Prolyl hydroxylase domain 2 deficiency promotes skeletal muscle fiber-type transition via a calcineurin/NFATc1-dependent pathway.
| Autor: | Junchul Shin1, Aki Nunomiya1, Yasuo Kitajima1, Takashi Dan2, Toshio Miyata2, Ryoichi Nagatomi1,3,4 nagatomi@med.tohoku.ac.jp |
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| Zdroj: | Skeletal Muscle. 3/5/2016, p1-16. 16p. |
| Databáze: | Academic Search Ultimate |
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