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Refinado por: Nome da Publicação: British Journal of Pharmacology remover Base de dados/Biblioteca: Wiley Online Library remover
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Therapeutic perspectives of epigenetically active nutrients
Therapeutic perspectives of epigenetically active nutrients
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Therapeutic perspectives of epigenetically active nutrients

Remely, M ; Lovrecic, L ; Garza, A L ; Migliore, L ; Peterlin, B ; Milagro, F I ; Martinez, A J ; Haslberger, A G

British journal of pharmacology, 2015-06, Vol.172 (11), p.2756-2768 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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2
Inhibition of phosphodiesterase‐3 by levosimendan is sufficient to account for its inotropic effect in failing human heart
Inhibition of phosphodiesterase‐3 by levosimendan is sufficient to account for its inotropic effect in failing human heart
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Inhibition of phosphodiesterase‐3 by levosimendan is sufficient to account for its inotropic effect in failing human heart

Ørstavik, Ø ; Ata, S H ; Riise, J ; Dahl, C P ; Andersen, G Ø ; Levy, F O ; Skomedal, T ; Osnes, J‐B ; Qvigstad, E

British journal of pharmacology, 2014-12, Vol.171 (23), p.5169-5181 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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3
Cannabidiol displays unexpectedly high potency as an antagonist of CB1 and CB2 receptor agonists in vitro
Cannabidiol displays unexpectedly high potency as an antagonist of CB1 and CB2 receptor agonists in vitro
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Cannabidiol displays unexpectedly high potency as an antagonist of CB1 and CB2 receptor agonists in vitro

Thomas, A ; Baillie, G L ; Phillips, A M ; Razdan, R K ; Ross, R A ; Pertwee, R G

British journal of pharmacology, 2007-03, Vol.150 (5), p.613-623 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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4
Corticosteroid insensitivity is reversed by formoterol via phosphoinositide‐3‐kinase inhibition
Corticosteroid insensitivity is reversed by formoterol via phosphoinositide‐3‐kinase inhibition
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Corticosteroid insensitivity is reversed by formoterol via phosphoinositide‐3‐kinase inhibition

Rossios, C ; To, Y ; Osoata, G ; Ito, M ; Barnes, PJ ; Ito, K

British journal of pharmacology, 2012-10, Vol.167 (4), p.775-786 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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5
Allosteric and orthosteric pharmacology of cannabidiol and cannabidiol‐dimethylheptyl at the type 1 and type 2 cannabinoid receptors
Allosteric and orthosteric pharmacology of cannabidiol and cannabidiol‐dimethylheptyl at the type 1 and type 2 cannabinoid receptors
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Allosteric and orthosteric pharmacology of cannabidiol and cannabidiol‐dimethylheptyl at the type 1 and type 2 cannabinoid receptors

Tham, Mylyne ; Yilmaz, Orhan ; Alaverdashvili, Mariam ; Kelly, Melanie E M ; Denovan‐Wright, Eileen M ; Laprairie, Robert B

British journal of pharmacology, 2019-05, Vol.176 (10), p.1455-1469 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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6
Acetylcholine‐induced endothelium‐dependent contractions in the SHR aorta: the Janus face of prostacyclin
Acetylcholine‐induced endothelium‐dependent contractions in the SHR aorta: the Janus face of prostacyclin
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Acetylcholine‐induced endothelium‐dependent contractions in the SHR aorta: the Janus face of prostacyclin

Gluais, Pascale ; Lonchampt, Michel ; Morrow, Jason D ; Vanhoutte, Paul M ; Feletou, Michel

British journal of pharmacology, 2005-11, Vol.146 (6), p.834-845 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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7
Inhibition of COX‐2 expression by endocannabinoid 2‐arachidonoylglycerol is mediated via PPAR‐γ
Inhibition of COX‐2 expression by endocannabinoid 2‐arachidonoylglycerol is mediated via PPAR‐γ
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Inhibition of COX‐2 expression by endocannabinoid 2‐arachidonoylglycerol is mediated via PPAR‐γ

Du, Huizhi ; Chen, Xiaolei ; Zhang, Jian ; Chen, Chu

British journal of pharmacology, 2011-08, Vol.163 (7), p.1533-1549 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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8
Antidepressant-like effects of BU10119, a novel buprenorphine analogue with mixed κ/μ receptor antagonist properties, in mice
Antidepressant-like effects of BU10119, a novel buprenorphine analogue with mixed κ/μ receptor antagonist properties, in mice
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Antidepressant-like effects of BU10119, a novel buprenorphine analogue with mixed κ/μ receptor antagonist properties, in mice

Almatroudi, Abdulrahman Mohammed I ; Ostovar, Mehrnoosh ; Bailey, Christopher ; Husbands, Stephen ; Bailey, Sarah

British Journal of Pharmacology, 2018-07, Vol.175 (14), p.2869-2880 [Periódico revisado por pares]

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9
Non‐THC cannabinoids inhibit prostate carcinoma growth in vitro and in vivo: pro‐apoptotic effects and underlying mechanisms
Non‐THC cannabinoids inhibit prostate carcinoma growth in vitro and in vivo: pro‐apoptotic effects and underlying mechanisms
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Non‐THC cannabinoids inhibit prostate carcinoma growth in vitro and in vivo: pro‐apoptotic effects and underlying mechanisms

De Petrocellis, Luciano ; Ligresti, Alessia ; Schiano Moriello, Aniello ; Iappelli, Mariagrazia ; Verde, Roberta ; Stott, Colin G ; Cristino, Luigia ; Orlando, Pierangelo ; Di Marzo, Vincenzo

British journal of pharmacology, 2013-01, Vol.168 (1), p.79-102 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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