NARA KIYOMITSU 奈良清光

… Alternative Names

奈良清光ナラキヨミツ

NARA Kiyomitsu 奈良清光

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Researcher Number	40260327
Other IDs
Affiliation (Current)	2025: 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
Affiliation (based on the past Project Information) *help	2021 – 2023: 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 2018: 独立行政法人国立病院機構(東京医療センター臨床研究センター), 聴覚・平衡覚研究部, 研究員 2013: 福島県立医科大学, 生化学講座, 講師 2011 – 2013: 福島県立医科大学, 医学部, 講師 2008 – 2009: 公立大学法人福島県立医科大学, 医学部, 講師 … More 1995: 三菱化学, 生命科学研究所, 研究員 1995: Mitsubishi Kasei Life Science Institute Researcher, 研究員 1994 – 1995: 財団法人東京都臨床医学総合研究所, 生命情報研究部門, 研究員 Less
Review Section/Research Field	Principal Investigator Structural biochemistry Except Principal Investigator Basic Section 56050:Otorhinolaryngology-related / Medium-sized Section 56:Surgery related to the biological and sensory functions and related fields / General medical chemistry / Pathological medical chemistry / Biological Sciences
Keywords	Principal Investigator シアル酸転移酵素 / 分子生物学 / ガングリオシド / 糖鎖 / PCR / 遺伝子 / マウス / 糖脂質 / GD3 / メラノーマ / 癌関連抗原 / 糖転移酵素 / cDNAクローニング … More Except Principal Investigator … More 難聴 / アルツハイマー病 / 難聴遺伝子 / Copy Number Variant / ロングリードシーケンス / コピー数変異 / 遺伝子解析 / 相互作用分子 / モデル動物 / 網羅的発現遺伝子解析 / スプライシング / 発現遺伝子網羅的解析 / 疾患モデル動物 / ゲノム編集 / 原因遺伝子 / 分子病態 / PDZD7遺伝子 / アッシャー症候群 / USH2複合体 / PDZドメイン / 次世代シークエンサー / PDZD7 / 非症候群性難聴 / genome / sialyltransferase / ganglioside / galectin / tumor growth factor / 糖転移酵素 / シアル酸 / 糖脂質 / ゲノム / シアル酸転移酵素 / ガングリオシド / ガレクチン / 腫瘍化増殖因子 / スクリーニング法の開発 / 糖鎖マーカー / 認知症 / 髄液 / 診断マーカー / 軽度認知障害 / 質量分析 / SNAレクチン / 脳脊髄液 / α2, 6シアロ酸糖タンパク質 / α2,6-シアロ糖鎖 / 糖タンパク質 / βセクレターゼ Less

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
  
  務台英樹
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 56050:Otorhinolaryngology-related
- Research Institution
  Kitasato University
  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
  
  Matsunaga Tatsuo
- 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)
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)
Search for biomarkers of central nervous system diseases that show subtle morphological changes on MRI and CT.
- Principal Investigator
  
  HASHIMOTO Yasuhiro
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Fukushima Medical University
ベータ・セクレターゼ活性をモニターするバイオマーカーの分析
- Principal Investigator
  
  HASHIMOTO Yasuhiro
- Project Period (FY)
  2008 – 2009
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Review Section
  
  Biological Sciences
- Research Institution
  Fukushima Medical University
神経系におけるガングリオシドの機能解明を目的としたGD3合成酵素遺伝子の解析Principal Investigator
- Principal Investigator
  
  奈良清光
- Project Period (FY)
  1995
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Structural biochemistry
- Research Institution
  Tokyo Metropolitan Organization for Medical Research
ガングリオシドGD3の機能解明をめざしたGD3合成酵素のcDNAクローニングPrincipal Investigator
- Principal Investigator
  
  奈良清光
- Project Period (FY)
  1994
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Structural biochemistry
- Research Institution
  Tokyo Metropolitan Organization for Medical Research
Molecular regulatory mechanism of cell surface garbohydrate expression and its pathology.
- Principal Investigator
  
