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Familial Alzheimer’s disease–associated presenilin-1 alters cerebellar activity and calcium homeostasis

Familial Alzheimer’s disease (FAD) is characterized by autosomal dominant heritability and early disease onset. Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia w...

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Detalhes bibliográficos
Main Authors: Sepulveda-Falla, Diego, Barrera-Ocampo, Alvaro, Hagel, Christian, Korwitz, Anne, Vinueza-Veloz, Maria Fernanda, Zhou, Kuikui, Schonewille, Martijn, Zhou, Haibo, Velazquez-Perez, Luis, Rodriguez-Labrada, Roberto, Villegas, Andres, Ferrer, Isidro, Lopera, Francisco, Langer, Thomas, De Zeeuw, Chris I., Glatzel, Markus
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3973081/
https://ncbi.nlm.nih.gov/pubmed/24569455
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI66407
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