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 *

148 related articles for article (PubMed ID: 9718356)

  • 21. 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]  

  • 22. 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]  

  • 23. [Usher syndrome and possible heredity linked to X chromosome].
    Baldellou Vázquez A; Navarro Zapata C; Albalad Cebrian E; Mateo Blanco A
    An Esp Pediatr; 1993 Nov; 39(5):462-4. PubMed ID: 8285470
    [No Abstract]   [Full Text] [Related]  

  • 24. Identification of a new mutation of the myosin VII head region in Usher syndrome type 1.
    Liu XZ; Newton VE; Steel KP; Brown SD
    Hum Mutat; 1997; 10(2):168-70. PubMed ID: 9259201
    [No Abstract]   [Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation.
    Liu XZ; Hope C; Liang CY; Zou JM; Xu LR; Cole T; Mueller RF; Bundey S; Nance W; Steel KP; Brown SD
    Am J Hum Genet; 1999 Apr; 64(4):1221-5. PubMed ID: 10090909
    [No Abstract]   [Full Text] [Related]  

  • 30. Genetic heterogeneity of Usher syndrome.
    Kimberling WJ; Orten D; Pieke-Dahl S
    Adv Otorhinolaryngol; 2000; 56():11-8. PubMed ID: 10868209
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mouse models for Usher syndrome 1B.
    Lillo C; Kitamoto J; Liu X; Quint E; Steel KP; Williams DS
    Adv Exp Med Biol; 2003; 533():143-50. PubMed ID: 15180258
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. 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]  

  • 34. Schizophrenia and mental retardation associated in a pedigree with retinitis pigmentosa and sensorineural deafness.
    Sharp CW; Muir WJ; Blackwood DH; Walker M; Gosden C; St Clair DM
    Am J Med Genet; 1994 Dec; 54(4):354-60. PubMed ID: 7726208
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.
    Ebermann I; Scholl HP; Charbel Issa P; Becirovic E; Lamprecht J; Jurklies B; Millán JM; Aller E; Mitter D; Bolz H
    Hum Genet; 2007 Apr; 121(2):203-11. PubMed ID: 17171570
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis.
    Zwaenepoel I; Verpy E; Blanchard S; Meins M; Apfelstedt-Sylla E; Gal A; Petit C
    Hum Mutat; 2001; 17(1):34-41. PubMed ID: 11139240
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Unconventional myosins and the genetics of hearing loss.
    Friedman TB; Sellers JR; Avraham KB
    Am J Med Genet; 1999 Sep; 89(3):147-57. PubMed ID: 10704189
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome.
    Ben-Yosef T; Ness SL; Madeo AC; Bar-Lev A; Wolfman JH; Ahmed ZM; Desnick RJ; Willner JP; Avraham KB; Ostrer H; Oddoux C; Griffith AJ; Friedman TB
    N Engl J Med; 2003 Apr; 348(17):1664-70. PubMed ID: 12711741
    [No Abstract]   [Full Text] [Related]  

  • 39. RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections.
    Zito I; Downes SM; Patel RJ; Cheetham ME; Ebenezer ND; Jenkins SA; Bhattacharya SS; Webster AR; Holder GE; Bird AC; Bamiou DE; Hardcastle AJ
    J Med Genet; 2003 Aug; 40(8):609-15. PubMed ID: 12920075
    [No Abstract]   [Full Text] [Related]  

  • 40. Usher syndrome: from genetics to pathogenesis.
    Petit C
    Annu Rev Genomics Hum Genet; 2001; 2():271-97. PubMed ID: 11701652
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.