  YAMAOKA Kazuko, NAGAI Yoshitaka
- Project Period (FY)
  1993 – 1995
- Research Category
  
  Grant-in-Aid for General Scientific Research (B)
- Research Field
  
  General medical chemistry
- Research Institution
  Tokyo Metropolitan Institute of Medical Science

All 2023 2022 2021 2018 2013 2012 2011 2010 2009

All Journal Article Presentation Patent

[Journal Article] Correlation between genotype and phenotype with special attention to hearing in 14 Japanese cases of NF2-related schwannomatosis2023
- Author(s)
  Oishi Naoki、Noguchi Masaru、Fujioka Masato、Nara Kiyomitsu、Wasano Koichiro、Mutai Hideki、Kawakita Rie、Tamura Ryota、Karatsu Kosuke、Morimoto Yukina、Toda Masahiro、Ozawa Hiroyuki、Matsunaga Tatsuo
- Journal Title
  
  Scientific Reports
  
  Volume: 13 Issue: 1 Pages: 6595-6595
- DOI
  10.1038/s41598-023-33812-w
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K20409, KAKENHI-PROJECT-22K18399, KAKENHI-PROJECT-21H04839, KAKENHI-PROJECT-21K09574, KAKENHI-PROJECT-21K09598
[Journal Article] Phenotype-genotype correlation in patients with typical and atypical branchio-oto-renal syndrome2022
- Author(s)
  Masuda M, Kanno A, Nara K, Mutai H,Morisada N, Iijima K, Morimoto N, Nakano A, Sugiuchi T, Okamoto Y, Masuda S, Katsunuma S, Ogawa K, Matsunaga T
- Journal Title
  
  Scientific Reports
  
  Volume: 12 Issue: 1 Pages: 969-969
- DOI
  10.1038/s41598-022-04885-w
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K09644
[Journal Article] Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts2022
- Author(s)
  Nakano Atsuko、Arimoto Yukiko、Mutai Hideki、Nara Kiyomitsu、Inoue Satomi、Matsunaga Tatsuo
- Journal Title
  
  International Journal of Pediatric Otorhinolaryngology
  
  Volume: 152 Pages: 110975-110975
- DOI
  10.1016/j.ijporl.2021.110975
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20K19082, KAKENHI-PROJECT-21K09598
[Journal Article] Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes.2022
- Author(s)
  Hideki Mutai, Yukihide Momozawa, Yoichiro Kamatani, Atsuko Nakano, Hirokazu Sakamoto, Tetsuya Takiguchi, Kiyomitsu Nara, Michiaki Kubo, Tatsuo Matsunaga.
- Journal Title
  
  Orphanet Journal of Rare Diseases
  
  Volume: 17 Issue: 1 Pages: 114-114
- DOI
  10.1186/s13023-022-02262-4
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K09598, KAKENHI-PROJECT-21K09644
[Journal Article] Lectin-dependent inhibition of antigen-antibody reaction: application for measuringα2,6-sialylated glycoforms of transferrin2013
- Author(s)
  Kyoka Hoshi, Yoshinobu Kariya, Kiyomitsu Nara, Hiromi Ito, Keiro Shirotani, Yasuhiro Hashimoto, et al
- Journal Title
  
  J. Biochem.
  
  Volume: 154(3) Issue: 3 Pages: 229-232
- DOI
  10.1093/jb/mvt065
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23590367, KAKENHI-PROJECT-23592106, KAKENHI-PUBLICLY-24110511, KAKENHI-PUBLICLY-24110520, KAKENHI-PROJECT-25860243
[Journal Article] A unique N-glycan on human transferrin in CSF:a possible biomarker for iNPH2012
- Author(s)
  Satoshi Futakawa, Kiyomitsu Nara, Hiromi Ito, Keiro Shirotani, Yasuhiro Hashimoto, et al
- Journal Title
  
