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

doi:10.1016/j.toxlet.2014.06.614

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 journal › Meeting Abstract › peer-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 language	English
Pages (from-to)	S180-S180
Number of pages	1
Journal	Toxicology Letters
Volume	229
Early online date	17 Aug 2014
DOIs	https://doi.org/10.1016/j.toxlet.2014.06.614
Publication status	Published - 10 Sept 2014
Externally published	Yes

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10.1016/j.toxlet.2014.06.614

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title = "Tartrazine is not an activator of the mouse oestrogen ERα and ERβ receptors",

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.",

author = "Stephanie Meyer and Andrew Axon and Paul Jowsey and Faith Williams and Peter Blain and Matthew Wright",

year = "2014",

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day = "10",

doi = "10.1016/j.toxlet.2014.06.614",

language = "English",

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T1 - Tartrazine is not an activator of the mouse oestrogen ERα and ERβ receptors

AU - Meyer, Stephanie

AU - Axon, Andrew

AU - Jowsey, Paul

AU - Williams, Faith

AU - Blain, Peter

AU - Wright, Matthew

PY - 2014/9/10

Y1 - 2014/9/10

N2 - 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.

AB - 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.

U2 - 10.1016/j.toxlet.2014.06.614

DO - 10.1016/j.toxlet.2014.06.614

M3 - Meeting Abstract

SN - 0378-4274

VL - 229

SP - S180-S180

JO - Toxicology Letters

JF - Toxicology Letters

ER -

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

Abstract

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