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- Table of Contents
Information about Bile Duct Carcinoma: 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.
Most recent studies have shown that Bile Duct Carcinoma shares some biological mechanisms with adenocarcinoma, bile-duct-neoplasms, biliary-tract-neoplasm, carcinoma, cell-invasion, cholangiocarcinoma, cholangitis, ductal-carcinoma, gallbladder-neoplasm, icterus, liver-neoplasms, malignant-neoplasm-of-gallbladder, malignant-neoplasm-of-pancreas, malignant-neoplasms, malignant-paraganglionic-neoplasm, malignant-tumor-of-extrahepatic-bile-duct, neoplasm-metastasis, neoplasms, pancreatic-neoplasm.
Among the many pathways, these few ones have gauged particular interests from scientists studying Bile Duct Carcinoma, and have been seen in publications frequently: Cell Activation, Cell Adhesion, Cell Cycle, Cell Differentiation, Cell Growth, Cell Proliferation, Coagulation, Dedifferentiation, Dna Repair, Excretion, Gastric Emptying, Immune Response, Induction Of Apoptosis, Localization, Methylation, Pathogenesis, Regeneration, Reverse Transcription, Secretion, T Cell Activation
Quite a number of genes have been found to play important roles in Bile Duct Carcinoma, such as AFP, CCDC6, CD1B, CDKN2A, CEACAM5, CEACAM7, EGFR, F9, HRAS, MUC1, PCNA, PSG2, PTCH1, RET, SLC25A5, TAS2R38, TP53. 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.