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Plos Biology|June 13, 2017
Viral genetic variation accounts for a third of variability in HIV-1 set-point viral load in EuropeFrançois Blanquart, Chris Wymant, Marion Cornelissen, et al.
Plos Genetics|June 26, 2010
Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease geneNara L M Sobreira, Elizabeth T Cirulli, Dimitrios Avramopoulos, et al.
Human Molecular Genetics|September 8, 2009
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTABAnna C Need, Deborah K Attix, Jill M McEvoy, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|March 19, 2020
Whole-exome Sequencing for the Identification of Rare Variants in Primary Immunodeficiency Genes in Children With Sepsis: A Prospective, Population-based Cohort StudyAlessandro Borghesi, Johannes Trück, Samira Asgari, et al.
Virus Evolution|June 8, 2018
Easy and accurate reconstruction of whole HIV genomes from short-read sequence data with shiverChris Wymant, François Blanquart, Tanya Golubchik, et al.
Plos Genetics|March 8, 2014
LILRB2 interaction with HLA class I correlates with control of HIV-1 infectionArman A Bashirova, Enrique Martin-Gayo, Des C Jones, et al.
Medrxiv : the Preprint Server for Health Sciences|January 3, 2024
Lack of association between HLA and asymptomatic SARS-CoV-2 infectionAstrid Marchal, Elizabeth T Cirulli, Iva Neveux, et al.
HGG Advances|April 28, 2024
Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infectionAstrid Marchal, Elizabeth T Cirulli, Iva Neveux, et al.
Elife|October 31, 2013
A genome-to-genome analysis of associations between human genetic variation, HIV-1 sequence diversity, and viral controlIstván Bartha, Jonathan M Carlson, Chanson J Brumme, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2005
UCHL-1 gene in multiple system atrophy: a haplotype tagging approachDaniel G Healy, Patrick M Abou-Sleiman, Niall Quinn, et al.
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