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Descriptor en español: Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil
Descriptor proteína de la discapacidad intelectual del síndrome del cromosoma X frágil
Término(s) alternativo(s) proteína del retraso mental del síndrome del cromosoma X frágil
Nota de alcance: Proteína que se une al ARN y que se encuentra principalmente en el CITOPLASMA. Ayuda a regular la TRADUCCIÓN GENÉTICA en las NEURONAS y está ausente o infraexpresada en el SÍNDROME DEL CROMOSOMA X FRÁGIL.
Descriptor en inglés: Fragile X Mental Retardation Protein
Descriptor en portugués: Proteína do X Frágil da Deficiência Intelectual
Descriptor en francés: Protéine du syndrome X fragile
Término(s) alternativo(s): FMRP Protein
Fragile X Mental Retardation 1 Protein
Fragile X Mental Retardation-1 Protein
Código(s) jeráquico(s): D12.776.157.725.061
D12.776.631.299
D12.776.664.962.124
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D051860
Nota de alcance: 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. In DeCS, some entry terms may include outdated and offensive terms according to The United Nations Convention on the Rights of Persons with Disabilities (UNCRPD) in order to assist users who are interested in retrieving comprehensive search results for studies such as in longitudinal studies.
Calificadores permitidos: AD administration & dosage
AE adverse effects
AG agonists
AI antagonists & inhibitors
AN analysis
BI biosynthesis
BL blood
CF cerebrospinal fluid
CH chemistry
CL classification
CS chemical synthesis
DE drug effects
EC economics
GE genetics
HI history
IM immunology
IP isolation & purification
ME metabolism
PD pharmacology
PH physiology
PK pharmacokinetics
PO poisoning
RE radiation effects
SD supply & distribution
ST standards
TO toxicity
TU therapeutic use
UL ultrastructure
UR urine
Combinación alternativa: deficiency:Fragile X Syndrome
Número de registro: 139135-51-6
Nota Pública de MeSH: 2006; FRAGILE X MENTAL RETARDATION PROTEIN was indexed under NERVE TISSUE PROTEINS & RNA-BINDING PROTEINS 1991-2005
Nota de historia: 2006(1991)
Identificador de DeCS: 50923
ID del Descriptor: D051860
Documentos indizados en la Biblioteca Virtual de Salud (BVS): Haga clic aquí para acceder a los documentos de la BVS
Fecha de establecimiento: 01/01/2006
Fecha de entrada: 30/06/2005
Fecha de revisión: 23/11/2015
Fragile X Mental Retardation Protein - Concepto preferido
UI del concepto M0188653
Nota de alcance 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. In DeCS, some entry terms may include outdated and offensive terms according to The United Nations Convention on the Rights of Persons with Disabilities (UNCRPD) in order to assist users who are interested in retrieving comprehensive search results for studies such as in longitudinal studies.
Término preferido Fragile X Mental Retardation Protein
Término(s) alternativo(s) FMRP Protein
Fragile X Mental Retardation 1 Protein
Fragile X Mental Retardation-1 Protein



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