Biological redundancy of endogenous GPCR ligands in the gut and the potential for endogenous functional selectivity

Georgina Louise Thompson; Meritxell Canals; Daniel Philip Poole

doi:10.3389/fphar.2014.00262

Biological redundancy of endogenous GPCR ligands in the gut and the potential for endogenous functional selectivity

Georgina Louise Thompson, Meritxell Canals, Daniel Philip Poole

Drug Discovery Biology

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

21 Citations (Scopus)

Original language	English
Pages (from-to)	1 - 12
Number of pages	12
Journal	Frontiers in Pharmacology
Volume	5
DOIs	https://doi.org/10.3389/fphar.2014.00262
Publication status	Published - 2014

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10.3389/fphar.2014.00262

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title = "Biological redundancy of endogenous GPCR ligands in the gut and the potential for endogenous functional selectivity",

author = "Thompson, {Georgina Louise} and Meritxell Canals and Poole, {Daniel Philip}",

year = "2014",

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journal = "Frontiers in Pharmacology",

issn = "1663-9812",

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AU - Thompson, Georgina Louise

AU - Canals, Meritxell

AU - Poole, Daniel Philip

PY - 2014

Y1 - 2014

UR - http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4246669/pdf/fphar-05-00262.pdf

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DO - 10.3389/fphar.2014.00262

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EP - 12

JO - Frontiers in Pharmacology

JF - Frontiers in Pharmacology

SN - 1663-9812

ER -

Biological redundancy of endogenous GPCR ligands in the gut and the potential for endogenous functional selectivity

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Opiate-induced constipation: identifying key targets for therapy

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Biological redundancy of endogenous GPCR ligands in the gut and the potential for endogenous functional selectivity

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Opiate-induced constipation: identifying key targets for therapy

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