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Institution

Texas A&M University

EducationCollege Station, Texas, United States
About: Texas A&M University is a education organization based out in College Station, Texas, United States. It is known for research contribution in the topics: Population & Gene. The organization has 72169 authors who have published 164372 publications receiving 5764236 citations.


Papers
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Journal ArticleDOI
TL;DR: The authors empirically examined how capital affects a bank's performance (survival and market share), and how this effect varies across banking crises, market crises, and normal times that occurred in the U.S over the past quarter century.
Abstract: This paper empirically examines how capital affects a bank’s performance (survival and market share), and how this effect varies across banking crises, market crises, and normal times that occurred in the U.S. over the past quarter century. We have two main results. First, capital helps small banks to increase their probability of survival and market share at all times (during banking crises, market crises, and normal times). Second, capital enhances the performance of medium and large banks primarily during banking crises. Additional tests explore channels through which capital generates the documented effects. Numerous robustness checks and additional tests are performed.

1,080 citations

Book
16 Jun 2013
TL;DR: Results for Curvilinear Coordinates III are presented, showing clear trends in 3-D Incompressible Elasticity and Cellular Responses to Applied Loads and in Constitutive Framework, respectively.
Abstract: 1. INTRODUCTION. 1.1 Historical Prelude, 1.2 Basic Cell Biology, 1.3 The Extracellular Matrix, 1.4 Soft Tissue Behavior, 1.5 Needs and General Approach, 1.6 Exercises, 1.7 References. 2. MATHEMATICAL PRELIMINARIES 2.1 A Direct Tensor Notation, 2.2 Cartesian Components, 2.3 Further Results in Tensor Calculus, 2.4 Orthogonal Curvilinear Components, 2.5 Matrix Methods, 2.6 Exercises, 2.7 References, 3. CONTINUUM MECHANICS 3.1 Kinematics, 3.2 Forces, Tractions and Stresses, 3.3 Balance Relations, 3.4 Constitutive Formulations, 3.5 Boundary and Initial Conditions, 3.6 Exercises, 3.7 References, 4. FINITE ELASTICITY 4.1 Introduction, 4.2 Incompressible Isotropic Elasticity, 4.3 Solutions in 3-D Incompressible Elasticity, 4.4 Compressible Isotropic Elasticity, 4.5 Membrane Hyperelasticity, 4.6 Exercises, 4.7 References 5. EXPERIMENTAL METHODS 5.1 General Philosophy, 5.2 Measurement of Strain, 5.3 Measurement of Applied Loads, 5.4 Testing Conditions, 5.5 Parameter Estimation and Statistics, 5.6 Exercises, 5.7 References 6. Finite Element Methods 6.1 Fundamental Equations, 6.2 Interpolation, Integration, and Solvers, 6.3 An Illustrative Formulation, 6.4 Inflation of a Membrane, 6.5 Inverse Finite Elements, 6.6 Exercises, 6.7 References PART II - VASCULAR MECHANICS 7. THE NORMAL ARTERIAL WALL 7.1 Structure and Function, 7.2 General Characteristics, 7.3 Constitutive Framework, 7.4 Experimental Methods, 7.5 Specific Constitutive Relations, 7.6 Stress Analyses, 7.7 Exercises, 7.8 References 8. VASCULAR DISORDERS 8.1 Hypertension, 8.2 Intracranial Aneurysms, 8.3 Atherosclerosis, 8.4 Aortic Aneurysms, 8.5 Additional Topics, 8.6 Exercises, 8.7 References 9. VASCULAR ADAPTATION 9.1 Mechanical Preliminaries, 9.2 Cellular Responses to Applied Loads, 9.3 Arterial Response to Hypertension, 9.4 Arterial Response to Altered Flow, 9.5 Vessel Response to Injury, 9.6 Veins as Arterial Grafts, 9.7 Aging, 9.8 Exercises, 9.9 References PART III CARDIAC MECHANICS 10. THE NORMAL HEART 10.1 Structure and Function, 10.2 General Characteristics, 10.3 Constitutive Framework, 10.4 Constitutive Relations, 10.5 Stress Analyses, 10.6 Exercises, 10.7 References 11. EPILOGUE APPENDICES I. Nomenclature, Abbreviations, and Conversions II. Results for Curvilinear Coordinates III. Material Frame Indifference 11. CARDIAC DISORDERS 11.1 Ischemia 11.2 Volume Overload 11.3 Hypertrophy 11.4 Cardiac Aneurysms 11.5 Additional Topics

1,079 citations

Journal ArticleDOI
TL;DR: Using a meta-correlation matrix, the authors found that trait GO predicted job performance above and beyond cognitive ability and personality and demonstrate the value of GO to organizational researchers.
Abstract: The authors present an empirical review of the literature concerning trait and state goal orientation (GO). Three dimensions of GO were examined: learning, prove performance, and avoid performance along with presumed antecedents and proximal and distal consequences of these dimensions. Antecedent variables included cognitive ability, implicit theory of intelligence, need for achievement, self-esteem, general self-efficacy, and the Big Five personality characteristics. Proximal consequences included state GO, task-specific self-efficacy, self-set goal level, learning strategies, feedback seeking, and state anxiety. Distal consequences included learning, academic performance, task performance, and job performance. Generally speaking, learning GO was positively correlated, avoid performance GO was negatively correlated, and prove performance GO was uncorrelated with these variables. Consistent with theory, state GO tended to have stronger relationships with the distal consequences than did trait GO. Finally, using a meta-correlation matrix, the authors found that trait GO predicted job performance above and beyond cognitive ability and personality. These results demonstrate the value of GO to organizational researchers.

