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MUTAI Hideki  務台 英樹

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Researcher Number 60415891
Other IDs
Affiliation (Current) 2020: 独立行政法人国立病院機構(東京医療センター臨床研究センター), その他部局等, 研究員
Affiliation (based on the past Project Information) *help 2016 – 2018: 独立行政法人国立病院機構(東京医療センター臨床研究センター), その他部局等, 研究員
2014 – 2015: 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚平衡覚研究部, 研究員
2014: 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚・平衡覚研究部, 研究員
2014: 東京医療センター, 臨床研究センター聴覚障害研究室, 研究員
2013: 国立病院機構東京医療センター, 臨床研究センター・聴覚障害研究室, 研究員 … More
2013: 独立行政法人国立病院機構(東京医療センター臨床研究センター), その他部局等, 研究員
2012 – 2013: 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚障害研究室, 研究員
2012: 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚・平衡覚研究部・聴覚障害研究室, 研究員
2012: 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚平衡覚研究部, 研究員
2011: 国立病院機構東京医療センター臨床研究センター, 聴覚障害研究室, 研究員
2011: 独立行政法人国立病院機構東京医療センター(臨床研究センター), 聴覚平衡覚研究部, 研究員
2011: 独立行政法人国立病院機構東京医療センター臨床研究センター, 聴覚平衡覚研究部, 研究員
2010: 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚障害研究室, 研究員
2009 – 2010: 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚平衡覚研究部, 研究員
2009: 独立行政法人国立病院機構東京医療センター 臨床研究センター, 聴覚障害研究室, 研究員
2008: 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚平衡覚研究部, 研究員
2008: 独立行政法人国立病院機構, 東京医療センター臨床研究センター聴覚・平衡覚研究部聴覚障害研究室, 研究員
2008: 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚平衡覚研究部, 研究員
2007: 国立病院機構, 東京医療センター(臨床研究センター)・聴覚・平衡覚部・聴覚障害研究室, 研究員
2007: 独立行政法人国立病院機構(東京医療センター臨床研究センター), 東京医療センター(臨床研究センター)・聴覚平衡覚研究部, 研究員
2006: National Hospital Organization National Tokyo Medical Center National Institute of Sensory Organs, Division of Hearing and Balance Research, Laboratory of Auditory Disorders, Researcher, 聴覚・平衡覚研究部聴覚障害研究室, 研究員
2006: 独立行政法人国立病院機構東京医療センター(臨床研究センター), 聴覚平衡覚研究部聴覚障害研究室, 研究員 Less
Review Section/Research Field
Principal Investigator
Otorhinolaryngology / Basic Section 56050:Otorhinolaryngology-related
Except Principal Investigator
Otorhinolaryngology / Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields
Keywords
Principal Investigator
ゲノム / エピジェネティクス / 難聴 / ゲノム編集 / 耳鼻咽喉学 / 発生医学 / 脳・神経 / 発生・分化 / 遺伝学 / 発現制御 … More / 発生・文化 / 耳科学 / 神経科学 / 老化 / 加齢性難聴 / 亜鉛トランスポーター / 緑茶カテキン / EGCG / 薬剤標的 / 蝸牛 / マイクロアレイ / 内耳奇形 / 蝸牛神経 / 難聴遺伝子 / 神経芽腫細胞 / 胎生致死 / 遺伝性難聴 / 原因遺伝子 / モデルマウス / 動物モデル / スプライシング … More
Except Principal Investigator
遺伝性難聴 / DNA / 遺伝子 / ミトコンドリア / 非症候群性難聴 / 耳鼻咽喉学 / 聴覚医学 / 遺伝学 / 医療 / 遣伝学 / 耳科学 / 蝸牛神経 / 感音難聴 / 先天性難聴 / OTOF遺伝子 / Pejvakin遺伝子 / Auditory Neuropathy / 医療・福祉 / ゲノム / 脳神経疾患 / バイオテクノロジー / 蝸牛低形成 / 蝸牛神経低形成 / 次世代シーケンサー / エクソーム解析 / 新規疾患遺伝子 / 遺伝子解析 / SNP / MITOCHONDRIA / HEREDITARY HEARING LOSS / PDZD7遺伝子 / 次世代シークエンサー / PDZドメイン / USH2複合体 / アッシャー症候群 / 分子病態 Less
  • Research Projects

    (11 results)
  • Research Products

    (128 results)
  • Co-Researchers

    (25 People)
  •  新規難聴遺伝子候補SLC12A2の細胞・動物モデルを用いた分子病態解析Principal InvestigatorOngoing

    • Principal Investigator
      務台 英樹
    • Project Period (FY)
      2018 – 2020
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 56050:Otorhinolaryngology-related
    • Research Institution
      独立行政法人国立病院機構(東京医療センター臨床研究センター)
  •  Elucidation of prevalence, clinical features and pathogenic mechanism of PDZD7 mutations which was identified as a novel gene causing nonsyndromic hearing lossOngoing

    • Principal Investigator
      松永 達雄
    • Project Period (FY)
      2018 – 2019
    • Research Category
      Grant-in-Aid for Challenging Research (Exploratory)
    • Review Section
      Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields
    • Research Institution
      独立行政法人国立病院機構(東京医療センター臨床研究センター)
  •  Molecular functional analysis of ZBTB10, the novel candidate deafness gene associated with cochlear nerve hypoplasiaPrincipal Investigator

    • Principal Investigator
      Mutai Hideki
    • Project Period (FY)
      2015 – 2017
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Otorhinolaryngology
    • Research Institution
      独立行政法人国立病院機構(東京医療センター臨床研究センター)
  •  Elucidation of novel genes causing auditory neuropathy

    • Principal Investigator
      MATSUNAGA Tatsuo
    • Project Period (FY)
      2012 – 2014
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Otorhinolaryngology
    • Research Institution
      独立行政法人国立病院機構(東京医療センター臨床研究センター)
  •  Attenuation of Progressive Hearing Loss in DBA/2J Mice by Epigenetic-Modifying ReagentsPrincipal Investigator

    • Principal Investigator
      MUTAI Hideki
    • Project Period (FY)
      2012 – 2014
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Otorhinolaryngology
    • Research Institution
      独立行政法人国立病院機構(東京医療センター臨床研究センター)
  •  Study of responsible genes for cochlea and cochlear nerve dysplasia

    • Principal Investigator
      MATSUNAGA Tatsuo
    • Project Period (FY)
      2012 – 2013
    • Research Category
      Grant-in-Aid for Challenging Exploratory Research
    • Research Field
      Otorhinolaryngology
    • Research Institution
      独立行政法人国立病院機構(東京医療センター臨床研究センター)
  •  Elucidation of genetic backgrounds of auditory neuropathy specific to Japanese population

    • Principal Investigator
      MATSUNAGA Tatsuo
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Otorhinolaryngology
    • Research Institution
      独立行政法人国立病院機構東京医療センター(臨床研究センター)
      独立行政法人国立病院機構(東京医療センター臨床研究センター)
  •  Study of epigentic mechanism underlying age-related hearing lossPrincipal Investigator

    • Principal Investigator
      MUTAI Hideki
    • Project Period (FY)
      2009 – 2011
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Otorhinolaryngology
    • Research Institution
      独立行政法人国立病院機構東京医療センター(臨床研究センター)
      独立行政法人国立病院機構(東京医療センター臨床研究センター)
  •  General image of mitochondrial DNA mutations as a cause of deafness in Japanese deaf patients.

