BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

364 related articles for article (PubMed ID: 7568224)

  • 1. Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B.
    Hasson T; Heintzelman MB; Santos-Sacchi J; Corey DP; Mooseker MS
    Proc Natl Acad Sci U S A; 1995 Oct; 92(21):9815-9. PubMed ID: 7568224
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation analysis of the mouse myosin VIIA deafness gene.
    Mburu P; Liu XZ; Walsh J; Saw D; Cope MJ; Gibson F; Kendrick-Jones J; Steel KP; Brown SD
    Genes Funct; 1997 Jun; 1(3):191-203. PubMed ID: 9680294
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia.
    Weil D; Levy G; Sahly I; Levi-Acobas F; Blanchard S; El-Amraoui A; Crozet F; Philippe H; Abitbol M; Petit C
    Proc Natl Acad Sci U S A; 1996 Apr; 93(8):3232-7. PubMed ID: 8622919
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 374(6517):60-1. PubMed ID: 7870171
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression.
    Hasson T; Walsh J; Cable J; Mooseker MS; Brown SD; Steel KP
    Cell Motil Cytoskeleton; 1997; 37(2):127-38. PubMed ID: 9186010
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Myosin VIIa, the product of the Usher 1B syndrome gene, is concentrated in the connecting cilia of photoreceptor cells.
    Liu X; Vansant G; Udovichenko IP; Wolfrum U; Williams DS
    Cell Motil Cytoskeleton; 1997; 37(3):240-52. PubMed ID: 9227854
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B.
    Chen ZY; Hasson T; Kelley PM; Schwender BJ; Schwartz MF; Ramakrishnan M; Kimberling WJ; Mooseker MS; Corey DP
    Genomics; 1996 Sep; 36(3):440-8. PubMed ID: 8884267
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A human homologue of Drosophila kelch associates with myosin-VIIa in specialized adhesion junctions.
    Velichkova M; Guttman J; Warren C; Eng L; Kline K; Vogl AW; Hasson T
    Cell Motil Cytoskeleton; 2002 Mar; 51(3):147-64. PubMed ID: 11921171
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expression of myosin VIIA during mouse embryogenesis.
    Sahly I; El-Amraoui A; Abitbol M; Petit C; Dufier JL
    Anat Embryol (Berl); 1997 Aug; 196(2):159-70. PubMed ID: 9278160
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 16(2):191-3. PubMed ID: 9171833
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myosin VIIA gene: heterogeneity of the mutations responsible for Usher syndrome type IB.
    Lévy G; Levi-Acobas F; Blanchard S; Gerber S; Larget-Piet D; Chenal V; Liu XZ; Newton V; Steel KP; Brown SD; Munnich A; Kaplan J; Petit C; Weil D
    Hum Mol Genet; 1997 Jan; 6(1):111-6. PubMed ID: 9002678
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Myosin VIIa as a common component of cilia and microvilli.
    Wolfrum U; Liu X; Schmitt A; Udovichenko IP; Williams DS
    Cell Motil Cytoskeleton; 1998; 40(3):261-71. PubMed ID: 9678669
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness.
    Ernest S; Rauch GJ; Haffter P; Geisler R; Petit C; Nicolson T
    Hum Mol Genet; 2000 Sep; 9(14):2189-96. PubMed ID: 10958658
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.
    Liu XZ; Walsh J; Mburu P; Kendrick-Jones J; Cope MJ; Steel KP; Brown SD
    Nat Genet; 1997 Jun; 16(2):188-90. PubMed ID: 9171832
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease.
    Reiners J; Nagel-Wolfrum K; Jürgens K; Märker T; Wolfrum U
    Exp Eye Res; 2006 Jul; 83(1):97-119. PubMed ID: 16545802
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular motors: sensing a function for myosin-VIIa.
    Hasson T
    Curr Biol; 1999 Nov; 9(22):R838-41. PubMed ID: 10574757
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
    Riazuddin S; Nazli S; Ahmed ZM; Yang Y; Zulfiqar F; Shaikh RS; Zafar AU; Khan SN; Sabar F; Javid FT; Wilcox ER; Tsilou E; Boger ET; Sellers JR; Belyantseva IA; Riazuddin S; Friedman TB
    Hum Mutat; 2008 Apr; 29(4):502-11. PubMed ID: 18181211
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel myosin VI isoform is abundantly expressed in retina.
    Breckler J; Au K; Cheng J; Hasson T; Burnside B
    Exp Eye Res; 2000 Jan; 70(1):121-34. PubMed ID: 10644428
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome type I: confirmation of genetic heterogeneity.
    Janecke AR; Meins M; Sadeghi M; Grundmann K; Apfelstedt-Sylla E; Zrenner E; Rosenberg T; Gal A
    Hum Mutat; 1999; 13(2):133-40. PubMed ID: 10094549
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.