Literature DB >> 12223317

Mouse models for human deafness: current tools for new fashions.

Nadav Ahituv1, Karen B Avraham.   

Abstract

Mouse models are one of the major tools used for discovery and characterization of genes for non-syndromic deafness in humans. The similarities between the mouse and human genomes, and between the physiology and morphology of their auditory systems, are striking. This article describes the latest mouse models, including spontaneous, 'knockout' and ENU (N-ethyl-N-nitrosourea)-induced mutants, and the recent discovery of modifier genes that are involved in mouse deafness; this discovery is leading the search for genetic modifiers for human disorders.

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Year:  2002        PMID: 12223317     DOI: 10.1016/s1471-4914(02)02388-2

Source DB:  PubMed          Journal:  Trends Mol Med        ISSN: 1471-4914            Impact factor:   11.951


  9 in total

1.  Vestibular dysfunction, altered macular structure and trait localization in A/J inbred mice.

Authors:  Sarath Vijayakumar; Teresa E Lever; Jessica Pierce; Xing Zhao; David Bergstrom; Yunxia Wang Lundberg; Timothy A Jones; Sherri M Jones
Journal:  Mamm Genome       Date:  2015-02-03       Impact factor: 2.957

Review 2.  Strain background effects and genetic modifiers of hearing in mice.

Authors:  Kenneth R Johnson; Qing Yin Zheng; Konrad Noben-Trauth
Journal:  Brain Res       Date:  2006-03-31       Impact factor: 3.252

Review 3.  CRISPR/Cas9: targeted genome editing for the treatment of hereditary hearing loss.

Authors:  Rimsha Farooq; Khadim Hussain; Muhammad Tariq; Ali Farooq; Muhammad Mustafa
Journal:  J Appl Genet       Date:  2020-01-07       Impact factor: 3.240

Review 4.  Genetics of peripheral vestibular dysfunction: lessons from mutant mouse strains.

Authors:  Sherri M Jones; Timothy A Jones
Journal:  J Am Acad Audiol       Date:  2014-03       Impact factor: 1.664

5.  A comparison of vestibular and auditory phenotypes in inbred mouse strains.

Authors:  Sherri M Jones; Timothy A Jones; Kenneth R Johnson; Heping Yu; Lawrence C Erway; Qing Y Zheng
Journal:  Brain Res       Date:  2006-02-24       Impact factor: 3.252

6.  Deafness in Claudin 11-null mice reveals the critical contribution of basal cell tight junctions to stria vascularis function.

Authors:  Alexander Gow; Caroline Davies; Cherie M Southwood; Gregory Frolenkov; Mark Chrustowski; Lily Ng; Daisuke Yamauchi; Daniel C Marcus; Bechara Kachar
Journal:  J Neurosci       Date:  2004-08-11       Impact factor: 6.167

7.  GJB2 gene therapy and conditional deletion reveal developmental stage-dependent effects on inner ear structure and function.

Authors:  Jingying Guo; Xiaobo Ma; Jennifer M Skidmore; Jelka Cimerman; Diane M Prieskorn; Lisa A Beyer; Donald L Swiderski; David F Dolan; Donna M Martin; Yehoash Raphael
Journal:  Mol Ther Methods Clin Dev       Date:  2021-10-01       Impact factor: 5.849

8.  Inner ear morphology is perturbed in two novel mouse models of recessive deafness.

Authors:  Kerry A Miller; Louise H Williams; Elizabeth Rose; Michael Kuiper; Hans-Henrik M Dahl; Shehnaaz S M Manji
Journal:  PLoS One       Date:  2012-12-12       Impact factor: 3.240

9.  Eeyore: a novel mouse model of hereditary deafness.

Authors:  Kerry A Miller; Louise H Williams; Hans-Henrik M Dahl; Shehnaaz S M Manji
Journal:  PLoS One       Date:  2013-09-23       Impact factor: 3.240

  9 in total

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