    • Principal Investigator
      MATSUNAGA Tatsuo
    • Project Period (FY)
      2007 – 2008
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Otorhinolaryngology
    • Research Institution
      独立行政法人国立病院機構(東京医療センター臨床研究センター)
  •  Study of transcription factor Pou3f3 in developing mammalian inner ear and its regulation by epigenetic pathwayPrincipal Investigator

    • Principal Investigator
      MUTAI Hideki
    • Project Period (FY)
      2007 – 2008
    • Research Category
      Grant-in-Aid for Young Scientists (B)
    • Research Field
      Otorhinolaryngology
    • Research Institution
      独立行政法人国立病院機構(東京医療センター臨床研究センター)
  •  Analysis on genetic factors specific to Japanese population in deafness due to mitochondrial mutations.

    • Principal Investigator
      MATSUNAGA Tatsuo
    • Project Period (FY)
      2005 – 2006
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Otorhinolaryngology
    • Research Institution
      National Hospital Organization National Tokyo Medical Center National Institute of Sensory Organs

All 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 Other

All Journal Article Presentation Book Patent

  • [Book] 中耳細菌叢のメタ16S解析 in 実験医学別冊 NGSアプリケーション 今すぐ始める!メタゲノム解析 実験プロトコール 編:服部正平2016

    • Author(s)
      南修司郎、務台英樹
    • Total Pages
      229
    • Publisher
      羊土社
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Book] 病因と遺伝子 in 小耳症/外耳道閉鎖症に対する機能と形態の再建(朝戸裕貴、加我君孝編)2009

    • Author(s)
      松永達雄、孫コウイ、務台英樹
    • Publisher
      金原出版
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Journal Article] High-level heteroplasmy for the m.7445A>G mitochondrial DNA mutation can cause progressive sensorineural hearing loss in infancy2018

    • Author(s)
      Matsushima K, Nakano A, Arimoto Y, Mutai H, Yamazawa K, Murayama K, Matsunaga T.
    • Journal Title

      International Journal of Pediatric Otorhinolaryngology

      Volume: 108 Pages: 125-131

    • DOI

      10.1016/j.ijporl.2018.02.037

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16H05362, KAKENHI-PROJECT-15K10773, KAKENHI-PROJECT-15K15478
  • [Journal Article] IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis.2018

    • Author(s)
      Shigemizu D, Miya F, Akiyama S, Okuda S, Boroevich KA, Fujimoto A, Nakagawa H, Ozaki K, Niida S, Kanemura Y, Okamoto N, Saitoh S, Kato M, Yamasaki M, Matsunaga T, Mutai H, Kosaki K, Tsunoda T
    • Journal Title

      Sci Rep

      Volume: 8 Pages: 10367-10367

    • DOI

      10.1038/s41598-018-23978-z

    • NAID

      120006551758

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16H06299, KAKENHI-PROJECT-16K15530, KAKENHI-PROJECT-16K19068, KAKENHI-PROJECT-18K09336, KAKENHI-PLANNED-18H05511, KAKENHI-PROJECT-16H04726, KAKENHI-PROJECT-18H02680, KAKENHI-PROJECT-16K07211
  • [Journal Article] Spontaneous intramural duodenal hematoma as the manifestation of Noonan syndrome2018

    • Author(s)
      Yamazawa K, Yamada Y, Kuroda T, Mutai H, Matsunaga T, Komiyama O, Takahashi T.
    • Journal Title

      Am J Med Genet A

      Volume: 176 Pages: 496-498

    • DOI

      10.1002/ajmg.a.38556

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16H05362, KAKENHI-PROJECT-15K10773, KAKENHI-PROJECT-15K15478
  • [Journal Article] A case report of reversible generalized seizures in a patient with Waardenburg syndrome associated with a novel nonsense mutation in the penultimate exon of SOX102018

    • Author(s)
      Noriomi Suzuki, Hideki Mutai, Fuyuki Miya, Tatsuhiko Tsunoda, Hiroshi Terashima, Noriko Morimoto, and Tatsuo Matsunaga
    • Journal Title

      BMC Pediatrics

      Volume: 18 Pages: 171-171

    • DOI

      10.1186/s12887-018-1139-2

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K09336, KAKENHI-PROJECT-16K07211
  • [Journal Article] Gene expression dataset for whole cochlea of Macaca fascicularis2018

    • Author(s)
      Hideki Mutai, Fuyuki Miya, Hiroaki Shibata, Yasuhiro Yasutomi, Tatsuhiko Tsunoda, Tatsuo Matsunaga
    • Journal Title

      Scientific Reports

      Volume: 8 Pages: 15554-15554

    • DOI

      10.1038/s41598-018-33985-9

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K09336, KAKENHI-PROJECT-16K07211
  • [Journal Article] Deterioration in Distortion Product Otoacoustic Emissions in Auditory Neuropathy Patients with Distinct Clinical and Genetic Backgrounds2018

    • Author(s)
      Kyoko Kitao; Hideki Mutai; Kazunori Namba; Noriko Morimoto; Atsuko Nakano; Yukiko Arimoto; Tomoko Sugiuchi; Sawako Masuda; Yasuhide Okamoto; Noriko Morita; Hirokazu Sakamoto; Tomoko Shintani; Satoshi Fukuda; Kimitaka Kaga; Tatsuo Matsunaga
    • Journal Title

      Ear and Hearing

      Volume: Ahead of Print Pages: 0196-0202

    • DOI

      10.1097/aud.0000000000000586

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K10774, KAKENHI-PROJECT-18K09336
  • [Journal Article] Microbiomes of the normal middle ear and ears with chronic otitis media.2017

    • Author(s)
      Shujiro B. Minami, Hideki Mutai, Tomoko Suzuki Arata Horii, Naoki Oishi, Koichiro Wasano, Motoyasu Katsura, Fujinobu Tanaka, Tetsuya Takiguchi, Masato Fujii, Kimitaka Kaga
    • Journal Title

      Laryngoscope.

      Volume: 印刷中

    • DOI

      10.1002/lary.26579

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-15K10773, KAKENHI-PROJECT-16K11205
  • [Journal Article] WFS1 and GJB2 mutations in patients with bilateral low-frequency sensorineural hearing loss2017

    • Author(s)
      Natsuko Kasakura-Kimura, Masatsugu Masuda, Hideki Mutai, Sawako Masuda, Noriko Morimoto, Noboru Ogahara, Hayato Misawa, Hirokazu Sakamoto, Koichiro Saito, Tatsuo Matsunaga
    • Journal Title

      Laryngoscope

      Volume: 印刷中

    • DOI

      10.1002/lary.26528

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Journal Article] Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss2017

    • Author(s)
      Yamamoto N, Mutai H, Namba K, Morita N, Masuda S, Nishi Y, Nakano A, Masuda S, Fujioka M, Kaga K, Ogawa K, Matsunaga T.
    • Journal Title

      Orphanet Journal of Rare Diseases

      Volume: 25;12(1) Pages: 157-157

    • DOI

      10.1186/s13023-017-0708-z

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-17K19733, KAKENHI-PROJECT-17H07404, KAKENHI-PROJECT-15K10773, KAKENHI-PROJECT-15K15624
  • [Journal Article] Mitochondrial mutations in maternally inherited hearing loss2017

