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Multi-kinase inhibitor C1 triggers mitotic catastrophe of glioma stem cells mainly through MELK kinase inhibition

PloS one, 2014-04, Vol.9 (4), p.e92546-e92546

2014

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Aurora kinases orchestrate mitosis; who are the players?

Biomolecular concepts, 2010-08, Vol.1 (2), p.147-155

Molla, Annie

2010

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Weak but Uniform Enrichment of the Histone Variant macroH2A1 along the Inactive X Chromosome

Molecular and Cellular Biology, 2009-01, Vol.29 (1), p.150-156

2009

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Histone variant H2ABbd confers lower stability to the nucleosome

EMBO reports, 2004-07, Vol.5 (7), p.715-720

2004

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Role of Survivin Phosphorylation by Aurora B in Mitosis

Cell cycle (Georgetown, Tex.), 2007-08, Vol.6 (15), p.1878-1885

2007

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Benzo[e]pyridoindoles, novel inhibitors of the Aurora kinases

Cell cycle (Georgetown, Tex.), 2009-03, Vol.8 (5), p.765-772

2009

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Basal aurora kinase B activity is sufficient for histone H3 phosphorylation in prophase

Biology open, 2013-04, Vol.2 (4), p.379-386

2013

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Aurora B kinase, an immobile passenger

Cell cycle (Georgetown, Tex.), 2009-11, Vol.8 (21), p.3608-3609

2009

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Organs-on-chips dedicated to oncology

M.S. Médecine sciences, 2019-05, Vol.35 (5), p.419

2019

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Distinct Dynamics of Aurora B and Survivin During Mitosis

Cell cycle (Georgetown, Tex.), 2004-11, Vol.3 (11), p.1418-1426

2004

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In vitro high throughput screening, what next? Lessons from the screening for aurora kinase inhibitors

Biology (Basel, Switzerland), 2014-02, Vol.3 (1), p.167-175

2014

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Unsuccessful mitosis in multicellular tumour spheroids

Oncotarget, 2017-04, Vol.8 (17), p.28769-28784

2017

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Polyheteroaryl Oxazole/Pyridine-Based Compounds Selected in Vitro as G‑Quadruplex Ligands Inhibit Rock Kinase and Exhibit Antiproliferative Activity

Journal of medicinal chemistry, 2018-12, Vol.61 (23), p.10502-10518

2018

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The Histone Variant MacroH2A Interferes with Transcription Factor Binding and SWI/SNF Nucleosome Remodeling

Molecular cell, 2003-04, Vol.11 (4), p.1033-1041

2003

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Expression and function of receptors for extracellular matrix molecules in the differentiation of human megakaryocytes in vitro

British journal of haematology, 1997-09, Vol.98 (4), p.819-827

1997

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A Constrained Diketopiperazine as a New Scaffold for the Synthesis of Peptidomimetics

European journal of organic chemistry, 1998-05, Vol.1998 (5), p.853-859

1998

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Survivin reads the mitotic histone code

M.S. Médecine sciences, 2011-03, Vol.27 (3), p.241

2011

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Discovery of benzo[e]pyridoindolones as kinase inhibitors that disrupt mitosis exit while erasing AMPK-Thr172 phosphorylation on the spindle

Oncotarget, 2015-09, Vol.6 (26), p.22152-22166

2015

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Aurora B kinase, an immobile passenger: Aurora B kinase

Cell cycle (Georgetown, Tex.), 2009-11, Vol.8 (21), p.3600-1

2009

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The N-terminus of histone H2B, but not that of histone H3 or its phosphorylation, is essential for chromosome condensation

The EMBO journal, 2001-11, Vol.20 (22), p.6383-6393

2001

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Hydrosoluble Benzo[e]pyridoindolones as Potent Inhibitors of Aurora Kinases

ChemMedChem, 2013-02, Vol.8 (2), p.289-296

2013

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Calcium/calmodulin-dependent protein kinase II controls α5β1 integrin-mediated inside-out signaling

Journal of cell science, 1998-03, Vol.111 (5), p.657-665

1998

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Benzo[e]pyridoindoles, novel inhibitors of the aurora kinases

Cell cycle (Georgetown, Tex.), 2009-03, Vol.8 (5), p.765-72

2009

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Multi-Kinase Inhibitor C1 Triggers Mitotic Catastrophe of Glioma Stem Cells Mainly through MELK Kinase Inhibition: e92546

PloS one, 2014-04, Vol.9 (4)

2014

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Survivin, the starlet of the passenger-protein complex : check-up for its tenth anniversary

M.S. Médecine sciences, 2008-10, Vol.24 (10), p.828

2008

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Multi-kinase inhibitor C1 triggers mitotic catastrophe of glioma stem cells mainly through MELK kinase inhibition

Aurora kinases orchestrate mitosis; who are the players?

Weak but Uniform Enrichment of the Histone Variant macroH2A1 along the Inactive X Chromosome

Histone variant H2ABbd confers lower stability to the nucleosome

Role of Survivin Phosphorylation by Aurora B in Mitosis

Benzo[e]pyridoindoles, novel inhibitors of the Aurora kinases

Basal aurora kinase B activity is sufficient for histone H3 phosphorylation in prophase

Aurora B kinase, an immobile passenger

Organs-on-chips dedicated to oncology

Distinct Dynamics of Aurora B and Survivin During Mitosis

In vitro high throughput screening, what next? Lessons from the screening for aurora kinase inhibitors

Unsuccessful mitosis in multicellular tumour spheroids

Polyheteroaryl Oxazole/Pyridine-Based Compounds Selected in Vitro as G‑Quadruplex Ligands Inhibit Rock Kinase and Exhibit Antiproliferative Activity

The Histone Variant MacroH2A Interferes with Transcription Factor Binding and SWI/SNF Nucleosome Remodeling

Expression and function of receptors for extracellular matrix molecules in the differentiation of human megakaryocytes in vitro

A Constrained Diketopiperazine as a New Scaffold for the Synthesis of Peptidomimetics

Survivin reads the mitotic histone code

Discovery of benzo[e]pyridoindolones as kinase inhibitors that disrupt mitosis exit while erasing AMPK-Thr172 phosphorylation on the spindle

Aurora B kinase, an immobile passenger: Aurora B kinase

The N-terminus of histone H2B, but not that of histone H3 or its phosphorylation, is essential for chromosome condensation

Hydrosoluble Benzo[e]pyridoindolones as Potent Inhibitors of Aurora Kinases

Calcium/calmodulin-dependent protein kinase II controls α5β1 integrin-mediated inside-out signaling

Benzo[e]pyridoindoles, novel inhibitors of the aurora kinases

Multi-Kinase Inhibitor C1 Triggers Mitotic Catastrophe of Glioma Stem Cells Mainly through MELK Kinase Inhibition: e92546

Survivin, the starlet of the passenger-protein complex : check-up for its tenth anniversary

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