Emerging areas of opioid pharmacology

Eamonn Kelly; Graeme Henderson; Chris P. Bailey

doi:10.1111/bph.14343

Emerging areas of opioid pharmacology

Eamonn Kelly
, Graeme Henderson
, Chris P. Bailey

Department of Life Sciences

University of Bristol

Research output: Contribution to journal › Editorial › peer-review

3 Citations (SciVal)

243 Downloads (Pure)

Abstract

This themed section of the British Journal of Pharmacology stems from an International Narcotics Research Conference (INRC) meeting held in July 2016 at The Assembly Rooms in Bath, UK.

Original language	English
Pages (from-to)	2715-2716
Number of pages	2
Journal	British Journal of Pharmacology
Volume	175
Issue number	14
Early online date	22 Jun 2018
DOIs	https://doi.org/10.1111/bph.14343
Publication status	Published - 1 Jul 2018

Bibliographical note

ASJC Scopus subject areas

Pharmacology

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10.1111/bph.14343

BJP INRC Themed issue commentary
This is the peer reviewed version of the following article: Kelly, E., Henderson, G., and Bailey, C. P. ( 2018) Emerging areas of opioid pharmacology, British Journal of Pharmacology, 175: 2715– 2716, which has been published in final form at https://doi.org/10.1111/bph.14343. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
Submitted manuscript, 491 KB

Cite this

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title = "Emerging areas of opioid pharmacology",

abstract = "This themed section of the British Journal of Pharmacology stems from an International Narcotics Research Conference (INRC) meeting held in July 2016 at The Assembly Rooms in Bath, UK.",

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Emerging areas of opioid pharmacology

Abstract

Bibliographical note

ASJC Scopus subject areas

Access to Document

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Mu-Opioid Receptor Desensitization in Ventral Tegmental Neurones: Cellular Mechanisms and Functional Consequences

Cite this

Emerging areas of opioid pharmacology

Abstract

Bibliographical note

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Projects

Mu-Opioid Receptor Desensitization in Ventral Tegmental Neurones: Cellular Mechanisms and Functional Consequences

Cite this