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Disease Info Card
Wolfram Syndrome
Information about Wolfram 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 Wolfram Syndrome
Most recent studies have shown that Wolfram Syndrome shares some biological mechanisms with ataxia, atrophy, complete-hearing-loss, depressive-disorder, diabetes-mellitus, diabetes-mellitus-insulin-dependent, diabetes-mellitus-non-insulin-dependent, diabetic-retinopathy, hereditary-diseases, mental-disorders, mitochondrial-diseases, nervousness, neurodegenerative-disorders, optic-atrophy, pathological-dilatation, retinal-diseases, sensorineural-hearing-loss-(disorder), urologic-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Wolfram Syndrome, and have been seen in publications frequently: Aging, Autophagy, Cell Cycle, Cell Death, Cell Proliferation, Cognition, Diuresis, Exocytosis, Glucose Homeostasis, Insulin Secretion, Ion Homeostasis, Localization, Oxidative Phosphorylation, Pathogenesis, Platelet Aggregation, Programmed Cell Death, Protein Processing, Rna Interference, Secretion, Translation
Quite a number of genes have been found to play important roles in Wolfram Syndrome, such as ATF6, AVP, CDKN1A, CDKN2A, CISD2, DIAPH1, DMPK, ELN, GLUL, HSPA5, INS, KCNJ11, MTSS1, OPA1, POLG, POMC, SLC4A1, WFS1. 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.