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Disease Info Card
Shwachman Syndrome
Information about Shwachman 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 Shwachman Syndrome
Most recent studies have shown that Shwachman Syndrome shares some biological mechanisms with anxiety-disorders, carcinoma, depressive-disorder, diabetes-mellitus, dwarfism, exocrine-pancreatic-insufficiency, growth-disorders, growth-retardation, hypertensive-disease, kidney-failure-chronic, leukemia, malignant-neoplasms, malnutrition, neoplasms, obesity, pain, pituitary-diseases, somatotropin-deficiency.
Among the many pathways, these few ones have gauged particular interests from scientists studying Shwachman Syndrome, and have been seen in publications frequently: Aging, Bone Maturation, Cell Growth, Cell Proliferation, Coagulation, Excretion, Fermentation, Fertilization, Glomerular Filtration, Glycosylation, Immune Response, Localization, Menarche, Pathogenesis, Proteolysis, Regeneration, Secretion, Translation, Transport, Virulence
Quite a number of genes have been found to play important roles in Shwachman Syndrome, such as ALB, BEST1, DMD, FN1, GGH, GH1, GHR, IGF1, IGFBP3, INS, LYZ, MYH14, PLG, POMC, PRDM10, QPCT, RANGAP1, SLC17A5, 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.