Mariko Taniguchi-Ikeda 池田真理子 (谷口真理子)

… Alternative Names

Taniguchi-Ikeda Mariko 池田真理子

谷口真理子

谷口

TANIGUCHI-IKEDA Mariko 池田真理子(谷口真理子)

IKEDA Mariko 池田真理子

TANIGUCHI Mariko 谷口真理子

池田真理子(谷口真理子) イケダマリコ

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Researcher Number	00410738
Other IDs	https://orcid.org/0000-0002-1607-400X
Affiliation (Current)	2025: 高知大学, 教育研究部医療学系臨床医学部門, 教授 2025: 藤田医科大学, 大学病院, 准教授
Affiliation (based on the past Project Information) *help	2018 – 2024: 藤田医科大学, 大学病院, 准教授 2016 – 2017: 神戸大学, 医学研究科, 特命准教授 2015: 神戸大学, 医学(系)研究科(研究院), 准教授 2012 – 2014: 神戸大学, 医学(系)研究科(研究院), 講師 2013: 神戸大学, 大学院・医学研究科, 特命講師 … More 2011: 神戸大学, 医学研究科, 特命助教 2011: 神戸大学, 大学院・医学研究科, 特命助教 2008 – 2010: Osaka University, 医学系研究科, 特任助教(常勤) 2009: Osaka University, 医学研究科, 特任助教(常勤) Less
Review Section/Research Field	Principal Investigator Pediatrics / Medium-sized Section 52:General internal medicine and related fields / Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics / Embryonic/Neonatal medicine / Neurology
Keywords	Principal Investigator 福山型筋ジストロフィー / スプライシング異常 / RNA創薬 / 筋ジストロフィー / 先天性筋ジストロフィー / アンチセンス核酸 / 分子標的治療 / ドラッグデリバリーシステム / アンチセンス治療 / 糖鎖異常 … More / 低分子化合物 / バイオマーカー / ゲノム創薬 / キメラRNA分子 / 遺伝子治療 / RNA治療 / ホメオスタシス / Oマンノース型糖鎖 / 糖鎖修飾 / アルファジストログリカン / 糖鎖合成 / 糖鎖分解 / Oーマンノース型糖鎖 / 当鎖ホメオスタシス / スプライシングスイッチ療法 / dCas9 / ゲノム編集 / RNA / スプライシングスイッチ / 中枢奇形 / 中枢奇形を伴う筋ジストロフィー / バイオマーカー検索 / 疾患モデル / 創薬開発 / フクチン / ドラッグデリバリー / 中枢性疾患モデル / 核酸医薬 / 中枢異常 / 核酸治療 / 遺伝子 / 先天生筋ジストロフィー … More Except Principal Investigator レトロトランスポゾン / 福山型筋ジストロフィー / ゲノム編集 / アンチセンス療法 / SVA型レトロトランスポゾン / 尿中細胞 / ロングリードシークエンサー / SVA / フクチンマウス / シクロオキシゲナーゼ阻害薬 / 尿中プロスタグランジン代謝産物 / アラキドン酸カスケード / ステロイド / H-PGDS阻害薬 / アスピリン / ドラッグリポジショニング / プロスタノイド / 福山型先天性筋ジストロフィー / 臍帯 / 胎盤 / 周産期・新生児感染症 / 小児感染症 / 新生児感染症 / メタゲノミック診断法 / 次世代シークエンサー / ポストリン酸構造 / フクチン / アンチセンス治療 / ジストログリカノパチー Less

深部イントロン変異をもつ福山型筋ジストロフィー（FCMD）に対する新規治療法の開発Principal Investigator
- Principal Investigator
  
  池田真理子 (谷口真理子)
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 52:General internal medicine and related fields
- Research Institution
  Fujita Health University
Establishing Diagnostic Methods and Elucidating the Pathogenesis of Fukuyama Congenital Muscular Dystrophy Using Long-Read Sequencers
- Principal Investigator
  
  Nagasaka Miwako
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Aijinkai Healthcare Corporation Takatsuki General Hospital Clinical Research Center
Splicing switch therapy for FCMD by utilizing genome editor systemPrincipal Investigator
- Principal Investigator
  
  IKEDA-TANIGUCHI MARIKO
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Challenging Research (Exploratory)
- Review Section
  
