Disease Info Card

Choline Deficiency

Information about Choline 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 Choline Deficiency

Most recent studies have shown that Choline Deficiency shares some biological mechanisms with carcinogenesis, carcinoma, fatty-liver, fibrosis, folic-acid-deficiency, hepatocarcinogenesis, inflammation, injury-to-liver, liver-carcinoma, liver-cirrhosis, liver-cirrhosis-experimental, liver-diseases, liver-neoplasms, liver-neoplasms-experimental, macular-corneal-dystrophy-type-i, neoplasms, nonalcoholic-steatohepatitis, pancreatitis, steatohepatitis, steatosis.

Among the many pathways, these few ones have gauged particular interests from scientists studying Choline Deficiency, and have been seen in publications frequently: Brain Development, Cell Activation, Cell Cycle, Cell Death, Cell Growth, Cell Proliferation, Dna Methylation, Excretion, Fatty Acid Oxidation, Hepatocyte Proliferation, Inflammatory Response, Liver Regeneration, Localization, Methylation, Mitosis, Pathogenesis, Regeneration, Reverse Transcription, Secretion, Transport

Quite a number of genes have been found to play important roles in Choline Deficiency, such as ACHE, AFP, ALB, CASP3, CCK, CS, GGT1, GGT2, IL6, INS, MLYCD, MUC1, PEMT, PPARA, PPARG, SLC17A5, TNF. 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.