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A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.
Shore EM, Xu M, Feldman GJ, Fenstermacher DA, Cho TJ, Choi IH, Connor JM, Delai P, Glaser DL, LeMerrer M, Morhart R, Rogers JG, Smith R, Triffitt JT, Urtizberea JA, Zasloff M, Brown MA, Kaplan FS. Shore EM, et al. Among authors: kaplan fs. Nat Genet. 2006 May;38(5):525-7. doi: 10.1038/ng1783. Epub 2006 Apr 23. Nat Genet. 2006. PMID: 16642017
Hematopoietic stem-cell contribution to ectopic skeletogenesis.
Kaplan FS, Glaser DL, Shore EM, Pignolo RJ, Xu M, Zhang Y, Senitzer D, Forman SJ, Emerson SG. Kaplan FS, et al. J Bone Joint Surg Am. 2007 Feb;89(2):347-57. doi: 10.2106/JBJS.F.00472. J Bone Joint Surg Am. 2007. PMID: 17272450
Fibrodysplasia ossificans progressiva.
Kaplan FS, Le Merrer M, Glaser DL, Pignolo RJ, Goldsby RE, Kitterman JA, Groppe J, Shore EM. Kaplan FS, et al. Best Pract Res Clin Rheumatol. 2008 Mar;22(1):191-205. doi: 10.1016/j.berh.2007.11.007. Best Pract Res Clin Rheumatol. 2008. PMID: 18328989 Free PMC article. Review.
Skeletal metamorphosis in fibrodysplasia ossificans progressiva (FOP).
Kaplan FS, Shen Q, Lounev V, Seemann P, Groppe J, Katagiri T, Pignolo RJ, Shore EM. Kaplan FS, et al. J Bone Miner Metab. 2008;26(6):521-30. doi: 10.1007/s00774-008-0879-8. Epub 2008 Nov 1. J Bone Miner Metab. 2008. PMID: 18979151 Free PMC article. Review.
Viewing FOP through rosi-colored glasses.
Kaplan FS, Pignolo RJ, Shore EM. Kaplan FS, et al. J Bone Miner Res. 2010 Nov;25(11):2295-6. doi: 10.1002/jbmr.214. J Bone Miner Res. 2010. PMID: 20717980 Free PMC article. No abstract available.
274 results