MUTAI Hideki 務台英樹

Researcher Number	60415891
Other IDs
Affiliation (Current)	2021: 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 – 2021: 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
Review Section/Research Field	Principal Investigator Otorhinolaryngology / Basic Section 56050:Otorhinolaryngology-related Except Principal Investigator Otorhinolaryngology / Basic Section 56050:Otorhinolaryngology-related / Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields
Keywords	Principal Investigator 難聴 / ゲノム編集 / ゲノム / エピジェネティクス / スプライシング / 耳鼻咽喉学 / 発生医学 / 脳・神経 / 発生・分化 / 遺伝学 … 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 / 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 / PDZD7遺伝子 / 分子病態 / バリアント / 細胞死 / ロングリードシーケンス / Copy Number Variant / 難聴遺伝子 Less

KCNQ4関連遺伝性難聴の病態における細胞死の寄与を示す動物モデルと治療薬剤開発
- Principal Investigator
  
  和佐野浩一郎
- Project Period (FY)
  2021 – 2023
- 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)
新規難聴原因遺伝子SLC12A2の分子病態解析と治療標的の探索Principal Investigator
- Principal Investigator
  
  務台英樹
- Project Period (FY)
  2021 – 2023
- 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)
Identification of CNV of deafness gene and development of simple test method by long read sequencing
- Principal Investigator
  
  松永達雄
- Project Period (FY)
  2021 – 2023
- 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)
Molecular, Cellular, and in vivo analysis of SLC12A2, a novel candidate of deafness genePrincipal Investigator
- 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 loss
- Principal Investigator
  
  Matsunaga Tatsuo
- 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

[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] Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans2020
- Author(s)
  Mutai H, Wasano K, Momozawa Y, Kamatani Y, Miya F, Masuda S, Morimoto N, Nara K, Takahashi S, Tsunoda T, Homma K, Kubo M, Matsunaga T
- Journal Title
  
  PLOS Genetics
  
  Volume: 16
- DOI
  10.1371/journal.pgen.1008643
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K09336, KAKENHI-PROJECT-18K16869
[Journal Article] Clinical Profiles of DFNA11 at Diverse Stages of Development and Aging in a Large Family Identified by Linkage Analysis2020
- Author(s)
  Yamamoto Nobuko、Mutai Hideki、Namba Kazunori、Goto Fumiyuki、Ogawa Kaoru、Matsunaga Tatsuo
- Journal Title
  
  Otol Neurotol
  
  Volume: 41
- DOI
  10.1097/mao.0000000000002604
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09877, KAKENHI-PROJECT-18K09336
[Journal Article] Systematic quantification of the anion transport function of pendrin (SLC26A4) and its disease‐associated variants2020
- Author(s)
  Wasano K, Takahashi S, Rosenberg SK, Kojima T, Mutai H, Matsunaga T, Ogawa K, Homma K
- Journal Title
  
  Human Mutation
  
  Volume: 41 Pages: 316-331
- DOI
  10.1002/humu.23930
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K09336, KAKENHI-PROJECT-18K16869
[Journal Article] A clinical and genetic study of 16 Japanese families with Waardenburg syndrome2019
- Author(s)
  Minami SB, Nara K, Mutai H, Morimoto N, Sakamoto H, Takiguchi T, Kaga K, Matsunaga T.
- Journal Title
  
  Gene
  
  Volume: 704 Pages: 86-90
- DOI
  10.1016/j.gene.2019.04.023
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11205, KAKENHI-PROJECT-18K09336, KAKENHI-PROJECT-19K09881
[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] 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] 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] 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] 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 Daichi、Miya Fuyuki、Akiyama Shintaro、Okuda Shujiro、Boroevich Keith A、Fujimoto Akihiro、Nakagawa Hidewaki、Ozaki Kouichi、Niida Shumpei、Kanemura Yonehiro、Okamoto Nobuhiko、Saitoh Shinji、Kato Mitsuhiro、Yamasaki Mami、Matsunaga Tatsuo、Mutai Hideki、Kosaki Kenjiro、Tsunoda Tatsuhiko
- 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-16K15530, KAKENHI-PROJECT-16K19068, KAKENHI-PROJECT-18K09336, KAKENHI-PLANNED-18H05511, KAKENHI-PROJECT-16H04726, KAKENHI-PROJECT-18H02680, KAKENHI-PROJECT-16K07211, KAKENHI-PROJECT-16H06299
[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, KAKENHI-PROJECT-15H04991
[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] 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] 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] 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] 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] 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 mutation in patients with congenital high-frequency recessive or sporadic hereditary 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] 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 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] 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] 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] 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] 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] 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] 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] 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 J. Rare Dis
  
