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First PublishedTitleAuthor(s)Type
Mar-2009Orthosteric and allosteric binding sites of P2X receptors.Evans, RJJournal Article
20-Mar-2012Agonist binding evokes extensive conformational changes in the extracellular domain of the ATP-gated human P2X1 receptor ion channel.Roberts, JA; Allsopp, RC; El Ajouz S; Vial, C; Schmid, R; Young, MT; Evans, RJJournal Article
22-Sep-2000The role of positively charged amino acids in ATP recognition by human P2X(1) receptors.Ennion, S; Hagan, S; Evans, RJJournal Article
Jan-2009Characterisation of ATP analogues to cross-link and label P2X receptors.Agboh, KC; Powell, AJ; Evans, RJJournal Article
19-Aug-2011Cysteine scanning mutagenesis (residues Glu52-Gly96) of the human P2X1 receptor for ATP: mapping agonist binding and channel gating.Allsopp, RC; El Ajouz S; Schmid, R; Evans, RJJournal Article
Nov-2010Structural interpretation of P2X receptor mutagenesis studies on drug action.Evans, RJJournal Article
21-Mar-2014Malaria Protein Kinase CK2 (PfCK2) Shows Novel Mechanisms of RegulationGraciotti, Michele; Alam, Mahmood; Solyakov, Lev; Schmid, Ralf; Burley, G.; Bottrill, Andrew R.; Doerig, C.; Cullis, Paul; Tobin, Andrew B.Journal Article
16-Jan-2015Use of chimeras, point mutants, and molecular modeling to map the antagonist-binding site of 4,4',4″,4‴-(carbonylbis-(imino-5,1,3-benzenetriylbis(carbonylimino)))tetrakisbenzene-1,3-disulfonic acid (NF449) at P2X1 receptors for ATP.Farmer, Louise K.; Schmid, Ralf; Evans, Richard J.Journal Article