  Neurobiology of Aging
  
  Volume: 33(8) Pages: 1807-1815
- Data Source
  KAKENHI-PROJECT-23590367
[Journal Article] 糖タンパク質糖鎖をマーカーとする認知症の診断:特発性正常圧水頭症の新規マーカー2011
- Author(s)
  橋本康弘, 奈良清光, 城谷圭朗, 伊藤浩美, 他
- Journal Title
  
  老年期認知症研究会誌
  
  Volume: Vol.18 Pages: 115-116
- Data Source
  KAKENHI-PROJECT-23590367
[Journal Article] 認知症の髄液学-診断マーカーとしての糖鎖修飾-2011
- Author(s)
  奈良清光, 城谷圭朗, 橋本康弘, 他
- Journal Title
  
  認知症関連分子生物学各論「日本臨床」((株)日本臨床)
  
  Volume: 69巻,増刊号8 Pages: 69-73
- Data Source
  KAKENHI-PROJECT-23590367
[Journal Article] High Throughput ELISAs to Measure an Unique Glycan on Transferrin in Cerebrospinal fluid:A Possible Extension Toward Alzheimer's Disease Biomarker Development2011
- Author(s)
  Keiro Shirotani, Kiyomitsu Nara, Yasuhiro Hashimoto, et al
- Journal Title
  
