Concept information
Preferred term
beta-Hexosaminidase alpha Chain
Type
-
mesh:Descriptor
Definition
- The alpha subunit of hexosaminidase A. Mutations in the gene that encodes this protein can result in loss of hexosaminidase A activity and are linked to TAY-SACHS DISEASE.
Broader concept
Entry terms
- beta-N-Acetylhexosaminidase alpha Chain
- Hexosaminidase A, alpha Chain
Allowable Qualifier(s)
- administration & dosage (Qualifier)
- adverse effects (Qualifier)
- analysis (Qualifier)
- antagonists & inhibitors (Qualifier)
- biosynthesis (Qualifier)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemical synthesis (Qualifier)
- chemistry (Qualifier)
- classification (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
-
Chaine alpha de l'hexosaminidase A
-
Chaine alpha de la beta-hexosaminidase
-
Chaine alpha de la bêta-hexosaminidase
-
Chaîne alpha de la bêta-hexosaminidase
-
Chaine alpha de la bêta-N-acétylhexosaminidase
-
Sous-unité alpha de la bêta-hexosaminidase
URI
http://data.loterre.fr/ark:/67375/JVR-S4FVQS9J-N
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