  Medium-sized Section 52:General internal medicine and related fields
- Research Institution
  Fujita Health University
Homeostasis of alpha dystroglycan glycosylation in Fukuyama congenital muscular dystrophyPrincipal Investigator
- Principal Investigator
  
  池田真理子 (谷口真理子 / 谷口)
- Project Period (FY)
  2021 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Fujita Health University
Central Nervous System Involvement of Fukuyama type muscular dystrophyPrincipal Investigator
- Principal Investigator
  
  Ikeda Mariko
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Fujita Health University
Basic research aimed at developing a prostanoid synthetase inhibitor for patients with Fukuyama congenital muscular dystrophy
- Principal Investigator
  
  Ishigaki Keiko
- Project Period (FY)
  2016 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Tokyo Women's Medical University
Research on Fukuyama musucular dystrophy towards clincal trial using antisense oligonucleotidsPrincipal Investigator
- Principal Investigator
  
  Taniguchi-Ikeda Mariko
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
Pathogenic microorganism identification in neonatal infectious diseases by a meta-genomic analysis using the next generation sequencer
- Principal Investigator
  
  MORIOKA Ichiro
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Kobe University
Antisense oligonucleotide therapy for Fukuyama type congenital muscular dystrophyPrincipal Investigator
- Principal Investigator
  
  TANIGUCHI-IKEDA Mariko
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
Molecular targeting therapy and pathomechanism for Fukuyama muscular dystrophy and related disorders
- Principal Investigator
  
  TATSUSHI Toda
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Neurology
- Research Institution
  Kobe University
Establishment of radical therapy for Fukuyama Muscular DystrophyPrincipal Investigator
- Principal Investigator
  
  TANIGUCHI Mariko
- Project Period (FY)
  2010 – 2011
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
  Osaka University
New pathomechanism and the application of the treatment for Fukuyama-type congenital muscular dystrophyPrincipal Investigator
- Principal Investigator
  
  TANIGUCHI Mariko
- Project Period (FY)
  2008 – 2009
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Osaka University

[Book] 【遺伝学的検査の進歩とその応用】次世代シークエンサーの原理と出生前/出生後の臨床応用(解説)2023
- Author(s)
  長坂美和子　池田真理子
- Publisher
  日本新生児成育医学会雑誌
- Data Source
  KAKENHI-PROJECT-21K19457
[Book] 【小児科医が知っておくべき筋疾患診療:遺伝学的理解と治療の最新事情】代表的筋疾患　その他の先天性筋ジストロフィー(解説)2023
- Author(s)
  長坂美和子　池田真理子
- Publisher
  東京医学社
- Data Source
  KAKENHI-PROJECT-21K19457
[Book] Comprehensive Glycoscience (Second Edition)2021
- Author(s)
  Miwako Nagasaka, Mariko Ikeda-Taniguchi
- Total Pages
  2964
- Publisher
  ELSEVIER
- ISBN
  9780128194751
- Data Source
  KAKENHI-PROJECT-21K07789
[Book] 筋ジストロフィーと遺伝カウンセリング2020
- Author(s)
  池田　真理子
- Publisher
  遺伝子医学 MOOK別冊メディカル・ドゥ
- Data Source
  KAKENHI-PROJECT-18K07790
[Book] 福山型筋ジストロフィー治療の最前線2020
- Author(s)
  池田　真理子
- Publisher
  診断と治療社小児科診療
- Data Source
  KAKENHI-PROJECT-18K07790
[Book] 遺伝子医学 MOOK別冊2019
- Author(s)
  長坂美和子　池田真理子
- Total Pages
  6
- Publisher
  筋ジストロフィーと遺伝カウンセリング
- Data Source
  KAKENHI-PROJECT-18K07790
[Book] 小児疾患診療のための病態生理３　福山型筋ジストロフィー2016
- Author(s)
  池田真理子
- Publisher
  東京医学者
- Data Source
  KAKENHI-PROJECT-15K09621
[Book] 実験医学「SVA型レトロトランスポゾンによる病的エクソントラッピングと福山型筋ジストロフィーのアンチセンス療法」2012
- Author(s)
  池田(谷口)真理子・小林千浩・戸田達史
- Publisher
  羊土社(印刷中)(掲載確定)
- Data Source
  KAKENHI-PROJECT-22790980
[Book] THE LUNG perspective「福山型筋ジストロフィーのスプライシング異常に対するアンチセンス治療」2012
- Author(s)
  池田(谷口)真理子・小林千浩・戸田達史
- Publisher
  メディカルレビュー社(印刷中)(掲載確定)
- Data Source
  KAKENHI-PROJECT-22790980
[Book] 福山型筋ジストロフィーの病的スプライシング異常とアンチセンス療法2012
- Author(s)
  谷口真理子、小林千浩、戸田達史
- Publisher
  実験医学
- Data Source
  KAKENHI-PROJECT-22790980
[Book] 福山型筋ジストロフィーのスプライシング異常に対するアンチセンス治療2012
- Author(s)
  谷口真理子、小林千浩、戸田達史
- Publisher
  THE LUNG perspectives
- Data Source
  KAKENHI-PROJECT-22790980
[Book] 症候群ハンドブック「福山型筋ジストロフィー」2011
- Author(s)
  谷口真理子・戸田達史
- Total Pages
  757
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-22790980
[Book] 症候群ハンドブック福山型筋ジストロフィー2011
- Author(s)
  谷口真理子, 戸田達史
- Publisher
  中山書店(印刷中)
- Data Source
  KAKENHI-PROJECT-22790980
[Book] 福山型筋ジストロフィー症候群ハンドブック2011
- Author(s)
  谷口真理子, 戸田達史
- Total Pages
  68
- Publisher
  辻省次
- Data Source
  KAKENHI-PROJECT-22790980
[Journal Article] Molecular aggregation strategy for inhibiting DNase.2024
- Author(s)
  ③K. Morita, T. Moriwaki, S. Habe, M. Taniguchi-Ikeda, T. Hasegawa, Y. Minato, T. Aoi, T. Maruyama,
- Journal Title
  