  Volume: 8(1) Pages: 172-172
- 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 Jpn
  
  Volume: 23(5) Pages: 903-907
- NAID
  130005065221
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24659753
[Journal Article] A prevalent founder mutation and genotype-phenotype correlations of OTOFin Japanese patients with 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] 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] 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] 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] 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] 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] 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, 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] 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] 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] 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 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 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] 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] 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 wall.2009
- Author(s)
  Hideki Mutai, ほか
- Journal Title
  
  Neuroscience 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
  
  Pages: 415-421
- Data Source
  KAKENHI-PROJECT-19791251
[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] 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
  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・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
  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] Phenotypic presentation of DFNA11 at diverse stages of development and aging2020
- Author(s)
  Tatsuo Matsunaga, Nobuko Yamamoto, Hideki Mutai, Kazunori Namba, Fumiyuki Goto, Kaoru Ogawa
- Organizer
  第65回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] 難聴原因遺伝子候補SLC12A2モデル動物の作成2020
- Author(s)
  務台英樹、和佐野浩一郎、松永達雄
- Organizer
  第30回日本耳科学会
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] 視覚聴覚二重障害の医療向上への取り組み～難病プラットフォームによる全国多施設レジストリ～2020
- Author(s)
  松永達雄、和佐野浩一郎、務台英樹、南修司郎、加我君孝
- Organizer
  第30回日本耳科学会
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] Investigating the effects of exonic single nucleotide variants of SLC26A4 on pre-mRNA splicing2020
- Author(s)
  Koichiro Wasano, Takashi Kojima, Satoe Takahashi, Hideki Mutai, Tatsuo Matsunaga, Kazuaki Homma
- Organizer
  Association for Research in Otolaryngology 43rd Mid Winter Meeting
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] Elucidation of Genetic Background and Phenotypic Features in Patients with Hereditary Hearing Loss to Improve Diagnosis and Care2020
- Author(s)
  Tatsuo Matsunaga, Hideki Mutai, Kiyomitsu Nara , Koichiro Wasano, Shujiro Minami, Kimitaka Kaga
- Organizer
  Association for Research in Otolaryngology 43rd Mid Winter Meeting
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] BOR症候群の臨床遺伝学的検討：臨床症状と遺伝学的原因の関連性について2020
- Author(s)
  貫野彩子、増田正次、務台英樹、守本倫子、仲野敦子、杉内智子、岡本康秀、増田佐和子、勝沼紗矢香、小川郁、松永達雄
- Organizer
  第30回日本耳科学会
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] Investigating the effects of exonic and intronic variants of NF2 on pre-mRNA splicing2020
- Author(s)
  Masaru Noguchi , Masato Fujioka, Naoki Oishi, Hideki Mutai, Kiyomitsu Nara, Tatsuo Matsunaga, Kaoru Ogawa, Koichiro Wasano
- Organizer
  Association for Research in Otolaryngology 43rd Mid Winter Meetingg
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] Alport症候群9家系におけるサブタイプ別聴覚および聴力経過の検討2020
- Author(s)
  松﨑佐栄子、松永達雄、務台英樹、奈良清光、井上沙聡、細谷誠、藤岡正人、小川郁
- Organizer
  第30回日本耳科学会
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] Clinical and molecular characterization of a Japanese patient with auditory neuropathy spectrum disorder associated with m.7471dupC heteroplasmy2020
- Author(s)
  Shujiro Minami, Satomi Inoue, Kiyomitsu Nara, Hideki Mutai, Tatsuo Matsunaga
- Organizer
  第65回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] 国際研究チームによる164難聴遺伝子・疾患の組み合わせに対する臨床的妥当性の評価2019
- Author(s)
  松永達雄、奈良清光、務台英樹、細谷誠、小川郁、加我君孝
- Organizer
  第29回日本耳科学会
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] Multiple defects observed in postnatal Cbx2cterm/cterm mice2019
- Author(s)
  Yuko Katoh-Fukui, Hideki Mutai, Maki Fukami
- Organizer
  第42回日本分子生物学年会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] NLRP3遺伝子に原因variantを同定したクリオピリン関連周期熱症候群症例の長期聴力経過の検討2019
- Author(s)
  川崎泰士、和佐野浩一郎、松永達雄、務台英樹、奈良清光、平賀良彦
- Organizer
  第64回日本聴覚医学会総会
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] 霊長類蝸牛における高発現遺伝子群の探索2019
- Author(s)
  務台英樹、松永達雄
- Organizer
  第29回日本耳科学会
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] 病的意義不明GJB2遺伝子バリアントの解釈への国際共同研究による挑戦と成2019
- Author(s)
  松永達雄、奈良清光、務台英樹、井上沙聡、山本修子、和佐野浩一郎、南修司郎、加我君孝
- Organizer
  第64回日本聴覚医学会総会
- Data Source
  KAKENHI-PROJECT-18K09336
[Presentation] 極めて希少な遺伝子の病原性バリアントが原因として疑われた難聴の1家系2019
- Author(s)
  橋本陽介、奈良清光、和佐野浩一郎、南修司郎、務台英樹、松永達雄
- Organizer
  第29回日本耳科学会
- Data Source
  KAKENHI-PROJECT-18K09336
[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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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 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] 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] 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] 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] 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] 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] 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] 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・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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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/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] 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] 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] 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] 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] 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
[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

