CDH23 gene

Known as: Cadherin-Related 23 Gene, CADHERIN-RELATED FAMILY, MEMBER 23, cadherin-related family member 23 
This gene is involved in cell adhesion.

Topic mentions per year

Topic mentions per year

1995-2017
051019952017

Papers overview

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2008
2008
Mutations in the human gene encoding cadherin23 (CDH23) cause Usher syndrome type 1D (USH1D) and nonsyndromic hearing loss… (More)
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2007
Highly Cited
2007
Hair cells of the inner ear are mechanosensors that transduce mechanical forces arising from sound waves and head movement into… (More)
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2004
Highly Cited
2004
oskar messenger RNA localization at the posterior pole of the Drosophila oocyte is essential for germline and abdomen formation… (More)
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2004
Highly Cited
2004
Mechanoelectrical transduction, the conversion of mechanical force into electrochemical signals, underlies a range of sensory… (More)
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2004
2004
Usher syndrome type I (USH1), the most severe form of this syndrome, is characterized by profound congenital sensorineural… (More)
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2003
2003
Mutations in the cadherin 23 gene (CDH23) cause Usher syndrome type 1D in humans, a disease that results in retinitis pigmentosa… (More)
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2002
Highly Cited
2002
Usher syndrome type I is characterized by congenital hearing loss, retinitis pigmentosa (RP), and variable vestibular areflexia… (More)
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2001
Highly Cited
2001
Mouse chromosome 10 harbors several loci associated with hearing loss, including waltzer (v), modifier-of deaf waddler (mdfw) and… (More)
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2001
Highly Cited
2001
Usher syndrome type I (USH1) is an autosomal recessive disorder characterized by congenital sensorineural hearing loss… (More)
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2001
Highly Cited
2001
Genes causing nonsyndromic autosomal recessive deafness (DFNB12) and deafness associated with retinitis pigmentosa and vestibular… (More)
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