  JACS Au
  
  Volume: -
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K21430
[Journal Article] Antisense oligonucleotide induced pseudoexon skipping and restoration of functional protein for Fukuyama muscular dystrophy caused by a deep-intronic variant2022
- Author(s)
  Enkhjargal Sarantuya、Sugahara Kana、Khaledian Behnoush、Nagasaka Miwako、Inagaki Hidehito、Kurahashi Hiroki、Koshimizu Hisatsugu、Toda Tatsushi、Taniguchi-Ikeda Mariko
- Journal Title
  
  Human Molecular Genetics
  
  Volume: 32 Issue: 8 Pages: 1301-1312
- DOI
  10.1093/hmg/ddac286
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K21430, KAKENHI-PROJECT-23K08855
[Journal Article] Assessment of the upper limb muscles in patients with Fukuyama muscular dystrophy: Noninvasive assessment using visual ultrasound muscle analysis and shear wave elastography.2022
- Author(s)
  Risa Harada, Mariko Taniguchi-Ikeda, Miwako Nagasaka, Tatsiuya Nishii, Atsuyuki Inui, Tetsushi Yamamoto, Ichiro Morioka, Ryosuke Kuroda, Kazumoto Iijima, Kandai Nozu, Yoshitada Sakai, Tatsushi Toda,
- Journal Title
  
  Neuromuscular Disorders
  
  Volume: Inpress Issue: 9 Pages: 754-762
- DOI
  10.1016/j.nmd.2022.05.004
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K20673, KAKENHI-PROJECT-21K07789, KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-23K21430
[Journal Article] Restoration of the defect in radial glial fiber migration and cortical plate organization in a brain organoid model of Fukuyama muscular dystrophy2021
- Author(s)
  Taniguchi-Ikeda Mariko、Koyanagi-Aoi Michiyo、Maruyama Tatsuo、Takaori Toru、Hosoya Akiko、Tezuka Hiroyuki、Nagase Shotaro、Ishihara Takuma、Kadoshima Taisuke、Muguruma Keiko、Ishigaki Keiko、Sakurai Hidetoshi、Mizoguchi Akira、Novitch Bennett G.、Toda Tatsushi、Watanabe Momoko、Aoi Takashi
- Journal Title
  
  iScience
  
  Volume: 24 Issue: 10 Pages: 103140-103140
- DOI
  10.1016/j.isci.2021.103140
- NAID
  120007170807
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K07614, KAKENHI-PROJECT-21H03812, KAKENHI-PROJECT-21K19457, KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-23K21430
[Journal Article] Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy2021
- Author(s)
  1.Bonora E, Chakrabarty S, Tsutsumi M (他63名) Taniguchi-Ikeda M (Corresponding author) and Roberto De Giorgio.
- Journal Title
  
