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Disease Info Card
Vitamin K Deficiency
Information about Vitamin K 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 Vitamin K Deficiency
Most recent studies have shown that Vitamin K Deficiency shares some biological mechanisms with bleeding-tendency, blood-coagulation-disorders, cerebral-hemorrhage, cholestasis, disseminated-intravascular-coagulation, fibrosis, fracture, hemorrhage, hemorrhagic-disease-of-newborn, hemorrhagic-disorders, inherited-factor-ii-deficiency, intracranial-hemorrhages, liver-diseases, malabsorption-syndrome, malnutrition, neoplasms, potassium-deficiency, vitamin-d-deficiency, vitamin-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Vitamin K Deficiency, and have been seen in publications frequently: Aging, Blood Coagulation, Bone Mineralization, Bone Resorption, Coagulation, Excretion, Fibrinolysis, Hemostasis, Hypersensitivity, Intestinal Absorption, Lactation, Localization, Oxidative Phosphorylation, Pathogenesis, Platelet Aggregation, Protein Carboxylation, Response To Vitamin, Response To Vitamin K, Secretion, Transport
Quite a number of genes have been found to play important roles in Vitamin K Deficiency, such as AFP, ALB, BEST1, BGLAP, DMD, F2, GGCX, GLA, KRT1, MGP, NAT8, NR1I2, PTH, PTRH1, SLC25A10, VKORC1. 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.