Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1-Reference-Cited by-同舟云学术

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Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1

Published:2008-12-09 Issue:3 Volume:30 Page:379-390
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Kaplan Frederick S.,Xu Meiqi,Seemann Petra,Connor J. Michael,Glaser David L.,Carroll Liam,Delai Patricia,Fastnacht-Urban Elisabeth,Forman Stephen J.,Gillessen-Kaesbach Gabriele,Hoover-Fong Julie,Köster Bernhard,Pauli Richard M.,Reardon William,Zaidi Syed-Adeel,Zasloff Michael,Morhart Rolf,Mundlos Stefan,Groppe Jay,Shore Eileen M.

Funder

Center for Research in FOP and Related Disorders

International FOP Association

Ian Cali Endowment

Weldon Family Endowment

Isaac and Rose Nassau Professorship of Orthopaedic Molecular Medicine

Rita Allen Foundation

National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference73 articles.

1. Paresis of a bone morphogenetic protein-antagonist response in a genetic disorder of heterotopic skeletogenesis;Ahn;J Bone Joint Surg (Am),2003

2. Expression of bone morphogenetic proteins (BMPs), their receptors, and activins in normal and scarred conjunctiva: role of BMP-6 and activin-A in conjunctival scarring?;Andreev;Exp Eye Res,2006

3. Signaling by bone morphogenetic proteins and Smad1 modulates the postnatal differentiation of cerebellar cells;Angley;J Neurosci,2003

4. Mutations in BMP4 cause eye, brain, and digit developmental anomalies: overlap between the BMP4 and Hedgehog signaling pathways;Bakrania;Am J Hum Genet,2008

5. Combinatorial signaling through BMP receptor IB and GDF5: shaping of the distal mouse limb and the genetics of distal limb diversity;Baur;Development,2000

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