Disease Info Card

Epiretinal Membrane

Information about Epiretinal Membrane: 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 Epiretinal Membrane

Most recent studies have shown that Epiretinal Membrane shares some biological mechanisms with cataract, diabetic-retinopathy, disorder-of-eye, edema, hemorrhage, intraocular-pressure-disorder, macular-edema-cystoid, macular-hole, macular-puckering, macular-retinal-edema, macule, pathologic-neovascularization, posterior-vitreous-detachment, proliferative-diabetic-retinopathy, proliferative-vitreoretinopathy, retinal-detachment, retinal-diseases, retinal-perforations, vitreous-detachment, vitreous-hemorrhage.

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

Quite a number of genes have been found to play important roles in Epiretinal Membrane, such as COX5A, ERG, ERMAP, FN1, GFAP, IL6, KCNH2, MID1, PEX7, PHYH, PLXNA2, PVR, RPE, TNF, TNFSF14, VEGFA, VIM. 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.