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Disease Info Card
Pellagra
Information about Pellagra: 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 Pellagra
Most recent studies have shown that Pellagra shares some biological mechanisms with anemia, avitaminosis, beriberi, deficiency-diseases, dementia, dermatitis, dermatologic-disorders, diarrhea, disorders-of-porphyrin-metabolism, encephalopathies, erythema, hartnup-disease, kwashiorkor, malabsorption-syndrome, malignant-neoplasms, malnutrition, nutrition-disorders, photosensitivity-disorders, vitamin-b-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Pellagra, and have been seen in publications frequently: Aging, Amino Acid Transport, Cell Cycle, Cell Cycle Arrest, Cell Death, Cell Killing, Cell Proliferation, Cognition, Dna Repair, Excretion, Glucose Transport, Glycolysis, Hypersensitivity, Intestinal Absorption, Lactation, Neutral Amino Acid Transport, Pathogenesis, Pigmentation, Secretion, Transport
Quite a number of genes have been found to play important roles in Pellagra, such as ACMSD, ALB, BBS9, BLOC1S6, COL11A2, FECH, GAPDH, INS, KYNU, MS4A1, NDP, PARP1, PLEKHM1, POMC, QPCT, SLC6A19, SPANXB1, TDO2, TKT, TNFSF14. 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.