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Parvalbumin Interneurons of the Mouse Nucleus Accumbens are Required For Amphetamine-Induced Locomotor Sensitization and Conditioned Place Preference

Neuropsychopharmacology (New York, N.Y.), 2018-04, Vol.43 (5), p.953-963

2018

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LSD-stimulated behaviors in mice require β-arrestin 2 but not β-arrestin 1

Scientific reports, 2021-09, Vol.11 (1), p.17690-17690, Article 17690

2021

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Genetic disruption of both tryptophan hydroxylase genes dramatically reduces serotonin and affects behavior in models sensitive to antidepressants

PloS one, 2008-10, Vol.3 (10), p.e3301-e3301

2008

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Establishment of multi-stage intravenous self-administration paradigms in mice

Scientific reports, 2022-12, Vol.12 (1), p.21422-21422, Article 21422

2022

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The G protein biased serotonin 5-HT2A receptor agonist lisuride exerts anti-depressant drug-like activities in mice

Frontiers in molecular biosciences, 2023-10, Vol.10, p.1233743-1233743

2023

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Dopamine-Depleted Dopamine Transporter Knockout (DDD) Mice: Dyskinesia with L-DOPA and Dopamine D1 Agonists

Biomolecules (Basel, Switzerland), 2023-11, Vol.13 (11), p.1658

2023

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Mutant DISC1 affects methamphetamine-induced sensitization and conditioned place preference: a comorbidity model

Neuropharmacology, 2012-03, Vol.62 (3), p.1242-1251

2012

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Working memory deficits in neuronal nitric oxide synthase knockout mice: Potential impairments in prefrontal cortex mediated cognitive function

Biochemical and biophysical research communications, 2011-05, Vol.408 (4), p.707-712

2011

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Bespoke library docking for 5-HT2A receptor agonists with antidepressant activity

Nature (London), 2022-10, Vol.610 (7932), p.582-591

2022

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β-Arrestin-Biased Allosteric Modulator of NTSR1 Selectively Attenuates Addictive Behaviors

Cell, 2020-06, Vol.181 (6), p.1364-1379.e14

2020

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Parvalbumin Interneurons of the Mouse Nucleus Accumbens are Required For Amphetamine-Induced Locomotor Sensitization and Conditioned Place Preference

Neuropsychopharmacology (New York, N.Y.), 2018-04, Vol.43 (5), p.953-963

2018

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Characterization of PTPRG in knockdown and phosphatase-inactive mutant mice and substrate trapping analysis of PTPRG in mammalian cells

PloS one, 2012-09, Vol.7 (9), p.e45500

2012

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5-HT2C Agonists Modulate Schizophrenia-Like Behaviors in Mice

Neuropsychopharmacology (New York, N.Y.), 2017-10, Vol.42 (11), p.2163-2177

2017

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D2 Dopamine Receptor G Protein-Biased Partial Agonists Based on Cariprazine

Journal of medicinal chemistry, 2019-05, Vol.62 (9), p.4755-4771

2019

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D 2 Dopamine Receptor G Protein-Biased Partial Agonists Based on Cariprazine

Journal of medicinal chemistry, 2019-05, Vol.62 (9), p.4755-4771

2019

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Postsynaptic Mechanisms Render Syn I/II/III Mice Highly Responsive to Psychostimulants

The international journal of neuropsychopharmacology, 2019-07, Vol.22 (7), p.453-465

2019

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Distinct neuronal populations in the basolateral and central amygdala are activated with acute pain, conditioned fear, and fear-conditioned analgesia

Neuroscience letters, 2017-11, Vol.661, p.11-17

2017

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Optimization of 2‑Phenylcyclopropylmethylamines as Selective Serotonin 2C Receptor Agonists and Their Evaluation as Potential Antipsychotic Agents

Journal of medicinal chemistry, 2015-02, Vol.58 (4), p.1992-2002

2015

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Designing Functionally Selective Noncatechol Dopamine D 1 Receptor Agonists with Potent In Vivo Antiparkinsonian Activity

ACS chemical neuroscience, 2019-09, Vol.10 (9), p.4160-4182

2019

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Further Advances in Optimizing (2-Phenylcyclopropyl)methylamines as Novel Serotonin 2C Agonists: Effects on Hyperlocomotion, Prepulse Inhibition, and Cognition Models

Journal of medicinal chemistry, 2016-01, Vol.59 (2), p.578-591

2016

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Designing Functionally Selective Noncatechol Dopamine D1 Receptor Agonists with Potent In Vivo Antiparkinsonian Activity

