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Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|September 13, 2011
Hereditary hyperferritinemia-cataract syndrome in two large multigenerational American familiesJulia Shekunov, Piet C de Groen, Noralane M Lindor, et al.Journal of Neurochemistry|July 22, 2009
Human S-adenosylhomocysteine hydrolase: common gene sequence variation and functional genomic characterizationQiping Feng, Mani Keshtgarpour, Linda L Pelleymounter, et al.Biochemical and Biophysical Research Communications|September 11, 2004
Human SULT1A3 pharmacogenetics: gene duplication and functional genomic studiesMichelle A T Hildebrandt, Oreste E Salavaggione, Yvette N Martin, et al.Alcoholism, Clinical and Experimental Research|January 30, 2009
Sequence variations of the human MPDZ gene and association with alcoholism in subjects with European ancestryVictor M Karpyak, Jeong-Hyun Kim, Joanna M Biernacka, et al.Drug Metabolism and Disposition: the Biological Fate of Chemicals|April 28, 2006
Glutathione S-transferase omega 1 and omega 2 pharmacogenomicsBaidehi Mukherjee, Oreste E Salavaggione, Linda L Pelleymounter, et al.Gene|April 1, 2020
Transplant chimerism in porcine structural vascularized bone allotransplantsRudolph H Houben, Ross A Aleff, Patricia F Friedrich, et al.Oncotarget|April 17, 2017
Retinoic acid receptor alpha drives cell cycle progression and is associated with increased sensitivity to retinoids in T-cell lymphomaXueju Wang, Surendra Dasari, Grzegorz S Nowakowski, et al.The Journal of Clinical Endocrinology and Metabolism|May 14, 2009
Human glucocorticoid receptor alpha gene (NR3C1) pharmacogenomics: gene resequencing and functional genomicsNifang Niu, Venkatraman Manickam, Krishna R Kalari, et al.Pediatric Neurology|January 8, 2016
Whole Exome Sequencing and Heterologous Cellular Electrophysiology Studies Elucidate a Novel Loss-of-Function Mutation in the CACNA1A-Encoded Neuronal P/Q-Type Calcium Channel in a Child With Congenital Hypotonia and Developmental DelayDerek L Weyhrauch, Dan Ye, Nicole J Boczek, et al.Plos One|July 3, 2018
Gene expression in the corneal endothelium of Fuchs endothelial corneal dystrophy patients with and without expansion of a trinucleotide repeat in TCF4Eric D Wieben, Ross A Aleff, Xiaojia Tang, et al.Pageof 10