Literature DB >> 18283275

Quiet as a mouse: dissecting the molecular and genetic basis of hearing.

Steve D M Brown1, Rachel E Hardisty-Hughes, Philomena Mburu.   

Abstract

Mouse genetics has made crucial contributions to the understanding of the molecular mechanisms of hearing. With the help of a plethora of mouse mutants, many of the key genes that are involved in the development and functioning of the auditory system have been elucidated. Mouse mutants continue to shed light on the genetic and physiological bases of human hearing impairment, including both early- and late-onset deafness. A combination of genetic and physiological studies of mouse mutant lines, allied to investigations into the protein networks of the stereocilia bundle in the inner ear, are identifying key complexes that are crucial for auditory function and for providing profound insights into the underlying causes of hearing loss.

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Year:  2008        PMID: 18283275     DOI: 10.1038/nrg2309

Source DB:  PubMed          Journal:  Nat Rev Genet        ISSN: 1471-0056            Impact factor:   53.242


  74 in total

1.  Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity.

Authors:  Daniel Jagger; Gayle Collin; John Kelly; Emily Towers; Graham Nevill; Chantal Longo-Guess; Jennifer Benson; Karin Halsey; David Dolan; Jan Marshall; Jürgen Naggert; Andrew Forge
Journal:  Hum Mol Genet       Date:  2010-11-11       Impact factor: 6.150

2.  Functional Outcomes of Heparin-Binding Epidermal Growth Factor-Like Growth Factor for Regeneration of Chronic Tympanic Membrane Perforations in Mice.

Authors:  Peter Luke Santa Maria; Peter Gottlieb; Chloe Santa Maria; Sungwoo Kim; Sunil Puria; Yunzhi Peter Yang
Journal:  Tissue Eng Part A       Date:  2017-02-24       Impact factor: 3.845

Review 3.  MAGUKs, synaptic development, and synaptic plasticity.

Authors:  Chan-Ying Zheng; Gail K Seabold; Martin Horak; Ronald S Petralia
Journal:  Neuroscientist       Date:  2011-04-15       Impact factor: 7.519

Review 4.  Neurosensory mechanotransduction.

Authors:  Martin Chalfie
Journal:  Nat Rev Mol Cell Biol       Date:  2009-01       Impact factor: 94.444

Review 5.  Dynamic length regulation of sensory stereocilia.

Authors:  Uri Manor; Bechara Kachar
Journal:  Semin Cell Dev Biol       Date:  2008-07-25       Impact factor: 7.727

6.  The genetics of progressive hearing loss: a link between hearing impairment and dysfunction of mechanosensory hair cells.

Authors:  Ulrich Müller; Nicolas Grillet
Journal:  Future Neurol       Date:  2010-01-01

7.  A chimera analysis of prestin knock-out mice.

Authors:  Mary Ann Cheatham; Sharon Low-Zeddies; Khurram Naik; Roxanne Edge; Jing Zheng; Charles T Anderson; Peter Dallos
Journal:  J Neurosci       Date:  2009-09-23       Impact factor: 6.167

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

Authors:  Rachel E Hardisty-Hughes; Andrew Parker; Steve D M Brown
Journal:  Nat Protoc       Date:  2010-01-07       Impact factor: 13.491

9.  Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice.

Authors:  Jérôme Ruel; Sarah Emery; Régis Nouvian; Tiphaine Bersot; Bénédicte Amilhon; Jana M Van Rybroek; Guy Rebillard; Marc Lenoir; Michel Eybalin; Benjamin Delprat; Theru A Sivakumaran; Bruno Giros; Salah El Mestikawy; Tobias Moser; Richard J H Smith; Marci M Lesperance; Jean-Luc Puel
Journal:  Am J Hum Genet       Date:  2008-08       Impact factor: 11.025

10.  A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies.

Authors:  Daniel R Jensen; Donna M Martin; Stephen Gebarski; Trilochan Sahoo; Ellen K Brundage; A Craig Chinault; Edgar A Otto; Moumita Chaki; Friedhelm Hildebrandt; Sau Wai Cheung; Marci M Lesperance
Journal:  Am J Med Genet A       Date:  2009-03       Impact factor: 2.802

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