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Disease Info Card
Renal Dysplasia
Information about Renal Dysplasia: 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 Renal Dysplasia
Most recent studies have shown that Renal Dysplasia shares some biological mechanisms with congenital-abnormality, congenital-absence, congenital-absence-of-kidney, cystic-kidney-diseases, dysplasia, fetal-diseases, gastroesophageal-reflux-disease, hydronephrosis, hypertensive-disease, hypoplasia, kidney-diseases, kidney-failure, kidney-failure-chronic, multicystic-dysplastic-kidney, obstructive-uropathy, oligohydramnios, polycystic-kidney-diseases, urethral-diseases, urologic-diseases, vesico-ureteral-reflux.
Among the many pathways, these few ones have gauged particular interests from scientists studying Renal Dysplasia, and have been seen in publications frequently: Cell Death, Cell Proliferation, Developmental Process, Excretion, Glomerular Filtration, Inflammatory Response, Kidney Development, Kidney Morphogenesis, Localization, Lung Development, Lung Growth, Menarche, Micturition, Ossification, Pathogenesis, Secretion, System Development, Translation, Transport, Vasoconstriction
Quite a number of genes have been found to play important roles in Renal Dysplasia, such as ACE, AGT, AGTR1, AGTR2, BCL2, FGF7, GATA3, GDNF, GPC3, HNF1B, IGF2, MDK, PAX2, PTGS2, PTH, RAPGEF5, REN, RET. 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.