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Disease Info Card
Fallopian Tube Neoplasms
Information about Fallopian Tube Neoplasms: 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 Fallopian Tube Neoplasms
Most recent studies have shown that Fallopian Tube Neoplasms shares some biological mechanisms with adenocarcinoma, carcinoma, cystadenocarcinoma-serous, endometriosis-site-unspecified, epithelial-ovarian-cancer, fallopian-tube-carcinoma, fallopian-tube-diseases, genital-neoplasms-female, malignant-neoplasm-of-ovary, malignant-neoplasms, malignant-paraganglionic-neoplasm, neoplasm-metastasis, neoplasm-recurrence-local, neoplasms, ovarian-neoplasm, pain, peritoneal-neoplasms, uterine-cervical-neoplasm, uterine-neoplasms.
Among the many pathways, these few ones have gauged particular interests from scientists studying Fallopian Tube Neoplasms, and have been seen in publications frequently: Angiogenesis, Cell Cycle, Cell Death, Cell Proliferation, Coagulation, Drug Resistance, Enucleation, Fertilization, Hypersensitivity, Immune Response, Localization, Menarche, Menopause, Menstruation, Mitosis, Ovulation, Pathogenesis, Response To Paclitaxel, Response To Radiation, Secretion
Quite a number of genes have been found to play important roles in Fallopian Tube Neoplasms, such as BRCA1, BRCA2, CDAN1, CDKN2A, CEACAM5, CEACAM7, CSF3, ERBB2, MID1, MUC1, MUC16, PAX2, PGR, TP53, TUBE1, VEGFA, ZFP36. 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.