Cargando…
Expression, Purification, Characterization and Cellular Uptake of MeCP2 Variants
The transcriptional regulator Methyl-CpG-binding protein 2 (MeCP2) is an intrinsically disordered protein, mutations in which, are implicated in the onset of Rett Syndrome, a severe and debilitating neurodevelopmental disorder. Delivery of this protein fused to the cell-penetrating peptide TAT could...
Autores principales: | Beribisky, Alexander V., Steinkellner, Hannes, Geislberger, Sofia, Huber, Anna, Sarne, Victoria, Christodoulou, John, Laccone, Franco |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9122891/ https://www.ncbi.nlm.nih.gov/pubmed/35546650 http://dx.doi.org/10.1007/s10930-022-10054-9 |
Ejemplares similares
-
An electrochemiluminescence based assay for quantitative detection of endogenous and exogenously applied MeCP2 protein variants
por: Steinkellner, Hannes, et al.
Publicado: (2019) -
MeCP2 and Chromatin Compartmentalization
por: Schmidt, Annika, et al.
Publicado: (2020) -
The role of MeCP2 in learning and memory
por: Robinson, Holly A., et al.
Publicado: (2019) -
Rett Syndrome and MECP2 Duplication Syndrome: Disorders of MeCP2 Dosage
por: Collins, Bridget E, et al.
Publicado: (2022) -
Genetic Modifiers of MeCP2 Function in Drosophila
por: Cukier, Holly N., et al.
Publicado: (2008)