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Human Genomics|July 6, 2018
A novel LRAT mutation affecting splicing in a family with early onset retinitis pigmentosaYabin Chen, Li Huang, Xiaodong Jiao, et al.Human Genomics|June 5, 2019
IFITM5 pathogenic variant causes osteogenesis imperfecta V with various phenotype severity in Ukrainian and Vietnamese patientsLidiia Zhytnik, Katre Maasalu, Binh Ho Duy, et al.Human Genomics|January 29, 2021
High heterogeneity undermines generalization of differential expression results in RNA-Seq analysisWeitong Cui, Huaru Xue, Lei Wei, et al.Human Genomics|February 24, 2019
Association of HTRA1 and ARMS2 gene polymorphisms with response to intravitreal ranibizumab among neovascular age-related macular degenerative subjectsNur Afiqah Mohamad, Vasudevan Ramachandran, Hazlita Mohd Isa, et al.Human Genomics|April 21, 2011
Lysosomal storage disorders: molecular basis and laboratory testingMirella Filocamo, Amelia MorroneHuman Genomics|April 21, 2011
The human fatty acid-binding protein family: evolutionary divergences and functionsRebecca L Smathers, Dennis R PetersenHuman Genomics|November 26, 2010
A useful tool for drug interaction evaluation: the University of Washington Metabolism and Transport Drug Interaction DatabaseHouda Hachad, Isabelle Ragueneau-Majlessi, René H LevyHuman Genomics|February 8, 2011
Ancestry-informative markers on chromosomes 2, 8 and 15 are associated with insulin-related traits in a racially diverse sample of childrenYann C Klimentidis, Jasmin Divers, Krista Casazza, et al.Human Genomics|February 8, 2011
Naming 'junk': human non-protein coding RNA (ncRNA) gene nomenclatureMathew W Wright, Elspeth A BrufordHuman Genomics|February 8, 2011
Exploring the potential relevance of human-specific genes to complex diseaseDavid N Cooper, Hildegard Kehrer-SawatzkiPageof 112