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- Table of Contents
Information about Primary Angle-closure Glaucoma: 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.
Most recent studies have shown that Primary Angle-closure Glaucoma shares some biological mechanisms with acute-angle-closure-glaucoma, anatomical-narrow-angle-glaucoma, angle-closure-glaucoma, anterior-synechiae, blind-vision, cataract, corneal-diseases, disorder-of-the-optic-nerve, glaucoma, glaucoma-open-angle, hypertensive-disease, intraocular-pressure-disorder, ocular-hypertension, peripheral-anterior-synechiae, primary-open-angle-glaucoma, secondary-glaucoma, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Primary Angle-closure Glaucoma, and have been seen in publications frequently: Aging, Cell Death, Circadian Rhythm, Inflammatory Response, Mating, Pathogenesis, Pigment Accumulation, Pigmentation, Reflex, Regeneration, Translation, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Primary Angle-closure Glaucoma, such as ACD, APOE, ASAH1, BRCA1, CALCRL, CYP1B1, FUT2, LTA, MFRP, MMP9, MYOC, PISD, PLXNA2, PSD, RANGAP1, SLC17A5, SLC7A7, SQLE. 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.
Aging | Cell Death | Circadian Rhythm |
Inflammatory Response | Mating | Pathogenesis |
Pigment Accumulation | Pigmentation | Reflex |
Regeneration | Translation | Transport |
Wound Healing |