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Disease Info Card
Retinal Dysplasia
Information about Retinal 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 Retinal Dysplasia
Most recent studies have shown that Retinal Dysplasia shares some biological mechanisms with blind-vision, cataract, congenital-abnormality, congenital-ocular-coloboma-(disorder), disorder-of-eye, dog-diseases, dysplasia, eye-abnormalities, hydrocephalus, hyperplasia, hypoplasia, microphthalmos, neoplasms, norrie-disease, persistent-hyperplastic-primary-vitreous, retinal-degeneration, retinal-detachment, retinal-diseases, retinoblastoma.
Among the many pathways, these few ones have gauged particular interests from scientists studying Retinal Dysplasia, and have been seen in publications frequently: Aging, Angiogenesis, Brain Development, Cell Cycle, Cell Cycle Arrest, Cell Death, Cell Differentiation, Cell Proliferation, Enucleation, Eye Development, Eye Morphogenesis, Glycosylation, Hatching, Localization, Mitosis, Pathogenesis, Phototransduction, Pigmentation, Transport, Vasculogenesis
Quite a number of genes have been found to play important roles in Retinal Dysplasia, such as CAT, CDKN1B, CDKN2A, CDKN2D, CRAT, ERG, GFAP, GLYAT, IKBKG, KCNH2, NDP, NR2E3, RB1, RHO, RPE, TP53. 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.