tmc1 gene
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scholarly journals Molecular evolution of echolocation genes in cetaceans and bats

2019 ◽  
Author(s):  
Letícia Magpali Moura Estevão ◽  
Mariana Freitas Nery
Keyword(s):  
Molecular Evolution ◽  
Molecular Level ◽  
Tmc1 Gene

This study aims to understand the molecular evolution of hearing genes associated with echolocation in dolphins and bats. The convergence between these groups suggests that TMC1 gene is central to the evolution of echolocation and a case of convergence occurring on a molecular level.

scholarly journals Publisher Correction: Improved TMC1 gene therapy restores hearing and balance in mice with genetic inner ear disorders

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Carl A. Nist-Lund ◽  
Bifeng Pan ◽  
Amy Patterson ◽  
Yukako Asai ◽  
Tianwen Chen ◽  
...  
Keyword(s):  
Gene Therapy ◽  
Inner Ear ◽  
Tmc1 Gene ◽  
Inner Ear Disorders

scholarly journals Improved TMC1 gene therapy restores hearing and balance in mice with genetic inner ear disorders

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Carl A. Nist-Lund ◽  
Bifeng Pan ◽  
Amy Patterson ◽  
Yukako Asai ◽  
Tianwen Chen ◽  
...  
Keyword(s):  
Gene Therapy ◽  
Inner Ear ◽  
Tmc1 Gene ◽  
Inner Ear Disorders

scholarly journals Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran

2016 ◽  
Vol 18 (3) ◽  
Author(s):  
Negar Moradipour ◽  
Payam Ghasemi-Dehkordi ◽  
Fatemeh Heibati ◽  
Shahrbanuo Parchami-Barjui ◽  
Marziyeh Abolhasani ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Autosomal Recessive ◽  
Mutation Screening ◽  
Syndromic Hearing Loss ◽  
Tmc1 Gene

A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.

Gene ◽  
2015 ◽  
Vol 574 (1) ◽  
pp. 28-33 ◽  
Author(s):  
Amina Bakhchane ◽  
Hicham Charoute ◽  
Halima Nahili ◽  
Rachida Roky ◽  
Hassan Rouba ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Novel Mutation ◽  
Syndromic Hearing Loss ◽  
Moroccan Family ◽  
Tmc1 Gene

Identification of Three Novel Hearing Loss Mouse Strains with Mutations in the Tmc1 Gene

2012 ◽  
Vol 180 (4) ◽  
pp. 1560-1569 ◽  
Author(s):  
Shehnaaz S.M. Manji ◽  
Kerry A. Miller ◽  
Louise H. Williams ◽  
Hans-Henrik M. Dahl
Keyword(s):  
Hearing Loss ◽  
Mouse Strains ◽  
Tmc1 Gene

Molecular analysis of TMC1 gene in the Korean patients with nonsyndromic hearing loss

2011 ◽  
Vol 33 (2) ◽  
pp. 205-207 ◽  
Author(s):  
Hyo-Kyeong Kim ◽  
Yee Hyuk Kim ◽  
Borum Sagong ◽  
Tae-Jun Kwon ◽  
Se-Kyung Oh ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Molecular Analysis ◽  
Nonsyndromic Hearing Loss ◽  
Korean Patients ◽  
Tmc1 Gene

scholarly journals High Frequency of the p.R34X Mutation in the TMC1 Gene Associated with Nonsyndromic Hearing Loss Is Due to Founder Effects

2010 ◽  
Vol 14 (3) ◽  
pp. 307-311 ◽  
Author(s):  
Mariem Ben Saïd ◽  
Mounira Hmani-Aifa ◽  
Imen Amar ◽  
Shahid Mahmood Baig ◽  
Mirna Mustapha ◽  
...  
Keyword(s):  
Hearing Loss ◽  
High Frequency ◽  
Nonsyndromic Hearing Loss ◽  
Founder Effects ◽  
Tmc1 Gene
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