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

Papers overview

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2011
2011
OBJECTIVE The pathophysiology underlying the chromosome (Chr) 9p21 locus of atherosclerosis susceptibility is presently unknown… (More)
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2009
2009
BACKGROUND Mitochondrial neurogastrointestinal encephalopathy (MNGIE) is a progressive neurodegenerative disorder associated with… (More)
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2008
2008
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
The transcriptional coactivator peroxisome proliferator-activated receptor gamma coactivator-1alpha (PGC-1alpha) has been… (More)
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2004
2004
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
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
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 is an inherited disease that results from a lack of functional muscle glycogen phosphorylase. We report here… (More)
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1978
1978
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 conversion of skeletal muscle phosphorylase b to phosphorylase a is catalyzed by an enzyme requiring ATP’ and a divalent… (More)
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