Cornelia de Lange Syndrome as Paradigm of Chromatinopathies
Chromatinopathies can be defined as a class of neurodevelopmental disorders caused by mutations affecting proteins responsible for chromatin remodeling and transcriptional regulation. The resulting dysregulation of gene expression favors the onset of a series of clinical features such as development...
Guardado en:
Autores principales: | Ilaria Parenti, Frank J. Kaiser |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/9381370b66754a9fa61b4585cd03da18 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
Ejemplares similares
-
Síndrome Cornelia de Lange
por: D,Broitman, et al.
Publicado: (1980) -
Cohesin Mutations Induce Chromatin Conformation Perturbation of the <i>H19</i>/<i>IGF2</i> Imprinted Region and Gene Expression Dysregulation in Cornelia de Lange Syndrome Cell Lines
por: Silvana Pileggi, et al.
Publicado: (2021) -
Diagnostico prenatal en Sindrome de Cornelia de Lange a propósito de 2 casos
por: Taqua R.,Blanca, et al.
Publicado: (2018) -
The development of early social cognitive skills in neurogenetic syndromes associated with autism: Cornelia de Lange, fragile X and Rubinstein–Taybi syndromes
por: Katherine Ellis, et al.
Publicado: (2021) -
Más allá del criticismo radical. Lange y la herencia kantiana en Nietzsche
por: Villarroel Soto,Raúl, et al.
Publicado: (2020)