Cargando…
Comprehensive Analysis of GABA(A)-A1R Developmental Alterations in Rett Syndrome: Setting the Focus for Therapeutic Targets in the Time Frame of the Disease
Rett syndrome, a serious neurodevelopmental disorder, has been associated with an altered expression of different synaptic-related proteins and aberrant glutamatergic and γ-aminobutyric acid (GABA)ergic neurotransmission. Despite its severity, it lacks a therapeutic option. Through this work we aime...
Autores principales: | Oyarzabal, Alfonso, Xiol, Clara, Castells, Alba Aina, Grau, Cristina, O’Callaghan, Mar, Fernández, Guerau, Alcántara, Soledad, Pineda, Mercè, Armstrong, Judith, Altafaj, Xavier, García-Cazorla, Angels |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014188/ https://www.ncbi.nlm.nih.gov/pubmed/31947619 http://dx.doi.org/10.3390/ijms21020518 |
Ejemplares similares
-
Mitochondrial modulation with leriglitazone as a potential treatment for Rett syndrome
por: Musokhranova, Uliana, et al.
Publicado: (2023) -
Genetic Landscape of Rett Syndrome Spectrum: Improvements and Challenges
por: Vidal, Silvia, et al.
Publicado: (2019) -
The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome
por: Vidal, Silvia, et al.
Publicado: (2017) -
Unraveling Molecular Pathways Altered in MeCP2-Related Syndromes, in the Search for New Potential Avenues for Therapy
por: Castells, Alba-Aina, et al.
Publicado: (2021) -
X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients
por: Xiol, Clara, et al.
Publicado: (2019)