Pesquisa
Descritor em português: Proteína do X Frágil da Deficiência Intelectual
Descritor em inglês: Fragile X Mental Retardation Protein
Descritor em espanhol: Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil
Descritor proteína de la discapacidad intelectual del síndrome del cromosoma X frágil
Termo(s) alternativo(s) proteína del retraso mental del síndrome del cromosoma X frágil
Nota de escopo: 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.
Descritor em francês: Protéine du syndrome X fragile
Termo(s) alternativo(s): FMRP Protein
Fragile X Mental Retardation 1 Protein
Fragile X Mental Retardation-1 Protein
Código(s) hierárquico(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 escopo: 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 In DeCS, some entry terms may include outdated and offensive terms according to The United Nations Convention on the Rights of Persons with Disabilities (UNCRPD) in order to assist users who are interested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.
Qualificadores 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
Combinação de entrada: deficiency:Fragile X Syndrome
Número de registro: 139135-51-6
Nota MeSH pública: 2006; FRAGILE X MENTAL RETARDATION PROTEIN was indexed under NERVE TISSUE PROTEINS & RNA-BINDING PROTEINS 1991-2005
Nota histórica: 2006(1991)
Identificador DeCS: 50923
ID do descritor: D051860
Documentos indexados na Biblioteca Virtual em Saúde (BVS): Clique aqui para acessar os documentos da BVS
Data de estabelecimento: 01/01/2006
Data de entrada: 30/06/2005
Data de revisão: 23/11/2015
Fragile X Mental Retardation Protein - Conceito preferido
Identificador do conceito M0188653
Nota de escopo 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.
Termo preferido Fragile X Mental Retardation Protein
Termo(s) alternativo(s) FMRP Protein
Fragile X Mental Retardation 1 Protein
Fragile X Mental Retardation-1 Protein



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