P. Gaillard

发表

A cellular assay for measuring the modulation of glucose production in H4IIE cells.

K. Yeow, A. Scheer, Paul Lang, 2006, Assay and drug development technologies.

Inhibition of c‐Jun N‐terminal kinase decreases cardiomyocyte apoptosis and infarct size after myocardial ischemia and reperfusion in anaesthetized rats

C. Giachetti, P. Vitte, S. Carboni, 2004, British journal of pharmacology.

Control of death receptor and mitochondrial‐dependent apoptosis by c‐Jun N‐terminal kinase in hippocampal CA1 neurones following global transient ischaemia

B. Antonsson, P. Vitte, S. Carboni, 2005, Journal of neurochemistry.

The p110δ crystal structure uncovers mechanisms for selectivity and potency of novel PI3K inhibitors

Yi Liu, Kevan M. Shokat, Fabrice Gorrec, 2009, Nature chemical biology.

Synthesis of Novel C‐Methylflavones

M. Duclos, P. Gaillard, M. Kaouadji, 2006 .

The p110delta structure: mechanisms for selectivity and potency of new PI(3)K inhibitors.

Fabrice Gorrec, Simon Miller, Kevan M Shokat, 2010, Nature chemical biology.

the p 110 structure : mechanisms for selectivity and potency of new pI ( 3 ) K inhibitors

K. Shokat, C. Rommel, D. Le, 2010 .

Characterization of Novel PI3Kδ Inhibitors as Potential Therapeutics for SLE and Lupus Nephritis in Pre-Clinical Studies

M. Camps, H. Ji, C. Waltzinger, 2014, Front. Immunol..

AS601245 (1,3-Benzothiazol-2-yl (2-{[2-(3-pyridinyl) ethyl] amino}-4 pyrimidinyl) Acetonitrile): A c-Jun NH2-Terminal Protein Kinase Inhibitor with Neuroprotective Properties

Jean-Pierre Gotteland, P. Vitte, A. Hiver, 2004, Journal of Pharmacology and Experimental Therapeutics.

A cellular assay for measuring the inhibition of glycogen synthase kinase-3 via the accumulation of beta-catenin in Chinese hamster ovary clone K1 cells.

K. Yeow, A. Scheer, Paul Lang, 2006, Assay and drug development technologies.

AS601245, a c‐Jun NH2‐terminal kinase (JNK) inhibitor, reduces axon/dendrite damage and cognitive deficits after global cerebral ischaemia in gerbils

U. Boschert, P. Vitte, S. Carboni, 2008, British journal of pharmacology.

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.

Jean-Pierre Gotteland, Anthony Nichols, Serge Halazy, 2005, Journal of medicinal chemistry.

A novel synthesis of 1‐(2,4,6‐trihydroxy‐3,5‐dimethylphenyl)ethanone (di‐C‐methylphloracetophenone) and two new non‐aromatic C‐benzylated derivatives

M. Duclos, R. Stomberg, P. Gaillard, 1995 .

Synthesis of Novel C-Methylflavones.

M. Duclos, P. Gaillard, M. Kaouadji, 1996 .

Corrigendum: The p110[delta] structure: mechanisms for selectivity and potency of new PI(3)K inhibitors

K. Shokat, Roger L. Williams, S. Miller, 2010 .

Corrigendum: The p110[delta] structure: mechanisms for selectivity and potency of new PI(3)K inhibitors

K. Shokat, Roger L. Williams, S. Miller, 2010 .

The p110delta structure: mechanisms for selectivity and potency of new PI(3)K inhibitors.

K. Shokat, C. Rommel, J. Shaw, 2010, Nature chemical biology.