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Shin-Ichi Usami

Showing results (191-200 of 241) with videos related to

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Genes|September 19, 2019
Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of <i>OTOA</i>-Associated Hearing LossKenjiro Sugiyama, Hideaki Moteki, Shin-Ichiro Kitajiri, et al.
Scientific Reports|April 29, 2020
Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing lossHiroki Miyajima, Hideaki Moteki, Timothy Day, et al.
Genes|January 25, 2025
The Heterozygous p.A684V Variant in the <i>WFS1</i> Gene Is a Mutational Hotspot Causing a Severe Hearing Loss PhenotypeShintaro Otsuka, Chihiro Morimoto, Shin-Ya Nishio, et al.
Plos One|March 13, 2014
Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1Hidekane Yoshimura, Satoshi Iwasaki, Shin-Ya Nishio, et al.
The Annals of Otology, Rhinology, and Laryngology|July 30, 2016
Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic HybridizationHideaki Moteki, Hela Azaiez, Christina M Sloan-Heggen, et al.
Genes|September 25, 2019
Mutational Spectrum and Clinical Features of Patients with <i>LOXHD1</i> Variants Identified in an 8074 Hearing Loss Patient CohortKaruna Maekawa, Shin-Ya Nishio, Satoko Abe, et al.
Plos One|January 30, 2018
The diagnostic performance of a novel ELISA for human CTP (Cochlin-tomoprotein) to detect perilymph leakageTetsuo Ikezono, Tomohiro Matsumura, Han Matsuda, et al.
Acta Oto-Laryngologica|April 11, 2017
Differences between acoustic trauma and other types of acute noise-induced hearing loss in terms of treatment and hearing prognosisTetsuro Wada, Hajime Sano, Shin-Ya Nishio, et al.
Acta Oto-Laryngologica|October 22, 2024
HEARRING group genetic marker study: genetic background of CI patientsShin-Ichi Usami, Shin-Ya Nishio, Javier Gavilán, et al.
The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing lossNaoko Sakuma, Hideaki Moteki, Hela Azaiez, et al.
Pageof 25

Showing results (191-200 of 241) with videos related to

Sort By:
Pageof 25
Genes|September 19, 2019
Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of <i>OTOA</i>-Associated Hearing LossKenjiro Sugiyama, Hideaki Moteki, Shin-Ichiro Kitajiri, et al.
Scientific Reports|April 29, 2020
Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing lossHiroki Miyajima, Hideaki Moteki, Timothy Day, et al.
Genes|January 25, 2025
The Heterozygous p.A684V Variant in the <i>WFS1</i> Gene Is a Mutational Hotspot Causing a Severe Hearing Loss PhenotypeShintaro Otsuka, Chihiro Morimoto, Shin-Ya Nishio, et al.
Plos One|March 13, 2014
Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1Hidekane Yoshimura, Satoshi Iwasaki, Shin-Ya Nishio, et al.
The Annals of Otology, Rhinology, and Laryngology|July 30, 2016
Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic HybridizationHideaki Moteki, Hela Azaiez, Christina M Sloan-Heggen, et al.
Genes|September 25, 2019
Mutational Spectrum and Clinical Features of Patients with <i>LOXHD1</i> Variants Identified in an 8074 Hearing Loss Patient CohortKaruna Maekawa, Shin-Ya Nishio, Satoko Abe, et al.
Plos One|January 30, 2018
The diagnostic performance of a novel ELISA for human CTP (Cochlin-tomoprotein) to detect perilymph leakageTetsuo Ikezono, Tomohiro Matsumura, Han Matsuda, et al.
Acta Oto-Laryngologica|April 11, 2017
Differences between acoustic trauma and other types of acute noise-induced hearing loss in terms of treatment and hearing prognosisTetsuro Wada, Hajime Sano, Shin-Ya Nishio, et al.
Acta Oto-Laryngologica|October 22, 2024
HEARRING group genetic marker study: genetic background of CI patientsShin-Ichi Usami, Shin-Ya Nishio, Javier Gavilán, et al.
The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Novel PTPRQ mutations identified in three congenital hearing loss patients with various types of hearing lossNaoko Sakuma, Hideaki Moteki, Hela Azaiez, et al.
Pageof 25