Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Louis CARREGA"'
Autor:
Jean-Louis Bonnet, Thomas Cuisset, Christopher Mielot, Colette Monserrat, Jacques Quilici, Jean-Philippe Mouret, Roch Giorgi, Marc Lambert, Louis Carrega, Laurent Bali, Régis Guieu, Lyassine Nait-Saidi
Publikováno v:
Archives of Cardiovascular Diseases. 101(10):645-651
Objectif. - L'albumine modifiee par l'ischemie (IMA) est un biomarqueur diagnostique precoce de l'ischemie myocardique. Notre etude avait pour objectif d'evaluer la valeur pronostique de l'IMA chez les patients hospitalises pour syndrome coronaire ai
Autor:
Youlet By, Régis Guieu, Frederic Collard, François Benard, Pierre-Jean Lejeune, François Kerbaul, A Saadjian, Jean-Louis Bonnet, Frauck Paganelli, Colette Monserrat, Ibrahim Zouher, Bernard Mallet, Louis Carrega, Jean Ruf
Publikováno v:
Journal of Investigative Medicine. 55:195-201
Myocardial damage is a frequent complication of cardiac surgery by direct mechanical trauma during the surgical procedure and by myocardial ischemia, which occurs during the cardiopulmonary bypass (CBP). Because the concentrations of biomarkers in th
Autor:
Nicolas Andreotti, Hervé Rochat, H. Vacher, T. Pham, N. Sauze, Imed Regaya, Marie-France Martin-Eauclaire, Christiane Devaux, Régis Guieu, Besma Jouirou, J. C. Peragut, Jean-Marc Sabatier, Louis Carrega
Publikováno v:
Life Sciences. 76:367-377
It has been shown that A2A adenosine receptors are implicated in pain modulation. The precise mechanism by which activation of A2A receptors produces analgesic effects, however, remains unclear. The aim of this study was to investigate the possible i
Autor:
Laurence Mercier, Emmanuel Fenouillet, Radj Purgus, Nicole Sauze, Régis Guieu, Ibrahim Zouher, Guy Bechis, Yvon Berland, Phillippe Brunet, Louis Carrega, Bertrand Dussol
Publikováno v:
Kidney International. 66(4):1640-1646
Kinetic study of adenosine concentrations and the expression of adenosine deaminase in mononuclear cells during hemodialysis. Background We previously showed that high intralymphocytic adenosine (Ado) concentrations are found in hemodialyzed patients
Autor:
Christiane Devaux, Odile Fund-Saunier, Régis Guieu, Jean-Claude Peragut, Louis Carrega, A Saadjian, Nicole Sauze, Thao Pham
Publikováno v:
Anesthesiology. 98:459-464
Background The modulation of extracellular adenosine concentration by opioids provides evidence that the antinociceptive effects of these compounds involve endogenous adenosine. The aim of this study was to determine whether there is a relation betwe
Autor:
Eric DI LUCCIO, Alessandra MATAVEL, Sandrine OPI, Imed REGAYA, Guillaume SANDOZ, Sarrah M'BAREK, Edmond CARLIER, Eric ESTÈVE, Louis CARREGA, Ziad FAJLOUN, Hervé ROCHAT, Erwann LORET, Michel DE WAARD, Jean-Marc SABATIER
Publikováno v:
Biochemical Journal. 361:409-416
Maurotoxin (MTX) is a 34-mer scorpion toxin cross-linked by four disulphide bridges that acts on various K+ channels, including the voltage-gated Shaker B subtype. In the present study, we have investigated over 80h: (1) the time-course of folding of
Autor:
Bertrand Dussol, J. L. Mege, D. Lerda, Emmanuel Fenouillet, Hervé Rochat, Christian Capo, Joana Vitte, Philippe Brunet, Guy Bechis, Jerome Sampol, Louis Carrega, Yvon Berland, Zouher Ibrahim, Régis Guieu
Publikováno v:
Journal of Investigative Medicine. 49:56-67
