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Institution

University of Texas Health Science Center at Houston

EducationHouston, Texas, United States
About: University of Texas Health Science Center at Houston is a education organization based out in Houston, Texas, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 27309 authors who have published 42520 publications receiving 2151596 citations. The organization is also known as: UTHealth & The UT Health Science Center at Houston.


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Journal ArticleDOI
TL;DR: IDSA considers adherence to these guidelines to be voluntary, with the ultimate determination regarding their application to be made by the physician in the light of each patient's individual circumstances.
Abstract: It is important to realize that guidelines cannot always account for individual variation among patients. They are not intended to supplant physician judgment with respect to particular patients or special clinical situations. IDSA considers adherence to these guidelines to be voluntary, with the ultimate determination regarding their application to be made by the physician in the light of each patient's individual circumstances.

1,124 citations

Journal ArticleDOI
TL;DR: An important role is shown for neutrophils in lupus pathogenesis, whereby neutrophil activated by anti-self antibodies release NETs, which contain antimicrobial peptides complexed with self-DNA and can entrap bacteria, enabling them to be killed.
Abstract: Systemic lupus erythematosus (SLE) is a severe and incurable autoimmune disease characterized by chronic activation of plasmacytoid dendritic cells (pDCs) and production of autoantibodies against nuclear self-antigens by hyperreactive B cells. Neutrophils are also implicated in disease pathogenesis; however, the mechanisms involved are unknown. Here, we identified in the sera of SLE patients immunogenic complexes composed of neutrophil-derived antimicrobial peptides and self-DNA. These complexes were produced by activated neutrophils in the form of web-like structures known as neutrophil extracellular traps (NETs) and efficiently triggered innate pDC activation via Toll-like receptor 9 (TLR9). SLE patients were found to develop autoantibodies to both the self-DNA and antimicrobial peptides in NETs, indicating that these complexes could also serve as autoantigens to trigger B cell activation. Circulating neutrophils from SLE patients released more NETs than those from healthy donors; this was further stimulated by the antimicrobial autoantibodies, suggesting a mechanism for the chronic release of immunogenic complexes in SLE. Our data establish a link between neutrophils, pDC activation, and autoimmunity in SLE, providing new potential targets for the treatment of this devastating disease.

1,104 citations

Journal ArticleDOI
Helena Furberg1, Yunjung Kim1, Jennifer Dackor1, Eric Boerwinkle2, Nora Franceschini1, Diego Ardissino, Luisa Bernardinelli3, Luisa Bernardinelli4, Pier Mannuccio Mannucci5, Francesco Mauri, Piera Angelica Merlini, Devin Absher, Themistocles L. Assimes6, Stephen P. Fortmann6, Carlos Iribarren7, Joshua W. Knowles6, Thomas Quertermous6, Luigi Ferrucci8, Toshiko Tanaka8, Joshua C. Bis9, Curt D. Furberg10, Talin Haritunians11, Barbara McKnight9, Bruce M. Psaty9, Bruce M. Psaty12, Kent D. Taylor11, Evan L. Thacker9, Peter Almgren13, Leif Groop13, Claes Ladenvall13, Michael Boehnke14, Anne U. Jackson14, Karen L. Mohlke1, Heather M. Stringham14, Jaakko Tuomilehto15, Jaakko Tuomilehto16, Emelia J. Benjamin17, Shih-Jen Hwang8, Daniel Levy17, Sarah R. Preis8, Ramachandran S. Vasan17, Jubao Duan18, Pablo V. Gejman18, Douglas F. Levinson6, Alan R. Sanders18, Jianxin Shi8, Esther H. Lips19, James McKay19, Antonio Agudo, Luigi Barzan, Vladimir Bencko20, Simone Benhamou21, Simone Benhamou22, Xavier Castellsagué, Cristina Canova23, David I. Conway24, Eleonora Fabianova, Lenka Foretova, Vladimir Janout25, Claire M. Healy26, Ivana Holcatova20, Kristina Kjærheim, Pagona Lagiou27, Jolanta Lissowska, Ray Lowry28, Tatiana V. Macfarlane29, Dana Mates, Lorenzo Richiardi30, Peter Rudnai, Neonilia Szeszenia-Dabrowska31, David Zaridze32, Ariana Znaor, Mark Lathrop, Paul Brennan19, Stefania Bandinelli, Timothy M. Frayling33, Jack M. Guralnik8, Yuri Milaneschi, John R. B. Perry33, David Altshuler34, David Altshuler35, Roberto Elosua, S. Kathiresan35, S. Kathiresan34, Gavin Lucas, Olle Melander13, Christopher J. O'Donnell8, Veikko Salomaa16, Stephen M. Schwartz9, Benjamin F. Voight36, Brenda W.J.H. Penninx37, Johannes H. Smit37, Nicole Vogelzangs37, Dorret I. Boomsma37, Eco J. C. de Geus37, Jacqueline M. Vink37, Gonneke Willemsen37, Stephen J. Chanock8, Fangyi Gu34, Susan E. Hankinson34, David J. Hunter34, Albert Hofman38, Henning Tiemeier38, André G. Uitterlinden38, Cornelia M. van Duijn38, Stefan Walter38, Daniel I. Chasman34, Brendan M. Everett34, Guillaume Paré34, Paul M. Ridker34, Ming D. Li39, Hermine H. Maes40, Janet Audrain-McGovern41, Danielle Posthuma37, Laura M. Thornton1, Caryn Lerman41, Jaakko Kaprio16, Jaakko Kaprio15, Jed E. Rose42, John P. A. Ioannidis43, John P. A. Ioannidis44, Peter Kraft34, Danyu Lin1, Patrick F. Sullivan1 
TL;DR: A meta-analyses of several smoking phenotypes within cohorts of the Tobacco and Genetics Consortium found the strongest association was a synonymous 15q25 SNP in the nicotinic receptor gene CHRNA3, and three loci associated with number of cigarettes smoked per day were identified.
Abstract: Consistent but indirect evidence has implicated genetic factors in smoking behavior1,2. We report meta-analyses of several smoking phenotypes within cohorts of the Tobacco and Genetics Consortium (n = 74,053). We also partnered with the European Network of Genetic and Genomic Epidemiology (ENGAGE) and Oxford-GlaxoSmithKline (Ox-GSK) consortia to follow up the 15 most significant regions (n > 140,000). We identified three loci associated with number of cigarettes smoked per day. The strongest association was a synonymous 15q25 SNP in the nicotinic receptor gene CHRNA3 (rs1051730[A], b = 1.03, standard error (s.e.) = 0.053, beta = 2.8 x 10(-73)). Two 10q25 SNPs (rs1329650[G], b = 0.367, s. e. = 0.059, beta = 5.7 x 10(-10); and rs1028936[A], b = 0.446, s. e. = 0.074, beta = 1.3 x 10(-9)) and one 9q13 SNP in EGLN2 (rs3733829[G], b = 0.333, s. e. = 0.058, P = 1.0 x 10(-8)) also exceeded genome-wide significance for cigarettes per day. For smoking initiation, eight SNPs exceeded genome-wide significance, with the strongest association at a nonsynonymous SNP in BDNF on chromosome 11 (rs6265[C], odds ratio (OR) = 1.06, 95% confidence interval (Cl) 1.04-1.08, P = 1.8 x 10(-8)). One SNP located near DBH on chromosome 9 (rs3025343[G], OR = 1.12, 95% Cl 1.08-1.18, P = 3.6 x 10(-8)) was significantly associated with smoking cessation.

