Gene interactions and pathways from curated databases and text-mining

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FOS — OXTR

Pathways - manually collected, often from reviews:

Text-mined interactions from Literome

Hoare et al., Endocrinology 1999 (Breast Neoplasms) : We showed the requirement for GABP alpha/beta and c-Fos/c-Jun in endogenous OTR gene expression, using oligonucleotide GABP and AP-1 binding decoys to inhibit serum induced increases in 125I labeled OT antagonist binding to Hs578T cells
Terzidou et al., J Clin Endocrinol Metab 2006 : In transient transfection studies, OTR promoter activity was increased by C/EBPbeta and NF-kappaB, but not by AP-1