Deafness, Autosomal Dominant 4

Known as: DEAFNESS, AUTOSOMAL DOMINANT 4A, DFNA4, DFNA4A 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1995-2015
012319952015

Papers overview

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2011
2011
We report on a secreted protein found in mammalian cochlear outer hair cells (OHC) that is a member of the carcinoembryonic… (More)
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2011
2011
Both peripheral neuropathy and distal myopathy are well-established inherited neuromuscular disorders characterized by… (More)
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2008
2008
Autosomal dominant inheritance is described in about 20% of all nonsyndromic hearing loss with currently 54 distinct loci (DFNA1… (More)
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2005
2005
Mutations in the heavy chain of the class II nonmuscle myosin, MYH14, cause autosomal dominant hearing loss in families linked to… (More)
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2004
2004
Myosins have been implicated in various motile processes, including organelle translocation, ion-channel gating, and cytoskeleton… (More)
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2001
2001
The mammalian mitochondrial ribosome (mitoribosome) has a highly protein-rich composition with a small sedimentation coefficient… (More)
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2001
2001
Two genes for components of the mitochondrial translational apparatus, mitochondrial seryl-tRNA synthetase (SARSM) and… (More)
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2000
2000
Animal mitochondrial protein synthesis systems contain two serine tRNAs (tRNAs(Ser)) corresponding to the codons AGY and UCN… (More)
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2000
2000
Stereocilia of the inner ear play an integral role in the mechanotransduction of sound. Their structural support is derived from… (More)
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1995
1995
Inherited hearing impairment can occur either in the presence of other clinical features (syndromic hearing loss, SHL) or in… (More)
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