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Identification of key clinical phenotypes of breast cancer using a reduced panel of protein biomarkers

British journal of cancer, 2013-10, Vol.109 (7), p.1886-1894

2013

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HAGE (DDX43) is a biomarker for poor prognosis and a predictor of chemotherapy response in breast cancer

British journal of cancer, 2014-05, Vol.110 (10), p.2450-2461

2014

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Lack of expression of the proteins GMPR2 and PPARα are associated with the basal phenotype and patient outcome in breast cancer

Breast cancer research and treatment, 2013, Vol.137 (1), p.127-137

2013

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Erratum to: Nottingham prognostic index plus (NPI+) predicts risk of distant metastases in primary breast cancer

Breast cancer research and treatment, 2016-08, Vol.159 (1), p.199-199

2016

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L-743, 726 (DMP-266): a novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase

Antimicrobial Agents and Chemotherapy, 1995-12, Vol.39 (12), p.2602-2605

1995

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Asymmetric Synthesis of CDP840 by Jacobsen Epoxidation. An Unusual Syn Selective Reduction of an Epoxide

Journal of organic chemistry, 1997-12, Vol.62 (26), p.9223-9228

1997

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Identification of non-linear influences on the seasonal ozone dose–response of sensitive and resistant clover clones using artificial neural networks

Ecological modelling, 2000-05, Vol.129 (2), p.153-168

2000

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Stereoselective Total Synthesis of (±)-Thielocin Alβ

Journal of the American Chemical Society, 2001-11, Vol.123 (46), p.11381-11387

2001

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Identifying factors which modify the effects of ambient ozone on white clover ( Trifolium repens) in Europe

Environmental pollution (1987), 1998-01, Vol.103 (1), p.7-16

1998

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Synthesis and structure of [(η-C5Me5)Ir(CO)]2

Inorganic chemistry, 1990-05, Vol.29 (10), p.2023-2025

1990

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5-(Piperidin-2-yl)- and 5-(Homopiperidin-2-yl)-1,4-benzodiazepines: High-Affinity, Basic Ligands for the Cholecystokinin-B Receptor

Journal of medicinal chemistry, 1997-08, Vol.40 (16), p.2491-2501

1997

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A new series of selective COX-2 inhibitors: 5,6-diarylthiazolo[3,2-b][1,2,4]triazoles

Bioorganic & medicinal chemistry letters, 1997-01, Vol.7 (1), p.57-62

1997

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Tryptophan-Derived NK1 Antagonists: Conformationally Constrained Heterocyclic Bioisosteres of the Ester Linkage

Journal of medicinal chemistry, 1995-03, Vol.38 (6), p.923-933

1995

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Identification of 3,5-Dihydro-2-aryl-1H-pyrazolo[3,4-c]quinoline-1,4(2H)-diones as Novel High-Affinity Glycine Site N-Methyl-D-aspartate Antagonists

Journal of medicinal chemistry, 1995-06, Vol.38 (12), p.2239-2243

1995

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Methoxylation of cocaine reduces binding affinity and produces compounds of differential binding and dopamine uptake inhibitory activity: discovery of a weak cocaine "antagonist"

Journal of medicinal chemistry, 1993-11, Vol.36 (24), p.3975-3977

1993

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The question of reversible formation of bromonium ions during the course of electrophilic bromination of olefins. 2. The crystal and molecular structure of the bromonium ion of adamantylideneadamantane

Journal of the American Chemical Society, 1985-07, Vol.107 (15), p.4504-4508

1985

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Polyazamacrocycles. V. Structure of Isomeric 3,5,7,7,10,12,14,14-Octamethyl-1,4,8,11-tetraazacyclotetradecanes

Bulletin of the Chemical Society of Japan, 1989-11, Vol.62 (11), p.3701-3705

1989

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An introduction to artificial neural networks in bioinformatics-application to complex microarray and mass spectrometry datasets in cancer studies

Briefings in bioinformatics, 2009-05, Vol.10 (3), p.315-329

2009

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Structural and defect studies in solid oxide electrolytes

Solid state ionics, 1992-05, Vol.52 (1), p.213-218

1992

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Isolation, Structure, and Absolute Stereochemistry of Platensimycin, A Broad Spectrum Antibiotic Discovered Using an Antisense Differential Sensitivity Strategy

Journal of the American Chemical Society, 2006-09, Vol.128 (36), p.11916-11920

2006

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Receptor ligands which bind the oxytocin receptor with selectivity and high affinity. Chemical modification of a Streptomyces silvensis derived cyclic hexapeptide

