Disease Info Card

Duodenal Neoplasms

Information about Duodenal 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 Duodenal Neoplasms

Most recent studies have shown that Duodenal Neoplasms shares some biological mechanisms with adenocarcinoma, adenoma, carcinoid-tumor, carcinoma, duodenal-cancer, gastrointestinal-hemorrhage, hemorrhage, intestinal-neoplasms, intestinal-polyps, jejunal-neoplasms, lymphoma, malignant-neoplasms, malignant-paraganglionic-neoplasm, neoplasm-metastasis, neoplasms, pancreatic-neoplasm, polyposis, polyps, stomach-neoplasms, ulcer.

Among the many pathways, these few ones have gauged particular interests from scientists studying Duodenal Neoplasms, and have been seen in publications frequently: Acid Secretion, Cell Cycle, Cell Differentiation, Cell Proliferation, Coagulation, Dehiscence, Enucleation, Excretion, Gastric Acid Secretion, Gastric Emptying, Hemostasis, Localization, Methylation, Mismatch Repair, Mitosis, Pathogenesis, Peristalsis, Pigmentation, Secretion

Quite a number of genes have been found to play important roles in Duodenal Neoplasms, such as APC, CEL, ELL, ENO2, FAP, GAST, GCG, GLMN, GNAI1, INS, KIT, MEN1, POMC, PPY, PROC, SCT, 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.

Duodenal Neoplasms Related Genes

click to see detail information for each gene

APC CEL ELL
ENO2 FAP GAST
GCG GLMN GNAI1
INS KIT MEN1
POMC PPY PROC
SCT SST SYP
TP53