Disease Info Card

Coagulation Protein Disorders

Information about Coagulation Protein Disorders: 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 Coagulation Protein Disorders

Most recent studies have shown that Coagulation Protein Disorders shares some biological mechanisms with afibrinogenemia, bleeding-tendency, blood-coagulation-disorders, blood-coagulation-disorders-inherited, blood-platelet-disorders, coagulation-factor-deficiency, disseminated-intravascular-coagulation, dysfibrinogenemia, factor-vii-deficiency, hemophilia-a, hemophilia-b, hemorrhage, hemorrhagic-disorders, liver-diseases, pregnancy-complications-hematologic, thrombophilia, thrombosis, venous-thrombosis, vitamin-k-deficiency, von-willebrand-disease.

Among the many pathways, these few ones have gauged particular interests from scientists studying Coagulation Protein Disorders, and have been seen in publications frequently: Blood Coagulation, Coagulation, Complement Activation, Fibrinolysis, Hemostasis, Inflammatory Response, Lipid Glycosylation, Menarche, Parturition, Pathogenesis, Platelet Activation, Platelet Aggregation, Protein Carboxylation, Regulation Of Hemostasis, Regulation Of Wound Healing, Secretion, Secretory Pathway, Translation, Vasoconstriction, Wound Healing

Quite a number of genes have been found to play important roles in Coagulation Protein Disorders, such as F10, F11, F2, F3, F5, F8, GGCX, PLG, PROC, TF, TMSB4X, TSTA3, VKORC1, 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.