    • Author(s)
      Hideki Mutai, Takahisa Watabe, Kenjiro Kosaki, Kaoru Ogawa and Tatsuo Matsunaga
    • Journal Title

      BMC Medical Genetics

      Volume: 18 Pages: 32-32

    • DOI

      10.1186/s12881-017-0389-4

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Journal Article] Homozygous EDNRB Mutation in a Patient with Waardenburg Syndrome Type 12017

    • Author(s)
      Noriko Morimoto, Hideki Mutai, Kazunori Namba, Hiroki Kaneko, Rika Kosaki, Tatsuo Matsunaga
    • Journal Title

      Auris Nasus Larynx

      Volume: 印刷中

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Journal Article] Frequency and Specific Characteristics of the Incomplete Partition Type III Inner Ear Anomaly in Children with Hearing Loss2017

    • Author(s)
      Ayako Kanno, Hideki Mutai, Kazunori Namba, Noriko Morita, Atsuko Nakano, Noboru Ogahara, Tomoko Sugiuchi, Kaoru Ogawa, Tatsuo Matsunaga
    • Journal Title

      Laryngoscope

      Volume: 印刷中

    • DOI

      10.1002/lary.26245

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Journal Article] A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 92016

    • Author(s)
      Masuda M, Mutai H, Arimoto Y, Nakano A, Matsunaga T
    • Journal Title

      Biochem Biophys Res Commun.

      Volume: 469 Pages: 270-274

    • DOI

      10.1016/j.bbrc.2015.11.106

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Journal Article] A novel nonsense mutation in the NOG gene causes familial NOG-related symphalangism spectrum disorder2016

    • Author(s)
      Kenichi Takano, Noriko Ogasawara, Tatsuo Matsunaga, Hideki Mutai, Akihiro Sakurai, Aki Ishikawa, and Tetsuo Himi
    • Journal Title

      Human Genome Variation

      Volume: 3 Pages: 16023-16023

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Journal Article] Clinical characteristics of a Japanese family with hearing loss accompanied by compound heterozygous mutations in LOXHD12016

    • Author(s)
      Minami S, Mutai H, Namba M, Sakamoto H, Matsunaga T
    • Journal Title

      Auris Nasus Larynx.

      Volume: S0385-8146 Pages: 30065-7

    • DOI

      10.1016/j.anl.2016.02.010

    • NAID

      130005773901

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-15K10773, KAKENHI-PROJECT-25462657
  • [Journal Article] High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss.2015

    • Author(s)
      Mizutari K, Mutai H., Namba K., Miyanaga Y., Nakano A., Arimoto Y., Masuda S., Morimoto N., Sakamoto H., Kaga K., Matsunaga T.
    • Journal Title

      Orphanet J Rare Dis.

      Volume: 10 Pages: 60-60

    • DOI

      10.1186/s13023-015-0276-z

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-24592573, KAKENHI-PROJECT-15K10773, KAKENHI-PROJECT-26462572
  • [Journal Article] A novel frameshift mutation in KCNQ4 in a family with autosomal recessive non-syndromic hearing loss2015

    • Author(s)
      Wasano K, Mutai H, Obuchi C, Masuda S, Matsunaga T
    • Journal Title

      Biochem Biophys Res Comm

      Volume: 463 Pages: 582-586

    • DOI

      10.1016/j.bbrc.2015.05.099

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Journal Article] Attenuation of Progressive Hearing Loss in DBA/2J Mice by Reagents that Affect Epigenetic Modifications Is Associated with Up-Regulation of the Zinc Importer Zip42015

    • Author(s)
      Mutai H., Miya F., Fujii M., Tsunoda T., Matsunaga T.
    • Journal Title

      PLOS ONE

      Volume: 10

    • DOI

      10.1371/journal.pone.0124301

    • Peer Reviewed / Acknowledgement Compliant / Open Access
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Journal Article] A mutation in the heparin-binding site of noggin as a novel mechanism of proximal symphalangism and conductive hearing loss2014

    • Author(s)
      Masuda S., Namba K., Mutai H., Usui S., Miyanaga Y., Kaneko H., Matsunaga T.
    • Journal Title

      Biochemical and Biophysical Research Communications

      Volume: 447 Pages: 196-502

    • DOI

      10.1016/j.bbrc.2014.04.015

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-24592573, KAKENHI-PROJECT-26280108
  • [Journal Article] Subgroups of enlarged vestibular aqueduct in relation with SLC26A4 mutations and hearing loss2014

    • Author(s)
      Yasuhide Okamoto, Hideki Mutai, Atsuko Nakano, Yukiko Arimoto, , Tomoko Sugiuchi, Sawako Masuda, Noriko Morimoto, Hirokazu Sakamoto, , Noboru Ogahara, Akira Takagi, Hidenobu Taiji, Kimitaka Kaga, Kaoru Ogawa, Tatsuo Matsunaga
    • Journal Title

      Laryngoscope

      Volume: 124

    • DOI

      10.1002/lary.24368

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Journal Article] 次世代シークエンサーを用いた難聴の遺伝子診断に関する検討2013

    • Author(s)
      松永達雄、鈴木直大、務台英樹、難波一徳、加我君孝
    • Journal Title

      Otol Jpn

      Volume: 23(5) Pages: 903-907

    • NAID

      130005065221

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24659753
  • [Journal Article] 次世代シークエンサーを用いた難聴の遺伝子診断に関する検討2013

    • Author(s)
      松永達雄、鈴木直大、務台英樹、難波一徳、加我君孝
    • Journal Title

      Otol Japan

      Volume: 23 Pages: 903-907

    • NAID

      130005065221

    • Data Source
      KAKENHI-PROJECT-24592573
  • [Journal Article] 次世代シークエンサーを用いた難聴の遺伝子診断に関する検討2013

    • Author(s)
      松永達雄、鈴木直大、務台英樹、難波一徳、加我君孝
    • Journal Title

      Otol Jpn

      Volume: 23(5) Pages: 903-907

    • NAID

      130005065221

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390391
  • [Journal Article] GJB2-associated hearing loss undetected by hearing screening of newborns.2013

    • Author(s)
      Shujiro B Minami, Hideki Mutai, Atsuko Nakano, Yukiko Arimoto, Hidenobu Taiji, Noriko Morimoto, Hideaki Sakata, Nodoka Adachi, Sawako Masuda, Hirokazu Sakamoto, Haruo Yoshida, Fujinobu Tanaka, Tomoko Sugiuchi, Kimitaka Kaga, Tatsuo Matsunaga
    • Journal Title

      Gene

      Volume: 532 Pages: 41-45

    • DOI

      10.1016/j.gene.2013.08.094

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24592573, KAKENHI-PROJECT-25462657
  • [Journal Article] Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients : A cross-sectional, multi-center next-generation sequencing study2013

    • Author(s)
      Mutai H, Suzuki N, Shimizu A, Torii C, Namba K, Morimoto N, Kudoh J, Kaga K, Kosaki K, Matsunaga T
    • Journal Title

      Orphanet J. Rare Dis

      Volume: 8(1) Pages: 172-172

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24659753
  • [Journal Article] Genetic analysis of PAX3 for diagnosis of Waardenburg syndrome type I2013

