BMP type I receptor inhibition reduces heterotopic ossification-Reference-Cited by-同舟云学术

BMP type I receptor inhibition reduces heterotopic ossification

Published:2008-11-30 Issue:12 Volume:14 Page:1363-1369
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Yu Paul B,Deng Donna Y,Lai Carol S,Hong Charles C,Cuny Gregory D,Bouxsein Mary L,Hong Deborah W,McManus Patrick M,Katagiri Takenobu,Sachidanandan Chetana,Kamiya Nobuhiro,Fukuda Tomokazu,Mishina Yuji,Peterson Randall T,Bloch Kenneth D

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm.1888.pdf

Reference33 articles.

1. Shore, E.M. & Kaplan, F.S. Insights from a rare genetic disorder of extra-skeletal bone formation, fibrodysplasia ossificans progressiva (FOP). Bone 43, 427–433 (2008).

2. Buyse, G., Silberstein, J., Goemans, N. & Casaer, P. Fibrodysplasia ossificans progressiva: still turning into wood after 300 years? Eur. J. Pediatr. 154, 694–699 (1995).

3. Kaplan, F.S., Glaser, D.L., Pignolo, R.J. & Shore, E.M. A new era for fibrodysplasia ossificans progressiva: a druggable target for the second skeleton. Expert Opin. Biol. Ther. 7, 705–712 (2007).

4. Kaplan, F.S. et al. Fibrodysplasia ossificans progressiva. Best Pract. Res. Clin. Rheumatol. 22, 191–205 (2008).

5. Shore, E.M. et al. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nat. Genet. 38, 525–527 (2006).

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