Pin1-mediated Runx2 modification is critical for skeletal development

Runx2 is the master transcription factor for bone formation. Haploinsufficiency of RUNX2 is the genetic cause of cleidocranial dysplasia (CCD) that is characterized by hypoplastic clavicles and open fontanels. In this study, we found that Pin1, peptidyl prolyl cis-trans isomerase, is a critical regu...

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Detalhes bibliográficos
Main Authors: Yoon, Won-Joon, Islam, Rabia, Cho, Young-Dan, Woo, Kyung-Mi, Baek, Jeong-Hwa, Uchida, Takafumi, Komori, Toshihisa, van Wijnen, Andre, Stein, Janet L., Lian, Jane B., Stein, Gary S., Choi, Je-Yong, Bae, Suk-Chul, Ryoo, Hyun-Mo
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4051422/
https://ncbi.nlm.nih.gov/pubmed/23702614
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcp.24403
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