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Disease Info Card
Protein C Deficiency
Information about Protein C Deficiency: 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 Protein C Deficiency
Most recent studies have shown that Protein C Deficiency shares some biological mechanisms with activated-protein-c-resistance, antithrombin-iii-deficiency, blood-coagulation-disorders, cerebrovascular-accident, deep-vein-thrombosis, disseminated-intravascular-coagulation, embolism, hemorrhage, infarction, lupus-erythematosus-systemic, protein-s-deficiency, pulmonary-embolism, purpura, thromboembolism, thrombophilia, thrombophlebitis, thrombosis, venous-thromboembolism, venous-thrombosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Protein C Deficiency, and have been seen in publications frequently: Blood Coagulation, Cell Activation, Cell Adhesion, Coagulation, Fibrinolysis, Glycosylation, Hemostasis, Inflammatory Response, Localization, Oxygen Transport, Pathogenesis, Platelet Activation, Platelet Aggregation, Protein Folding, Proteolysis, Regulation Of Blood Coagulation, Regulation Of Hemostasis, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Protein C Deficiency, such as APC, F2, F5, LPA, MTHFR, PLG, PROC, PROCR, SERPINA5, SERPINC1, SERPINE1, SLC25A10, THBD, VWF. 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.