1,104 citations

Journal ArticleDOI
TL;DR: This Review gives an overview of selected recent developments and applications of nanomedicine.
Abstract: The application of nanotechnology concepts to medicine joins two large cross-disciplinary fields with an unprecedented societal and economical potential arising from the natural combination of specific achievements in the respective fields. The common basis evolves from the molecular-scale properties relevant to the two fields. Local probes and molecular imaging techniques allow surface and interface properties to be characterized on a nanometer scale at predefined locations, while chemical approaches offer the opportunity to elaborate and address surfaces, for example, for targeted drug delivery, enhanced biocompatibility, and neuroprosthetic purposes. However, concerns arise in this cross-disciplinary area about toxicological aspects and ethical implications. This Review gives an overview of selected recent developments and applications of nanomedicine.

1,101 citations

Journal ArticleDOI
TL;DR: Two new indexes are developed: the first quantitates rapid shallow breathing as the ratio of respiratory frequency to tidal volume (f/VT), and the second is termed CROP, because it integrates thoracic compliance, respiratory ṟate, arterial oxygenation, and P1max.
Abstract: Background. The traditional predictors of the outcome of weaning from mechanical ventilation — minute ventilation (VE) and maximal inspiratory pressure (P1max) — are frequently inaccurate. We developed two new indexes: the first quantitates rapid shallow breathing as the ratio of respiratory frequency to tidal volume (f/VT), and the second is termed CROP, because it integrates thoracic compliance, respiratory ṟate, arterial oxygenation, and P1max. Methods. The threshold values for each index that discriminated best between a successful and an unsuccessful outcome of weaning were determined in 36 patients, and the predictive accuracy of these values was then tested prospectively in an additional 64 patients. Sensitivity and specificity were calculated, and the data were also analyzed with receiver-operating-characteristic (ROC) curves, in which the proportions of true positive results and false positive results are plotted against each other for a number of threshold values of an index; the area...

1,093 citations


Authors

Showing all 27450 results

NameH-indexPapersCitations
Paul M. Ridker2331242245097
Eugene Braunwald2301711264576
Eric N. Olson206814144586
Hagop M. Kantarjian2043708210208
André G. Uitterlinden1991229156747
Gordon B. Mills1871273186451
Eric Boerwinkle1831321170971
Bruce M. Psaty1811205138244
Aaron R. Folsom1811118134044
Daniel R. Weinberger177879128450
Bharat B. Aggarwal175706116213
Richard A. Gibbs172889249708
Russel J. Reiter1691646121010
James F. Sallis169825144836
Steven N. Blair165879132929
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202342
2022231
20213,048
20202,807
20192,467
20182,224