Published in Dev Biol on February 10, 2010
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The deaf mouse mutant whirler suggests a role for whirlin in actin filament dynamics and stereocilia development. Cell Motil Cytoskeleton (2007) 1.13
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The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss. PLoS Genet (2008) 1.08
The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice. Hum Mol Genet (2010) 1.07
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Two new mouse mutants with vestibular defects that map to the highly mutable locus on chromosome 4. Int J Audiol (2005) 0.90
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A novel stereocilia defect in sensory hair cells of the deaf mouse mutant Tasmanian devil. Eur J Neurosci (2002) 0.87
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The future role of genetic screening to detect newborns at risk of childhood-onset hearing loss. Int J Audiol (2012) 0.83
Myosin VI is required for normal retinal function. Exp Eye Res (2005) 0.83
A missense mutation in Fgfr1 causes ear and skull defects in hush puppy mice. Mamm Genome (2011) 0.82
A reduction in Ptprq associated with specific features of the deafness phenotype of the miR-96 mutant mouse diminuendo. Eur J Neurosci (2014) 0.81
Auditory function in the Tc1 mouse model of down syndrome suggests a limited region of human chromosome 21 involved in otitis media. PLoS One (2012) 0.80
Mice deficient in H+-ATPase a4 subunit have severe hearing impairment associated with enlarged endolymphatic compartments within the inner ear. Dis Model Mech (2012) 0.80
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Use of mouse genetics for studying inner ear development. Curr Top Dev Biol (2003) 0.77
Early development and degeneration of vestibular hair cells in bronx waltzer mutant mice. Hear Res (2002) 0.77
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Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) are two new mutations of Lmx1a causing severe cochlear and vestibular defects. PLoS One (2012) 0.76
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A cornucopia of candidates for deafness. Cell (2012) 0.75