Noguchi Yoshihiro 野口佳裕

… Alternative Names

NOGUCHI Yoshihiro 野口佳裕

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Researcher Number	50282752
Other IDs
External Links
Affiliation (Current)	2025: 信州大学, 医学部, 特任教授 2025: 国際医療福祉大学, 医学部, 教授
Affiliation (based on the past Project Information) *help	2022: 国際医療福祉大学, 医学部, 教授 2015 – 2021: 信州大学, 医学部, 特任教授 2014 – 2015: 信州大学, 医学部, 教授 2007 – 2014: Tokyo Medical and Dental University, 医学部附属病院, 講師 2008 – 2011: 東京医科歯科大学, 医学部付属病院, 講師 … More 2009: Tokyo Medical and Dental University, 医学部・附属病院, 講師 2003: 医科歯科大, 講師 2000 – 2002: 東京医科歯科大学, 大学院・医歯学総合研究科, 講師 2001: Tokyo Medical & Dental University, Department of Otolaryngology, Assistant Professor, 大学院・歯学総合研究科, 講師 1999: 東京医科歯科大学, 大学院・医歯学総合研究科, 助手 Less
Review Section/Research Field	Principal Investigator Otorhinolaryngology / Otorhinolaryngology / Basic Section 56050:Otorhinolaryngology-related Except Principal Investigator Otorhinolaryngology / Otorhinolaryngology / Laboratory animal science / Neurophysiology / General neuroscience / Biological Sciences
Keywords	Principal Investigator 難聴 / 蝸牛 / auditory neuropathy / ANSD / 遺伝子 / マウス / マイクロRNA / C57BL/6 / 発現解析 / mRNA … More / 加齢 / 内耳 / 老人性難聴 / 蝸牛マイクロフォン電位 / 蝸電図 / cochlear implant / hereditary hearing loss / 内耳奇形 / 遺伝学 / 遺伝子解析 / エクソーム解析 / 中耳奇形 / マイクロCT / miRNA / マイクロ RNA / マウスモデル / 平衡障害 / 聴覚障害 / PMCA2 / Atp2b2 / 難聴遺伝子 / 遺伝性難聴 / 聴力保存手術 / 聴神経腫瘍 … More Except Principal Investigator 遺伝子 / 難聴 / 内耳 / 有毛細胞 / 神経科学 / 脳・神経 / マウス / NKCC / CLC-KB / イオンチャネル / Six1 / 転写因子 / 内耳奇形マウス / DPOAE / メカノセンサー / ゲノム / 医療・福祉 / 加齢性難聴 / 解剖学 / 耳科学 / ASIC / 機械刺激電気変換 / Otic Gene / Six 1 / Homeobox / Endolymph / Deafness / Mice / トランスジェニックマウス / Cl^-チャンネル / Furosemide / Na-K-Cl cotransporter / 増感方法論 / 細胞生物学 / イオン輸送 / Spiral ligament / Stria / EGFP / cochlea / 6 / C57BL / mice / db / Lepr db / ob / Lepr ob / ラセン神経節 / 血管条 / 静止電位 / II型糖尿病 / ドメイン / 内リンパ / 蝸牛 / Cranial Nerve / Brain・Nerve / Neurology / Genome / Gene / protein / Scaffold / Scaffold protein / ホメオボックス遺伝子 / 脳神経疾患 / 神経科 / myosin / transcription factor / mutant mouse / gene / deafness / 感音難聴 / 遺伝子変異 / 実験動物 / 内耳奇形 / ミオシン / アミノ / 機械電気変換イオンチャネル / 機会電気変換イオンチャネル / 内耳有毛細胞 / TMC2 / TMC1 / アミノグリコシド系抗菌薬 / パッチクランプ / 機械刺激電流 / MET channel / ASIC4 / 英国 / 国際研究者交流 / 機械刺激受容チャネル / 聴覚受容体 / ASIC1b / ABR / ノックアウトマウス / 酸感受性イオンチャネル / Cadherin23 / 近交系マウス / モデルマウス / カドヘリン / Lrrc30 / コンソミック系統 / QTL / 難聴モデルマウス / 遺伝学 / 医療福祉 / 臨床 / マウス亜種間交配 / Myosin VI / Whirlin / Sans / 4.1蛋白質 / 2J / DBA / ゲルソリン / 修飾遺伝子 / カドヘリン23 / ミオシンVI / ヒト難聴モデルマウス / 難聴発症機構 / Stereocilia / 分子間相互作用 / 育種遺伝 / ミトコンドリア遺伝子 / ヒトゲノム Less

Identification of novel causative gene of auditory neuropathy spectrum disorderPrincipal Investigator
- Principal Investigator
  
  Noguchi Yoshihiro
- Project Period (FY)
  2019 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56050:Otorhinolaryngology-related
- Research Institution
  International University of Health and Welfare
  Shinshu University
omprehensive investigations of physiological roles of putative mechanosensory cation channels ASICs expressed in mouse auditory and vestibular hair cells
- Principal Investigator
  
  Ugawa Shinya
- Project Period (FY)
  2017 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Nagoya City University
Development of novel clasiffication based on genetic analysis for ANSD and middle ear anormalyPrincipal Investigator
- Principal Investigator
  
  Noguchi Yoshihiro
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Shinshu University
Systemic Fluorescent Gentamicin Enters Neonatal Mouse Hair Cells Predominantly Through Mechanoelectrical Transduction Channels
- Principal Investigator
  
  KAWASHIMA Yoshiyuki
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
A study of microRNAs regulating the pathogenesis of age-related hearing lossPrincipal Investigator
- Principal Investigator
  
  NOGUCHI Yoshihiro
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Shinshu University
  Tokyo Medical and Dental University
Comprehensive screening of genetic factors by using mouse models of age-related hearing loss in human for clinical application
- Principal Investigator
  
  KIKKAWA Yoshiaki
- Project Period (FY)
  2011 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Laboratory animal science
- Research Institution
  Tokyo Metropolitan Institute of Medical Science
Functional characterization of putative mechanoelectrical transducer channel proteins using knockout mice.
- Principal Investigator
  
  UGAWA SHINYA
- Project Period (FY)
  2011 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Neurophysiology / General neuroscience
- Research Institution
  Nagoya City University
Mouse microRNA expression study identifying the nature of age-related hearing lossPrincipal Investigator
- Principal Investigator
  
  NOGUCHI Yoshihiro
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
Analysis of pathophysiology of presbycusis by gene profile study of senescent cochlear cells
- Principal Investigator
  
  KITAMURA Ken
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
Extensive and rapid comprehensive screening for mitochondrial DNA point mutations in patients with hereditary hearing loss and quantitative analysis of mtDNA mutation in the cells of the inner ear
- Principal Investigator
  
