Cargando…
Genetic and epigenetic determinants of reactivation of Mecp2 and the inactive X chromosome in neural stem cells
Rett syndrome may be treated by reactivating the silent copy of Mecp2 from the inactive X chromosome in female cells. Most studies that model Mecp2 reactivation have used mouse fibroblasts rather than neural cells, which would be critical for phenotypic reversal, and rely on fluorescent reporters th...
Autores principales: | Mira-Bontenbal, H., Tan, B., Gontan, C., Goossens, S., Boers, R.G., Boers, J.B., Dupont, C., van Royen, M.E., IJcken, W.F.J., French, P., Bedalov, A., Gribnau, J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039756/ https://www.ncbi.nlm.nih.gov/pubmed/35148843 http://dx.doi.org/10.1016/j.stemcr.2022.01.008 |
Ejemplares similares
-
Perturbed maintenance of transcriptional repression on the inactive X-chromosome in the mouse brain after Xist deletion
por: Adrianse, Robin L., et al.
Publicado: (2018) -
REX1 is the critical target of RNF12 in imprinted X chromosome inactivation in mice
por: Gontan, Cristina, et al.
Publicado: (2018) -
Characterization of Histone Modifications Associated with Inactive X-Chromosome in Trophoblast Stem Cells, eXtra-Embryonic Endoderm Cells and in In Vitro Derived Undifferentiated and Differentiated Epiblast Like Stem Cells
por: Dupont, Cathérine, et al.
Publicado: (2016) -
Genome-wide analysis toward the epigenetic aetiology of myelodysplastic syndrome disease progression and pharmacoepigenomic basis of hypomethylating agents drug treatment response
por: Siamoglou, Stavroula, et al.
Publicado: (2023) -
Genome wide DNA methylation analysis of alveolar capillary dysplasia lung tissue reveals aberrant methylation of genes involved in development including the FOXF1 locus
por: Slot, Evelien, et al.
Publicado: (2021)