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Disease Info Card
Lipochrome Pigmentation
Information about Lipochrome Pigmentation: 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 Lipochrome Pigmentation
Most recent studies have shown that Lipochrome Pigmentation shares some biological mechanisms with abnormal-degeneration, age-related-macular-degeneration, albinism, alzheimers-disease, atrophy, blind-vision, diabetes-mellitus, dystrophy, hyperplasia, inflammation, malnutrition, neoplasms, nerve-degeneration, nervousness, neurodegenerative-disorders, retinal-degeneration, retinal-diseases, stargardts-disease, vitamin-e-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Lipochrome Pigmentation, and have been seen in publications frequently: Aging, Autophagy, Cell Aging, Cell Death, Cell Division, Cell Proliferation, Cellular Senescence, Complement Activation, Exocytosis, Localization, Pathogenesis, Phagocytosis, Pigment Accumulation, Pigmentation, Proteolysis, Regeneration, Replicative Senescence, Secretion, Senescence, Transport
Quite a number of genes have been found to play important roles in Lipochrome Pigmentation, such as ABCA4, BEST1, CA1, CA3, CAT, CDKN1A, CP, CTSD, ERG, FANCF, GSR, INS, KCNH2, MAOB, RHO, RPE, RPE65, SOD1, TNFSF14. 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.