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Publications by Mirei Taniguchi

Carrier Frequency of the GJB2 Mutations That Cause Hereditary Hearing Loss in the Japanese Population

Journal of Human Genetics

Genetics

2015

English

In Vivo Imaging of Mouse Cochlea by Optical Coherence Tomography

Otology and Neurotology

English

Related publications

GJB2 ‐related Hearing Loss in Central Iran: Review of the Spectrum and Frequency of Gene Mutations

Annals of Human Genetics

Genetics

2019

English

GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss

Revista Romana de Medicina de Laborator

2017

English

Absence of GJB2 Gene Mutations, the GJB6 Deletion (GJB6-D13S1830) and Four Common Mitochondrial Mutations in Nonsyndromic Genetic Hearing Loss in a South African Population

International Journal of Pediatric Otorhinolaryngology

English

Whole-Exome Sequencing to Identify the Cause of Congenital Sensorineural Hearing Loss in Carriers of a Heterozygous GJB2 Mutation

European Archives of Oto-Rhino-Laryngology

Medicine

Otorhinolaryngology

2017

English

Population Carrier Frequency of hMSH2 and hMLH1 Mutations

British Journal of Cancer

Cancer Research

Oncology

2000

English

Mutations in the First MyTH4 Domain ofMYO15Aare a Common Cause of DFNB3 Hearing Loss

Laryngoscope

Otorhinolaryngology

2009

English

Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of C.299-300delAT Mutation in Kurdish Population of Iran

Journal of audiology and otology

English

Myo1c Mutations Associated With Hearing Loss Cause Defects in the Interaction With Nucleotide and Actin

Cellular and Molecular Life Sciences

Molecular Neuroscience

English

Opinions of Hearing Parents About the Causes of Hearing Impairment of Their Children With Biallelic GJB2 Mutations

Journal of Community Genetics

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Mirei Taniguchi

Carrier Frequency of the GJB2 Mutations That Cause Hereditary Hearing Loss in the Japanese Population

In Vivo Imaging of Mouse Cochlea by Optical Coherence Tomography

Related publications

GJB2 ‐related Hearing Loss in Central Iran: Review of the Spectrum and Frequency of Gene Mutations

GJB2 and GJB6 Genes Mutations in Children With Non-Syndromic Hearing Loss

Absence of GJB2 Gene Mutations, the GJB6 Deletion (GJB6-D13S1830) and Four Common Mitochondrial Mutations in Nonsyndromic Genetic Hearing Loss in a South African Population

Whole-Exome Sequencing to Identify the Cause of Congenital Sensorineural Hearing Loss in Carriers of a Heterozygous GJB2 Mutation

Population Carrier Frequency of hMSH2 and hMLH1 Mutations

Mutations in the First MyTH4 Domain ofMYO15Aare a Common Cause of DFNB3 Hearing Loss

Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of C.299-300delAT Mutation in Kurdish Population of Iran

Myo1c Mutations Associated With Hearing Loss Cause Defects in the Interaction With Nucleotide and Actin

Opinions of Hearing Parents About the Causes of Hearing Impairment of Their Children With Biallelic GJB2 Mutations