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PUBMED FOR HANDHELDS

Journal Abstract Search


241 related items for PubMed ID: 15897456

  • 1. A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.
    Hemara-Wahanui A, Berjukow S, Hope CI, Dearden PK, Wu SB, Wilson-Wheeler J, Sharp DM, Lundon-Treweek P, Clover GM, Hoda JC, Striessnig J, Marksteiner R, Hering S, Maw MA.
    Proc Natl Acad Sci U S A; 2005 May 24; 102(21):7553-8. PubMed ID: 15897456
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  • 2. Clinical manifestations of a unique X-linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2.
    Hope CI, Sharp DM, Hemara-Wahanui A, Sissingh JI, Lundon P, Mitchell EA, Maw MA, Clover GM.
    Clin Exp Ophthalmol; 2005 Apr 24; 33(2):129-36. PubMed ID: 15807819
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  • 3. Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2.
    Regus-Leidig H, Atorf J, Feigenspan A, Kremers J, Maw MA, Brandstätter JH.
    PLoS One; 2014 Apr 24; 9(1):e86769. PubMed ID: 24466230
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  • 8. Congenital stationary night blindness type 2 mutations S229P, G369D, L1068P, and W1440X alter channel gating or functional expression of Ca(v)1.4 L-type Ca2+ channels.
    Hoda JC, Zaghetto F, Koschak A, Striessnig J.
    J Neurosci; 2005 Jan 05; 25(1):252-9. PubMed ID: 15634789
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  • 9. A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness.
    Jacobi FK, Hamel CP, Arnaud B, Blin N, Broghammer M, Jacobi PC, Apfelstedt-Sylla E, Pusch CM.
    Am J Ophthalmol; 2003 May 05; 135(5):733-6. PubMed ID: 12719097
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  • 11. The Ca(v)1.4 calcium channel: more than meets the eye.
    Doering CJ, Peloquin JB, McRory JE.
    Channels (Austin); 2007 May 05; 1(1):3-10. PubMed ID: 19151588
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  • 16. Cacna1f gene decreased contractility of skeletal muscle in rat model with congenital stationary night blindness.
    An J, Zhang L, Jiao B, Lu F, Xia F, Yu Z, Zhang Z.
    Gene; 2015 May 15; 562(2):210-9. PubMed ID: 25748727
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  • 17. Cav1.4 dysfunction and congenital stationary night blindness type 2.
    Koschak A, Fernandez-Quintero ML, Heigl T, Ruzza M, Seitter H, Zanetti L.
    Pflugers Arch; 2021 Sep 15; 473(9):1437-1454. PubMed ID: 34212239
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