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Structure and assembly mechanism for heteromeric kainate receptors. , Kumar J, Schuck P, Mayer ML., Neuron. July 28, 2011; 71 (2): 319-31.
Different structural requirements for functional ion pore transplantation suggest different gating mechanisms of NMDA and kainate receptors. , Villmann C, Hoffmann J, Werner M, Kott S, Strutz-Seebohm N, Nilsson T, Hollmann M., J Neurochem. October 1, 2008; 107 (2): 453-65.
pH-dependent inhibition of kainate receptors by zinc. , Mott DD, Benveniste M, Dingledine RJ., J Neurosci. February 13, 2008; 28 (7): 1659-71.
Crystal structures of the kainate receptor GluR5 ligand binding core dimer with novel GluR5-selective antagonists. , Mayer ML, Ghosal A, Dolman NP, Jane DE., J Neurosci. March 15, 2006; 26 (11): 2852-61.
Pore block versus intrinsic gating in the mechanism of inward rectification in strongly rectifying IRK1 channels. , Guo D, Lu Z., J Gen Physiol. October 1, 2000; 116 (4): 561-8.
Mechanism of IRK1 channel block by intracellular polyamines. , Guo D, Lu Z., J Gen Physiol. June 1, 2000; 115 (6): 799-814.
Acute effects of ethanol on kainate receptors with different subunit compositions. , Valenzuela CF, Cardoso RA., J Pharmacol Exp Ther. March 1, 1999; 288 (3): 1199-206.
New developments in the molecular pharmacology of alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionate and kainate receptors. , Fletcher EJ, Lodge D., Pharmacol Ther. January 1, 1996; 70 (1): 65-89.