    • Author(s)
      Matsunaga T, Mutai H, Namba K, Morita N, Masuda S.
    • Journal Title

      Acta Oto-Laryngologica

      Volume: 133 Pages: 345-351

    • DOI

      10.3109/00016489.2012.744470

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Journal Article] Moderate hearing loss associated with a novel KCNQ4 non-truncating mutation located near the N-terminus of the pore helix.2013

    • Author(s)
      Takahisa Watabe,Tatsuo Matsunaga, Kazunori Namba, Hideki Mutai, Yasuhiro Inoue, Kaoru Ogawa
    • Journal Title

      Biochemical and Biophysical Research Communications

      Volume: 432

    • DOI

      10.1016/j.bbrc.2013.01.118

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Journal Article] Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: A cross-sectional, multi-center next-generation sequencing study2013

    • Author(s)
      Mutai H, Suzuki N, Shimizu A, Torii C, Namba K, Morimoto N, Kudoh J, Kaga K, Kosaki K, Matsunaga T
    • Journal Title

      Orphanet Journal of Rare Diseases

      Volume: 8 Pages: 172-172

    • DOI

      10.1186/1750-1172-8-172

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24390391, KAKENHI-PROJECT-24592573, KAKENHI-PROJECT-24659753
  • [Journal Article] A novel animal model of hearing loss caused by acute endoplasmic reticulum stress in the cochlea2012

    • Author(s)
      Fujinami Y, Mutai H, Mizutari K, Nakagawa S, and Matsunaga T
    • Journal Title

      Journal of Pharmacological Sciences

      Volume: 118 Pages: 363-72

    • NAID

      10030455675

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] A prevalent founder mutation of OTOF and additional genotype-phenotype correlations identified in Japanese patients with congenital or early-onset auditory neuropathy.2012

    • Author(s)
      Matsunaga T, Mutai H, Kunishima S, Namba K, Morimoto N, Shinjo Y, Arimoto Y, Kataoka Y, Shintani T, Morita N, Sugiuchi T, Masuda S, Nakano A, Taiji H, Kaga K.
    • Journal Title

      Clinical Genetics

      Volume: 82(5) Pages: 425-32

    • DOI

      10.1111/j.1399-0004.2012.01897.x

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22791641, KAKENHI-PROJECT-23591429, KAKENHI-PROJECT-24390391, KAKENHI-PROJECT-24592573
  • [Journal Article] In silico Modeling of the Pore Region of a KCNQ4 Missense Mutant from a Patient with Hearing Loss2012

    • Author(s)
      Namba K., Mutai H(equal contributor), et al
    • Journal Title

      BMC Research Notes

      Volume: 5 Pages: 145-145

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] Comorbid of GJB2 and WFS1 mutations in one family.2012

    • Author(s)
      Shujiro B Minami1, Sawako Masuda, Tomoko Usui, Hideki Mutai, Tatsuo Matsunaga.
    • Journal Title

      Gene

      Volume: 501 Pages: 193-197

    • DOI

      10.1016/j.gene.2012.03.060

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Journal Article] In silico Modeling of the Pore Region of a KCNQ4 Missense Mutant from a Patient with Hearing Loss2012

    • Author(s)
      Namba K, Mutai H, Kaneko H, Hashimoto S, Matsunaga T
    • Journal Title

      BMC Research Notes

      Volume: 5 Pages: 145-145

    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population : dHPLC reveals a new candidate mutation2011

    • Author(s)
      Mutai H, Kouike H, Teruya E, Takahashi-Kodomoari I, Kakishima H, Taiji H, Usami SI, Okuyama T, Matsunaga T
    • Journal Title

      BMC Med Genet

      Volume: 12 Pages: 135-135

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21592172
  • [Journal Article] Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population : dHPLC reveals a new candidate mutation2011

    • Author(s)
      Mutai H, Kouike H, Teruya E, Takahashi-Kodomoari I, Kakishima H, Taiji H, Usami S, Okuyama T and Matsunaga T
    • Journal Title

      BMC Medical Genetics

      Volume: 12 Pages: 135-135

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population : dHPLC reveals a new candidate mutation2011

    • Author(s)
      Mutai H
    • Journal Title

      BMC Medical Genetics

      Volume: 12 Pages: 135-135

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] Late-phase recovery in the cochlear lateral wall following severe degeneration by acute energy failure2011

    • Author(s)
      Mizutari K, Nakagawa S, Mutai H, Fujii M, Ogawa K, Matsunaga T
    • Journal Title

      Brain Res

      Volume: 1419 Pages: 1-11

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population : dHPLC reveals a new candidate mutation2011

    • Author(s)
      Mutai H
    • Journal Title

      BMC Med Genet

      Volume: 12 Pages: 135-135

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21592172
  • [Journal Article] Enhanced expression of C/EBP homologous protein(CHOP) precedes degeneration of fibrocytes in the lateral wall after acute cochlear mitochondrial dysfunction induced by 3-nitropropionic acid2010

    • Author(s)
      Fujinami Y, Mutai H, Kamiya K, Mizutari K, Fujii M, Matsunaga T
    • Journal Title

      Neurochemistry International

      Volume: 56 Pages: 487-494

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] Expression of Pou3f3/Brn-1 and its genomic methylation in developing auditory epithelium.2009

    • Author(s)
      Hideki Mutai, ほか
    • Journal Title

      Developmental Neurobiology 69

      Pages: 913-930

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] Expression of Pou3f3/Brn-1 and its genomic methylation in developing auditory epithelium2009

    • Author(s)
      Mutai H, Nagashima R, Sugitani Y, Noda T, Fujii M, Matsunaga T.
    • Journal Title

      Develop. Neurobiol

      Volume: 69 Pages: 913-930

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] Mitotic activity and specification of fibrocyte subtypes in the developing rat cochlear lateral wall.2009

    • Author(s)
      Hideki Mutai, ほか
    • Journal Title

      Neuroscience 163

      Pages: 1255-1263

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] Mitotic activity and specification of fibrocyte subtypes in the developing rat cochlear lateral wall2009

    • Author(s)
      Hideki Mutai, Masato Fujii, Tatsuo Matsunaga
    • Journal Title

      Neuroscience (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Journal Article] Promoted cell Proliferation by Connexin 30 Gene Transfection fo Head-and-Neck Cancer Cell Line2009

    • Author(s)
      Ozawa H, Mutai H, Tatsuo Matsunaga T, Tokumaru Y, Fujii M, Sakamoto K, Tomita T, Ogawa K
    • Journal Title

      Anticancer Res

      Volume: 29 Pages: 1981-1986

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] Expression of Pou3f3/Brn-1 and its genomic methylation in developing auditory epithelium2009

    • Author(s)
      Hideki Mutai, Reiko Nagashima, Yoshinobu Sugitani, Tetsuo Noda, Masato Fujii, Tatsuo Matsunaga
    • Journal Title

      Developmental Neurobiology (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Journal Article] Mitotic activity and specification of fibrocyte subtypes in the developing rat cochlear lateral wall2009

    • Author(s)
      Mutai H, Nagashima R, Fujii M, Matsunaga T
    • Journal Title

      Neuroscience

      Volume: 163 Pages: 1255-1263

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Journal Article] 難聴の遺伝子検査2008

    • Author(s)
      松永達雄、幸池浩子、務台英樹
    • Journal Title

      神経内科 68(5)