Journal of medicinal chemistry, 1990-09, Vol.33 (9), p.2321-2323

1990

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An Efficient Preparation of Vinamidinium Hexafluorophosphate Salts

Journal of organic chemistry, 2000-07, Vol.65 (15), p.4571-4574

2000

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Optimization of a Tertiary Alcohol Series of Phosphodiesterase-4 (PDE4) Inhibitors: Structure−Activity Relationship Related to PDE4 Inhibition and Human Ether-a-go-go Related Gene Potassium Channel Binding Affinity

Journal of medicinal chemistry, 2003-06, Vol.46 (12), p.2413-2426

2003

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Synthesis and muscarinic receptor pharmacology of a series of 4,5,6,7-tetrahydroisothiazolo[4,5- c]pyridine bioisosteres of arecoline

Bioorganic & medicinal chemistry, 1999-05, Vol.7 (5), p.795-809

1999

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Novel 5-HT3 antagonists: indol-3-ylspiro(azabicycloalkane-3,5'(4'H)oxazoles)

Journal of medicinal chemistry, 1992-03, Vol.35 (6), p.1019-1031

1992

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Identification of key clinical phenotypes of breast cancer using a reduced panel of protein biomarkers

HAGE (DDX43) is a biomarker for poor prognosis and a predictor of chemotherapy response in breast cancer

Lack of expression of the proteins GMPR2 and PPARα are associated with the basal phenotype and patient outcome in breast cancer

Erratum to: Nottingham prognostic index plus (NPI+) predicts risk of distant metastases in primary breast cancer

L-743, 726 (DMP-266): a novel, highly potent nonnucleoside inhibitor of the human immunodeficiency virus type 1 reverse transcriptase

Asymmetric Synthesis of CDP840 by Jacobsen Epoxidation. An Unusual Syn Selective Reduction of an Epoxide

Identification of non-linear influences on the seasonal ozone dose–response of sensitive and resistant clover clones using artificial neural networks

Stereoselective Total Synthesis of (±)-Thielocin Alβ

Identifying factors which modify the effects of ambient ozone on white clover ( Trifolium repens) in Europe

Synthesis and structure of [(η-C5Me5)Ir(CO)]2

5-(Piperidin-2-yl)- and 5-(Homopiperidin-2-yl)-1,4-benzodiazepines: High-Affinity, Basic Ligands for the Cholecystokinin-B Receptor

A new series of selective COX-2 inhibitors: 5,6-diarylthiazolo[3,2-b][1,2,4]triazoles

Tryptophan-Derived NK1 Antagonists: Conformationally Constrained Heterocyclic Bioisosteres of the Ester Linkage

Identification of 3,5-Dihydro-2-aryl-1H-pyrazolo[3,4-c]quinoline-1,4(2H)-diones as Novel High-Affinity Glycine Site N-Methyl-D-aspartate Antagonists

Methoxylation of cocaine reduces binding affinity and produces compounds of differential binding and dopamine uptake inhibitory activity: discovery of a weak cocaine "antagonist"

The question of reversible formation of bromonium ions during the course of electrophilic bromination of olefins. 2. The crystal and molecular structure of the bromonium ion of adamantylideneadamantane

Polyazamacrocycles. V. Structure of Isomeric 3,5,7,7,10,12,14,14-Octamethyl-1,4,8,11-tetraazacyclotetradecanes

An introduction to artificial neural networks in bioinformatics-application to complex microarray and mass spectrometry datasets in cancer studies

Structural and defect studies in solid oxide electrolytes

Isolation, Structure, and Absolute Stereochemistry of Platensimycin, A Broad Spectrum Antibiotic Discovered Using an Antisense Differential Sensitivity Strategy

Receptor ligands which bind the oxytocin receptor with selectivity and high affinity. Chemical modification of a Streptomyces silvensis derived cyclic hexapeptide

An Efficient Preparation of Vinamidinium Hexafluorophosphate Salts

Optimization of a Tertiary Alcohol Series of Phosphodiesterase-4 (PDE4) Inhibitors: Structure−Activity Relationship Related to PDE4 Inhibition and Human Ether-a-go-go Related Gene Potassium Channel Binding Affinity

Synthesis and muscarinic receptor pharmacology of a series of 4,5,6,7-tetrahydroisothiazolo[4,5- c]pyridine bioisosteres of arecoline

Novel 5-HT3 antagonists: indol-3-ylspiro(azabicycloalkane-3,5'(4'H)oxazoles)

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