Biochemical, Ultrastructural, and Reversibility Studies on Huntingtin Filaments Isolated from Mouse and Human Brain

Huntington's disease (HD) and eight additional inherited neurological disorders are caused by CAG triplet-repeat expansions leading to expanded polyglutamine-sequences in their respective proteins. These triplet-CAG repeat disorders have in common the formation of aberrant intraneuronal protein...

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Detalhes bibliográficos
Publicado no:J Neurosci
Main Authors: Díaz-Hernández, Miguel, Moreno-Herrero, Fernando, Gómez-Ramos, Pilar, Morán, María A., Ferrer, Isidro, Baró, Arturo M., Avila, Jesús, Hernández, Félix, Lucas, José J.
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2004
Assuntos:
Neurobiology of Disease
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6730096/
https://ncbi.nlm.nih.gov/pubmed/15496672
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.2365-04.2004
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