Fatigue and critical thinking on eight-and twelve-hour shifts

Phenylethanolamines inhibit NMDA receptors by enhancing proton inhibition.

Nature neuroscience·1999

Structure and functional characterization of a novel human low-voltage activated calcium channel.

Journal of neurochemistry·1999

Conformationally restricted analogues of nicotine and anabasine.

Bioorganic & medicinal chemistry letters·1999

The potential of subtype-selective neuronal nicotinic acetylcholine receptor agonists as therapeutic agents.

Life sciences·1998

Differential dependence on GluR2 expression of three characteristic features of AMPA receptors.

The Journal of neuroscience : the official journal of the Society for Neuroscience·1998

Pharmacological characterization of recombinant human neuronal nicotinic acetylcholine receptors h alpha 2 beta 2, h alpha 2 beta 4, h alpha 3 beta 2, h alpha 3 beta 4, h alpha 4 beta 2, h alpha 4 beta 4 and h alpha 7 expressed in Xenopus oocytes.

The Journal of pharmacology and experimental therapeutics·1997

Nursing work environment as a determinant of health care outcomes: A scoping review.

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Frailty index deficit interchangeability: an empirical test using random survival forests in adults with cardiovascular disease.

Age and ageing·2026

Beyond complications: the mayo adhesive probability (MAP) score as an imaging biomarker of surgical complexity in percutaneous nephrolithotomy.

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Journal of visualized experiments : JoVE·2026

Persona-prompted LLM agents achieve modest but genuine prediction of human social media reactions.

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The Lancet. Digital health·2026

Contrastive learning of adverse events to provide effective and interpretable vector representations for machine-assisted pharmacovigilance.

Briefings in bioinformatics·2026

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Phenylethanolamines inhibit NMDA receptors by enhancing proton inhibition.

Structure and functional characterization of a novel human low-voltage activated calcium channel.

Conformationally restricted analogues of nicotine and anabasine.

The potential of subtype-selective neuronal nicotinic acetylcholine receptor agonists as therapeutic agents.

Differential dependence on GluR2 expression of three characteristic features of AMPA receptors.

Pharmacological characterization of recombinant human neuronal nicotinic acetylcholine receptors h alpha 2 beta 2, h alpha 2 beta 4, h alpha 3 beta 2, h alpha 3 beta 4, h alpha 4 beta 2, h alpha 4 beta 4 and h alpha 7 expressed in Xenopus oocytes.

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