Disease Info Card

Appendiceal Neoplasms

Information about Appendiceal 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 Appendiceal Neoplasms

Most recent studies have shown that Appendiceal Neoplasms shares some biological mechanisms with adenocarcinoma, adenoma, appendicitis, appendix-adenocarcinoma, carcinoid-tumor, carcinoma, colonic-neoplasms, cystadenocarcinoma, cystadenoma, cystadenoma-mucinous, malignant-neoplasms, malignant-paraganglionic-neoplasm, mucinous-adenocarcinoma, mucocele, neoplasm-metastasis, neoplasms, ovarian-neoplasm, pain, peritoneal-neoplasms, pseudomyxoma-peritonei.

Among the many pathways, these few ones have gauged particular interests from scientists studying Appendiceal Neoplasms, and have been seen in publications frequently: Aging, Angiogenesis, Cell Cycle, Cell Cycle Arrest, Cell Differentiation, Cell Proliferation, Circadian Rhythm, Dedifferentiation, Enucleation, Excretion, Heat Generation, Localization, Methylation, Mismatch Repair, Pathogenesis, Pigmentation, Regeneration, Secretion, Smooth Muscle Hyperplasia

Quite a number of genes have been found to play important roles in Appendiceal Neoplasms, such as CEACAM5, CEACAM7, ENO2, GNAI1, KIT, KRT20, KRT7, MID1, MUC2, MUC5AC, POMC, PSG2, SERPINA5, SST, SYP, 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.