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BMC Medical Genetics|May 10, 2018
Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathyPatricia S Graham, Georgia Kaidonis, Sotoodeh Abhary, et al.
Human Molecular Genetics|July 30, 2014
Risk for ACPA-positive rheumatoid arthritis is driven by shared HLA amino acid polymorphisms in Asian and European populationsYukinori Okada, Kwangwoo Kim, Buhm Han, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 30, 2022
Reduction of New Heterotopic Ossification (HO) in the Open-Label, Phase 3 MOVE Trial of Palovarotene for Fibrodysplasia Ossificans Progressiva (FOP)Robert J Pignolo, Edward C Hsiao, Mona Al Mukaddam, et al.
American Journal of Human Genetics|March 6, 2012
Multicentric carpotarsal osteolysis is caused by mutations clustering in the amino-terminal transcriptional activation domain of MAFBAndreas Zankl, Emma L Duncan, Paul J Leo, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 10, 2004
Influence of LRP5 polymorphisms on normal variation in BMDM Audrey Koay, Peng Y Woon, Yun Zhang, et al.
Annals of the Rheumatic Diseases|May 15, 2020
Normal human enthesis harbours conventional CD4+ and CD8+ T cells with regulatory features and inducible IL-17A and TNF expressionAbdulla Watad, Hannah Rowe, Tobias Russell, et al.
Life Science Alliance|June 11, 2020
Multiple sclerosis risk variants regulate gene expression in innate and adaptive immune cellsMelissa M Gresle, Margaret A Jordan, Jim Stankovich, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|August 7, 2020
Septic Shock: A Genomewide Association Study and Polygenic Risk Score AnalysisShannon D'Urso, Dorrilyn Rajbhandari, Elizabeth Peach, et al.
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