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Neuroinflammation, body temperature and behavioural changes in CD1 male mice undergoing acute restraint stress: An exploratory study

PloS one, 2021-11, Vol.16 (11), p.e0259938-e0259938

2021

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PHA-739358, a potent inhibitor of Aurora kinases with a selective target inhibition profile relevant to cancer

Molecular cancer therapeutics, 2007-12, Vol.6 (12), p.3158-3168

2007

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FOXM1 expression is significantly associated with chemotherapy resistance and adverse prognosis in non-serous epithelial ovarian cancer patients

Journal of experimental & clinical cancer research, 2017-05, Vol.36 (1), p.63-63, Article 63

2017

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In vivo imaging of early stage apoptosis by measuring real-time caspase-3/7 activation

Apoptosis (London), 2011-02, Vol.16 (2), p.198-207

2011

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novel method based on click chemistry, which overcomes limitations of cell cycle analysis by classical determination of BrdU incorporation, allowing multiplex antibody staining

Cytometry. Part A, 2008-07, Vol.73A (7), p.626-636

2008

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PHA-680632, a Novel Aurora Kinase Inhibitor with Potent Antitumoral Activity

Clinical cancer research, 2006-07, Vol.12 (13), p.4080-4089

2006

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Identification of 4,5-Dihydro-1H-pyrazolo[4,3-h]quinazoline Derivatives as a New Class of Orally and Selective Polo-Like Kinase 1 Inhibitors

Journal of medicinal chemistry, 2010-05, Vol.53 (9), p.3532-3551

2010

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A Novel High-Content Immunofluorescence Assay as a Tool to Identify at the Single Cell Level γ-Globin Inducing Compounds

PloS one, 2015-10, Vol.10 (10), p.e0141083-e0141083

2015

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Cell Proliferation Method: Click Chemistry Based on BrdU Coupling for Multiplex Antibody Staining

Current Protocols in Cytometry, 2015-04, Vol.72 (1), p.7.34.1-7.34.17

2015

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Highly multiplexed phenotypic imaging for cell proliferation studies

Journal of biomolecular screening, 2014-01, Vol.19 (1), p.145-157

2014

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Interpreting cell cycle effects of drugs : the case of melphalan

Cancer chemotherapy and pharmacology, 2006-04, Vol.57 (4), p.443-457

2006

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Targeting the mitotic checkpoint for cancer therapy with NMS-P715, an inhibitor of MPS1 kinase

Cancer research (Chicago, Ill.), 2010-12, Vol.70 (24), p.10255-10264

2010

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NMS-P937, an orally available, specific small-molecule polo-like kinase 1 inhibitor with antitumor activity in solid and hematologic malignancies

Molecular cancer therapeutics, 2012-04, Vol.11 (4), p.1006-1016

2012

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Multiparametric cell cycle analysis by automated microscopy

Journal of biomolecular screening, 2006-09, Vol.11 (6), p.586-598

2006

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1,4,5,6-Tetrahydropyrrolo[3,4-c]pyrazoles: Identification of a Potent Aurora Kinase Inhibitor with a Favorable Antitumor Kinase Inhibition Profile

Journal of medicinal chemistry, 2006-11, Vol.49 (24), p.7247-7251

2006

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CyTOF Mass Cytometry for Click Proliferation Assays

Current Protocols in Cytometry, 2017-07, Vol.81 (1), p.7.50.1-7.50.14

2017

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From “Click” to “Fenton” chemistry for 5‐bromo‐2′‐deoxyuridine determination

Cytometry. Part A, 2013-11, Vol.83 (11), p.989-1000

2013

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Identification of 4,5-Dihydro-1 H -pyrazolo[4,3- h ]quinazoline Derivatives as a New Class of Orally and Selective Polo-Like Kinase 1 Inhibitors

Journal of medicinal chemistry, 2010-05, Vol.53 (9), p.3532-3551

2010

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Application of Click Chemistry Conditions for 5‐Bromo‐2′‐Deoxyuridine Determination Through Fenton and Related Reactions

