Cargando…
Oligomerization, trans-reduction, and instability of mutant NOTCH3 in inherited vascular dementia
Cerebral small vessel disease (SVD) is a prevalent disease of aging and a major contributor to stroke and dementia. The most commonly inherited SVD, CADASIL, is caused by dominantly acting cysteine-altering mutations in NOTCH3. These mutations change the number of cysteines from an even to an odd nu...
Autores principales: | Young, Kelly Z., Rojas Ramírez, Carolina, Keep, Simon G., Gatti, John R., Lee, Soo Jung, Zhang, Xiaojie, Ivanova, Magdalena I., Ruotolo, Brandon T., Wang, Michael M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8991201/ https://www.ncbi.nlm.nih.gov/pubmed/35393494 http://dx.doi.org/10.1038/s42003-022-03259-2 |
Ejemplares similares
-
Hydrolysis of a second Asp-Pro site at the N-terminus of NOTCH3 in inherited vascular dementia
por: Zhang, Xiaojie, et al.
Publicado: (2021) -
Trans-Reduction of Cerebral Small Vessel Disease Proteins by Notch-Derived EGF-like Sequences
por: Cartee, Naw May Pearl, et al.
Publicado: (2022) -
FSHR Trans-Activation and Oligomerization
por: Szymańska, Kamila, et al.
Publicado: (2018) -
Biochemical Characterization and Cellular Effects of CADASIL Mutants of NOTCH3
por: Meng, He, et al.
Publicado: (2012) -
A midposition NOTCH3 truncation in inherited cerebral small vessel disease may affect the protein interactome
por: Lee, Soo Jung, et al.
Publicado: (2022)