      Pages: 415-421

    • Data Source
      KAKENHI-PROJECT-19592001
  • [Journal Article] 難聴の遺伝子検査2008

    • Author(s)
      松永達雄, 幸池浩子, 務台英樹
    • Journal Title

      神経内科 68(5)

      Pages: 415-421

    • Data Source
      KAKENHI-PROJECT-19592001
  • [Journal Article] 難聴の遺伝子検査2008

    • Author(s)
      松永達雄、幸池浩子、務台英樹
    • Journal Title

      神経内科 68

      Pages: 415-421

    • Data Source
      KAKENHI-PROJECT-19791251
  • [Journal Article] Auditory neuropathyの遺伝子研究の動向2008

    • Author(s)
      松永達雄、務台英樹
    • Journal Title

      Monthly Book ENTONI 93

      Pages: 11-16

    • Data Source
      KAKENHI-PROJECT-19791251
  • [Journal Article] Auditory Neuropathyの遺伝子研究の動向2008

    • Author(s)
      松永達雄、務台英樹
    • Journal Title

      MB ENT 93

      Pages: 11-16

    • Data Source
      KAKENHI-PROJECT-19592001
  • [Journal Article] Auditory Neuropathy の遺伝子研究の動向2008

    • Author(s)
      松永達雄, 務台英樹
    • Journal Title

      MB ENT 93

      Pages: 11-16

    • Data Source
      KAKENHI-PROJECT-19592001
  • [Journal Article] Comorbidity of GJB2 and WFS1 mutations in one family

    • Author(s)
      Minami SB, Masuda S, Usui S, Mutai H, Matsunaga T
    • Journal Title

      Gene

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-21592172
  • [Journal Article] A prevalent founder mutation and genotype-phenotype correlations of OTOF in Japanese patients with auditory neuropathy

    • Author(s)
      Matsunaga T, Mutai H, Kunishima S, Namba K, Morimoto N, Shinjo Y, Arimoto Y, Kataoka Y, Shintani T, Morita N, Sugiuchi T, Masuda S, Nakano A, Taiji H, Kaga K
    • Journal Title

      Clin Genet

    • Data Source
      KAKENHI-PROJECT-21592172
  • [Patent] 難聴疾患の予防又は治療剤2011

    • Inventor(s)
      務台英樹、藤井正人、松永達雄
    • Industrial Property Rights Holder
      独立行政法人国立病院機構
    • Filing Date
      2011-01-18
    • Data Source
      KAKENHI-PROJECT-21592172
  • [Patent] 難聴疾患の予防又は治療剤2011

    • Inventor(s)
      務台・藤井・松永
    • Industrial Property Rights Holder
      国立病院機構
    • Industrial Property Number
      2011-007581
    • Filing Date
      2011-01-18
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Patent] 難聴疾患の予防又は治療剤2011

    • Inventor(s)
      務台英樹、藤井正人、松永達雄
    • Industrial Property Rights Holder
      財団法人ヒューマンサイエンス振興財団
    • Industrial Property Number
      2011-000758
    • Filing Date
      2011-01-18
    • Data Source
      KAKENHI-PROJECT-21592172
  • [Patent] 難聴疾患の予防又は治療剤2011

    • Inventor(s)
      務台英樹、松永達雄、藤井正人
    • Industrial Property Rights Holder
      国立病院機構
    • Filing Date
      2011-01-18
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] Identification of SLC12A2 as a candidate of deafness gene in human2019

    • Author(s)
      Hideki Mutai, Koichiro Wasano, Yukihide Momozawa, Yoichiro Kamatani, Fuyuki Miya, Sawako Masuda, Noriko Morimoto, Kiyomitsu Nara, Satoe Takahashi, Tatsuhiko Tsunoda, Kazuaki Homma, Mitsuaki Kubo, Tatsuo Matsunaga
    • Organizer
      42nd Annual Midwinter Meeting, Association for Research in Otolaryngology
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K09336
  • [Presentation] Whole Exome Sequencing to Discover Novel Genes Associated with Hearing Loss2018

    • Author(s)
      Hideki Mutai, Yukihide Momozawa, Yoichiro Kamatani, Michiaki Kubo, Tatsuo Matsunaga
    • Organizer
      41th annual midwinter meeting, Association for Research in Otolaryngology
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Presentation] Exome解析により同定された新規難聴原因候補SLC12A2変異とその機能解析2018

    • Author(s)
      務台英樹、和佐野浩一郎、奈良清光、松永達雄
    • Organizer
      第28回日本耳科学会
    • Data Source
      KAKENHI-PROJECT-18K09336
  • [Presentation] Whole Exome Sequencingにより同定された新規難聴原因候補SLC12A2とその変異2018

    • Author(s)
      務台英樹、和佐野浩一郎、桃沢幸秀、鎌谷洋一郎、宮冬樹、奈良清光、角田達彦、本間和明、久保充明、松永達雄
    • Organizer
      第63回日本人類遺伝学会
    • Data Source
      KAKENHI-PROJECT-18K09336
  • [Presentation] Multiple defects observed in postnatal Cbx2cterm/cterm mice2018

    • Author(s)
      Yuko Katoh-Fukui, Hideki Mutai and Maki Fukami
    • Organizer
      2nd INFRAFRONTIER / IMPC Stakeholder Meeting
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K09336
  • [Presentation] Identification of novel candidate deafness genes by whole exome sequencing in patients with hearing loss.2018

    • Author(s)
      Matsunaga T, Nara K, Inoue S, Yamamoto N, Minami S, Kaga K, Mutai H
    • Organizer
      Corlas Annual Meeting 2018
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-18K19626
  • [Presentation] Apoptosis is Associated with Decreased BDNF Signal in the Spiral Ganglion of Otof -deficient Mouse2018

    • Author(s)
      Kazunori Namba, Hideki Mutai, Tatsuo Matsunaga
    • Organizer
      41th annual midwinter meeting, Association for Research in Otolaryngology
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Presentation] 3家系より同定された新規難聴原因候補SLC12A2と変異の機能解析2018

    • Author(s)
      務台英樹、和佐野浩一郎、桃沢幸秀、鎌谷洋一郎、宮冬樹、奈良清光、高橋里枝、角田達彦、本間和明、久保充明、松永達雄
    • Organizer
      第41回日本分子生物学会
    • Data Source
      KAKENHI-PROJECT-18K09336
  • [Presentation] Exome解析を用いた新規難聴原因遺伝子の探索2017

    • Author(s)
      務台英樹 松永達雄
    • Organizer
      第27回日本耳科学会
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Presentation] 臨床検体を用いた中耳細菌叢のメタ16S解析2017

    • Author(s)
      務台英樹、鈴木朋子、南修司郎
    • Organizer
      NGS現場の会 第5回研究会
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Presentation] 混合難聴の進行により、人工内耳埋め込み術を施行した中耳・内耳奇形・内耳道狭窄の3症例の検討2017

    • Author(s)
      利國桂太郎、南修司郎、山本修子、和佐野浩一郎、務台英樹、松永達雄、加我君孝
    • Organizer
      第27回日本耳科学会
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Presentation] TECTA蛋白の構造解析による新規変異の分子病態予測2017

