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Shin-Ya Nishio

Showing results (81-90 of 142) with videos related to

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BMC Medical Genetics|September 24, 2013
OTOF mutation screening in Japanese severe to profound recessive hearing loss patientsYoh-ichiro Iwasa, Shin-ya Nishio, Hidekane Yoshimura, et al.
International Journal of Pediatric Otorhinolaryngology|December 15, 2012
An Usher syndrome type 1 patient diagnosed before the appearance of visual symptoms by MYO7A mutation analysisHidekane Yoshimura, Satoshi Iwasaki, Yukihiko Kanda, et al.
The Annals of Otology, Rhinology, and Laryngology|March 18, 2015
Detailed hearing and vestibular profiles in the patients with COCH mutationsKeita Tsukada, Aya Ichinose, Maiko Miyagawa, 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 JapanYasunori Maeda, Akira Sasaki, Shuya Kasai, et al.
Acta Oto-Laryngologica|April 4, 2017
Etiology of single-sided deafness and asymmetrical hearing lossShin-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 LossKaruna Maekawa, Shin-Ya Nishio, Kotaro Ishikawa, 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 analysisMaiko Miyagawa, Shin-Ya Nishio, Mitsuru Hattori, 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 JapanYasunori Maeda, Akira Sasaki, Shuya Kasai, 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 TissueClaudia Steinacher, Dietmar Rieder, Jasmin E Turner, et al.
Genes|October 23, 2021
Prevalence and Clinical Characteristics of Hearing Loss Caused by <i>MYH14</i> VariantsKen Hiramatsu, Shin-Ya Nishio, Shin-Ichiro Kitajiri, et al.
Pageof 15

Showing results (81-90 of 142) with videos related to

Sort By:
Pageof 15
BMC Medical Genetics|September 24, 2013
OTOF mutation screening in Japanese severe to profound recessive hearing loss patientsYoh-ichiro Iwasa, Shin-ya Nishio, Hidekane Yoshimura, et al.
International Journal of Pediatric Otorhinolaryngology|December 15, 2012
An Usher syndrome type 1 patient diagnosed before the appearance of visual symptoms by MYO7A mutation analysisHidekane Yoshimura, Satoshi Iwasaki, Yukihiko Kanda, et al.
The Annals of Otology, Rhinology, and Laryngology|March 18, 2015
Detailed hearing and vestibular profiles in the patients with COCH mutationsKeita Tsukada, Aya Ichinose, Maiko Miyagawa, 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 JapanYasunori Maeda, Akira Sasaki, Shuya Kasai, et al.
Acta Oto-Laryngologica|April 4, 2017
Etiology of single-sided deafness and asymmetrical hearing lossShin-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 LossKaruna Maekawa, Shin-Ya Nishio, Kotaro Ishikawa, 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 analysisMaiko Miyagawa, Shin-Ya Nishio, Mitsuru Hattori, 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 JapanYasunori Maeda, Akira Sasaki, Shuya Kasai, 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 TissueClaudia Steinacher, Dietmar Rieder, Jasmin E Turner, et al.
Genes|October 23, 2021
Prevalence and Clinical Characteristics of Hearing Loss Caused by <i>MYH14</i> VariantsKen Hiramatsu, Shin-Ya Nishio, Shin-Ichiro Kitajiri, et al.
Pageof 15