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Molecular & Cellular Proteomics : MCP|July 10, 2010
Naturally occurring human urinary peptides for use in diagnosis of chronic kidney diseaseDavid M Good, Petra Zürbig, Angel Argilés, et al.
Nature Genetics|June 20, 2017
Variants in the fetal genome near FLT1 are associated with risk of preeclampsiaRalph McGinnis, Valgerdur Steinthorsdottir, Nicholas O Williams, et al.
Science Translational Medicine|August 27, 2010
Recommendations for biomarker identification and qualification in clinical proteomicsHarald Mischak, Günter Allmaier, Rolf Apweiler, et al.
JCI Insight|October 11, 2019
KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization patternAlexander Teumer, Teresa Trenkwalder, Thorsten Kessler, et al.
American Journal of Human Genetics|November 20, 2012
Copy-number disorders are a common cause of congenital kidney malformationsSimone Sanna-Cherchi, Krzysztof Kiryluk, Katelyn E Burgess, et al.
American Journal of Respiratory and Critical Care Medicine|October 4, 2011
Effect of five genetic variants associated with lung function on the risk of chronic obstructive lung disease, and their joint effects on lung functionMaría Soler Artigas, Louise V Wain, Emmanouela Repapi, et al.
Nature Genetics|May 28, 2013
Combined sequence-based and genetic mapping analysis of complex traits in outbred rats, Amelie Baud, Roel Hermsen, et al.
European Heart Journal|January 30, 2014
Mendelian randomization of blood lipids for coronary heart diseaseMichael V Holmes, Folkert W Asselbergs, Tom M Palmer, et al.
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