The Endocannabinoids Anandamide and Virodhamine Modulate the Activity of the Candidate Cannabinoid Receptor GPR55
Published 2012 View Full Article
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Title
The Endocannabinoids Anandamide and Virodhamine Modulate the Activity of the Candidate Cannabinoid Receptor GPR55
Authors
Keywords
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Journal
Journal of Neuroimmune Pharmacology
Volume 7, Issue 4, Pages 856-865
Publisher
Springer Nature
Online
2012-03-27
DOI
10.1007/s11481-012-9351-6
References
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Note: Only part of the references are listed.- Identification of the GPR55 Agonist Binding Site Using a Novel Set of High-Potency GPR55 Selective Ligands
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- Cannabinoid receptor 2 undergoes Rab5-mediated internalization and recycles via a Rab11-dependent pathway
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- New blood brothers: the GPR55 and CB2 partnership
- (2011) Andy Irving CELL RESEARCH
- GPR55 regulates cannabinoid 2 receptor-mediated responses in human neutrophils
- (2011) Nariman A B Balenga et al. CELL RESEARCH
- Modulation of l-α-Lysophosphatidylinositol/GPR55 Mitogen-activated Protein Kinase (MAPK) Signaling by Cannabinoids
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- Anandamide exerts its antiproliferative actions on cholangiocarcinoma by activation of the GPR55 receptor
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- The putative cannabinoid receptor GPR55 defines a novel autocrine loop in cancer cell proliferation
- (2010) R Piñeiro et al. ONCOGENE
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- Differential changes in GPR55 during microglial cell activation
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- Lipid G Protein-coupled Receptor Ligand Identification Using β-Arrestin PathHunter™ Assay
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- Atypical Responsiveness of the Orphan Receptor GPR55 to Cannabinoid Ligands
- (2009) Ankur Kapur et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The putative cannabinoid receptor GPR55 affects osteoclast function in vitro and bone mass in vivo
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- The GPR55 ligand l-α-lysophosphatidylinositol promotes RhoA-dependent Ca2+ signaling and NFAT activation
- (2008) Christopher M. Henstridge et al. FASEB JOURNAL
- The putative cannabinoid receptor GPR55 plays a role in mechanical hyperalgesia associated with inflammatory and neuropathic pain
- (2008) Penny C. Staton et al. PAIN
- GPR55 is a cannabinoid receptor that increases intracellular calcium and inhibits M current
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- (2007) E Ryberg et al. BRITISH JOURNAL OF PHARMACOLOGY
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