  KITAMURA Ken
- Project Period (FY)
  2009 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
Establishment and characterization of mouse models for hearing loss based on Molecular interaction
- Principal Investigator
  
  KIKKAWA Yoshiaki
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Laboratory animal science
- Research Institution
  Tokyo University of Agriculture
Age-related balance disorders in Atp2b2 mutant mouse with no otoconiaPrincipal Investigator
- Principal Investigator
  
  NOGUCHI Yoshihiro
- Project Period (FY)
  2007 – 2009
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
分子生物学的および電気生理学的手法を用いた遺伝性難聴発症機構の研究Principal Investigator
- Principal Investigator
  
  野口佳裕
- Project Period (FY)
  2003
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
Analysis of deafness using homeobox and molecular motor gene, and knockout mouse
- Principal Investigator
  
  KITAMURA Ken
- Project Period (FY)
  2002 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
Maintenance in the Endolynph Iron Environment of the Mutant mice
- Principal Investigator
  
  UZAWA Masamichi, 岡村洋沖
- Project Period (FY)
  2002 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University Hospital
難聴遺伝子の解析による内耳聴覚・前庭の分子機構
- Principal Investigator
  
  KITAMURA Ken
- Project Period (FY)
  2001
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas (C)
- Review Section
  
  Biological Sciences
- Research Institution
  Tokyo Medical and Dental University
非症候群性遺伝性難聴の分子生物学的および電気生理学的手法による難聴発症機構の解明Principal Investigator
- Principal Investigator
  
  野口佳裕
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
蝸電図による聴神経腫瘍の蝸牛病態の解明と聴力保存手術適応の確立Principal Investigator
- Principal Investigator
  
  野口佳裕
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical and Dental University
Study of deafness mechanism by genetic analysis of gene knockout mouse and homeobox a well as molecular motor gene
- Principal Investigator
  
  KITAMURA Ken
- Project Period (FY)
  1999 – 2001
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Otorhinolaryngology
- Research Institution
  Tokyo Medical & Dental University

[Book] 感覚器聴覚;脳・神経系;疾患モデルマウス:臓器・疾患別解析・実験法;生命科学研究の戦略:疾患モデルマウスと表現型
- Author(s)
  吉川欣亮・鈴木沙理・野口佳裕
- Publisher
  中山書店(印刷中)
- Data Source
  KAKENHI-PROJECT-20300147
[Journal Article] Auditory Attention Ability under Dichotic Dual-Task Situation in Adults with Listening Difficulties2022
- Author(s)
  Obuchi Chie、Kawase Tetsuaki、Kaga Kimitaka、Noguchi Yoshihiro
- Journal Title
  
  Audiology and Neurotology
  
  Volume: 27 Issue: 3 Pages: 1-8
- DOI
  10.1159/000528050
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K03006, KAKENHI-PROJECT-20H03831, KAKENHI-PROJECT-19K09865
[Journal Article] 特集この1冊でわかる遺伝学的検査-基礎知識と臨床応用《臨床への応用》遺伝性難聴2022
- Author(s)
  野口佳裕, 上斗米愛美
- Journal Title
  
  耳鼻咽喉科・頭頸部外科
  
  Volume: 94 Issue: 12 Pages: 1024-1027
- DOI
  10.11477/mf.1411203181
- ISSN
  0914-3491, 1882-1316
- Year and Date
  2022-11-20
- Data Source
  KAKENHI-PROJECT-19K09865
[Journal Article] An introduction to hereditary hearing loss2022
- Author(s)
  野口佳裕
- Journal Title
  
  AUDIOLOGY JAPAN
  
  Volume: 65 Issue: 3 Pages: 169
- DOI
  10.4295/audiology.65.169
- NAID
  130008119005
- ISSN
  0303-8106, 1883-7301
- Year and Date
  2022-06-30
- Language
  Japanese
- Open Access
- Data Source
  KAKENHI-PROJECT-19K09865
[Journal Article] Usefulness and pitfalls of genetic testing using next-generation sequencing2021
- Author(s)
  野口佳裕，西尾信哉，宇佐美真一
- Journal Title
  
  Otology Japan
  
  Volume: 31 Issue: 2 Pages: 125-130
- DOI
  10.11289/otoljpn.31.125
- NAID
  130008120525
- ISSN
  0917-2025, 1884-1457
- Language
  Japanese
- Data Source
  KAKENHI-PROJECT-19K09865
[Journal Article] 特集副腎皮質ステロイド-どこに注意し,どう使う? 《ステロイド投与の実際》急性感音難聴2021
- Author(s)
  岡　愛子，鬼頭良輔，野口佳裕
- Journal Title
  
  耳鼻咽喉科・頭頸部外科
  
  Volume: 93 Issue: 9 Pages: 694-698
- DOI
  10.11477/mf.1411202779
- ISSN
  0914-3491, 1882-1316
- Year and Date
  2021-08-20
- Data Source
  KAKENHI-PROJECT-19K09865
[Journal Article] 増刊号術前画像と術中解剖-カンファレンスで突っ込まれないための知識〔特別付録Web動画〕 1.耳領域人工聴覚器手術2021
- Author(s)
  野口佳裕, 岡　愛子，宇佐美真一
- Journal Title
  
  耳鼻咽喉科・頭頸部外科
  
  Volume: 93 Issue: 5 Pages: 42-50
- DOI
  10.11477/mf.1411202674
- ISSN
  0914-3491, 1882-1316
- Year and Date
  2021-04-30
- Data Source
  KAKENHI-PROJECT-19K09865
[Journal Article] 急性感音難聴（突発性難聴、低音障害型感音難聴、外リンパ瘻など）2021
- Author(s)
  野口佳裕，岡　愛子
- Journal Title
  
  JOHNS
  
  Volume: 37 Pages: 1063-1070
- Data Source
  KAKENHI-PROJECT-19K09865
[Journal Article] 急性感音難聴の診断と治療2020
- Author(s)
  野口佳裕
- Journal Title
  
  Nippon Jibiinkoka Gakkai Kaiho
  
  Volume: 123 Issue: 1 Pages: 71-77
- DOI
  10.3950/jibiinkoka.123.71
- NAID
  130007795169
- ISSN
  0030-6622, 1883-0854
- Year and Date
  2020-01-20
- Language
  Japanese
- Open Access
- Data Source
  KAKENHI-PROJECT-19K09865
[Journal Article] Haplotype Analysis of GJB2 Mutations: Founder Effect or Mutational Hot Spot?2020
- Author(s)
  Shinagawa J, Moteki H, Nishio SY, Noguchi Y, Usami SI.
- Journal Title
  
