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Mice Carrying a Ubiquitous R235W Mutation of Wnt1 Display a Bone-Specific Phenotype.
Yorgan TA, Rolvien T, Stürznickel J, Vollersen N, Lange F, Zhao W, Baranowsky A, Rosenthal L, Hermans-Borgmeyer I, Sharaf A, Karsak M, David JP, Oheim R, Amling M, Schinke T. Yorgan TA, et al. J Bone Miner Res. 2020 Sep;35(9):1726-1737. doi: 10.1002/jbmr.4043. Epub 2020 May 20. J Bone Miner Res. 2020. PMID: 32369212 Free article.
The WNT1G177C mutation specifically affects skeletal integrity in a mouse model of osteogenesis imperfecta type XV.
Vollersen N, Zhao W, Rolvien T, Lange F, Schmidt FN, Sonntag S, Shmerling D, von Kroge S, Stockhausen KE, Sharaf A, Schweizer M, Karsak M, Busse B, Bockamp E, Semler O, Amling M, Oheim R, Schinke T, Yorgan TA. Vollersen N, et al. Bone Res. 2021 Nov 10;9(1):48. doi: 10.1038/s41413-021-00170-0. Bone Res. 2021. PMID: 34759273 Free PMC article.