Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Shin-Ya Nishio

Showing results (31-40 of 142) with videos related to

Pageof 15
Sort By:
Scientific Reports|May 8, 2024
Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variantsKeita Tsukada, Shin-Ya Nishio, Yutaka Takumi, et al.
The Annals of Otology, Rhinology, and Laryngology|May 23, 2015
Massively parallel DNA sequencing successfully identified seven families with deafness-associated MYO6 mutations: the mutational spectrum and clinical characteristicsMaiko Miyagawa, Shin-Ya Nishio, Kozo Kumakawa, et al.
Genetic Testing and Molecular Biomarkers|January 15, 2015
Clinical application of a custom AmpliSeq library and ion torrent PGM sequencing to comprehensive mutation screening for deafness genesShin-Ya Nishio, Yoshiharu Hayashi, Manabu Watanabe, et al.
Audiology Research|September 22, 2025
Use of the FLEX 28 Dexamethasone-Eluting Cochlear Implant Electrode in Electric-Acoustic Stimulation: A Case ReportShin-Ichi Usami, Yutaka Takumi, Hidekane Yoshimura, et al.
Acta Oto-Laryngologica|January 20, 2023
Sound localization in patients with idiopathic sudden hearing lossRyosuke Kitoh, Yutaka Takumi, Shin-Ya Nishio, et al.
International Journal of Molecular Sciences|September 19, 2019
Detailed Clinical Features of Deafness Caused by a Claudin-14 VariantTomohiro Kitano, Shin-Ichiro Kitajiri, Shin-Ya Nishio, et al.
Plos One|September 15, 2016
Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss PatientsKentaro Mori, Hideaki Moteki, Maiko Miyagawa, et al.
Genes|February 26, 2025
Auditory Neuropathy Caused by a Structural Variation in the <i>OTOF</i> Gene, Identified Using Oxford Nanopore Adaptive SamplingTakumi Kumai, Shin-Ya Nishio, Hideaki Moteki, et al.
Plos One|March 3, 2012
Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter studyShin-ichi Usami, Shin-ya Nishio, Makoto Nagano, et al.
Acta Oto-Laryngologica|August 28, 2021
A nationwide epidemiologic, clinical, genetic study of Usher syndrome in JapanHidekane Yoshimura, Shin-Ya Nishio, Yuichi Isaka, et al.
Pageof 15

Showing results (31-40 of 142) with videos related to

Sort By:
Pageof 15
Scientific Reports|May 8, 2024
Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variantsKeita Tsukada, Shin-Ya Nishio, Yutaka Takumi, et al.
The Annals of Otology, Rhinology, and Laryngology|May 23, 2015
Massively parallel DNA sequencing successfully identified seven families with deafness-associated MYO6 mutations: the mutational spectrum and clinical characteristicsMaiko Miyagawa, Shin-Ya Nishio, Kozo Kumakawa, et al.
Genetic Testing and Molecular Biomarkers|January 15, 2015
Clinical application of a custom AmpliSeq library and ion torrent PGM sequencing to comprehensive mutation screening for deafness genesShin-Ya Nishio, Yoshiharu Hayashi, Manabu Watanabe, et al.
Audiology Research|September 22, 2025
Use of the FLEX 28 Dexamethasone-Eluting Cochlear Implant Electrode in Electric-Acoustic Stimulation: A Case ReportShin-Ichi Usami, Yutaka Takumi, Hidekane Yoshimura, et al.
Acta Oto-Laryngologica|January 20, 2023
Sound localization in patients with idiopathic sudden hearing lossRyosuke Kitoh, Yutaka Takumi, Shin-Ya Nishio, et al.
International Journal of Molecular Sciences|September 19, 2019
Detailed Clinical Features of Deafness Caused by a Claudin-14 VariantTomohiro Kitano, Shin-Ichiro Kitajiri, Shin-Ya Nishio, et al.
Plos One|September 15, 2016
Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss PatientsKentaro Mori, Hideaki Moteki, Maiko Miyagawa, et al.
Genes|February 26, 2025
Auditory Neuropathy Caused by a Structural Variation in the <i>OTOF</i> Gene, Identified Using Oxford Nanopore Adaptive SamplingTakumi Kumai, Shin-Ya Nishio, Hideaki Moteki, et al.
Plos One|March 3, 2012
Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter studyShin-ichi Usami, Shin-ya Nishio, Makoto Nagano, et al.
Acta Oto-Laryngologica|August 28, 2021
A nationwide epidemiologic, clinical, genetic study of Usher syndrome in JapanHidekane Yoshimura, Shin-Ya Nishio, Yuichi Isaka, et al.
Pageof 15