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Oxytocin attenuates phencyclidine hyperactivity and increases social interaction and nucleus accumben dopamine release in rats

Neuropsychopharmacology (New York, N.Y.), 2019-01, Vol.44 (2), p.295-305

2019

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Induction of Metabolic Hypofunction and Neurochemical Deficits after Chronic Intermittent Exposure to Phencyclidine: Differential Modulation by Antipsychotic Drugs

Neuropsychopharmacology (New York, N.Y.), 2003-02, Vol.28 (2), p.265-275

2003

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The atypical antipsychotic risperidone reverses the recognition memory deficits induced by post-weaning social isolation in rats

Psychopharmacology, 2013-07, Vol.228 (1), p.31-42

2013

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Chronic phencyclidine (PCP)-induced modulation of muscarinic receptor mRNAs in rat brain : Impact of antipsychotic drug treatment

Neuropharmacology, 2012-03, Vol.62 (3), p.1554-1563

2012

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Poster #7 CLOZAPINE REVERSES RECOGNITIONMEMORY BUT NOT SOCIAL INTERACTION DEFICITS IN A “DUAL-HIT” RAT MODEL OF SCHIZOPHRENIA

Schizophrenia research, 2012-04, Vol.136, p.S282-S283

2012

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G protein-coupled receptor transmembrane binding pockets and their applications in GPCR research and drug discovery: a survey

Current topics in medicinal chemistry, 2011-08, Vol.11 (15), p.1902

2011

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The atypical antipsychotic drug clozapine enhances chronic PCP-induced regulation of prefrontal cortex 5-HT2A receptors

Neuropharmacology, 2004-09, Vol.47 (4), p.527-537

2004

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Diversity oriented biosynthesis via accelerated evolution of modular gene clusters

Nature communications, 2017-10, Vol.8 (1), p.1206-10, Article 1206

2017

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Ability of angiotensin II to modulate striatal dopamine release via the AT1 receptor in vitro and in vivo

British journal of pharmacology, 1996-05, Vol.118 (2), p.414-420

1996

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Cyclic guanidines as dual 5-HT5A/5-HT7 receptor ligands : Optimising brain penetration

Bioorganic & medicinal chemistry letters, 2008, Vol.18 (1), p.262-266

2008

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Discovery of potent, balanced and orally active dual NK1/NK3 receptor ligands

Bioorganic & medicinal chemistry letters, 2010-06, Vol.20 (11), p.3405-3408

2010

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Cyclic guanidines as dual 5-HT5A/5-HT7 receptor ligands : Structure-activity relationship elucidation

Bioorganic & medicinal chemistry letters, 2008, Vol.18 (1), p.256-261

2008

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Synthesis and SAR evaluation of 1,2,4-triazoles as A2A receptor antagonists

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (3), p.817-821

2004

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CHARACTERIZATION OF RO4583298 AS A HIGHLY POTENT, DUAL ANTAGONIST WITH IN VIVO ACTIVITY AT TACHYKININ NK1 AND NK3 RECEPTORS

Schizophrenia research, 2010-04, Vol.117 (2-3), p.485-486

2010

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CHARACTERIZATION OF RO4583298 AS A HIGHLY POTENT, DUAL ANTAGONIST WITH IN VIVO ACTIVITY AT TACHYKININ NK1AND NK3RECEPTORS

Schizophrenia research, 2010-04, Vol.117 (2-3), p.485-486

2010

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Discovery of potent, balanced and orally active dual NK sub(1)/NK sub(3) receptor ligands

Bioorganic & medicinal chemistry letters, 2010-06, Vol.20 (11), p.3405-3408

2010

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CHARACTERIZATION OF RO4583298 AS A HIGHLY POTENT, DUAL ANTAGONIST WITH IN VIVO ACTIVITY AT TACHYKININ NK 1 AND NK 3 RECEPTORS

Schizophrenia research, 2010, Vol.117 (2), p.485-486

2010

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CLONING AND PHARMACOLOGICAL PROFILE OF THE GERBIL (MERIONESUNGUICULATUS) NK3 RECEPTOR: COMPARISON WITH HUMAN, RAT ANDMOUSE NK3 RECEPTORS

Schizophrenia research, 2008, Vol.102 (1), p.209-209

2008

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Cyclic guanidines as dual 5-HT sub(5A)/5-HT sub(7) receptor ligands: Optimising brain penetration

Bioorganic & medicinal chemistry, 2008-01, Vol.18 (1), p.262-266

2008

Volltextzugriff (PDF)

Cyclic guanidines as dual 5-HT sub(5A)/5-HT sub(7) receptor ligands: Structure-activity relationship elucidation

