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Disease Info Card
Breast Microcalcification
Information about Breast Microcalcification: 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 Breast Microcalcification
Most recent studies have shown that Breast Microcalcification shares some biological mechanisms with breast-diseases, breast-fibrocystic-disease, calcinosis, carcinoma, carcinoma-in-situ, carcinoma-lobular, ductal-breast-carcinoma, ductal-carcinoma, hyperplasia, intraductal-hyperplasia, malignant-neoplasm-of-breast, malignant-neoplasm-of-thyroid, malignant-neoplasms, malignant-paraganglionic-neoplasm, mammary-neoplasms, neoplasm-metastasis, neoplasms, noninfiltrating-intraductal-carcinoma, thyroid-neoplasm, thyroid-nodule.
Among the many pathways, these few ones have gauged particular interests from scientists studying Breast Microcalcification, and have been seen in publications frequently: Aging, Angiogenesis, Cell Death, Cell Proliferation, Coagulation, Excretion, Glomerular Filtration, Inflammatory Response, Lactation, Localization, Menopause, Pathogenesis, Pigmentation, Regeneration, Secretion, Segmentation, Spermatogenesis, Transport, Visual Perception
Quite a number of genes have been found to play important roles in Breast Microcalcification, such as ACR, AGA, AVP, CALR, DBT, ERBB2, ESR1, IBSP, PGR, POMC, PTGFR, RUNX2, SDHA, SLC6A8, SPP1, TG, TMEM37. 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.