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Proteomics. Clinical Applications|February 5, 2010
CE-MS analysis of the human urinary proteome for biomarker discovery and disease diagnosticsJoshua J Coon, Petra Zürbig, Mohammed Dakna, et al.
BMC Medical Genetics|October 4, 2006
Generation Scotland: the Scottish Family Health Study; a new resource for researching genes and heritabilityBlair H Smith, Harry Campbell, Douglas Blackwood, et al.
Hypertension (Dallas, Tex. : 1979)|November 2, 2016
Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to HydrochlorothiazideErika Salvi, Zhiying Wang, Federica Rizzi, et al.
Lancet (London, England)|February 14, 2012
Inheritance of coronary artery disease in men: an analysis of the role of the Y chromosomeFadi J Charchar, Lisa Ds Bloomer, Timothy A Barnes, et al.
Hypertension (Dallas, Tex. : 1979)|June 12, 2013
Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazideStephen T Turner, Eric Boerwinkle, Jeffrey R O'Connell, et al.
Hypertension (Dallas, Tex. : 1979)|June 3, 2015
Metabolomic identification of a novel pathway of blood pressure regulation involving hexadecanedioateCristina Menni, Delyth Graham, Gabi Kastenmüller, et al.
Human Molecular Genetics|January 31, 2015
Mosaic structural variation in children with developmental disordersDaniel A King, Wendy D Jones, Yanick J Crow, et al.
Plos One|April 7, 2009
Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretionStephen Newhouse, Martin Farrall, Chris Wallace, et al.
Journal of Hypertension|February 20, 2015
TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensivesMartina Chittani, Roberta Zaninello, Chiara Lanzani, et al.
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