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Shin-Ya Nishio

Showing results (21-30 of 142) with videos related to

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Journal of Human Genetics|January 10, 2014
Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screeningTakuya Yano, Shin-ya Nishio, Shin-ichi Usami, et al.
Scientific Reports|December 22, 2025
Targeted long-read nanopore sequencing as a complementary approach for detecting STRC variants and distinguishing the STRCP1 pseudogeneHideaki Moteki, Shin-Ya Nishio, Shin-Ichi Usami
Genes|March 28, 2026
Clinical Details of Low-Frequency Hearing Loss Observed in Autosomal Dominant <i>MYO7A</i>-Associated Hearing Loss PatientsHiromi Koizumi, Shin-Ya Nishio, Shin-Ichi Usami, et al.
Plos One|December 3, 2016
Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss PatientsYoh-Ichiro Iwasa, Shin-Ya Nishio, Shin-Ichi Usami
Acta Oto-Laryngologica|June 6, 2020
Electric-acoustic stimulation with longer electrodes for potential deterioration in low-frequency hearingHidekane Yoshimura, Hideaki Moteki, Shin-Ya Nishio, et al.
Human Genetics|January 12, 2022
Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing lossShin-Ichi Usami, Yuichi Isaka, Maiko Miyagawa, et al.
Journal of Visualized Experiments : Jove|October 28, 2024
Enhanced Cochlear Coverage and Hearing Preservation in High-Frequency Hearing Loss via Electric Acoustic Stimulation with Longer ElectrodeHidekane Yoshimura, Yutaka Takumi, Shin-Ya Nishio, et al.
The Annals of Otology, Rhinology, and Laryngology|May 23, 2015
Ethnic-specific spectrum of GJB2 and SLC26A4 mutations: their origin and a literature reviewKeita Tsukada, Shin-Ya Nishio, Mitsuru Hattori, et al.
Human Genome Variation|August 30, 2018
Sensorineural hearing loss and mild cardiac phenotype caused by an <i>EYA4</i> mutationSatoko Abe, Hidehiko Takeda, Shin-Ya Nishio, et al.
International Journal of Molecular Sciences|February 27, 2026
Inflammation and Oxidative-Stress Pathways Are Associated with Idiopathic Sudden Hearing Loss: A Genome-Wide Association Study in 15,494 Japanese IndividualsRyosuke Kitoh, Shin-Ya Nishio, Yutaka Takumi, et al.
Pageof 15

Showing results (21-30 of 142) with videos related to

Sort By:
Pageof 15
Journal of Human Genetics|January 10, 2014
Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screeningTakuya Yano, Shin-ya Nishio, Shin-ichi Usami, et al.
Scientific Reports|December 22, 2025
Targeted long-read nanopore sequencing as a complementary approach for detecting STRC variants and distinguishing the STRCP1 pseudogeneHideaki Moteki, Shin-Ya Nishio, Shin-Ichi Usami
Genes|March 28, 2026
Clinical Details of Low-Frequency Hearing Loss Observed in Autosomal Dominant <i>MYO7A</i>-Associated Hearing Loss PatientsHiromi Koizumi, Shin-Ya Nishio, Shin-Ichi Usami, et al.
Plos One|December 3, 2016
Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss PatientsYoh-Ichiro Iwasa, Shin-Ya Nishio, Shin-Ichi Usami
Acta Oto-Laryngologica|June 6, 2020
Electric-acoustic stimulation with longer electrodes for potential deterioration in low-frequency hearingHidekane Yoshimura, Hideaki Moteki, Shin-Ya Nishio, et al.
Human Genetics|January 12, 2022
Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing lossShin-Ichi Usami, Yuichi Isaka, Maiko Miyagawa, et al.
Journal of Visualized Experiments : Jove|October 28, 2024
Enhanced Cochlear Coverage and Hearing Preservation in High-Frequency Hearing Loss via Electric Acoustic Stimulation with Longer ElectrodeHidekane Yoshimura, Yutaka Takumi, Shin-Ya Nishio, et al.
The Annals of Otology, Rhinology, and Laryngology|May 23, 2015
Ethnic-specific spectrum of GJB2 and SLC26A4 mutations: their origin and a literature reviewKeita Tsukada, Shin-Ya Nishio, Mitsuru Hattori, et al.
Human Genome Variation|August 30, 2018
Sensorineural hearing loss and mild cardiac phenotype caused by an <i>EYA4</i> mutationSatoko Abe, Hidehiko Takeda, Shin-Ya Nishio, et al.
International Journal of Molecular Sciences|February 27, 2026
Inflammation and Oxidative-Stress Pathways Are Associated with Idiopathic Sudden Hearing Loss: A Genome-Wide Association Study in 15,494 Japanese IndividualsRyosuke Kitoh, Shin-Ya Nishio, Yutaka Takumi, et al.
Pageof 15