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Jesse Loverme

Showing results (1-10 of 10) with videos related to

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The Journal of Biological Chemistry|June 21, 2006
Cold exposure stimulates synthesis of the bioactive lipid oleoylethanolamide in rat adipose tissueJesse LoVerme, Manuel Guzmán, Silvana Gaetani, et al.
Anesthesia and Analgesia|May 22, 2007
The antinociceptive effects of local injections of propofol in rats are mediated in part by cannabinoid CB1 and CB2 receptorsJosée Guindon, Jesse LoVerme, Daniele Piomelli, et al.
European Journal of Pharmacology|October 10, 2006
Synergistic antinociceptive effects of anandamide, an endocannabinoid, and nonsteroidal anti-inflammatory drugs in peripheral tissue: a role for endogenous fatty-acid ethanolamides?Josée Guindon, Jesse LoVerme, André De Léan, et al.
Life Sciences|June 21, 2005
The search for the palmitoylethanolamide receptorJesse LoVerme, Giovanna La Rana, Roberto Russo, et al.
Brain Research Reviews|January 24, 2009
Rapid pain modulation with nuclear receptor ligandsJill C Fehrenbacher, Jesse Loverme, William Clarke, et al.
European Journal of Pharmacology|April 17, 2007
Synergistic antinociception by the cannabinoid receptor agonist anandamide and the PPAR-alpha receptor agonist GW7647Roberto Russo, Jesse LoVerme, Giovanna La Rana, et al.
Bioorganic & Medicinal Chemistry Letters|January 9, 2009
Synthesis and characterization of a peripherally restricted CB1 cannabinoid antagonist, URB447, that reduces feeding and body-weight gain in miceJesse LoVerme, Andrea Duranti, Andrea Tontini, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 26, 2006
Rapid broad-spectrum analgesia through activation of peroxisome proliferator-activated receptor-alphaJesse LoVerme, Roberto Russo, Giovanna La Rana, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 7, 2007
The fatty acid amide hydrolase inhibitor URB597 (cyclohexylcarbamic acid 3'-carbamoylbiphenyl-3-yl ester) reduces neuropathic pain after oral administration in miceRoberto Russo, Jesse Loverme, Giovanna La Rana, et al.
European Journal of Pharmacology|April 24, 2009
Central administration of palmitoylethanolamide reduces hyperalgesia in mice via inhibition of NF-kappaB nuclear signalling in dorsal root gangliaGiuseppe D'Agostino, Giovanna La Rana, Roberto Russo, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
The Journal of Biological Chemistry|June 21, 2006
Cold exposure stimulates synthesis of the bioactive lipid oleoylethanolamide in rat adipose tissueJesse LoVerme, Manuel Guzmán, Silvana Gaetani, et al.
Anesthesia and Analgesia|May 22, 2007
The antinociceptive effects of local injections of propofol in rats are mediated in part by cannabinoid CB1 and CB2 receptorsJosée Guindon, Jesse LoVerme, Daniele Piomelli, et al.
European Journal of Pharmacology|October 10, 2006
Synergistic antinociceptive effects of anandamide, an endocannabinoid, and nonsteroidal anti-inflammatory drugs in peripheral tissue: a role for endogenous fatty-acid ethanolamides?Josée Guindon, Jesse LoVerme, André De Léan, et al.
Life Sciences|June 21, 2005
The search for the palmitoylethanolamide receptorJesse LoVerme, Giovanna La Rana, Roberto Russo, et al.
Brain Research Reviews|January 24, 2009
Rapid pain modulation with nuclear receptor ligandsJill C Fehrenbacher, Jesse Loverme, William Clarke, et al.
European Journal of Pharmacology|April 17, 2007
Synergistic antinociception by the cannabinoid receptor agonist anandamide and the PPAR-alpha receptor agonist GW7647Roberto Russo, Jesse LoVerme, Giovanna La Rana, et al.
Bioorganic & Medicinal Chemistry Letters|January 9, 2009
Synthesis and characterization of a peripherally restricted CB1 cannabinoid antagonist, URB447, that reduces feeding and body-weight gain in miceJesse LoVerme, Andrea Duranti, Andrea Tontini, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 26, 2006
Rapid broad-spectrum analgesia through activation of peroxisome proliferator-activated receptor-alphaJesse LoVerme, Roberto Russo, Giovanna La Rana, et al.
The Journal of Pharmacology and Experimental Therapeutics|April 7, 2007
The fatty acid amide hydrolase inhibitor URB597 (cyclohexylcarbamic acid 3'-carbamoylbiphenyl-3-yl ester) reduces neuropathic pain after oral administration in miceRoberto Russo, Jesse Loverme, Giovanna La Rana, et al.
European Journal of Pharmacology|April 24, 2009
Central administration of palmitoylethanolamide reduces hyperalgesia in mice via inhibition of NF-kappaB nuclear signalling in dorsal root gangliaGiuseppe D'Agostino, Giovanna La Rana, Roberto Russo, et al.
Pageof 1