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Glycogen Phosphorylase, Liver Form
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.
推出的年份: 2002
副标题
administration and dosage
adverse effects
analysis
antagonists and inhibitors
biosynthesis
blood
cerebrospinal fluid
chemical synthesis
chemistry
classification
deficiency
drug effects
economics
genetics
history
immunology
isolation and purification
metabolism
pharmacokinetics
pharmacology
physiology
poisoning
radiation effects
standards
supply and distribution
therapeutic use
toxicity
ultrastructure
urine
树号:
D08.811.913.400.450.460.400.186.124
MeSH 单一 ID:
D025001
进入的组:
Glycogen Phosphorylase b, Liver Form
Glycogen Phosphorylase a, Liver Form
早前的内容:
Glucosyltransferases (1966-1971)
Phosphorylases (1972-2001)
All MeSH Categories
Chemicals and Drugs Category
Enzymes and Coenzymes [D08]
Enzymes [D08.811]
Transferases [D08.811.913]
Glycosyltransferases [D08.811.913.400]
Hexosyltransferases [D08.811.913.400.450]
Glucosyltransferases [D08.811.913.400.450.460]
Phosphorylases [D08.811.913.400.450.460.400]
Glycogen Phosphorylase [D08.811.913.400.450.460.400.186]
Glycogen Phosphorylase, Brain Form [D08.811.913.400.450.460.400.186.061]
Glycogen Phosphorylase, Liver Form [D08.811.913.400.450.460.400.186.124]
Glycogen Phosphorylase, Muscle Form [D08.811.913.400.450.460.400.186.312]
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