| DEBRA | Dystrophic Epidermolysis Bulosa Research Association |
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| debrancher deficiency | Type of glycogen storage disease, due to deficiency of amylo-1,4-1,6-transglucosidase (brancher enzyme). Synonym: brancher deficiency glycogenosis, debrancher deficiency. (05 Mar 2000) |
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| debranching enzymes | Enzyme's that bring about destruction of branches in glycogen; formerly considered to be one enzyme, now known to be a mixture of transferases (4-alpha-d-glucanotransferase) and hydrolases (amylo-1,6-glucosidase). Synonym: debranching factors. (05 Mar 2000) |
| debranching factors | Enzyme's that bring about destruction of branches in glycogen; formerly considered to be one enzyme, now known to be a mixture of transferases (4-alpha-d-glucanotransferase) and hydrolases (amylo-1,6-glucosidase). Synonym: debranching factors. (05 Mar 2000) |
| debranching enzyme |
An enzyme, dextrin-1-6-glucosidase, that removes a carbohydrate unit from molecules that contain short carbohydrate units attached as side chains.
Ãâó:
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| debrancher d. |
glycogen storage disease, type III.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| debrancher e. |
1. amylo-1,6-glucosidase. 2. a term used to describe any enzyme removing branches from macromolecules, usually polysaccharides, by cleaving at branch points.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| debrancher enzyme |
see under enzyme.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| debrancher enzyme deficiency |
glycogen storage disease, type III.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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