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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 10, 2013
The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disordersVandana Shashi, Allyn McConkie-Rosell, Bruce Rosell, et al.Plos One|March 3, 2011
Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophagesSebastiaan M Bol, Perry D Moerland, Sophie Limou, et al.Epilepsy Research|May 6, 2006
A pharmacogenetic exploration of vigabatrin-induced visual field constrictionPeter Kinirons, Gianpiero L Cavalleri, Rinki Singh, et al.Plos One|April 12, 2022
A genome-wide screen for variants influencing certolizumab pegol response in a moderate to severe rheumatoid arthritis populationIan R White, Sarah E Kleinstein, Christophe Praet, et al.The Journal of Experimental Medicine|July 17, 2024
Loss of tolerance precedes triggering and lifelong persistence of pathogenic type I interferon autoantibodiesSonja Fernbach, Nina K Mair, Irene A Abela, et al.Plos Pathogens|August 8, 2024
Using viral diversity to identify HIV-1 variants under HLA-dependent selection in a systematic viral genome-wide screenNadia Neuner-Jehle, Marius Zeeb, Christian W Thorball, et al.American Journal of Human Genetics|January 17, 2024
A common NFKB1 variant detected through antibody analysis in UK Biobank predicts risk of infection and allergyAmanda Y Chong, Nicole Brenner, Andres Jimenez-Kaufmann, et al.Genome Research|August 13, 2016
Inhibition of microRNA 128 promotes excitability of cultured cortical neuronal networksK Melodi McSweeney, Ayal B Gussow, Shelton S Bradrick, et al.Journal of Genetic Counseling|February 13, 2016
Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed DisordersAllyn McConkie Rosell, Loren D M Pena, Kelly Schoch, et al.Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|March 21, 2006
No association of DYNC1H1 with sporadic ALS in a case-control study of a northern European derived population: a tagging SNP approachParesh R Shah, Azlina Ahmad-Annuar, Kourosh R Ahmadi, et al.Pageof 51