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Disease Info Card
Occlusion, Middle Cerebral Artery
Information about Occlusion, Middle Cerebral Artery: 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 Occlusion, Middle Cerebral Artery
Most recent studies have shown that Occlusion, Middle Cerebral Artery shares some biological mechanisms with arterial-occlusion, arterial-occlusive-diseases, brain-edema, brain-infarction, brain-injuries, brain-ischemia, cerebral-artery-occlusion, cerebral-infarction, cerebral-ischemia, cerebrovascular-accident, edema, infarction, infarction-middle-cerebral-artery, inflammation, ischemia, ischemic-stroke, malnutrition, reperfusion-injury, transient-ischemic-attack.
Among the many pathways, these few ones have gauged particular interests from scientists studying Occlusion, Middle Cerebral Artery, and have been seen in publications frequently: Aging, Angiogenesis, Cell Adhesion, Cell Death, Cell Migration, Cell Proliferation, Coagulation, Immune Response, Inflammatory Response, Localization, Neurogenesis, Neuroprotection, Pathogenesis, Platelet Aggregation, Reflex, Regeneration, Reverse Transcription, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Occlusion, Middle Cerebral Artery, such as BCL2, BDNF, CASP3, CAT, FGFR1, GFAP, IL6, MMP9, NOS1, NOS2, PLAT, RANGAP1, SLC17A5, SOD1, TNF, VEGFA. 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.