Institution
University of Arkansas
Education•Fayetteville, Arkansas, United States•
About: University of Arkansas is a education organization based out in Fayetteville, Arkansas, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 17225 authors who have published 33329 publications receiving 941102 citations. The organization is also known as: Arkansas & UA.
Topics: Population, Poison control, Quantum dot, Broiler, Supply chain
Papers published on a yearly basis
Papers
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TL;DR: For example, the authors found that contamination fear was best predicted by seven different disgust domains, thereby suggesting that the contamination fear is accounted for by generalized, rather than domain-specific, disgust elicitors.
202 citations
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University of California, Los Angeles1, Brigham Young University2, University of Arkansas3, University of Washington4, Kaiserslautern University of Technology5, Stanford University6, University of Western Australia7, University of Southern California8, Pennsylvania State University9, University of California, Berkeley10
TL;DR: The configurable computing community should focus on refining the emerging architectures, producing more effective software/hardware APIs, better tools for application development that incorporate the models of hardware reconfiguration, and effective benchmarking strategies.
Abstract: Configurable computing offers the potential of producing powerful new computing systems. Will current research overcome the dearth of commercial applicability to make such systems a reality? Unfortunately, no system to date has yet proven attractive or competitive enough to establish a commercial presence. We believe that ample opportunity exists for work in a broad range of areas. In particular, the configurable computing community should focus on refining the emerging architectures, producing more effective software/hardware APIs, better tools for application development that incorporate the models of hardware reconfiguration, and effective benchmarking strategies.
201 citations
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TL;DR: Green chemistry principles have gradually been implemented into the development of the synthetic chemistry of high-quality semiconductor nanocrystals and the resulting alternative routes are safe, simple, inexpensive, reproducible, versatile, "user friendly", and yield nanocrystal with well-controlled size, shape, and size/shape distribution.
Abstract: Green chemistry principles have gradually been implemented into the development of the synthetic chemistry of high-quality semiconductor nanocrystals. In comparison with the original organometallic approach, the resulting alternative routes are safe, simple, inexpensive, reproducible, versatile, "user friendly", and yield nanocrystals with well-controlled size, shape, and size/shape distribution. Further developments in this direction will promote the understanding of crystallization in general.
201 citations
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TL;DR: THYLAKOID FORMATION1 (THF1) is demonstrated in vivo as a Gα interaction partner that functions downstream of the plasma membrane–delimited heterotrimeric G-protein (GPA1) in a d-glucose signaling pathway and provides evidence of a sugar-signaling mechanism between plastids and the plasma membranes.
Abstract: Mutations in genes encoding components of the heterotrimeric G-protein complex were previously shown to confer altered sensitivity to increased levels of d-glucose. This suggests that G-protein coupling may be a novel sugar-signaling mechanism in Arabidopsis thaliana. THYLAKOID FORMATION1 (THF1) is here demonstrated in vivo as a Gα interaction partner that functions downstream of the plasma membrane–delimited heterotrimeric G-protein (GPA1) in a d-glucose signaling pathway. THF1 is a plastid protein localized to both the outer plastid membrane and the stroma. Contact between root plastidic THF1 and GPA1 at the plasma membrane occurs at sites where the plastid membrane abuts the plasma membrane, as demonstrated by Forster resonance energy transfer (FRET). A probable role for THF1 in sugar signaling is demonstrated by both biochemical and genetic evidence. Root growth in the thf1-1 null mutant is hypersensitive to exogenous d-glucose, and THF1-overexpressing roots are resistant to inhibition of growth rate by high d-glucose. Additionally, THF1 levels are rapidly degraded by d-glucose but not l-glucose. The interaction between THF1 and GPA1 has been confirmed by in vitro and in vivo coimmunoprecipitation, FRET analysis, and genetic epistasis and provides evidence of a sugar-signaling mechanism between plastids and the plasma membrane.
200 citations
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TL;DR: The authors found a negative association between CEO inside debt holdings and the volatility of future firm stock returns, R&D expenditures, and financial leverage, and a positive association between inside debt holders and the extent of diversification and asset liquidity.
200 citations
Authors
Showing all 17387 results
Name | H-index | Papers | Citations |
---|---|---|---|
Robert M. Califf | 196 | 1561 | 167961 |
Hugh A. Sampson | 147 | 816 | 76492 |
Stephen Boyd | 138 | 822 | 151205 |
Nikhil C. Munshi | 134 | 906 | 67349 |
Jian-Guo Bian | 128 | 1219 | 80964 |
Bart Barlogie | 126 | 779 | 57803 |
Robert R. Wolfe | 124 | 566 | 54000 |
Daniel B. Mark | 124 | 576 | 78385 |
E. Magnus Ohman | 124 | 622 | 68976 |
Benoît Roux | 120 | 493 | 62215 |
Robert C. Haddon | 112 | 577 | 52712 |
Rodney J. Bartlett | 109 | 700 | 56154 |
Baoshan Xing | 109 | 823 | 48944 |
Gareth J. Morgan | 109 | 1019 | 52957 |
Josep Dalmau | 108 | 568 | 49331 |