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Disease Info Card
North Carolina Macular Dystrophy
Information about North Carolina Macular Dystrophy: 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 North Carolina Macular Dystrophy
Most recent studies have shown that North Carolina Macular Dystrophy shares some biological mechanisms with age-related-macular-degeneration, atrophy, blind-vision, chorioretinal-atrophy, chorioretinal-atrophy-progressive-bifocal, choroidal-neovascularization, dystrophy, geographic-atrophy, hemorrhage, macule, maculopathy, pathologic-neovascularization, retinal-degeneration, retinal-detachment, retinal-diseases, retinal-drusen, retinal-dystrophies, stargardts-disease, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying North Carolina Macular Dystrophy, and have been seen in publications frequently: Localization, Pathogenesis, Pigmentation, Transdifferentiation
Quite a number of genes have been found to play important roles in North Carolina Macular Dystrophy, such as ABCA4, BEST1, COIL, COX5A, ELOVL4, ERG, EXOSC1, IL1R1, IMPG1, KCNH2, KIR3DL2, PLXNA2, RANGAP1, RIMS1, RPE, SLC17A5, SMC2, SRCIN1, WDR48. 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.
Pathways Related to North Carolina Macular Dystrophy
This information is being compiled and will come in a future update
| Localization | Pathogenesis | Pigmentation |
| Transdifferentiation |