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Vincent A. Chiappinelli

Researcher at George Washington University

Publications -  74
Citations -  3405

Vincent A. Chiappinelli is an academic researcher from George Washington University. The author has contributed to research in topics: Nicotinic agonist & Ganglion type nicotinic receptor. The author has an hindex of 31, co-authored 74 publications receiving 3361 citations. Previous affiliations of Vincent A. Chiappinelli include University of Connecticut & Washington University in St. Louis.

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Journal Article

International Union of Pharmacology. XX. Current Status of the Nomenclature for Nicotinic Acetylcholine Receptors and Their Subunits

TL;DR: Nicotinic acetylcholine receptors in jawed vertebrates are prototypical members of the multisubunit, neurotransmitter-gated superfamily of ion channels (ionotropic neurotransmitter receptors; see Section IV for selected seminal papers, reviews, and collections).
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Kappa-bungarotoxin: a probe for the neuronal nicotinic receptor in the avian ciliary ganglion.

TL;DR: The interaction of snake alpha-neurotoxins with neuronal membranes has been examined in the chick ciliary ganglion and two binding sites are blocked following pre-treatment of ganglia with the irreversible nicotinic affinity agent bromoacetylcholine, proposed to account for these observations.
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Glutamate and GABA Release Are Enhanced by Different Subtypes of Presynaptic Nicotinic Receptors in the Lateral Geniculate Nucleus

TL;DR: The results demonstrate that the LGNv neurons receive both glutamatergic and GABAergic inputs and that the release of these transmitters can be modulated by different presynaptic nAChRs, demonstrating the regulation of synaptic efficacy in the brain by presycholine receptors can be complex.
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Nicotinic acetylcholine receptor subtypes in human frontal cortex: changes in Alzheimer's disease.

TL;DR: Alzheimer's disease does not affect all subtypes of nicotinic receptors in the frontal cortex to the same extent, and it is concluded that 125I‐κ‐bungarotoxin sites are not significantly different in number from age‐matched control brains.