TY  - GEN
AU  - Shin,Junchul
AU  - Nunomiya,Aki
AU  - Kitajima,Yasuo
AU  - Dan,Takashi
AU  - Miyata,Toshio
AU  - Nagatomi,Ryoichi
TI  - Prolyl hydroxylase domain 2 deficiency promotes skeletal muscle fiber-type transition via a calcineurin/NFATc1-dependent pathway
SN  - 2044-5040
PY  - 2016///0928
KW  - Animals
KW  - Calcineurin
KW  - metabolism
KW  - Calcineurin Inhibitors
KW  - pharmacology
KW  - Capillaries
KW  - Cell Hypoxia
KW  - Cell Line
KW  - Genotype
KW  - Hydroxylation
KW  - Hypoxia-Inducible Factor 1, alpha Subunit
KW  - Hypoxia-Inducible Factor-Proline Dioxygenases
KW  - deficiency
KW  - Mice, Knockout
KW  - Muscle Fibers, Slow-Twitch
KW  - drug effects
KW  - Muscle, Skeletal
KW  - blood supply
KW  - NFATC Transcription Factors
KW  - Neovascularization, Physiologic
KW  - Phenotype
KW  - Protein Stability
KW  - Signal Transduction
KW  - Tacrolimus
KW  - Time Factors
KW  - Vascular Endothelial Growth Factor A
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1186/s13395-016-0079-5
ER  -