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The IMPROVE Guidelines (Ischaemia Models: Procedural Refinements Of in Vivo Experiments)

Journal of Cerebral Blood Flow & Metabolism, 2017-11, Vol.37 (11), p.3488-3517

2017

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What should we do about student use of cognitive enhancers? An analysis of current evidence

Neuropharmacology, 2013-01, Vol.64, p.588-595

2013

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Production of Superoxide Radicals and Hydrogen Peroxide by NADH- Ubiquinone Reductase and Ubiquinol-Cytochrome c Reductase from Beef-Heart Mitochondria

Archives of biochemistry and biophysics, 2022-09, p.109231

2022

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Reprint of: Production of Superoxide Radicals and Hydrogen Peroxide by NADH- Ubiquinone Reductase and Ubiquinol-Cytochrome c Reductase from Beef-Heart Mitochondria

Archives of biochemistry and biophysics, 2022-09, Vol.726, p.109231-109231, Article 109231

2022

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The design of chronic toxicology studies of monoclonal antibodies: Implications for the reduction in use of non-human primates

Regulatory toxicology and pharmacology, 2012-03, Vol.62 (2), p.347-354

2012

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Replacement of in vivo human rabies vaccine potency testing by in vitro glycoprotein quantification using ELISA – Results of an international collaborative study

Vaccine, 2017-02, Vol.35 (6), p.966-971

2017

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Refinements to rodent head fixation and fluid/food control for neuroscience

Journal of neuroscience methods, 2022-11, Vol.381, p.109705-109705, Article 109705

2022

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Techniques for the Analysis of Membrane Proteins

1, 1986

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URF6, Last Unidentified Reading Frame of Human mtDNA, Codes for an NADH Dehydrogenase Subunit

Science (American Association for the Advancement of Science), 1986-10, Vol.234 (4776), p.614-618

1986

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Can GM marmoset use be justified?

Nature (London), 2014-10, Vol.514 (7524), p.567-567

2014

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Biological profile of L-745,870, a selective antagonist with high affinity for the dopamine D4 receptor

The Journal of pharmacology and experimental therapeutics, 1997-11, Vol.283 (2), p.636

1997

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5-(4-Chlorophenyl)-4-methyl-3-(1-(2- phenylethyl)piperidin-4-yl)isoxazole: A Potent, Selective Antagonist at Human Cloned Dopamine D4 Receptors

Journal of medicinal chemistry, 1996-05, Vol.39 (10), p.1943-1945

1996

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Pharmacological and functional characterisation of dopamine D4 receptors in the rat retina

Neuropharmacology, 2003-06, Vol.44 (8), p.1038-1046

2003

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L-745,870, a subtype selective dopamine D4 receptor antagonist, does not exhibit a neuroleptic-like profile in rodent behavioral tests

The Journal of pharmacology and experimental therapeutics, 1997-12, Vol.283 (3), p.1256

1997

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Corrigendum to “What should we do about student use of cognitive enhancers?: An analysis of current evidence” [Neuropharmacology 64 (2012) 588–595]

Neuropharmacology, 2013-02, Vol.65, p.28-28

2013

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GABAA receptor subtypes immunopurified from rat brain with α subunit-specific antibodies have unique pharmacological properties

Neuron (Cambridge, Mass.), 1991-10, Vol.7 (4), p.667-676

1991

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Lab animals: Can GM marmoset use be justified?

Nature (London), 2014-10, Vol.514 (7524), p.567-567

2014

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Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase

Nature (London), 1985-04, Vol.314 (6012), p.592-597

1985

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3-(1-piperazinyl)-4,5-dihydro-1H-benzo[g]indazoles: high affinity ligands for the human dopamine D4 receptor with improved selectivity over ion channels

Bioorganic & medicinal chemistry, 1998-06, Vol.6 (6), p.743-753

1998

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Solubilisation of the 5‐Hydroxytryptamine3 Receptor from Pooled Rat Cortical and Hippocampal Membranes

Journal of neurochemistry, 1990-03, Vol.54 (3), p.924-930

1990

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Inhibition of PC12 Cell Redox Activity is a Specific, Early Indicator of the Mechanism of β-Amyloid-Mediated Cell Death

Proceedings of the National Academy of Sciences - PNAS, 1994-02, Vol.91 (4), p.1470-1474

1994

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Alcohol alternatives – a goal for psychopharmacology?

