Glycogen Phosphorylase, Muscle Form

Known as: phosphorylase, polyphosphorylase, amylophosphorylase 
An isoenzyme of GLYCOGEN PHOSPHORYLASE that catalyzes the degradation of GLYCOGEN in muscle. Mutation of the gene coding this enzyme is the cause of… (More)
National Institutes of Health

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16 relations
Glycogen PhosphorylaseGlycogen Storage Disease Type VIn BloodPYGM gene
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Broader (2)

Phosphorylaseshexosyltransferase

Papers overview

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2011
2011
Expression of Chr9p21 genes CDKN2B (p15(INK4b)), CDKN2A (p16(INK4a), p14(ARF)) and MTAP in human atherosclerotic plaque.
OBJECTIVE The pathophysiology underlying the chromosome (Chr) 9p21 locus of atherosclerosis susceptibility is presently unknown… (More)
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2009
2009
Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B.
BACKGROUND Mitochondrial neurogastrointestinal encephalopathy (MNGIE) is a progressive neurodegenerative disorder associated with… (More)
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2008
2008
Prognostic significance of thymidylate synthase, dihydropyrimidine dehydrogenase and thymidine phosphorylase protein expression in colorectal cancer patients treated with or without 5-fluorouracil…
BACKGROUND Low tumour expression levels of thymidylate synthase (TS), dihydropyrimidine dehydrogenase (DPD) and thymidine… (More)
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Highly Cited
2007
Highly Cited
2007
A role for the transcriptional coactivator PGC-1alpha in muscle refueling.
The transcriptional coactivator peroxisome proliferator-activated receptor gamma coactivator-1alpha (PGC-1alpha) has been… (More)
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2004
2004
Definitive diagnosis of mitochondrial neurogastrointestinal encephalomyopathy by biochemical assays.
BACKGROUND Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE) is caused by mutations in the gene encoding thymidine… (More)
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Highly Cited
2002
Highly Cited
2002
Spontaneous "second wind" and glucose-induced second "second wind" in McArdle disease: oxidative mechanisms.
BACKGROUND Blocked glycogen breakdown in McArdle disease impairs oxidative as well as anaerobic metabolism, but the contribution… (More)
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Highly Cited
1997
Highly Cited
1997
PTG, a protein phosphatase 1-binding protein with a role in glycogen metabolism.
Protein dephosphorylation by phosphatase PP1 plays a central role in mediating the effects of insulin on glucose and lipid… (More)
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1993
1993
McArdle's disease: a nonsense mutation in exon 1 of the muscle glycogen phosphorylase gene explains some but not all cases.
McArdle's disease is an inherited disease that results from a lack of functional muscle glycogen phosphorylase. We report here… (More)
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1978
1978
Fatal infantile form of muscle phosphorylase deficiency.
A girl had generalized, rapidly progressive weakness beginning at age 4 weeks, and causing severe respiratory insufficiency and… (More)
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1958
1958
The muscle phosphorylase b kinase reaction.
The conversion of skeletal muscle phosphorylase b to phosphorylase a is catalyzed by an enzyme requiring ATP’ and a divalent… (More)
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