Cargando…
Transcriptome alterations in myotonic dystrophy frontal cortex
Myotonic dystrophy (DM) is caused by expanded CTG/CCTG repeats, causing symptoms in skeletal muscle, heart, and central nervous system (CNS). CNS issues are debilitating and include hypersomnolence, executive dysfunction, white matter atrophy, and neurofibrillary tangles. Here, we generate RNA-seq t...
Autores principales: | Otero, Brittney A., Poukalov, Kiril, Hildebrandt, Ryan P., Thornton, Charles A., Jinnai, Kenji, Fujimura, Harutoshi, Kimura, Takashi, Hagerman, Katharine A., Sampson, Jacinda B., Day, John W., Wang, Eric T. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272850/ https://www.ncbi.nlm.nih.gov/pubmed/33472074 http://dx.doi.org/10.1016/j.celrep.2020.108634 |
Ejemplares similares
-
Differences in splicing defects between the grey and white matter in myotonic dystrophy type 1 patients
por: Nishi, Masamitsu, et al.
Publicado: (2020) -
Muscleblind-Like 1 Knockout Mice Reveal Novel Splicing Defects in the Myotonic Dystrophy Brain
por: Suenaga, Koichi, et al.
Publicado: (2012) -
The myotonic dystrophy experience: a North American cross‐sectional study
por: Hagerman, Katharine A., et al.
Publicado: (2019) -
The Impact of Pregnancy on Myotonic Dystrophy: A Registry-Based Study
por: Johnson, Nicholas E., et al.
Publicado: (2015) -
Molecular characterization of myotonic dystrophy fibroblast cell lines for use in small molecule screening
por: Jenquin, Jana R., et al.
Publicado: (2022)