1,078 citations

Journal ArticleDOI
Kathryn G. Roberts1, Yongjin Li, Debbie Payne-Turner1, Richard C. Harvey1, Yung-Li Yang1, Dehua Pei, Kelly McCastlain1, Li Ding2, Li Ding3, Changxue Lu3, Changxue Lu2, Guangchun Song1, Jing Ma1, Jared Becksfort, Michael Rusch, S. C. Chen1, John Easton, J. Cheng, Kristy Boggs, Natalia Santiago-Morales1, Ilaria Iacobucci1, Robert S. Fulton3, Robert S. Fulton2, Ji Wen1, Marcus B. Valentine, Cheng Cheng, Steven W. Paugh, Meenakshi Devidas4, Meenakshi Devidas5, I-Ming Chen4, S. Reshmi6, S. Reshmi4, Amy Smith6, Erin Hedlund, Pankaj Gupta, Panduka Nagahawatte, Gang Wu, Xiang Chen, Donald Yergeau, Bhavin Vadodaria, Heather L. Mulder, Naomi J. Winick7, Eric Larsen, William L. Carroll8, William L. Carroll4, Nyla A. Heerema, Andrew J. Carroll9, G. Grayson10, Sarah K. Tasian11, Andrew S. Moore12, F. Keller13, Melissa Frei-Jones14, J. A. Whitlock15, Elizabeth A. Raetz, Deborah L. White, Timothy P. Hughes16, J. M. Guidry Auvil4, Malcolm A. Smith17, Malcolm A. Smith4, Guido Marcucci7, Clara D. Bloomfield7, Krzysztof Mrózek7, Jessica Kohlschmidt7, Jessica Kohlschmidt17, Wendy Stock18, Steven M. Kornblau19, Marina Konopleva20, Elisabeth Paietta21, Ching-Hon Pui, Sima Jeha, Mary V. Relling4, William E. Evans, Daniela S. Gerhard4, Julie M. Gastier-Foster6, Julie M. Gastier-Foster4, Elaine R. Mardis, Richard K. Wilson, Mignon L. Loh22, Mignon L. Loh4, James R. Downing1, James R. Downing4, Stephen P. Hunger4, Stephen P. Hunger23, Cheryl L. Willman1, Cheryl L. Willman4, Jinghui Zhang4, Charles G. Mullighan1, Charles G. Mullighan4 
TL;DR: Ph-like ALL was found to be characterized by a range of genomic alterations that activate a limited number of signaling pathways, all of which may be amenable to inhibition with approved tyrosine kinase inhibitors.
Abstract: BACKGROUND Philadelphia chromosome–like acute lymphoblastic leukemia (Ph-like ALL) is characterized by a gene-expression profile similar to that of BCR–ABL1–positive ALL, alterations of lymphoid transcription factor genes, and a poor outcome. The frequency and spectrum of genetic alterations in Ph-like ALL and its responsiveness to tyrosine kinase inhibition are undefined, especially in adolescents and adults. METHODS We performed genomic profiling of 1725 patients with precursor B-cell ALL and detailed genomic analysis of 154 patients with Ph-like ALL. We examined the functional effects of fusion proteins and the efficacy of tyrosine kinase inhibitors in mouse pre-B cells and xenografts of human Ph-like ALL. RESULTS Ph-like ALL increased in frequency from 10% among children with standard-risk ALL to 27% among young adults with ALL and was associated with a poor outcome. Kinase-activating alterations were identified in 91% of patients with Ph-like ALL; rearrangements involving ABL1, ABL2, CRLF2, CSF1R, EPOR, JAK2, NTRK3, PDGFRB, PTK2B, TSLP, or TYK2 and sequence mutations involving FLT3, IL7R, or SH2B3 were most common. Expression of ABL1, ABL2, CSF1R, JAK2, and PDGFRB fusions resulted in cytokine-independent proliferation and activation of phosphorylated STAT5. Cell lines and human leukemic cells expressing ABL1, ABL2, CSF1R, and PDGFRB fusions were sensitive in vitro to dasatinib, EPOR and JAK2 rearrangements were sensitive to ruxolitinib, and the ETV6–NTRK3 fusion was sensitive to crizotinib. CONCLUSIONS Ph-like ALL was found to be characterized by a range of genomic alterations that activate a limited number of signaling pathways, all of which may be amenable to inhibition with approved tyrosine kinase inhibitors. Trials identifying Ph-like ALL are needed to assess whether adding tyrosine kinase inhibitors to current therapy will improve the survival of patients with this type of leukemia. (Funded by the American Lebanese Syrian Associated Charities and others.)

1,077 citations

Journal ArticleDOI
13 Sep 2001-Nature
TL;DR: This work describes how engineered membrane pores can be used to make rapid and sensitive biosensors with potential applications that range from the detection of biological warfare agents to pharmaceutical screening.
Abstract: Sensory systems use a variety of membrane-bound receptors, including responsive ion channels, to discriminate between a multitude of stimuli Here we describe how engineered membrane pores can be used to make rapid and sensitive biosensors with potential applications that range from the detection of biological warfare agents to pharmaceutical screening Notably, use of the engineered pores in stochastic sensing, a single-molecule detection technology, reveals the identity of an analyte as well as its concentration

1,076 citations


Authors

Showing all 72708 results

NameH-indexPapersCitations
Yi Chen2174342293080
Scott M. Grundy187841231821
Evan E. Eichler170567150409
Yang Yang1642704144071
Martin Karplus163831138492
Robert Stone1601756167901
Philip Cohen154555110856
Claude Bouchard1531076115307
Jongmin Lee1502257134772
Zhenwei Yang150956109344
Vivek Sharma1503030136228
Frede Blaabjerg1472161112017
Steven L. Salzberg147407231756
Mikhail D. Lukin14660681034
John F. Hartwig14571466472
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20241
2023211
2022938
20218,666
20208,925
20198,426