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In vitro and in silico analysis of the effects of D2 receptor antagonist target binding kinetics on the cellular response to fluctuating dopamine concentrations

British journal of pharmacology, 2018-11, Vol.175 (21), p.4121-4136

2018

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Blood‐Based Biomarkers of Quinpirole Pharmacology: Cluster‐Based PK/PD and Metabolomics to Unravel the Underlying Dynamics in Rat Plasma and Brain

CPT: pharmacometrics and systems pharmacology, 2019-02, Vol.8 (2), p.107-117

2019

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Online solid phase extraction with liquid chromatography–tandem mass spectrometry to analyze remoxipride in small plasma-, brain homogenate-, and brain microdialysate samples

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2010-04, Vol.878 (13), p.969-975

2010

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Drug Disposition in Obesity: Toward Evidence-Based Dosing

Annual review of pharmacology and toxicology, 2015-01, Vol.55 (1), p.149-167

2015

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The Pharmacodynamic Effects of a Dopamine–Somatostatin Chimera Agonist on the Cardiovascular System

Journal of cardiovascular pharmacology, 2019-08, Vol.74 (2), p.128-136

2019

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In vitro and in silico analysis of the effects of D 2 receptor antagonist target binding kinetics on the cellular response to fluctuating dopamine concentrations

British journal of pharmacology, 2018-11, Vol.175 (21), p.4121-4136

2018

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Individual differences in male rat ejaculatory behaviour: searching for models to study ejaculation disorders

The European journal of neuroscience, 2005-08, Vol.22 (3), p.724-734

2005

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Mechanism-based modeling of functional adaptation upon chronic treatment with midazolam

Pharmaceutical research, 2000-03, Vol.17 (3), p.321-327

2000

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Mechanism-based modeling of adaptive changes in the pharmacodynamics of midazolam in the kindling model of epilepsy

Pharmaceutical research, 1999-11, Vol.16 (11), p.1702-1709

1999

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A New Minimal-Stress Freely-Moving Rat Model for Preclinical Studies on Intranasal Administration of CNS Drugs

Pharmaceutical research, 2009-08, Vol.26 (8), p.1911-1917

2009

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Modulation of agonist responses at the A1 adenosine receptor by an irreversible antagonist, receptor-G protein uncoupling and by the G protein activation state

Biochemical pharmacology, 2002-10, Vol.64 (8), p.1251-1265

2002

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Modulation of agonist responses at the A(1) adenosine receptor by an irreversible antagonist, receptor-G protein uncoupling and by the G protein activation state

Biochemical pharmacology, 2002-10, Vol.64 (8), p.1251-1265

2002

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Modulation of agonist responses at the A 1 adenosine receptor by an irreversible antagonist, receptor–G protein uncoupling and by the G protein activation state

Biochemical pharmacology, 2002, Vol.64 (8), p.1251-1265

2002

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Multivariate calibration of reversed-phase chromatographic systems. Some designs based on three-way data analysis

Analytica chimica acta, 1990, Vol.235 (1), p.41-51

1990

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In vitro and in silico analysis of the effects of D2 receptor antagonist target binding kinetics on the cellular response to fluctuating dopamine concentrations

Blood‐Based Biomarkers of Quinpirole Pharmacology: Cluster‐Based PK/PD and Metabolomics to Unravel the Underlying Dynamics in Rat Plasma and Brain

Online solid phase extraction with liquid chromatography–tandem mass spectrometry to analyze remoxipride in small plasma-, brain homogenate-, and brain microdialysate samples

Drug Disposition in Obesity: Toward Evidence-Based Dosing

The Pharmacodynamic Effects of a Dopamine–Somatostatin Chimera Agonist on the Cardiovascular System

In vitro and in silico analysis of the effects of D 2 receptor antagonist target binding kinetics on the cellular response to fluctuating dopamine concentrations

Individual differences in male rat ejaculatory behaviour: searching for models to study ejaculation disorders

Mechanism-based modeling of functional adaptation upon chronic treatment with midazolam

Mechanism-based modeling of adaptive changes in the pharmacodynamics of midazolam in the kindling model of epilepsy

A New Minimal-Stress Freely-Moving Rat Model for Preclinical Studies on Intranasal Administration of CNS Drugs

Modulation of agonist responses at the A1 adenosine receptor by an irreversible antagonist, receptor-G protein uncoupling and by the G protein activation state

Modulation of agonist responses at the A(1) adenosine receptor by an irreversible antagonist, receptor-G protein uncoupling and by the G protein activation state

Modulation of agonist responses at the A 1 adenosine receptor by an irreversible antagonist, receptor–G protein uncoupling and by the G protein activation state

Multivariate calibration of reversed-phase chromatographic systems. Some designs based on three-way data analysis

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