  Genes
  
  Volume: 11 Issue: 3 Pages: 250-250
- DOI
  10.3390/genes11030250
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K09865
[Journal Article] Gender categorization by children with normal hearing and children with cochlear implants2020
- Author(s)
  佐藤友貴, 小渕千絵, 籠宮隆之, 大金さや香, 城間将江, 野口佳裕, 加我君孝
- Journal Title
  
  AUDIOLOGY JAPAN
  
  Volume: 63 Issue: 3 Pages: 181-188
- DOI
  10.4295/audiology.63.181
- NAID
  130007876892
- ISSN
  0303-8106, 1883-7301
- Year and Date
  2020-06-30
- Language
  Japanese
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K00552, KAKENHI-PROJECT-19K09865
[Journal Article] 遺伝性疾患としての内耳奇形の診断2019
- Author(s)
  野口佳裕
- Journal Title
  
  Nippon Jibiinkoka Gakkai Kaiho
  
  Volume: 123 Issue: 3 Pages: 210-216
- DOI
  10.3950/jibiinkoka.123.210
- NAID
  130007829483
- ISSN
  0030-6622, 1883-0854
- Year and Date
  2019-03-20
- Language
  Japanese
- Open Access
- Data Source
  KAKENHI-PROJECT-19K09865
[Journal Article] POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss.2017
- Author(s)
  Kitano T, Miyagawa M, Nishio SY, Moteki H, Oda K, Ohyama K, Miyazaki H, Hidaka H, Nakamura KI, Murata T, Matsuoka R, Ohta Y, Nishiyama N, Kumakawa K, Furutate S, Iwasaki S, Yamada T, Ohta Y, Uehara N, Noguchi Y, Usami SI.
- Journal Title
  
  PLoS One.
  
  Volume: 12 Issue: 5 Pages: e0177636-e0177636
- DOI
  10.1371/journal.pone.0177636
- NAID
  120006373770
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K11176, KAKENHI-PROJECT-17K11322, KAKENHI-PROJECT-15H02565, KAKENHI-PROJECT-26861365, KAKENHI-PROJECT-17K11356
[Journal Article] A nationwide study on enlargement of the vestibular aqueduct in Japan.2017
- Author(s)
  Noguchi Y, Fukuda S, Fukushima K, Gyo K, Hara A, Nakashima T, Ogawa K, Okamoto M, Sato H, Usami S, Yamasoba T, Yokoyama T, Kitamura K.
- Journal Title
  
  Auris Nasus Larynx
  
  Volume: 44 Pages: 33-39
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11176
[Journal Article] 日常診療における遺伝子診断ー診療の手引きをふまえて2017
- Author(s)
  野口佳裕
- Journal Title
  
  Otol Jpn
  
  Volume: 27 Pages: 43-48
- NAID
  130007592427
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11176
[Journal Article] 難聴遺伝子検査2017
- Author(s)
  野口佳裕
- Journal Title
  
  耳鼻咽喉科頭頸部外科
  
  Volume: 89 Pages: 95-99
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K11176
[Journal Article] 軽度難聴の急性感音難聴症例の検討2014
- Author(s)
  野口佳裕，籾山直子，高橋正時，喜多村　健
- Journal Title
  
  Audiology Japan
  
  Volume: 57 Pages: 63-70
- NAID
  130004714067
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] A DFNA5 Mutation Identified in Japanese Families with Autosomal Dominant Hereditary Hearing Loss2014
- Author(s)
  Nishio A, Noguchi Y, Sato T, Naruse T, Kimura A, Takagi A, Kitamura K
- Journal Title
  
  Ann Hum Genet
  
  Volume: 78 Issue: 2 Pages: 83-91
- DOI
  10.1111/ahg.12053
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459, KAKENHI-PROJECT-24590398
[Journal Article] Audiovestibular findings in patients with Vogt-Koyanagi-Harada disease2014
- Author(s)
  Noguchi Y, Nishio A, Takase H, Miyanaga M, Takahashi H, Mochizuki M, Kitamura K
- Journal Title
  
  Acta Otolaryngol
  
  Volume: 134(4) Pages: 339-44
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] 埋込型骨導補聴器術後皮膚合併症に対する再手術例の検討2013
- Author(s)
  吉本亮一，野口佳裕，岩崎朱見，喜多村健
- Journal Title
  
  Otology Japan
  
  Volume: 23 Pages: 834-40
- NAID
  130005065209
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] 前庭水管拡大症を伴うSLC26A4, ATP6V1B1, SIX1 変異例の聴平衡覚所見の検討2013
- Author(s)
  野口佳裕, 伊藤卓, 川島慶之, 西尾綾子, 本田圭司, 喜多村健
- Journal Title
  
  Equilibrium Res
  
  Volume: 72(2) Pages: 97-106
- NAID
  10031167657
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] 前庭水管拡大症を伴うSLC26A4, ATP6V1B1, SIX1変異例の聴平衡覚所見の検討2013
- Author(s)
  野口佳裕，伊藤卓，川島慶之，西尾綾子，本田圭司，喜多村健
- Journal Title
  
  Equilibrium Res
  
  Volume: 72 Pages: 97-106
- NAID
  10031167657
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] 網羅的解析により診断された耳小骨奇形を合併したミトコンドリア3243 変異例2013
- Author(s)
  本田圭司, 野口佳裕, 加藤智史, 奥野秀次, 喜多村健
- Journal Title
  
  Otology Japan
  
  Volume: 23(3) Pages: 227-32
- NAID
  10031189730
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] 網羅的解析により診断された耳小骨奇形を合併したミトコンドリア3243変異例2013
- Author(s)
  本田圭司，野口佳裕，加藤智史，奥野秀次，喜多村健
- Journal Title
  
  Otology Japan
  
  Volume: 23 Pages: 227-32
- NAID
  10031189730
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] 熱湯による外傷性鼓膜穿孔例2013
- Author(s)
  籾山直子，高橋正時，野口佳裕，喜多村健
- Journal Title
  
  耳鼻臨床
  
  Volume: 106 Pages: 1077-82
- NAID
  130003386096
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] Extended screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.2012
- Author(s)
  Kato T, Nishigaki Y, Noguchi Y, Fuku N, Ito T, Mikami E, Kitamura K, Tanaka M.
- Journal Title
  
  J Hum Genet
  
  Volume: 57 Issue: 12 Pages: 772-775
- DOI
  10.1038/jhg.2012.109
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-11J04771, KAKENHI-PROJECT-22240072, KAKENHI-PROJECT-22659305, KAKENHI-PROJECT-22791577, KAKENHI-PROJECT-24650414
[Journal Article] Mitochondrial DNA haplogroup associated with hereditary hearing loss in a Japanese population.2012
- Author(s)
  Kato T, Fuku N, Noguchi Y, Murakami H, Miyachi M, Kimura Y, Tanaka M and Kitamura K
- Journal Title
  
  Acta Otolaryngol.
  
