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Journal Abstract Search

267 related items for PubMed ID: 23552282

  • 21. Structural and functional characterization of an achromatopsia-associated mutation in a phototransduction channel.
    Zheng X, Li H, Hu Z, Su D, Yang J.
    Commun Biol; 2022 Mar 01; 5(1):190. PubMed ID: 35233102
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  • 25. Loss of cone cyclic nucleotide-gated channel leads to alterations in light response modulating system and cellular stress response pathways: a gene expression profiling study.
    Ma H, Thapa A, Morris LM, Michalakis S, Biel M, Frank MB, Bebak M, Ding XQ.
    Hum Mol Genet; 2013 Oct 01; 22(19):3906-19. PubMed ID: 23740940
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  • 26. The B3 Subunit of the Cone Cyclic Nucleotide-gated Channel Regulates the Light Responses of Cones and Contributes to the Channel Structural Flexibility.
    Ding XQ, Thapa A, Ma H, Xu J, Elliott MH, Rodgers KK, Smith ML, Wang JS, Pittler SJ, Kefalov VJ.
    J Biol Chem; 2016 Apr 15; 291(16):8721-34. PubMed ID: 26893377
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  • 27. Regulation of human cone cyclic nucleotide-gated channels by endogenous phospholipids and exogenously applied phosphatidylinositol 3,4,5-trisphosphate.
    Bright SR, Rich ED, Varnum MD.
    Mol Pharmacol; 2007 Jan 15; 71(1):176-83. PubMed ID: 17018579
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  • 30. Endoplasmic reticulum stress-associated cone photoreceptor degeneration in cyclic nucleotide-gated channel deficiency.
    Thapa A, Morris L, Xu J, Ma H, Michalakis S, Biel M, Ding XQ.
    J Biol Chem; 2012 May 25; 287(22):18018-29. PubMed ID: 22493484
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  • 32. Impaired cone function and cone degeneration resulting from CNGB3 deficiency: down-regulation of CNGA3 biosynthesis as a potential mechanism.
    Ding XQ, Harry CS, Umino Y, Matveev AV, Fliesler SJ, Barlow RB.
    Hum Mol Genet; 2009 Dec 15; 18(24):4770-80. PubMed ID: 19767295
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  • 34. Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.
    Kohl S, Baumann B, Broghammer M, Jägle H, Sieving P, Kellner U, Spegal R, Anastasi M, Zrenner E, Sharpe LT, Wissinger B.
    Hum Mol Genet; 2000 Sep 01; 9(14):2107-16. PubMed ID: 10958649
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  • 35. Mouse Models of Achromatopsia in Addressing Temporal "Point of No Return" in Gene-Therapy.
    Wang NK, Liu PK, Kong Y, Levi SR, Huang WC, Hsu CW, Wang HH, Chen N, Tseng YJ, Quinn PMJ, Tai MH, Lin CS, Tsang SH.
    Int J Mol Sci; 2021 Jul 28; 22(15):. PubMed ID: 34360834
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  • 36. Potential contribution of ryanodine receptor 2 upregulation to cGMP/PKG signaling-induced cone degeneration in cyclic nucleotide-gated channel deficiency.
    Yang F, Ma H, Butler MR, Ding XQ.
    FASEB J; 2020 May 28; 34(5):6335-6350. PubMed ID: 32173907
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  • 39. Ryanodine Receptor 2 Contributes to Impaired Protein Localization in Cyclic Nucleotide-Gated Channel Deficiency.
    Ma H, Yang F, Butler MR, Rapp J, Le YZ, Ding XQ.
    eNeuro; 2019 May 28; 6(3):. PubMed ID: 31182474
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