  Brain
  
  Volume: 0 Issue: 5 Pages: 0-0
- DOI
  10.1093/brain/awab056
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07790, KAKENHI-PROJECT-21K06283, KAKENHI-PROJECT-19H03362, KAKENHI-PROJECT-21K07807, KAKENHI-PROJECT-21K19457, KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-23K21430
[Journal Article] Acute rhabdomyolysis following viral infection with coxsackie A4 in a 50-day-old infant with Fukuyama congenital muscular dystrophy2020
- Author(s)
  Yamaguchi H, Taniguchi-Ikeda M, Nagase H, Ito Y, Tokumoto S, Toyoshima D, Enkhjargal S, Nishiyama M, Awano H, Kurosawa H, Kasai M, Maruyama A, Iijima K
- Journal Title
  
  J Infect Chemother
  
  Volume: 26 Issue: 5 Pages: 516-519
- DOI
  10.1016/j.jiac.2019.12.015
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K15711, KAKENHI-PROJECT-18K07790
[Journal Article] α-Dystroglycanopathy. Comprehensive Glycoscience.2020
- Author(s)
  Nagasaka Miwako、Taniguchi-Ikeda Mariko
- Journal Title
  
  Elsevier.
  
  Volume: 2
- Data Source
  KAKENHI-PROJECT-18K07790
[Journal Article] A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia.2020
- Author(s)
  Rie Kawamura,Takema Kato,Shunsuke Miyai,Fumihiko Suzuki,Yuki Naru,Maki Kato,Keiko Tanaka,Miwako Nagasaka,Makiko Tsutsumi,Hidehito Inagaki,Tomoaki Ioroi,Makiko Yoshida,Tomoya Nao,Laura K Conlin,Kazumoto Iijima,Hiroki Kurahashi,Mariko Taniguchi-Ikeda
- Journal Title
  
  Journal of human genetics
  
  Volume: －
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07790
[Journal Article] Congenital hearing impairment associated with peripheral cochlear nerve dysmyelination in glycosylation-deficient muscular dystrophy2020
- Author(s)
  Morioka Shigefumi、Sakaguchi Hirofumi、Mohri Hiroaki、Taniguchi-Ikeda Mariko、Kanagawa Motoi、Suzuki Toshiaki、Miyagoe-Suzuki Yuko、Toda Tatsushi、Saito Naoaki、Ueyama Takehiko
- Journal Title
  
  PLOS Genetics
  
  Volume: 16 Issue: 5 Pages: 1-28
- DOI
  10.1371/journal.pgen.1008826
- NAID
  120006863578
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K22472, KAKENHI-PROJECT-20H00526, KAKENHI-PROJECT-18H02616, KAKENHI-PROJECT-18K07790, KAKENHI-PROJECT-18K09383, KAKENHI-PLANNED-17H06421, KAKENHI-PROJECT-19K07519
[Journal Article] Muscular Dystrophy2020
- Author(s)
  Nagasaka Miwako、Taniguchi-Ikeda Mariko
- Journal Title
  
  Spring Nature
  
  Volume: 0 Pages: 103-119
- DOI
  10.1007/978-981-15-8171-7_8
- ISBN
  9789811581700, 9789811581717
- Data Source
  KAKENHI-PROJECT-18K07790
[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] Cryptic exon activation in SLC12A3 in Gitelman syndrome.2017
- Author(s)
  Nozu K, Nozu Y, Nakanishi K, Konomoto T, Horinouchi T, Shono A, Morisada N, Minamikawa S, Yamamura T, Fujimura J, Nakanishi K, Ninchoji T, Kaito H, Morioka I, Taniguchi-Ikeda M, Vorechovsky I, Iijima K
- Journal Title
  
  J Hum Genet.
  
