encyclopedia of medical concepts
ψ 

Glycogen Phosphorylase, Liver Form

More information in Books or onNLM PubMed
Definition: An isoenzyme of GLYCOGEN PHOSPHORYLASE that catalyzes the degradation of GLYCOGEN in liver tissue. Mutation of the gene coding this enzyme on chromosome 14 is the cause of GLYCOGEN STORAGE DISEASE TYPE VI.     
See Also Glycogen Storage Disease Type VI 		Other names Glycogen Phosphorylase b, Liver Form; Glycogen Phosphorylase a, Liver Form
 
SubstanceCAS Registry & nameCategoriesSourceDrugs*
N-(1-benzyl-3-(3,4-dihydroxypyrrolidin-1-yl)-2-hydroxy-3-oxopropyl)-5-chloro-1H-indole-2-carboxamide  0   *Indoles *Pyrrolidines Glycogen Phosphorylase, Liver Form/antagonists & inhibitors. J Pharmacol Toxicol Methods 2007 Jan-Feb;55(1):71-7

To share this definition, click "text" (Facebook, Twitter) or "link" (blog, mail) then paste text link
Ads by Google

Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012
Warning: the drugs or drug combinations referred to here may be similar or related, but are not be the same ones and may not have the same pharmacological action as other substances described on the same page or in the same row. Please refer to product monograph or to your doctor
This website is accredited by Health On the Net Foundation. Click to verify. We comply with the HONcode standard for trustworthy health information: verify here.
About Reference.MD Privacy