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- Table of Contents
, No Gclids
pathway Info Card
Donor Selection
Information about Donor Selection: 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 Donor Selection
Most recent studies have shown that Donor Selection shares some biological mechanisms with aging, coagulation, complement-dependent-cytotoxicity, cytokine-secretion, fertilization, glomerular-filtration, hemostasis, immune-response, inflammatory-response, insemination, liver-regeneration, localization, mating, pathogenesis, regeneration, secretion, sensitization, sperm-motility, sulfate-reduction, transport.
Among the many pathways, these few ones have gauged particular interests from scientists studying Donor Selection, and have been seen in publications frequently: aging, coagulation, complement-dependent-cytotoxicity, cytokine-secretion, fertilization, glomerular-filtration, hemostasis, immune-response, inflammatory-response, insemination, liver-regeneration, localization, mating, pathogenesis, regeneration, secretion, sensitization, sperm-motility, sulfate-reduction, transport
Quite a number of genes have been found to play important roles in Donor Selection, such as ABO, FUT1, GEM, HLA-A, HLA-B, HLA-C, HLA-DPB1, HLA-DRB1, HLA-DRB3, HLA-DRB4, HLA-DRB5, HLA-E, IFNG, IL10, IL2, IL4, KIR3DL1, NOD2, PRNP, 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 pathway. Plesae stay updated.