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Journal Abstract Search

204 related items for PubMed ID: 21955162

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  • 5. Propofol restores the function of "hyperekplexic" mutant glycine receptors in Xenopus oocytes and mice.
    O'Shea SM, Becker L, Weiher H, Betz H, Laube B.
    J Neurosci; 2004 Mar 03; 24(9):2322-7. PubMed ID: 14999083
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  • 6. Correlating structural and energetic changes in glycine receptor activation.
    Scott S, Lynch JW, Keramidas A.
    J Biol Chem; 2015 Feb 27; 290(9):5621-34. PubMed ID: 25572390
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  • 7. Pair of Residue Substitutions at the Outer Mouth of the Channel Pore Act as Inputs for a Boolean Logic "OR" Gate Based on the Glycine Receptor.
    Han L, Shan Q.
    ACS Chem Neurosci; 2020 Oct 21; 11(20):3409-3417. PubMed ID: 32970400
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  • 8. Novel GLRA1 missense mutation (P250T) in dominant hyperekplexia defines an intracellular determinant of glycine receptor channel gating.
    Saul B, Kuner T, Sobetzko D, Brune W, Hanefeld F, Meinck HM, Becker CM.
    J Neurosci; 1999 Feb 01; 19(3):869-77. PubMed ID: 9920650
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  • 9. Murine startle mutant Nmf11 affects the structural stability of the glycine receptor and increases deactivation.
    Wilkins ME, Caley A, Gielen MC, Harvey RJ, Smart TG.
    J Physiol; 2016 Jul 01; 594(13):3589-607. PubMed ID: 27028707
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  • 10. Charged residues at the pore extracellular half of the glycine receptor facilitate channel gating: a potential role played by electrostatic repulsion.
    Tian Y, Chen S, Shan Q.
    J Physiol; 2020 Oct 01; 598(20):4643-4661. PubMed ID: 32844405
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  • 11. New hyperekplexia mutations provide insight into glycine receptor assembly, trafficking, and activation mechanisms.
    Bode A, Wood SE, Mullins JGL, Keramidas A, Cushion TD, Thomas RH, Pickrell WO, Drew CJG, Masri A, Jones EA, Vassallo G, Born AP, Alehan F, Aharoni S, Bannasch G, Bartsch M, Kara B, Krause A, Karam EG, Matta S, Jain V, Mandel H, Freilinger M, Graham GE, Hobson E, Chatfield S, Vincent-Delorme C, Rahme JE, Afawi Z, Berkovic SF, Howell OW, Vanbellinghen JF, Rees MI, Chung SK, Lynch JW.
    J Biol Chem; 2013 Nov 22; 288(47):33745-33759. PubMed ID: 24108130
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  • 12. Effects of a mutation in the TM2-TM3 linker region of the glycine receptor alpha1 subunit on gating and allosteric modulation.
    Dupre ML, Broyles JM, Mihic SJ.
    Brain Res; 2007 Jun 04; 1152():1-9. PubMed ID: 17434460
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  • 15. Different Behaviors of a Glycine Receptor Channel Pore Residue between Wild-Type-Mimicking and Disease-Type-Mimicking Formats.
    Han L, Shan Q.
    ACS Chem Neurosci; 2021 Sep 15; 12(18):3397-3409. PubMed ID: 34460217
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  • 16. The basic property of Lys385 is important for potentiation of the human α1 glycine receptor by ethanol.
    Castro PA, Figueroa M, Yevenes GE, San Martin LS, Aguayo LG.
    J Pharmacol Exp Ther; 2012 Feb 15; 340(2):339-49. PubMed ID: 22040678
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  • 17. Recessive hyperekplexia mutations of the glycine receptor alpha1 subunit affect cell surface integration and stability.
    Villmann C, Oertel J, Melzer N, Becker CM.
    J Neurochem; 2009 Nov 15; 111(3):837-47. PubMed ID: 19732286
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  • 19. A novel hyperekplexia-causing mutation in the pre-transmembrane segment 1 of the human glycine receptor alpha1 subunit reduces membrane expression and impairs gating by agonists.
    Castaldo P, Stefanoni P, Miceli F, Coppola G, Del Giudice EM, Bellini G, Pascotto A, Trudell JR, Harrison NL, Annunziato L, Taglialatela M.
    J Biol Chem; 2004 Jun 11; 279(24):25598-604. PubMed ID: 15066993
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  • 20. Ligand-specific conformational changes in the alpha1 glycine receptor ligand-binding domain.
    Pless SA, Lynch JW.
    J Biol Chem; 2009 Jun 05; 284(23):15847-56. PubMed ID: 19286654
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