Journal of psychopharmacology (Oxford), 2006-05, Vol.20 (3), p.325-326

Ragan, Ian

2006

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Sulphated compounds attenuate β-amyloid toxicity by inhibiting its association with cells

Neuroreport, 1995-12, Vol.7 (1), p.49-53

1995

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3-[[4-(4-Chlorophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine: An Antagonist with High Affinity and Selectivity for the Human Dopamine D4 Receptor

Journal of medicinal chemistry, 1996-05, Vol.39 (10), p.1941-1942

1996

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The IMPROVE Guidelines (Ischaemia Models: Procedural Refinements Of in Vivo Experiments)

What should we do about student use of cognitive enhancers? An analysis of current evidence

Production of Superoxide Radicals and Hydrogen Peroxide by NADH- Ubiquinone Reductase and Ubiquinol-Cytochrome c Reductase from Beef-Heart Mitochondria

Reprint of: Production of Superoxide Radicals and Hydrogen Peroxide by NADH- Ubiquinone Reductase and Ubiquinol-Cytochrome c Reductase from Beef-Heart Mitochondria

The design of chronic toxicology studies of monoclonal antibodies: Implications for the reduction in use of non-human primates

Replacement of in vivo human rabies vaccine potency testing by in vitro glycoprotein quantification using ELISA – Results of an international collaborative study

Refinements to rodent head fixation and fluid/food control for neuroscience

Techniques for the Analysis of Membrane Proteins

URF6, Last Unidentified Reading Frame of Human mtDNA, Codes for an NADH Dehydrogenase Subunit

Can GM marmoset use be justified?

7-(1,1-Dimethylethyl)-6-(2-ethyl-2H-1,2,4- triazol-3-ylmethoxy)-3-(2-fluorophenyl)- 1,2,4-triazolo[4,3-b]pyridazine: A Functionally Selective γ-Aminobutyric AcidA (GABAA) α2/α3-Subtype Selective Agonist That Exhibits Potent Anxiolytic Activity but Is Not Sedating in Animal Models

Biological profile of L-745,870, a selective antagonist with high affinity for the dopamine D4 receptor

5-(4-Chlorophenyl)-4-methyl-3-(1-(2- phenylethyl)piperidin-4-yl)isoxazole: A Potent, Selective Antagonist at Human Cloned Dopamine D4 Receptors

Pharmacological and functional characterisation of dopamine D4 receptors in the rat retina

L-745,870, a subtype selective dopamine D4 receptor antagonist, does not exhibit a neuroleptic-like profile in rodent behavioral tests

Corrigendum to “What should we do about student use of cognitive enhancers?: An analysis of current evidence” [Neuropharmacology 64 (2012) 588–595]

GABAA receptor subtypes immunopurified from rat brain with α subunit-specific antibodies have unique pharmacological properties

Lab animals: Can GM marmoset use be justified?

Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase

3-(1-piperazinyl)-4,5-dihydro-1H-benzo[g]indazoles: high affinity ligands for the human dopamine D4 receptor with improved selectivity over ion channels

Solubilisation of the 5‐Hydroxytryptamine3 Receptor from Pooled Rat Cortical and Hippocampal Membranes

Inhibition of PC12 Cell Redox Activity is a Specific, Early Indicator of the Mechanism of β-Amyloid-Mediated Cell Death

Alcohol alternatives – a goal for psychopharmacology?

Sulphated compounds attenuate β-amyloid toxicity by inhibiting its association with cells

3-[[4-(4-Chlorophenyl)piperazin-1-yl]methyl]-1H-pyrrolo[2,3-b]pyridine: An Antagonist with High Affinity and Selectivity for the Human Dopamine D4 Receptor

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