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Publications by Eric A Barnard
The P2Y1receptor Closes the N-Type Ca2+channel in Neurones, With Both Adenosine Triphosphates and Diphosphates as Potent Agonists
British Journal of Pharmacology
Pharmacology
Related publications
A Functional Screening of Adenosine Analogues at the Adenosine A2BReceptor: A Search for Potent Agonists
Nucleosides and Nucleotides
P2Y2Nucleotide Receptors Expressed Heterologously in Sympathetic Neurons Inhibit Both N-Type Ca2+and M-Type K+Currents
Journal of Neuroscience
Neuroscience
Electrophysiological Characterization of Potent Agonists and Antagonists at Pre- And Postsynaptic GABAB Receptors on Neurones in Rat Brain Slices
British Journal of Pharmacology
Pharmacology
Purine (N)Methanocarba Nucleoside Derivatives Lacking an Exocyclic Amine as Selective A3 Adenosine Receptor Agonists
Purine (N)Methanocarba Nucleoside Derivatives Lacking an Exocyclic Amine as Selective A3 Adenosine Receptor Agonists
Ca2+ Signaling in Cardiac Myocytes Overexpressing the Alpha1 Subunit of L-Type Ca2+ Channel
Circulation Research
Cardiovascular Medicine
Physiology
Cardiology
[3]5?-N-Ethylcarboxamide Adenosine Binds to Both Ra and Ri Adenosine Receptors in Rat Striatum
Naunyn-Schmiedeberg's Archives of Pharmacology
Medicine
Pharmacology
Biarylaniline Phenethanolamines as Potent and Selective B3 Adrenergic Receptor Agonists
A Single Non-L-, Non-N-Type Ca2+ Channel in Rat Insulin-Secreting RINm5F Cells
Pflugers Archiv European Journal of Physiology
Clinical Biochemistry
Physiology