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Journal Abstract Search

121 related items for PubMed ID: 15180258

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  • 2. Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B.
    Libby RT, Steel KP.
    Invest Ophthalmol Vis Sci; 2001 Mar; 42(3):770-8. PubMed ID: 11222540
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  • 5. Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells.
    el-Amraoui A, Sahly I, Picaud S, Sahel J, Abitbol M, Petit C.
    Hum Mol Genet; 1996 Aug; 5(8):1171-8. PubMed ID: 8842737
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  • 6. Defective myosin VIIA gene responsible for Usher syndrome type 1B.
    Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD.
    Nature; 1995 Mar 02; 374(6517):60-1. PubMed ID: 7870171
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  • 9. Mutations in myosin VIIA (MYO7A) and usherin (USH2A) in Spanish patients with Usher syndrome types I and II, respectively.
    Nájera C, Beneyto M, Blanca J, Aller E, Fontcuberta A, Millán JM, Ayuso C.
    Hum Mutat; 2002 Jul 02; 20(1):76-7. PubMed ID: 12112664
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  • 14. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene.
    Weil D, Küssel P, Blanchard S, Lévy G, Levi-Acobas F, Drira M, Ayadi H, Petit C.
    Nat Genet; 1997 Jun 02; 16(2):191-3. PubMed ID: 9171833
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  • 19. Abnormal phagocytosis by retinal pigmented epithelium that lacks myosin VIIa, the Usher syndrome 1B protein.
    Gibbs D, Kitamoto J, Williams DS.
    Proc Natl Acad Sci U S A; 2003 May 27; 100(11):6481-6. PubMed ID: 12743369
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  • 20. Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type I.
    Jaijo T, Aller E, Oltra S, Beneyto M, Nájera C, Ayuso C, Baiget M, Carballo M, Antiñolo G, Valverde D, Moreno F, Vilela C, Perez-Garrigues H, Navea A, Millán JM.
    Hum Mutat; 2006 Mar 27; 27(3):290-1. PubMed ID: 16470552
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