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P5384Postnatal mouse aorta contains yolk sac-derived haemangioblasts with myeloid and endothelial plasticity and vasculogenic capacity

European heart journal, 2019-10, Vol.40 (Supplement_1)

2019

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Fibrinolysis or Primary PCI in ST-Segment Elevation Myocardial Infarction

The New England journal of medicine, 2013-04, Vol.368 (15), p.1379-1387

2013

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037 Eukaryotic Elongation Factor 2 Kinase (eEF2k) Regulates Foam Cell Formation and Atherosclerosis by Promoting Translation and Glycosylation of CD36 Scavenger Receptor Expression in Macrophages

Heart, lung & circulation, 2020, Vol.29, p.S54-S54

2020

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723 Colchicine Exerts Anti-Atherosclerotic and Plaque-Stabilising Effects in Mice by Inhibiting Macrophage Foam Cell Formation and Cholesterol Crystal-Induced NLRP3 Activation

Heart, lung & circulation, 2020, Vol.29, p.S361-S362

2020

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Postnatal Mouse Aorta Contains Yolk Sac-Derived Haemangioblasts with Myeloid and Endothelial Plasticity and Vasculogenic Capacity

Heart, lung & circulation, 2019, Vol.28, p.S330-S331

2019

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Eukaryotic Elongation Factor 2 Kinase (eEF2k) Regulates Cholesterol Uptake by Macrophages via CD36 Scavenger Receptor Expression

Heart, lung & circulation, 2019, Vol.28, p.S329-S329

2019

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ST-segment-elevation myocardial infarction patients randomized to a pharmaco-invasive strategy or primary percutaneous coronary intervention: Strategic Reperfusion Early After Myocardial Infarction (STREAM) 1-year mortality follow-up

Circulation (New York, N.Y.), 2014-09, Vol.130 (14), p.1139-1145

2014

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Indirect Polarographic Determination of Aluminum

Analytical chemistry (Washington), 1966-01, Vol.38 (1), p.64-66

1966

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Pyruvate kinase M2 activators promote tetramer formation and suppress tumorigenesis

Nature chemical biology, 2012-10, Vol.8 (10), p.839

2012

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Evaluation of Substituted N,N′-Diarylsulfonamides as Activators of the Tumor Cell Specific M2 Isoform of Pyruvate Kinase

Journal of medicinal chemistry, 2010-02, Vol.53 (3), p.1048-1055

2010

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Evaluation of thieno[3,2-b]pyrrole[3,2-d]pyridazinones as activators of the tumor cell specific M2 isoform of pyruvate kinase

Bioorganic & medicinal chemistry letters, 2010-06, Vol.20 (11), p.3387-3393

2010

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Extending Pummerer Reaction Chemistry. Synthesis of (±)-Dibromophakellstatin by Oxidative Cyclization of an Imidazole Derivative

Organic letters, 2005-03, Vol.7 (5), p.929-931

2005

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Palau’amine and Related Oroidin Alkaloids Dibromophakellin and Dibromophakellstatin Inhibit the Human 20S Proteasome

Journal of natural products (Washington, D.C.), 2012-05, Vol.75 (5), p.980-985

2012

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Elucidation of the structural basis of interaction of the BCR-ABL kinase inhibitor, nilotinib (Tasigna) with the human ABC drug transporter P-glycoprotein

Leukemia, 2014-04, Vol.28 (4), p.961-964

2014

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A Virtual Screen for Diverse Ligands: Discovery of Selective G Protein-Coupled Receptor Antagonists

Journal of the American Chemical Society, 2008-04, Vol.130 (15), p.5115-5123

2008

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Extending Pummerer Reaction Chemistry. Synthesis Studies in the Phakellin Alkaloid Area

Journal of organic chemistry, 2007-10, Vol.72 (21), p.8076-8086

2007

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A new facile method for the synthesis of 1-arylimidazole-5-carboxylates

Tetrahedron letters, 2000-07, Vol.41 (29), p.5453-5456

2000

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Exploration and optimization of substituted triazolothiadiazines and triazolopyridazines as PDE4 inhibitors

Bioorganic & medicinal chemistry letters, 2009-07, Vol.19 (13), p.3686-3692

2009

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The Integration of Multiple Stimulus Features by V1 Neurons

The Journal of neuroscience, 2004-10, Vol.24 (41), p.9185-9194

2004

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Synthesis and Characterization of a BODIPY Conjugate of the BCR-ABL Kinase Inhibitor Tasigna (Nilotinib): Evidence for Transport of Tasigna and Its Fluorescent Derivative by ABC Drug Transporters