    • Author(s)
      山本修子、難波一徳、務台英樹、森田訓子、松永達雄
    • Organizer
      第27回日本耳科学会
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Presentation] 臨床像を起点とした遺伝性難聴診療の確立2017

    • Author(s)
      松永達雄、加我君孝、務台英樹、奈良清光、南修司郎、山本修子、藤岡正人、小川郁
    • Organizer
      第27回日本耳科学会
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Presentation] Microbiomes in the normal middle ear and chronic otitis media2016

    • Author(s)
      Minami S, Mutai H, Suzuki T, HoriiA, Oishi N, Katsura M, Wasano K, Tanaka F, Takiguchi T, Fujii M.
    • Organizer
      Association for Research in Otolaryngology 39th Midwiner Meeting
    • Place of Presentation
      Manchester Grand Hyatt, San Diego, CA, USA
    • Year and Date
      2016-02-20
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Presentation] Exome解析を用いた症候群性難聴に対する原因遺伝子同定の試み2015

    • Author(s)
      務台英樹、仲野敦子、有本友希子、松永達雄
    • Organizer
      第25回日本耳科学会総会
    • Place of Presentation
      長崎ブリックホール
    • Year and Date
      2015-10-07
    • Data Source
      KAKENHI-PROJECT-15K10773
  • [Presentation] Target-captured next generation sequencing of reported deafness genes reveals variability of genetic background of hereditary hearing loss in Japan.2013

    • Author(s)
      Mutai H, Suzuki N, Shimizu A, Torii C, Namba K, Kudoh J, Kosaki K, Matsunaga T
    • Organizer
      9th Molecular Biology of Hearing & Deafness Conference the Stanford School of Medicine in Stanford
    • Place of Presentation
      California, USA
    • Data Source
      KAKENHI-PROJECT-24390391
  • [Presentation] 孤発例の先天性難聴患者における稀少難聴遺伝子変異の同定2013

    • Author(s)
      務台英樹、難波一徳、加我君孝、松永達雄
    • Organizer
      第23回日本耳科学会
    • Place of Presentation
      宮崎県宮崎市 シーガイアコンヴェンションセンター
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Presentation] Target-captured next generation sequencing of reported deafness genes reveals variability of genetic background of hereditary hearing loss in Japan.2013

    • Author(s)
      Mutai H, Suzuki N, Shimizu A, Torii C, Namba K, Kudoh J, Kosaki K, Matsunaga T
    • Organizer
      9th Molecular Biology of Hearing & Deafness Conference the Stanford School of Medicine in Stanford
    • Place of Presentation
      California, USA
    • Data Source
      KAKENHI-PROJECT-24659753
  • [Presentation] Target-captured next generation sequencing of reported deafness genes reveals variability of genetic background of hereditary hearing loss in Japan2013

    • Author(s)
      Hideki Mutai, Naohiro Suzuki, Atsushi Shimizu, Chiharu Torii, Kazunori Namba, Jun Kudoh, Kenjiro Kosaki,Tatsuo Matsunaga
    • Organizer
      9th Molecular Biology of Hearing and Deafness
    • Place of Presentation
      Stanford University, Palo Alto, California, USA
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Presentation] 次世代シークエンスデータにおける難聴遺伝子変異の探索2012

    • Author(s)
      鈴木直大、務台英樹、松永達雄
    • Organizer
      第22回日本耳科学会
    • Place of Presentation
      名古屋国際会議場
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Presentation] カスタムターゲットリシーケンスによる難聴関連遺伝子の変異探索2012

    • Author(s)
      鈴木直大、務台英樹、鳥居千春、清水厚志、宮冬樹、難波一徳、工藤純、小崎健次郎、松永達雄
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      京王プラザホテル
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Presentation] Noggin蛋白質のin silico解析から推測されたSYM-1におけるアブミ骨を含む骨固着の分子病態2012

    • Author(s)
      難波一徳、務台英樹、増田佐和子、臼井智子、藤井正人、松永達雄
    • Organizer
      第22回日本耳科学会
    • Place of Presentation
      名古屋国際会議場
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Presentation] Genotype and Phenotype Correlation in GJB2 Mutations(DFNB1) and Structural Analysis of Non-Inactivating Mutations2012

    • Author(s)
      Shujiro Minami, Kazunori Namba ; Hideki Mutai ; Tatsuo Matsunaga
    • Organizer
      第35回北米耳鼻咽喉科学会
    • Place of Presentation
      サンディエゴ、米国
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] Rapid and efficient mutation detection in the hundreds of target genes by bench-top next generation sequencer with custom target capture method2012

    • Author(s)
      Shimizu A, Torii C, Suzuki N, Mutai H, Kudoh J, Kosaki R, Matsunaga T, Kosaki K
    • Organizer
      62nd Annual Meeting of the American Society of Human Genetics (ASHG)
    • Place of Presentation
      San Francisco, California, USA
    • Data Source
      KAKENHI-PROJECT-24659753
  • [Presentation] 次世代シークエンサーを用いた難聴の遺伝子診断に関する検討2012

    • Author(s)
      松永達雄、鈴木直大、務台英樹、難波一徳、加我君孝
    • Organizer
      第22回日本耳科学会
    • Place of Presentation
      名古屋国際会議場
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Presentation] 難聴モデルDBA/2Jマウスに対するエピジェネティクス調節と聴力変化の検討2012

    • Author(s)
      務台英樹・藤井正人・松永達雄
    • Organizer
      第22回日本耳科学会
    • Place of Presentation
      名古屋国際会議場
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Presentation] dHPLC法を用いた日本人難聴者におけるミトコンドリア遺伝子多型解析2011

    • Author(s)
      務台英樹・泰地秀信、宇佐美真一、松永達雄
    • Organizer
      第21回日本耳科学会総会
    • Place of Presentation
      沖縄コンベンションセンター
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] dHPLC法を用いた日本人難聴者におけるミトコンドリア遺伝子多型解析2011

    • Author(s)
      務台英樹
    • Organizer
      第21回日本耳科学会
    • Place of Presentation
      沖縄コンベンションセンター
    • Year and Date
      2011-11-24
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] 温度感受性Auditory NeuropathyにおけるOTOF遺伝子の新規特異的変異の同定2011

    • Author(s)
      松永達雄、新正由紀子、山本聡、難波一徳、務台英樹、加我君孝
    • Organizer
      第21回日本耳科学会総会
    • Place of Presentation
      沖縄コンベンションセンター
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] Expression of DNA methyltransferases(Dnmts) in developing auditory epithelium and possible role for maintenance of hearing2011

    • Author(s)
      Hideki Mutai, Susumu Nakagawa Kazunori Namba, Masato Fujii, Tatsuo Matsunaga
    • Organizer
      第34回北米耳鼻咽喉科学会
    • Place of Presentation
      バルチモア米国
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] 加齢性難聴動物モデルを用いたDNAメチル化解析2011

    • Author(s)
      務台英樹
    • Organizer
      第6回 感覚器センターシンポジウム
    • Place of Presentation
      東京医療センター
    • Year and Date
      2011-03-04
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] Expression of DNA methyltransferases (Dnmts) in developing auditory epithelium and possible role for maintenance of hearing2011

    • Author(s)
      務台英樹
    • Organizer
      第34回 北米耳鼻咽喉科学会
    • Place of Presentation
      Marriot Waterfront Hotel, Baltimore, MA, USA
    • Year and Date
      2011-02-20
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] dHPLC法を用いた日本人難聴者におけるミトコンドリア遺伝子多型解析2011

