Loss of tafazzin results in decreased myoblast differentiation in C2C12 cells: A myoblast model of Barth syndrome and cardiolipin deficiency

Barth syndrome (BTHS) is an X-linked genetic disorder resulting from mutations in the tafazzin gene (TAZ), which encodes the transacylase that remodels the mitochondrial phospholipid cardiolipin (CL). While most BTHS patients exhibit pronounced skeletal myopathy, the mechanisms linking defective CL...

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Publicado en:Biochim Biophys Acta
Main Authors: Lou, Wenjia, Reynolds, Christian A., Li, Yiran, Liu, Jenney, Hüttemann, Maik, Schlame, Michael, Stevenson, David, Strathdee, Douglas, Greenberg, Miriam L.
Formato: Artigo
Idioma:Inglês
Publicado: 2018
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5976547/
https://ncbi.nlm.nih.gov/pubmed/29694924
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbalip.2018.04.015
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