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Disease Info Card
Mucocutaneous Lymph Node Syndrome
Information about Mucocutaneous Lymph Node 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 Mucocutaneous Lymph Node Syndrome
Most recent studies have shown that Mucocutaneous Lymph Node Syndrome shares some biological mechanisms with aneurysm, arteritis, coronary-aneurysm, coronary-artery-disease, coronary-heart-disease, edema, exanthema, heart-diseases, infarction, inflammation, ischemia, lymphatic-diseases, malignant-lymphoma-lymphocytic-intermediate-differentiation-diffuse, myocardial-infarction, pathological-dilatation, polyarteritis-nodosa, sequelae-aspects, stenosis, vasculitis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mucocutaneous Lymph Node Syndrome, and have been seen in publications frequently: B Cell Activation, Cell Activation, Cell Adhesion, Cell Cycle, Cell Proliferation, Coagulation, Cytokine Production, Excretion, Hypersensitivity, Immune Response, Inflammatory Response, Localization, Lymphocyte Activation, Macrophage Activation, Pathogenesis, Platelet Aggregation, Reverse Transcription, Secretion, T Cell Activation, Transport
Quite a number of genes have been found to play important roles in Mucocutaneous Lymph Node Syndrome, such as ALB, CCND1, CD4, CD8A, CLEC4D, CRP, CSRP1, CTLA4, FBLIM1, FH, GOPC, HLA-DQA1, IFNG, IL10, IL2, IL4, IL6, NOD2, TNF, VEGFA. 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.