Research of Cadasil Syndrome has been linked to Arteriopathic Disease, Leukoencephalopathies, Dementia, Cerebrovascular Accident, Multi-infarct Dementia. The study of Cadasil Syndrome has been mentioned in research publications which can be found using our bioinformatics tool below. Researched pathways related to Cadasil Syndrome include Pathogenesis, Cognition, Notch Signaling Pathway, Aging, Segmentation. These pathways complement our catalog of research reagents for the study of Cadasil Syndrome including antibodies and ELISA kits against NOTCH, ACAT1, JAG1, SLC25A5, APOE.
Cadasil Syndrome Bioinformatics Tool
Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Cadasil Syndrome below!
For more information on how to use Laverne, please read the How to Guide.
We have 1042 products for the study of Cadasil Syndrome that can be applied to Western Blot, Immunocytochemistry/Immunofluorescence, Flow Cytometry, Chromatin Immunoprecipitation (ChIP), Immunohistochemistry from our catalog of antibodies and ELISA kits.
Cadasil Syndrome is also known as Cadasil, Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy, Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And Leucoencephalopathy, Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And Leukoencephalopathy.