Emerging Role of NLRP3 Inflammasome/Pyroptosis in Huntington’s Disease

Huntington’s disease (HD) is a neurodegenerative disease characterized by several symptoms encompassing movement, cognition, and behavior. The mutation of the IT15 gene encoding for the huntingtin protein is the cause of HD. Mutant huntingtin interacts with and impairs the function of several transc...

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Detalles Bibliográficos
Autores principales: Paldino, Emanuela, Fusco, Francesca Romana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368941/
https://www.ncbi.nlm.nih.gov/pubmed/35955494
http://dx.doi.org/10.3390/ijms23158363

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368941/
https://www.ncbi.nlm.nih.gov/pubmed/35955494
http://dx.doi.org/10.3390/ijms23158363

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