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See Latest ArticlesA non-desensitizing kainate receptor point mutant
Molecular Pharmacology, 06/29/09
Nayeem N et al. - The authors therefore hypothesize that the unexpected phenotype of this charge-reversal mutation results from the substitution of the sodium ions bound within the dimer interface by the introduced lysine NH3+ groups. The non-desensitizing D776K mutant provides insights into kainate receptor gating, as well as representing a potentially useful new tool for dissecting kainate receptor function.
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Polymorphism of Human Cytochrome P450 2D6 and Its Clinical Significance: Part II
Clinical Pharmacokinetics, 12/01/09
Pharmacokinetics, metabolism and bioavailability of the triazole antifungal agent voriconazole in relation to CYP2C19 genotype
British Journal of Clinical Pharmacology, 11/30/09
A Conserved Motif in the Membrane Proximal C-Terminal Tail of Human Muscarinic M1 Acetylcholine Receptors Affects Plasma Membrane Expression
Journal of Pharmacology and Experimental Therapeutics, 11/25/09
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