Literature DB >> 9770442

Identifying the genes of hearing, deafness, and dysequilibrium.

J T Corwin1.   

Abstract

Entities:  

Mesh:

Year:  1998        PMID: 9770442      PMCID: PMC33905          DOI: 10.1073/pnas.95.21.12080

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


× No keyword cloud information.
  32 in total

1.  Identification of mutations in the COL4A5 collagen gene in Alport syndrome.

Authors:  D F Barker; S L Hostikka; J Zhou; L T Chow; A R Oliphant; S C Gerken; M C Gregory; M H Skolnick; C L Atkin; K Tryggvason
Journal:  Science       Date:  1990-06-08       Impact factor: 47.728

Review 2.  Genetic epidemiology of hearing impairment.

Authors:  N E Morton
Journal:  Ann N Y Acad Sci       Date:  1991       Impact factor: 5.691

3.  Molecular markers for cell types of the inner ear and candidate genes for hearing disorders.

Authors:  S Heller; C A Sheane; Z Javed; A J Hudspeth
Journal:  Proc Natl Acad Sci U S A       Date:  1998-09-15       Impact factor: 11.205

4.  Hair cell distributions in the normal human cochlea.

Authors:  A Wright; A Davis; G Bredberg; L Ulehlova; H Spencer
Journal:  Acta Otolaryngol Suppl       Date:  1987

Review 5.  Hearing loss.

Authors:  J B Nadol
Journal:  N Engl J Med       Date:  1993-10-07       Impact factor: 91.245

6.  Defective myosin VIIA gene responsible for Usher syndrome type 1B.

Authors:  D Weil; S Blanchard; J Kaplan; P Guilford; F Gibson; J Walsh; P Mburu; A Varela; J Levilliers; M D Weston
Journal:  Nature       Date:  1995-03-02       Impact factor: 49.962

7.  Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness.

Authors:  T R Prezant; J V Agapian; M C Bohlman; X Bu; S Oztas; W Q Qiu; K S Arnos; G A Cortopassi; L Jaber; J I Rotter
Journal:  Nat Genet       Date:  1993-07       Impact factor: 38.330

8.  Brain-derived neurotrophic factor and neurotrophin 3 mRNAs in the peripheral target fields of developing inner ear ganglia.

Authors:  U Pirvola; J Ylikoski; J Palgi; E Lehtonen; U Arumäe; M Saarma
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-15       Impact factor: 11.205

9.  Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene.

Authors:  M Tassabehji; A P Read; V E Newton; R Harris; R Balling; P Gruss; T Strachan
Journal:  Nature       Date:  1992-02-13       Impact factor: 49.962

10.  Mice homozygous for a targeted disruption of the proto-oncogene int-2 have developmental defects in the tail and inner ear.

Authors:  S L Mansour; J M Goddard; M R Capecchi
Journal:  Development       Date:  1993-01       Impact factor: 6.868

View more
  1 in total

1.  Identification of genes expressed in the Xenopus inner ear.

Authors:  E E Serrano; C Trujillo-Provencio; D R Sultemeier; W M Bullock; Q A Quick
Journal:  Cell Mol Biol (Noisy-le-grand)       Date:  2001-11       Impact factor: 1.770

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.