Literature DB >> 6613551

Inner ear pathology in the deafness mutant mouse.

G R Bock, K P Steel.   

Abstract

A distinctive cochlear pathology was found in deafness mutant mice. There was a delay in the formation of the fluid-filled Nuel and tunnel spaces in the organ of Corti, the hair cells were distorted and degenerate, and there was poor maintenance of synapses. No hair cells appeared normal by TEM, but SEM revealed some areas where stereocilia appeared relatively normal, suggesting that SEM of the surface of the organ of Corti is not necessarily a good indicator of hair cell pathology in hereditary hearing impairment. Mutant mice show normal development of endocochlear potential, but have no measurable cochlear microphonics or compound action potential. The data suggest that the deafness gene affects the organ of Corti and that cochlear hair cells in deafness mice are never functional.

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Year:  1983        PMID: 6613551     DOI: 10.3109/00016488309132873

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN: 0001-6489            Impact factor:   1.494


  14 in total

1.  Tmc1 is necessary for normal functional maturation and survival of inner and outer hair cells in the mouse cochlea.

Authors:  Walter Marcotti; Alexandra Erven; Stuart L Johnson; Karen P Steel; Corné J Kros
Journal:  J Physiol       Date:  2006-04-20       Impact factor: 5.182

2.  Tmc proteins are essential for zebrafish hearing where Tmc1 is not obligatory.

Authors:  Zongwei Chen; Shaoyuan Zhu; Kayla Kindig; Shengxuan Wang; Shih-Wei Chou; Robin Woods Davis; Michael R Dercoli; Hannah Weaver; Ruben Stepanyan; Brian M McDermott
Journal:  Hum Mol Genet       Date:  2020-07-29       Impact factor: 6.150

3.  Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36.

Authors:  Yoshihiro Noguchi; Kiyoto Kurima; Tomoko Makishima; Martin Hrabé de Angelis; Helmut Fuchs; Gregory Frolenkov; Ken Kitamura; Andrew J Griffith
Journal:  Genetics       Date:  2006-04-28       Impact factor: 4.562

4.  Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairment.

Authors:  Regie Lyn P Santos; Muhammad Wajid; Mohammad Nasim Khan; Nathan McArthur; Thanh L Pham; Attya Bhatti; Kwanghyuk Lee; Saba Irshad; Asif Mir; Kai Yan; Maria H Chahrour; Muhammad Ansar; Wasim Ahmad; Suzanne M Leal
Journal:  Hum Mutat       Date:  2005-10       Impact factor: 4.878

5.  The deafness locus (dn) maps to mouse chromosome 19.

Authors:  B J Keats; N Nouri; J M Huang; M Money; D B Webster; C I Berlin
Journal:  Mamm Genome       Date:  1995-01       Impact factor: 2.957

6.  Ellis-van Creveld syndrome and profound deafness resulted by sequence variants in the EVC/EVC2 and TMC1 genes.

Authors:  Muhammad Umair; Heide Seidel; Ishtiaq Ahmed; Asmat Ullah; Tobias B Haack; Bader Alhaddad; Abid Jan; Afzal Rafique; Tim M Strom; Farooq Ahmad; Thomas Meitinger; Wasim Ahmad
Journal:  J Genet       Date:  2017-12       Impact factor: 1.166

7.  A new Atp2b2 deafwaddler allele, dfw(i5), interacts strongly with Cdh23 and other auditory modifiers.

Authors:  Claire J Watson; Bruce L Tempel
Journal:  Hear Res       Date:  2013-06-18       Impact factor: 3.208

8.  A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness.

Authors:  Ellen Knierim; Esther Gill; Franziska Seifert; Susanne Morales-Gonzalez; Sathya D Unudurthi; Thomas J Hund; Werner Stenzel; Markus Schuelke
Journal:  Hum Genet       Date:  2017-05-24       Impact factor: 4.132

9.  Mutations of TMC1 cause deafness by disrupting mechanoelectrical transduction.

Authors:  Hiroshi Nakanishi; Kiyoto Kurima; Yoshiyuki Kawashima; Andrew J Griffith
Journal:  Auris Nasus Larynx       Date:  2014-06-02       Impact factor: 1.863

10.  An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice.

Authors:  Morag A Lewis; Elizabeth Quint; Anne M Glazier; Helmut Fuchs; Martin Hrabé De Angelis; Cordelia Langford; Stijn van Dongen; Cei Abreu-Goodger; Matias Piipari; Nick Redshaw; Tamas Dalmay; Miguel Angel Moreno-Pelayo; Anton J Enright; Karen P Steel
Journal:  Nat Genet       Date:  2009-04-12       Impact factor: 38.330

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