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Disease Info Card
Cadasil Syndrome
Information about Cadasil Syndrome: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Cadasil Syndrome
Most recent studies have shown that Cadasil Syndrome shares some biological mechanisms with alzheimers-disease, arteriopathic-disease, cerebral-arterial-diseases, cerebral-infarction, cerebrovascular-accident, cerebrovascular-disorders, cognition-disorders, dementia, dementia-vascular, hypertensive-disease, impaired-cognition, infarction, ischemic-stroke, lacunar-infarction, leukoencephalopathies, leukoencephalopathy-progressive-multifocal, migraine-disorders, migraine-with-aura, multi-infarct-dementia, vascular-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cadasil Syndrome, and have been seen in publications frequently: Aging, Angiogenesis, Cell Adhesion, Cell Death, Cell Fate Determination, Cell Fate Specification, Cell Proliferation, Coagulation, Cognition, Endocytosis, Glycosylation, Localization, Neurogenesis, Notch Signaling Pathway, Pathogenesis, Reflex, Segmentation, Somitogenesis, Vasculogenesis, Vasodilation
Quite a number of genes have been found to play important roles in Cadasil Syndrome, such as ACAT1, APOE, APP, AURKA, CSF1R, CSF2, EGF, HTRA1, JAG1, KCNJ13, LAMC2, MAPT, MTHFR, NOTCH1, NOTCH3, NOTCH4, RBPJ, SLC25A5, TREX1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.