Bioorganic & medicinal chemistry, 2008-01, Vol.18 (1), p.256-261

2008

Volltextzugriff (PDF)

Cyclic guanidines as dual 5-HT 5A/5-HT 7 receptor ligands: Optimising brain penetration

Bioorganic & medicinal chemistry letters, 2008, Vol.18 (1), p.262-266

2008

Volltextzugriff (PDF)

Cyclic guanidines as dual 5-HT 5A/5-HT 7 receptor ligands: Structure–activity relationship elucidation

Bioorganic & medicinal chemistry letters, 2008, Vol.18 (1), p.256-261

2008

Volltextzugriff (PDF)

Synthesis and SAR evaluation of 1,2,4-triazoles as A(2A) receptor antagonists

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (3), p.817-821

2004

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MAPPING THE BINDING SITE FOR TACHYKININ NK3 RECEPTOR ANTAGONISTS

Schizophrenia research, 2008, Vol.102 (1), p.65-65

2008

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The atypical antipsychotic drug clozapine enhances chronic PCP-induced regulation of prefrontal cortex 5-HT2 A receptors

Neuropharmacology, 2004, Vol.47 (4), p.527-537

2004

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Oxytocin attenuates phencyclidine hyperactivity and increases social interaction and nucleus accumben dopamine release in rats

Induction of Metabolic Hypofunction and Neurochemical Deficits after Chronic Intermittent Exposure to Phencyclidine: Differential Modulation by Antipsychotic Drugs

The atypical antipsychotic risperidone reverses the recognition memory deficits induced by post-weaning social isolation in rats

Chronic phencyclidine (PCP)-induced modulation of muscarinic receptor mRNAs in rat brain : Impact of antipsychotic drug treatment

Poster #7 CLOZAPINE REVERSES RECOGNITIONMEMORY BUT NOT SOCIAL INTERACTION DEFICITS IN A “DUAL-HIT” RAT MODEL OF SCHIZOPHRENIA

G protein-coupled receptor transmembrane binding pockets and their applications in GPCR research and drug discovery: a survey

The atypical antipsychotic drug clozapine enhances chronic PCP-induced regulation of prefrontal cortex 5-HT2A receptors

Diversity oriented biosynthesis via accelerated evolution of modular gene clusters

Ability of angiotensin II to modulate striatal dopamine release via the AT1 receptor in vitro and in vivo

Cyclic guanidines as dual 5-HT5A/5-HT7 receptor ligands : Optimising brain penetration

Discovery of potent, balanced and orally active dual NK1/NK3 receptor ligands

Cyclic guanidines as dual 5-HT5A/5-HT7 receptor ligands : Structure-activity relationship elucidation

Synthesis and SAR evaluation of 1,2,4-triazoles as A2A receptor antagonists

CHARACTERIZATION OF RO4583298 AS A HIGHLY POTENT, DUAL ANTAGONIST WITH IN VIVO ACTIVITY AT TACHYKININ NK1 AND NK3 RECEPTORS

CHARACTERIZATION OF RO4583298 AS A HIGHLY POTENT, DUAL ANTAGONIST WITH IN VIVO ACTIVITY AT TACHYKININ NK1AND NK3RECEPTORS

Discovery of potent, balanced and orally active dual NK sub(1)/NK sub(3) receptor ligands

CHARACTERIZATION OF RO4583298 AS A HIGHLY POTENT, DUAL ANTAGONIST WITH IN VIVO ACTIVITY AT TACHYKININ NK 1 AND NK 3 RECEPTORS

CLONING AND PHARMACOLOGICAL PROFILE OF THE GERBIL (MERIONESUNGUICULATUS) NK3 RECEPTOR: COMPARISON WITH HUMAN, RAT ANDMOUSE NK3 RECEPTORS

Cyclic guanidines as dual 5-HT sub(5A)/5-HT sub(7) receptor ligands: Optimising brain penetration

Cyclic guanidines as dual 5-HT sub(5A)/5-HT sub(7) receptor ligands: Structure-activity relationship elucidation

Cyclic guanidines as dual 5-HT 5A/5-HT 7 receptor ligands: Optimising brain penetration

Cyclic guanidines as dual 5-HT 5A/5-HT 7 receptor ligands: Structure–activity relationship elucidation

Synthesis and SAR evaluation of 1,2,4-triazoles as A(2A) receptor antagonists

MAPPING THE BINDING SITE FOR TACHYKININ NK3 RECEPTOR ANTAGONISTS

The atypical antipsychotic drug clozapine enhances chronic PCP-induced regulation of prefrontal cortex 5-HT2 A receptors

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