Literature DB >> 12350347

A compendium of mouse knockouts with inner ear defects.

Anna V Anagnostopoulos1.   

Abstract

Genetically engineered strains of mice, modified by gene targeting (knockouts), are increasingly being employed as alternative effective research tools in elucidating the genetic basis of human deafness. An impressive array of auditory and vestibular mouse knockouts is already available as a valuable resource for studying the ontogenesis, morphogenesis and function of the mammalian inner ear. This article provides a current catalog of mouse knockouts with inner ear morphogenetic malformations and hearing or balance deficits resulting from ablation of genes that are regionally expressed in the inner ear and/or within surrounding tissues, such as the hindbrain, neural crest and mesenchyme.

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Year:  2002        PMID: 12350347     DOI: 10.1016/s0168-9525(02)02753-1

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  18 in total

1.  Toward a systems biology of mouse inner ear organogenesis: gene expression pathways, patterns and network analysis.

Authors:  Samin A Sajan; Mark E Warchol; Michael Lovett
Journal:  Genetics       Date:  2007-07-29       Impact factor: 4.562

2.  Head bobber: an insertional mutation causes inner ear defects, hyperactive circling, and deafness.

Authors:  Giuseppina Somma; Heather M Alger; Ryan M McGuire; Jim D Kretlow; Fernanda R Ruiz; Svetlana A Yatsenko; Pawel Stankiewicz; Wilbur Harrison; Etai Funk; Antonio Bergamaschi; John S Oghalai; Antonios G Mikos; Paul A Overbeek; Fred A Pereira
Journal:  J Assoc Res Otolaryngol       Date:  2012-03-02

3.  Preserved otolith organ function in caspase-3-deficient mice with impaired horizontal semicircular canal function.

Authors:  Patrick A Armstrong; Scott J Wood; Naoki Shimizu; Kael Kuster; Adrian Perachio; Tomoko Makishima
Journal:  Exp Brain Res       Date:  2015-04-01       Impact factor: 1.972

Review 4.  Integration of human and mouse genetics reveals pendrin function in hearing and deafness.

Authors:  Amiel A Dror; Zippora Brownstein; Karen B Avraham
Journal:  Cell Physiol Biochem       Date:  2011-11-18

5.  Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.

Authors:  M I Shabbir; Z M Ahmed; S Y Khan; Saima Riazuddin; A M Waryah; S N Khan; R D Camps; M Ghosh; M Kabra; I A Belyantseva; T B Friedman; Sheikh Riazuddin
Journal:  J Med Genet       Date:  2006-02-03       Impact factor: 6.318

6.  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

Review 7.  A symphony of inner ear developmental control genes.

Authors:  Sumantra Chatterjee; Petra Kraus; Thomas Lufkin
Journal:  BMC Genet       Date:  2010-07-16       Impact factor: 2.797

8.  Rotational responses of vestibular-nerve afferents innervating the semicircular canals in the C57BL/6 mouse.

Authors:  David M Lasker; Gyu Cheol Han; Hong Ju Park; Lloyd B Minor
Journal:  J Assoc Res Otolaryngol       Date:  2008-05-13

9.  Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).

Authors:  M Zhu; T Yang; S Wei; A T DeWan; R J Morell; J L Elfenbein; R A Fisher; S M Leal; R J H Smith; K H Friderici
Journal:  Am J Hum Genet       Date:  2003-09-16       Impact factor: 11.025

10.  Catweasel mice: a novel role for Six1 in sensory patch development and a model for branchio-oto-renal syndrome.

Authors:  Erika A Bosman; Elizabeth Quint; Helmut Fuchs; Martin Hrabé de Angelis; Karen P Steel
Journal:  Dev Biol       Date:  2009-02-02       Impact factor: 3.582

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