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Published in 2018 at "Journal of the Neurological Sciences"
DOI: 10.1016/j.jns.2018.04.027
Abstract: AIM CADASIL is an inherited cerebrovascular disease caused by mutations in the NOTCH3 gene. Notch signaling is involved in a broad spectrum of function, from the cell proliferation to apoptosis. Thus far, because the molecular…
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Keywords:
protein expression;
cadasil patients;
notch3 protein;
expression ... See more keywords