Prolyl hydroxylase domain 2 deficiency promotes skeletal muscle fiber-type transition via a calcineurin/NFATc1-dependent pathway

Overview of attention for article published in Skeletal Muscle, March 2016

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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

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