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Proceedings of the National Academy of Sciences of the United States of America|December 29, 2011
Lupus-associated causal mutation in neutrophil cytosolic factor 2 (NCF2) brings unique insights to the structure and function of NADPH oxidaseChaim O Jacob, Miriam Eisenstein, Mary C Dinauer, et al.
Genes and Immunity|June 16, 2018
Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitisLeah C Kottyan, Avery Maddox, Julian R Braxton, et al.
American Journal of Human Genetics|October 23, 2012
Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in EuropeansDavid L Morris, Kimberly E Taylor, Michelle M A Fernando, et al.
American Journal of Human Genetics|July 30, 2002
Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosusRobert R Graham, Ward A Ortmann, Carl D Langefeld, et al.
Nature Genetics|January 31, 2017
A missense variant in NCF1 is associated with susceptibility to multiple autoimmune diseasesJian Zhao, Jianyang Ma, Yun Deng, et al.
Nature Genetics|October 9, 2012
CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B-cell signaling and activationNataly Manjarrez-Orduño, Emiliano Marasco, Sharon A Chung, et al.
Genes and Immunity|March 7, 2014
MHC associations with clinical and autoantibody manifestations in European SLED L Morris, M M A Fernando, K E Taylor, et al.
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