Cargando…
Epigenomic signature of adrenoleukodystrophy predicts compromised oligodendrocyte differentiation
Epigenomic changes may either cause disease or modulate its expressivity, adding a layer of complexity to mendelian diseases. X‐linked adrenoleukodystrophy (X‐ALD) is a rare neurometabolic condition exhibiting discordant phenotypes, ranging from a childhood cerebral inflammatory demyelination (cALD)...
Autores principales: | Schlüter, Agatha, Sandoval, Juan, Fourcade, Stéphane, Díaz‐Lagares, Angel, Ruiz, Montserrat, Casaccia, Patrizia, Esteller, Manel, Pujol, Aurora |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6857458/ https://www.ncbi.nlm.nih.gov/pubmed/29476661 http://dx.doi.org/10.1111/bpa.12595 |
Ejemplares similares
-
Antioxidants Halt Axonal Degeneration in a Mouse Model of X-Adrenoleukodystrophy
por: López-Erauskin, Jone, et al.
Publicado: (2011) -
Functional genomic analysis unravels a metabolic-inflammatory interplay in adrenoleukodystrophy
por: Schlüter, Agatha, et al.
Publicado: (2012) -
Autophagy induction halts axonal degeneration in a mouse model of X-adrenoleukodystrophy
por: Launay, Nathalie, et al.
Publicado: (2014) -
Oxidative stress modulates mitochondrial failure and cyclophilin D function in X-linked adrenoleukodystrophy
por: López-Erauskin, Jone, et al.
Publicado: (2012) -
Complete loss of KCNA1 activity causes neonatal epileptic encephalopathy and dyskinesia
por: Verdura, Edgard, et al.
Publicado: (2020)