Gain and Loss of Function of P2X7 Receptors: Mechanisms, Pharmacology and Relevance to Diabetic Neuropathic Pain-Reference-Cited by-同舟云学术

Gain and Loss of Function of P2X7 Receptors: Mechanisms, Pharmacology and Relevance to Diabetic Neuropathic Pain

Published:2014-01 Issue: Volume:10 Page:1744-8069-10-37
ISSN:1744-8069
Container-title:Molecular Pain
language:en
Short-container-title:Mol Pain

Author:

Ursu Daniel¹,Ebert Philip²,Langron Emily¹,Ruble Cara²,Munsie Leanne²,Zou Wei³,Fijal Bonnie²,Qian Yue-Wei²,McNearney Terry A²,Mogg Adrian¹,Grubisha Olivera¹,Merchant Kalpana²,Sher Emanuele¹

Affiliation:

1. Lilly Research Centre, Eli Lilly & Co. Ltd., Sunninghill Road, GU20 6PH Windlesham, Surrey, UK

2. Lilly Corporate Center, Eli Lilly and Company, 46285 Indianapolis, Indiana, USA

3. InVentiv Clinical Health, LLC, 504 Carnegie Center, 08540 Princeton, NJ, USA

Publisher

SAGE Publications

Subject

Anesthesiology and Pain Medicine,Cellular and Molecular Neuroscience,Molecular Medicine

Link

http://journals.sagepub.com/doi/pdf/10.1186/1744-8069-10-37

Reference47 articles.

1. Molecular Physiology of P2X Receptors

2. Antinociceptive effect of a new P2Z/P2X7 antagonist, oxidized ATP, in arthritic rats

3. Disruption of the P2X7 purinoceptor gene abolishes chronic inflammatory and neuropathic pain

4. A-740003 [N-(1-{[(Cyanoimino)(5-quinolinylamino) methyl]amino}-2,2-dimethylpropyl)-2-(3,4-dimethoxyphenyl)acetamide], a Novel and Selective P2X7Receptor Antagonist, Dose-Dependently Reduces Neuropathic Pain in the Rat

5. P2X7 Receptor Signaling Pathway as a Therapeutic Target for Neurodegenerative Diseases

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