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Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|September 25, 2021
Novel variant in glycophorin c gene protects against ribavirin-induced anemia during chronic hepatitis C treatmentJennifer J Lin, Catrina M Loucks, Jessica N Trueman, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 21, 2018
The molecular epidemiology of Huntington disease is related to intermediate allele frequency and haplotype in the general populationChris Kay, Jennifer A Collins, Galen E B Wright, et al.
American Journal of Human Genetics|May 21, 2019
Length of Uninterrupted CAG, Independent of Polyglutamine Size, Results in Increased Somatic Instability, Hastening Onset of Huntington DiseaseGalen E B Wright, Jennifer A Collins, Chris Kay, et al.
JAMA Oncology|April 28, 2017
Association Between SLC16A5 Genetic Variation and Cisplatin-Induced Ototoxic Effects in Adult Patients With Testicular CancerBritt I Drögemöller, Jose G Monzon, Amit P Bhavsar, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|February 2, 2022
Patient-specific genetic factors predict treatment failure in sofosbuvir-treated patients with chronic hepatitis CCatrina M Loucks, Jennifer J Lin, Jessica N Trueman, et al.
Nature Genetics|July 18, 2018
Common variation near IRF6 is associated with IFN-β-induced liver injury in multiple sclerosisKaarina Kowalec, Galen E B Wright, Britt I Drögemöller, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|February 12, 2022
A pharmacogenomic investigation of the cardiac safety profile of ondansetron in children and pregnant womenBritt I Drögemöller, Galen E B Wright, Jessica Trueman, et al.
Frontiers in Pharmacology|November 1, 2021
The Extent and Impact of Variation in ADME Genes in Sub-Saharan African PopulationsJorge E B da Rocha, Houcemeddine Othman, Gerrit Botha, et al.
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