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Disease Info Card
Lymphangioleiomyomatosis
Information about Lymphangioleiomyomatosis: 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 Lymphangioleiomyomatosis
Most recent studies have shown that Lymphangioleiomyomatosis shares some biological mechanisms with angiomyolipoma, dyspnea, fibrosis, kidney-neoplasm, lung-diseases, lung-lymphangioleiomyomatosis, lung-neoplasms, lymphangiomyoma, lymphoproliferative-disorders, neoplasms, pleural-effusion-disorder, pulmonary-emphysema, pulmonary-fibrosis, renal-angiomyolipoma, respiratory-failure, sclerosis, tuberous-sclerosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Lymphangioleiomyomatosis, and have been seen in publications frequently: Angiogenesis, Cell Adhesion, Cell Cycle, Cell Differentiation, Cell Growth, Cell Migration, Cell Proliferation, Dehiscence, Hyperphosphorylation, Hypersensitivity, Localization, Lymphangiogenesis, Menopause, Mitosis, Muscle Cell Proliferation, Muscle Hyperplasia, Pathogenesis, Smooth Muscle Cell Proliferation, Smooth Muscle Hyperplasia, Translation
Quite a number of genes have been found to play important roles in Lymphangioleiomyomatosis, such as AKT1, DES, ESR1, FEV, MLANA, MMP2, MTOR, PGR, PSMC4, RHEB, RPS6, SLC12A3, TESC, TSC1, TSC2, VEGFA, VIM. 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.