  Volume: 132 Issue: 11 Pages: 1178-82
- DOI
  10.3109/00016489.2012.693624
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22659305, KAKENHI-PROJECT-23791953, KAKENHI-PROJECT-24650414
[Journal Article] Extended screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss2012
- Author(s)
  Kato T, Nishigaki Y, Noguchi Y, Fuku N, Ito T, Mikami E, Kitamura K and Tanaka M
- Journal Title
  
  J Hum Genet
  
  Volume: 57 Pages: 772-5
- NAID
  10031145884
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] Mitochondrial DNA haplogroup associated with hereditary hearing loss in a Japanese population2012
- Author(s)
  Kato T, Fuku N, Noguchi Y, Murakami H, Miyachi M, Kimura Y, Tanaka M and Kitamura K
- Journal Title
  
  Acta Otolaryngol
  
  Volume: 132 Pages: 1178-82
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] Long term follow-up study of mastoid obliteration using bone pate in cholesteatoma2011
- Author(s)
  Kitamura K, Nakamura Y, Noguchi Y, Takahashi M
- Journal Title
  
  The Journal of International Advanced Otology
  
  Volume: 7, (3), supplement 2 Pages: 42-3
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] Audiovestibular findings in a branchio-oto syndrome patient with a SIX1 mutation2011
- Author(s)
  Noguchi Y, Ito T, Nishio A, Honda K, Kitamura K
- Journal Title
  
  Acta Otolaryngol Apr
  
  Volume: 131(4) Pages: 413-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] Long term follow-up study of mastoid obliteration using bone pate in cholesteatoma2011
- Author(s)
  Kitamura K, Nakamura Y, Noguchi Y, Takahashi M
- Journal Title
  
  The Journal of International Advanced Otology
  
  Volume: 7(3) Pages: 42-3
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22659305
[Journal Article] Long term follow-up study of mastoid obliteration using bone pate in cholesteatoma.2011
- Author(s)
  Kitamura K, Nakamura Y, Noguchi Y, Takahashi M
- Journal Title
  
  The Journal of International Advanced Otology
  
  Volume: 7(3) Pages: 42-3
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22659305
[Journal Article] Audiovestibular findings in a branchio-oto syndrome patient with a SIX1 mutation2011
- Author(s)
  Noguchi Y, Ito T, Nishio A, Honda K, Kitamura K
- Journal Title
  
  Acta Otolaryngol
  
  Volume: 131(4) Issue: 4 Pages: 413-8
- DOI
  10.3109/00016489.2010.543146
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459, KAKENHI-PROJECT-22659305
[Journal Article] Audiological Analysis and Peri-and Postoperative Complications in Bone-Anchored Hearing Aid Surgery2011
- Author(s)
  野口佳裕, 高橋正時, 喜多村健
- Journal Title
  
  Nippon Jibiinkoka Gakkai Kaiho
  
  Volume: 114 Issue: 7 Pages: 607-614
- DOI
  10.3950/jibiinkoka.114.607
- NAID
  10029380923
- ISSN
  0030-6622, 1883-0854
- Language
  Japanese
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459, KAKENHI-PROJECT-22659305
[Journal Article] Novel ATP6V1B1 mutations in distal renal tubular acidosis and hearing loss2010
- Author(s)
  Yashima T, Noguchi Y, Kawashima Y, Rai T, Ito T, Kitamura K
- Journal Title
  
  Acta Otolaryngol
  
  Volume: 130 Pages: 1002-1008
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22659305
[Journal Article] Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss2010
- Author(s)
  Kato T, Nishigaki Y, Noguchi Y, Ueno H, Hosoya H, Ito T, Kimura Y, Kitamura K, Tanaka M
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Pages: 147-154
- NAID
  10030733907
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22659305
[Journal Article] Hereditary hearing loss and deafness genes in Japan2010
- Author(s)
  Ito T, Noguchi Y, Yashima T, Ohno K, Kitamura K
- Journal Title
  
  J Med Dent Sci
  
  Volume: 57 Pages: 1-10
- NAID
  110007544677
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.2010
- Author(s)
  Kato T, Nishigaki Y, Noguchi Y, Ueno H, Hosoya H, Ito T, Kimura Y, Kitamura K and Tanaka M
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Pages: 147-154
- NAID
  10030733907
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22659305
[Journal Article] Novel ATP6V1B1 mutations in distal renal tubular acidosis and hearing loss.2010
- Author(s)
  Yashima T, Noguchi Y, Kawashima Y, Rai T, Ito T, Kitamura K
- Journal Title
  
  Acta Otolaryngol
  
  Volume: 130 Pages: 1002-1008
- URL
  http://informahealthcare.com/doi/abs/10.3109/00016481003631529
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22659305
[Journal Article] Additional heterozygous 2507A>C mutation of WFS1 in progressive hearing loss at lower frequencies2010
- Author(s)
  Fujikawa T, Noguchi Y, Ito T, Takahashi M, Kitamura K
- Journal Title
  
  Laryngoscope
  
  Volume: 120 Pages: 166-171
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] What do patients with hereditary deafness think of genetic studies?2010
- Author(s)
  Abe S, Noguchi Y, Kitamura K
- Journal Title
  
  Auris Nasus Larynx
  
  Volume: 37 Pages: 422-426
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] Novel ATP6V1B1 mutations in distal renal tubular acidosis and hearing loss2010
- Author(s)
  Yashima T, Noguchi Y, Kawashima Y, Rai T, Ito T, Kitamura K
- Journal Title
  
  Acta Otolaryngol
  
  Volume: 130 Pages: 1002-1008
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss2010
- Author(s)
  Kato T, Nishigaki Y, Noguchi Y, Ueno H, Hosoya H, Ito T, Kimura Y, Kitamura K and Tanaka M
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Pages: 147-154
- NAID
  10030733907
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] What do patients with hereditary deafness think of genetic studies?2010
- Author(s)
  Abe S, Noguchi Y, Kitamura K
- Journal Title
  
  Auris Nasus Larynx
  
  Volume: 37 Pages: 422-426
- URL
  http://www.aurisnasuslarynx.com/
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22659305
[Journal Article] Hereditary Hearing Loss and Deafness Genes in Japan2010
- Author(s)
  Ito T, Noguchi Y, Yashima T, Ohno K, Kitamura K
- Journal Title
  