1. MATSUNAGA Tatsuo (90245580)

# of Collaborated Projects: 7 results

# of Collaborated Products: 29 results
2. MIYA Fuyuki (50415311)

# of Collaborated Projects: 3 results

# of Collaborated Products: 9 results
3. 奈良清光 (40260327)

# of Collaborated Projects: 3 results

# of Collaborated Products: 1 results
4. KUDOH Jun (80178003)

# of Collaborated Projects: 2 results

# of Collaborated Products: 5 results
5. SUZUKI Naohiro (90611195)

# of Collaborated Projects: 2 results

# of Collaborated Products: 7 results
6. SHIMIZU Atsushi (30327655)

# of Collaborated Projects: 2 results

# of Collaborated Products: 5 results
7. KOUIKE Hiroko (70415892)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
8. KAGA Kimitaka (80082238)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
9. FUJINAMI Yoshiaki (80392801)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. 神谷和作 (10374159)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. 難波一徳 (60425684)

# of Collaborated Projects: 1 results

# of Collaborated Products: 9 results
12. 和佐野浩一郎 (40528866)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
13. 小島敬史 (60528660)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. YAMAZAWA Kazuki

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
15. OGAWA Kaoru

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
16. OZAKI Kouichi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
17. NAKAGAWA Hidewaki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
18. GOTO Fumiyuki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
19. 國島伸治

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
20. 藤岡正人

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
21. 山本修子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
22. 水足邦雄

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
23. 金子寛生

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
24. 南修司郎

# of Collaborated Projects: 0 results

# of Collaborated Products: 4 results
25. 斉藤伸治

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. 重水大智

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
27. 藤本明洋

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
28. 角田達彦

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

MUTAI Hideki 務台 英樹

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新規難聴原因遺伝子SLC12A2の分子病態解析と治療標的の探索Principal Investigator

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Molecular, Cellular, and in vivo analysis of SLC12A2, a novel candidate of deafness genePrincipal Investigator

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Molecular functional analysis of ZBTB10, the novel candidate deafness gene associated with cochlear nerve hypoplasiaPrincipal Investigator

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Attenuation of Progressive Hearing Loss in DBA/2J Mice by Epigenetic-Modifying ReagentsPrincipal Investigator

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Study of epigentic mechanism underlying age-related hearing lossPrincipal Investigator

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Study of transcription factor Pou3f3 in developing mammalian inner ear and its regulation by epigenetic pathwayPrincipal Investigator

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MUTAI Hideki 務台英樹

[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