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Human Genomics|April 27, 2018
Evaluation of a bone morphogenetic protein 6 variant as a cause of iron loadingCameron J McDonald, Gautam Rishi, Eriza S Secondes, et al.Human Genomics|May 26, 2018
Integrating rare genetic variants into pharmacogenetic drug response predictionsMagnus Ingelman-Sundberg, Souren Mkrtchian, Yitian Zhou, et al.Human Genomics|April 11, 2018
Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi communityNasser A Elhawary, Essam H Jiffri, Samira Jambi, et al.Human Genomics|July 13, 2017
Inferring clonal structure in HTLV-1-infected individuals: towards bridging the gap between analysis and visualizationAmir Farmanbar, Sanaz Firouzi, Wojciech Makałowski, et al.Human Genomics|July 5, 2018
Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patientsJakub Piotr Fichna, Anna Macias, Marcin Piechota, et al.Human Genomics|April 13, 2018
Correlation of gene expression and associated mutation profiles of APOBEC3A, APOBEC3B, REV1, UNG, and FHIT with chemosensitivity of cancer cell lines to drug treatmentSuleyman Vural, Richard Simon, Julia KrushkalHuman Genomics|April 19, 2018
Tensions in ethics and policy created by National Precision Medicine ProgramsJusaku Minari, Kyle B Brothers, Michael MorrisonHuman Genomics|June 20, 2018
Associations between hypertension and the peroxisome proliferator-activated receptor-δ (PPARD) gene rs7770619 C>T polymorphism in a Korean populationMinjoo Kim, Minkyung Kim, Hye Jin Yoo, et al.Human Genomics|January 9, 2009
Influence of SLCO1B1 and CYP2C8 gene polymorphisms on rosiglitazone pharmacokinetics in healthy volunteersChristina L Aquilante, Lane R Bushman, Shannon D Knutsen, et al.Human Genomics|January 9, 2009
A high incidence of polymorphic CYP2C19 variants in archival blood samples from Papua New GuineaHuai-Ling Hsu, Kathryn J Woad, D Graeme Woodfield, et al.Pageof 112