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Journal Abstract Search

113 related items for PubMed ID: 14996542

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  • 2. Mutations at F637 in the NMDA receptor NR2A subunit M3 domain influence agonist potency, ion channel gating and alcohol action.
    Ren H, Salous AK, Paul JM, Lipsky RH, Peoples RW.
    Br J Pharmacol; 2007 Jul; 151(6):749-57. PubMed ID: 17519952
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  • 4. Structural features of the glutamate binding site in recombinant NR1/NR2A N-methyl-D-aspartate receptors determined by site-directed mutagenesis and molecular modeling.
    Chen PE, Geballe MT, Stansfeld PJ, Johnston AR, Yuan H, Jacob AL, Snyder JP, Traynelis SF, Wyllie DJ.
    Mol Pharmacol; 2005 May; 67(5):1470-84. PubMed ID: 15703381
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  • 5. Molecular determinants of proton-sensitive N-methyl-D-aspartate receptor gating.
    Low CM, Lyuboslavsky P, French A, Le P, Wyatte K, Thiel WH, Marchan EM, Igarashi K, Kashiwagi K, Gernert K, Williams K, Traynelis SF, Zheng F.
    Mol Pharmacol; 2003 Jun; 63(6):1212-22. PubMed ID: 12761330
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  • 7. Site within N-Methyl-D-aspartate receptor pore modulates channel gating.
    Chen N, Li B, Murphy TH, Raymond LA.
    Mol Pharmacol; 2004 Jan; 65(1):157-64. PubMed ID: 14722247
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  • 8. Delineation of additional PSD-95 binding domains within NMDA receptor NR2 subunits reveals differences between NR2A/PSD-95 and NR2B/PSD-95 association.
    Cousins SL, Kenny AV, Stephenson FA.
    Neuroscience; 2009 Jan 12; 158(1):89-95. PubMed ID: 18308477
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  • 10. Two adjacent phenylalanines in the NMDA receptor GluN2A subunit M3 domain interactively regulate alcohol sensitivity and ion channel gating.
    Ren H, Zhao Y, Wu M, Dwyer DS, Peoples RW.
    Neuropharmacology; 2017 Mar 01; 114():20-33. PubMed ID: 27876530
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  • 11. Protein kinase C enhances glycine-insensitive desensitization of NMDA receptors independently of previously identified protein kinase C sites.
    Jackson MF, Konarski JZ, Weerapura M, Czerwinski W, MacDonald JF.
    J Neurochem; 2006 Mar 01; 96(6):1509-18. PubMed ID: 16417568
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  • 12. Equilibrium constants for (R)-[(S)-1-(4-bromo-phenyl)-ethylamino]-(2,3-dioxo-1,2,3,4-tetrahydroquinoxalin-5-yl)-methyl]-phosphonic acid (NVP-AAM077) acting at recombinant NR1/NR2A and NR1/NR2B N-methyl-D-aspartate receptors: Implications for studies of synaptic transmission.
    Frizelle PA, Chen PE, Wyllie DJ.
    Mol Pharmacol; 2006 Sep 01; 70(3):1022-32. PubMed ID: 16778008
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  • 13. Molecular determinants of glycine-independent desensitization of NR1/NR2A receptors.
    Hu B, Zheng F.
    J Pharmacol Exp Ther; 2005 May 01; 313(2):563-9. PubMed ID: 15650113
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  • 14. Effects of amino acid substitutions in transmembrane domains of the NR1 subunit on the ethanol inhibition of recombinant N-methyl-D-aspartate receptors.
    Smothers CT, Woodward JJ.
    Alcohol Clin Exp Res; 2006 Mar 01; 30(3):523-30. PubMed ID: 16499494
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  • 15. The function of the amino terminal domain in NMDA receptor modulation.
    Huggins DJ, Grant GH.
    J Mol Graph Model; 2005 Jan 01; 23(4):381-8. PubMed ID: 15670959
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  • 19. Differential actions of ethanol and trichloroethanol at sites in the M3 and M4 domains of the NMDA receptor GluN2A (NR2A) subunit.
    Salous AK, Ren H, Lamb KA, Hu XQ, Lipsky RH, Peoples RW.
    Br J Pharmacol; 2009 Nov 01; 158(5):1395-404. PubMed ID: 19788495
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  • 20. Inhibition of NMDA-gated ion channels by bis(7)-tacrine: whole-cell and single-channel studies.
    Liu YW, Luo JL, Ren H, Peoples RW, Ai YX, Liu LJ, Pang YP, Li ZW, Han YF, Li CY.
    Neuropharmacology; 2008 Jun 01; 54(7):1086-94. PubMed ID: 18407299
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