Ontology highlight
ABSTRACT:
SUBMITTER: Kim H
PROVIDER: S-EPMC9505916 | biostudies-literature | 2022 Sep
REPOSITORIES: biostudies-literature
Kim Hyesung H Jang Bogun B Kim Yang-Ji YJ Choi Jay Chol JC
International journal of molecular sciences 20220911 18
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 pathway have not been investigated extensively in CADASIL. In this study, we measured the serum and plasma levels of NOTCH3 extracellular domain (N3ECD) and its ligand, Jagged-1, in 279 healthy subje ...[more]