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RT @davidjglassMD: Prolyl hydroxylase domain 2 deficiency causes skeletal muscle transition via a calcineurin/NFATc1-dependent pathway htt…
RT @davidjglassMD: Prolyl hydroxylase domain 2 deficiency causes skeletal muscle transition via a calcineurin/NFATc1-dependent pathway htt…
New #SkeletalMuscle paper on PHD2-deficiency resulting in fiber-type transition via a calcineurin/NFATc1-dep.pathway https://t.co/7fLtFH0LpC
Prolyl hydroxylase domain 2 deficiency causes skeletal muscle transition via a calcineurin/NFATc1-dependent pathway https://t.co/xhhjje3Qgr