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Disease Info Card
Reperfusion Injury
Information about Reperfusion Injury: 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 Reperfusion Injury
Most recent studies have shown that Reperfusion Injury shares some biological mechanisms with arterial-occlusion, brain-injuries, brain-ischemia, cerebral-ischemia, cerebrovascular-accident, edema, hepatic-ischaemia, hypoxia, infarction, inflammation, inflammatory-response, injury-to-kidney, injury-to-liver, ischemia, lung-injury, myocardial-infarction, myocardial-ischemia, myocardial-reperfusion-injury, tissue-adhesions.
Among the many pathways, these few ones have gauged particular interests from scientists studying Reperfusion Injury, and have been seen in publications frequently: Angiogenesis, Cell Activation, Cell Adhesion, Cell Death, Cell Proliferation, Coagulation, Complement Activation, Excretion, Glomerular Filtration, Immune Response, Inflammatory Response, Localization, Neuroprotection, Neutrophil Activation, Pathogenesis, Regeneration, Secretion, Transport, Vasoconstriction, Vasodilation
Quite a number of genes have been found to play important roles in Reperfusion Injury, such as AKT1, BCL2, CASP3, CAT, HMOX1, ICAM1, IL10, IL6, ITGB2, MPO, NFKB1, NOS1, NOS2, NOS3, SLC17A5, SOD1, TNF, XDH. 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.