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Elife|February 7, 2018
Wilms Tumor 1b defines a wound-specific sheath cell subpopulation associated with notochord repairJuan Carlos Lopez-Baez, Daniel J Simpson, Laura LLeras Forero, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
Genome-wide analysis of epistasis in body mass index using multiple human populationsWen-Hua Wei, Gib Hemani, Attila Gyenesei, et al.
Human Molecular Genetics|September 13, 2011
Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adultsJennifer E Huffman, Ana Knezevic, Veronique Vitart, et al.
Journal of the American Society of Nephrology : JASN|March 1, 2014
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysisMatthias Olden, Tanguy Corre, Caroline Hayward, et al.
Human Molecular Genetics|July 16, 2015
Homozygous loss-of-function variants in European cosmopolitan and isolate populationsVera B Kaiser, Victoria Svinti, James G Prendergast, et al.
Human Molecular Genetics|July 23, 2013
Genetic influences on plasma CFH and CFHR1 concentrations and their role in susceptibility to age-related macular degenerationMorad Ansari, Paul M McKeigue, Christine Skerka, et al.
Nature Genetics|February 24, 2009
Highly conserved non-coding elements on either side of SOX9 associated with Pierre Robin sequenceSabina Benko, Judy A Fantes, Jeanne Amiel, et al.
Nature Genetics|March 11, 2008
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and goutVeronique Vitart, Igor Rudan, Caroline Hayward, et al.
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