Characterization of Contractile P2 Receptors in Human Coronary Arteries by Use of the Stable Pyrimidines Uridine 5′-O-Thiodiphosphate and Uridine 5′-O-3-Thiotriphosphate

This publication has 35 references indexed in Scilit:

• The use of the slowly degradable analog, α,β-methylene ATP, to produce desensitisation of the P2-purinoceptor: Effect on non-adrenergic, non-cholinergic responses of the guinea-pig urinary bladder
  Published by Elsevier ,2002
• Involvement of pyrimidinoceptors in the regulation of cell functions by uridine and by uracil nucleotides
  Published by Elsevier ,2002
• Phenotype Changes of the Vascular Smooth Muscle Cell Regulate P2 Receptor Expression as Measured by Quantitative RT-PCR
  Biochemical and Biophysical Research Communications, 1998
• Pharmacological analysis of responses to ATP in the isolated and perfused canine coronary artery
  European Journal of Pharmacology, 1997
• The P2Y1 receptor is an ADP receptor antagonized by ATP and expressed in platelets and megakaryoblastic cells
  Published by Wiley ,1997
• Cloning and sequencing of a human cDNA encoding endothelial P2Y1 purinoceptor
  Gene, 1996
• Cloning, Functional Expression and Tissue Distribution of the Human P2Y6Receptor
  Biochemical and Biophysical Research Communications, 1996
• ATP mediates coronary vasoconstriction via P2x-purinoceptors and coronary vasodilatation via P2y-purinoceptors in the isolated perfused rat heart
  European Journal of Pharmacology, 1987
• Direct evidence for ATP release from non-adrenergic, non-cholinergic (“purinergic”) nerves in the guinea-pig taenia coli and bladder
  European Journal of Pharmacology, 1978
• The enzymatic synthesis of thiophosphate analogs of nucleotides
  Biochimica et Biophysica Acta (BBA) - Enzymology, 1972