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-Ichi Usami

Showing results (131-140 of 241) with videos related to

Pageof 25
Sort By:
Acta Oto-Laryngologica|July 7, 2011
Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutationsHideaki Moteki, Yasushi Naito, Keizo Fujiwara, et al.
Plos One|July 29, 2025
A novel incision design for Vibrant SoundBridge®︎ implantation prior to auricular reconstruction for microtiaNaohiro Ueda, Takatoshi Yotsuyanagi, Ken Yamashita, et al.
Neuroreport|April 13, 2004
The effect of hypergravity on the inner ear: CREB and syntaxin are up-regulatedNaoya Iijima, Nobuyoshi Suzuki, Tomohiro Oguchi, et al.
Journal of Leukocyte Biology|May 2, 2009
Pivotal Advance: Eosinophilia in the MES rat strain is caused by a loss-of-function mutation in the gene for cytochrome b(-245), alpha polypeptide (Cyba)Masayuki Mori, Guixin Li, Maiko Hashimoto, et al.
Clinical Case Reports|January 25, 2021
Cochlear implantation in a patient with a <i>POU4F3</i> mutationKeitaro Miyake, Kyoko Shirai, Nobuhiro Nishiyama, et al.
Audiology & Neuro-Otology|June 8, 2002
Molecular diagnosis of deafness: impact of gene identificationShin-ichi Usami, Eiko Koda, Koji Tsukamoto, et al.
Brain Research. Molecular Brain Research|December 14, 2002
Microtubule associated protein (MAP1A) mRNA was up-regulated by hypergravity in the rat inner earYutaka Takumi, Naoya Iijima, Nobuyoshi Suzuki, et al.
Human Genetics|February 1, 2003
GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutationAkihiro Ohtsuka, Isamu Yuge, Shinobu Kimura, et al.
Acta Oto-Laryngologica|April 14, 2009
Semi-quantitative evaluation of endolymphatic hydrops by bilateral intratympanic gadolinium-based contrast agent (GBCA) administration with MRI for Meniere's diseaseHisakuni Fukuoka, Keita Tsukada, Maiko Miyagawa, et al.
Acta Oto-Laryngologica|October 30, 2009
Endolymphatic hydrops and therapeutic effects are visualized in 'atypical' Meniere's diseaseMaiko Miyagawa, Hisakuni Fukuoka, Keita Tsukada, et al.
Pageof 25

Showing results (131-140 of 241) with videos related to

Sort By:
Pageof 25
Acta Oto-Laryngologica|July 7, 2011
Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutationsHideaki Moteki, Yasushi Naito, Keizo Fujiwara, et al.
Plos One|July 29, 2025
A novel incision design for Vibrant SoundBridge®︎ implantation prior to auricular reconstruction for microtiaNaohiro Ueda, Takatoshi Yotsuyanagi, Ken Yamashita, et al.
Neuroreport|April 13, 2004
The effect of hypergravity on the inner ear: CREB and syntaxin are up-regulatedNaoya Iijima, Nobuyoshi Suzuki, Tomohiro Oguchi, et al.
Journal of Leukocyte Biology|May 2, 2009
Pivotal Advance: Eosinophilia in the MES rat strain is caused by a loss-of-function mutation in the gene for cytochrome b(-245), alpha polypeptide (Cyba)Masayuki Mori, Guixin Li, Maiko Hashimoto, et al.
Clinical Case Reports|January 25, 2021
Cochlear implantation in a patient with a <i>POU4F3</i> mutationKeitaro Miyake, Kyoko Shirai, Nobuhiro Nishiyama, et al.
Audiology & Neuro-Otology|June 8, 2002
Molecular diagnosis of deafness: impact of gene identificationShin-ichi Usami, Eiko Koda, Koji Tsukamoto, et al.
Brain Research. Molecular Brain Research|December 14, 2002
Microtubule associated protein (MAP1A) mRNA was up-regulated by hypergravity in the rat inner earYutaka Takumi, Naoya Iijima, Nobuyoshi Suzuki, et al.
Human Genetics|February 1, 2003
GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutationAkihiro Ohtsuka, Isamu Yuge, Shinobu Kimura, et al.
Acta Oto-Laryngologica|April 14, 2009
Semi-quantitative evaluation of endolymphatic hydrops by bilateral intratympanic gadolinium-based contrast agent (GBCA) administration with MRI for Meniere's diseaseHisakuni Fukuoka, Keita Tsukada, Maiko Miyagawa, et al.
Acta Oto-Laryngologica|October 30, 2009
Endolymphatic hydrops and therapeutic effects are visualized in 'atypical' Meniere's diseaseMaiko Miyagawa, Hisakuni Fukuoka, Keita Tsukada, et al.
Pageof 25