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Journal Abstract Search

175 related items for PubMed ID: 17898294

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  • 23. Mouse bestrophin-2 is a bona fide Cl(-) channel: identification of a residue important in anion binding and conduction.
    Qu Z, Fischmeister R, Hartzell C.
    J Gen Physiol; 2004 Apr; 123(4):327-40. PubMed ID: 15051805
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  • 24. Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications.
    Iannaccone A, Kerr NC, Kinnick TR, Calzada JI, Stone EM.
    Arch Ophthalmol; 2011 Feb; 129(2):211-7. PubMed ID: 21320969
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  • 25. The light peak of the electroretinogram is dependent on voltage-gated calcium channels and antagonized by bestrophin (best-1).
    Marmorstein LY, Wu J, McLaughlin P, Yocom J, Karl MO, Neussert R, Wimmers S, Stanton JB, Gregg RG, Strauss O, Peachey NS, Marmorstein AD.
    J Gen Physiol; 2006 May; 127(5):577-89. PubMed ID: 16636205
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  • 30. [Function of bestrophin].
    Strauss O, Rosenthal R.
    Ophthalmologe; 2005 Feb; 102(2):122-6. PubMed ID: 15627200
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  • 31. Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene.
    Eksandh L, Bakall B, Bauer B, Wadelius C, Andréasson S.
    Ophthalmic Genet; 2001 Jun; 22(2):107-15. PubMed ID: 11449320
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  • 33. 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; 29(3):139-44. PubMed ID: 18766995
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  • 34. [Best's disease. Overview of pathology and its causes].
    Lorenz B, Preising MN.
    Ophthalmologe; 2005 Feb; 102(2):111-5. PubMed ID: 15657691
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  • 36. Autosomal Recessive Bestrophinopathy Is Not Associated With the Loss of Bestrophin-1 Anion Channel Function in a Patient With a Novel BEST1 Mutation.
    Johnson AA, Bachman LA, Gilles BJ, Cross SD, Stelzig KE, Resch ZT, Marmorstein LY, Pulido JS, Marmorstein AD.
    Invest Ophthalmol Vis Sci; 2015 Jul; 56(8):4619-30. PubMed ID: 26200502
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  • 39. Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease).
    Marquardt A, Stöhr H, Passmore LA, Krämer F, Rivera A, Weber BH.
    Hum Mol Genet; 1998 Sep; 7(9):1517-25. PubMed ID: 9700209
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  • 40. Suppression of Ca2+ signaling in a mouse model of Best disease.
    Zhang Y, Stanton JB, Wu J, Yu K, Hartzell HC, Peachey NS, Marmorstein LY, Marmorstein AD.
    Hum Mol Genet; 2010 Mar 15; 19(6):1108-18. PubMed ID: 20053664
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