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Journal Abstract Search


152 related items for PubMed ID: 9354337

  • 1. Identification of amino acid residues that control functional behavior in GluR5 and GluR6 kainate receptors.
    Swanson GT, Gereau RW, Green T, Heinemann SF.
    Neuron; 1997 Oct; 19(4):913-26. PubMed ID: 9354337
    [Abstract] [Full Text] [Related]

  • 2. Interface interactions modulating desensitization of the kainate-selective ionotropic glutamate receptor subunit GluR6.
    Zhang Y, Nayeem N, Nanao MH, Green T.
    J Neurosci; 2006 Sep 27; 26(39):10033-42. PubMed ID: 17005866
    [Abstract] [Full Text] [Related]

  • 3. Heteromeric kainate receptors formed by the coassembly of GluR5, GluR6, and GluR7.
    Cui C, Mayer ML.
    J Neurosci; 1999 Oct 01; 19(19):8281-91. PubMed ID: 10493729
    [Abstract] [Full Text] [Related]

  • 4. Effect of RNA editing and subunit co-assembly single-channel properties of recombinant kainate receptors.
    Swanson GT, Feldmeyer D, Kaneda M, Cull-Candy SG.
    J Physiol; 1996 Apr 01; 492 ( Pt 1)(Pt 1):129-42. PubMed ID: 8730589
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  • 5. Functional consequences of natural substitutions in the GluR6 kainate receptor subunit ligand-binding site.
    Kistler T, Fleck MW.
    Channels (Austin); 2007 Apr 01; 1(6):417-28. PubMed ID: 18690046
    [Abstract] [Full Text] [Related]

  • 6. Amino acid substitutions in the pore helix of GluR6 control inhibition by membrane fatty acids.
    Wilding TJ, Fulling E, Zhou Y, Huettner JE.
    J Gen Physiol; 2008 Jul 01; 132(1):85-99. PubMed ID: 18562501
    [Abstract] [Full Text] [Related]

  • 7. Crystal structures of the GluR5 and GluR6 ligand binding cores: molecular mechanisms underlying kainate receptor selectivity.
    Mayer ML.
    Neuron; 2005 Feb 17; 45(4):539-52. PubMed ID: 15721240
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  • 11. Amino-acid residues involved in glutamate receptor 6 kainate receptor gating and desensitization.
    Fleck MW, Cornell E, Mah SJ.
    J Neurosci; 2003 Feb 15; 23(4):1219-27. PubMed ID: 12598610
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  • 12. Mutations to the kainate receptor subunit GluR6 binding pocket that selectively affect domoate binding.
    Zhang Y, Nayeem N, Green T.
    Mol Pharmacol; 2008 Oct 15; 74(4):1163-9. PubMed ID: 18664604
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  • 13. Identification of domains and amino acids involved in GLuR7 ion channel function.
    Strutz N, Villmann C, Thalhammer A, Kizelsztein P, Eisenstein M, Teichberg VI, Hollmann M.
    J Neurosci; 2001 Jan 15; 21(2):401-11. PubMed ID: 11160421
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  • 16. Pharmacological characterization of a GluR6 kainate receptor in cultured hippocampal neurons.
    Bleakman D, Ogden AM, Ornstein PL, Hoo K.
    Eur J Pharmacol; 1999 Aug 13; 378(3):331-7. PubMed ID: 10493110
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  • 18. Pharmacological characterization of glutamatergic agonists and antagonists at recombinant human homomeric and heteromeric kainate receptors in vitro.
    Alt A, Weiss B, Ogden AM, Knauss JL, Oler J, Ho K, Large TH, Bleakman D.
    Neuropharmacology; 2004 May 13; 46(6):793-806. PubMed ID: 15033339
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  • 19. 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; 2008 Oct 13; 107(2):453-65. PubMed ID: 18710418
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  • 20. Subunit-dependent modulation of kainate receptors by extracellular protons and polyamines.
    Mott DD, Washburn MS, Zhang S, Dingledine RJ.
    J Neurosci; 2003 Feb 15; 23(4):1179-88. PubMed ID: 12598606
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