Cargando…
Contribution of “Omic” Studies to the Understanding of Cadasil. A Systematic Review
CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) is a small vessel disease caused by mutations in NOTCH3 that lead to an odd number of cysteines in the epidermal growth factor (EGF)-like repeat domain, causing protein misfolding and aggregation. Th...
Autores principales: | Muiño, Elena, Fernández-Cadenas, Israel, Arboix, Adrià |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8304933/ https://www.ncbi.nlm.nih.gov/pubmed/34298974 http://dx.doi.org/10.3390/ijms22147357 |
Ejemplares similares
-
Systematic Review of Cysteine-Sparing NOTCH3 Missense Mutations in Patients with Clinical Suspicion of CADASIL
por: Muiño, Elena, et al.
Publicado: (2017) -
Intravenous thrombolysis in CADASIL: report of two cases and a systematic review
por: Pescini, Francesca, et al.
Publicado: (2022) -
Acute Effects of Wearing Bite-Aligning Mouthguards on Muscular Strength, Power, Agility and Quickness in a Trained Population: A Systematic Review
por: Miró, Adrià, et al.
Publicado: (2021) -
Genome-wide transcriptome study in skin biopsies reveals an association of E2F4 with cadasil and cognitive impairment
por: Muiño, Elena, et al.
Publicado: (2021) -
CADASIL and CARASIL
por: Tikka, Saara, et al.
Publicado: (2014)