  International Journal of Alzheimer's Disease
  
  Volume: 2011 Issue: 1 Pages: 352787-352787
- DOI
  10.4061/2011/352787
- Data Source
  KAKENHI-PROJECT-23590367
[Patent] 糖鎖アイソフォーム検出方法及び糖鎖アイソフォーム検出装置2012
- Inventor(s)
  橋本康弘, 城谷圭朗, 奈良清光, 苅谷慶喜, 伊藤浩美, (他4名)
- Industrial Property Rights Holder
  独立行政法人産業技術総合研究所, 公立大学法人福島県立医科大学
- Filing Date
  2012-08-10
- Overseas
- Data Source
  KAKENHI-PROJECT-23590367
[Patent] 糖鎖アイソフォーム検出方法及び糖鎖アイソフォーム検出装置2012
- Inventor(s)
  成松久、橋本康弘、城谷圭朗、奈良清光、苅谷慶喜、伊藤浩美　他３名
- Industrial Property Rights Holder
  独立行政法人産業技術総合研究所、公立大学法人福島県立医科大学
- Industrial Property Rights Type
  特許
- Industrial Property Number
  2012-178722
- Filing Date
  2012-08-10
- Data Source
  KAKENHI-PROJECT-23590367
[Presentation] Efficient identification of causative genes of hearing loss by phenotype similarity analysis.2023
- Author(s)
  Mutai H, Miya F, Nara K, Muramatsu R, Inoue S, Murakami H, Minami S, Nakano A, Arimoto Y, Morimoto N, Kawasaki T, Wasano K, Sakamoto H, Katsunuma S, Masuda S, Yamazawa K, Kosaki K, Tsunoda T, Matsunaga T
- Organizer
  Human Genetics Asia 2023 (The 68th Annual Meeting of the Japan Society of Human Genetics).
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K09644
[Presentation] MYO6新規バリアントが同定された成人期軽度感音難聴の１例2023
- Author(s)
  川畑満里奈、宇田川友克、茂木雅臣、中澤宝、奈良清光、務台英樹、櫻井結華、小島博己、松永達雄
- Organizer
  第68回日本聴覚医学会総会・学術講演会
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] Genetic approach to improve clinical practice for deafblindness in Japan2023
- Author(s)
  Tatsuo Matsunaga, Kiyomitsu Nara, Hideki Mutai, Haruka Murakami, Satomi Inoue, et al.
- Organizer
  Human Genetics Asia 2023
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] Efficient identification of causative genes of hearing loss by phenotype similarity analysis2023
- Author(s)
  Hideki Mutai, Fuyuki Miya, Kiyomitsu Nara, Reiko Muramatsu, Satomi Inoue, Haruka Murakami, Shujiro Minami, Atsuko Nakano, Yukiko Arimoto, Noriko Morimoto, Taiji Kawasaki, Koichiro Wasano, Hirokazu Sakamoto, Sayaka Katsunuma, Sawako Masuda, Kazuki Yamazawa, Kenjiro Kosaki, Tatsuhiko Tsunoda, Tatsuo Matsunaga
- Organizer
  Human Genetics Asia 2023
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] アッシャー症候群の原因遺伝子が検出された小児難聴症例の検討2023
- Author(s)
  仲野敦子、有本友季子、外池百合恵、村松玲子、奈良清光、務台英樹、松永達雄
- Organizer
  第68回日本聴覚医学会総会・学術講演会
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] 難聴原因遺伝子の全エクソーム解析による効率的な同定2023
- Author(s)
  務台英樹、奈良清光、南修司郎、仲野敦子、有本友季子、守本倫子、川﨑泰士、和佐野浩一郎、阪本浩一、勝沼紗矢香、増田佐和子、松永達雄
- Organizer
  第33回日本耳科学会総会・学術講演会
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] 新たなPOU4F3遺伝子バリアントを同定した顕性（優性）遺伝形式の難聴1家系2023
- Author(s)
  高津南美子、茂木雅臣、宇田川友克、櫻井結華、小島博己、奈良清光、務台英樹、松永達雄
- Organizer
  第68回日本聴覚医学会総会・学術講演会
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] 難聴の原因として報告されたミトコンドリア遺伝子変異に対する国際基準を用いた評価2022
- Author(s)
  奈良清光、務台英樹、瀧口哲也、守本倫子、仲野敦子、有本友季子、森田訓子、南修司郎、加我君孝、松永達雄
- Organizer
  第17回日本小児耳鼻咽喉学会
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] 聴患者におけるAxenfeld-Rieger症候群の遺伝学的診断2022
- Author(s)
  松永達雄、奈良清光、務台英樹、村上遥香、村松玲子、守本倫子、小笠原徳子、高野賢一
- Organizer
  第67回日本聴覚医学会
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] 視覚聴覚二重障害を持つ小児の診療における遺伝学的検査の意義2022
- Author(s)
  松永達雄、奈良清光、務台英樹、泉修司、山岸達矢、堀井新、江崎友子、土橋奈々、中川尚志、上原奈津美、丹生健一、山本修子、和佐野浩一郎、南修司郎、加我君孝
- Organizer
  第17回日本小児耳鼻咽喉学会
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] Auditory neuropathy あるいはそれに類似した聴覚検査所見を呈した MTTS1 遺伝子変異3 家系5 例2021
