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Disease Info Card
Retinopathy Of Prematurity
Information about Retinopathy Of Prematurity: 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 Retinopathy Of Prematurity
Most recent studies have shown that Retinopathy Of Prematurity shares some biological mechanisms with blind-vision, bronchopulmonary-dysplasia, diabetic-retinopathy, disorder-of-eye, dysplasia, enterocolitis, enterocolitis-necrotizing, fibrosis, hemorrhage, infant-very-low-birth-weight, intraventricular-brain-hemorrhage, lung-diseases, myopia, pathologic-neovascularization, respiratory-distress, respiratory-distress-syndrome-newborn, retinal-detachment, retinal-diseases, retinal-neovascularization, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Retinopathy Of Prematurity, and have been seen in publications frequently: Aging, Angiogenesis, Cell Death, Cell Growth, Cell Migration, Cell Proliferation, Coagulation, Endothelial Cell Proliferation, Exocytosis, Inflammatory Response, Localization, Pathogenesis, Pollen Tube Growth, Protein Folding, Reflex, Secretion, Transport, Tube Formation, Vasculogenesis, Vasoconstriction
Quite a number of genes have been found to play important roles in Retinopathy Of Prematurity, such as AGA, EPO, ERMAP, GLS2, IGF1, INSL3, NDP, OPN1LW, PEX7, PHYH, POLE3, RHO, RHOD, RLF, SUB1, 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.