  J Med Dent Sci 57
  
  Pages: 1-10
- NAID
  110007544677
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19591960
[Journal Article] Deficiency of Vlgr1 resulted in deafness and susceptibility to audiogenic seizures while the degree of hearing impairment was not correlated with seizure severity in C57BL/6- and 129-backcrossed lines of Vlgr1 knockout mice2009
- Author(s)
  Yagi H, Noguchi Y, Kitamura K, Sato M
- Journal Title
  
  Neurosci Lett
  
  Volume: 461 Pages: 190-195
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] Vestibular evoked myogenic potentials in patients with the mitochondrial A1555G mutation2009
- Author(s)
  Kawashima Y, Noguchi Y, Ito T, Kitamura K
- Journal Title
  
  Laryngoscope
  
  Volume: 119 Pages: 1874-1879
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] Audiovestibular findings in patients with mitochondrial A1555G mutation.2004
- Author(s)
  Noguchi Y, Yashima T, Ito T, Sumi t, Tsuzuku T, Kitamura K.
- Journal Title
  
  Laryngoscope 114
  
  Pages: 344-348
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14571608
[Journal Article] Audiovestibular findings in patients with mitochondrial A1555G mutation.2004
- Author(s)
  Noguchi Y
- Journal Title
  
  Laryngoscope 114
  
  Pages: 344-348
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14370539
[Journal Article] Audiovestibular findings in patients with mitochondrial A1555G mutation.2004
- Author(s)
  Noguchi Y, Yashima T, Ito T, Sumi T, Tsuzuku T, Kitamura K
- Journal Title
  
  Laryngoscope 114
  
  Pages: 344-348
- Data Source
  KAKENHI-PROJECT-14370539
[Journal Article] Audiovestibular findings in patients with mitochondrial A1555G mutation.2004
- Author(s)
  Noguchi Y, Yashima T, Ito T, Sumi T, Tsuzuku T, Kitamura K.
- Journal Title
  
  Laryngoscope. 114
  
  Pages: 344-348
- Data Source
  KAKENHI-PROJECT-14571608
[Journal Article] A comparison of acute low-tone sensorineural hearing loss versus Meniere's disease in electrocochleography.2004
- Author(s)
  Noguchi Y, Nishida H, Tokano H, Kawashima Y, Kitamura K
- Journal Title
  
  Ann Otol Rhinol Laryngol 113
  
  Pages: 194-199
- Data Source
  KAKENHI-PROJECT-14370539
[Journal Article] A comparison of acute low-tone sensorineural hearing loss versus Meniere' s disease in electrocochleography.2004
- Author(s)
  Noguchi Y, Nishida H, Tokano H, Kawashima Y, Kitamura K.
- Journal Title
  
  Ann Otol Rhinol Laryngol. 113
  
  Pages: 194-199
- Data Source
  KAKENHI-PROJECT-14571608
[Journal Article] Audiovestibular findings in patients with mitochondrlal A1555G mutation.2004
- Author(s)
  Noguchi Y, Yashima T, Ito T, Sumi T, Tsuzuku T, Kitamura K.
- Journal Title
  
  Laryngoscope 114
  
  Pages: 344-348
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14571608
[Journal Article] A Mutation of the EYA1 gene in patients with Branchio-oto syndrome.2003
- Author(s)
  Yashima T, Noguchi Y, Ishikawa K, et al.
- Journal Title
  
  Acta Otolaryngologica 123
  
  Pages: 279-282
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14370539
[Journal Article] Ex Vivo Visualization of the Mouse Otoconial Layer Compared to Micro-computed Tomography
- Author(s)
  Honda K, Noguchi Y, Kawashima Y, Takahashi M, Nishio A, Kitamura K
- Journal Title
  
  Otol Neurotol
  
  Volume: (accepted)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Journal Article] A DFNA5 Mutation Identified in Japanese Families with Autosomal Dominant Hereditary Hearing Loss
- Author(s)
  Nishio A, Noguchi Y, Sato T, Naruse T, Kimura A, Takagi A, Kitamura K
- Journal Title
  
