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Eleonora Distrutti

Showing results (91-100 of 139) with videos related to

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The Journal of Pharmacology and Experimental Therapeutics|July 21, 2006
5-Amino-2-hydroxybenzoic acid 4-(5-thioxo-5H-[1,2]dithiol-3yl)-phenyl ester (ATB-429), a hydrogen sulfide-releasing derivative of mesalamine, exerts antinociceptive effects in a model of postinflammatory hypersensitivityEleonora Distrutti, Luca Sediari, Andrea Mencarelli, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 28, 2020
The Bile Acid Receptor GPBAR1 Modulates CCL2/CCR2 Signaling at the Liver Sinusoidal/Macrophage Interface and Reverses Acetaminophen-Induced Liver ToxicityMichele Biagioli, Adriana Carino, Chiara Fiorucci, et al.
European Journal of Pharmacology|May 11, 2011
Development of non-antibiotic macrolide that corrects inflammation-driven immune dysfunction in models of inflammatory bowel diseases and arthritisAndrea Mencarelli, Eleonora Distrutti, Barbara Renga, et al.
Journal of Hepatology|December 4, 2003
NCX-1000, a nitric oxide-releasing derivative of ursodeoxycholic acid, ameliorates portal hypertension and lowers norepinephrine-induced intrahepatic resistance in the isolated and perfused rat liverStefano Fiorucci, Elisabetta Antonelli, Vincenzo Brancaleone, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 30, 2005
Evidence that hydrogen sulfide exerts antinociceptive effects in the gastrointestinal tract by activating KATP channelsEleonora Distrutti, Luca Sediari, Andrea Mencarelli, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 11, 2018
Agonism for the bile acid receptor GPBAR1 reverses liver and vascular damage in a mouse model of steatohepatitisAdriana Carino, Silvia Marchianò, Michele Biagioli, et al.
Diabetes|July 10, 2013
Dissociation of intestinal and hepatic activities of FXR and LXRα supports metabolic effects of terminal ileum interposition in rodentsAndrea Mencarelli, Barbara Renga, Claudio D'Amore, et al.
Oncotarget|July 14, 2016
The bile acid receptor GPBAR1 (TGR5) is expressed in human gastric cancers and promotes epithelial-mesenchymal transition in gastric cancer cell linesAdriana Carino, Luigina Graziosi, Claudio D'Amore, et al.
American Journal of Physiology. Heart and Circulatory Physiology|May 3, 2015
Cystathionine γ-lyase, a H2S-generating enzyme, is a GPBAR1-regulated gene and contributes to vasodilation caused by secondary bile acidsBarbara Renga, Mariarosaria Bucci, Sabrina Cipriani, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 4, 2021
Atorvastatin protects against liver and vascular damage in a model of diet induced steatohepatitis by resetting FXR and GPBAR1 signalingSilvia Marchianò, Michele Biagioli, Rosalinda Roselli, et al.
Pageof 14

Showing results (91-100 of 139) with videos related to

Sort By:
Pageof 14
The Journal of Pharmacology and Experimental Therapeutics|July 21, 2006
5-Amino-2-hydroxybenzoic acid 4-(5-thioxo-5H-[1,2]dithiol-3yl)-phenyl ester (ATB-429), a hydrogen sulfide-releasing derivative of mesalamine, exerts antinociceptive effects in a model of postinflammatory hypersensitivityEleonora Distrutti, Luca Sediari, Andrea Mencarelli, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 28, 2020
The Bile Acid Receptor GPBAR1 Modulates CCL2/CCR2 Signaling at the Liver Sinusoidal/Macrophage Interface and Reverses Acetaminophen-Induced Liver ToxicityMichele Biagioli, Adriana Carino, Chiara Fiorucci, et al.
European Journal of Pharmacology|May 11, 2011
Development of non-antibiotic macrolide that corrects inflammation-driven immune dysfunction in models of inflammatory bowel diseases and arthritisAndrea Mencarelli, Eleonora Distrutti, Barbara Renga, et al.
Journal of Hepatology|December 4, 2003
NCX-1000, a nitric oxide-releasing derivative of ursodeoxycholic acid, ameliorates portal hypertension and lowers norepinephrine-induced intrahepatic resistance in the isolated and perfused rat liverStefano Fiorucci, Elisabetta Antonelli, Vincenzo Brancaleone, et al.
The Journal of Pharmacology and Experimental Therapeutics|September 30, 2005
Evidence that hydrogen sulfide exerts antinociceptive effects in the gastrointestinal tract by activating KATP channelsEleonora Distrutti, Luca Sediari, Andrea Mencarelli, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|October 11, 2018
Agonism for the bile acid receptor GPBAR1 reverses liver and vascular damage in a mouse model of steatohepatitisAdriana Carino, Silvia Marchianò, Michele Biagioli, et al.
Diabetes|July 10, 2013
Dissociation of intestinal and hepatic activities of FXR and LXRα supports metabolic effects of terminal ileum interposition in rodentsAndrea Mencarelli, Barbara Renga, Claudio D'Amore, et al.
Oncotarget|July 14, 2016
The bile acid receptor GPBAR1 (TGR5) is expressed in human gastric cancers and promotes epithelial-mesenchymal transition in gastric cancer cell linesAdriana Carino, Luigina Graziosi, Claudio D'Amore, et al.
American Journal of Physiology. Heart and Circulatory Physiology|May 3, 2015
Cystathionine γ-lyase, a H2S-generating enzyme, is a GPBAR1-regulated gene and contributes to vasodilation caused by secondary bile acidsBarbara Renga, Mariarosaria Bucci, Sabrina Cipriani, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 4, 2021
Atorvastatin protects against liver and vascular damage in a model of diet induced steatohepatitis by resetting FXR and GPBAR1 signalingSilvia Marchianò, Michele Biagioli, Rosalinda Roselli, et al.
Pageof 14