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Enduring disruption of reward and stress circuit activities by early-life adversity in male rats
Enduring disruption of reward and stress circuit activities by early-life adversity in male rats
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Enduring disruption of reward and stress circuit activities by early-life adversity in male rats

Levis, Sophia C ; Birnie, Matthew T ; Bolton, Jessica L ; Perrone, Christina R ; Montesinos, Johanna S ; Baram, Tallie Z ; Mahler, Stephen V

Translational psychiatry, 2022-06, Vol.12 (1), p.251-251, Article 251 [Periódico revisado por pares]

United States: Nature Publishing Group

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2
The synthesis and characterization of BMS-204352 (MaxiPost) and related 3-fluorooxindoles as openers of maxi-K potassium channels
The synthesis and characterization of BMS-204352 (MaxiPost) and related 3-fluorooxindoles as openers of maxi-K potassium channels
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The synthesis and characterization of BMS-204352 (MaxiPost) and related 3-fluorooxindoles as openers of maxi-K potassium channels

HEWAWASAM, Piyasena ; GRIBKOFF, Valentin K ; PAJOR, Lorraine M ; KNIPE, Jay ; QI GAO ; PERRONE, Robert ; STARRETT, John E ; PENDRI, Yadagiri ; DWORETZKY, Steven I ; MEANWELL, Nicholas A ; MARTINEZ, Eduardo ; BOISSARD, Christopher G ; POST-MUNSON, Debra J ; TROJNACKI, Joanne T ; YELESWARAM, Krishnaswamy

Bioorganic & medicinal chemistry letters, 2002-04, Vol.12 (7), p.1023-1026 [Periódico revisado por pares]

Oxford: Elsevier

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3
New σ and 5-HT1A Receptor Ligands:  ω-(Tetralin-1-yl)-n-alkylamine Derivatives
New σ and 5-HT1A Receptor Ligands:  ω-(Tetralin-1-yl)-n-alkylamine Derivatives
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New σ and 5-HT1A Receptor Ligands:  ω-(Tetralin-1-yl)-n-alkylamine Derivatives

Berardi, Francesco ; Colabufo, Nicola A ; Giudice, Giuseppe ; Perrone, Roberto ; Tortorella, Vincenzo ; Govoni, Stefano ; Lucchi, Laura

Journal of medicinal chemistry, 1996-01, Vol.39 (1), p.176-182 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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4
High Affinity and Selectivity on 5-HT1A Receptor of 1-Aryl-4-[(1-tetralin)alkyl]piperazines. 2
High Affinity and Selectivity on 5-HT1A Receptor of 1-Aryl-4-[(1-tetralin)alkyl]piperazines. 2
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High Affinity and Selectivity on 5-HT1A Receptor of 1-Aryl-4-[(1-tetralin)alkyl]piperazines. 2

Perrone, Roberto ; Berardi, Francesco ; Colabufo, Nicola A ; Leopoldo, Marcello ; Tortorella, Vincenzo ; Fiorentini, Francesco ; Olgiati, Vincenzo ; Ghiglieri, Alberto ; Govoni, Stefano

Journal of medicinal chemistry, 1995-03, Vol.38 (6), p.942-949 [Periódico revisado por pares]

United States: American Chemical Society

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5
N-[omega-(Tetralin-1-yl)alkyl] derivatives of 3,3-dimethylpiperidine are highly potent and selective sigma1 or sigma2 ligands
N-[omega-(Tetralin-1-yl)alkyl] derivatives of 3,3-dimethylpiperidine are highly potent and selective sigma1 or sigma2 ligands
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N-[omega-(Tetralin-1-yl)alkyl] derivatives of 3,3-dimethylpiperidine are highly potent and selective sigma1 or sigma2 ligands

Berardi, F ; Santoro, S ; Perrone, R ; Tortorella, V ; Govoni, S ; Lucchi, L

Journal of medicinal chemistry, 1998-10, Vol.41 (21), p.3940-3947 [Periódico revisado por pares]

