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Institution

University of Texas Southwestern Medical Center

HealthcareDallas, Texas, United States
About: University of Texas Southwestern Medical Center is a healthcare organization based out in Dallas, Texas, United States. It is known for research contribution in the topics: Population & Cancer. The organization has 39107 authors who have published 75242 publications receiving 4497256 citations. The organization is also known as: UT Southwestern & UT Southwestern Medical School.
Topics: Population, Cancer, Medicine, Gene, Receptor


Papers
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Journal ArticleDOI
Jeffrey W. Tyner1, Cristina E. Tognon2, Cristina E. Tognon1, Daniel Bottomly1, Beth Wilmot1, Stephen E. Kurtz1, Samantha L. Savage1, Nicola Long1, Anna Reister Schultz1, Elie Traer1, Melissa L. Abel1, Anupriya Agarwal1, Aurora Blucher1, Uma Borate1, Jade Bryant1, Russell T. Burke1, Amy S. Carlos1, Richie Carpenter1, Joseph Carroll1, Bill H. Chang1, Cody Coblentz1, Amanda d’Almeida1, Rachel J. Cook1, Alexey V. Danilov1, Kim Hien T. Dao1, Michie Degnin1, Deirdre Devine1, James Dibb1, David K. Edwards1, Christopher A. Eide1, Christopher A. Eide2, Isabel English1, Jason M. Glover1, Rachel Henson1, Hibery Ho1, Abdusebur Jemal1, Kara Johnson1, Ryan C. Johnson1, Brian Junio1, Andy Kaempf1, Jessica Leonard1, Chenwei Lin1, Selina Qiuying Liu1, Pierrette Lo1, Marc M. Loriaux1, Samuel B. Luty1, Tara A. Macey1, Jason D. MacManiman1, Jacqueline Martinez1, Motomi Mori1, Dylan Nelson3, Ceilidh Nichols1, Jill Peters1, Justin Ramsdill1, Angela Rofelty1, Robert Schuff1, Robert P. Searles1, Erik Segerdell1, Rebecca Smith1, Stephen E. Spurgeon1, Tyler Sweeney1, Aashis Thapa1, Corinne Visser1, Jake Wagner1, Kevin Watanabe-Smith1, Kristen Werth1, Joelle Wolf1, Libbey White1, Amy Yates1, Haijiao Zhang1, Christopher R. Cogle4, Robert H. Collins5, Denise C. Connolly6, Michael W. Deininger7, Leylah Drusbosky4, Christopher S. Hourigan8, Craig T. Jordan9, Patricia Kropf6, Tara L. Lin10, Micaela E. Martinez11, Bruno C. Medeiros12, Rachel R. Pallapati11, Daniel A. Pollyea9, Ronan T. Swords11, Justin M. Watts11, Scott Weir10, David L. Wiest6, Ryan M. Winters6, Shannon K. McWeeney1, Brian J. Druker1, Brian J. Druker2 
17 Oct 2018-Nature
TL;DR: Analyses of samples from patients with acute myeloid leukaemia reveal that drug response is associated with mutational status and gene expression; the generated dataset provides a basis for future clinical and functional studies of this disease.
Abstract: The implementation of targeted therapies for acute myeloid leukaemia (AML) has been challenging because of the complex mutational patterns within and across patients as well as a dearth of pharmacologic agents for most mutational events. Here we report initial findings from the Beat AML programme on a cohort of 672 tumour specimens collected from 562 patients. We assessed these specimens using whole-exome sequencing, RNA sequencing and analyses of ex vivo drug sensitivity. Our data reveal mutational events that have not previously been detected in AML. We show that the response to drugs is associated with mutational status, including instances of drug sensitivity that are specific to combinatorial mutational events. Integration with RNA sequencing also revealed gene expression signatures, which predict a role for specific gene networks in the drug response. Collectively, we have generated a dataset—accessible through the Beat AML data viewer (Vizome)—that can be leveraged to address clinical, genomic, transcriptomic and functional analyses of the biology of AML. Analyses of samples from patients with acute myeloid leukaemia reveal that drug response is associated with mutational status and gene expression; the generated dataset provides a basis for future clinical and functional studies of this disease.

763 citations

Journal ArticleDOI
TL;DR: Localization to this microdomain is likely to optimize eNOS activation and the extracellular release of nitric oxide and that both myristoylation and palmitoylation are required to target the enzyme to caveolae and that each acylation process enhances targeting by 10-fold.

763 citations

Journal ArticleDOI
TL;DR: Data are consistent with a model in which PCSK9 binding to EGF-A interferes with an acid-dependent conformational change required for receptor recycling, and the LDLR is rerouted from the endosome to the lysosome where it is degraded.

762 citations

Journal ArticleDOI
05 Oct 1989-Nature
TL;DR: Biophysical studies suggest that mechanical forces control the opening and closing of transduction channels by acting through elastic components in each hair cell's mechanoreceptive hair bundle.
Abstract: The senses of hearing and equilibrium depend on sensory receptors called hair cells which can detect motions of atomic dimensions and respond more than 100,000 times a second. Biophysical studies suggest that mechanical forces control the opening and closing of transduction channels by acting through elastic components in each hair cell's mechanoreceptive hair bundle. Other ion channels, as well as the mechanical and hydrodynamic properties of hair bundles, tune individual hair cells to particular frequencies of stimulation.

761 citations

Journal ArticleDOI
TL;DR: A reiterative selection procedure is used to identify new specific binding sites for p53, using nuclear extracts from normal human fibroblasts as the source of p53 protein, and the preferred consensus is the palindrome GGACATGCCCGGGCATGTCC.
Abstract: Recent studies have demonstrated transcriptional activation domains within the tumor suppressor protein p53, while others have described specific DNA-binding sites for p53, implying that the protein may act as a transcriptional regulatory factor. We have used a reiterative selection procedure (CASTing: cyclic amplification and selection of targets) to identify new specific binding sites for p53, using nuclear extracts from normal human fibroblasts as the source of p53 protein. The preferred consensus is the palindrome GGACATGCCCGGGCATGTCC. In vitro-translated p53 binds to this sequence only when mixed with nuclear extracts, suggesting that p53 may bind DNA after posttranslational modification or as a complex with other protein partners. When placed upstream of a reporter construct, this sequence promotes p53-dependent transcription in transient transfection assays.

761 citations


Authors

Showing all 39410 results

NameH-indexPapersCitations
Eugene Braunwald2301711264576
Joseph L. Goldstein207556149527
Eric N. Olson206814144586
Craig B. Thompson195557173172
Thomas C. Südhof191653118007
Scott M. Grundy187841231821
Michael S. Brown185422123723
Eric Boerwinkle1831321170971
Jiaguo Yu178730113300
John J.V. McMurray1781389184502
Eric J. Nestler178748116947
John D. Minna169951106363
Yuh Nung Jan16246074818
Andrew P. McMahon16241590650
Elliott M. Antman161716179462
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023114
2022407
20215,247
20204,674
20194,094
20183,400