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Disease Info Card
Intraductal Hyperplasia
Information about Intraductal Hyperplasia: 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 Intraductal Hyperplasia
Most recent studies have shown that Intraductal Hyperplasia shares some biological mechanisms with atypical-ductal-breast-hyperplasia, breast-diseases, carcinoma, carcinoma-in-situ, carcinoma-lobular, ductal-breast-carcinoma, ductal-carcinoma, hyperplasia, invasive-ductal-breast-carcinoma, lobular-carcinoma-in-situ-of-breast, lobular-hyperplasia, malignant-neoplasm-of-breast, malignant-neoplasms, malignant-paraganglionic-neoplasm, mammary-neoplasms, neoplasms, noninfiltrating-intraductal-carcinoma, papilloma, precancerous-conditions.
Among the many pathways, these few ones have gauged particular interests from scientists studying Intraductal Hyperplasia, and have been seen in publications frequently: Aging, Angiogenesis, Cell Adhesion, Cell Cycle, Cell Death, Cell Growth, Cell Proliferation, Dna Methylation, Gland Development, Lactation, Localization, Mammary Gland Development, Menopause, Methylation, Oncogenesis, Pathogenesis, Secretion, Segmentation, Senescence, Tissue Remodeling
Quite a number of genes have been found to play important roles in Intraductal Hyperplasia, such as AR, AVP, BCL2, BRCA1, CCND1, CDH1, CKAP4, ERBB2, ESR1, LMNA, MUC1, PGR, TMEM37, TP53, TP63, UVRAG. 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.