pathway Info Card

Response To Irinotecan

Information about Response To Irinotecan: 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 Response To Irinotecan

Most recent studies have shown that Response To Irinotecan shares some biological mechanisms with cell-cycle, cell-death, cellular-senescence, dna-damage-checkpoint, dna-repair, drug-resistance, localization, mismatch-repair, response-to-5-fluorouracil, reverse-transcription, senescence, sensitization, transport.

Among the many pathways, these few ones have gauged particular interests from scientists studying Response To Irinotecan, and have been seen in publications frequently: cell-cycle, cell-death, cellular-senescence, dna-damage-checkpoint, dna-repair, drug-resistance, localization, mismatch-repair, response-to-5-fluorouracil, reverse-transcription, senescence, sensitization, transport

Quite a number of genes have been found to play important roles in Response To Irinotecan, such as ABCB1, ABCG2, CDKN2A, CES2, CHEK1, CYP3A4, DPYD, FGF7, GLP2R, IGF1, MSH2, PGR, PTGS2, SLC35A2, SPARC, TP53, TYMP, TYMS, UGT1A9, Ugt1a1. 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 pathway. Plesae stay updated.

Response To Irinotecan Related Genes

click to see detail information for each gene

ABCB1 ABCG2 CDKN2A
CES2 CHEK1 CYP3A4
DPYD FGF7 GLP2R
IGF1 MSH2 PGR
PTGS2 SLC35A2 SPARC
TP53 TYMP TYMS
UGT1A9 Ugt1a1