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Chronic neuropathic pain is accompanied by global changes in gene expression and shares pathobiology with neurodegenerative diseases

Neuroscience, 2002-01, Vol.114 (3), p.529-546

2002

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Assessment of human abuse potential of dasotraline compared to methylphenidate and placebo in recreational stimulant users

Drug and alcohol dependence, 2016-02, Vol.159, p.26-34

2016

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Functional neuroimaging study of a new compound for schizophrenia in healthy volunteers with high or low schizotypy

European neuropsychopharmacology, 2017-03, Vol.27, p.S60-S60

2017

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The effects of a novel histamine-3 receptor inverse agonist on essential tremor in comparison to stable levels of alcohol

Journal of psychopharmacology (Oxford), 2012-02, Vol.26 (2), p.292-302

2012

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Cloning, characterization and central nervous system distribution of receptor activity modifying proteins in the rat

The European journal of neuroscience, 2001-08, Vol.14 (4), p.618-628

2001

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P.0450 The safety profile of the trace amine–associated receptor 1 agonist, SEP-363856, is distinct from atypical antipsychotics

European neuropsychopharmacology, 2021-12, Vol.53, p.S329-S329

2021

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Tuberoinfundibular peptide of 39 residues (TIP39): molecular structure and activity for parathyroid hormone 2 receptor

Neuropharmacology, 2003, Vol.44 (1), p.141-153

2003

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P.163 SEP-363856, a novel psychotropic agent with a unique, non-d2 mechanism of action

European neuropsychopharmacology, 2019-12, Vol.29, p.S126-S127

2019

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Mouse mammary tumor virus-Ki-rasB transgenic mice develop mammary carcinomas that can be growth-inhibited by a farnesyl :protein transferase inhibitor

Cancer research (Chicago, Ill.), 2000-05, Vol.60 (10), p.2680-2688

2000

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Imidazole-containing diarylether and diarylsulfone inhibitors of farnesyl-protein transferase

Bioorganic & medicinal chemistry letters, 1999-12, Vol.9 (23), p.3301-3306

1999

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P.100 Efficacy and safety of SEP-363856, a novel non-D2 agent, in the treatment of schizophrenia: A 4-week, randomized, placebo-controlled trial

European neuropsychopharmacology, 2019-12, Vol.29, p.S85-S86

2019

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Transformed PANSS Factors Intended to Reduce Pseudospecificity Among Symptom Domains and Enhance Understanding of Symptom Change in Antipsychotic-Treated Patients With Schizophrenia

Schizophrenia bulletin, 2018-04, Vol.44 (3), p.593-602

2018

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Sub-chronic administration of zolpidem affects modifications to rat sleep architecture

Brain research, 2004-06, Vol.1010 (1), p.45-54

2004

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A Farnesyltransferase Inhibitor Induces Tumor Regression in Transgenic Mice Harboring Multiple Oncogenic Mutations by Mediating Alterations in Both Cell Cycle Control and Apoptosis

Molecular and Cellular Biology, 1998-01, Vol.18 (1), p.85-92

1998

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Characterization and localization of a human serine racemase

Brain research. Molecular brain research., 2004-06, Vol.125 (1), p.96-104

2004

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Design and in Vivo Analysis of Potent Non-Thiol Inhibitors of Farnesyl Protein Transferase

Journal of medicinal chemistry, 1999-08, Vol.42 (17), p.3356-3368

1999

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Effect of the inflammatory biomarker C-reactive protein on response to lurasidone treatment in patients with bipolar depression

European neuropsychopharmacology, 2017-10, Vol.27, p.S839

2017

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P.2.d.043 - Effect of the inflammatory biomarker C-reactive protein on response to lurasidone treatment in patients with bipolar depression

European neuropsychopharmacology, 2017-10, Vol.27, p.S839-S839

2017

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Characterisation of the effects of a non-peptide CGRP receptor antagonist in SK-N-MC cells and isolated human cerebral arteries

European journal of pharmacology, 2001-03, Vol.415 (1), p.39-44

2001

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P.3.012 - Functional neuroimaging study of a new compound for schizophrenia in healthy volunteers with high or low schizotypy

