Disease Info Card

Riboflavin Deficiency

Information about Riboflavin 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 Riboflavin Deficiency

Most recent studies have shown that Riboflavin Deficiency shares some biological mechanisms with anemia, ascorbic-acid-deficiency, avitaminosis, deficiency-diseases, folic-acid-deficiency, malaria, malignant-neoplasms, malnutrition, neoplasms, nutrition-disorders, pregnancy-complications, protein-deficiency, stomatitis, thiamine-deficiency, vitamin-a-deficiency, vitamin-b-12-deficiency, vitamin-b-6-deficiency, vitamin-b-deficiency, vitamin-deficiency, vitamin-e-deficiency.

Among the many pathways, these few ones have gauged particular interests from scientists studying Riboflavin Deficiency, and have been seen in publications frequently: Aging, Cell Cycle, Cell Proliferation, Electron Transport, Excretion, Fatty Acid Beta-oxidation, Fatty Acid Oxidation, Hypersensitivity, Immune Response, Intestinal Absorption, Lactation, Mating, Oxidative Phosphorylation, Parturition, Pathogenesis, Regeneration, Riboflavin Transport, Secretion, Transport, Wound Healing

Quite a number of genes have been found to play important roles in Riboflavin Deficiency, such as ACADS, ALB, ASAH1, BBS9, BRCA2, DAO, FANCD2, FMN1, G6PD, GSR, INS, MS4A1, NR3C1, PLEKHM1, PSEN1, SLC52A1, SPANXB1, TKT, XDH. 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.