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2003 | 1 |
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Page 1
Chemical genetics: toward the next generation of molecular medicines.
Pharmacogenomics. 2004 Oct;5(7):757-61. doi: 10.1517/14622416.5.7.757.
Pharmacogenomics. 2004.
PMID: 15469399
Free article.
Review.
No abstract available.
GLEPP1/protein-tyrosine phosphatase phi inhibitors block chemotaxis in vitro and in vivo and improve murine ulcerative colitis.
Gobert RP, van den Eijnden M, Szyndralewiez C, Jorand-Lebrun C, Swinnen D, Chen L, Gillieron C, Pixley F, Juillard P, Gerber P, Johnson-Léger C, Halazy S, Camps M, Bombrun A, Shipp M, Vitte PA, Ardissone V, Ferrandi C, Perrin D, Rommel C, Hooft van Huijsduijnen R.
Gobert RP, et al. Among authors: halazy s.
J Biol Chem. 2009 Apr 24;284(17):11385-95. doi: 10.1074/jbc.M807241200. Epub 2009 Feb 20.
J Biol Chem. 2009.
PMID: 19233845
Free PMC article.
Item in Clipboard
Discovery and development of a new class of potent, selective, orally active oxytocin receptor antagonists.
Quattropani A, Dorbais J, Covini D, Pittet PA, Colovray V, Thomas RJ, Coxhead R, Halazy S, Scheer A, Missotten M, Ayala G, Bradshaw C, De Raemy-Schenk AM, Nichols A, Cirillo R, Tos EG, Giachetti C, Golzio L, Marinelli P, Church DJ, Barberis C, Chollet A, Schwarz MK.
Quattropani A, et al. Among authors: halazy s.
J Med Chem. 2005 Dec 1;48(24):7882-905. doi: 10.1021/jm050645f.
J Med Chem. 2005.
PMID: 16302826
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3,6-dibromocarbazole piperazine derivatives of 2-propanol as first inhibitors of cytochrome c release via Bax channel modulation.
Bombrun A, Gerber P, Casi G, Terradillos O, Antonsson B, Halazy S.
Bombrun A, et al. Among authors: halazy s.
J Med Chem. 2003 Oct 9;46(21):4365-8. doi: 10.1021/jm034107j.
J Med Chem. 2003.
PMID: 14521400
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In vitro and in vivo pharmacological profile of AS057278, a selective d-amino acid oxidase inhibitor with potential anti-psychotic properties.
Adage T, Trillat AC, Quattropani A, Perrin D, Cavarec L, Shaw J, Guerassimenko O, Giachetti C, Gréco B, Chumakov I, Halazy S, Roach A, Zaratin P.
Adage T, et al. Among authors: halazy s.
Eur Neuropsychopharmacol. 2008 Mar;18(3):200-14. doi: 10.1016/j.euroneuro.2007.06.006. Epub 2007 Aug 2.
Eur Neuropsychopharmacol. 2008.
PMID: 17681761
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Design, synthesis, and biological activity of novel, potent, and selective (benzoylaminomethyl)thiophene sulfonamide inhibitors of c-Jun-N-terminal kinase.
Rückle T, Biamonte M, Grippi-Vallotton T, Arkinstall S, Cambet Y, Camps M, Chabert C, Church DJ, Halazy S, Jiang X, Martinou I, Nichols A, Sauer W, Gotteland JP.
Rückle T, et al. Among authors: halazy s.
J Med Chem. 2004 Dec 30;47(27):6921-34. doi: 10.1021/jm031112e.
J Med Chem. 2004.
PMID: 15615541
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Design and synthesis of the first generation of novel potent, selective, and in vivo active (benzothiazol-2-yl)acetonitrile inhibitors of the c-Jun N-terminal kinase.
Gaillard P, Jeanclaude-Etter I, Ardissone V, Arkinstall S, Cambet Y, Camps M, Chabert C, Church D, Cirillo R, Gretener D, Halazy S, Nichols A, Szyndralewiez C, Vitte PA, Gotteland JP.
Gaillard P, et al. Among authors: halazy s.
J Med Chem. 2005 Jul 14;48(14):4596-607. doi: 10.1021/jm0310986.
J Med Chem. 2005.
PMID: 15999997
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