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Annals of the Rheumatic Diseases|January 17, 2023
Efficacy and safety of bimekizumab in axial spondyloarthritis: results of two parallel phase 3 randomised controlled trialsDésirée van der Heijde, Atul Deodhar, Xenofon Baraliakos, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|November 6, 2018
An N-Ethyl-N-Nitrosourea (ENU)-Induced Tyr265Stop Mutation of the DNA Polymerase Accessory Subunit Gamma 2 (Polg2) Is Associated With Renal Calcification in MiceCaroline M Gorvin, Bushra N Ahmad, Michael J Stechman, et al.Human Molecular Genetics|July 18, 2021
Germline ERBB3 mutation in familial non-small-cell lung carcinoma: expanding ErbB's role in oncogenesisAideen M McInerney-Leo, Hui Yi Chew, Po-Ling Inglis, et al.American Journal of Human Genetics|August 4, 2016
Contribution of a Non-classical HLA Gene, HLA-DOA, to the Risk of Rheumatoid ArthritisYukinori Okada, Akari Suzuki, Katsunori Ikari, et al.Diabetologia|July 20, 2015
Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near the GRB2 geneKathryn P Burdon, Rhys D Fogarty, Weiyong Shen, et al.Nature Genetics|May 3, 2011
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1Kathryn P Burdon, Stuart Macgregor, Alex W Hewitt, et al.ACR Open Rheumatology|March 30, 2022
47XXY and 47XXX in Scleroderma and MyositisR Hal Scofield, Valerie M Lewis, Joshua Cavitt, et al.Plos Genetics|April 5, 2019
Genome-wide association study in Turkish and Iranian populations identify rare familial Mediterranean fever gene (MEFV) polymorphisms associated with ankylosing spondylitisZhixiu Li, Servet Akar, Handan Yarkan, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 27, 2011
A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutationChristopher T Esapa, Tertius A Hough, Sarah Testori, et al.Ebiomedicine|June 25, 2020
Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han populationXiu-Yu Shi, Geng Wang, Ting Li, et al.Pageof 38