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Disease Info Card
Histiocytosis, Langerhans-cell
Information about Histiocytosis, Langerhans-cell: 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 Histiocytosis, Langerhans-cell
Most recent studies have shown that Histiocytosis, Langerhans-cell shares some biological mechanisms with bone-diseases, dermatologic-disorders, diabetes-mellitus, eosinophilic-granuloma, fibrosis, granuloma, histiocytosis, leukemia, lung-diseases, lymphatic-diseases, lymphoma, malignant-neoplasms, malignant-paraganglionic-neoplasm, neoplasms, nervousness, pain, pituitary-diseases, pulmonary-fibrosis, sarcoidosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Histiocytosis, Langerhans-cell, and have been seen in publications frequently: Angiogenesis, Cell Differentiation, Cell Proliferation, Coagulation, Cytokine Production, Excretion, Glycosylation, Hypersensitivity, Immune Response, Inflammatory Response, Leydig Cell Differentiation, Lipid Storage, Localization, Macrophage Activation, Mitosis, Pathogenesis, Phagocytosis, Proteolysis, Secretion, Transdifferentiation
Quite a number of genes have been found to play important roles in Histiocytosis, Langerhans-cell, such as AVP, CD1A, CD1B, CD1C, CD207, CD4, CD68, CTLA4, DCX, GGH, GH1, HLA-DQA1, LYZ, NOD2, POMC, S100A1, S100B, 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.