Tdp-43 cryptic exons are highly variable between cell types

BACKGROUND: TDP-43 proteinopathy is a prominent pathological feature that occurs in a number of human diseases including amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTD), and inclusion body myositis (IBM). Our recent finding that TDP-43 represses nonconserved cryptic exons led us t...

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Detalles Bibliográficos
Autores principales: Jeong, Yun Ha, Ling, Jonathan P., Lin, Sophie Z., Donde, Aneesh N., Braunstein, Kerstin E., Majounie, Elisa, Traynor, Bryan J., LaClair, Katherine D., Lloyd, Thomas E., Wong, Philip C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289002/
https://www.ncbi.nlm.nih.gov/pubmed/28153034
http://dx.doi.org/10.1186/s13024-016-0144-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289002/
https://www.ncbi.nlm.nih.gov/pubmed/28153034
http://dx.doi.org/10.1186/s13024-016-0144-x

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