Apobec2 deficiency causes mitochondrial defects and mitophagy in skeletal muscle

Apobec2 is a member of the activation-induced deaminase/apolipoprotein B mRNA editing enzyme catalytic polypeptide cytidine deaminase family expressed in differentiated skeletal and cardiac muscle. We previously reported that Apobec2 deficiency in mice leads to a shift in muscle fiber type, myopathy...

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Detalles Bibliográficos
Autores principales: Sato, Yusuke, Ohtsubo, Hideaki, Nihei, Naohiro, Kaneko, Takane, Sato, Yoriko, Adachi, Shin-Ichi, Kondo, Shinji, Nakamura, Mako, Mizunoya, Wataru, Iida, Hiroshi, Tatsumi, Ryuichi, Rada, Cristina, Yoshizawa, Fumiaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Federation of American Societies for Experimental Biology 2018
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892721/
https://www.ncbi.nlm.nih.gov/pubmed/29127187
http://dx.doi.org/10.1096/fj.201700493R

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5892721/
https://www.ncbi.nlm.nih.gov/pubmed/29127187
http://dx.doi.org/10.1096/fj.201700493R

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