Literature DB >> 20057387

A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment.

Rachel E Hardisty-Hughes1, Andrew Parker, Steve D M Brown.   

Abstract

We describe a protocol for the production of mice carrying N-ethyl-N-nitrosourea (ENU) mutations and their screening for auditory and vestibular phenotypes. In comparison with the procedures describing individual phenotyping tests, this protocol integrates a set of tests for the comprehensive determination of the causes of hearing loss. It comprises a primary screen of relatively simple auditory and vestibular tests. A variety of secondary phenotyping protocols are also described for further investigating the deaf and vestibular mutants identified in the primary screen. The screen can be applied to potentially thousands of mutant mice, produced either by ENU or other mutagenesis approaches. Primary screening protocols take no longer than a few minutes, apart from ABR testing which takes upto 3.5 h per mouse. These protocols have been applied for the identification of mouse models of human deafness and are a key component for investigating the genes and genetic pathways involved in hereditary deafness.

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Year:  2010        PMID: 20057387     DOI: 10.1038/nprot.2009.204

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  37 in total

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Journal:  Hum Mol Genet       Date:  2001-03-01       Impact factor: 6.150

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4.  A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse.

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Journal:  Nat Genet       Date:  2000-08       Impact factor: 38.330

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Journal:  Eur J Neurosci       Date:  2002-10       Impact factor: 3.386

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Authors:  Q Y Zheng; K R Johnson; L C Erway
Journal:  Hear Res       Date:  1999-04       Impact factor: 3.208

Review 7.  ENU mutagenesis, a way forward to understand gene function.

Authors:  Abraham Acevedo-Arozena; Sara Wells; Paul Potter; Michelle Kelly; Roger D Cox; Steve D M Brown
Journal:  Annu Rev Genomics Hum Genet       Date:  2008       Impact factor: 8.929

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Journal:  Nat Genet       Date:  2005-11       Impact factor: 38.330

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  54 in total

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Journal:  Hum Mol Genet       Date:  2013-12-11       Impact factor: 6.150

7.  Sodium salicylate alters temporal integration measured through increasing stimulus presentation rates.

Authors:  Nicole J Wood; Andrea S Lowe; Joseph P Walton
Journal:  Int J Audiol       Date:  2019-03       Impact factor: 2.117

8.  Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G.

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Journal:  Hum Mol Genet       Date:  2014-08-11       Impact factor: 6.150

10.  The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in mice.

Authors:  Mario Bortolozzi; Marisa Brini; Nick Parkinson; Giulia Crispino; Pietro Scimemi; Romolo Daniele De Siati; Francesca Di Leva; Andrew Parker; Saida Ortolano; Edoardo Arslan; Steve D Brown; Ernesto Carafoli; Fabio Mammano
Journal:  J Biol Chem       Date:  2010-09-08       Impact factor: 5.157

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