Precaution Code - Deaf

Known as: Deaf 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2004-2018
02420042018

Papers overview

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2016
2016
UNLABELLED The genetic correction of induced pluripotent stem cells (iPSCs) induced from somatic cells of patients with… (More)
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2016
2016
Early auditory deprivation may drive the auditory cortex into cross-modal processing of non-auditory sensory information. In a… (More)
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2015
2015
Sensorineural hearing loss is a common and currently irreversible disorder, because mammalian hair cells (HCs) do not regenerate… (More)
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2015
2015
OBJECTIVES Infants with slight/mild or late-onset hearing impairment might be missed in universal newborn hearing screening (UNHS… (More)
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2014
2014
Identification of the causative mutations in patients affected by autosomal recessive non syndromic deafness (DFNB forms), is… (More)
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2013
2013
BACKGROUND Although over 60 non-syndromic deafness genes have been identified to date, the etiologic contribution of most… (More)
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2010
2010
We screened the GJB2 gene for mutations in 534 (108 multiplex and 426 simplex) probands with non-syndromic sensorineural deafness… (More)
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2004
2004
Pou4f3 (Brn3.1, Brn3c) is a class IV POU domain transcription factor that has a central function in the development of all hair… (More)
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2004
2004
Large calyceal synapses are often regarded as simple relay points, built for high-fidelity and high-frequency synaptic… (More)
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2004
2004
Recent investigations identified a large deletion of the GJB6 gene in trans to a mutation of GJB2 in deaf patients. We looked for… (More)
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