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Journal Abstract Search

175 related items for PubMed ID: 17898294

  • 1. Chloride channel activity of bestrophin mutants associated with mild or late-onset macular degeneration.
    Yu K, Qu Z, Cui Y, Hartzell HC.
    Invest Ophthalmol Vis Sci; 2007 Oct; 48(10):4694-705. PubMed ID: 17898294
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  • 2. The bestrophin mutation A243V, linked to adult-onset vitelliform macular dystrophy, impairs its chloride channel function.
    Yu K, Cui Y, Hartzell HC.
    Invest Ophthalmol Vis Sci; 2006 Nov; 47(11):4956-61. PubMed ID: 17065513
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  • 4. The best disease-linked Cl- channel hBest1 regulates Ca V 1 (L-type) Ca2+ channels via src-homology-binding domains.
    Yu K, Xiao Q, Cui G, Lee A, Hartzell HC.
    J Neurosci; 2008 May 28; 28(22):5660-70. PubMed ID: 18509027
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  • 5. Bestrophins and retinopathies.
    Xiao Q, Hartzell HC, Yu K.
    Pflugers Arch; 2010 Jul 28; 460(2):559-69. PubMed ID: 20349192
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  • 6. Human disease-causing mutations disrupt an N-C-terminal interaction and channel function of bestrophin 1.
    Qu Z, Cheng W, Cui Y, Cui Y, Zheng J.
    J Biol Chem; 2009 Jun 12; 284(24):16473-16481. PubMed ID: 19372599
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  • 7. Assessment of mutations in the Best macular dystrophy (VMD2) gene in patients with adult-onset foveomacular vitelliform dystrophy, age-related maculopathy, and bull's-eye maculopathy.
    Seddon JM, Afshari MA, Sharma S, Bernstein PS, Chong S, Hutchinson A, Petrukhin K, Allikmets R.
    Ophthalmology; 2001 Nov 12; 108(11):2060-7. PubMed ID: 11713080
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  • 10. Bestrophin-1 influences transepithelial electrical properties and Ca2+ signaling in human retinal pigment epithelium.
    Marmorstein AD, Kinnick TR, Stanton JB, Johnson AA, Lynch RM, Marmorstein LY.
    Mol Vis; 2015 Nov 12; 21():347-59. PubMed ID: 25878489
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  • 11. Volume sensitivity of the bestrophin family of chloride channels.
    Fischmeister R, Hartzell HC.
    J Physiol; 2005 Jan 15; 562(Pt 2):477-91. PubMed ID: 15564283
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  • 12. Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration.
    Krämer F, White K, Pauleikhoff D, Gehrig A, Passmore L, Rivera A, Rudolph G, Kellner U, Andrassi M, Lorenz B, Rohrschneider K, Blankenagel A, Jurklies B, Schilling H, Schütt F, Holz FG, Weber BH.
    Eur J Hum Genet; 2000 Apr 15; 8(4):286-92. PubMed ID: 10854112
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  • 13. Late onset is common in best macular dystrophy associated with VMD2 gene mutations.
    Renner AB, Tillack H, Kraus H, Krämer F, Mohr N, Weber BH, Foerster MH, Kellner U.
    Ophthalmology; 2005 Apr 15; 112(4):586-92. PubMed ID: 15808248
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  • 14. A model of best vitelliform macular dystrophy in rats.
    Marmorstein AD, Stanton JB, Yocom J, Bakall B, Schiavone MT, Wadelius C, Marmorstein LY, Peachey NS.
    Invest Ophthalmol Vis Sci; 2004 Oct 15; 45(10):3733-9. PubMed ID: 15452084
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  • 15. Regulation of bestrophin Cl channels by calcium: role of the C terminus.
    Xiao Q, Prussia A, Yu K, Cui YY, Hartzell HC.
    J Gen Physiol; 2008 Dec 15; 132(6):681-92. PubMed ID: 19029375
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  • 16. Clinical expression of Best's vitelliform macular dystrophy in Swedish families with mutations in the bestrophin gene.
    Ponjavic V, Eksandh L, Andréasson S, Sjöström K, Bakall B, Ingvast S, Wadelius C, Ehinger B.
    Ophthalmic Genet; 1999 Dec 15; 20(4):251-7. PubMed ID: 10617923
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  • 17. Functional assembly and purinergic activation of bestrophins.
    Milenkovic VM, Soria RB, Aldehni F, Schreiber R, Kunzelmann K.
    Pflugers Arch; 2009 Jun 15; 458(2):431-41. PubMed ID: 19130075
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  • 18. Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium.
    Marmorstein AD, Marmorstein LY, Rayborn M, Wang X, Hollyfield JG, Petrukhin K.
    Proc Natl Acad Sci U S A; 2000 Nov 07; 97(23):12758-63. PubMed ID: 11050159
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  • 19. VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies.
    White K, Marquardt A, Weber BH.
    Hum Mutat; 2000 Nov 07; 15(4):301-8. PubMed ID: 10737974
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  • 20. Novel BEST1 Mutations and Special Clinical Features of Best Vitelliform Macular Dystrophy.
    Liu J, Zhang Y, Xuan Y, Liu W, Wang M.
    Ophthalmic Res; 2016 Nov 07; 56(4):178-185. PubMed ID: 27078032
    [Abstract] [Full Text] [Related]

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