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Nature Communications|November 10, 2023
A large meta-analysis identifies genes associated with anterior uveitisSahar Gelfman, Arden Moscati, Santiago Mendez Huergo, et al.Human Molecular Genetics|October 2, 2007
Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorderSven Cichon, Ingeborg Winge, Manuel Mattheisen, et al.American Journal of Human Genetics|May 20, 2005
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopeciaAxel M Hillmer, Sandra Hanneken, Sibylle Ritzmann, et al.Scientific Reports|March 17, 2016
C9orf72 ablation causes immune dysregulation characterized by leukocyte expansion, autoantibody production, and glomerulonephropathy in miceAmanda Atanasio, Vilma Decman, Derek White, et al.American Journal of Human Genetics|February 28, 2012
Use of a multiethnic approach to identify rheumatoid- arthritis-susceptibility loci, 1p36 and 17q12Fina A S Kurreeman, Eli A Stahl, Yukinori Okada, 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.Nature|June 18, 2010
Functionally defective germline variants of sialic acid acetylesterase in autoimmunityIra Surolia, Stephan P Pirnie, Vasant Chellappa, et al.Nature Genetics|March 10, 2009
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24Stefanie Birnbaum, Kerstin U Ludwig, Heiko Reutter, et al.Nature Communications|January 30, 2024
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implicationsRosalie B T M Sterenborg, Inga Steinbrenner, Yong Li, et al.Pageof 32