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Disease Info Card
Delayed Graft Function
Information about Delayed Graft Function: 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 Delayed Graft Function
Most recent studies have shown that Delayed Graft Function shares some biological mechanisms with brain-death, cardiac-death, cold-ischemia, cytomegalovirus-infections, decreased-immunologic-activity-[pe], diabetes-mellitus, graft-failure, hemorrhage, hypertensive-disease, infective-disorder, ischemia, kidney-diseases, kidney-failure, kidney-failure-chronic, kidney-tubular-necrosis-acute, renal-tubular-necrosis, reperfusion-injury, thrombosis, warm-ischemia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Delayed Graft Function, and have been seen in publications frequently: Aging, Cell Activation, Cell Adhesion, Cell Death, Cell Proliferation, Coagulation, Complement-dependent Cytotoxicity, Dehiscence, Diuresis, Donor Selection, Excretion, Glomerular Filtration, Immune Response, Inflammatory Response, Pathogenesis, Regeneration, Secretion, Sensitization, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Delayed Graft Function, such as AKR1B1, AR, AREG, CABIN1, CIT, CS, DHDDS, ECD, EPO, FDXR, GNL3, HLA-DRB4, IL2, IL6, KRAS, LCN2, RAPGEF5, S100A6, TNF. 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.