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Institution

Vanderbilt University

EducationNashville, Tennessee, United States
About: Vanderbilt University is a education organization based out in Nashville, Tennessee, United States. It is known for research contribution in the topics: Population & Cancer. The organization has 45066 authors who have published 106528 publications receiving 5435039 citations. The organization is also known as: Vandy.


Papers
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Journal ArticleDOI
TL;DR: Progress has been made in understanding the mechanisms responsible for the pathogenesis and the resolution of lung injury, including the contribution of environmental and genetic factors, and on developing novel therapeutics that can facilitate and enhance lung repair.
Abstract: The acute respiratory distress syndrome (ARDS) is an important cause of acute respiratory failure that is often associated with multiple organ failure. Several clinical disorders can precipitate ARDS, including pneumonia, sepsis, aspiration of gastric contents, and major trauma. Physiologically, ARDS is characterized by increased permeability pulmonary edema, severe arterial hypoxemia, and impaired carbon dioxide excretion. Based on both experimental and clinical studies, progress has been made in understanding the mechanisms responsible for the pathogenesis and the resolution of lung injury, including the contribution of environmental and genetic factors. Improved survival has been achieved with the use of lung-protective ventilation. Future progress will depend on developing novel therapeutics that can facilitate and enhance lung repair.

1,506 citations

Journal ArticleDOI
Julie George1, Jing Shan Lim2, Se Jin Jang3, Yupeng Cun1, Luka Ozretić, Gu Kong4, Frauke Leenders1, Xin Lu1, Lynnette Fernandez-Cuesta1, Graziella Bosco1, Christian Müller1, Ilona Dahmen1, Nadine Jahchan2, Kwon-Sik Park2, Dian Yang2, Anthony N. Karnezis5, Dedeepya Vaka2, Ángela Torres2, Maia Segura Wang, Jan O. Korbel, Roopika Menon6, Sung-Min Chun3, Deokhoon Kim3, Matthew D. Wilkerson7, Neil Hayes7, David Engelmann8, Brigitte M. Pützer8, Marc Bos1, Sebastian Michels6, Ignacija Vlasic, Danila Seidel1, Berit Pinther1, Philipp Schaub1, Christian Becker1, Janine Altmüller1, Jun Yokota9, Takashi Kohno, Reika Iwakawa, Koji Tsuta, Masayuki Noguchi10, Thomas Muley11, Hans Hoffmann11, Philipp A. Schnabel12, Iver Petersen13, Yuan Chen13, Alex Soltermann14, Verena Tischler14, Chang-Min Choi3, Yong-Hee Kim3, Pierre P. Massion15, Yong Zou15, Dragana Jovanovic16, Milica Kontic16, Gavin M. Wright17, Prudence A. Russell17, Benjamin Solomon17, Ina Koch, Michael Lindner, Lucia Anna Muscarella18, Annamaria la Torre18, John K. Field19, Marko Jakopović20, Jelena Knezevic, Esmeralda Castaños-Vélez21, Luca Roz, Ugo Pastorino, O.T. Brustugun22, Marius Lund-Iversen22, Erik Thunnissen23, Jens Köhler, Martin Schuler, Johan Botling24, Martin Sandelin24, Montserrat Sanchez-Cespedes, Helga B. Salvesen25, Viktor Achter1, Ulrich Lang1, Magdalena Bogus1, Peter M. Schneider1, Thomas Zander, Sascha Ansén6, Michael Hallek1, Jürgen Wolf6, Martin Vingron26, Yasushi Yatabe, William D. Travis27, Peter Nürnberg1, Christian Reinhardt, Sven Perner3, Lukas C. Heukamp, Reinhard Büttner, Stefan A. Haas26, Elisabeth Brambilla28, Martin Peifer1, Julien Sage2, Roman K. Thomas1 
06 Aug 2015-Nature
TL;DR: This first comprehensive study of somatic genome alterations in SCLC uncovers several key biological processes and identifies candidate therapeutic targets in this highly lethal form of cancer.
Abstract: We have sequenced the genomes of 110 small cell lung cancers (SCLC), one of the deadliest human cancers. In nearly all the tumours analysed we found bi-allelic inactivation of TP53 and RB1, sometimes by complex genomic rearrangements. Two tumours with wild-type RB1 had evidence of chromothripsis leading to overexpression of cyclin D1 (encoded by the CCND1 gene), revealing an alternative mechanism of Rb1 deregulation. Thus, loss of the tumour suppressors TP53 and RB1 is obligatory in SCLC. We discovered somatic genomic rearrangements of TP73 that create an oncogenic version of this gene, TP73Δex2/3. In rare cases, SCLC tumours exhibited kinase gene mutations, providing a possible therapeutic opportunity for individual patients. Finally, we observed inactivating mutations in NOTCH family genes in 25% of human SCLC. Accordingly, activation of Notch signalling in a pre-clinical SCLC mouse model strikingly reduced the number of tumours and extended the survival of the mutant mice. Furthermore, neuroendocrine gene expression was abrogated by Notch activity in SCLC cells. This first comprehensive study of somatic genome alterations in SCLC uncovers several key biological processes and identifies candidate therapeutic targets in this highly lethal form of cancer.

