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Ubiquitin ligase RNF146 coordinates bone dynamics and energy metabolism

Cleidocranial dysplasia (CCD) is an autosomal dominant human disorder characterized by abnormal bone development that is mainly due to defective intramembranous bone formation by osteoblasts. Here, we describe a mouse strain lacking the E3 ubiquitin ligase RNF146 that shows phenotypic similarities t...

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Bibliografiske detaljer
Udgivet i:J Clin Invest
Main Authors: Matsumoto, Yoshinori, La Rose, Jose, Lim, Melissa, Adissu, Hibret A., Law, Napoleon, Mao, Xiaohong, Cong, Feng, Mera, Paula, Karsenty, Gerard, Goltzman, David, Changoor, Adele, Zhang, Lucia, Stajkowski, Megan, Grynpas, Marc D., Bergmann, Carsten, Rottapel, Robert
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Clinical Investigation 2017
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5490759/
https://ncbi.nlm.nih.gov/pubmed/28581440
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI92233
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