Random Lasing Detection of Mutant Huntingtin Expression in Cells

Huntington’s disease (HD) is an autosomal dominant, incurable neurodegenerative disease caused by mutation in the huntingtin gene (HTT). HTT mutation leads to protein misfolding and aggregation, which affect cells’ functions and structural features. Because these changes might modify the scattering...

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Detalles Bibliográficos
Autores principales: de Armas-Rillo, Sergio, Fumagallo-Reading, Felipe, Luis-Ravelo, Diego, Abdul-Jalbar, Beatriz, González-Hernández, Tomás, Lahoz, Fernando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8198928/
https://www.ncbi.nlm.nih.gov/pubmed/34073127
http://dx.doi.org/10.3390/s21113825

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8198928/
https://www.ncbi.nlm.nih.gov/pubmed/34073127
http://dx.doi.org/10.3390/s21113825

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