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STRC gene

Known as: STEREOCILIN, STRC 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Rapid screening of copy number variations in STRC by droplet digital PCR in patients with mild-to-moderate hearing loss
Copy number variations (CNVs) are commonly reported in STRC, the causal gene for DFNB16. Various techniques are used clinically… 
2019
2019
Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene
Hearing loss is the most frequent sensory disorder and is genetically extremely heterogeneous. By far the most frequent cause of… 
2019
2019
Phenotypic Characterization of DFNB16-associated Hearing Loss.
HYPOTHESIS We hypothesized that patients with DFNB16 caused hearing loss show characteristical audiological findings depending on… 
2017
2017
STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic.
OBJECTIVE This study aimed to clarify the molecular epidemiology of hearing loss by identifying the responsible genes in patients… 
2017
2017
Combined genetic approaches yield a 48% diagnostic rate in a large cohort of French hearing-impaired patients
Hearing loss is the most common sensory disorder and because of its high genetic heterogeneity, implementation of Massively… 
2016
2016
Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic Hybridization
Objective: Copy number variations (CNVs), a major cause of genetic hearing loss, most frequently involve the STRC gene, located… 
2015
2015
Visualization of Stereocilin in the Developing Zebrafish Ear
Purpose:  In the vertebrate inner ear, the protein stereocilin is expressed in the tips of mechanotransducing stereocilia that… 
Highly Cited
2014
Highly Cited
2014
Comprehensive diagnostic testing for stereocilin: an approach for analyzing medically important genes with high homology.
2011
2011
Structural and mechanical analysis of tectorial membrane Tecta mutants.
Review
2011
Review
2011
Nonlinear models of development, amplification and compression in the mammalian cochlea
This paper reviews current understanding and presents new results on some of the nonlinear processes that underlie the function… 
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