C. Delorme

发表

Glycosphingolipid Binding Specificities of Rotavirus: Identification of a Sialic Acid-Binding Epitope

N. Roche, S. Teneberg, K. Karlsson, 2001, Journal of Virology.

Concomitant Inhibition of PI3Kβ and BRAF or MEK in PTEN-Deficient/BRAF-Mutant Melanoma Treatment: Preclinical Assessment of SAR260301 Oral PI3Kβ-Selective Inhibitor

C. García-echeverría, C. Lengauer, L. Vincent, 2016, Molecular Cancer Therapeutics.

KRAS G12C fragment screening renders new binding pockets

M. Mathieu, L. Debussche, M. Lowinski, 2021, Small GTPases.

Mechanism-based inactivation of bovine cytochrome P-450(11beta) by 18-unsaturated progesterone derivatives.

F. Sobrio, A. Piffeteau, A. Marquet, 1997, European journal of biochemistry.

Inhibition of bovine cytochrome P-450(11 beta) by 18-unsaturated progesterone derivatives.

A. Piffeteau, A. Marquet, C. Delorme, 1995, European journal of biochemistry.

A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions

P. Yu-Wai-Man, A. Chaussenot, S. Bannwarth, 2017, Human molecular genetics.

Regulation of oxidative phosphorylation: The flexible respiratory network ofParacoccus denitrificans

H. Westerhoff, J. Oost, A. H. Stouthamer, 1995, Journal of bioenergetics and biomembranes.

SAR156497, an exquisitely selective inhibitor of aurora kinases.

Sébastien Maignan, François Clerc, Thomas Bertrand, 2014, Journal of medicinal chemistry.

Discovery and optimization of new benzimidazole- and benzoxazole-pyrimidone selective PI3Kβ inhibitors for the treatment of phosphatase and TENsin homologue (PTEN)-deficient cancers.

J. Nicolas, C. Lengauer, L. Vincent, 2012, Journal of medicinal chemistry.

Discovery and optimization of pyrimidone indoline amide PI3Kβ inhibitors for the treatment of phosphatase and tensin homologue (PTEN)-deficient cancers.

Jean-Pierre Marquette, Magali Mathieu, Thomas Bertrand, 2014, Journal of medicinal chemistry.

Tricyclic series of heat shock protein 90 (Hsp90) inhibitors part I: discovery of tricyclic imidazo[4,5-c]pyridines as potent inhibitors of the Hsp90 molecular chaperone.

Paul Ferrari, Patrick Mailliet, Hervé Minoux, 2011, Journal of medicinal chemistry.

AI4DR: Development and Implementation of an Annotation System for High-Throughput Dose-Response Experiments

H. Minoux, M. Bianciotto, S. Vougier, 2023, Artificial Intelligence in the Life Sciences.

Specific inhibition of the last steps of aldosterone biosynthesis by 18-vinylprogesterone in bovine adrenocortical cells

A. Piffeteau, G. Defaye, A. Marquet, 1996, The Journal of Steroid Biochemistry and Molecular Biology.

The use of virtual screening and differential scanning fluorimetry for the rapid identification of fragments active against MEK1.

Maryse Lowinski, A. Rak, F. Vallée, 2013, Bioorganic & medicinal chemistry letters.

Concomitant Inhibition of PI3Kβ and BRAF or MEK in PTEN-Deficient/BRAF-Mutant Melanoma Treatment: Preclinical Assessment of SAR260301 Oral PI3Kβ-Selective Inhibitor

C. García-echeverría, C. Lengauer, L. Vincent, 2016, Molecular Cancer Therapeutics.

Preparation and optimization of new 4-(morpholin-4-yl)-(6-oxo-1,6-dihydropyrimidin-2-yl)amide derivatives as PI3Kβ inhibitors.

J. Nicolas, C. Lengauer, L. Vincent, 2012, Bioorganic & medicinal chemistry letters.