  Volume: 62 Issue: 2 Pages: 335-337
- DOI
  10.1038/jhg.2016.129
- NAID
  40021065185
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-16K10066
[Journal Article] Two patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia2017
- Author(s)
  Taniguchi-Ikeda M.、Morisada N.、Inagaki H.、Ouchi Y.、Takami Y.、Tachikawa M.、Satake W.、Kobayashi K.、Tsuneishi S.、Takada S.、Yamaguchi H.、Nagase H.、Nozu K.、Okamoto N.、Nishio H.、Toda T.、Morioka I.、Wada H.、Kurahashi H.、Iijima K.
- Journal Title
  
  Clinical Genetics
  
  Volume: 93 Issue: 4 Pages: 931-933
- DOI
  10.1111/cge.13106
- Data Source
  KAKENHI-PROJECT-15K09621
[Journal Article] Deep-intronic variant of fukutin is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in Japan2017
- Author(s)
  Kobayashi Kazuhiro、Kato Reiko、Kondo-Iida Eri、Taniguchi-Ikeda Mariko、Osawa Makiko、Saito Kayoko、Toda Tatsushi
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 62 Issue: 11 Pages: 945-948
- DOI
  10.1038/jhg.2017.71
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-16H05353, KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-17H01563
[Journal Article] Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.2017
- Author(s)
  Taniguchi-Ikeda M, Nagasaka M, Inagaki H, Ouchi Y, Kurokawa D, Yamana K, Harada R, Nozu K, Sakai Y, Mishra SK, Yamaguchi Y, Morikoka I, Toda T, Kurahashi H, Iijima K.
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 未定 Issue: 9 Pages: 851-855
- DOI
  10.1038/jhg.2017.48
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-15K08287, KAKENHI-PROJECT-16H04758
[Journal Article] Novel missense mutation in DLL4 in a Japanese sporadic case of Adams-Oliver syndrome.2017
- Author(s)
  Nagasaka M, Taniguchi-Ikeda M, Inagaki H, Ouchi Y, Kuroda D, Yamana K, Harada R, Nozu K, Sakai Y, Morikoka I, Toda T, Kurahashi H, Iijima K
- Journal Title
  
  J Hum Genet.
  
  Volume: 印刷中
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461632
[Journal Article] Changes in the numbers of patients with acute gastroenteritis after voluntary introduction of the rotavirus vaccine in a Japanese children’s primary emergency medical center.2017
- Author(s)
  Morioka I, Kamiyoshi N, Nishiyama M, Yamamura T, Minamikawa S, Iwatani S, Nagase H, Nozu K, Nishimura N, Taniguchi-Ikeda M, Ishibashi K, Ishida A, Iijima K
- Journal Title
  
  Environ Health Prev Med.
  
  Volume: 22 Issue: 1 Pages: 15-15
- DOI
  10.1186/s12199-017-0638-3
- NAID
  120006377650
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26461632
[Journal Article] The Generation of Human γδT Cell-Derived Induced Pluripotent Stem Cells from Whole Peripheral Blood Mononuclear Cell Culture2017
- Author(s)
  Watanabe Daisuke、Koyanagi-Aoi Michiyo、Taniguchi-Ikeda Mariko、Yoshida Yukiko、Azuma Takeshi、Aoi Takashi
- Journal Title
  
  STEM CELLS Translational Medicine
  
  Volume: 7 Issue: 1 Pages: 34-44
- DOI
  10.1002/sctm.17-0021
- NAID
  120006382346
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26293117, KAKENHI-PROJECT-15K09621
[Journal Article] Comprehensive analysis of serum cytokines/chemokines in febrile children with primary human herpes virus-6B infection.2016
- Author(s)
  Nagasaka M, Morioka I, Kawabata A, Yamagishi Y, Iwatani S, Taniguchi-Ikeda M, Ishida A, Iijima K, Mori Y
- Journal Title
  
  J Infect Chemother.
  
  Volume: 22 Issue: 9 Pages: 593-598
- DOI
  10.1016/j.jiac.2016.05.010
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-15K19613
[Journal Article] A pediatric patient with interstitial pneumonia due to enterovirus D68.2016
- Author(s)
  Matsumoto M, Awano H, Ogi M, Tomioka K, Unzaki A, Nishiyama M, Toyoshima D, Taniguchi-Ikeda M, Ishida A, Nagase H, Morioka I, Iijima K
- Journal Title
  
  J Infect Chemother.
  
