Literature DB >> 11489639

Mechanisms that regulate mechanosensory hair cell differentiation.

U Müller1, A Littlewood-Evans.   

Abstract

Hair cells of the vertebrate inner ear are mechanosensors that detect sound, gravity and acceleration. They have a specialized cytoskeleton optimized for the transmission of mechanical force. Hair cell defects are a major cause of deafness. The cloning of disease genes and studies of model organisms have provided insights into the mechanisms that regulate the differentiation of hair cells and their cytoskeleton. The studies have also provided new insights into the function of receptors such as integrins and protocadherins, and cytoplasmic proteins such as Rho-type GTPases and unconventional myosins, in organizing the actin cytoskeleton.

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Year:  2001        PMID: 11489639     DOI: 10.1016/s0962-8924(01)02046-3

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  17 in total

Review 1.  Cells, molecules and morphogenesis: the making of the vertebrate ear.

Authors:  Bernd Fritzsch; Sarah Pauley; Kirk W Beisel
Journal:  Brain Res       Date:  2006-04-27       Impact factor: 3.252

2.  The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions.

Authors:  Jan Siemens; Piotr Kazmierczak; Anna Reynolds; Melanie Sticker; Amanda Littlewood-Evans; Ulrich Müller
Journal:  Proc Natl Acad Sci U S A       Date:  2002-10-29       Impact factor: 11.205

Review 3.  Hearing loss and renal syndromes.

Authors:  Paul J Phelan; Michelle N Rheault
Journal:  Pediatr Nephrol       Date:  2017-11-12       Impact factor: 3.714

Review 4.  Extracellular inhibitors, repellents, and semaphorin/plexin/MICAL-mediated actin filament disassembly.

Authors:  Ruei-Jiun Hung; Jonathan R Terman
Journal:  Cytoskeleton (Hoboken)       Date:  2011-08-25

5.  A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice.

Authors:  Chantal M Longo-Guess; Leona H Gagnon; Susan A Cook; Jian Wu; Qing Y Zheng; Kenneth R Johnson
Journal:  Proc Natl Acad Sci U S A       Date:  2005-05-19       Impact factor: 11.205

6.  Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.

Authors:  Hashem Shahin; Tom Walsh; Tama Sobe; Judeh Abu Sa'ed; Amal Abu Rayan; Eric D Lynch; Ming K Lee; Karen B Avraham; Mary-Claire King; Moein Kanaan
Journal:  Am J Hum Genet       Date:  2005-11-21       Impact factor: 11.025

7.  Physical and functional interaction between protocadherin 15 and myosin VIIa in mechanosensory hair cells.

Authors:  Mathias Senften; Martin Schwander; Piotr Kazmierczak; Concepcion Lillo; Jung-Bum Shin; Tama Hasson; Gwenaëlle S G Géléoc; Peter G Gillespie; David Williams; Jeffrey R Holt; Ulrich Müller
Journal:  J Neurosci       Date:  2006-02-15       Impact factor: 6.167

Review 8.  Cadherins and mechanotransduction by hair cells.

Authors:  Ulrich Müller
Journal:  Curr Opin Cell Biol       Date:  2008-07-30       Impact factor: 8.382

9.  Allele-specific effects of human deafness gamma-actin mutations (DFNA20/26) on the actin/cofilin interaction.

Authors:  Keith E Bryan; Peter A Rubenstein
Journal:  J Biol Chem       Date:  2009-05-06       Impact factor: 5.157

10.  Propagation of F-actin disassembly via Myosin15-Mical interactions.

Authors:  Shannon K Rich; Raju Baskar; Jonathan R Terman
Journal:  Sci Adv       Date:  2021-05-12       Impact factor: 14.136

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