Lee Tomoko 李知子

… Alternative Names

LEE TOMOKO 李知子

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Researcher Number	10596042
Other IDs
Affiliation (Current)	2025: 兵庫医科大学, 医学部, 准教授
Affiliation (based on the past Project Information) *help	2023 – 2024: 兵庫医科大学, 医学部, 准教授 2020 – 2022: 兵庫医科大学, 医学部, 講師 2014 – 2019: 兵庫医科大学, 医学部, 助教
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics / Human genetics
Keywords	Principal Investigator デュシェンヌ型筋ジストロフィー / アンチセンスオリゴヌクレオチド / イントロン内スプライシング制御配列 / スプライシング / エクソンスキッピング治療 / アンチセンス核酸 / ナンセンス変異依存mRNA分解機構 / ナンセンス変異リードスルー治療 / ナンセンス変異 / リードスルー / リードスルー治療 / ナンセンス変異依存性mRNA分解 / Duchenne型筋ジストロフィー … More Except Principal Investigator … More 筋ジストロフィー / 分子治療 / アンチセンスオリゴヌクレオチド / エクソンスキッピング / スプライシング / 小児神経学 / Duchenne型筋ジストロフィー / 治療評価系 / バイオマーカー / セルフリーRNA / 血管内皮増殖因子 / 血管作動性因子 / 尿中exRNA / extracellular RNA / extracelluar RNA / 次世代シークエンサー / exon skipping / splicing / molecular therapy / muscular dystrophy / データベース / 遺伝学 / 分子疫学 / 東アジア / 遺伝子診断 / ナンセンス変異リードスルー誘導治療 / エクソンスキッピング誘導治療 / ジストロフィン / プロスタグランジン / 炎症性物質 Less

アンチセンス核酸による筋ジストロフィーナンセンス変異リードスルー治療効率化の検証Principal Investigator
- Principal Investigator
  
  李知子
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hyogo Medical University
循環血中セルフリーRNAをバイオマーカーとした筋ジストロフィー治療評価系の検証
- Principal Investigator
  
  竹島泰弘
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hyogo Medical University
エクソンスキッピング誘導治療の有効性を予測する残存イントロン解析システムの検証Principal Investigator
- Principal Investigator
  
  李知子
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hyogo Medical University
Validation of a treatment evaluation system for muscular dystrophy using urinary splicing products as biomarkers
- Principal Investigator
  
  TANAKA Yasuhiko
- Project Period (FY)
  2020 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hyogo Medical University
Splicing dynamics of vasoactive factors in muscular dystrophy and therapeutic application in muscular dystrophy
- Principal Investigator
  
  Takeshima Yasuhiro
- Project Period (FY)
  2020 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hyogo Medical University
Enhancement of exon skipping therapy by controlling intronic sequencesPrincipal Investigator
- Principal Investigator
  
  Lee Tomoko
- Project Period (FY)
  2018 – 2021
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hyogo Medical University
Non-invasive system for predicting effectiveness of the exon skipping therapy for muscular dystrophy
- Principal Investigator
  
  Yasuhiro Takeshima
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Hyogo Medical University
東アジアにおける筋ジストロフィーオーダーメイド治療開発のための分子疫学的調査
- Principal Investigator
  
  竹島泰弘
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Human genetics
- Research Institution
  Hyogo Medical University
Improvement of the nonsense read-through therapy for muscular dystrophy by controlling nonsense mediated mRNA decayPrincipal Investigator
- Principal Investigator
  
  LEE TOMOKO
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Hyogo Medical University
Investigation of inflammatory factors affecting the efficacy of the molecular therapies for muscular dystrophy
- Principal Investigator
  
  Yasuhiro Takeshima
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Hyogo Medical University

All 2024 2023 2022 2021 2020 2019 2018 2017 2016

All Journal Article Presentation Book

[Book] MDフロンティア2021
- Author(s)
  李　知子
- Total Pages
  4
- Publisher
  メディカルレビュー社
- ISBN
  9784779225598
- Data Source
  KAKENHI-PROJECT-18K15734
[Journal Article] Longitudinal data of serum creatine kinase levels and motor, pulmonary, and cardiac functions in 337 patients with Duchenne muscular dystrophy2024
- Author(s)
  Awano Hiroyuki、Nambu Yoshinori、Itoh Chieko、Kida Akihiro、Yamamoto Tetsushi、Lee Tomoko、Takeshima Yasuhiro、Nozu Kandai、Matsuo Masafumi
- Journal Title
  
