Cargando…
Oral administration of erythromycin decreases RNA toxicity in myotonic dystrophy
OBJECTIVE: Myotonic dystrophy type 1 (DM1) is caused by the expansion of a CTG repeat in the 3′ untranslated region of DMPK. The transcripts containing an expanded CUG repeat (CUG (exp)) result in a toxic gain‐of‐function by forming ribonuclear foci that sequester the alternative splicing factor mus...
Autores principales: | Nakamori, Masayuki, Taylor, Katarzyna, Mochizuki, Hideki, Sobczak, Krzysztof, Takahashi, Masanori P. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4704483/ https://www.ncbi.nlm.nih.gov/pubmed/26783549 http://dx.doi.org/10.1002/acn3.271 |
Ejemplares similares
-
Cellular Senescence and Aging in Myotonic Dystrophy
por: Hasuike, Yuhei, et al.
Publicado: (2022) -
Expanded CUG Repeat RNA Induces Premature Senescence in Myotonic Dystrophy Model Cells
por: Hasuike, Yuhei, et al.
Publicado: (2022) -
Global Increase in Circular RNA Levels in Myotonic Dystrophy
por: Czubak, Karol, et al.
Publicado: (2019) -
Pharmacotherapy alleviates pathological changes in human direct reprogrammed neuronal cell model of myotonic dystrophy type 1
por: Eltahir, Mougina K., et al.
Publicado: (2022) -
Cell type-specific abnormalities of central nervous system in myotonic dystrophy type 1
por: Nakamori, Masayuki, et al.
Publicado: (2022)