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Disease Info Card
Renal Hypoplasia
Information about Renal Hypoplasia: 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 Hypoplasia
Most recent studies have shown that Renal Hypoplasia shares some biological mechanisms with ask-upmark-kidney, congenital-abnormality, congenital-absence, congenital-absence-of-kidney, dysplasia, gastroesophageal-reflux-disease, hydronephrosis, hypertensive-disease, hypoplasia, infection-of-kidney, kidney-diseases, kidney-failure, kidney-failure-chronic, renal-dysplasia, renal-hypertension, renal-insufficiency, stenosis, unilateral-renal-hypoplasia, vesico-ureteral-reflux.
Among the many pathways, these few ones have gauged particular interests from scientists studying Renal Hypoplasia, and have been seen in publications frequently: Angiogenesis, Axon Guidance, Cardiac Conduction, Cell Adhesion, Cell Death, Cell Migration, Cell Proliferation, Excretion, Glomerular Filtration, Hypersensitivity, Kidney Development, Localization, Menarche, Mitosis, Nephron Development, Ossification, Pathogenesis, Pigmentation, Programmed Cell Death, Sex Determination
Quite a number of genes have been found to play important roles in Renal Hypoplasia, such as BCL2, BMP4, CDKN2A, CST3, DBH, EYA1, FBXW4, GDNF, HNF1B, ITGA2, PAX2, RAPGEF5, REN, RET, SIX2, SLIT3. 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.