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Disease Info Card
Hereditary Factor I Deficiency Disease
Information about Hereditary Factor I Deficiency Disease: 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 Hereditary Factor I Deficiency Disease
Most recent studies have shown that Hereditary Factor I Deficiency Disease shares some biological mechanisms with afibrinogenemia, bleeding-tendency, blood-coagulation-disorders, cerebral-hemorrhage, dysfibrinogenemia, hematoma, hemophilia-a, hemorrhage, hemorrhagic-disorders, hypofibrinogenemia, infarction, intracranial-hemorrhages, pregnancy-complications-hematologic, rupture-spontaneous, thrombasthenia, thrombosis, tissue-adhesions, von-willebrand-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hereditary Factor I Deficiency Disease, and have been seen in publications frequently: Blood Coagulation, Cell Migration, Coagulation, Endothelial Cell Proliferation, Fibrinolysis, Hemostasis, Hypersensitivity, Localization, Menstruation, Mrna Splicing, Ovulation, Pathogenesis, Platelet Activation, Platelet Aggregation, Protein Phosphorylation, Protein Secretion, Reverse Transcription, Secretion, Translation, Wound Healing
Quite a number of genes have been found to play important roles in Hereditary Factor I Deficiency Disease, such as ABCB6, ALB, CARD14, F2, FGA, FGB, FGG, FN1, ITGA2B, PLG, PRDX2, PRNP, RNF130, TNC, 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.