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Geoffrey Burnstock

Researcher at University of Melbourne

Publications -  1489
Citations -  103269

Geoffrey Burnstock is an academic researcher from University of Melbourne. The author has contributed to research in topics: Purinergic receptor & Receptor. The author has an hindex of 141, co-authored 1488 publications receiving 99525 citations. Previous affiliations of Geoffrey Burnstock include National Institutes of Health & Second Military Medical University.

Papers
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Book ChapterDOI

Receptors for Purines and Pyrimidines

TL;DR: In this review particular emphasis is placed on the discrepancy between the concentrations ofadenosine, ADP, and ATP in the purine receptors of UDP and UTP.
Journal Article

Nomenclature and classification of purinoceptors

TL;DR: The evidence is now compelling that ATP plays important physiological and/ or pathophysiological roles in a variety of biological systems, and the presence of receptors for ADP and adenosine (presumably A2) receptors exist on platelets is compelling.
Journal ArticleDOI

Physiology and Pathophysiology of Purinergic Neurotransmission

TL;DR: This review is focused on purinergic neurotransmission, i.e., ATP released from nerves as a transmitter or cotransmitter to act as an extracellular signaling molecule on both pre- and postjunctional membranes at neuroeffector junctions and synapses, as well as acting as a trophic factor during development and regeneration.
Journal ArticleDOI

Is there a basis for distinguishing two types of P2-purinoceptor?

TL;DR: Differences in the structure of the P2-purinoceptor in various tissues may be useful in the development of drugs for the treatment of vascular, gastrointestinal and urinoglenital disorders.
Journal ArticleDOI

International Union of Pharmacology LVIII: Update on the P2Y G Protein-Coupled Nucleotide Receptors: From Molecular Mechanisms and Pathophysiology to Therapy

TL;DR: There have been many advances in knowledge about different aspects of P2Y receptor signaling since the last review published by the International Union of Pharmacology subcommittee, and more receptor subtypes have been cloned and characterized and most orphan receptors deorphanized, so that it is now possible to provide a basis for a future subdivision of P 2Y receptor sub types.