  Ann Hum Genet
  
  Volume: (in press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] 難聴・めまいに関連する遺伝子2022
- Author(s)
  野口佳裕
- Organizer
  第22回Auditory Neuroscience Meeting
- Invited
- Data Source
  KAKENHI-PROJECT-19K09865
[Presentation] 遺伝性難聴入門2022
- Author(s)
  野口佳裕
- Organizer
  第76回宮崎県耳鼻咽喉科懇話会臨床セミナー
- Invited
- Data Source
  KAKENHI-PROJECT-19K09865
[Presentation] 日常臨床における難聴の遺伝医療2022
- Author(s)
  野口佳裕
- Organizer
  第200回御茶ノ水耳鼻咽喉・頭頸科治療研究会
- Invited
- Data Source
  KAKENHI-PROJECT-19K09865
[Presentation] 教育セミナー2　遺伝性難聴入門2021
- Author(s)
  野口佳裕
- Organizer
  第66回日本聴覚医学会総会・学術講演会
- Invited
- Data Source
  KAKENHI-PROJECT-19K09865
[Presentation] 臨床セミナー　めまい・平衡障害にかかわる遺伝性疾患2021
- Author(s)
  野口佳裕
- Organizer
  第80回日本めまい平衡医学会総会・学術講演会
- Invited
- Data Source
  KAKENHI-PROJECT-19K09865
[Presentation] 日本耳科学会30周年記念シンポジウム1　遺伝性難聴2020
- Author(s)
  野口佳裕
- Organizer
  第30回日本耳科学会総会学術講演会
- Invited
- Data Source
  KAKENHI-PROJECT-19K09865
[Presentation] 教育セミナー5　人工聴覚器手術2020
- Author(s)
  野口佳裕
- Organizer
  第30回日本耳科学会総会学術講演会
- Invited
- Data Source
  KAKENHI-PROJECT-19K09865
[Presentation] テーマセッション1　「次世代シーケンサー時代の難聴遺伝子診断と臨床応用」　Keynote2　次世代シークエンサーによる遺伝子診断の有用性とピットフォール2020
- Author(s)
  野口佳裕
- Organizer
  第30回日本耳科学会総会学術講演会
- Invited
- Data Source
  KAKENHI-PROJECT-19K09865
[Presentation] Two Different Sequencing Platforms Identified an Additional Phenotype Caused by a HOXA2 Variant in a Family with Mixed Hearing Loss and Middle Ear Anomaly without Microtia2019
- Author(s)
  Yoshihiro Noguchi, Shin-ya Nishio, Shin-ichi Usami
- Organizer
  Association for Research in Otolaryngology(ARO) 2019
- Data Source
  KAKENHI-PROJECT-16K11176
[Presentation] TNCバリアントによる常染色体優性非症候群性遺伝性難聴2019
- Author(s)
  野口佳裕、西尾信哉、茂木英明、藤川太朗、宇佐美真一
- Organizer
  第29回　日本耳科学会学術講演会
- Data Source
  KAKENHI-PROJECT-19K09865
[Presentation] ２つの全エクソーム解析技術によりHOXA2バリアントが同定された常染色体優性混合性難聴家系2019
- Author(s)
  野口佳裕、西尾信哉、宇佐美真一
- Organizer
  第81回　耳鼻咽喉科臨床学会
- Data Source
  KAKENHI-PROJECT-19K09865
[Presentation] 一側混合性難聴に対する人工中耳（Vbrant Soundbridge）の１症例2018
- Author(s)
  高橋優宏、岩崎聡、古舘佐起子、野口佳裕、岡野光博、宇佐美真一
- Organizer
  第28回日本耳科学会
- Data Source
  KAKENHI-PROJECT-16K11176
[Presentation] A duplication mutation in HOXA2 causes autosomal dominant nonsyndromic mixed hearing loss and middle ear anomaly.2018
- Author(s)
  Noguchi Y, Usami S
- Organizer
  Association for Research in Otolaryngology 2018
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K11176
[Presentation] 回転性めまいの有無による前庭水管拡大症例の臨床的検討2017
- Author(s)
  野口佳裕、喜多村健、宇佐美真一
- Organizer
  第76回日本めまい平衡医学会
- Data Source
  KAKENHI-PROJECT-16K11176
[Presentation] ヌーナン症候群および類縁疾患における人工内耳2017
- Author(s)
  野口佳裕、宮川麻衣子、茂木英明、宇佐美真一
- Organizer
  第62回　日本聴覚医学会総会
- Data Source
  KAKENHI-PROJECT-16K11176
[Presentation] HOXA2重複変異は常染色体優性非症候群性混合性難聴と中耳奇形を引き起こす2017
- Author(s)
  野口佳裕、西尾信哉、和佐野浩一郎、藤川太郎、木村彰方
- Organizer
  第62回　日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-16K11176
[Presentation] 次世代シーケンサーにより見出されたPOU4F3遺伝子変異症例2017
- Author(s)
  北野友裕、宮川麻衣子、西尾信哉、茂木英明、野口佳裕、宇佐美真一
- Organizer
  第118回日本耳鼻咽喉科学会学術講演会
- Data Source
  KAKENHI-PROJECT-16K11176
[Presentation] 外耳、中耳奇形例に対するHOXA2遺伝子解析2017
- Author(s)
  野口佳裕、西尾信哉、和佐野浩一郎、宇佐美真一
- Organizer
  第118回日本耳鼻咽喉科学会学術講演会
- Data Source
  KAKENHI-PROJECT-16K11176
[Presentation] HOXA2変異によるアブミ骨奇形を呈する常染色体優性遺伝性混合性難聴2016
- Author(s)
  野口佳裕、西尾信哉、宇佐美真一
- Organizer
  第26回日本耳科学会
- Place of Presentation
  ホテル国際21（長野市）
- Year and Date
  2016-10-05
- Data Source
  KAKENHI-PROJECT-16K11176
[Presentation] 次世代シーケンサーにより見出されたPOU4F3遺伝子変異症例の臨床像2016
- Author(s)
  北野友裕、宮川麻衣子、西尾信哉、茂木英明、野口佳裕、宇佐美真一
- Organizer
  第26回日本耳科学会
- Place of Presentation
  ホテル国際21（長野市）
- Year and Date
  2016-10-05
- Data Source
  KAKENHI-PROJECT-16K11176
[Presentation] 日常診療における遺伝子診断ー診療の手引きをふまえて2016
- Author(s)
  野口佳裕
- Organizer
  第26回日本耳科学会
- Place of Presentation
  ホテル国際21（長野市）
- Year and Date
  2016-10-05
- Data Source
  KAKENHI-PROJECT-16K11176
[Presentation] Delayed restoration of speech discrimination score in sudden sensorineural hearing loss2013
- Author(s)
  Noguchi Y, Takahashi M, Ito T, Tokano H, Nishio A, Yamamoto K, Kitamura K
- Organizer
  20th IFOS World Congress
- Place of Presentation
  Seoul, Korea
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] Comprehensibe analyses for mitochondrial DNA in patients with hereditary hearing loss2013
- Author(s)
  Kato T, Noguchi Y, Kimura Y, Kitamura K
- Organizer
  13th Triennial Meeting of the International Otopathology Society
- Place of Presentation
  Boston, USA
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] A DFNA5 mutation in two Japanese families with autosomal dominant hereditary hearing loss2013
- Author(s)
  Kitamura K, Sato T, Noguchi Y, Nishio A, Naruse T, Kimura A, Takagi A
- Organizer
  29th Politzer Society Meeting
- Place of Presentation
  Antalya Turkey
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] microRNAexpression in the aging mouse cochlea2012
- Author(s)
  Noguchi Y, Takahashi M, Honda K,Nishio A, Kitamura K
- Organizer
  35th Annual Midwinter Meeting of the Association for Research in Otolaryngology
- Place of Presentation
  San Diego
- Data Source
  KAKENHI-PROJECT-22591876
[Presentation] 加齢性難聴モデルマウスにおける加齢に伴うmiRNA発現の変化2012
- Author(s)
  野口佳裕,本田圭司,高橋正時,川島慶之,喜多村健
- Organizer
  第22回日本耳科学会総会
- Place of Presentation
  名古屋
- Data Source
  KAKENHI-PROJECT-22591876
[Presentation] microRNA expression in the aging mouse cochlea2012
- Author(s)
  Noguchi Y, et al
- Organizer
  35^<th> Annual Midwinter Meeting of the Association for Research in Otolaryngology
- Place of Presentation
  サンディエゴ、米国
- Year and Date
  2012-02-26
- Data Source
  KAKENHI-PROJECT-22591876
[Presentation] Evaluation of Baha efficacy by self-assessment questionnaires2011
- Author(s)
  Noguchi Y, Sawada M, Takahashi M, Tokano H, Kitamura K
- Organizer
  The 8^<th> Asia Pacific Symposium on Cochlear Implant and Related Sciences
- Place of Presentation
  Daegu Korea
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] Long term follow-up study of mastoid obliteration using bone pate in cholesteatoma.2011
- Author(s)
  Kitamura K, Y Nakamura Y, Noguchi Y, Takahashi M
- Organizer
  28th Politzer Society Meeting
- Place of Presentation
  Athens Greece
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] Evaluation of Baha efficacy by self-assessment questionnaires2011
- Author(s)
  Noguchi Y, Sawada M, Takahashi M, Tokano H, Kitamura K
- Organizer
  The 8^<th> Asia Pacific Symposium on Cochlear Implant and Related Sciences
- Place of Presentation
  Daegu Korea
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] 遺伝性難聴疑い症例のミトコンドリアハプログループ解析.2011
- Author(s)
  加藤智史,野口佳裕,木村百合香,喜多村健
- Organizer
  第21回日本耳科学会総会・学術講演会
- Place of Presentation
  沖縄
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] 遺伝性難聴疑い症例のミトコンドリアハプログループ解析2011
- Author(s)
  加藤智史, 野口佳裕, 木村百合香, 喜多村健
- Organizer
  第21回日本耳科学会総会・学術講演会
- Place of Presentation
  沖縄(招待講演)
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] Long term follow-up study of mastoid obliteration using bone pate in cholesteatoma2011
- Author(s)
  Kitamura K, Y Nakamura Y, Noguchi Y, Takahashi M
- Organizer
  28^<th> Politzer Society Meeting
- Place of Presentation
  Athens Greece(招待講演)
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] A DFNA5 mutation in two Japanese families with autosomal dominant hereditary hearing loss2011
- Author(s)
  Nishio A, Noguchi Y, Kitamura K
