Fragile X-like behaviors and abnormal cortical dendritic spines in cytoplasmic FMR1-interacting protein 2-mutant mice.

Han, Kihoon; Chen, Hogmei; Gennarino, Vincenzo A; Richman, Ronald; Lu, Hui-Chen; Zoghbi, Huda Y

Han, Kihoon; Chen, Hogmei; Gennarino, Vincenzo A; Richman, Ronald; Lu, Hui-Chen; Zoghbi, Huda Y.

Afiliación

Han K; Department of Molecular and Human Genetics, The Howard Hughes Medical Institute, Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA kihoonh@bcm.edu hzoghbi@bcm.edu.
Chen H; Departments of Pediatrics and, The Cain Foundation Laboratories Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA.
Gennarino VA; Department of Molecular and Human Genetics, Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA.
Richman R; Department of Molecular and Human Genetics, The Howard Hughes Medical Institute, Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA.
Lu HC; Departments of Pediatrics and, Program in Developmental Biology and Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA, The Cain Foundation Laboratories Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA.
Zoghbi HY; Department of Molecular and Human Genetics, The Howard Hughes Medical Institute, Departments of Pediatrics and, Program in Developmental Biology and Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030, USA, Jan and Dan Duncan Neurological Research Institute, Texas Children's Ho

Hum Mol Genet ; 24(7): 1813-23, 2015 Apr 01.

Article en En | MEDLINE | ID: mdl-25432536

Asunto(s)

Corteza Cerebral/metabolismo; Citoplasma/metabolismo; Espinas Dendríticas/metabolismo; Síndrome del Cromosoma X Frágil/metabolismo; Proteínas del Tejido Nervioso/genética; Proteínas Adaptadoras Transductoras de Señales; Animales; Conducta Animal; Corteza Cerebral/anomalías; Citoplasma/genética; Modelos Animales de Enfermedad; Femenino; Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil/genética; Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil/metabolismo; Síndrome del Cromosoma X Frágil/genética; Síndrome del Cromosoma X Frágil/fisiopatología; Humanos; Masculino; Ratones; Ratones Endogámicos C57BL; Ratones Noqueados; Proteínas del Tejido Nervioso/deficiencia

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Corteza Cerebral / Citoplasma / Espinas Dendríticas / Síndrome del Cromosoma X Frágil / Proteínas del Tejido Nervioso Límite: Animals / Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2015 Tipo del documento: Article

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google