  Muscle and Nerve
  
  Volume: 69 Issue: 5 Pages: 604-612
- DOI
  10.1002/mus.28073
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K17203, KAKENHI-PROJECT-23K07237, KAKENHI-PROJECT-20K08243
[Journal Article] Underlying diseases in sporadic presentation of high creatine kinase levels in girls2021
- Author(s)
  Lee Tomoko、Tokunaga Sachi、Taniguchi Naoko、Misaki Maiko、Shimomura Hideki、Nishino Ichizo、Itoh Kyoko、Takeshima Yasuhiro
- Journal Title
  
  Clinica Chimica Acta
  
  Volume: 519 Pages: 198-203
- DOI
  10.1016/j.cca.2021.05.003
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K15734
[Journal Article] Duchenne型筋ジストロフィーにおける生後早期の血清クレアチンキナーゼ値の推移2021
- Author(s)
  片山慈之, 李知子, 徳永沙知, 谷口直子, 下村英毅, 柴田暁男, 峰淳史, 石井良樹, 藤坂方葉, 吉井勝彦, 奥田真珠美, 竹島泰弘
- Journal Title
  
  日本小児科学会雑誌
  
  Volume: 125 Pages: 1301-1305
- NAID
  40022711657
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K15734
[Journal Article] Two closely spaced mutations in cis result in Ullrich congenital muscular dystrophy2019
- Author(s)
  Shimomura Hideki、Lee Tomoko、Tanaka Yasuhiko、Awano Hiroyuki、Itoh Kyoko、Nishino Ichizo、Takeshima Yasuhiro
- Journal Title
  
  Human Genome Variation
  
  Volume: 6 Issue: 1 Pages: 21-21
- DOI
  10.1038/s41439-019-0052-z
- NAID
  120006644105
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K10087, KAKENHI-PROJECT-16K21524
[Journal Article] Ambulatory capacity in Japanese patients with Duchenne muscular dystrophy2018
- Author(s)
  Awano H, Itoh C, Takeshima Y, Lee T, Matsumoto M, Kida A, Kaise T, Suzuki T, Matsuo M.
- Journal Title
  
  Brain and Development
  
  Volume: 40 Issue: 6 Pages: 465-472
- DOI
  10.1016/j.braindev.2018.02.011
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10087, KAKENHI-PROJECT-16H05814
[Journal Article] Cardiac involvement in Fukuyama muscular dystrophy is less severe than in Duchenne muscular dystrophy.2017
- Author(s)
  Yamamoto T, Taniguchi-Ikeda M, Awano H, Matsumoto M, Lee T, Harada R, Imanishi T, Hayashi N, Sakai Y, Morioka I, Takeshima Y, Iijima K, Saegusa J, Toda T.
- Journal Title
  
  Brain and Development
  
  Volume: 39 Issue: 10 Pages: 861-868
- DOI
  10.1016/j.braindev.2017.05.008
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K10087, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-16H05814, KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-17H01563
[Journal Article] 2′-O-Methyl RNA/Ethylene-Bridged Nucleic Acid Chimera Antisense Oligonucleotides to Induce Dystrophin Exon 45 Skipping2017
- Author(s)
  Tomoko Lee, Hiroyuki Awano, Mariko Yagi, Masaaki Matsumoto, Nobuaki Watanabe, Ryoya Goda, Makoto Koizumi, Yasuhiro Takeshima and Masafumi Matsuo
- Journal Title
  
  Genes
  
  Volume: 8 Issue: 2 Pages: 67-67
- DOI
  10.3390/genes8020067
- NAID
  120006373782
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26461545, KAKENHI-PROJECT-15K19641
[Journal Article] Patients with Duchenne muscular dystrophy are significantly shorter than those with Becker muscular dystrophy, with the higher incidence of short stature in Dp71 mutated subgroup2017
- Author(s)
  Matsumoto M, Awano H, Lee T, Takeshima Y, Matsuo M, Iijima K.
- Journal Title
  
