Prolyl hydroxylase domain 2 deficiency promotes skeletal muscle fiber-type transition via a calcineurin/NFATc1-dependent pathwayJunchul Shin(Tohoku University), Ryoichi Nagatomi(Tohoku University)Skeletal MuscleDecember 1, 201510.1186/s13395-016-0079-5Cited by 29SaveCiteExport RISWatch citationsRelated PapersActivation of the hypoxia‐inducible factor pathway induced by prolyl hydroxylase domain 2 deficiency enhances the effect of running training in mice|Acta Physiologica|2016|25Flow-induced endothelial mitochondrial remodeling mitigates mitochondrial reactive oxygen species production and promotes mitochondrial DNA integrity in a p53-dependent manner|Redox Biology|2022|18