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Journal Abstract Search

158 related items for PubMed ID: 24009494

  • 1. Network and atomistic simulations unveil the structural determinants of mutations linked to retinal diseases.
    Mariani S, Dell'Orco D, Felline A, Raimondi F, Fanelli F.
    PLoS Comput Biol; 2013; 9(8):e1003207. PubMed ID: 24009494
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  • 2. A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit.
    Manes G, Cheguru P, Majumder A, Bocquet B, Sénéchal A, Artemyev NO, Hamel CP, Brabet P.
    PLoS One; 2014; 9(4):e95768. PubMed ID: 24760071
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  • 3. Phototransduction in a transgenic mouse model of Nougaret night blindness.
    Moussaif M, Rubin WW, Kerov V, Reh R, Chen D, Lem J, Chen CK, Hurley JB, Burns ME, Artemyev NO.
    J Neurosci; 2006 Jun 21; 26(25):6863-72. PubMed ID: 16793893
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  • 5. Mutation R238E in transducin-alpha yields a GTPase and effector-deficient, but not dominant-negative, G-protein alpha-subunit.
    Barren B, Natochin M, Artemyev NO.
    Mol Vis; 2006 May 12; 12():492-8. PubMed ID: 16735989
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  • 7. Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness.
    Dryja TP, Hahn LB, Reboul T, Arnaud B.
    Nat Genet; 1996 Jul 12; 13(3):358-60. PubMed ID: 8673138
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  • 10. Structural Determinants of Constitutive Activation of Gα Proteins: Transducin as a Paradigm.
    Felline A, Mariani S, Raimondi F, Bellucci L, Fanelli F.
    J Chem Theory Comput; 2017 Feb 14; 13(2):886-899. PubMed ID: 28001387
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  • 12. A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function.
    Peachey NS, Hasan N, FitzMaurice B, Burrill S, Pangeni G, Karst SY, Reinholdt L, Berry ML, Strobel M, Gregg RG, McCall MA, Chang B.
    J Neurophysiol; 2017 Aug 01; 118(2):845-854. PubMed ID: 28490646
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  • 13. The molecular architecture of photoreceptor phosphodiesterase 6 (PDE6) with activated G protein elucidates the mechanism of visual excitation.
    Irwin MJ, Gupta R, Gao XZ, Cahill KB, Chu F, Cote RH.
    J Biol Chem; 2019 Dec 20; 294(51):19486-19497. PubMed ID: 31690623
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  • 17. The retinal cGMP phosphodiesterase gamma-subunit - a chameleon.
    Guo LW, Ruoho AE.
    Curr Protein Pept Sci; 2008 Dec 20; 9(6):611-25. PubMed ID: 19075750
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  • 18. Slowed recovery of rod photoresponse in mice lacking the GTPase accelerating protein RGS9-1.
    Chen CK, Burns ME, He W, Wensel TG, Baylor DA, Simon MI.
    Nature; 2000 Feb 03; 403(6769):557-60. PubMed ID: 10676965
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  • 19. Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness.
    Scalabrino ML, Boye SL, Fransen KM, Noel JM, Dyka FM, Min SH, Ruan Q, De Leeuw CN, Simpson EM, Gregg RG, McCall MA, Peachey NS, Boye SE.
    Hum Mol Genet; 2015 Nov 01; 24(21):6229-39. PubMed ID: 26310623
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  • 20. A Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night Blindness.
    Kondo M, Das G, Imai R, Santana E, Nakashita T, Imawaka M, Ueda K, Ohtsuka H, Sakai K, Aihara T, Kato K, Sugimoto M, Ueno S, Nishizawa Y, Aguirre GD, Miyadera K.
    PLoS One; 2015 Nov 01; 10(9):e0137072. PubMed ID: 26368928
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