Concept information
Preferred term
alpha-Glucosidases
Type
-
mesh:Descriptor
Definition
- Enzymes that catalyze the exohydrolysis of 1,4-alpha-glucosidic linkages with release of alpha-glucose. Deficiency of alpha-1,4-glucosidase may cause GLYCOGEN STORAGE DISEASE TYPE II.
Broader concept
Synonym(s)
- alpha-D-Glucoside glucohydrolases
- alpha-Glucosidase
- Maltase
- Maltase-Glucoamylase
- Maltases
Allowable Qualifier(s)
- administration & dosage (Qualifier)
- adverse effects (Qualifier)
- analysis (Qualifier)
- biosynthesis (Qualifier)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemical synthesis (Qualifier)
- chemistry (Qualifier)
- classification (Qualifier)
- deficiency (Qualifier)
- drug effects (Qualifier)
- economics (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- isolation & purification (Qualifier)
- metabolism (Qualifier)
- pharmacokinetics (Qualifier)
- pharmacology (Qualifier)
- physiology (Qualifier)
- poisoning (Qualifier)
- radiation effects (Qualifier)
- standards (Qualifier)
- supply & distribution (Qualifier)
- therapeutic use (Qualifier)
- toxicity (Qualifier)
- ultrastructure (Qualifier)
- urine (Qualifier)
In other languages
-
French
-
Alpha-D-glucoside glucohydrolase
-
alpha-D-Glucoside glucohydrolases
-
Glucoinvertase
-
Glucosidosucrase
-
Maltase
URI
http://data.loterre.fr/ark:/67375/JVR-QJKPM4J1-8
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