Disease Info Card

Ascorbic Acid Deficiency

Information about Ascorbic Acid 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 Ascorbic Acid Deficiency

Most recent studies have shown that Ascorbic Acid Deficiency shares some biological mechanisms with anemia, avitaminosis, deficiency-diseases, folic-acid-deficiency, hemorrhage, malignant-neoplasms, malnutrition, neoplasms, nutrition-disorders, periodontal-diseases, riboflavin-deficiency, scurvy, thiamine-deficiency, vitamin-a-deficiency, vitamin-b-12-deficiency, vitamin-b-6-deficiency, vitamin-b-deficiency, vitamin-d-deficiency, vitamin-deficiency, vitamin-e-deficiency.

Among the many pathways, these few ones have gauged particular interests from scientists studying Ascorbic Acid Deficiency, and have been seen in publications frequently: Aging, Blood Coagulation, Bone Resorption, Cell Proliferation, Coagulation, Dentinogenesis, Disease Resistance, Excretion, Gallstone Formation, Hypersensitivity, Immune Response, Inflammatory Response, Ossification, Pathogenesis, Phagocytosis, Regeneration, Secretion, Senescence, Transport, Wound Healing

Quite a number of genes have been found to play important roles in Ascorbic Acid Deficiency, such as ALB, BBS9, CAT, CP, CRP, EPO, GSR, GULO, HP, INS, MS4A1, POMC, PYCARD, RGN, SPANXB1, STS, TEAD1, TF. 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.