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Bioorganic & Medicinal Chemistry Letters|April 13, 2000
Inhibition of the ras-dependent mitogenic pathway by phosphopeptide prodrugs with antiproliferative propertiesW Q Liu, M Vidal, C Mathé, et al.
Biochemical Pharmacology|April 15, 1992
Increase of neutral endopeptidase-24.11 with cellular density and enzyme modulation with an inhibitor on human Reh6 cell lineP E Milhiet, A Beaumont, C Garbay-Jaureguiberry, et al.
British Journal of Pharmacology|August 28, 1998
Opposite effects of CCK(B) agonists in grooming behaviour in rats: further evidence for two CCK(B) subsitesN Ladurelle, A Sebret, C Garbay, et al.
Biochemistry|April 5, 1977
A proton magnetic resonance study of the conformation of methionine-enkephalin as a function of pHM Anteunis, A K Lala, C Garbay-Jaureguiberry, et al.
Analytical Biochemistry|February 17, 2006
Affinity chromatography for purification of the modular protein growth factor receptor-bound protein 2 and development of a screening test for growth factor receptor-bound protein 2 Src homology 3 domain inhibitor using peroxidase-linked ligandB Gril, W Q Liu, C Lenoir, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1984
Highly selective photoaffinity labeling of mu and delta opioid receptorsC Garbay-Jaureguiberry, A Robichon, V Daugé, et al.
Anti-Cancer Drug Design|June 1, 1988
Relationship between the size and position of substituents on 7H-pyrido[4,3-c]carbazole monomers and dimers and their DNA binding and anti-tumor propertiesP Léon, C Garbay-Jaureguiberry, J B Le Pecq, et al.
Journal of Molecular Biology|July 9, 1999
Molecular and cellular analysis of Grb2 SH3 domain mutants: interaction with Sos and dynaminM Vidal, N Goudreau, F Cornille, et al.
Journal of Molecular Biology|November 5, 1989
1H and 31P nuclear magnetic resonance studies of the differences in DNA deformation induced by anti-tumoral 7H-pyrido[4,3-c]carbazole dimersM Delepierre, R Maroun, C Garbay-Jaureguiberry, et al.
Journal of Medicinal Chemistry|September 10, 1999
Small peptides containing phosphotyrosine and adjacent alphaMe-phosphotyrosine or its mimetics as highly potent inhibitors of Grb2 SH2 domainW Q Liu, M Vidal, N Gresh, et al.
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