  Volume: 22 Issue: 10 Pages: 712-715
- DOI
  10.1016/j.jiac.2016.03.009
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26461632
[Journal Article] Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencing.2016
- Author(s)
  Yamamura T, Morisada N, Nozu K, Minamikawa S, Ishimori S, Toyoshima D, Ninchoji T, Yasui M, Taniguchi-Ikeda M, Morioka I, Nakanishi K, Nishio H, Iijima K.
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: 20 Issue: 1 Pages: 136-142
- DOI
  10.1007/s10157-016-1256-x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-15K09261
[Journal Article] Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother.2016
- Author(s)
  Taniguchi-Ikeda M, Takeshima Y, Lee T, Nishiyama M, Awano H, Yagi M, Unzaki A, Nozu K, Nishio H, Matsuo M, Kurahashi H, Toda T, Morioka I, Iijima K.
- Journal Title
  
  J Hum Genet.
  
  Volume: 61 Issue: 4 Pages: 351-355
- DOI
  10.1038/jhg.2015.157
- NAID
  40020802923
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-26461632
[Journal Article] Mechanistic aspects of the formation of α-dystroglycan and therapeutic research for the treatment of α-dystroglycanopathy: A review.2016
- Author(s)
  Taniguchi-Ikeda M, Morioka I, Iijima K, Toda T.
- Journal Title
  
  Mol Aspects Med.
  
  Volume: 51 Pages: 115-124
- DOI
  10.1016/j.mam.2016.07.003
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-26253057
[Journal Article] Thr72Ala polymorphism in the NKG2D gene is associated with congenital cytomegalovirus disease2015
- Author(s)
  Taniguchi R, Koyano S, Suzutani T, Goishi K, Ito Y, Morioka I, Nakamura H, Yamada Y, Oka A, Inoue N
- Journal Title
  
  Infection
  
  Volume: In press
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461632
[Journal Article] A novel PIGN mutation and prenatal diagnosis of inherited glycosylphosphatidylinositol deficiency.2015
- Author(s)
  Nakagawa T, Taniguchi-Ikeda M, Murakami Y, Nakamura S, Motooka D, Emoto T, Satake W, Nishiyama M, Toyoshima D, Morisada N, Takada S, Tairaku S, Okamoto N, Morioka I, Kurahashi H, Toda T, Kinoshita T, Iijima K.
- Journal Title
  
  American Journal of Medical Genetics PartA
  
  Volume: 170 Issue: 1 Pages: 183-188
- DOI
  10.1002/ajmg.a.37397
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-25713015
[Journal Article] Genetic mutations in adipose triglyceride lipase and myocardial up-regulation of peroxisome proliferated activated receptor-γ in patients with triglyceride deposit cardiomyovasculopathy.2014
- Author(s)
  Hirano K, Tanaka T, Ikeda Y, Yamaguchi S, Zaima N, Kobayashi K, Suzuki A, Sakata Y, Sakata Y, Kobayashi K, Toda T, Fukushima N, Ishibashi-Ueda H, Tavian D, Nagasaka H, Hui SP, Chiba H, Sawa Y, Hori M.
- Journal Title
  
  Biochem Biophys Res Commun.
  
  Volume: 443 Issue: 2 Pages: 574-579
- DOI
  10.1016/j.bbrc.2013.12.003
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23617010
[Journal Article] 福山型筋ジストロフィー　遺伝子・病態の解明、分子標的治療を目指して2013
- Author(s)
  戸田達史, 谷口真理子(池田), 金川基, 小林千浩
- Journal Title
  
  生化学
  
  Volume: 85 Pages: 253-260
- NAID
  10031169565
- Data Source
  KAKENHI-PROJECT-23249049
[Journal Article] 福山型筋ジストロフィーの新たな病態と分子標的治療2013
- Author(s)
  戸田達史, 池田真理子, 小林千浩
- Journal Title
  
  小児科診療
  
  Volume: 76 Pages: 671-671
- Data Source
  KAKENHI-PROJECT-23249049
[Journal Article] 【遺伝性筋疾患の新たな治療戦略】福山型筋ジストロフィーの新たな病態とアンチセンス療法2012
- Author(s)
  戸田達史, 谷口真理子(池田), 小林千浩
- Journal Title
  
  神経内科
  
  Volume: 76 Pages: 361-366
- Data Source
  KAKENHI-PROJECT-23249049
[Journal Article] 福山型先天性筋ジストロフィーの発症機序と治療戦略2012
- Author(s)
  池田真理子,戸田達史
- Journal Title
  