Molecular pharmaceutics, 2011-08, Vol.8 (4), p.1292-1302

2011

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Synthesis and biological evaluation of analogues of the kinase inhibitor nilotinib as Abl and Kit inhibitors

Bioorganic & medicinal chemistry letters, 2013-02, Vol.23 (3), p.682-686

2013

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Identification of a potent new chemotype for the selective inhibition of PDE4

Bioorganic & medicinal chemistry, 2008-02, Vol.18 (4), p.1297-1303

2008

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Synthesis of substituted 2-phenylhistamines via a microwave promoted Suzuki coupling

Tetrahedron letters, 2007-12, Vol.48 (52), p.9140-9143

2007

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The inhibition and treatment of breast cancer with poly (ADP-ribose) polymerase (PARP-1) inhibitors

International journal of biological sciences, 2006-01, Vol.2 (4), p.179-185

2006

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Synthesis of Dibromophakellin, Dibromophakellstatin, and Dibromoagelaspongin via Oxidative Cyclization of Dihydrooroidin Derivatives

Synthesis (Stuttgart), 2009-09, Vol.2009 (18), p.3162-3173

2009

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P5384Postnatal mouse aorta contains yolk sac-derived haemangioblasts with myeloid and endothelial plasticity and vasculogenic capacity

Fibrinolysis or Primary PCI in ST-Segment Elevation Myocardial Infarction

037 Eukaryotic Elongation Factor 2 Kinase (eEF2k) Regulates Foam Cell Formation and Atherosclerosis by Promoting Translation and Glycosylation of CD36 Scavenger Receptor Expression in Macrophages

723 Colchicine Exerts Anti-Atherosclerotic and Plaque-Stabilising Effects in Mice by Inhibiting Macrophage Foam Cell Formation and Cholesterol Crystal-Induced NLRP3 Activation

Postnatal Mouse Aorta Contains Yolk Sac-Derived Haemangioblasts with Myeloid and Endothelial Plasticity and Vasculogenic Capacity

Eukaryotic Elongation Factor 2 Kinase (eEF2k) Regulates Cholesterol Uptake by Macrophages via CD36 Scavenger Receptor Expression

ST-segment-elevation myocardial infarction patients randomized to a pharmaco-invasive strategy or primary percutaneous coronary intervention: Strategic Reperfusion Early After Myocardial Infarction (STREAM) 1-year mortality follow-up

Indirect Polarographic Determination of Aluminum

Pyruvate kinase M2 activators promote tetramer formation and suppress tumorigenesis

Evaluation of Substituted N,N′-Diarylsulfonamides as Activators of the Tumor Cell Specific M2 Isoform of Pyruvate Kinase

Evaluation of thieno[3,2-b]pyrrole[3,2-d]pyridazinones as activators of the tumor cell specific M2 isoform of pyruvate kinase

Extending Pummerer Reaction Chemistry. Synthesis of (±)-Dibromophakellstatin by Oxidative Cyclization of an Imidazole Derivative

Palau’amine and Related Oroidin Alkaloids Dibromophakellin and Dibromophakellstatin Inhibit the Human 20S Proteasome

Elucidation of the structural basis of interaction of the BCR-ABL kinase inhibitor, nilotinib (Tasigna) with the human ABC drug transporter P-glycoprotein

A Virtual Screen for Diverse Ligands: Discovery of Selective G Protein-Coupled Receptor Antagonists

Extending Pummerer Reaction Chemistry. Synthesis Studies in the Phakellin Alkaloid Area

A new facile method for the synthesis of 1-arylimidazole-5-carboxylates

Exploration and optimization of substituted triazolothiadiazines and triazolopyridazines as PDE4 inhibitors

The Integration of Multiple Stimulus Features by V1 Neurons

Synthesis and Characterization of a BODIPY Conjugate of the BCR-ABL Kinase Inhibitor Tasigna (Nilotinib): Evidence for Transport of Tasigna and Its Fluorescent Derivative by ABC Drug Transporters

Synthesis and biological evaluation of analogues of the kinase inhibitor nilotinib as Abl and Kit inhibitors

Identification of a potent new chemotype for the selective inhibition of PDE4

Synthesis of substituted 2-phenylhistamines via a microwave promoted Suzuki coupling

The inhibition and treatment of breast cancer with poly (ADP-ribose) polymerase (PARP-1) inhibitors

Synthesis of Dibromophakellin, Dibromophakellstatin, and Dibromoagelaspongin via Oxidative Cyclization of Dihydrooroidin Derivatives

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