Fibrodysplasia ossificans progressiva: Basic understanding and experimental models-Reference-Cited by-同舟云学术

Fibrodysplasia ossificans progressiva: Basic understanding and experimental models

Published:2017 Issue:4 Volume:6 Page:242-248
ISSN:2186-361X
Container-title:Intractable & Rare Diseases Research
language:en
Short-container-title:IRDR

Author:

Qi Zijuan¹²,Luan Jing²,Zhou Xiaoyan²,Cui Yazhou²,Han Jinxiang²

Affiliation:

1. School of Medicine and Life Sciences, University of Jinan-Shandong Academy of Medical Science

2. Key Laboratory for Rare Disease Research of Shandong Province, Key Laboratory for Biotech Drugs of the Ministry of Health, Shandong Medical Biotechnological Center, Shandong Academy of Medical Sciences

Publisher

International Research and Cooperation Association for Bio & Socio-Sciences Advancement (IRCA-BSSA)

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/irdr/6/4/6_2017.01055/_pdf

Reference54 articles.

1. 1. Nilsson OS. Heterotopic ossification. Acta Orthop Scand. 1998; 69:103-106.

2. 2. Miao J, Zhang C, Wu S, Peng Z, Tania M. Genetic abnormalities in fibrodysplasia ossificans progressiva. Genes Genet Syst. 2012; 87:213-219.

3. 3. Pignolo R J, Bedford-Gay C, Liljesthröm M, Durbin-Johnson B P, Shore E M, Rocke DM, Kaplan FS. The natural history of flare-ups in fibrodysplasia ossificans progressiva (FOP): A comprehensive global assessmen. J Bone Miner Res. 2016; 31:650-656.

4. 4. Shore EM, Gannon FH, Kaplan FS. Fibrodysplasia ossificans progressiva: Why do some people have two skeletons? Rev Rhum Engl Ed. 1997; 64(Suppl 6):92S-97S.

5. 5. Shore EM, Xu M, Feldman GJ, et al. A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.Nat Genet. 2006; 38:525-527.

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