Pharmacological characterization of recombinant human and rat P2X receptor subtypes-Reference-Cited by-同舟云学术

Pharmacological characterization of recombinant human and rat P2X receptor subtypes

Published:1999-07 Issue:1-2 Volume:376 Page:127-138
ISSN:0014-2999
Container-title:European Journal of Pharmacology
language:en
Short-container-title:European Journal of Pharmacology

Author:

Bianchi Bruce R,Lynch Kevin J,Touma Edward,Niforatos Wende,Burgard Edward C,Alexander Karen M,Park Helen S,Yu Haixia,Metzger Randy,Kowaluk Elizabeth,Jarvis Michael F,van Biesen Tim

Publisher

Elsevier BV

Subject

Pharmacology

Reference47 articles.

1. Radioligand binding assays using [35S]ATPγS and [35S]ADPβS are non-selective for ionotropic or metabotropic P2 receptor subtypes;Bianchi;FASEB J.,1998

2. A P2X purinoceptor cDNA conferring a novel pharmacological profile;Bo;FEBS Lett.,1995

3. New structural motif for ligand-gated ion channels defined by an ionotropic ATP receptor;Brake;Nature,1994

4. An antagonist-insensitive P2X receptor expressed in epithelia and brain;Buell;EMBO J.,1996

5. P2-purinoceptor antagonists: III. Blockade of P2-purinoceptor subtypes and ecto-nucleotidases by compounds related to suramin;Bultmann;Naunyn-Schmiedeberg's Arch. Pharmacol.,1996

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