Disease Info Card

Bile Duct Neoplasms

Information about Bile Duct 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 Bile Duct Neoplasms

Most recent studies have shown that Bile Duct Neoplasms shares some biological mechanisms with adenocarcinoma, bile-duct-adenoma, bile-duct-carcinoma, carcinoma, cholangiocarcinoma, cholangitis, cholestasis, gallbladder-neoplasm, icterus, intrahepatic-cholangiocarcinoma, jaundice-obstructive, klatskins-tumor, liver-carcinoma, liver-neoplasms, malignant-neoplasms, malignant-paraganglionic-neoplasm, neoplasm-metastasis, neoplasms, pancreatic-neoplasm, stenosis.

Among the many pathways, these few ones have gauged particular interests from scientists studying Bile Duct Neoplasms, and have been seen in publications frequently: Angiogenesis, Cell Adhesion, Cell Cycle, Cell Death, Cell Growth, Cell Proliferation, Coagulation, Dedifferentiation, Dna Repair, Excretion, Gastric Emptying, Induction Of Apoptosis, Invasive Growth, Liver Regeneration, Localization, Methylation, Pathogenesis, Regeneration, Reverse Transcription, Secretion

Quite a number of genes have been found to play important roles in Bile Duct Neoplasms, such as AFP, ALB, CCDC6, CDKN2A, CEACAM5, CEACAM7, EGFR, F9, IL6, KRT19, KRT7, MUC1, MUC2, PSG2, PTCH1, RET, 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.