  Neuromuscular disorders
  
  Volume: 27 Issue: 11 Pages: 1023-1028
- DOI
  10.1016/j.nmd.2017.06.007
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10087, KAKENHI-PROJECT-16H05814
[Presentation] 5歳からビルトラルセン治療を開始したデュシェンヌ型筋ジストロフィー2例の約3年間の経過2024
- Author(s)
  岩本真太郎,李知子, 長谷川佳奈, 角田朋大, 松井美樹, 徳永沙知, 谷口直子, 下村英毅, 中野さやか, 竹島泰弘
- Organizer
  第37回近畿小児科学会
- Data Source
  KAKENHI-PROJECT-21K07831
[Presentation] 5歳からビルトラルセン治療を開始したデュシェンヌ型筋ジストロフィー2例の約3年間の経過2024
- Author(s)
  岩本真太郎,李知子, 長谷川佳奈, 角田朋大, 松井美樹, 徳永沙知, 谷口直子, 下村英毅, 中野さやか, 竹島泰弘
- Organizer
  第37回近畿小児科学会
- Data Source
  KAKENHI-PROJECT-23K07237
[Presentation] 家族歴のないジストロフィン遺伝子変異を有する女児における母親の保因者頻度2023
- Author(s)
  李知子, 徳永沙知, 谷口直子, 下村英毅, 竹島泰弘
- Organizer
  保因者頻度第65回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08243
[Presentation] Duchenne型筋ジストロフィー小児例における約3年間のビルトラルセン治療経過2023
- Author(s)
  李　知子、徳永沙知、谷口直子、下村英毅、竹島泰弘
- Organizer
  国立研究開発法人国立精神・神経医療研究センター精神・神経疾患研究開発費『筋ジストロフィーの臨床開発推進の基盤整備』班　2023年度班会議
- Data Source
  KAKENHI-PROJECT-21K07831
[Presentation] Cases of Becker muscular dystrophy with nonsense mutations in the dystrophin gene2023
- Author(s)
  Yoshiyuki Katayama, Tomoko Lee, Miki Matsui, Sachi Tokunaga, Naoko Taniguchi, Hideki Shimomura, Yoko Yokoyama, Yukihiro Noda, Jun Matsui, Katsuhiko Yoshii, Yasuhiko Takeshima
- Organizer
  Human Genetics Asia 2023
- Data Source
  KAKENHI-PROJECT-20K08243
[Presentation] Cases of Becker muscular dystrophy with nonsense mutations in the dystrophin gene2023
- Author(s)
  oshiyuki Katayama, Tomoko Lee, Miki Matsui, Sachi Tokunaga, Naoko Taniguchi, Hideki Shimomura, Yoko Yokoyama, Yukihiro Noda, Jun Matsui, Katsuhiko Yoshii, Yasuhiko Takeshima
- Organizer
  Human Genetics Asia 2023
- Data Source
  KAKENHI-PROJECT-23K07237
[Presentation] 家族歴のないジストロフィン遺伝子変異を有する女児における母親の保因者頻度2023
- Author(s)
  李知子, 徳永沙知, 谷口直子, 下村英毅, 竹島泰弘
- Organizer
  第65回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-23K07237
[Presentation] ビルトラルセン治療中のデュシェンヌ型筋ジストロフィー患者・保護者へのアンケート調査2022
- Author(s)
  李　知子、田中めぐみ、堀部拓哉、徳永沙知、谷口直子、下村英毅、竹島泰弘
- Organizer
  第64回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-21K07831
[Presentation] ビルトラルセン治療中のDuchennne型筋ジストロフィー(DMD)患者6例の経過2022
- Author(s)
  谷口直子, 田中めぐみ, 堀部拓哉, 佐浦龍太郎, 角田朋大, 徳永沙知, 李知子, 下村英毅, 竹島泰弘
- Organizer
  第35回近畿小児科学会
- Data Source
  KAKENHI-PROJECT-21K07831
[Presentation] Duchenne型筋ジストロフィーにおける生後早期のCK値の推移2020
- Author(s)
  李　知子、下村英毅、谷口直子、徳永沙知子、牟禮慎子、柴田暁男、峰淳史、石井良樹、藤坂方葉、吉井勝彦、奥田真珠美、竹島泰弘
- Organizer
  第123回日本小児科学会
- Data Source
  KAKENHI-PROJECT-18K15734
[Presentation] Clinical background of hyper-creatine-kinase-emia girls without a family history of genetic muscular diseases2019
- Author(s)
  李知子、徳永沙知、牟禮慎子、三﨑真生子、下村英毅、西野一三、伊東恭子、竹島泰弘
- Organizer
  European Human Genetics Conference 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K15734
[Presentation] A manifesting carrier of Duchenne Muscular Dystrophy with a balanced X- autosome translocation with a breakpoint in the dystrophin gene2019
- Author(s)
  李　知子、底田　辰之、三崎真生子、下村英毅、竹島泰弘
- Organizer
  24th International Annual Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K15734
[Presentation] 家族歴のない高ＣＫ血症女児の臨床背景の検討2019
- Author(s)
  李知子, 徳永沙知, 牟禮慎子, 三﨑真生子, 下村英毅, 西野一三, 伊東恭子, 竹島泰弘
- Organizer
  第61回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-17K10087
[Presentation] A manifesting carrier of Duchenne Muscular Dystrophy with a balanced X-autosome translocation with a breakpoint in the dystrophin gene2019
- Author(s)
  Lee T., Sokoda T., Misaki M., Shimomura H., Takeshima Y.
- Organizer
