Concept information
Terme préférentiel
Fragile X Mental Retardation Protein
Type
-
mesh:Descriptor
Définition
- A RNA-binding protein that is found predominately in the CYTOPLASM. It helps regulate GENETIC TRANSLATION in NEURONS and is absent or under-expressed in FRAGILE X SYNDROME.
Concept générique
Synonyme(s)
- 139135-51-6
- FMRP Protein
- Fragile X Mental Retardation-1 Protein
Qualificatif(s) autorisé(s)
- administration & dosage (Qualifier)
- adverse effects (Qualifier)
- agonists (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)
Traductions
-
français
-
139135-51-6
-
Protéine du retard metal lié au chromosome X
-
Protéine du syndrome de l'X fragile
-
Protéine du syndrome X-fragile
-
Protéine FMR-1
-
Protéine FMR1
-
Protéine FMRP
-
Protéine FMRP du syndrome X-fragile
URI
http://data.loterre.fr/ark:/67375/JVR-W2WF3TBF-R
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