Variant BMP receptor mutations causing fibrodysplasia ossificans progressiva (FOP) in humans show BMP ligand-independent receptor activation in zebrafish-Reference-Cited by-同舟云学术

Variant BMP receptor mutations causing fibrodysplasia ossificans progressiva (FOP) in humans show BMP ligand-independent receptor activation in zebrafish

Published:2018-04 Issue: Volume:109 Page:225-231
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Mucha Bettina E.,Hashiguchi Megumi,Zinski Joseph,Shore Eileen M.,Mullins Mary C.

Funder

NIH/NIGMS

NIH

Cali Developmental Grant

International Fibrodysplasia Ossificans Progressiva Association

Center for Research in FOP and Related Disorders

Cali/Weldon Professorship

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference49 articles.

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3. Structure of the bone morphogenetic protein receptor ALK2 and implications for fibrodysplasia ossificans progressiva;Chaikuad;J. Biol. Chem.,2012

4. An Acvr1 R206H knock-in mouse has fibrodysplasia ossificans progressiva;Chakkalakal;J. Bone Miner. Res.,2012

5. The role of tolloid/minifin in dorsoventral pattern formation of the zebrafish embryo;Connors;Development,1999

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