- Author(s)
  喜田有未来，南修司郎，奈良清光，井上沙聡，務台英樹，和佐野浩一郎，森田訓子，加我君孝，松永達雄
- Organizer
  第31回日本耳科学会
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] CDH23遺伝子のバリアントが原因と考えられた難聴の一家系についての検討2021
- Author(s)
  髙野さくらこ，阪本浩一，坂下哲史，小杉祐季、務台英樹，奈良清光，松永達雄，角南貴司子
- Organizer
  第66回日本聴覚医学会
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] 当院を受診した難聴者に対する遺伝子診断と遺伝カウンセリングの現況2021
- Author(s)
  井上沙聡、奈良清光、務台英樹、南修司郎、加我君孝、和佐野浩一郎、松永達雄
- Organizer
  第31回日本耳科学会
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] 若年発症型両側性感音難聴の発症後早期の臨床的特徴2021
- Author(s)
  松永達雄、務台英樹、奈良清光、井上沙聡、森田訓子、内田育恵、南修司郎、山本修子、和佐野浩一郎、加我君孝
- Organizer
  第66回日本聴覚医学会
- Data Source
  KAKENHI-PROJECT-21K09598
[Presentation] 当院を受診した難聴者に対する遺伝子診断と遺伝カウンセリングの現況2021
- Author(s)
  井上沙聡、奈良清光、務台英樹、南修司郎、加我君孝、和佐野浩一郎、松永達雄
- Organizer
  第 31 回日本耳科学会総会・学術講演会
- Data Source
  KAKENHI-PROJECT-21K09644
[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] SSAレクチンによる抗原-抗体反応の阻害:髄液中α2,6-シアル酸化トランスフェリン測定への応用2013
- Author(s)
  星京香, 苅谷慶喜, 奈良清光, 伊藤浩美, 城谷圭朗, 橋本康弘, 他
- Organizer
  第7回東北糖鎖研究会
- Place of Presentation
  新潟
- Data Source
  KAKENHI-PROJECT-23590367
[Presentation] SAレクチンによる抗原-抗体反応の阻害：髄液中α2,6-シアル酸化トランスフェリン測定への応用2013
- Author(s)
  星京香、苅谷慶喜、奈良清光、伊藤浩美、松本加奈、長江雅倫、山口芳樹、中島円、宮嶋雅一、新井一、久野敦、成松久、城谷圭朗、橋本康弘
- Organizer
  第7回東北糖鎖研究会
- Place of Presentation
  新潟
- Data Source
  KAKENHI-PROJECT-23590367
[Presentation] 認知症マーカーとしてのα2,6シアル酸化トランスフェリンの新規測定法2013
- Author(s)
  星京香, 苅谷慶喜, 奈良清光, 伊藤浩美, 城谷圭朗, 橋本康弘, 他
- Organizer
  第86回日本生化学会大会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23590367
[Presentation] 認知症の糖鎖バイオマーカーのハイスループット測定法2013
- Author(s)
  城谷圭朗, 奈良清光, 橋本康弘, 他
- Organizer
  日本薬学会第133年会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-23590367
[Presentation] 次世代ポストゲノムの時代, 糖鎖研究はおもしろい2012
- Author(s)
  奈良清光, 城谷圭朗, 伊藤浩美, 橋本康弘, 他
- Organizer
  第75回日本皮膚科学会東京支部学会
- Place of Presentation
  東京
- Invited
- Data Source
  KAKENHI-PROJECT-23590367
[Presentation] 脳型糖タンパク質の中枢神経疾患マーカーとしての意義2012
- Author(s)
  奈良清光, 苅谷慶喜, 伊藤浩美, 橋本康弘, 他
- Organizer
  第6回東北糖鎖研究会
- Place of Presentation
  弘前
- Data Source
  KAKENHI-PROJECT-23590367
[Presentation] 髄液に特徴的な脳型トランスフェリンの認知症マーカーとしての意義2012
- Author(s)
  橋本康弘, 城谷圭朗, 奈良清光, 伊藤浩美, 苅谷慶喜, 他
- Organizer
  第31回日本糖質学会年会
- Place of Presentation
  鹿児島
- Data Source
  KAKENHI-PROJECT-23590367
[Presentation] A unique N-glycan on human transferrin in CSF:a possible biomarker for iNPH2012
- Author(s)
  Satoshi Futakawa, Kiyomitsu Nara, Hiromi Ito, Keiro Shirotani, Yasuhiro Hashimoto, et al
- Organizer
  Hydrocephalus 2012
- Place of Presentation
  Kyoto, Japan
- Data Source
  KAKENHI-PROJECT-23590367
[Presentation] 認知症糖鎖マーカーのハイスループット測定法2011
- Author(s)
  城谷圭朗, 奈良清光, 伊藤浩美, 苅谷慶喜, 橋本康弘, 他
- Organizer
  第5回東北糖鎖研究会
- Place of Presentation
  仙台
- Data Source
  KAKENHI-PROJECT-23590367
[Presentation] がん糖鎖によるシダリック-7を介し免疫細胞死の誘導2010
- Author(s)
  橋本康弘、奈良清光
- Organizer
  第5回臨床糖鎖研究会(特別講演)
- Place of Presentation
  弘前市
- Year and Date
  2010-03-04
- Data Source
  KAKENHI-PROJECT-20023023
[Presentation] 糖鎖と疾患:神経疾患とガンを例にして2009
- Author(s)
  奈良清光、菅野真由美、橋本康弘
- Organizer
  第7回日本糖鎖科学コンソーシアムシンポジウム
- Place of Presentation
  豊中市
- Data Source
  KAKENHI-PROJECT-20023023
[Presentation] Siglec-7によるITIM依存性および非依存性まの新規シグナル伝達2009
- Author(s)
  橋本康弘、菅野真田美、山口芳樹、奈良清光
- Organizer
  第29回日本糖質学会年会
- Place of Presentation
  高山市
- Data Source
  KAKENHI-PROJECT-20023023

