Calpains as novel players in the molecular pathogenesis of spinocerebellar ataxia type 17

Spinocerebellar ataxia type 17 (SCA17) is a neurodegenerative disease caused by a polyglutamine-encoding trinucleotide repeat expansion in the gene of transcription factor TATA box-binding protein (TBP). While its underlying pathomechanism is elusive, polyglutamine-expanded TBP fragments of unknown...

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Detalles Bibliográficos
Autores principales: Weber, Jonasz Jeremiasz, Anger, Stefanie Cari, Pereira Sena, Priscila, Incebacak Eltemur, Rana Dilara, Huridou, Chrisovalantou, Fath, Florian, Gross, Caspar, Casadei, Nicolas, Riess, Olaf, Nguyen, Huu Phuc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050766/
https://www.ncbi.nlm.nih.gov/pubmed/35482253
http://dx.doi.org/10.1007/s00018-022-04274-6

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