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Nature Genetics|May 31, 2001
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4K Mykytyn, T Braun, R Carmi, et al.Plos One|October 15, 2011
Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiologyGyungah Jun, Michael Nicolaou, Margaux A Morrison, et al.Vision Research|September 30, 2009
Convergence of linkage, gene expression and association data demonstrates the influence of the RAR-related orphan receptor alpha (RORA) gene on neovascular AMD: a systems biology based approachAlexandra C Silveira, Margaux A Morrison, Fei Ji, et al.Investigative Ophthalmology & Visual Science|May 10, 2014
FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expressionLeah A Owen, Margaux A Morrison, Jeeyun Ahn, et al.Human Molecular Genetics|April 4, 2001
Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)D Y Nishimura, C C Searby, R Carmi, et al.Human Genomics|December 14, 2011
Systems biology-based analysis implicates a novel role for vitamin D metabolism in the pathogenesis of age-related macular degenerationMargaux A Morrison, Alexandra C Silveira, Nancy Huynh, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 11, 2019
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorderLloyd B Williams, Asif Javed, Amin Sabri, et al.Pageof 14