Cargando…
Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset inherited neurodegenerative disorder characterized by progressive intention tremor, gait ataxia and dementia associated with mild brain atrophy. The cause of FXTAS is a premutation expansion, of 55 to 200 CGG repeats localized withi...
Autores principales: | Glineburg, M. Rebecca, Todd, Peter K., Charlet-Berguerand, Nicolas, Sellier, Chantal |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier/North-Holland Biomedical Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010627/ https://www.ncbi.nlm.nih.gov/pubmed/29453961 http://dx.doi.org/10.1016/j.brainres.2018.02.006 |
Ejemplares similares
-
The multiple molecular facets of fragile X-associated tremor/ataxia syndrome
por: Sellier, Chantal, et al.
Publicado: (2014) -
Neuropathology of RAN translation proteins in fragile X-associated tremor/ataxia syndrome
por: Krans, Amy, et al.
Publicado: (2019) -
Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome
por: Sellier, Chantal, et al.
Publicado: (2017) -
FMRpolyG-positive inclusions in CNS and non-CNS organs of a fragile X premutation carrier with fragile X-associated tremor/ataxia syndrome
por: Buijsen, Ronald AM, et al.
Publicado: (2014) -
Curcumin Regulates the r(CGG)(exp) RNA Hairpin Structure and Ameliorate Defects in Fragile X-Associated Tremor Ataxia Syndrome
por: Verma, Arun Kumar, et al.
Publicado: (2020)