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Disease Info Card
Whipple Disease
Information about Whipple Disease: 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 Whipple Disease
Most recent studies have shown that Whipple Disease shares some biological mechanisms with arthralgia, arthritis, bacterial-infections, brain-diseases, celiac-disease, communicable-diseases, crohn-disease, diarrhea, endocarditis, gastrointestinal-diseases, infective-disorder, inflammation, intestinal-diseases, lipodystrophy, lymphoma, malabsorption-syndrome, nervousness, pain, sarcoidosis, ulcerative-colitis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Whipple Disease, and have been seen in publications frequently: Cell Adhesion, Excretion, Glycosylation, Hormone Secretion, Hypersensitivity, Immune Response, Inflammatory Response, Intestinal Absorption, Lipid Storage, Lipid Transport, Localization, Macrophage Activation, Pathogenesis, Peristalsis, Phagocytosis, Pigmentation, Reflex, Secretion, Transport, Virulence
Quite a number of genes have been found to play important roles in Whipple Disease, such as ALB, ATP7B, AVP, BCL2, CD4, CRP, CSF2, ESR1, GNAI1, HSPD1, IFNG, IL10, IL2, IL4, LAMC2, MRAP, POMC, SLC4A1, 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.