  細胞
  
  Volume: 44 Pages: 22-26
- Data Source
  KAKENHI-PROJECT-24591510
[Journal Article] Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytes.2012
- Author(s)
  Tsutsumi M, Kowa-Sugiyama H, Bolor H, Kogo H, Inagaki H, Ohye T, Yamada K, Taniguchi-Ikeda M, Toda T, Kurahashi H.
- Journal Title
  
  J Hum Genet
  
  Volume: 57 Issue: 8 Pages: 515-522
- DOI
  10.1038/jhg.2012.61
- NAID
  10031056588
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-22129006, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23659182, KAKENHI-PROJECT-24390085, KAKENHI-PROJECT-24590263
[Journal Article] MEDICAL TOPICS(第42回)　福山型筋ジストロフィーのスプライシング異常に対するアンチセンス治療2012
- Author(s)
  谷口真理子(池田), 小林千浩, 戸田達史
- Journal Title
  
  THE LUNG-perspectives
  
  Volume: 20 Pages: 186-191
- Data Source
  KAKENHI-PROJECT-23249049
[Journal Article] 【RNAバイオロジーの最先端】福山型先天性筋ジストロフィーの発症機序と治療戦略2012
- Author(s)
  谷口真理子(池田), 戸田達史
- Journal Title
  
  細胞
  
  Volume: 44 Pages: 598-602
- Data Source
  KAKENHI-PROJECT-23249049
[Journal Article] 福山型筋ジストロフィーのスプライシング異常に対するアンチセンス治療2012
- Author(s)
  池田真理子,小林千浩,戸田達史
- Journal Title
  
  The LUNG perspective
  
  Volume: 20 Pages: 186-192
- Data Source
  KAKENHI-PROJECT-24591510
[Journal Article] [Molecular targeting therapy for Fukuyama muscular dystrophy2012
- Author(s)
  Toda T, Taniguchi-Ikeda M, Kobayashi K.
- Journal Title
  
  Rinsho Shinkeigaku
  
  Volume: 52 Pages: 1158-1158
- NAID
  130004505090
- Data Source
  KAKENHI-PROJECT-24591510
[Journal Article] Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytes.2012
- Author(s)
  Tsutsumi M, Kowa-Sugiyama H, Bolor H, Kogo H, Inagaki H, Ohye T, Yamada K, Taniguchi-Ikeda M, Toda T, Kurahashi H.
- Journal Title
  
  J Hum Genet.
  
  Volume: 57 Pages: 515-522
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591510
[Journal Article] 福山型筋ジストロフィーの病的スプライシング異常とアンチセンス療法2012
- Author(s)
  池田真理子,小林千浩,戸田達史
- Journal Title
  
  実験医学
  
  Volume: 30 Pages: 950-953
- Data Source
  KAKENHI-PROJECT-24591510
[Journal Article] 福山型筋ジストロフィーの病的スプライシング異常とアンチセンス療法2012
- Author(s)
  谷口(池田)真理子, 小林千浩, 戸田達史
- Journal Title
  
  実験医学
  
  Volume: 30 Pages: 950-953
- Data Source
  KAKENHI-PROJECT-23249049
[Journal Article] 【神経筋疾患の分子標的治療開発】福山型筋ジストロフィーの分子標的治療2012
- Author(s)
  戸田達史, 谷口真理子(池田), 小林千浩
- Journal Title
  
  BIO Clinica
  
  Volume: 27 Pages: 925-929
- Data Source
  KAKENHI-PROJECT-23249049
[Journal Article] Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy2011
- Author(s)
  Taniguchi-Ikeda M, Kobayashi K, Kanagawa M, Yu CC, Mori K, Oda T, Kuga A, Kurahashi H, Akman HO, DiMauro S, Kaji R, Yokota T, Takeda S, Toda T
- Journal Title
  
