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European Journal of Pharmacology|April 9, 2002
Arvanil-induced inhibition of spasticity and persistent pain: evidence for therapeutic sites of action different from the vanilloid VR1 receptor and cannabinoid CB(1)/CB(2) receptorsJason W Brooks, Gareth Pryce, Tiziana Bisogno, et al.Frontiers in Pharmacology|April 5, 2018
Oral Ultramicronized Palmitoylethanolamide: Plasma and Tissue Levels and Spinal Anti-hyperalgesic EffectStefania Petrosino, Marika Cordaro, Roberta Verde, et al.Cells|May 24, 2020
Hepatic NAPE-PLD Is a Key Regulator of Liver Lipid MetabolismCharlotte Lefort, Martin Roumain, Matthias Van Hul, et al.Journal of Translational Medicine|June 6, 2026
Bacteroides-derived endocannabinoid-like commendamide attenuates skeletal muscle ferroptosis in vitro: implications for Duchenne muscular dystrophyNoemi Di Muraglia, Martina De Vito, Elisabetta Panza, et al.European Journal of Medicinal Chemistry|November 21, 2012
2-Arylbenzofuran-based molecules as multipotent Alzheimer's disease modifying agentsStefano Rizzo, Andrea Tarozzi, Manuela Bartolini, et al.The New Microbiologica|October 6, 2020
SARS-CoV-2 pandemic: implications in the management of patients with colorectal cancerFrancesco Di Marzo, Enrico Fiori, Massimo Sartelli, et al.Frontiers in Pharmacology|March 13, 2020
Treatment With 2-Pentadecyl-2-Oxazoline Restores Mild Traumatic Brain Injury-Induced Sensorial and Neuropsychiatric DysfunctionsSerena Boccella, Monica Iannotta, Claudia Cristiano, et al.Molecular Metabolism|January 16, 2022
Adipocyte-specific Nos2 deletion improves insulin resistance and dyslipidemia through brown fat activation in diet-induced obese miceVanessa Rodrigues Vilela, Nolwenn Samson, Renato Nachbar, et al.Nature Communications|September 29, 2018
Genetic and pharmacological regulation of the endocannabinoid CB1 receptor in Duchenne muscular dystrophyFabio A Iannotti, Ester Pagano, Ombretta Guardiola, et al.Allergy|June 27, 2024
Altered levels of phospholipases C, diacylglycerols, endocannabinoids, and N-acylethanolamines in patients with hereditary angioedema due to FXII mutationAnne Lise Ferrara, Francesco Palestra, Fabiana Piscitelli, et al.Pageof 116