United States

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6
Mixed 5-HT1A/D-2 activity of a new model of arylpiperazines: 1-aryl-4-[3-(1,2-dihydronaphthalen-4-yl)-n-propyl]piperazines. 1. Synthesis and structure-activity relationships
Mixed 5-HT1A/D-2 activity of a new model of arylpiperazines: 1-aryl-4-[3-(1,2-dihydronaphthalen-4-yl)-n-propyl]piperazines. 1. Synthesis and structure-activity relationships
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Mixed 5-HT1A/D-2 activity of a new model of arylpiperazines: 1-aryl-4-[3-(1,2-dihydronaphthalen-4-yl)-n-propyl]piperazines. 1. Synthesis and structure-activity relationships

Perrone, Roberto ; Berardi, Francesco ; Colabufo, Nicola A ; Tortorella, Vincenzo ; Fiorentini, Francesco ; Olgiati, Vincenzo ; Vanotti, Ermes ; Govoni, Stefano

Journal of medicinal chemistry, 1994-01, Vol.37 (1), p.99-104 [Periódico revisado por pares]

United States: American Chemical Society

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7
Experimental renal failure in the rat modulates cardiac Na,K-ATPase alpha 2 mRNA but not protein
Experimental renal failure in the rat modulates cardiac Na,K-ATPase alpha 2 mRNA but not protein
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Experimental renal failure in the rat modulates cardiac Na,K-ATPase alpha 2 mRNA but not protein

da Silva, Jr, J C ; Shi, X J ; Johns, C A ; Jefferson, D M ; Grubman, S A ; Madias, N E ; Perrone, R D

Journal of the American Society of Nephrology, 1994-07, Vol.5 (1), p.27-35 [Periódico revisado por pares]

United States

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8
In silico identification and in vivo validation of miR-495 as a novel regulator of motivation for cocaine that targets multiple addiction-related networks in the nucleus accumbens
In silico identification and in vivo validation of miR-495 as a novel regulator of motivation for cocaine that targets multiple addiction-related networks in the nucleus accumbens
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In silico identification and in vivo validation of miR-495 as a novel regulator of motivation for cocaine that targets multiple addiction-related networks in the nucleus accumbens

Bastle, R M ; Oliver, R J ; Gardiner, A S ; Pentkowski, N S ; Bolognani, F ; Allan, A M ; Chaudhury, T ; St Peter, M ; Galles, N ; Smith, C ; Neisewander, J L ; Perrone-Bizzozero, N I

Molecular psychiatry, 2018-02, Vol.23 (2), p.434-443 [Periódico revisado por pares]

England: Nature Publishing Group

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9
The Discovery of LML134, a Histamine H3 Receptor Inverse Agonist for the Clinical Treatment of Excessive Sleep Disorders
The Discovery of LML134, a Histamine H3 Receptor Inverse Agonist for the Clinical Treatment of Excessive Sleep Disorders
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The Discovery of LML134, a Histamine H3 Receptor Inverse Agonist for the Clinical Treatment of Excessive Sleep Disorders

Troxler, Thomas ; Feuerbach, Dominik ; Zhang, Xuechun ; Yang, Charles R. ; Lagu, Bharat ; Perrone, Mark ; Wang, Tie‐Lin ; Briner, Karin ; Bock, Mark G. ; Auberson, Yves P.

ChemMedChem, 2019-07, Vol.14 (13), p.1238-1247 [Periódico revisado por pares]

Germany: Wiley Subscription Services, Inc

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10
Ergoline-Derived Inverse Agonists of the Human H3 Receptor for the Treatment of Narcolepsy
Ergoline-Derived Inverse Agonists of the Human H3 Receptor for the Treatment of Narcolepsy
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Ergoline-Derived Inverse Agonists of the Human H3 Receptor for the Treatment of Narcolepsy

Auberson, Yves P. ; Troxler, Thomas ; Zhang, Xuechun ; Yang, Charles R. ; Fendt, Markus ; Feuerbach, Dominik ; Liu, Yu-Chih ; Lagu, Bharat ; Lerchner, Andreas ; Perrone, Mark ; Lei, Lijun ; Zhang, Chao ; Wang, Chunxiu ; Wang, Tie-Lin ; Bock, Mark G.

ChemMedChem, 2014-08, Vol.9 (8), p.1683-1696 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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