galaxy's bulge.
3,901 citations
••
TL;DR: The authors' data provide clues as to how neurons and astrocytes differ in their ability to dynamically regulate glycolytic flux and lactate generation attributable to unique splicing of PKM2, the gene encoding the glycoleytic enzyme pyruvate kinase.
Abstract: The major cell classes of the brain differ in their developmental processes, metabolism, signaling, and function To better understand the functions and interactions of the cell types that comprise these classes, we acutely purified representative populations of neurons, astrocytes, oligodendrocyte precursor cells, newly formed oligodendrocytes, myelinating oligodendrocytes, microglia, endothelial cells, and pericytes from mouse cerebral cortex We generated a transcriptome database for these eight cell types by RNA sequencing and used a sensitive algorithm to detect alternative splicing events in each cell type Bioinformatic analyses identified thousands of new cell type-enriched genes and splicing isoforms that will provide novel markers for cell identification, tools for genetic manipulation, and insights into the biology of the brain For example, our data provide clues as to how neurons and astrocytes differ in their ability to dynamically regulate glycolytic flux and lactate generation attributable to unique splicing of PKM2, the gene encoding the glycolytic enzyme pyruvate kinase This dataset will provide a powerful new resource for understanding the development and function of the brain To ensure the widespread distribution of these datasets, we have created a user-friendly website (http://webstanfordedu/group/barres_lab/brain_rnaseqhtml) that provides a platform for analyzing and comparing transciption and alternative splicing profiles for various cell classes in the brain
3,891 citations
Authors
Showing all 95138 results
Name | H-index | Papers | Citations |
---|---|---|---|
George M. Whitesides | 240 | 1739 | 269833 |
Eugene Braunwald | 230 | 1711 | 264576 |
Yi Chen | 217 | 4342 | 293080 |
Robert J. Lefkowitz | 214 | 860 | 147995 |
Joseph L. Goldstein | 207 | 556 | 149527 |
Eric N. Olson | 206 | 814 | 144586 |
Hagop M. Kantarjian | 204 | 3708 | 210208 |
Rakesh K. Jain | 200 | 1467 | 177727 |
Francis S. Collins | 196 | 743 | 250787 |
Gordon B. Mills | 187 | 1273 | 186451 |
Scott M. Grundy | 187 | 841 | 231821 |
Michael S. Brown | 185 | 422 | 123723 |
Eric Boerwinkle | 183 | 1321 | 170971 |
Aaron R. Folsom | 181 | 1118 | 134044 |
Jiaguo Yu | 178 | 730 | 113300 |