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Disease Info Card
Gitelman Syndrome
Information about Gitelman Syndrome: 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 Gitelman Syndrome
Most recent studies have shown that Gitelman Syndrome shares some biological mechanisms with alkalosis, bartter-disease, calcium-pyrophosphate-deposition-disease, hyperaldosteronism, hypercalciuria, hypertensive-disease, hypocalcemia, hypotension-adverse-event, kidney-diseases, magnesium-deficiency, metabolic-alkalosis, muscle-weakness, nephrocalcinosis, renal-tubular-disorder, tetany, tuberous-sclerosis, vomiting, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Gitelman Syndrome, and have been seen in publications frequently: Chloride Transport, Diuresis, Excretion, Glomerular Filtration, Hypersensitivity, Intestinal Absorption, Ion Transport, Localization, Natriuresis, Pathogenesis, Reflex, Regulation Of Ion Transport, Renal Potassium Excretion, Secretion, Senescence, Translation, Transport, Tubuloglomerular Feedback, Vasoconstriction, Vasodilation
Quite a number of genes have been found to play important roles in Gitelman Syndrome, such as AGT, ANG, APC, BLM, BSND, CLCNKB, CLDN16, DCT, GLUL, GP1BB, KCNJ1, PTH, REN, SLC12A1, SLC12A3, STK39, TESC, TRPM6, TSC1, WNK1. 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.