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Adherence-resistance relationships for protease and non-nucleoside reverse transcriptase inhibitors explained by virological fitness

AIDS (London), 2006-01, Vol.20 (2), p.223-231

2006

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Effects of 1-Year Treatment with Cyclophosphamide on Outcomes at 2 Years in Scleroderma Lung Disease

American journal of respiratory and critical care medicine, 2007-11, Vol.176 (10), p.1026-1034

2007

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Characterization of SB‐269970‐A, a selective 5‐HT7 receptor antagonist

British journal of pharmacology, 2000-06, Vol.130 (3), p.539-548

2000

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From ATP to AZD6140 : The discovery of an orally active reversible P2Y12 receptor antagonist for the prevention of thrombosis

Bioorganic & medicinal chemistry letters, 2007-11, Vol.17 (21), p.6013-6018

2007

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Decreased susceptibility to cephalosporins among gonococci: data from the Gonococcal Resistance to Antimicrobials Surveillance Programme (GRASP) in England and Wales, 2007–2011

The Lancet infectious diseases, 2013-09, Vol.13 (9), p.762-768

2013

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Sensitivity of the cervical transformation zone to estrogen-induced squamous carcinogenesis

Cancer research (Chicago, Ill.), 2000-03, Vol.60 (5), p.1267-1275

2000

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Exploratory randomized clinical study of pagoclone in persistent developmental stuttering: the EXamining Pagoclone for peRsistent dEvelopmental Stuttering Study

Journal of clinical psychopharmacology, 2010-02, Vol.30 (1), p.48-56

2010

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SB-399885 is a potent, selective 5-HT6 receptor antagonist with cognitive enhancing properties in aged rat water maze and novel object recognition models

European journal of pharmacology, 2006-12, Vol.553 (1-3), p.109-119

2006

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(R)-3,N-Dimethyl-N-[1-methyl-3-(4-methylpiperidin-1-yl)propyl]benzenesulfonamide: The First Selective 5-HT7 Receptor Antagonist

Journal of medicinal chemistry, 1998-02, Vol.41 (5), p.655-657

1998

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Risperidone for the treatment of stuttering

Journal of clinical psychopharmacology, 2000-08, Vol.20 (4), p.479-482

2000

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Acetaminophen toxicity in children

Pediatrics (Evanston), 2001-10, Vol.108 (4), p.1020-1024

2001

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Nonpeptidic urotensin‐II receptor antagonists I: in vitro pharmacological characterization of SB‐706375

British journal of pharmacology, 2005-07, Vol.145 (5), p.620-635

2005

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3,4-Dihydro-2H-benzoxazinones are 5-HT1A receptor antagonists with potent 5-HT reuptake inhibitory activity

Bioorganic & medicinal chemistry letters, 2005-02, Vol.15 (3), p.737-741

2005

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Identification of a novel series of selective 5-HT7 receptor antagonists

Bioorganic & medicinal chemistry letters, 2003-03, Vol.13 (6), p.1055-1058

2003

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SB-656104-A: A novel 5-HT7 receptor antagonist with improved in vivo properties

Bioorganic & medicinal chemistry letters, 2002-11, Vol.12 (22), p.3341-3344

2002

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Studies towards the identification of a new generation of atypical antipsychotic agents

Bioorganic & medicinal chemistry letters, 2007-01, Vol.17 (2), p.400-405

2007

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Novel and Selective 5-HT2C/2B Receptor Antagonists as Potential Anxiolytic Agents: Synthesis, Quantitative Structure−Activity Relationships, and Molecular Modeling of Substituted 1-(3-Pyridylcarbamoyl)indolines

Journal of medicinal chemistry, 1998-05, Vol.41 (10), p.1598-1612

1998

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Design of novel and potent cPLA2α inhibitors containing an α-methyl-2-ketothiazole as a metabolically stable serine trap

Bioorganic & medicinal chemistry letters, 2011-05, Vol.21 (10), p.3128-3133

2011

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Design and Synthesis of 2-Naphthoate Esters as Selective Dopamine D4 Antagonists

Journal of medicinal chemistry, 1996-05, Vol.39 (10), p.1946-1948

1996

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Hepatobiliary damage and changes in hepatic gene expression caused by the antitumor drug ecteinascidin-743 (ET-743) in the female rat

