Prolyl hydroxylase domain 2 deficiency promotes skeletal muscle fiber-type transition via a calcineurin/NFATc1-dependent pathway
Crossref DOI link: https://doi.org/10.1186/s13395-016-0079-5
Published Online: 2016-03-05
Published Print: 2015-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Shin, Junchul
Nunomiya, Aki
Kitajima, Yasuo
Dan, Takashi
Miyata, Toshio
Nagatomi, Ryoichi