Current Protocols in Cytometry, 2015-01, Vol.71 (1), p.7.43.1-7.43.17

2015

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A Novel High-Content Immunofluorescence Assay as a Tool to Identify at the Single Cell Level [gamma]-Globin Inducing Compounds

PloS one, 2015-10, Vol.10 (10)

2015

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Neuroinflammation, body temperature and behavioural changes in CD1 male mice undergoing acute restraint stress: An exploratory study

PloS one, 2021-01, Vol.16 (11), p.e0259938

2021

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Potent and Selective Aurora Inhibitors Identified by the Expansion of a Novel Scaffold for Protein Kinase Inhibition

Journal of medicinal chemistry, 2005-04, Vol.48 (8), p.3080-3084

2005

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Quantitative Assessment of the Complex Dynamics of G1, S, and G2-M Checkpoint Activities

Cancer research (Chicago, Ill.), 2009-06, Vol.69 (12), p.5234-5240

2009

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Identification of Myb-binding Protein 1A (MYBBP1A) as a Novel Substrate for Aurora B Kinase

The Journal of biological chemistry, 2010-04, Vol.285 (16), p.11775-11785

2010

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Phosphorylation of TCTP as a Marker for Polo-like Kinase-1 Activity In Vivo

Anticancer research, 2010-12, Vol.30 (12), p.4973-4985

2010

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Neuroinflammation, body temperature and behavioural changes in CD1 male mice undergoing acute restraint stress: An exploratory study

PHA-739358, a potent inhibitor of Aurora kinases with a selective target inhibition profile relevant to cancer

FOXM1 expression is significantly associated with chemotherapy resistance and adverse prognosis in non-serous epithelial ovarian cancer patients

In vivo imaging of early stage apoptosis by measuring real-time caspase-3/7 activation

novel method based on click chemistry, which overcomes limitations of cell cycle analysis by classical determination of BrdU incorporation, allowing multiplex antibody staining

PHA-680632, a Novel Aurora Kinase Inhibitor with Potent Antitumoral Activity

Identification of 4,5-Dihydro-1H-pyrazolo[4,3-h]quinazoline Derivatives as a New Class of Orally and Selective Polo-Like Kinase 1 Inhibitors

A Novel High-Content Immunofluorescence Assay as a Tool to Identify at the Single Cell Level γ-Globin Inducing Compounds

Cell Proliferation Method: Click Chemistry Based on BrdU Coupling for Multiplex Antibody Staining

Highly multiplexed phenotypic imaging for cell proliferation studies

Interpreting cell cycle effects of drugs : the case of melphalan

Targeting the mitotic checkpoint for cancer therapy with NMS-P715, an inhibitor of MPS1 kinase

NMS-P937, an orally available, specific small-molecule polo-like kinase 1 inhibitor with antitumor activity in solid and hematologic malignancies

Multiparametric cell cycle analysis by automated microscopy

1,4,5,6-Tetrahydropyrrolo[3,4-c]pyrazoles: Identification of a Potent Aurora Kinase Inhibitor with a Favorable Antitumor Kinase Inhibition Profile

CyTOF Mass Cytometry for Click Proliferation Assays

From “Click” to “Fenton” chemistry for 5‐bromo‐2′‐deoxyuridine determination

Identification of 4,5-Dihydro-1 H -pyrazolo[4,3- h ]quinazoline Derivatives as a New Class of Orally and Selective Polo-Like Kinase 1 Inhibitors

Application of Click Chemistry Conditions for 5‐Bromo‐2′‐Deoxyuridine Determination Through Fenton and Related Reactions

A Novel High-Content Immunofluorescence Assay as a Tool to Identify at the Single Cell Level [gamma]-Globin Inducing Compounds

Neuroinflammation, body temperature and behavioural changes in CD1 male mice undergoing acute restraint stress: An exploratory study

Potent and Selective Aurora Inhibitors Identified by the Expansion of a Novel Scaffold for Protein Kinase Inhibition

Quantitative Assessment of the Complex Dynamics of G1, S, and G2-M Checkpoint Activities

Identification of Myb-binding Protein 1A (MYBBP1A) as a Novel Substrate for Aurora B Kinase

Phosphorylation of TCTP as a Marker for Polo-like Kinase-1 Activity In Vivo

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