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Journal Abstract Search

225 related items for PubMed ID: 17591911

  • 1. Differential macular and peripheral expression of bestrophin in human eyes and its implication for best disease.
    Mullins RF, Kuehn MH, Faidley EA, Syed NA, Stone EM.
    Invest Ophthalmol Vis Sci; 2007 Jul; 48(7):3372-80. PubMed ID: 17591911
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  • 2. Functional characterization of bestrophin-1 missense mutations associated with autosomal recessive bestrophinopathy.
    Davidson AE, Millar ID, Burgess-Mullan R, Maher GJ, Urquhart JE, Brown PD, Black GC, Manson FD.
    Invest Ophthalmol Vis Sci; 2011 Jun 01; 52(6):3730-6. PubMed ID: 21330666
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  • 3. High-definition optical coherence tomography features in vitelliform macular dystrophy.
    Querques G, Regenbogen M, Quijano C, Delphin N, Soubrane G, Souied EH.
    Am J Ophthalmol; 2008 Oct 01; 146(4):501-507. PubMed ID: 18619572
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  • 4. Deposition of exon-skipping splice isoform of human retinal G protein-coupled receptor from retinal pigment epithelium into Bruch's membrane.
    Lin MY, Kochounian H, Moore RE, Lee TD, Rao N, Fong HK.
    Mol Vis; 2007 Jul 19; 13():1203-14. PubMed ID: 17679941
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  • 5. 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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  • 6. Indocyanine green angiography abnormality of the periphery in vitelliform macular dystrophy.
    Maruko I, Iida T, Spaide RF, Kishi S.
    Am J Ophthalmol; 2006 May 07; 141(5):976-8. PubMed ID: 16678528
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  • 8. The role of bestrophin in airway epithelial ion transport.
    Duta V, Szkotak AJ, Nahirney D, Duszyk M.
    FEBS Lett; 2004 Nov 19; 577(3):551-4. PubMed ID: 15556645
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  • 9. Variant phenotype of Best vitelliform macular dystrophy associated with compound heterozygous mutations in VMD2.
    Schatz P, Klar J, Andréasson S, Ponjavic V, Dahl N.
    Ophthalmic Genet; 2006 Jun 19; 27(2):51-6. PubMed ID: 16754206
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  • 11. Late-onset macular degeneration and long anterior lens zonules result from a CTRP5 gene mutation.
    Ayyagari R, Mandal MN, Karoukis AJ, Chen L, McLaren NC, Lichter M, Wong DT, Hitchcock PF, Caruso RC, Moroi SE, Maumenee IH, Sieving PA.
    Invest Ophthalmol Vis Sci; 2005 Sep 19; 46(9):3363-71. PubMed ID: 16123441
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  • 12. Mutation analysis of the VMD2 gene in thai families with best macular dystrophy.
    Atchaneeyasakul LO, Jinda W, Sakolsatayadorn N, Trinavarat A, Ruangvoravate N, Thanasombatskul N, Thongnoppakhun W, Limwongse C.
    Ophthalmic Genet; 2008 Sep 19; 29(3):139-44. PubMed ID: 18766995
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  • 13. Looking chloride channels straight in the eye: bestrophins, lipofuscinosis, and retinal degeneration.
    Hartzell C, Qu Z, Putzier I, Artinian L, Chien LT, Cui Y.
    Physiology (Bethesda); 2005 Oct 19; 20():292-302. PubMed ID: 16174869
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  • 16. Novel retinal and cone photoreceptor transcripts revealed by human macular expression profiling.
    Hornan DM, Peirson SN, Hardcastle AJ, Molday RS, Cheetham ME, Webster AR.
    Invest Ophthalmol Vis Sci; 2007 Dec 19; 48(12):5388-96. PubMed ID: 18055785
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  • 18. Similarity of mRNA phenotypes of morphologically normal macular and peripheral retinal pigment epithelial cells in older human eyes.
    Ishibashi K, Tian J, Handa JT.
    Invest Ophthalmol Vis Sci; 2004 Sep 19; 45(9):3291-301. PubMed ID: 15326154
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  • 19. 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 19; 47(11):4956-61. PubMed ID: 17065513
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