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Austin, TX, United States

The University of Texas at Austin is a state research university and the flagship institution of The University of Texas System. Founded in 1883 as "The University of Texas," its campus is located in Austin—approximately 1 mile from the Texas State Capitol. The institution has the fifth-largest single-campus enrollment in the nation, with over 50,000 undergraduate and graduate students and over 24,000 faculty and staff. The university has been labeled one of the "Public Ivies," a publicly funded university considered as providing a quality of education comparable to those of the Ivy League.UT Austin was inducted into the American Association of Universities in 1929, becoming only the third university in the American South to be elected. It is a major center for academic research, with research expenditures exceeding $640 million for the 2009–2010 school year. The university houses seven museums and seventeen libraries, including the Lyndon Baines Johnson Library and Museum and the Blanton Museum of Art, and operates various auxiliary research facilities, such as the J. J. Pickle Research Campus and the McDonald Observatory. Among university faculty are recipients of the Nobel Prize, Pulitzer Prize, the Wolf Prize, and the National Medal of Science, as well as many other awards.UT Austin student athletes compete as the Texas Longhorns and are members of the Big 12 Conference. Its Longhorn Network is unique in that it is the only sports network featuring the college sports of a single university. The Longhorns have won four NCAA Division I National Football Championships, six NCAA Division I National Baseball Championships and has claimed more titles in men's and women's sports than any other school in the Big 12 since the league was founded in 1996. Current and former UT Austin athletes have won 130 Olympic medals, including 14 in Beijing in 2008 and 13 in London in 2012. The university was recognized by Sports Illustrated as "America's Best Sports College" in 2002. Wikipedia.


Vogel C.,New York University | Marcotte E.M.,University of Texas at Austin
Nature Reviews Genetics | Year: 2012

Recent advances in next-generation DNA sequencing and proteomics provide an unprecedented ability to survey mRNA and protein abundances. Such proteome-wide surveys are illuminating the extent to which different aspects of gene expression help to regulate cellular protein abundances. Current data demonstrate a substantial role for regulatory processes occurring after mRNA is made-that is, post-transcriptional, translational and protein degradation regulation-in controlling steady-state protein abundances. Intriguing observations are also emerging in relation to cells following perturbation, single-cell studies and the apparent evolutionary conservation of protein and mRNA abundances. Here, we summarize current understanding of the major factors regulating protein expression. © 2012 Macmillan Publishers Limited. All rights reserved. Source


Matz M.V.,University of Texas at Austin
Physiological Reviews | Year: 2010

Green fluorescent protein (GFP) from the jellyfish Aequorea victoria and its homologs from diverse marine animals are widely used as universal genetically encoded fluorescent labels. Many laboratories have focused their efforts on identification and development of fluorescent proteins with novel characteristics and enhanced properties, resulting in a powerful toolkit for visualization of structural organization and dynamic processes in living cells and organisms. The diversity of currently available fluorescent proteins covers nearly the entire visible spectrum, providing numerous alternative possibilities for multicolor labeling and studies of protein interactions. Photoactivatable fluorescent proteins enable tracking of photolabeled molecules and cells in space and time and can also be used for super-resolution imaging. Genetically encoded sensors make it possible to monitor the activity of enzymes and the concentrations of various analytes. Fast-maturing fluorescent proteins, cell clocks, and timers further expand the options for real time studies in living tissues. Here we focus on the structure, evolution, and function of GFP-like proteins and their numerous applications for in vivo imaging, with particular attention to recent techniques. Copyright © 2010 the American Physiological Society. Source


Andrews J.G.,University of Texas at Austin
IEEE Communications Magazine | Year: 2013

Imagine a world with more base stations than cell phones: this is where cellular technology is headed in 10-20 years. This mega-trend requires many fundamental differences in visualizing, modeling, analyzing, simulating, and designing cellular networks vs. the current textbook approach. In this article, the most important shifts are distilled down to seven key factors, with the implications described and new models and techniques proposed for some, while others are ripe areas for future exploration. © 1979-2012 IEEE. Source


Brodbelt J.S.,University of Texas at Austin
Chemical Society Reviews | Year: 2014

Photodissociation mass spectrometry combines the ability to activate and fragment ions using photons with the sensitive detection of the resulting product ions by mass spectrometry. This combination affords a versatile tool for characterization of biological molecules. The scope and breadth of photodissociation mass spectrometry have increased substantially over the past decade as new research groups have entered the field and developed a number of innovative applications that illustrate the ability of photodissociation to produce rich fragmentation patterns, to cleave bonds selectively, and to target specific molecules based on incorporation of chromophores. This review focuses on many of the key developments in photodissociation mass spectrometry over the past decade with a particular emphasis on its applications to biological molecules. This journal is © the Partner Organisations 2014. Source


Goodenough J.B.,University of Texas at Austin
Energy and Environmental Science | Year: 2014

The storage of electrical energy in a rechargeable battery is subject to the limitations of reversible chemical reactions in an electrochemical cell. The limiting constraints on the design of a rechargeable battery also depend on the application of the battery. Of particular interest for a sustainable modern society are (1) powering electric vehicles that can compete with cars powered by the internal combustion engine and (2) stationary storage of electrical energy from renewable energy sources that can compete with energy stored in fossil fuels. Existing design strategies for the rechargeable battery have enabled the wireless revolution and the plug-in hybrid electric car, but they show little promise of providing safe, adequate capacity with an acceptable shelf and cycle life to compete in cost and convenience with the chemical energy stored in fossil fuels. Electric vehicles that are charged overnight (plug-in vehicles) offer a distributed energy storage, but larger battery packs are needed for stationary storage of electrical energy generated from wind or solar farms and for stand-by power. This paper outlines the limitations of existing commercial strategies and some developing strategies that may overcome these limitations. © 2014 The Royal Society of Chemistry. Source

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