Disease Info Card

Retinal Perforations

Information about Retinal Perforations: 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 Perforations

Most recent studies have shown that Retinal Perforations shares some biological mechanisms with cataract, diabetic-retinopathy, disorder-of-eye, edema, epiretinal-membrane, eye-injuries, giving-way, hemorrhage, intraocular-pressure-disorder, macular-hole, macular-retinal-edema, macule, myopia, posterior-vitreous-detachment, proliferative-vitreoretinopathy, retinal-detachment, retinal-diseases, rhegmatogenous-retinal-detachment, vitreous-detachment, vitreous-hemorrhage.

Among the many pathways, these few ones have gauged particular interests from scientists studying Retinal Perforations, and have been seen in publications frequently: Aging, Angiogenesis, Cell Death, Cell Migration, Cell Proliferation, Coagulation, Dehiscence, Delamination, Enucleation, Glial Cell Proliferation, Inflammatory Response, Localization, Pathogenesis, Phagocytosis, Pigmentation, Reflex, Regeneration, Segmentation, Transport, Wound Healing

Quite a number of genes have been found to play important roles in Retinal Perforations, such as COX5A, ERG, ERMAP, GFAP, HNRNPC, KCNH2, MID1, PEX7, PHYH, PLXNA2, PVR, RPE, SLC17A5, TNFSF14, 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.