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Elife|June 1, 2021
Systematic screening of viral and human genetic variation identifies antiretroviral resistance and immune escape linkHuyen Nguyen, Christian Wandell Thorball, Jacques Fellay, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 19, 2022
A Baseline Cellular Antiviral State Is Maintained by cGAS and Its Most Frequent Naturally Occurring Variant rs610913Julia Kazmierski, Carina Elsner, Katinka Döhner, et al.
Ophthalmic Genetics|October 3, 2019
Modification of the <i>PROM1</i> disease phenotype by a mutation in <i>ABCA4</i>Winston Lee, Maarjaliis Paavo, Jana Zernant, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 31, 2019
A case-control collapsing analysis identifies retinal dystrophy genes associated with ophthalmic disease in patients with no pathogenic ABCA4 variantsCharles J Wolock, Nicholas Stong, Chu Jian Ma, et al.
Journal of Hepatology|June 28, 2011
Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patientsAlexander J Thompson, Paul J Clark, Abanish Singh, et al.
Plos Computational Biology|January 13, 2022
Using population-specific add-on polymorphisms to improve genotype imputation in underrepresented populationsZhi Ming Xu, Sina Rüeger, Michaela Zwyer, et al.
American Journal of Human Genetics|April 5, 2011
A genome-wide comparison of the functional properties of rare and common genetic variants in humansQianqian Zhu, Dongliang Ge, Jessica M Maia, et al.
Genomics|August 2, 2011
A whole-genome analysis of premature termination codonsElizabeth T Cirulli, Erin L Heinzen, Fred S Dietrich, et al.
Hepatology (Baltimore, Md.)|March 2, 2011
Estimating the net contribution of interleukin-28B variation to spontaneous hepatitis C virus clearanceJulia di Iulio, Angela Ciuffi, Karen Fitzmaurice, et al.
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