Cancer research (Chicago, Ill.), 2002-08, Vol.62 (15), p.4256-4262

2002

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A series of bisaryl imidazolidin-2-ones has shown to be selective and orally active 5-HT2C receptor antagonists

Bioorganic & medicinal chemistry letters, 2005-11, Vol.15 (22), p.4989-4993

2005

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Functional characterisation of the human cloned 5‐HT7 receptor (long form); antagonist profile of SB‐258719

British journal of pharmacology, 1998-07, Vol.124 (6), p.1300-1306

1998

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Heterocyclic analogues of 2-aminotetralins with high affinity and selectivity for the dopamine D3 receptor

Bioorganic & medicinal chemistry letters, 1999-09, Vol.9 (18), p.2715-2720

1999

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Design and synthesis of novel 2,3-dihydro-1H-isoindoles with high affinity and selectivity for the dopamine D3 receptor

Bioorganic & medicinal chemistry letters, 2001-03, Vol.11 (5), p.685-688

2001

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Adherence-resistance relationships for protease and non-nucleoside reverse transcriptase inhibitors explained by virological fitness

Effects of 1-Year Treatment with Cyclophosphamide on Outcomes at 2 Years in Scleroderma Lung Disease

Characterization of SB‐269970‐A, a selective 5‐HT7 receptor antagonist

From ATP to AZD6140 : The discovery of an orally active reversible P2Y12 receptor antagonist for the prevention of thrombosis

Decreased susceptibility to cephalosporins among gonococci: data from the Gonococcal Resistance to Antimicrobials Surveillance Programme (GRASP) in England and Wales, 2007–2011

Sensitivity of the cervical transformation zone to estrogen-induced squamous carcinogenesis

Exploratory randomized clinical study of pagoclone in persistent developmental stuttering: the EXamining Pagoclone for peRsistent dEvelopmental Stuttering Study

SB-399885 is a potent, selective 5-HT6 receptor antagonist with cognitive enhancing properties in aged rat water maze and novel object recognition models

(R)-3,N-Dimethyl-N-[1-methyl-3-(4-methylpiperidin-1-yl)propyl]benzenesulfonamide: The First Selective 5-HT7 Receptor Antagonist

Risperidone for the treatment of stuttering

Biarylcarbamoylindolines Are Novel and Selective 5-HT2C Receptor Inverse Agonists: Identification of 5-Methyl-1-[[2-[(2-methyl-3-pyridyl)oxy]- 5-pyridyl]carbamoyl]-6-trifluoromethylindoline (SB-243213) as a Potential Antidepressant/Anxiolytic Agent

Acetaminophen toxicity in children

Nonpeptidic urotensin‐II receptor antagonists I: in vitro pharmacological characterization of SB‐706375

3,4-Dihydro-2H-benzoxazinones are 5-HT1A receptor antagonists with potent 5-HT reuptake inhibitory activity

Identification of a novel series of selective 5-HT7 receptor antagonists

SB-656104-A: A novel 5-HT7 receptor antagonist with improved in vivo properties

Studies towards the identification of a new generation of atypical antipsychotic agents

Novel and Selective 5-HT2C/2B Receptor Antagonists as Potential Anxiolytic Agents: Synthesis, Quantitative Structure−Activity Relationships, and Molecular Modeling of Substituted 1-(3-Pyridylcarbamoyl)indolines

Design of novel and potent cPLA2α inhibitors containing an α-methyl-2-ketothiazole as a metabolically stable serine trap

Design and Synthesis of 2-Naphthoate Esters as Selective Dopamine D4 Antagonists

Hepatobiliary damage and changes in hepatic gene expression caused by the antitumor drug ecteinascidin-743 (ET-743) in the female rat

A series of bisaryl imidazolidin-2-ones has shown to be selective and orally active 5-HT2C receptor antagonists

Functional characterisation of the human cloned 5‐HT7 receptor (long form); antagonist profile of SB‐258719

Heterocyclic analogues of 2-aminotetralins with high affinity and selectivity for the dopamine D3 receptor

Design and synthesis of novel 2,3-dihydro-1H-isoindoles with high affinity and selectivity for the dopamine D3 receptor

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