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Vaccinia virus protein C4 inhibits NF-κB activation and promotes virus virulence

Journal of general virology, 2012-10, Vol.93 (Pt 10), p.2098-2108

2012

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Vaccinia virus immune evasion: mechanisms, virulence and immunogenicity

Journal of general virology, 2013-11, Vol.94 (Pt 11), p.2367-2392

2013

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Acetyl-lysine Binding Site of Bromodomain-Containing Protein 4 (BRD4) Interacts with Diverse Kinase Inhibitors

ACS chemical biology, 2014-05, Vol.9 (5), p.1160-1171

2014

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Identification of a Novel Class of BRD4 Inhibitors by Computational Screening and Binding Simulations

ACS omega, 2017-08, Vol.2 (8), p.4760-4771

2017

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A mechanism for induction of a hypoxic response by vaccinia virus

Proceedings of the National Academy of Sciences - PNAS, 2013-07, Vol.110 (30), p.12444-12449

2013

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Fluorescence lifetime imaging of quantum dot labeled DNA microarrays

International journal of molecular sciences, 2009-04, Vol.10 (4), p.1930-1941

2009

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Fluorinated Aromatic Amino Acids Are Sensitive 19F NMR Probes for Bromodomain-Ligand Interactions

ACS chemical biology, 2014-12, Vol.9 (12), p.2755-2760

2014

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Assessment of Bromodomain Target Engagement by a Series of BI2536 Analogues with Miniaturized BET-BRET

ChemMedChem, 2016-12, Vol.11 (23), p.2575-2581

2016

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Fast DNA and protein microarray tests for the diagnosis of hepatitis C virus infection on a single platform

Analytical and bioanalytical chemistry, 2011-11, Vol.401 (8), p.2549-2559

2011

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Correction to Letter: Fluorinated Aromatic Amino Acids Are Sensitive 19F NMR Probes for Bromodomain–Ligand Interactions

ACS chemical biology, 2016-04, Vol.11 (4), p.1149-1149

2016

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Back Cover: Assessment of Bromodomain Target Engagement by a Series of BI2536 Analogues with Miniaturized BET-BRET (ChemMedChem 23/2016)

ChemMedChem, 2016-12, Vol.11 (23), p.2638-2638

2016

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Correction to Letter: Fluorinated Aromatic Amino Acids Are Sensitive 19 F NMR Probes for Bromodomain–Ligand Interactions

ACS chemical biology, 2016-04, Vol.11 (4), p.1149-1149

2016

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Fluorinated Aromatic Amino Acids Are Sensitive 19 F NMR Probes for Bromodomain-Ligand Interactions

ACS chemical biology, 2014-12, Vol.9 (12), p.2755-2760

2014

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Abstract 3643: Targeting the acetyl-lysine binding site of BRD4 with dual nanomolar BET-JAK2 inhibitors: A new anticancer therapeutic strategy

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.3643-3643

2015

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Solution state hybridization detection using time-resolved fluorescence anisotropy of quantum dot-DNA bioconjugates

Chemical physics letters, 2010-01, Vol.484 (4), p.309-314

2010

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Correction to Letter: Fluorinated Aromatic Amino Acids Are Sensitive (19)F NMR Probes for Bromodomain-Ligand Interactions

ACS chemical biology, 2016-04, Vol.11 (4), p.1149-1149

2016

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MULTI-FACTORIAL ANALYSIS OF CLASS PREDICTION ERROR: ESTIMATING OPTIMAL NUMBER OF BIOMARKERS FOR VARIOUS CLASSIFICATION RULES

Journal of bioinformatics and computational biology, 2010-12, Vol.8 (6), p.945-965

2010

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Multi-factorial analysis of class prediction error: estimating optimal number of biomarkers for various classification rules

Journal of bioinformatics and computational biology, 2010-12, Vol.8 (6), p.945

2010

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Potent Dual BET Bromodomain-Kinase Inhibitors as Value-Added Multitargeted Chemical Probes and Cancer Therapeutics

Molecular cancer therapeutics, 2017-06, Vol.16 (6), p.1054-1067

2017

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Potent dual BET bromodomain-kinase inhibitors as value added multi-targeted chemical probes and cancer therapeutics

Molecular cancer therapeutics, 2017-03, Vol.16 (6), p.1054-1067

2017

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Single Molecule Dual JAK2-BET Inhibition As an MPN Therapeutic

Blood, 2015-12, Vol.126 (23), p.2826-2826

2015

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Vaccinia virus protein C4 inhibits NF-κB activation and promotes virus virulence

Vaccinia virus immune evasion: mechanisms, virulence and immunogenicity

Acetyl-lysine Binding Site of Bromodomain-Containing Protein 4 (BRD4) Interacts with Diverse Kinase Inhibitors

Identification of a Novel Class of BRD4 Inhibitors by Computational Screening and Binding Simulations

A mechanism for induction of a hypoxic response by vaccinia virus

Fluorescence lifetime imaging of quantum dot labeled DNA microarrays

Fluorinated Aromatic Amino Acids Are Sensitive 19F NMR Probes for Bromodomain-Ligand Interactions

Assessment of Bromodomain Target Engagement by a Series of BI2536 Analogues with Miniaturized BET-BRET

Fast DNA and protein microarray tests for the diagnosis of hepatitis C virus infection on a single platform

Correction to Letter: Fluorinated Aromatic Amino Acids Are Sensitive 19F NMR Probes for Bromodomain–Ligand Interactions

Back Cover: Assessment of Bromodomain Target Engagement by a Series of BI2536 Analogues with Miniaturized BET-BRET (ChemMedChem 23/2016)

Correction to Letter: Fluorinated Aromatic Amino Acids Are Sensitive 19 F NMR Probes for Bromodomain–Ligand Interactions

Fluorinated Aromatic Amino Acids Are Sensitive 19 F NMR Probes for Bromodomain-Ligand Interactions

Abstract 3643: Targeting the acetyl-lysine binding site of BRD4 with dual nanomolar BET-JAK2 inhibitors: A new anticancer therapeutic strategy

Solution state hybridization detection using time-resolved fluorescence anisotropy of quantum dot-DNA bioconjugates

Correction to Letter: Fluorinated Aromatic Amino Acids Are Sensitive (19)F NMR Probes for Bromodomain-Ligand Interactions

MULTI-FACTORIAL ANALYSIS OF CLASS PREDICTION ERROR: ESTIMATING OPTIMAL NUMBER OF BIOMARKERS FOR VARIOUS CLASSIFICATION RULES

Peptide-tags for enhanced DNA microarray performanceElectronic supplementary information (ESI) available: Calibration plots obtained with differentially functionalized HCMV and HCV probes hybridized with Cy3-labelled complementary targets. See DOI: 10.1039/c005491g

Multi-factorial analysis of class prediction error: estimating optimal number of biomarkers for various classification rules

Potent Dual BET Bromodomain-Kinase Inhibitors as Value-Added Multitargeted Chemical Probes and Cancer Therapeutics

Potent dual BET bromodomain-kinase inhibitors as value added multi-targeted chemical probes and cancer therapeutics

Single Molecule Dual JAK2-BET Inhibition As an MPN Therapeutic

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