  24th International Annual Congress of the World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10087
[Presentation] ジストロフェン遺伝子内に切断点を有するＸ染色体-常染色体均衡型転座によるデュシェンヌ型筋ジストロフィー女児2019
- Author(s)
  李知子, 底田辰之, 三﨑真生子, 下村英毅, 奥野美佐子, 竹島泰弘
- Organizer
  第60回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-17K10087
[Presentation] ジストロフィン遺伝子内に切断点を有するX染色体―常染色体均衡型転座によるデュシェンヌ型筋ジストロフィー女児2019
- Author(s)
  李　知子、底田　辰之、三崎真生子、下村英毅、奥野美佐子、竹島泰弘
- Organizer
  第64回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-18K15734
[Presentation] 高CK血症を契機に受診した男児例の検討2019
- Author(s)
  李　知子、谷口直子、徳永沙知、下村英毅、奥野美佐子、竹島泰弘
- Organizer
  筋ジストロフィー研究小牧班班会議
- Data Source
  KAKENHI-PROJECT-18K15734
[Presentation] 家族歴のない高CK血症女児の臨床背景の検討2019
- Author(s)
  李知子、徳永沙知、牟禮慎子、三﨑真生子、下村英毅、西野一三、伊東恭子、竹島泰弘
- Organizer
  第６１回日本小児神経学会
- Data Source
  KAKENHI-PROJECT-18K15734
[Presentation] 新規変異を同定した重症型LMNA-related congenital muscular dystrophyの一例2018
- Author(s)
  李　知子、下村英毅、牟禮慎子、三崎真生子、香田　翼、柴田暁男、
- Organizer
  第60回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-17K10087
[Presentation] 家族歴のない無症候性高CK血症女児の検討2018
- Author(s)
  李知子、三崎真生子、下村英毅、伊東恭子、竹島泰弘
- Organizer
  第121回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-17K10087
[Presentation] 次世代シークエンサーを用いた遺伝子解析によりCalpain-3遺伝子変異を同定した筋症状のない高CK血症女児2018
- Author(s)
  李知子、西岡　隆文、三崎真生子、下村英毅、竹島泰弘
- Organizer
  日本人類遺伝学会第63回大会
- Data Source
  KAKENHI-PROJECT-17K10087
[Presentation] 新規変異を同定した重症型LMNA-related congenital muscular dystrophyの一例2018
- Author(s)
  李知子、下村英毅、牟禮慎子、三崎真生子、香田翼、柴田暁男、川本久美、岡田陽子、小泉真琴、伊東恭子、竹島泰弘
- Organizer
  日本小児神経学会
- Data Source
  KAKENHI-PROJECT-16H05814
[Presentation] 新規変異を同定した重症型LMNA-related congenital muscular dystrophyの一例2018
- Author(s)
  李　知子、下村英毅、牟禮慎子、三崎真生子、香田　翼、柴田暁男、川本久美、岡田陽子、小泉真琴、伊東恭子、竹島泰弘
- Organizer
  日本小児神経学会
- Data Source
  KAKENHI-PROJECT-17K10087
[Presentation] 筋疾患の家族歴のない無症候性高CK血症女児の検討2018
- Author(s)
  李知子, 三崎真生子, 下村英毅, 伊東恭子, 竹島泰弘
- Organizer
  日本小児科学会
- Data Source
  KAKENHI-PROJECT-16H05814
[Presentation] Duchenne型筋ジストロフィーに対するENAアンチセンスオリゴヌクレオチド(AO85)投与の効果2017
- Author(s)
  李知子, 下村英毅, 粟野宏之, 飯島一誠, 荻寛志, 伊東恭子, 松尾雅文, 竹島泰弘
- Organizer
  日本小児神経学会
- Data Source
  KAKENHI-PROJECT-16H05814
[Presentation] 片側アレルに近接した2つの遺伝子異常を認めたUllrich型先天性筋ジストロフィーの1例2017
- Author(s)
  下村英毅, 李知子, 松本真明, 粟野宏之, 伊東恭子, 西一三, 竹島泰弘
- Organizer
  日本小児神経学会
- Data Source
  KAKENHI-PROJECT-16H05814
[Presentation] RNA/ENA chimera antisense oligonucleotide (AO85) was safely administered and shown to induce dystrophin exon 45 skipping in Duchenne muscular dystrophy patient: the first clinical study2016
- Author(s)
  Yasuhiro Takeshima, Tomoko Lee, Hideki Shimomura, Yasuhiko Tanaka, Hiroyuki Awano, Atsushi Nishida, Isao Ojima, Satoshi Minami, Akio Nakagawa, Kazumoto Iijima, Masafumi Matsuo
- Organizer
  The 13th International Congress of Human Genetics
- Place of Presentation
  Kyoto International Conference Center（京都府京都市）
- Year and Date
  2016-04-04
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461545
[Presentation] A new antisense oligonucleotide composed of RNA/ENA chimera (AO85) against dystrophin exon 45 significantly increased six-minute walk distance in Duchenne muscular dystrophy2016
- Author(s)
  Yasuhiro Takeshima, Tomoko Lee, Hideki shimomura, Yasuhiko Tanaka, Hiroyuki Awano, Atsushi Nishida, Isao Ojima, Satoshi Minami, Akio Nakagawa, Kazumoto Iijima, Masafumi Matsuo
- Organizer
  5th　International Congress of Myology
- Place of Presentation
  Lyon, France
- Year and Date
  2016-03-14
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461545

