SnapShot: FMRP interacting proteins.

Pasciuto, Emanuela; Bagni, Claudia

Pasciuto, Emanuela; Bagni, Claudia.

Afiliação

Pasciuto E; VIB Center for the Biology of Disease, 3000 Leuven, Belgium; Center for Human Genetics and Leuven Institute for Neurodegenerative Diseases (LIND), KU Leuven, 3000 Leuven, Belgium.
Bagni C; VIB Center for the Biology of Disease, 3000 Leuven, Belgium; Center for Human Genetics and Leuven Institute for Neurodegenerative Diseases (LIND), KU Leuven, 3000 Leuven, Belgium; Department of Biomedicine and Prevention, University of Rome "Tor Vergata," 00133 Rome, Italy.

Cell ; 159(1): 218-218.e1, 2014 Sep 25.

Article em En | MEDLINE | ID: mdl-25259928

ABSTRACT

ABSTRACT

The Fragile X syndrome, caused by the absence or mutation of fragile X mental retardation protein, FMRP, is a the common component of inherited intellectual disability and autism. This SnapShot surveys the protein interaction partners of FMRP, focusing on the cellular pathways in which they are involved.

Assuntos

Proteína do X Frágil da Deficiência Intelectual/metabolismo; Animais; Síndrome do Cromossomo X Frágil/metabolismo; Humanos; Mapas de Interação de Proteínas; RNA Mensageiro/metabolismo

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína do X Frágil da Deficiência Intelectual Limite: Animals / Humans Idioma: En Ano de publicação: 2014 Tipo de documento: Article

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