Background Infections and hypotension are serious complications that develop during hemodialysis (HD) treatment. Adenosine (ADO), a strong hypotensive and immunosuppressive agent, may participate in these two HD complications, because high concentrat
Autor:
Laurent Commeiras, Smitha C. Mathew, Gaëlle Chouraqui, Marie-Alice Virolleaud, Jocelyne Condo, Jean Rodriguez, Anouk Gaudel-Siri, Youlet By, Jean Ruf, Régis Guieu, Jean-Luc Parrain, Aurélie Berthault, Mireille Attolini, Louis Carrega
Publikováno v:
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2010, 8 (17), pp.3874-81. ⟨10.1039/c0ob00017e⟩
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2010, 8, pp.3874. ⟨10.1039/c0ob00017e⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2010, 8 (17), pp.3874-81. ⟨10.1039/c0ob00017e⟩
Organic & Biomolecular Chemistry, 2010, 8, pp.3874. ⟨10.1039/c0ob00017e⟩
Organic & Biomolecular Chemistry, 2010, 8 (17), pp.3874-81. ⟨10.1039/c0ob00017e⟩
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2010, 8, pp.3874. ⟨10.1039/c0ob00017e⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2010, 8 (17), pp.3874-81. ⟨10.1039/c0ob00017e⟩
Organic & Biomolecular Chemistry, 2010, 8, pp.3874. ⟨10.1039/c0ob00017e⟩
International audience; The synthesis of new C-6 1,2,3-triazole adenosine derivatives via microwave assisted 1,3-dipolar cycloaddition as key step is described. The binding on membranes of cells that over express A(1) adenosine receptors (A(1)AR) was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72328199fbe978ce388af8f881b6a75d
https://hal.science/hal-00682114
https://hal.science/hal-00682114
Autor:
Louis Carrega, Jocelyne Condo, Aurélie Berthault, Laurent Commeiras, Mireille Attolini, Gaëlle Chouraqui, Jean Ruf, Régis Guieu, Youlet By, Nandita Ghosh, Jean-Luc Parrain, Jean Rodriguez, Smitha C. Mathew, Anouk Gaudel-Siri, Marie-Alice Virolleaud
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, 2009, 19, pp.6736. ⟨10.1016/j.bmcl.2009.09.112⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2009, 19, pp.6736. ⟨10.1016/j.bmcl.2009.09.112⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2009, 19, pp.6736-6739. ⟨10.1016/j.bmcl.2009.09.112⟩
Bioorganic and Medicinal Chemistry Letters, 2009, 19, pp.6736-6739. ⟨10.1016/j.bmcl.2009.09.112⟩
Bioorganic and Medicinal Chemistry Letters, 2009, 19, pp.6736. ⟨10.1016/j.bmcl.2009.09.112⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2009, 19, pp.6736. ⟨10.1016/j.bmcl.2009.09.112⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2009, 19, pp.6736-6739. ⟨10.1016/j.bmcl.2009.09.112⟩
Bioorganic and Medicinal Chemistry Letters, 2009, 19, pp.6736-6739. ⟨10.1016/j.bmcl.2009.09.112⟩
The cross talk between different membrane receptors is the source of increasing research. We designed and synthesized a new hetero-bivalent ligand that has antagonist properties on both A(1) adenosine and mu opiate receptors with a K(i) of 0.8+/-0.05
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61dca52f1f35f9d3891ec9961903b68b
https://hal.science/hal-01407732
https://hal.science/hal-01407732
Autor:
Roch Giorgi, V. Gerolami, Dorothée Blayac, Fréderic Benard, Louis Carrega, François Kerbaul, Ibrahim Zouher, Vincent Bénas, Youlet, Régis Guieu, Vlad Gariboldi, Laurence Mercier, Frederic Collart
Publikováno v:
ResearcherID
Objective Adenosine (ADO) is an endogenous nucleoside, which has been involved in blood pressure failure during severe systemic inflammatory response syndrome (severe SIRS) after cardiac surgery with cardiopulmonary bypass (CPB). Adenosine acts via i