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Disease Info Card
Nephrotic Syndrome
Information about Nephrotic Syndrome: 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 Nephrotic Syndrome
Most recent studies have shown that Nephrotic Syndrome shares some biological mechanisms with amyloidosis, edema, focal-glomerulosclerosis, glomerulonephritis, glomerulonephritis-membranoproliferative, glomerulosclerosis-(disorder), hypertensive-disease, kidney-diseases, kidney-failure, kidney-failure-chronic, lipoid-nephrosis, lupus-erythematosus-systemic, membranous-glomerulonephritis, nephritis, nephrosis, proteinuria-of-undiagnosed-cause, renal-glomerular-disease, sclerosis, segmental-glomerulosclerosis, thrombosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Nephrotic Syndrome, and have been seen in publications frequently: Aging, Blood Coagulation, Cell Activation, Cell Proliferation, Coagulation, Complement Activation, Diuresis, Excretion, Fibrinolysis, Glomerular Filtration, Hemostasis, Hypersensitivity, Immune Response, Localization, Natriuresis, Pathogenesis, Platelet Aggregation, Secretion, Transport, Vasoconstriction
Quite a number of genes have been found to play important roles in Nephrotic Syndrome, such as ACE, ACTN4, AGT, ALB, C3, GNL3, IL2, INS, KRAS, LPA, LYZ, NPHS1, NPHS2, POMC, RAPGEF5, REN, SERPINC1, 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.