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Rosiglitazone induces mitochondrial biogenesis in mouse brain

Journal of Alzheimer's disease, 2007-03, Vol.11 (1), p.45-51

2007

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Self-prescribing by doctors

Health trends, 1988-11, Vol.20 (4), p.128

Selley, P

1988

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Patient alarm bell

British journal of general practice, 1992-07, Vol.42 (360), p.304-304

Selley, Peter

1992

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Vocational training: a trainee's view

Practitioner, 1981-03, Vol.225 (1353), p.281

Selley, P

1981

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Training the trainee

BMJ, 1980-06, Vol.280 (6231), p.1621-1621

1980

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Hazards of sulphinpyrazone

BMJ, 1978-12, Vol.2 (6154), p.1786-1787

1978

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Self-prescribing by doctors

Health Trends, 1988-11, Vol.4 (Nov 88), p.128-129

Selley, P

1988

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Differential Tolerance to FTY720-Induced Antinociception in Acute Thermal and Nerve Injury Mouse Pain Models: Role of Sphingosine-1-Phosphate Receptor Adaptation

The Journal of pharmacology and experimental therapeutics, 2018-09, Vol.366 (3), p.509-518

2018

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An essential role for ΔFosB in the nucleus accumbens in morphine action

Nature neuroscience, 2006-02, Vol.9 (2), p.205-211

2006

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Statistical Parametric Mapping reveals ligand and region-specific activation of G-proteins by CB1 receptors and non-CB1 sites in the 3D reconstructed mouse brain

NeuroImage (Orlando, Fla.), 2010-10, Vol.52 (4), p.1243-1251

2010

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Sphingosine-1-phosphate receptors as emerging targets for treatment of pain

Biochemical pharmacology, 2012-12, Vol.84 (12), p.1551-1562

2012

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Sphingosine lysolipids in the CNS: Endogenous cannabinoid antagonists or a parallel pain modulatory system?

Life sciences (1973), 2013-08, Vol.93 (5-6), p.187-193

2013

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Region‐dependent attenuation of μ opioid receptor‐mediated G‐protein activation in mouse CNS as a function of morphine tolerance

British journal of pharmacology, 2007-08, Vol.151 (8), p.1324-1333

2007

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Global Translational Responses to Oxidative Stress Impact upon Multiple Levels of Protein Synthesis

The Journal of biological chemistry, 2006-09, Vol.281 (39), p.29011-29021

2006

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Manipulating Pharmacodynamic Efficacy with Agonist + Antagonist Mixtures: In Vitro and In Vivo Studies with Opioids and Cannabinoids

The Journal of pharmacology and experimental therapeutics, 2021-03, Vol.376 (3), p.374-384

2021

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Upstream sequence elements direct post-transcriptional regulation of gene expression under stress conditions in yeast

BMC genomics, 2009-01, Vol.10 (1), p.7-7, Article 7

2009

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Sphingosine and Its Analog, the Immunosuppressant 2-Amino-2-(2-[4-octylphenyl]ethyl)-1,3-propanediol, Interact with the CB1 Cannabinoid Receptor

Molecular pharmacology, 2006-07, Vol.70 (1), p.41

2006

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Treatment of Autoimmune Neuroinflammation with a Synthetic Tryptophan Metabolite

Science (American Association for the Advancement of Science), 2005-11, Vol.310 (5749), p.850-855

2005

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N-arachidonyl maleimide potentiates the pharmacological and biochemical effects of the endocannabinoid 2-arachidonylglycerol through inhibition of monoacylglycerol lipase

The Journal of pharmacology and experimental therapeutics, 2008-11, Vol.327 (2), p.546-553

2008

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Sphingosine-1-phosphate receptors mediate neuromodulatory functions in the CNS

Journal of neurochemistry, 2009-08, Vol.110 (4), p.1191-1202

2009

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Inhibition of monoacylglycerol lipase reduces nicotine withdrawal

British journal of pharmacology, 2015-02, Vol.172 (3), p.869-882

2015

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Systematic Structure–Activity Relationship Study of Nalfurafine Analogues toward Development of Potentially Nonaddictive Pain Management Treatments

Journal of medicinal chemistry, 2024-06, Vol.67 (11), p.9552-9574

2024

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Structural Alterations of the “Address” Moiety of NAN Leading to the Discovery of a Novel Opioid Receptor Modulator with Reduced hERG Toxicity

Journal of medicinal chemistry, 2023-01, Vol.66 (1), p.577-595

2023

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Glucose depletion inhibits translation initiation via eIF4A loss and subsequent 48S preinitiation complex accumulation, while the pentose phosphate pathway is coordinately up-regulated

Molecular biology of the cell, 2011-09, Vol.22 (18), p.3379-3393

2011

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Molecular Pharmacology Profiling of Phenylfentanil and Its Analogues to Understand the Putative Involvement of an Adrenergic Mechanism in Fentanyl-Induced Respiratory Depression

Journal of medicinal chemistry, 2024-01, Vol.67 (1), p.603-619

2024

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Rosiglitazone induces mitochondrial biogenesis in mouse brain

Self-prescribing by doctors

Patient alarm bell

Vocational training: a trainee's view

Training the trainee

Hazards of sulphinpyrazone

Self-prescribing by doctors

Differential Tolerance to FTY720-Induced Antinociception in Acute Thermal and Nerve Injury Mouse Pain Models: Role of Sphingosine-1-Phosphate Receptor Adaptation

An essential role for ΔFosB in the nucleus accumbens in morphine action

Statistical Parametric Mapping reveals ligand and region-specific activation of G-proteins by CB1 receptors and non-CB1 sites in the 3D reconstructed mouse brain

Sphingosine-1-phosphate receptors as emerging targets for treatment of pain

Sphingosine lysolipids in the CNS: Endogenous cannabinoid antagonists or a parallel pain modulatory system?

Region‐dependent attenuation of μ opioid receptor‐mediated G‐protein activation in mouse CNS as a function of morphine tolerance

Global Translational Responses to Oxidative Stress Impact upon Multiple Levels of Protein Synthesis

Manipulating Pharmacodynamic Efficacy with Agonist + Antagonist Mixtures: In Vitro and In Vivo Studies with Opioids and Cannabinoids

Upstream sequence elements direct post-transcriptional regulation of gene expression under stress conditions in yeast

Sphingosine and Its Analog, the Immunosuppressant 2-Amino-2-(2-[4-octylphenyl]ethyl)-1,3-propanediol, Interact with the CB1 Cannabinoid Receptor

Treatment of Autoimmune Neuroinflammation with a Synthetic Tryptophan Metabolite

N-arachidonyl maleimide potentiates the pharmacological and biochemical effects of the endocannabinoid 2-arachidonylglycerol through inhibition of monoacylglycerol lipase

Sphingosine-1-phosphate receptors mediate neuromodulatory functions in the CNS

Inhibition of monoacylglycerol lipase reduces nicotine withdrawal

Systematic Structure–Activity Relationship Study of Nalfurafine Analogues toward Development of Potentially Nonaddictive Pain Management Treatments

Structural Alterations of the “Address” Moiety of NAN Leading to the Discovery of a Novel Opioid Receptor Modulator with Reduced hERG Toxicity

Glucose depletion inhibits translation initiation via eIF4A loss and subsequent 48S preinitiation complex accumulation, while the pentose phosphate pathway is coordinately up-regulated

Molecular Pharmacology Profiling of Phenylfentanil and Its Analogues to Understand the Putative Involvement of an Adrenergic Mechanism in Fentanyl-Induced Respiratory Depression

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