Angiotensins and Huntington’s Disease: A Study on Immortalized Progenitor Striatal Cell Lines

Neurons from mouse models of Huntington’s disease (HD) exhibit altered electrophysiological properties, potentially contributing to neuronal dysfunction and neurodegeneration. The renin–angiotensin system (RAS) is a potential contributor to the pathophysiology of neurodegenerative diseases. However,...

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Detalles Bibliográficos
Autores principales: De Mello, Walmor C., Gerena, Yamil, Ayala-Peña, Sylvette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442183/
https://www.ncbi.nlm.nih.gov/pubmed/28596754
http://dx.doi.org/10.3389/fendo.2017.00108

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5442183/
https://www.ncbi.nlm.nih.gov/pubmed/28596754
http://dx.doi.org/10.3389/fendo.2017.00108

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