1,504 citations

Journal ArticleDOI
TL;DR: Pulmonary arterial hypertension has a multifactorial pathobiology and recent genetic and pathophysiologic studies have emphasized the relevance of several mediators in this condition, including prostacyclin, nitric oxide, ET-1, angiopoietin- 1, serotonin, cytokines, chemokines, and members of the transforming-growth-factor-beta superfamily.

1,501 citations

Journal ArticleDOI
TL;DR: Patients with melanoma in whom fatal myocarditis developed after treatment with ipilimumab and nivolumab were having a rare, potentially fatal, T-cell-driven drug reaction, according to Pharmacovigilance studies.
Abstract: Immune checkpoint inhibitors have improved clinical outcomes associated with numerous cancers, but high-grade, immune-related adverse events can occur, particularly with combination immunotherapy. We report the cases of two patients with melanoma in whom fatal myocarditis developed after treatment with ipilimumab and nivolumab. In both patients, there was development of myositis with rhabdomyolysis, early progressive and refractory cardiac electrical instability, and myocarditis with a robust presence of T-cell and macrophage infiltrates. Selective clonal T-cell populations infiltrating the myocardium were identical to those present in tumors and skeletal muscle. Pharmacovigilance studies show that myocarditis occurred in 0.27% of patients treated with a combination of ipilimumab and nivolumab, which suggests that our patients were having a rare, potentially fatal, T-cell-driven drug reaction. (Funded by Vanderbilt-Ingram Cancer Center Ambassadors and others.).

1,498 citations

Journal ArticleDOI
16 Dec 2004-Nature
TL;DR: It is suggested that lower crustal foundering occurred within the North China craton during the Late Jurassic, and thus provides constraints on the timing of lithosphere removal beneath the NorthChina craton.
Abstract: Foundering of mafic lower continental crust into underlying convecting mantle has been proposed as one means to explain the unusually evolved chemical composition of Earth's continental crust, yet direct evidence of this process has been scarce. Here we report that Late Jurassic high-magnesium andesites, dacites and adakites (siliceous lavas with high strontium and low heavy-rare-earth element and yttrium contents) from the North China craton have chemical and petrographic features consistent with their origin as partial melts of eclogite that subsequently interacted with mantle peridotite. Similar features observed in adakites and some Archaean sodium-rich granitoids of the tonalite-trondhjemite-granodiorite series have been interpreted to result from interaction of slab melts with the mantle wedge. Unlike their arc-related counterparts, however, the Chinese magmas carry inherited Archaean zircons and have neodymium and strontium isotopic compositions overlapping those of eclogite xenoliths derived from the lower crust of the North China craton. Such features cannot be produced by crustal assimilation of slab melts, given the high Mg#, nickel and chromium contents of the lavas. We infer that the Chinese lavas derive from ancient mafic lower crust that foundered into the convecting mantle and subsequently melted and interacted with peridotite. We suggest that lower crustal foundering occurred within the North China craton during the Late Jurassic, and thus provides constraints on the timing of lithosphere removal beneath the North China craton.

1,495 citations


Authors

Showing all 45403 results

NameH-indexPapersCitations
Walter C. Willett3342399413322
Meir J. Stampfer2771414283776
John Q. Trojanowski2261467213948
Robert M. Califf1961561167961
Matthew Meyerson194553243726
Scott M. Grundy187841231821
Tony Hunter175593124726
David R. Jacobs1651262113892
Donald E. Ingber164610100682
L. Joseph Melton16153197861
Ralph A. DeFronzo160759132993
David W. Bates1591239116698
Charles N. Serhan15872884810
David Cella1561258106402
Jay Hauser1552145132683
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023141
2022540
20215,134
20205,232
20194,883
20184,649