Epigallocatechin-3-gallate improves cardiac hypertrophy and short-term memory deficits in a Williams-Beuren syndrome mouse model

Williams-Beuren syndrome (WBS) is a neurodevelopmental disorder caused by a heterozygous deletion of 26–28 genes at chromosome band 7q11.23. The complete deletion (CD) mouse model mimics the most common deletion found in WBS patients and recapitulates most neurologic features of the disorder along w...

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Detalles Bibliográficos
Autores principales: Ortiz-Romero, Paula, Borralleras, Cristina, Bosch-Morató, Mònica, Guivernau, Biuse, Albericio, Guillermo, Muñoz, Francisco J., Pérez-Jurado, Luis A., Campuzano, Victoria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858783/
https://www.ncbi.nlm.nih.gov/pubmed/29554110
http://dx.doi.org/10.1371/journal.pone.0194476

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5858783/
https://www.ncbi.nlm.nih.gov/pubmed/29554110
http://dx.doi.org/10.1371/journal.pone.0194476

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