1. Yasuhiro Takeshima (40281141)

# of Collaborated Projects: 8 results

# of Collaborated Products: 26 results
2. 下村英毅 (30441273)

# of Collaborated Projects: 7 results

# of Collaborated Products: 23 results
3. TANAKA Yasuhiko (20595045)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. 三崎真生子 (50595048)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
5. 奥野美佐子 (60646553)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 山本哲志

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Lee Tomoko 李 知子

LEE TOMOKO 李 知子

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アンチセンス核酸による筋ジストロフィーナンセンス変異リードスルー治療効率化の検証Principal Investigator

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循環血中セルフリーRNAをバイオマーカーとした筋ジストロフィー治療評価系の検証

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エクソンスキッピング誘導治療の有効性を予測する残存イントロン解析システムの検証Principal Investigator

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Validation of a treatment evaluation system for muscular dystrophy using urinary splicing products as biomarkers

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Splicing dynamics of vasoactive factors in muscular dystrophy and therapeutic application in muscular dystrophy

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Enhancement of exon skipping therapy by controlling intronic sequencesPrincipal Investigator

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Non-invasive system for predicting effectiveness of the exon skipping therapy for muscular dystrophy

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東アジアにおける筋ジストロフィーオーダーメイド治療開発のための分子疫学的調査

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Improvement of the nonsense read-through therapy for muscular dystrophy by controlling nonsense mediated mRNA decayPrincipal Investigator

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Investigation of inflammatory factors affecting the efficacy of the molecular therapies for muscular dystrophy

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[Book] MDフロンティア2021

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[Journal Article] Longitudinal data of serum creatine kinase levels and motor, pulmonary, and cardiac functions in 337 patients with Duchenne muscular dystrophy2024

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[Journal Article] Underlying diseases in sporadic presentation of high creatine kinase levels in girls2021

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Lee Tomoko 李知子

LEE TOMOKO 李知子