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Shin-Ichi Usami

Showing results (41-50 of 256) with videos related to

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Auris, Nasus, Larynx|April 23, 2018
Pneumolabyrinth, intracochlear and vestibular fluid loss after cochlear implantationHideaki Moteki, Yasunari Fujinaga, Tetsuya Goto, et al.
Auris, Nasus, Larynx|October 24, 2002
Identification of 605ins46, a novel GJB2 mutation in a Japanese familyIsamu Yuge, Akihiro Ohtsuka, Tatsuo Matsunaga, 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
Journal of Human Genetics|March 8, 2003
Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplificationSatoko Abe, Kumiko Koyama, Shin-ichi Usami, et al.
Journal of Human Genetics|May 12, 2007
Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in JapaneseHisakuni Fukuoka, Yukihiko Kanda, Shuji Ohta, 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.
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 26

Showing results (41-50 of 256) with videos related to

Sort By:
Pageof 26
Auris, Nasus, Larynx|April 23, 2018
Pneumolabyrinth, intracochlear and vestibular fluid loss after cochlear implantationHideaki Moteki, Yasunari Fujinaga, Tetsuya Goto, et al.
Auris, Nasus, Larynx|October 24, 2002
Identification of 605ins46, a novel GJB2 mutation in a Japanese familyIsamu Yuge, Akihiro Ohtsuka, Tatsuo Matsunaga, 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
Journal of Human Genetics|March 8, 2003
Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplificationSatoko Abe, Kumiko Koyama, Shin-ichi Usami, et al.
Journal of Human Genetics|May 12, 2007
Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in JapaneseHisakuni Fukuoka, Yukihiko Kanda, Shuji Ohta, 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.
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 26