Analysis of mutant and total huntingtin expression in Huntington’s disease murine models
Abstract Huntington’s disease (HD) is a monogenetic neurodegenerative disorder that is caused by the expansion of a polyglutamine region within the huntingtin (HTT) protein, but there is still an incomplete understanding of the molecular mechanisms that drive pathology. Expression of the mutant form...
Enregistré dans:
Auteurs principaux: | Valentina Fodale, Roberta Pintauro, Manuel Daldin, Roberta Altobelli, Maria Carolina Spiezia, Monica Bisbocci, Douglas Macdonald, Alberto Bresciani |
---|---|
Format: | article |
Langue: | EN |
Publié: |
Nature Portfolio
2020
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/f0f9716e3bb54bde98e7f84e35b5a6f0 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
Polyglutamine expansion affects huntingtin conformation in multiple Huntington’s disease models
par: Manuel Daldin, et autres
Publié: (2017) -
Salivary levels of total huntingtin are elevated in Huntington’s disease patients
par: Jody Corey-Bloom, et autres
Publié: (2018) -
Mutant Huntingtin stalls ribosomes and represses protein synthesis in a cellular model of Huntington disease
par: Mehdi Eshraghi, et autres
Publié: (2021) -
Normal aging modulates the neurotoxicity of mutant huntingtin.
par: Elsa Diguet, et autres
Publié: (2009) -
Truncation of mutant huntingtin in knock-in mice demonstrates exon1 huntingtin is a key pathogenic form
par: Huiming Yang, et autres
Publié: (2020)