European neuropsychopharmacology, 2017-03, Vol.27, p.S60-S60

2017

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2-Substituted Piperazines as Constrained Amino Acids. Application to the Synthesis of Potent, Non Carboxylic Acid Inhibitors of Farnesyltransferase

Journal of medicinal chemistry, 1996-03, Vol.39 (7), p.1345-1348

1996

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Localization of a Binding Site for Phosphatidylinositol 4,5-Bisphosphate on Human Profilin (∗)

The Journal of biological chemistry, 1995-09, Vol.270 (36), p.21114-21120

1995

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Site-specific enthalpic regulation of DNA transcription at bacteriophage .lambda. OR

Biochemistry (Easton), 1992-01, Vol.31 (1), p.57-65

1992

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Non-thiol 3-aminomethylbenzamide inhibitors of farnesyl-protein transferase

Bioorganic & medicinal chemistry letters, 1999-07, Vol.9 (14), p.1991-1996

1999

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Chronic neuropathic pain is accompanied by global changes in gene expression and shares pathobiology with neurodegenerative diseases

Assessment of human abuse potential of dasotraline compared to methylphenidate and placebo in recreational stimulant users

Functional neuroimaging study of a new compound for schizophrenia in healthy volunteers with high or low schizotypy

The effects of a novel histamine-3 receptor inverse agonist on essential tremor in comparison to stable levels of alcohol

Cloning, characterization and central nervous system distribution of receptor activity modifying proteins in the rat

P.0450 The safety profile of the trace amine–associated receptor 1 agonist, SEP-363856, is distinct from atypical antipsychotics

Tuberoinfundibular peptide of 39 residues (TIP39): molecular structure and activity for parathyroid hormone 2 receptor

P.163 SEP-363856, a novel psychotropic agent with a unique, non-d2 mechanism of action

Mouse mammary tumor virus-Ki-rasB transgenic mice develop mammary carcinomas that can be growth-inhibited by a farnesyl :protein transferase inhibitor

Imidazole-containing diarylether and diarylsulfone inhibitors of farnesyl-protein transferase

P.100 Efficacy and safety of SEP-363856, a novel non-D2 agent, in the treatment of schizophrenia: A 4-week, randomized, placebo-controlled trial

Transformed PANSS Factors Intended to Reduce Pseudospecificity Among Symptom Domains and Enhance Understanding of Symptom Change in Antipsychotic-Treated Patients With Schizophrenia

Sub-chronic administration of zolpidem affects modifications to rat sleep architecture

A Farnesyltransferase Inhibitor Induces Tumor Regression in Transgenic Mice Harboring Multiple Oncogenic Mutations by Mediating Alterations in Both Cell Cycle Control and Apoptosis

Characterization and localization of a human serine racemase

Design and in Vivo Analysis of Potent Non-Thiol Inhibitors of Farnesyl Protein Transferase

Effect of the inflammatory biomarker C-reactive protein on response to lurasidone treatment in patients with bipolar depression

P.2.d.043 - Effect of the inflammatory biomarker C-reactive protein on response to lurasidone treatment in patients with bipolar depression

Design and Biological Activity of (S)-4-(5-{[1-(3-Chlorobenzyl)-2- oxopyrrolidin-3-ylamino]methyl}imidazol-1-ylmethyl)benzonitrile, a 3-Aminopyrrolidinone Farnesyltransferase Inhibitor with Excellent Cell Potency

Characterisation of the effects of a non-peptide CGRP receptor antagonist in SK-N-MC cells and isolated human cerebral arteries

P.3.012 - Functional neuroimaging study of a new compound for schizophrenia in healthy volunteers with high or low schizotypy

2-Substituted Piperazines as Constrained Amino Acids. Application to the Synthesis of Potent, Non Carboxylic Acid Inhibitors of Farnesyltransferase

Localization of a Binding Site for Phosphatidylinositol 4,5-Bisphosphate on Human Profilin (∗)

Site-specific enthalpic regulation of DNA transcription at bacteriophage .lambda. OR

Non-thiol 3-aminomethylbenzamide inhibitors of farnesyl-protein transferase

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