- Organizer
  11th Japan-Taiwan Conference on Otolaryngology-Head and Neck Surgery
- Place of Presentation
  Kobe
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] Evaluation of Baha efficacy by self-assessment questionnaires.2011
- Author(s)
  Noguchi Y, Sawada M, Takahashi M, Tokano H, Kitamura K
- Organizer
  The 8th Asia Pacific Symposium on Cochlear Implant and Related Sciences
- Place of Presentation
  Daegu Korea
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] 遺伝性難聴疑い症例のミトコンドリアハプログループ解析2011
- Author(s)
  加藤智史, 野口佳裕, 木村百合香, 喜多村健
- Organizer
  第21回日本耳科学会総会・学術講演会
- Place of Presentation
  沖縄(特別講演)
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] A DFNA5 mutation in two Japanese families with autosomal dominanthereditary hearing loss2011
- Author(s)
  Nishio A, Noguchi Y, Kitamura K
- Organizer
  11th Japan-Taiwan Conference on Otolaryngology-Head and Neck Surgery
- Place of Presentation
  Kobe
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] ADFNA5 mutation in two Japanese familieswith autosomal dominant hereditary hearing loss.2011
- Author(s)
  Nishio A, Noguchi Y, Kitamura K
- Organizer
  11th Japan-Taiwan Conference on Otolaryngology-Head and Neck Surgery.
- Place of Presentation
  Kobe
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] Long term follow-up study of mastoid obliteration using bone pate in cholesteatoma2011
- Author(s)
  Kitamura K, Y Nakamura Y, Noguchi Y, Takahashi M
- Organizer
  28^<th> Politzer Society Meeting
- Place of Presentation
  Athens Greece(招待講演)
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] Variable audiovestibular findings in patients with enlargement of the vestibular aqueduct caused bymutations of SLC26A4, SIX1, and ATP6V1B1.2010
- Author(s)
  Noguchi Y, Ito T, Nishio A, Honda K, Kitamura K
- Organizer
  Sixth international symposium on Meniere's disease and inner ear disorders.
- Place of Presentation
  Kyoto
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] MicroRNA expression in the cochlea of age related hearing loss mouse2010
- Author(s)
  Noguchi Y, et al
- Organizer
  20th Triennial Meeting The International Otopathology Society
- Place of Presentation
  Massachusetts Eye and Ear Infirmary(ボストン)
- Year and Date
  2010-06-08
- Data Source
  KAKENHI-PROJECT-22591876
[Presentation] Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.2010
- Author(s)
  Kato T, Nishigaki Y, Fuku N, Ueno H, Noguchi Y, Kitamura K, Tanaka M
- Organizer
  The 7^<th> Conference of Asian Society for Mitochondrial Research and Medicine
- Place of Presentation
  Fukuoka
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss2010
- Author(s)
  Kato T, Nishigaki Y, Fuku N, Ueno H, Noguchi Y, Kitamura K, Tanaka M
- Organizer
  The 7^<th> Conference of Asian Society for Mitochondrial Research and Medicine
- Place of Presentation
  Fukuoka
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] Audiovestibular findings in a Branchio-Oto syndrome patient with SIX1 mutation.2010
- Author(s)
  Noguchi Y, Ito T, Nishio A, Kitamura K
- Organizer
  Collegium Oto-Rhino-Laryngologicum Amicitiae Sacrum
- Place of Presentation
  Budapest, Hungary
- Year and Date
  2010-08-25
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] 加齢性難聴モデルマウスC57BL/6JにおけるmiRNA発現解析2010
- Author(s)
  野口佳裕、高橋正時、喜多村健
- Organizer
  第20回日本耳科学会総会
- Place of Presentation
  ひめぎんホール(松山市)
- Year and Date
  2010-10-08
- Data Source
  KAKENHI-PROJECT-22591876
[Presentation] Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.2010
- Author(s)
  Kato T, Nishigaki Y, Fuku N, Ueno H, Noguchi Y, Kitamura K, Tanaka M
- Organizer
  The 7th Conference of Asian Society for Mitochondrial Reseach and Medicine.
- Place of Presentation
  Fukuoka
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] Variable audiovestibular findings in patients with enlargement of the vestibular aqueduct caused by mutations of SLC26A4, SIXI, and ATP6V1B12010
- Author(s)
  Noguchi Y, Ito T, Nishio AHonda K, Kitamura K
- Organizer
  Sixth international symposium on Meniere' sdisease and inner ear disorders
- Place of Presentation
  Kyoto
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] Audiovestibular findings in a Branchio-Oto syndrome patientwith SIX1 mutation2010
- Author(s)
  Noguchi Y, Ito T, Nishio A, Kitamura K
- Organizer
  Collegium Oto-Rhino-LaryngologicumAmicitiae Sacrum
- Place of Presentation
  Budapest
- Year and Date
  2010-08-25
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] Audiovestibular findings in a Branchio-Oto syndrome patient with STX1 mutation2010
- Author(s)
  Noguchi Y, Ito T, Nishio A, Kitamura K
- Organizer
  Collegium Oto-Rhino-Laryngologicum Amicitiae Sacrum
- Place of Presentation
  Budapest
- Year and Date
  2010-08-25
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss2010
- Author(s)
  Kato T, Nishigaki Y, Noguchi Y, Ito T, Tanaka M, Kitamura K
- Organizer
  2^<nd> East Asian Symposium on Otology
- Place of Presentation
  Taipei Taiwan November 2010
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss2010
- Author(s)
  Kato T, Nishigaki Y, Noguchi Y, Ito T, Tanaka M, Kitamura K
- Organizer
  2^<nd> East Asian Symposium on Otology
- Place of Presentation
  Taipei Taiwan
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.2010
- Author(s)
  Kato T, Nishigaki Y, Noguchi Y, Ito T, Tanaka M, Kitamura K
- Organizer
  2nd East Asian Symposium on Otology
- Place of Presentation
  Taipei Taiwan
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] Variable audiovestibular findings in patients with enlargemeni of the vestibular aqueduct caused by mutations of SLC26A4, SIX1, and ATP6V1B12010
- Author(s)
  Noguchi Y, Ito T, Nishio A, Honda K, Kitamura K
- Organizer
  Sixth international symposium on Meniere's disease and inner ear disorders
- Place of Presentation
  Kyota
- Data Source
  KAKENHI-PROJECT-22659305
[Presentation] 加齢性難聴モデルマウスC57BL/6JにおけるmiRNA発現解析2010
- Author(s)
  野口佳裕,高橋正時,喜多村健
- Organizer
  第20回日本耳科学会総会
- Place of Presentation
  松山
- Data Source
  KAKENHI-PROJECT-22591876
[Presentation] Whirlin and Sans functions in planar cell polarity regulation at the apical surface of inner ear hair cells.2009
- Author(s)
  Kazuhiro Okumura, Yuki Miyasaka, Yasuhiro Oshiba, Yoshihiro Noguchi, Ken Kitamura, Philomena Mburu, Steve D.M.Brown, Hiromichi Yonekawa, Yoshiaki Kikkawa
- Organizer
  第32回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜(横浜)
- Year and Date
  2009-12-11
- Data Source
  KAKENHI-PROJECT-20300147
[Presentation] 進行性難聴モデルマウスにおける経時的歪成分耳音響放射2009
- Author(s)
  野口佳裕, 大野十央, 高橋正時, Andrew J. Giffith, 喜多村健
- Organizer
  第4回ERA・OAE研究会
- Place of Presentation
  東京
- Year and Date
  2009-07-05
- Data Source
  KAKENHI-PROJECT-19591960
[Presentation] 前庭水管拡大症を伴うSIX1変異によるBranchio-oto症候群の聴平衡覚検査所見2009
- Author(s)
  野口佳裕
- Organizer
  第68回日本めまい平衡医学会・学術講演会
- Place of Presentation
  徳島
- Year and Date
  2009-11-26
- Data Source
  KAKENHI-PROJECT-21390459
[Presentation] 前庭水管拡大症を伴うSIX1変異による Branchio-oto 症候群の聴平衡覚検査所見2009
- Author(s)
  野口佳裕, 伊藤卓, 喜多村健
- Organizer
  第68回めまい平衡医学会総会
- Place of Presentation
  徳島
- Year and Date
  2009-11-26
- Data Source
  KAKENHI-PROJECT-19591960
[Presentation] 平衡障害を示したミトコンドリアDNA1555点変異の1例2008
- Author(s)
  野口佳裕, 川島慶之, 伊藤卓, 喜多村健
- Organizer
  第67回めまい平衡医学会総会
- Place of Presentation
  秋田
- Year and Date
  2008-10-30
- Data Source
  KAKENHI-PROJECT-19591960
[]

