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Disease Info Card
Norrie Disease
Information about Norrie Disease: 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 Norrie Disease
Most recent studies have shown that Norrie Disease shares some biological mechanisms with blind-vision, blindness-congenital, complete-hearing-loss, disorder-of-eye, dysplasia, eye-abnormalities, eye-diseases-hereditary, eye-neoplasms, glioma, hearing-problem, nervous-system-disorder, osteoporosis, retinal-detachment, retinal-diseases, retinal-dysplasia, retinoblastoma, retinopathy-of-prematurity, sensorineural-hearing-loss-(disorder).
Among the many pathways, these few ones have gauged particular interests from scientists studying Norrie Disease, and have been seen in publications frequently: Angiogenesis, Bone Resorption, Brain Development, Cell Adhesion, Cell Differentiation, Cell Migration, Cell Proliferation, Endothelial Cell Migration, Enucleation, Eye Development, Localization, Osteoblast Proliferation, Pathogenesis, Pigmentation, Programmed Cell Death, Reflex, Secretion, Stem Cell Maintenance, Translation, Vasculogenesis
Quite a number of genes have been found to play important roles in Norrie Disease, such as BEST1, CHM, DAND5, DMD, FAM49B, FZD1, FZD4, IKBKG, LRP5, MAOA, MAOB, MVP, NDP, OAT, OPN1LW, POU3F4, VEGFA, VWF. 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.