These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 9678669)

  • 1. 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]  

  • 2. 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]  

  • 3. Rhodopsin transport in the membrane of the connecting cilium of mammalian photoreceptor cells.
    Wolfrum U; Schmitt A
    Cell Motil Cytoskeleton; 2000 Jun; 46(2):95-107. PubMed ID: 10891855
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Interactions in the network of Usher syndrome type 1 proteins.
    Adato A; Michel V; Kikkawa Y; Reiners J; Alagramam KN; Weil D; Yonekawa H; Wolfrum U; El-Amraoui A; Petit C
    Hum Mol Genet; 2005 Feb; 14(3):347-56. PubMed ID: 15590703
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of DNA elements that modulate myosin VIIA expression in humans.
    Orten DJ; Weston MD; Kelley PM; Cremers CW; Wagenaar M; Jacobson SG; Kimberling WJ
    Hum Mutat; 1999 Oct; 14(4):354. PubMed ID: 10502787
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Erratum: analysis of DNA elements that modulate myosin VIIa expression in humans.
    Orten DJ; Weston MD; Kelley PM; Cremers CW; Wagenaar M; Jacobson SG; Kimberling WJ
    Hum Mutat; 2000 Jan; 15(1):114-5. PubMed ID: 10612833
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Identification of three novel mutations in the MYO7A gene.
    Cuevas JM; Espinós C; Millán JM; Sánchez F; Trujillo MJ; Ayuso C; Beneyto M; Nájera C
    Hum Mutat; 1999 Aug; 14(2):181. PubMed ID: 10447383
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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; 20(1):76-7. PubMed ID: 12112664
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A missense mutation in myosin VIIA prevents aminoglycoside accumulation in early postnatal cochlear hair cells.
    Richardson GP; Forge A; Kros CJ; Marcotti W; Becker D; Williams DS; Thorpe J; Fleming J; Brown SD; Steel KP
    Ann N Y Acad Sci; 1999 Nov; 884():110-24. PubMed ID: 10842588
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ala397Asp mutation of myosin VIIA gene segregating in a Spanish family with type-Ib Usher syndrome.
    Espinós C; Millán JM; Sánchez F; Beneyto M; Nájera C
    Hum Genet; 1998 Jun; 102(6):691-4. PubMed ID: 9703432
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation.
    Tamagawa Y; Ishikawa K; Ishikawa K; Ishida T; Kitamura K; Makino S; Tsuru T; Ichimura K
    Laryngoscope; 2002 Feb; 112(2):292-7. PubMed ID: 11889386
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.