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Disease Info Card
Hamartoma
Information about Hamartoma: 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 Hamartoma
Most recent studies have shown that Hamartoma shares some biological mechanisms with adenoma, benign-neoplasm, carcinoma, epilepsy, hemangioma, hyperplasia, hypothalamic-hamartoma, kidney-neoplasm, lipoma, liver-neoplasms, lung-neoplasms, malignant-neoplasms, malignant-paraganglionic-neoplasm, melanocytic-nevus, neoplasms, polyps, sclerosis, skin-neoplasms, tuberous-sclerosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hamartoma, and have been seen in publications frequently: Angiogenesis, Bone Maturation, Cell Cycle, Cell Differentiation, Cell Growth, Cell Proliferation, Coagulation, Cognition, Enucleation, Keratinization, Localization, Menarche, Methylation, Ossification, Pathogenesis, Pigmentation, Secretion, Short-term Memory, Translation
Quite a number of genes have been found to play important roles in Hamartoma, such as AKT1, CD34, DES, FLCN, FUT1, GFAP, GLI3, HFE, HMGA2, MTOR, NF1, PTEN, SLC12A3, STK11, TESC, TP53, TSC1, TSC2, 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.