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European Journal of Medicinal Chemistry|April 5, 2011
New ferrocenic pyrrolo[1,2-a]quinoxaline derivatives: synthesis, and in vitro antimalarial activity--Part IIJean Guillon, Elisabeth Mouray, Stéphane Moreau, et al.
The Journal of Pathology|May 13, 2015
CBL controls a tyrosine kinase network involving AXL, SYK and LYN in nilotinib-resistant chronic myeloid leukaemiaRomain Gioia, Claire Trégoat, Pierre-Yves Dumas, et al.
Oncotarget|December 13, 2017
Chronic myeloid leukemia progenitor cells require autophagy when leaving hypoxia-induced quiescenceAngela Ianniciello, Pierre-Yves Dumas, Claire Drullion, et al.
Chemmedchem|December 6, 2016
Design, Synthesis, and Evaluation of 2,9-Bis[(substituted-aminomethyl)phenyl]-1,10-phenanthroline Derivatives as G-Quadruplex LigandsNassima Meriem Gueddouda, Miyanou Rosales Hurtado, Stéphane Moreau, et al.
Archiv Der Pharmazie|April 14, 2021
Design, synthesis, and antiproliferative effect of 2,9-bis[4-(pyridinylalkylaminomethyl)phenyl]-1,10-phenanthroline derivatives on human leukemic cells by targeting G-quadruplexJean Guillon, Caroline Denevault-Sabourin, Edith Chevret, et al.
Haematologica|March 30, 2019
Hematopoietic niche drives FLT3-ITD acute myeloid leukemia resistance to quizartinib <i>via</i> STAT5-and hypoxia-dependent upregulation of AXLPierre-Yves Dumas, Cécile Naudin, Séverine Martin-Lannerée, et al.
Blood|March 29, 2014
A new human mast cell line expressing a functional IgE receptor converts to tumorigenic growth by KIT D816V transfectionRosine Saleh, Ghaith Wedeh, Harald Herrmann, et al.
Pharmaceuticals (Basel, Switzerland)|January 23, 2024
New 2,4-bis[(substituted-aminomethyl)phenyl]phenylquinazoline and 2,4-bis[(substituted-aminomethyl)phenyl]phenylquinoline Derivatives: Synthesis and Biological Evaluation as Novel Anticancer Agents by Targeting G-QuadruplexJean Guillon, Marc Le Borgne, Vittoria Milano, et al.
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