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Disease Info Card
Punctate Inner Choroidopathy
Information about Punctate Inner Choroidopathy: 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 Punctate Inner Choroidopathy
Most recent studies have shown that Punctate Inner Choroidopathy shares some biological mechanisms with carcinoma, choroid-diseases, choroidal-neovascularization, choroiditis, diabetes-mellitus, disseminated-intravascular-coagulation, dysequilibrium-syndrome, hiv-infections, hypertensive-disease, immunologic-deficiency-syndromes, infarction, infective-disorder, inflammation, leukemia, malignant-neoplasms, neoplasms, pathologic-neovascularization, thrombosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Punctate Inner Choroidopathy, and have been seen in publications frequently: Blood Coagulation, Cell Cycle, Cell Death, Cell Proliferation, Chromatin Remodeling, Coagulation, Fibrinolysis, Hemostasis, Immune Response, Lactation, Localization, Nuclear Import, Pathogenesis, Reflex, Reverse Transcription, Secretion, Translation, Transport, Viral Replication, Virulence
Quite a number of genes have been found to play important roles in Punctate Inner Choroidopathy, such as AP3B1, ATAT1, CD55, DSP, INS, PLAT, PLCB1, PLCB4, PLCG1, PLG, PREP, PTGDR, SERPINC1, SERPINE1, SERPINF2, STATH, TAT, TBP, TNF. 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.