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Journal of Bone and Mineral Metabolism|November 4, 2008
Skeletal metamorphosis in fibrodysplasia ossificans progressiva (FOP)Frederick S Kaplan, Qi Shen, Vitali Lounev, et al.Human Molecular Genetics|January 22, 2008
Brachydactyly type A2 associated with a defect in proGDF5 processingFrank Plöger, Petra Seemann, Mareen Schmidt-von Kegler, et al.International Journal of Molecular Sciences|December 10, 2021
Natural Autoimmunity to Selenoprotein P Impairs Selenium Transport in Hashimoto's ThyroiditisQian Sun, Sebastian Mehl, Kostja Renko, et al.Orphanet Journal of Rare Diseases|June 25, 2015
A hypomorphic BMPR1B mutation causes du Pan acromesomelic dysplasiaKatja Stange, Julie Désir, Naseebullah Kakar, et al.Journal of Molecular Biology|August 6, 2014
Molecular analysis of two novel missense mutations in the GDF5 proregion that reduce protein activity and are associated with brachydactyly type CKatja Stange, Tino Thieme, Karen Hertel, et al.The Journal of Clinical Investigation|October 27, 2009
The fibrodysplasia ossificans progressiva R206H ACVR1 mutation activates BMP-independent chondrogenesis and zebrafish embryo ventralizationQi Shen, Shawn C Little, Meiqi Xu, et al.Redox Biology|February 9, 2022
Humoral immune response to COVID-19 mRNA vaccination in relation to selenium statusKamil Demircan, Thilo Samson Chillon, Qian Sun, et al.Redox Biology|May 31, 2022
Autoimmunity to selenoprotein P predicts breast cancer recurrenceKamil Demircan, Qian Sun, Ylva Bengtsson, et al.Proceedings of the National Academy of Sciences of the United States of America|October 3, 2003
Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2Katarina Lehmann, Petra Seemann, Sigmar Stricker, et al.American Journal of Human Genetics|March 31, 2009
Duplications involving a conserved regulatory element downstream of BMP2 are associated with brachydactyly type A2Katarina Dathe, Klaus W Kjaer, Anja Brehm, et al.Pageof 5