ACS chemical neuroscience, 2019-09, Vol.10 (9), p.4160-4182

2019

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Addition to "Designing Functionally Selective Noncatechol Dopamine D 1 Receptor Agonists with Potent In Vivo Antiparkinsonian Activity"

ACS chemical neuroscience, 2021-04, Vol.12 (8), p.1464-1464

2021

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Novelty seeking and stereotypic activation of behavior in mice with disruption of the Dat1 gene

Neuropsychopharmacology (New York, N.Y.), 2005-10, Vol.30 (10), p.1818-1831

2005

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Identification and Characterization of ML321: A Novel and Highly Selective D2 Dopamine Receptor Antagonist with Efficacy in Animal Models That Predict Atypical Antipsychotic Activity

ACS pharmacology & translational science, 2023-01, Vol.6 (1), p.151-170

2023

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Identification and Characterization of ML321: A Novel and Highly Selective D 2 Dopamine Receptor Antagonist with Efficacy in Animal Models That Predict Atypical Antipsychotic Activity

ACS pharmacology & translational science, 2023-01, Vol.6 (1), p.151-170

2023

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Parvalbumin Interneurons of the Mouse Nucleus Accumbens are Required For Amphetamine-Induced Locomotor Sensitization and Conditioned Place Preference

LSD-stimulated behaviors in mice require β-arrestin 2 but not β-arrestin 1

Genetic disruption of both tryptophan hydroxylase genes dramatically reduces serotonin and affects behavior in models sensitive to antidepressants

Establishment of multi-stage intravenous self-administration paradigms in mice

The G protein biased serotonin 5-HT2A receptor agonist lisuride exerts anti-depressant drug-like activities in mice

Dopamine-Depleted Dopamine Transporter Knockout (DDD) Mice: Dyskinesia with L-DOPA and Dopamine D1 Agonists

Mutant DISC1 affects methamphetamine-induced sensitization and conditioned place preference: a comorbidity model

Working memory deficits in neuronal nitric oxide synthase knockout mice: Potential impairments in prefrontal cortex mediated cognitive function

Bespoke library docking for 5-HT2A receptor agonists with antidepressant activity

β-Arrestin-Biased Allosteric Modulator of NTSR1 Selectively Attenuates Addictive Behaviors

Parvalbumin Interneurons of the Mouse Nucleus Accumbens are Required For Amphetamine-Induced Locomotor Sensitization and Conditioned Place Preference

Characterization of PTPRG in knockdown and phosphatase-inactive mutant mice and substrate trapping analysis of PTPRG in mammalian cells

5-HT2C Agonists Modulate Schizophrenia-Like Behaviors in Mice

D2 Dopamine Receptor G Protein-Biased Partial Agonists Based on Cariprazine

D 2 Dopamine Receptor G Protein-Biased Partial Agonists Based on Cariprazine

Postsynaptic Mechanisms Render Syn I/II/III Mice Highly Responsive to Psychostimulants

Distinct neuronal populations in the basolateral and central amygdala are activated with acute pain, conditioned fear, and fear-conditioned analgesia

Optimization of 2‑Phenylcyclopropylmethylamines as Selective Serotonin 2C Receptor Agonists and Their Evaluation as Potential Antipsychotic Agents

Designing Functionally Selective Noncatechol Dopamine D 1 Receptor Agonists with Potent In Vivo Antiparkinsonian Activity

Further Advances in Optimizing (2-Phenylcyclopropyl)methylamines as Novel Serotonin 2C Agonists: Effects on Hyperlocomotion, Prepulse Inhibition, and Cognition Models

Designing Functionally Selective Noncatechol Dopamine D1 Receptor Agonists with Potent In Vivo Antiparkinsonian Activity

Addition to "Designing Functionally Selective Noncatechol Dopamine D 1 Receptor Agonists with Potent In Vivo Antiparkinsonian Activity"

Novelty seeking and stereotypic activation of behavior in mice with disruption of the Dat1 gene

Identification and Characterization of ML321: A Novel and Highly Selective D2 Dopamine Receptor Antagonist with Efficacy in Animal Models That Predict Atypical Antipsychotic Activity

Identification and Characterization of ML321: A Novel and Highly Selective D 2 Dopamine Receptor Antagonist with Efficacy in Animal Models That Predict Atypical Antipsychotic Activity

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