    • Author(s)
      務台英樹
    • Organizer
      第21回日本耳科学会
    • Place of Presentation
      沖縄県宜野湾市
    • Data Source
      KAKENHI-PROJECT-21592172
  • [Presentation] 聴覚発達とエピジェネティック制御機構2010

    • Author(s)
      務台英樹
    • Organizer
      第5回感覚器シンポジウム
    • Place of Presentation
      東京医療センター(東京都)
    • Year and Date
      2010-03-11
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] 聴覚発達・老化と関連するDNAメチル化修飾とメチル化酵素Dnmt3a/3bの発現2010

    • Author(s)
      務台英樹・藤井正人・松永達雄
    • Organizer
      第20回日本耳科学会総会
    • Place of Presentation
      愛媛県ひめぎんホール
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] 日本人小児Auditory Neuropathyの遺伝的要因の解明2010

    • Author(s)
      務台英樹
    • Organizer
      第55回人類遺伝学会
    • Place of Presentation
      大宮ソニックシティ
    • Year and Date
      2010-10-28
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] 聴覚発達・老化と関連するDNAメチル化修飾とメチル化酵素Dnmt3a/3bの発現2010

    • Author(s)
      務台英樹
    • Organizer
      第20回日本耳科学会総会
    • Place of Presentation
      愛媛県・ひめぎんホール
    • Year and Date
      2010-10-08
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] 日本人小児Auditory Neuropathyの遺伝的要因の解明2010

    • Author(s)
      松永達雄、加我君孝、務台英樹、泰地秀信、守本倫子、新正由紀子、武腰英樹、仲野敦子、新谷朋子、難波一徳、増田佐和子、新田清一
    • Organizer
      第20回日本耳科学会総会・学術講演会
    • Place of Presentation
      ひめぎんホール(松山市)
    • Data Source
      KAKENHI-PROJECT-21592172
  • [Presentation] 発達中および成熟個体聴覚上皮におけるDNAメチル化酵素Dnmt3a/3bの発現2010

    • Author(s)
      務台英樹、藤井正人、松永達雄
    • Organizer
      第4回日本エピジェネティクス研究会年会
    • Place of Presentation
      米子市文化ホール
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] 日本人小児Auditory NeuropathyにおけるOTOF遺伝子解析と治療法選択2010

    • Author(s)
      松永達雄、國島伸治、務台英樹、難波一徳、加我君孝
    • Organizer
      第55回日本人類遺伝学会
    • Place of Presentation
      大宮ソニックシティ(さいたま市)
    • Data Source
      KAKENHI-PROJECT-21592172
  • [Presentation] 日本人小児Auditory NeuropathyにおけるOTOF遺伝子解析と治療法選択への活用2010

    • Author(s)
      松永達雄、國島伸治、務台英樹、難波一徳、加我君孝
    • Organizer
      第55回人類遺伝学会埼玉県さいたま市大宮区桜木町1-7-5
    • Place of Presentation
      大宮ソニックシティ
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] 発達中および成熟個体聴覚上皮におけるDNAメチル化酵素Dnmt3a/3bの発現2010

    • Author(s)
      務台英樹
    • Organizer
      第4回 日本エピジェネティクス研究会年会
    • Place of Presentation
      米子市文化ホール
    • Year and Date
      2010-05-28
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] ラット蝸牛外側壁線維細胞の生後発達様式2009

    • Author(s)
      務台英樹, ほか
    • Organizer
      第32回日本耳科学会総会
    • Place of Presentation
      京王プラザホテル(東京都)
    • Year and Date
      2009-10-08
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] Genomic DNA of Pou3f3/Brn-1 is highly methylated in the CpG island at the 3'-flanking region in the developing auditory epithelium2009

    • Author(s)
      Hideki Mutai, Masato Fujii, Tatsuo Matsunaga
    • Organizer
      32^<nd> meeting, Association for Research in Otolaryngology
    • Place of Presentation
      Baltimore, MA, USA
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] 聴覚のエイジングと全身疾患-基礎的検討と臨床研究2009

    • Author(s)
      藤井正人、務台英樹
    • Organizer
      第4回感覚器シンポジウム
    • Place of Presentation
      東京
    • Year and Date
      2009-03-13
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] Genomic DNA of Pou3f3/Brn-1 is highly methylated in the CpG island at the 3'-flanking region in the developing auditory epithehum2009

    • Author(s)
      務台英樹
    • Organizer
      第32回北米耳鼻咽喉科学会
    • Place of Presentation
      米国メリーランド州ボルチモア・マリオットホテル
    • Year and Date
      2009-02-17
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] Expression of Pou3f3/Brn-1 and its genomic methylation in developing auditory epithelium2009

    • Author(s)
      務台英樹, ほか
    • Organizer
      第32回日本分子生物学会年年会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2009-12-09
    • Data Source
      KAKENHI-PROJECT-21791659
  • [Presentation] 小児難聴に対する系統的遺伝子解析の第1次解析の検討2008

    • Author(s)
      松永達雄、加我君孝、務台英樹、孫コウイ、守本倫子、泰地秀信、竹腰英樹、藤井正人、井上泰宏、小川郁
    • Organizer
      第53回日本聴覚医学会
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] 幼小児難聴の系統的遺伝子解析と診療への活用2008

    • Author(s)
      松永達雄、加我君孝、藤井正人、務台英樹、孫こうい、橋本省、三沢逸人、瀧口哲也、中原はるか、上田勉、竹腰英樹、徳丸裕、羽生昇、矢島陽子、泰地秀信、守本倫子
    • Organizer
      第62回国立病院総合医学会
    • Place of Presentation
      東京国際フォーラム、東京
    • Year and Date
      2008-11-22
    • Data Source
      KAKENHI-PROJECT-19592001
  • [Presentation] Expression of Pou3f3/Brn1 and its possible epigenetic regulation in the developing mammalian cochlea2008

    • Author(s)
      Hideki Mutai, Masato Fujii, Tatsuo Matsunaga
    • Organizer
      31^<st> meeting, Association for Research in Otolaryngology
    • Place of Presentation
      Phoenix, AZ, USA
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] Expression of Pou3f3/Brn1 and its possible epigenetic regulation in the developing mammalian cochlea2008

    • Author(s)
      務台 英樹、藤井 正人、松永 達雄
    • Organizer
      第31回北米耳鼻咽喉学会
    • Place of Presentation
      フェニックス・コンベンションセンター
    • Year and Date
      2008-02-19
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] 小児難聴に対する系統的遺伝子解析の第一次解析の検討2008

    • Author(s)
      松永達雄、加我君孝、務台英樹、孫こうい、守本倫子、泰地秀信、竹腰英樹、藤井正人、井上泰宏、小川郁
    • Organizer
      第53回日本聴覚医学会総会
    • Place of Presentation
      明治記念館、東京
    • Data Source
      KAKENHI-PROJECT-19592001
  • [Presentation] 生後発達期の聴覚上皮におけるエピジェネティック遺伝子制御機構2008

    • Author(s)
      務台英樹、藤井正人、松永達雄
    • Organizer
      第18回日本耳科学会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] 新生児・乳幼児難聴に対するGJB2遺伝子およびミトコンドリアDNA変異の遺伝子診断2008

