Cargando…
341 Repeats Is Not Enough for Methylation in a New Fragile X Mouse Model
Fragile X syndrome (FXS) is a leading monogenic cause of intellectual disability and autism spectrum disorders, spurring decades of intense research and a multitude of mouse models. So far, these models do not recapitulate the genetic underpinning of classical FXS—CGG repeat-induced methylation of t...
Autores principales: | Colvin, Steven, Lea, Nick, Zhang, Qiangge, Wienisch, Martin, Kaiser, Tobias, Aida, Tomomi, Feng, Guoping |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9469916/ https://www.ncbi.nlm.nih.gov/pubmed/35977823 http://dx.doi.org/10.1523/ENEURO.0142-22.2022 |
Ejemplares similares
-
Lovastatin, not Simvastatin, Corrects Core Phenotypes in the Fragile X Mouse Model
por: Muscas, Melania, et al.
Publicado: (2019) -
Impaired Reliability and Precision of Spiking in Adults But Not Juveniles in a Mouse Model of Fragile X Syndrome
por: Dwivedi, Deepanjali, et al.
Publicado: (2019) -
BC RNA Mislocalization in the Fragile X Premutation
por: Muslimov, Ilham A., et al.
Publicado: (2018) -
Cell-Type Specific Channelopathies in the Prefrontal Cortex of the fmr1-/y Mouse Model of Fragile X Syndrome(1,2,3)
por: Kalmbach, Brian E., et al.
Publicado: (2015) -
A quantitative homogeneous assay for fragile X mental retardation 1 protein
por: Schutzius, Gabi, et al.
Publicado: (2013)