Disease Info Card

Factor Xi Deficiency

Information about Factor Xi 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 Factor Xi Deficiency

Most recent studies have shown that Factor Xi Deficiency shares some biological mechanisms with afibrinogenemia, bleeding-tendency, blood-coagulation-disorders, blood-coagulation-disorders-inherited, blood-loss-surgical, cattle-diseases, factor-v-deficiency, factor-vii-deficiency, factor-x-deficiency, factor-xii-deficiency, hemophilia-a, hemophilia-b, hemorrhage, hemorrhagic-disorders, inherited-factor-ii-deficiency, menorrhagia, postoperative-hemorrhage, pregnancy-complications-hematologic, thrombosis, von-willebrand-disease.

Among the many pathways, these few ones have gauged particular interests from scientists studying Factor Xi Deficiency, and have been seen in publications frequently: Blood Coagulation, Cellular Homeostasis, Coagulation, Fibrinolysis, Hemostasis, Hypersensitivity, Localization, Mating, Menarche, Menstruation, Mrna Splicing, Neutrophil Degranulation, Pathogenesis, Platelet Activation, Platelet Aggregation, Proteolysis, Response To Heparin, Secretion, Translation, Zymogen Activation

Quite a number of genes have been found to play important roles in Factor Xi Deficiency, such as F10, F11, F12, F2, F3, F8, KLK4, KNG1, PLG, PTCRA, SERPINC1, TF, VWF, ZNF160. 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.