Literature DB >> 11120747

A genetic approach to understanding inner ear function.

J F Battey1.   

Abstract

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Year:  2000        PMID: 11120747      PMCID: PMC381476          DOI: 10.1172/JCI11763

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


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  16 in total

1.  Perspectives: biomedicine. The benefits of recycling.

Authors:  K P Steel
Journal:  Science       Date:  1999-08-27       Impact factor: 47.728

2.  Prestin is the motor protein of cochlear outer hair cells.

Authors:  J Zheng; W Shen; D Z He; K B Long; L D Madison; P Dallos
Journal:  Nature       Date:  2000-05-11       Impact factor: 49.962

3.  Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

Authors:  A Wang; Y Liang; R A Fridell; F J Probst; E R Wilcox; J W Touchman; C C Morton; R J Morell; K Noben-Trauth; S A Camper; T B Friedman
Journal:  Science       Date:  1998-05-29       Impact factor: 47.728

4.  Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

Authors:  F J Probst; R A Fridell; Y Raphael; T L Saunders; A Wang; Y Liang; R J Morell; J W Touchman; R H Lyons; K Noben-Trauth; T B Friedman; S A Camper
Journal:  Science       Date:  1998-05-29       Impact factor: 47.728

5.  Inner ear defects induced by null mutation of the isk gene.

Authors:  D E Vetter; J R Mann; P Wangemann; J Liu; K J McLaughlin; F Lesage; D C Marcus; M Lazdunski; S F Heinemann; J Barhanin
Journal:  Neuron       Date:  1996-12       Impact factor: 17.173

6.  Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9.

Authors:  N G Robertson; A B Skvorak; Y Yin; S Weremowicz; K R Johnson; K A Kovatch; J F Battey; F R Bieber; C C Morton
Journal:  Genomics       Date:  1997-12-15       Impact factor: 5.736

7.  A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.

Authors:  N Neyroud; F Tesson; I Denjoy; M Leibovici; C Donger; J Barhanin; S Fauré; F Gary; P Coumel; C Petit; K Schwartz; P Guicheney
Journal:  Nat Genet       Date:  1997-02       Impact factor: 38.330

8.  Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice.

Authors:  M P Lee; J D Ravenel; R J Hu; L R Lustig; G Tomaselli; R D Berger; S A Brandenburg; T J Litzi; T E Bunton; C Limb; H Francis; M Gorelikow; H Gu; K Washington; P Argani; J R Goldenring; R J Coffey; A P Feinberg
Journal:  J Clin Invest       Date:  2000-12       Impact factor: 14.808

9.  Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness.

Authors:  R J Morell; H J Kim; L J Hood; L Goforth; K Friderici; R Fisher; G Van Camp; C I Berlin; C Oddoux; H Ostrer; B Keats; T B Friedman
Journal:  N Engl J Med       Date:  1998-11-19       Impact factor: 91.245

10.  Connexin-26 mutations in sporadic and inherited sensorineural deafness.

Authors:  X Estivill; P Fortina; S Surrey; R Rabionet; S Melchionda; L D'Agruma; E Mansfield; E Rappaport; N Govea; M Milà; L Zelante; P Gasparini
Journal:  Lancet       Date:  1998-02-07       Impact factor: 79.321

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