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Increased body weight in mice with fragile X messenger ribonucleoprotein 1 (Fmr1) gene mutation is associated with hypothalamic dysfunction.
Ruggiero-Ruff, Rebecca E; Villa, Pedro A; Hijleh, Sarah Abu; Avalos, Bryant; DiPatrizio, Nicholas V; Haga-Yamanaka, Sachiko; Coss, Djurdjica.
Afiliación
  • Ruggiero-Ruff RE; Division of Biomedical Sciences, School of Medicine, University of California, Riverside, Riverside, CA, 92521, USA.
  • Villa PA; Division of Biomedical Sciences, School of Medicine, University of California, Riverside, Riverside, CA, 92521, USA.
  • Hijleh SA; Division of Biomedical Sciences, School of Medicine, University of California, Riverside, Riverside, CA, 92521, USA.
  • Avalos B; Division of Biomedical Sciences, School of Medicine, University of California, Riverside, Riverside, CA, 92521, USA.
  • DiPatrizio NV; Division of Biomedical Sciences, School of Medicine, University of California, Riverside, Riverside, CA, 92521, USA.
  • Haga-Yamanaka S; Department of Molecular, Cell, and Systems Biology, College of Natural and Agricultural Sciences, University of California, Riverside, Riverside, USA.
  • Coss D; Division of Biomedical Sciences, School of Medicine, University of California, Riverside, Riverside, CA, 92521, USA. djurdjica.coss@ucr.edu.
Sci Rep ; 13(1): 12666, 2023 08 04.
Article en En | MEDLINE | ID: mdl-37542065
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proopiomelanocortina / Síndrome del Cromosoma X Frágil Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: Sci Rep Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proopiomelanocortina / Síndrome del Cromosoma X Frágil Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: Sci Rep Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos