S. Vispé

发表

A cellular defense pathway regulating transcription through poly(ADP-ribosyl)ation in response to DNA damage.

M. Satoh, H. Serizawa, S. Vispé, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Design, Synthesis and Biological Evaluation of 4-Amino-N-(4-aminophenyl)benzamide Analogues of Quinoline-Based SGI-1027 as Inhibitors of DNA Methylation

F. Sautel, A. Jeltsch, P. Arimondo, 2014, ChemMedChem.

Consequences of combining siRNA-mediated DNA methyltransferase 1 depletion with 5-aza-2′-deoxycytidine in human leukemic KG1 cells

D. Cussac, J. Tost, P. Arimondo, 2015, Oncotarget.

DNA methylation inhibitors in cancer: recent and future approaches.

Jean-Marc Gregoire, Christina Gros, P. Arimondo, 2012, Biochimie.

Physalin B, a novel inhibitor of the ubiquitin-proteasome pathway, triggers NOXA-associated apoptosis.

J. Annereau, C. Bailly, L. Créancier, 2008, Biochemical pharmacology.

F14512, a potent antitumor agent targeting topoisomerase II vectored into cancer cells via the polyamine transport system.

J. Annereau, C. Bailly, J. Barret, 2008, Cancer research.

Cytotoxicity and cell death mechanisms induced by the polyamine-vectorized anti-cancer drug F14512 targeting topoisomerase II.

J. Annereau, C. Bailly, A. Kruczynski, 2011, Biochemical pharmacology.

Semisynthetic neoboutomellerone derivatives as ubiquitin-proteasome pathway inhibitors.

F. Sautel, L. Marcourt, P. Arimondo, 2012, Bioorganic & medicinal chemistry.

Novel tetra-acridine derivatives as dual inhibitors of topoisomerase II and the human proteasome.

J. Annereau, C. Bailly, L. Créancier, 2007, Biochemical pharmacology.

Synthesis and biological evaluation of bengacarboline derivatives.

J. Annereau, C. Bailly, J. Barret, 2008, Bioorganic & Medicinal Chemistry Letters.

An Integrated Drosophila Model System Reveals Unique Properties for F14512, a Novel Polyamine-Containing Anticancer Drug That Targets Topoisomerase II

C. Bailly, J. Barret, E. Käs, 2011, PloS one.

Overexpression of Rad51 protein stimulates homologous recombination and increases resistance of mammalian cells to ionizing radiation.

S. Vispé, C. Cazaux, M. Defais, 1998, Nucleic acids research.

A fluorescent biomarker of the polyamine transport system to select patients with AML for F14512 treatment.

J. Annereau, C. Bailly, J. Barret, 2010, Leukemia research.

Synthesis of conjugated spermine derivatives with 7-nitrobenzoxadiazole (NBD), rhodamine and bodipy as new fluorescent probes for the polyamine transport system.

J. Annereau, C. Bailly, J. Barret, 2009, Bioorganic & medicinal chemistry letters.

Poly(ADP-ribose) Polymerase-1 Is a Negative Regulator of HIV-1 Transcription through Competitive Binding to TAR RNA with Tat·Positive Transcription Elongation Factor b (p-TEFb) Complex*

Hiroshi Handa, Tadashi Wada, Ann Rancourt, 2005, Journal of Biological Chemistry.

Antitumor activity of pyridoisoquinoline derivatives F91873 and F91874, novel multikinase inhibitors with activity against the anaplastic lymphoma kinase

J. Annereau, C. Bailly, A. Marchand, 2009, Anti-cancer drugs.

Triptolide is an inhibitor of RNA polymerase I and II–dependent transcription leading predominantly to down-regulation of short-lived mRNA

J. Annereau, D. Cussac, C. Bailly, 2009, Molecular Cancer Therapeutics.

DNA repair patch-mediated double strand DNA break formation in human cells.

M. Satoh, S. Vispé, S. Vispé, 2000, The Journal of biological chemistry.

Double-strand DNA Break Formation Mediated by Flap Endonuclease-1*

M. Satoh, S. Vispé, T. M. Yung, 2003, Journal of Biological Chemistry.

Mammalian Rad51 protein: a RecA homologue with pleiotropic functions.

S. Vispé, M. Defais, S. Vispé, 1997, Biochimie.

Characterization of the sensitivity to various genotoxic agents of the UVU1-CHO cell line, a double mutant from UV complementation group 1.

S. Vispé, M. Defais, C. Lesca, 1997, Biochimie.