Determination of Blood NOTCH3 Extracellular Domain and Jagged-1 Levels in Healthy Subjects

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most common genetic disorder among those responsible for hereditary strokes, and it is caused by a mutation in the NOTCH3 gene on chromosome 19. Blood biomarkers related to the Notch signaling...

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Detalles Bibliográficos
Autores principales: Kim, Hyesung, Jang, Bogun, Kim, Yang-Ji, Choi, Jay Chol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505916/
https://www.ncbi.nlm.nih.gov/pubmed/36142458
http://dx.doi.org/10.3390/ijms231810547

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505916/
https://www.ncbi.nlm.nih.gov/pubmed/36142458
http://dx.doi.org/10.3390/ijms231810547

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