James P. Pearson
0009-0001-5927-8395
Publication & Citation Trends
Publications
0 total
FAAH inhibitor URB597 shows anti‐hyperalgesic action and increases brain and intestinal tissues fatty acid amides in a model of CRF1 agonist mediated visceral hypersensitivity in male rats OA
Cited by 4
Semantic Scholar
Attenuation of persistent pain-related behavior by fatty acid amide hydrolase (FAAH) inhibitors in a rat model of HIV sensory neuropathy. OA
Cited by 41
Semantic Scholar
Fatty Acid Amide Hydrolase (FAAH) Inhibitors Exert Pharmacological Effects, but Lack Antinociceptive Efficacy in Rats with Neuropathic Spinal Cord Injury Pain OA
Cited by 14
Semantic Scholar
Effects of repeated dosing with mechanistically distinct antinociceptive ligands in a rat model of neuropathic spinal cord injury pain OA
Cited by 7
Semantic Scholar
Fatty Acid Amide Hydrolase (FAAH) Inhibition Reduces l-3,4-Dihydroxyphenylalanine-Induced Hyperactivity in the 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-Lesioned Non-Human Primate Model of Parkinson's Disease
Cited by 39
Semantic Scholar
S1808 Analgesic Effect of URB597, a Selective Inhibitor of Fatty Acid Amide Hydrolase (FAAH) on Colorectal Pain in a Rat Model of Irritable Bowel Syndrome (IBS) Induced by the Selective Corticotropin Releasing Factor Receptor 1 (CRF1) Agonist, Cortagine OA
Cited by 0
Semantic Scholar
Composes indole utiles
Cited by 0
Semantic Scholar
Modulateurs de crth2, de cox-2 et de faah
Cited by 0
Semantic Scholar
Research Topics
Bacterial biofilms and quorum sensing
(13)
Bacterial Genetics and Biotechnology
(11)
Bacteriophages and microbial interactions
(5)
Cannabis and Cannabinoid Research
(4)
Pain Mechanisms and Treatments
(2)
Affiliations
University of Iowa
Ironwood Pharmaceuticals (United States)
East Carolina University
Montana State University
University of Oxford