1. 務台英樹 (60415891)

# of Collaborated Projects: 3 results

# of Collaborated Products: 18 results
2. HASHIMOTO Yasuhiro (80164797)

# of Collaborated Projects: 2 results

# of Collaborated Products: 17 results
3. SHIROTANI Keiro (20322696)

# of Collaborated Projects: 2 results

# of Collaborated Products: 13 results
4. YAMAOKA Kazuko (00124438)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
5. NAGAI Yoshitaka (80072974)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
6. Matsunaga Tatsuo (90245580)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
7. KARIYA Yoshinobu (00458217)

# of Collaborated Projects: 1 results

# of Collaborated Products: 7 results
8. ITO Hiromi (00450669)

# of Collaborated Projects: 1 results

# of Collaborated Products: 11 results
9. WATANABE Yumiko (90250216)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. KASAHARA Kohji (60250213)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. SANAI Yutaka (40150289)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. 二川了次 (90533167)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. 森努 (60244373)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. 梶山泰生 (70250214)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. 小山内たか (60126018)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. 井上沙聡

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
18. 野口勝

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

NARA KIYOMITSU 奈良 清光

奈良 清光 ナラ キヨミツ

NARA Kiyomitsu 奈良 清光

Research Projects

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Co-Researchers

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

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Identification of CNV of deafness gene and development of simple test method by long read sequencing

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Elucidation of prevalence, clinical features and pathogenic mechanism of PDZD7 mutations which was identified as a novel gene causing nonsyndromic hearing loss

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Search for biomarkers of central nervous system diseases that show subtle morphological changes on MRI and CT.

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ベータ・セクレターゼ活性をモニターするバイオマーカーの分析

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神経系におけるガングリオシドの機能解明を目的としたGD3合成酵素遺伝子の解析Principal Investigator

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ガングリオシドGD3の機能解明をめざしたGD3合成酵素のcDNAクローニングPrincipal Investigator

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Molecular regulatory mechanism of cell surface garbohydrate expression and its pathology.

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[Journal Article] Correlation between genotype and phenotype with special attention to hearing in 14 Japanese cases of NF2-related schwannomatosis2023

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[Journal Article] Phenotype-genotype correlation in patients with typical and atypical branchio-oto-renal syndrome2022

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[Journal Article] Clinical and genetic analysis of children with hearing loss and bilateral enlarged vestibular aqueducts2022

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[Journal Article] Whole exome analysis of patients in Japan with hearing loss reveals high heterogeneity among responsible and novel candidate genes.2022

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[Journal Article] Lectin-dependent inhibition of antigen-antibody reaction: application for measuringα2,6-sialylated glycoforms of transferrin2013

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[Journal Article] A unique N-glycan on human transferrin in CSF:a possible biomarker for iNPH2012

NARA KIYOMITSU 奈良清光

奈良清光ナラキヨミツ

NARA Kiyomitsu 奈良清光