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Hydrolysis of a second Asp-Pro site at the N-terminus of NOTCH3 in inherited vascular dementia

Cerebrovascular pathology at the biochemical level has been informed by the study of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a vascular disorder caused by NOTCH3 mutations. Previous work in CADASIL described N-terminal proteolysis of NOTC...

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Detalles Bibliográficos
Autores principales: Zhang, Xiaojie, Lee, Soo Jung, Wang, Michael M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8390697/
https://www.ncbi.nlm.nih.gov/pubmed/34446744
http://dx.doi.org/10.1038/s41598-021-96679-9