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4. Mutations of the noggin (NOG) and of the activin A type I receptor (ACVR1) genes in a series of twenty-seven French fibrodysplasia ossificans progressiva (FOP) patients. Lucotte G; Houzet A; Hubans C; Lagarde JP; Lenoir G Genet Couns; 2009; 20(1):53-62. PubMed ID: 19400542 [TBL] [Abstract][Full Text] [Related]
5. Neofunction of ACVR1 in fibrodysplasia ossificans progressiva. Hino K; Ikeya M; Horigome K; Matsumoto Y; Ebise H; Nishio M; Sekiguchi K; Shibata M; Nagata S; Matsuda S; Toguchida J Proc Natl Acad Sci U S A; 2015 Dec; 112(50):15438-43. PubMed ID: 26621707 [TBL] [Abstract][Full Text] [Related]
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11. ACVR1-Fc suppresses BMP signaling and chondro-osseous differentiation in an in vitro model of Fibrodysplasia ossificans progressiva. Pang J; Zuo Y; Chen Y; Song L; Zhu Q; Yu J; Shan C; Cai Z; Hao J; Kaplan FS; Shore EM; Zhang K Bone; 2016 Nov; 92():29-36. PubMed ID: 27492611 [TBL] [Abstract][Full Text] [Related]
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14. ALK2: A Therapeutic Target for Fibrodysplasia Ossificans Progressiva and Diffuse Intrinsic Pontine Glioma. Sekimata K; Sato T; Sakai N Chem Pharm Bull (Tokyo); 2020; 68(3):194-200. PubMed ID: 32115526 [TBL] [Abstract][Full Text] [Related]
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19. Fibrodysplasia ossificans progressiva: middle-age onset of heterotopic ossification from a unique missense mutation (c.974G>C, p.G325A) in ACVR1. Whyte MP; Wenkert D; Demertzis JL; DiCarlo EF; Westenberg E; Mumm S J Bone Miner Res; 2012 Mar; 27(3):729-37. PubMed ID: 22131272 [TBL] [Abstract][Full Text] [Related]
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