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SUBSTITUTION OF A CHARGED RESIDUE, LYSINE-282, IN THE M2 DOMAIN OF THE 5-HT3 RECEPTOR AFFECTS THE RATE OF DESENSITIZATION
Authors: GUNTHORPE MJ LUMMIS SCR
Citation: Mj. Gunthorpe et Scr. Lummis, SUBSTITUTION OF A CHARGED RESIDUE, LYSINE-282, IN THE M2 DOMAIN OF THE 5-HT3 RECEPTOR AFFECTS THE RATE OF DESENSITIZATION, British Journal of Pharmacology, 122, 1997, pp. 252-252
DIRECT INHIBITION OF 5-HYDROXYTRYPTAMINE(3) RECEPTORS BY ANTAGONISTS OF L-TYPE CA2+ CHANNELS
Authors: HARGREAVES AC GUNTHORPE MJ TAYLOR CW LUMMIS SCR
Citation: Ac. Hargreaves et al., DIRECT INHIBITION OF 5-HYDROXYTRYPTAMINE(3) RECEPTORS BY ANTAGONISTS OF L-TYPE CA2+ CHANNELS, Molecular pharmacology, 50(5), 1996, pp. 1284-1294
CONVERSION OF THE ION SELECTIVITY OF THE 5-HT3 RECEPTOR FROM CATIONICTO ANIONIC - A CONSERVED FEATURE OF THE LIGAND-GATED ION-CHANNEL SUPERFAMILY
Authors: GUNTHORPE MJ FLETCHER EJ LUMMIS SCR
Citation: Mj. Gunthorpe et al., CONVERSION OF THE ION SELECTIVITY OF THE 5-HT3 RECEPTOR FROM CATIONICTO ANIONIC - A CONSERVED FEATURE OF THE LIGAND-GATED ION-CHANNEL SUPERFAMILY, British Journal of Pharmacology, 119, 1996, pp. 259-259
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