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 *

138 related articles for article (PubMed ID: 9070921)

  • 1. The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A).
    Kelley PM; Weston MD; Chen ZY; Orten DJ; Hasson T; Overbeck LD; Pinnt J; Talmadge CB; Ing P; Mooseker MS; Corey D; Sumegi J; Kimberling WJ
    Genomics; 1997 Feb; 40(1):73-9. PubMed ID: 9070921
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic analysis of a four generation Indian family with Usher syndrome: a novel insertion mutation in MYO7A.
    Kumar A; Babu M; Kimberling WJ; Venkatesh CP
    Mol Vis; 2004 Nov; 10():910-6. PubMed ID: 15592175
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. A sequence-ready map of the Usher syndrome type III critical region on chromosome 3q.
    Joensuu T; Hämäläinen R; Lehesjoki AE; de la Chapelle A; Sankila EM
    Genomics; 2000 Feb; 63(3):409-16. PubMed ID: 10704288
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.
    Bitner-Glindzicz M; Lindley KJ; Rutland P; Blaydon D; Smith VV; Milla PJ; Hussain K; Furth-Lavi J; Cosgrove KE; Shepherd RM; Barnes PD; O'Brien RE; Farndon PA; Sowden J; Liu XZ; Scanlan MJ; Malcolm S; Dunne MJ; Aynsley-Green A; Glaser B
    Nat Genet; 2000 Sep; 26(1):56-60. PubMed ID: 10973248
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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(3):290-1. PubMed ID: 16470552
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
    Yu CE; Oshima J; Hisama FM; Matthews S; Trask BJ; Schellenberg GD
    Genomics; 1996 Aug; 35(3):431-40. PubMed ID: 8812476
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type I.
    Bharadwaj AK; Kasztejna JP; Huq S; Berson EL; Dryja TP
    Exp Eye Res; 2000 Aug; 71(2):173-81. PubMed ID: 10930322
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
    Verpy E; Leibovici M; Zwaenepoel I; Liu XZ; Gal A; Salem N; Mansour A; Blanchard S; Kobayashi I; Keats BJ; Slim R; Petit C
    Nat Genet; 2000 Sep; 26(1):51-5. PubMed ID: 10973247
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel mutations in MYO7A and USH2A in Usher syndrome.
    Maubaret C; Griffoin JM; Arnaud B; Hamel C
    Ophthalmic Genet; 2005 Mar; 26(1):25-9. PubMed ID: 15823922
    [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. 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]  

  • 20. Clinical and genetic linkage analysis of a large Venezuelan kindred with Usher syndrome.
    Keogh IJ; Godinho RN; Wu TP; Diaz de Palacios AM; Palacios N; Bello de Alford M; De Almada MI; MarPalacios N; Vazquez A; Mattei R; Seidman C; Seidman J; Eavey RD
    Int J Pediatr Otorhinolaryngol; 2004 Aug; 68(8):1063-8. PubMed ID: 15236894
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.