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...
Main Authors: | Paula Ortiz-Romero, Cristina Borralleras, Mònica Bosch-Morató, Biuse Guivernau, Guillermo Albericio, Francisco J Muñoz, Luis A Pérez-Jurado, Victoria Campuzano |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2018-01-01
|
Series: | PLoS ONE |
Online Access: | http://europepmc.org/articles/PMC5858783?pdf=render |
Similar Items
-
Co-Treatment With Verapamil and Curcumin Attenuates the Behavioral Alterations Observed in Williams–Beuren Syndrome Mice by Regulation of MAPK Pathway and Microglia Overexpression
by: Paula Ortiz-Romero, et al.
Published: (2021-08-01) -
Autistic disorder in patients with Williams-Beuren syndrome: a reconsideration of the Williams-Beuren syndrome phenotype.
by: Sylvie Tordjman, et al.
Published: (2012-01-01) -
Williams-Beuren Syndrome with Brain Dysplasia
by: J Gordon Millichap
Published: (2013-10-01) -
The Temperament of Children with Williams-Beuren Syndrome
by: Shu Chien, et al.
Published: (2006) -
Crystallization studies of epigallocatechin gallate
by: Kesani, Sheshanka
Published: (2007)