Tartrazine is not an activator of the mouse oestrogen ERα and ERβ receptors

Stephanie Meyer, Andrew Axon, Paul Jowsey, Faith Williams, Peter Blain, Matthew Wright

Research output: Contribution to journalMeeting Abstractpeer-review

Abstract

A major target for endocrine disruptor chemicals are the oestrogen receptors (ERs) and a variety of human-based reporter gene in vitro assay platforms have been developed that enable chemicals to be rapidly screened for potential oestrogenic activity in man.
Original languageEnglish
Pages (from-to)S180-S180
Number of pages1
JournalToxicology Letters
Volume229
Early online date17 Aug 2014
DOIs
Publication statusPublished - 10 Sep 2014
Externally publishedYes

Cite this