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TMC1 gene

Known as: transmembrane channel like 1, TRANSMEMBRANE COCHLEAR-EXPRESSED GENE 1, TMC1 
National Institutes of Health

Related topics

Related topics

5 relations
TMC2 geneTMC3 geneTMC4 geneTMC5 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Mutation spectra and founder effect of TMC1 in patients with non‐syndromic deafness in Xiamen area, China
To analyze the spectrum and founder effect of TMC1 mutations in patients with non‐syndromic deafness in the Xiamen area. Sporadic… 
2016
2016
Tmc1 Is a Dynamically Regulated Effector of the Rpn4 Proteotoxic Stress Response*
The ubiquitin-proteasome system represents the major pathway of selective intracellular protein degradation in eukaryotes… 
2016
2016
Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran
Background: Non-syndromic hearing loss (NSHL) is the most common birth defect and occurs in approximately 1/1,000 newborns. NSHL… 
2016
2016
[Advances in hereditary hearing loss caused by TMC1 mutations].
Hearing loss is the most frequent sensorineural disorder worldwild, among which about 50% are caused by genetic factors. TMC1 is… 
2015
2015
A TMC1 (transmembrane channel-like 1) mutation (p.S320R) in a Polish family with hearing impairment
After excluding frequent mutations in common genes like GJB2, SLC26A4 and MT-RNR1 by straightforward Sanger sequencing in about… 
2012
2012
The common TMC1 mutation c.100C>T (p.Arg34X) is not a significant cause of deafness in British Asians.
TMC1, a second-tier deafness gene below GJB2, is an appreciable cause of recessive nonsyndromic hearing loss (DFNB7/11) in North… 
2011
2011
Molecular analysis of TMC1 gene in the Korean patients with nonsyndromic hearing loss
Hereditary nonsyndromic hearing loss (NSHL) is a highly heterogeneous disorder in humans. Mutations of the transmembrane channel… 
2011
2011
Isolation of Ty1-copia retrotransposon in myrtle genome and development of S-SAP molecular marker
Long terminal repeat (LTR)-retrotransposons are mobile genetic elements that are ubiquitous in plants and constitute a major… 
2008
2008
Gene symbol: TMC1. Disease: Hearing loss.
Review
2003
Review
2003
Mouse tales from Kresge: the deafness mouse.
Mouse models for human deafness have not only proven instrumental in the identification of genes for hereditary hearing loss, but… 
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