1. KITAMURA Ken (90010470)

# of Collaborated Projects: 8 results

# of Collaborated Products: 64 results
2. OKAMURA Hiro-oki (50244372)

# of Collaborated Projects: 4 results

# of Collaborated Products: 0 results
3. ITO Taku (40401400)

# of Collaborated Projects: 3 results

# of Collaborated Products: 17 results
4. 宇佐美真一 (10184996)

# of Collaborated Projects: 3 results

# of Collaborated Products: 14 results
5. SUMI Takurou (20361701)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
6. KAWASHIMA Yoshiyuki (10376759)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
7. KIKKAWA Yoshiaki (20280787)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
8. SHITARA Hiroshi (90321885)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
9. KIMURA Yurika (40450564)

# of Collaborated Projects: 2 results

# of Collaborated Products: 12 results
10. UGAWA SHINYA (20326135)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
11. MURAKAMI Shingo (80157750)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
12. UEDA Takashi (90244540)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
13. UZAWA Masamichi (10361700)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
14. 西尾信哉 (70467166)

# of Collaborated Projects: 2 results

# of Collaborated Products: 10 results
15. TANAKA Masashi (60155166)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
16. KATO Tomofumi (80469965)

# of Collaborated Projects: 1 results

# of Collaborated Products: 9 results
17. TAKAHASHI Masatoki (80401355)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
18. SAWABE Motoji (30196331)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. WADA Kenta (20508113)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. KAJITA Kenji (80381820)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. SAKUMA Eisuke (90295585)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
22. NISHIO Ayako (00611576)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
23. HONDA Keiji (90621079)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
24. KAWAKAMI Kiyoshi (10161283)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
25. TSUTSUMI Takeshi (90302851)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
26. TSUNODA Atsunobu (00280983)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
27. KOUDA Hiroko (80334423)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
28. YASHIMA Takatoshi (50372438)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
29. 栫博幸 (40201412)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
30. 柴田泰宏 (10534745)

# of Collaborated Projects: 1 results

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31. 島田昌一 (20216063)

# of Collaborated Projects: 1 results

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32. 熊本奈都子 (30467584)

# of Collaborated Projects: 1 results

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33. SUZUKI Sari

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
34. MIYASAKA Yuki

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
35. OBARA Yo

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
36. STEVE Brown

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
37. 奥村和弘

# of Collaborated Projects: 1 results

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38. KROS Corne

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
39. OBUCHI Chie

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
40. 八島隆俊

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

Noguchi Yoshihiro 野口 佳裕

NOGUCHI Yoshihiro 野口 佳裕

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Identification of novel causative gene of auditory neuropathy spectrum disorderPrincipal Investigator

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Development of novel clasiffication based on genetic analysis for ANSD and middle ear anormalyPrincipal Investigator

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A study of microRNAs regulating the pathogenesis of age-related hearing lossPrincipal Investigator

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Mouse microRNA expression study identifying the nature of age-related hearing lossPrincipal Investigator

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Age-related balance disorders in Atp2b2 mutant mouse with no otoconiaPrincipal Investigator

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分子生物学的および電気生理学的手法を用いた遺伝性難聴発症機構の研究Principal Investigator

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Noguchi Yoshihiro 野口佳裕

NOGUCHI Yoshihiro 野口佳裕

[Book] 感覚器聴覚;脳・神経系;疾患モデルマウス:臓器・疾患別解析・実験法;生命科学研究の戦略:疾患モデルマウスと表現型

[Journal Article] 特集この1冊でわかる遺伝学的検査-基礎知識と臨床応用《臨床への応用》遺伝性難聴2022