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GS Glycogen synthase
GSK Glycogen synthase kinase
MeSH(Medical Subject Headings) ¸ÂÃã °Ë»ö (http://www.nlm.nih.gov) °á°ú : 5 ÆäÀÌÁö: 3
  • Glycogen Storage Disease Type III - »õâ An autosomal recessive metabolic disorder due to deficient expression of amylo-1,6-glucosidase (one part of the glycogen debranching enzyme system). The clinical course of the disease is similar to that of glycogen storage disease type I, but milder. Massive hepatomegaly, which is present in young children, diminishes and occasionally disappears with age. Levels of glycogen with short outer branches are elevated in muscle, liver, and erythrocytes. Six subgroups have been identified, with subgroups Type IIIa and Type IIIb being the most prevalent.
    Synonyms : Cori Disease, Deficiency, Debrancher, Coris Disease, Debrancher Deficiencies, Deficiencies, Debrancher, Dextrinoses, Limit, Dextrinosis, Limit, Disease, Cori, Disease, Cori's, Disease, Forbes, Limit Dextrinoses
  • Glycogen Storage Disease Type IV - »õâ An autosomal recessive metabolic disorder due to a deficiency in expression of GLYCOGEN BRANCHING ENZYME 1 (alpha-1,4-glucan-6-alpha-glucosyltransferase), resulting in an accumulation of abnormal GLYCOGEN with long outer branches. Clinical features are MUSCLE HYPOTONIA and CIRRHOSIS. Death from liver disease usually occurs before age 2.
    Synonyms : Andersen's Disease, Deficiency, Brancher, Type IV Glycogenosis, Amylopectinoses, Andersens Disease, Brancher Deficiencies, Deficiencies, Brancher, Disease, Andersen, Disease, Andersen's, Glycogenosis, Type IV
  • Glycogen Storage Disease Type V - »õâ Glycogenosis due to muscle phosphorylase deficiency. Characterized by painful cramps following sustained exercise.
    Synonyms : Deficiency, Muscle Phosphorylase, McArdle Disease, Muscle Phosphorylase Deficiency, 5, Glycogenosis, 5s, Glycogenosis, Deficiencies, Muscle Phosphorylase, Disease, McArdle, Disease, McArdle's, Glycogenosis 5s, McArdles Disease, Muscle Phosphorylase Deficiencies
  • Glycogen Storage Disease Type VI - »õâ A hepatic GLYCOGEN STORAGE DISEASE in which there is an apparent deficiency of hepatic phosphorylase (GLYCOGEN PHOSPHORYLASE, LIVER FORM) activity.
    Synonyms : Glycogenosis Type VI, Glycogenosis VI, Hers' Disease, Disease, Hers, Disease, Hers', Her Disease, Type VI, Glycogenosis
  • Glycogen Storage Disease Type VII - »õâ An autosomal recessive glycogen storage disease in which there is deficient expression of 6-phosphofructose 1-kinase in muscle (PHOSPHOFRUCTOKINASE-1, MUSCLE TYPE) resulting in abnormal deposition of glycogen in muscle tissue. These patients have severe congenital muscular dystrophy and are exercise intolerant.
    Synonyms : Deficiency, Muscle Phosphofructokinase, Muscle Phosphofructokinase Deficiency, Tarui's Disease, Deficiencies, Muscle Phosphofructokinase, Disease, Tarui, Disease, Tarui's, Muscle Phosphofructokinase Deficiencies, Phosphofructokinase Deficiencies, Muscle
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glycogenesis The process by which molecules of glucose combine to form a molecule called glycogen.
Ãâó: www.nutrabio.com/Definitions/definitions_g.htm
glycogenolysis The breakdown of glycogen into glucose molecules.
Ãâó: www.nutrabio.com/Definitions/definitions_g.htm
glycogenesis The process by which glycogen is formed from glucose. See also: Glycogen.
Ãâó: aspin.asu.edu/geneinfo/glos-g.htm
glycogen A food storage molecule. Glycogen is the main form in which carbohydrates are stored in the body. It can be broken down to form glucose to provide the body with energy.
Ãâó: www.spinalnet.co.uk/EEndCom/GBCON/homepage.nsf/0/C...
glycogen A starch that is stored in the muscles and liver that maintains blood sugar levels between meals. It is the form in which carbohydrates are stored in animals and humans.
Ãâó: www.pbs.org/wgbh/pages/frontline/teach/diet/worksh...
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