Хайлтын үр дүнгүүд - Shin‐ichi Usami

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  1. 1
    Prevalence of mitochondrial gene mutations among hearing impaired patients

    Prevalence of mitochondrial gene mutations among hearing impaired patients -н Shin‐ichi Usami

    Хэвлэсэн 2000
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    Artigo
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  2. 2
    The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients

    The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients -н Shin‐ichi Usami, Shin‐ya Nishio

    Хэвлэсэн 2021
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  3. 3
    Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing loss

    Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters’ cells and the fibrocytes, as the cause of nonsyndromic hearing loss -н Satoko Abe, Shin‐ichi Usami, Yusuke Nakamura

    Хэвлэсэн 2003
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    Artigo
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  4. 4
    Mutation spectrum and genotype–phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study

    Mutation spectrum and genotype–phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study -н Maiko Miyagawa, Shin‐ya Nishio, Shin‐ichi Usami

    Хэвлэсэн 2014
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    Artigo
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  5. 5
    Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study

    Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study -н Maiko Miyagawa, Shin‐ya Nishio, Shin‐ichi Usami

    Хэвлэсэн 2012
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  6. 6
    A Comprehensive Study on the Etiology of Patients Receiving Cochlear Implantation With Special Emphasis on Genetic Epidemiology

    A Comprehensive Study on the Etiology of Patients Receiving Cochlear Implantation With Special Emphasis on Genetic Epidemiology -н Maiko Miyagawa, Shin‐ya Nishio, Shin‐ichi Usami

    Хэвлэсэн 2016
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  7. 7
    Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese

    Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese -н Hisakuni Fukuoka, Yukihiko Kanda, Shuji Ohta, Shin‐ichi Usami

    Хэвлэсэн 2007
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  8. 8
    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 loss

    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 loss -н Shin‐ichi Usami, Yuichi Isaka, Maiko Miyagawa, Shin‐ya Nishio

    Хэвлэсэн 2022
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  9. 9
    Exacerbation of Noise-Induced Hearing Loss in Mice Lacking the Glutamate Transporter GLAST

    Exacerbation of Noise-Induced Hearing Loss in Mice Lacking the Glutamate Transporter GLAST -н Nobuhiro Hakuba, Kenichiro Koga, Kiyofumi Gyo, Shin‐ichi Usami, Kohichi Tanaka

    Хэвлэсэн 2000
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  10. 10
    IgG4-related chronic rhinosinusitis: A new clinical entity of nasal disease

    IgG4-related chronic rhinosinusitis: A new clinical entity of nasal disease -н Hideaki Moteki, Masanori Yasuo, Hideaki Hamano, Takeshi Uehara, Shin‐ichi Usami

    Хэвлэсэн 2010
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  11. 11
    Simultaneous Screening of Multiple Mutations by Invader Assay Improves Molecular Diagnosis of Hereditary Hearing Loss: A Multicenter Study

    Simultaneous Screening of Multiple Mutations by Invader Assay Improves Molecular Diagnosis of Hereditary Hearing Loss: A Multicenter Study -н Shin‐ichi Usami, Shin‐ya Nishio, Makoto Nagano, Satoko Abe, Toshikazu Yamaguchi

    Хэвлэсэн 2012
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  12. 12
    Targeted Exon Sequencing Successfully Discovers Rare Causative Genes and Clarifies the Molecular Epidemiology of Japanese Deafness Patients

    Targeted Exon Sequencing Successfully Discovers Rare Causative Genes and Clarifies the Molecular Epidemiology of Japanese Deafness Patients -н Maiko Miyagawa, Takehiko Naito, Shin‐ya Nishio, Naoyuki Kamatani, Shin‐ichi Usami

    Хэвлэсэн 2013
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  13. 13
    Massively Parallel DNA Sequencing Successfully Identifies New Causative Mutations in Deafness Genes in Patients with Cochlear Implantation and EAS

    Massively Parallel DNA Sequencing Successfully Identifies New Causative Mutations in Deafness Genes in Patients with Cochlear Implantation and EAS -н Maiko Miyagawa, Shin‐ya Nishio, Takuo Ikeda, Kunihiro Fukushima, Shin‐ichi Usami

    Хэвлэсэн 2013
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  14. 14
    Cochlear Implantation From the Perspective of Genetic Background

    Cochlear Implantation From the Perspective of Genetic Background -н Shin‐ichi Usami, Shin‐ya Nishio, Hideaki Moteki, Maiko Miyagawa, Hidekane Yoshimura

    Хэвлэсэн 2020
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  15. 15
    Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese

    Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutatio... -н Koji Tsukamoto, Hiroaki Suzuki, Daisuke Harada, Atsushi Namba, Satoko Abe, Shin‐ichi Usami

    Хэвлэсэн 2003
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  16. 16
    Organization of AMPA Receptor Subunits at a Glutamate Synapse: A Quantitative Immunogold Analysis of Hair Cell Synapses in the Rat Organ of Corti

    Organization of AMPA Receptor Subunits at a Glutamate Synapse: A Quantitative Immunogold Analysis of Hair Cell Synapses in the Rat Organ of Corti -н Atsushi Matsubara, Jon Henrik Laake, Svend Davanger, Shin‐ichi Usami, Ole Petter Ottersen

    Хэвлэсэн 1996
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  17. 17
    Epidemiology, aetiology and diagnosis of congenital hearing loss via hearing screening of 153 913 newborns

    Epidemiology, aetiology and diagnosis of congenital hearing loss via hearing screening of 153 913 newborns -н Hidekane Yoshimura, Takuya Okubo, Jun Shinagawa, Shin‐ya Nishio, Yutaka Takumi, Shin‐ichi Usami

    Хэвлэсэн 2024
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  18. 18
    Total-Circumference Intraoperative Frozen Section Analysis Reduces Margin-Positive Rate in Breast-Conservation Surgery

    Total-Circumference Intraoperative Frozen Section Analysis Reduces Margin-Positive Rate in Breast-Conservation Surgery -н Kiyotaka Fukamachi, Toru Ishida, Shin‐ichi Usami, Motohiro Takeda, Mika Watanabe, Hironobu Sasano, Noriaki Ohuchi

    Хэвлэсэн 2010
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  19. 19
    Identification of CRYM as a Candidate Responsible for Nonsyndromic Deafness, through cDNA Microarray Analysis of Human Cochlear and Vestibular Tissues**Nucleotide sequence data reported herein are available in the DDBJ/EMBL/GenBank databases; for details, see the Electronic-Database Information section of this article.

    Identification of CRYM as a Candidate Responsible for Nonsyndromic Deafness, through cDNA Microarray Analysis of Human Cochlear and Vestibular Tissues**Nucleotide sequence data rep... -н Satoko Abe, Toyomasa Katagiri, Akihiko Saito-Hisaminato, Shin‐ichi Usami, Yasuhiro Inoue, Tatsuhiko Tsunoda, Yusuke Nakamura

    Хэвлэсэн 2003
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  20. 20
    Clinical practice guidelines for the diagnosis and management of acute sensorineural hearing loss

    Clinical practice guidelines for the diagnosis and management of acute sensorineural hearing loss -н Ryosuke Kitoh, Shin-ya Nishio, Hiroaki Sato, Tetsuo Ikezono, Shinya Morita, Tetsuro Wada, Shin‐ichi Usami

    Хэвлэсэн 2024
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