检索结果 - Satoko Abe

  • Showing 1 - 8 results of 8
Refine Results
  1. 1
    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 由 Satoko Abe, Shin‐ichi Usami, Yusuke Nakamura

    出版 2003
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  2. 2
    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 由 Shin‐ichi Usami, Shin‐ya Nishio, Makoto Nagano, Satoko Abe, Toshikazu Yamaguchi

    出版 2012
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  3. 3
    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... 由 Koji Tsukamoto, Hiroaki Suzuki, Daisuke Harada, Atsushi Namba, Satoko Abe, Shin‐ichi Usami

    出版 2003
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  4. 4
    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... 由 Satoko Abe, Toyomasa Katagiri, Akihiko Saito-Hisaminato, Shin‐ichi Usami, Yasuhiro Inoue, Tatsuhiko Tsunoda, Yusuke Nakamura

    出版 2003
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  5. 5
    Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns

    Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns 由 Tomohiro Oguchi, Akihiro Ohtsuka, Shigenari Hashimoto, Aki Oshima, Satoko Abe, Yumiko Kobayashi, Kyoko Nagai, Tatsuo Matsunaga, Satoshi Iwasaki, Takashi Nakagawa, Shin‐ichi Usami

    出版 2005
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  6. 6
    Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort: Genotype-Phenotype Correlations and a Founder Mutation

    Comprehensive Genetic Screening of KCNQ4 in a Large Autosomal Dominant Nonsyndromic Hearing Loss Cohort: Genotype-Phenotype Correlations and a Founder Mutation 由 Takehiko Naito, Shin‐ya Nishio, Yoh-ichiro Iwasa, Takuya Yano, Kozo Kumakawa, Satoko Abe, Kotaro Ishikawa, Hiromi Kojima, Atsushi Namba, Chie Oshikawa, Shin‐ichi Usami

    出版 2013
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  7. 7
    Frequency and clinical features of hearing loss caused by STRC deletions

    Frequency and clinical features of hearing loss caused by STRC deletions 由 Yoh Yokota, Hideaki Moteki, Shin‐ya Nishio, Tomomi Yamaguchi, Keiko Wakui, Yumiko Kobayashi, Kenji Ohyama, Hiromitsu Miyazaki, Rina Matsuoka, Satoko Abe, Kozo Kumakawa, Masahiro Takahashi, Hirofumi Sakaguchi, Natsumi Uehara, Takashi Ishino, Tomoki Kosho, Yoshimitsu Fukushima, Shin‐ichi Usami

    出版 2019
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  8. 8
    OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients

    OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients 由 Yoh-ichiro Iwasa, Shin‐ya Nishio, Akiko Sugaya, Yuko Kataoka, Yukihiko Kanda, Mirei Taniguchi, Kyoko Nagai, Yasushi Naito, Tetsuo Ikezono, Rie Horie, Yuika Sakurai, Rina Matsuoka, Hidehiko Takeda, Satoko Abe, Chiharu Kihara, Takashi Ishino, Shin‐ya Morita, Satoshi Iwasaki, Masahiro Takahashi, Tsukasa Ito, Yasuhiro Arai, Shin‐ichi Usami

    出版 2019
    获取全文
    Artigo
    加到收藏夹
    Saved in:

检索工具: