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European Journal of Human Genetics : EJHG
|
September 27, 2003
Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease
Shin-ichi Usami, Kentaro Takahashi, Isamu Yuge, et al.
The Annals of Otology, Rhinology, and Laryngology
|
March 21, 2015
Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis
Maiko Miyagawa, Shin-Ya Nishio, Mitsuru Hattori, et al.
Human Genome Variation
|
November 2, 2020
Correction to: Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan
Yasunori Maeda, Akira Sasaki, Shuya Kasai, et al.
Acta Oto-Laryngologica
|
April 4, 2017
Etiology of single-sided deafness and asymmetrical hearing loss
Shin-Ichi Usami, Ryosuke Kitoh, Hideaki Moteki, et al.
Genes
|
February 26, 2025
Prevalence and Clinical Characteristics of <i>OTOGL</i>-Associated Hearing Loss Identified in a Cohort of 7065 Japanese Patients with Hearing Loss
Karuna Maekawa, Shin-Ya Nishio, Kotaro Ishikawa, et al.
Human Genome Variation
|
October 5, 2020
Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan
Yasunori Maeda, Akira Sasaki, Shuya Kasai, et al.
Stem Cell Research
|
April 26, 2023
Generation and characterization of a human iPSC line (JUFMDOi007-A) from a patient with Usher syndrome due to mutation in USH2A
Takao Ukaji, Mikako Takahashi-Shibata, Daisuke Arai, et al.
International Journal of Molecular Sciences
|
March 13, 2024
Validation of RNA Extraction Methods and Suitable Reference Genes for Gene Expression Studies in Developing Fetal Human Inner Ear Tissue
Claudia Steinacher, Dietmar Rieder, Jasmin E Turner, et al.
Nihon Jibiinkoka Gakkai Kaiho
|
February 2, 2016
[Multicenter Clinical Study of Vibrant Soundbridge in Japan: Analysis of Subjective Questionnaires]
Kozo Kumakawa, Sho Kanzaki, Shin-ichi Usami, et al.
Genes
|
October 23, 2021
Prevalence and Clinical Characteristics of Hearing Loss Caused by <i>MYH14</i> Variants
Ken Hiramatsu, Shin-Ya Nishio, Shin-Ichiro Kitajiri, et al.
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Search research articles
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Showing results (151-160 of 241) with videos related to
Sort By:
Page
of 25
European Journal of Human Genetics : EJHG
|
September 27, 2003
Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease
Shin-ichi Usami, Kentaro Takahashi, Isamu Yuge, et al.
The Annals of Otology, Rhinology, and Laryngology
|
March 21, 2015
Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis
Maiko Miyagawa, Shin-Ya Nishio, Mitsuru Hattori, et al.
Human Genome Variation
|
November 2, 2020
Correction to: Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan
Yasunori Maeda, Akira Sasaki, Shuya Kasai, et al.
Acta Oto-Laryngologica
|
April 4, 2017
Etiology of single-sided deafness and asymmetrical hearing loss
Shin-Ichi Usami, Ryosuke Kitoh, Hideaki Moteki, et al.
Genes
|
February 26, 2025
Prevalence and Clinical Characteristics of <i>OTOGL</i>-Associated Hearing Loss Identified in a Cohort of 7065 Japanese Patients with Hearing Loss
Karuna Maekawa, Shin-Ya Nishio, Kotaro Ishikawa, et al.
Human Genome Variation
|
October 5, 2020
Prevalence of the mitochondrial 1555 A>G and 1494 C>T mutations in a community-dwelling population in Japan
Yasunori Maeda, Akira Sasaki, Shuya Kasai, et al.
Stem Cell Research
|
April 26, 2023
Generation and characterization of a human iPSC line (JUFMDOi007-A) from a patient with Usher syndrome due to mutation in USH2A
Takao Ukaji, Mikako Takahashi-Shibata, Daisuke Arai, et al.
International Journal of Molecular Sciences
|
March 13, 2024
Validation of RNA Extraction Methods and Suitable Reference Genes for Gene Expression Studies in Developing Fetal Human Inner Ear Tissue
Claudia Steinacher, Dietmar Rieder, Jasmin E Turner, et al.
Nihon Jibiinkoka Gakkai Kaiho
|
February 2, 2016
[Multicenter Clinical Study of Vibrant Soundbridge in Japan: Analysis of Subjective Questionnaires]
Kozo Kumakawa, Sho Kanzaki, Shin-ichi Usami, et al.
Genes
|
October 23, 2021
Prevalence and Clinical Characteristics of Hearing Loss Caused by <i>MYH14</i> Variants
Ken Hiramatsu, Shin-Ya Nishio, Shin-Ichiro Kitajiri, et al.
Page
of 25