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JCI Insight|April 10, 2019
ERK1/2 signaling induces skeletal muscle slow fiber-type switching and reduces muscular dystrophy disease severityJustin G Boyer, Vikram Prasad, Taejeong Song, et al.
Human Molecular Genetics|May 31, 2014
P38α MAPK underlies muscular dystrophy and myofiber death through a Bax-dependent mechanismErin R Wissing, Justin G Boyer, Jennifer Q Kwong, et al.
Molecular Genetics and Metabolism Reports|February 7, 2019
Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiencyDelia Apatean, Bojana Rakic, Catherine Brunel-Guitton, et al.
Journal of Molecular and Cellular Cardiology|September 4, 2015
Cardiac-specific deletion of protein phosphatase 1β promotes increased myofilament protein phosphorylation and contractile alterationsRuijie Liu, Robert N Correll, Jennifer Davis, et al.
Molecular Genetics and Metabolism Reports|May 9, 2019
Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex 1 deficiencyDelia Apatean, Bojana Rakic, Catherine Brunel-Guitton, et al.
Human Molecular Genetics|February 22, 2014
Enhanced Ca²⁺ influx from STIM1-Orai1 induces muscle pathology in mouse models of muscular dystrophySanjeewa A Goonasekera, Jennifer Davis, Jennifer Q Kwong, et al.
Psychiatric Genetics|June 5, 2003
Quantitation of X-Y homologous genes in patients with schizophrenia by multiplex polymerase chain reactionNorman L J Ross, Lampros A Mavrogiannis, Carole A Sargent, et al.
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