Cargando…
Huntingtin and Its Role in Mechanisms of RNA-Mediated Toxicity
Huntington’s disease (HD) is caused by a CAG-repeat expansion mutation in the Huntingtin (HTT) gene. It is characterized by progressive psychiatric and neurological symptoms in combination with a progressive movement disorder. Despite the ubiquitous expression of HTT, pathological changes occur quit...
Autores principales: | Heinz, Annika, Nabariya, Deepti Kailash, Krauss, Sybille |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310054/ https://www.ncbi.nlm.nih.gov/pubmed/34357961 http://dx.doi.org/10.3390/toxins13070487 |
Ejemplares similares
-
Intracellular and intercellular transport of RNA organelles in CXG repeat disorders: The strength of weak ties
por: Nabariya, Deepti Kailash, et al.
Publicado: (2022) -
Huntingtin Ubiquitination Mechanisms and Novel Possible Therapies to Decrease the Toxic Effects of Mutated Huntingtin
por: Fiorillo, Annarita, et al.
Publicado: (2021) -
An in vitro perspective on the molecular mechanisms underlying mutant huntingtin protein toxicity
por: Cisbani, G, et al.
Publicado: (2012) -
Cdk5 phosphorylation of huntingtin reduces its cleavage by caspases: implications for mutant huntingtin toxicity
por: Luo, Shouqing, et al.
Publicado: (2005) -
Huntingtin and Its Partner Huntingtin-Associated Protein 40: Structural and Functional Considerations in Health and Disease
por: Seefelder, Manuel, et al.
Publicado: (2022)