    • Author(s)
      松永達雄、孫こうい、務台英樹、幸池浩子、守本倫子、松田明史、川城信子、山下大介、竹腰英樹、矢島陽子、羽生昇、徳丸裕、藤井正人、泰地秀信、加我君孝
    • Organizer
      第3回日本小児耳鼻咽喉科学会総会
    • Place of Presentation
      城山観光ホテル、鹿児島市
    • Data Source
      KAKENHI-PROJECT-19592001
  • [Presentation] 生後発達期の聴覚上皮におけるエピジェネティック遺伝子制御機構2008

    • Author(s)
      務台英樹
    • Organizer
      第18回日本耳科学会
    • Place of Presentation
      兵庫県・神戸国際会議場
    • Year and Date
      2008-10-16
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] Expression of Pou3f3/Brn1 and it'spossible epigenetic regulation in the developing mammalian cochlea.2008

    • Author(s)
      Mutai H, et. al.
    • Organizer
      31st Annual midwinter research meeting of the association for reaesrch in otolaryngology.
    • Place of Presentation
      Phoenix, Arizona, USA
    • Data Source
      KAKENHI-PROJECT-19592001
  • [Presentation] 急性内耳エネルギー不全による蝸牛外側壁線維細胞の可塑的変化2008

    • Author(s)
      瀧口洋一郎、孫コウイ、務台英樹、幸池浩子、水足邦雄、藤井正人、小川郁、松永達雄
    • Organizer
      第18回日本耳科学会
    • Place of Presentation
      神戸
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] ラット蝸牛外側壁線維細胞の生後発達と細胞増殖2007

    • Author(s)
      務台 英樹、藤井 正人、松永 達雄
    • Organizer
      第52回日本聴覚医学会総会・学術講演会
    • Place of Presentation
      名古屋国際会議場
    • Year and Date
      2007-10-05
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] POU3f3/Brm1の胎生内耳における発現分布と欠損マウスを用いた解析2007

    • Author(s)
      務台 英樹, 他
    • Organizer
      第17回日本耳科学会総会
    • Place of Presentation
      福岡
    • Data Source
      KAKENHI-PROJECT-19592001
  • [Presentation] Pou3f3/Brn1の胎生内耳における発現分布と欠損マウスを用いた解析2007

    • Author(s)
      務台 英樹、藤井 正人、松永 達雄
    • Organizer
      第17回日本耳科学会総会・学術講演会
    • Place of Presentation
      福岡国際会議場
    • Year and Date
      2007-10-18
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] 原因不明の両側性感音難聴に対して行う難聴遺伝子解析の臨床的意義2007

    • Author(s)
      松永達雄、藤井正人、幸池浩子、務台英樹、孫こうい、橋本省、三沢逸人、瀧口哲也、小室哲、永橋立望、竹内直信、上田勉、加我君孝
    • Organizer
      第61回国立病院総合医学会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-19592001
  • [Presentation] 原因不明の日本人難聴者における12S ribosomalRNA (MTRNR1)遺伝子変異解析2007

    • Author(s)
      松永達雄、幸池浩子、務台英樹、孫コウイ、藤井正人、守本倫子、泰地秀信、宇佐美真一、佐藤美奈子、小川郁、加我君孝
    • Organizer
      第17回日本耳科学会
    • Place of Presentation
      福岡
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] Pou3f3/Brn1の胎生内耳における発現分布と欠損マウスを用いた解析2007

    • Author(s)
      務台英樹、藤井正人、松永達雄
    • Organizer
      第17回日本耳科学会
    • Place of Presentation
      福岡
    • Data Source
      KAKENHI-PROJECT-19791251
  • [Presentation] A3243GtRNALeu(UUR)遺伝子変異による両側性感音難聴10家系の検討2007

    • Author(s)
      松永達雄、幸池浩子、孫こうい、務台英樹、藤井正人、加我君孝、武井泰彦、武井聡、相馬啓子、佐藤美奈子、小川郁
    • Organizer
      第52回日本聴覚医学会総会
    • Place of Presentation
      名古屋
    • Data Source
      KAKENHI-PROJECT-19592001
  • [Presentation] 原因不明の日本人難聴者における12S ribosomal RNA(MTRNR1)遺伝子変異解析2007

    • Author(s)
      松永達雄、幸池浩子、務台英樹、孫こうい、藤井正人、守本倫子、泰地秀信、宇佐美真一、佐藤美奈子、小川郁、加我君孝
    • Organizer
      第17回日本耳科学会総会
    • Place of Presentation
      福岡
    • Data Source
      KAKENHI-PROJECT-19592001
  • [Presentation] DBA/2Jマウスのメチオニン・バルプロ酸による難聴進行抑制と候補標的遺伝子の亜鉛トランスポーターZip4

    • Author(s)
      務台、宮、藤井、角田、松永
    • Organizer
      日本エピジェネティクス研究会第9回年会
    • Place of Presentation
      一ツ橋学術総合センター(東京)
    • Year and Date
      2015-05-25 – 2015-05-26
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Presentation] Attenuation of Progressive Hearing Loss in DBA/2J Mice by Epigenetic-Modifying Reagents Is Associated with Up-Regulation of the Zinc-Importer Zip4 /Slc39a4

    • Author(s)
      Mutai, Miya, Fujii, Tsunoda, Matsunaga
    • Organizer
      北米耳鼻咽喉科学会第38回年会
    • Place of Presentation
      ボルチモア(アメリカ合衆国メリーランド)
    • Year and Date
      2015-02-21 – 2015-02-25
    • Data Source
      KAKENHI-PROJECT-24592573
  • [Presentation] DBA/2Jマウスの難聴進行を抑制したエピジェネティクス調節剤の分子機構解析

    • Author(s)
      務台、藤井、松永
    • Organizer
      日本耳科学会第39回年会
    • Place of Presentation
      朱鷺メッセ (新潟)
    • Year and Date
      2014-10-15 – 2014-10-18
    • Data Source
      KAKENHI-PROJECT-24592573
  • 1.  MATSUNAGA Tatsuo (90245580)
    # of Collaborated Projects: 6 results
    # of Collaborated Products: 29 results
  • 2.  MIYA Fuyuki (50415311)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 9 results
  • 3.  KUDOH Jun (80178003)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 5 results
  • 4.  SUZUKI Naohiro (90611195)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 7 results
  • 5.  SHIMIZU Atsushi (30327655)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 5 results
  • 6.  KOUIKE Hiroko (70415892)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 6 results
  • 7.  KAGA Kimitaka (80082238)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 3 results
  • 8.  FUJINAMI Yoshiaki (80392801)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 9.  神谷 和作 (10374159)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 10.  難波 一徳 (60425684)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 9 results
  • 11.  奈良 清光 (40260327)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 1 results
  • 12.  YAMAZAWA Kazuki
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 13.  OZAKI Kouichi
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 14.  NAKAGAWA Hidewaki
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 15.  南 修司郎
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 3 results
  • 16.  角田 達彦
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 17.  斉藤 伸治
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 18.  重水 大智
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 19.  藤本 明洋
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 20.  水足 邦雄
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 21.  國島 伸治
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 22.  藤岡 正人
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 23.  小川 郁
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 24.  山本 修子
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 25.  金子 寛生
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results

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