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Disease Info Card
Migraine With Aura
Information about Migraine With Aura: 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 Migraine With Aura
Most recent studies have shown that Migraine With Aura shares some biological mechanisms with brain-ischemia, cadasil-syndrome, cerebrovascular-accident, common-migraine, depressive-disorder, epilepsy, familial-hemiplegic-migraine, foramen-ovale-patent, headache, headache-disorders, hemiplegia, infarction, ischemia, ischemic-stroke, migraine-disorders, nausea, pain, tension-headache.
Among the many pathways, these few ones have gauged particular interests from scientists studying Migraine With Aura, and have been seen in publications frequently: Coagulation, Foramen Ovale Closure, Habituation, Hypersensitivity, Ion Homeostasis, Ion Transport, Localization, Menarche, Menopause, Menstruation, Pathogenesis, Platelet Activation, Platelet Aggregation, Reflex, Secretion, Sensitization, Synaptic Transmission, Transport, Vasoconstriction, Vasodilation
Quite a number of genes have been found to play important roles in Migraine With Aura, such as ACE, ATP1A2, AURKA, CACNA1A, CALCA, CHM, CSAD, F2, GOLPH3, MTHFR, NOTCH3, NOTCH4, PMEL, PYCARD, S100A12, SCN1A, SLC6A4, TGFBI, TNF, TYMS. 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.