  Nature
  
  Volume: 478 Issue: 7367 Pages: 127-131
- DOI
  10.1038/nature10456
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21390101, KAKENHI-PROJECT-21390269, KAKENHI-PROJECT-21689030, KAKENHI-PLANNED-22129006, KAKENHI-PROJECT-22790980, KAKENHI-PUBLICLY-23013019, KAKENHI-PROJECT-23249049, KAKENHI-PROJECT-23659182
[Journal Article] Pathogenic exon-trapping by SVA retrotransoposon and rescue in Fukuyama2011
- Author(s)
  Taniguchi-Ikeda M., Kobayashi K., Kanagawa M., Yu CC., Mori K., Oda T., Kuga A., Kurahashi H., Akman HO., DiMauro S., Kaji R., Yokota T., Takeda S., Toda T.
- Journal Title
  
  muscular dystrophy Nature
  
  Volume: 478 Pages: 127-131
- Data Source
  KAKENHI-PROJECT-22790980
[Journal Article] Chromosomal instability mediated by non-B DNA: cruciform conformation and not DNA sequence is responsible for recurrent translocation in humans2009
- Author(s)
  Inagaki, H., Ohye, T., Kogo, T., Kato, T., Bolor, H., Taniguchi, M., Shaikh, T.H., Emanuel, B.S., Kurahashi, H.
- Journal Title
  
  Genome Res 19
  
  Pages: 191-198
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20790725
[Journal Article] Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy2009
- Author(s)
  Kanagawa, M., Nishimoto, A., Chiyonobu, T., Takeda, S., Miyagoe-Suzuki, Y., Wang, F., Fujikake, N., Taniguchi, M., Lu, Z., Tachikawa, M., Nagai, Y., Tashiro, F., Miyazaki, J., Tajima, Y., Takeda, S., Endo, T., Kobayashi, K., Campbell, K.P., Toda, T.
- Journal Title
  
  Hum. Mol. Genet 18
  
  Pages: 621-631
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20790725
[Patent] アンチセンス核酸およびその利用2023
- Inventor(s)
  池田真理子
- Industrial Property Rights Holder
  池田真理子
- Industrial Property Rights Type
  特許
- Filing Date
  2023
- Data Source
  KAKENHI-PROJECT-21K19457
[Patent] 福山型筋ジストロフィー治療用医薬組成物2012
- Inventor(s)
  戸田達史, 小林千浩, 池田真理子
- Industrial Property Rights Holder
  国立大学法人神戸大学
- Industrial Property Rights Type
  特許
- Filing Date
  2012-04-05
- Data Source
  KAKENHI-PROJECT-23249049
[Patent] 福山型筋ジストロフィー治療用医薬組成物2012
- Inventor(s)
  戸田　達史、　小林　千浩、池田　真理子
- Industrial Property Rights Holder
  戸田　達史、　小林　千浩、池田　真理子
- Industrial Property Rights Type
  特許
- Industrial Property Number
  2012-086891
- Filing Date
  2012-04-05
- Data Source
  KAKENHI-PROJECT-23249049
[Patent] 福山型筋ジストロフィー治療用医薬組成物2012
- Inventor(s)
  戸田達史、池田(谷口)真理子、小林千浩
- Industrial Property Rights Holder
  神戸大学
- Industrial Property Number
  2012-086891
- Filing Date
  2012-04-05
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] 福山型筋ジストロフィーの治療法開発研究2024
- Author(s)
  池田真理子
- Organizer
  広島臨床遺伝セミナー
- Invited
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] Finding cures for Fukuyama muscular dystrophy2023
- Author(s)
  池田真理子
- Organizer
  アジアオセアニア国際人類遺伝学会
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] Mn007 restores O-mannosyl glycosylation of alpha dystroglycan in FCMD patient’s cell and model mice2023
- Author(s)
  Mariko Taniguchi-Ikeda
- Organizer
  7th International Workshop for Glycosylation Defects in Muscular Dystrophies symposium
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] 福山型筋ジストロフィーの治療法開発研究2023
- Author(s)
  池田真理子
- Organizer
  新潟県国立病院機構セミナー
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] Finding cures for Fukuyama muscular dystrophy2023
- Author(s)
  池田真理子
- Organizer
  アジアオセアニア　人類遺伝学会
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] 福山型筋ジストロフィーの治療法開発研究2023
- Author(s)
  池田真理子
- Organizer
  小児神経学会
- Invited
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] 福山型筋ジストロフィーの中枢神経系の疾患モデル構築と低分子化合物を用いたレスキュー2022
- Author(s)
  池田　真理子
- Organizer
  CNS障害研究会
- Invited
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] 福山型筋ジストロフィーのエラストグラフィーを用いた骨格筋画像評価2022
- Author(s)
  池田真理子、原田理沙、長坂美和子、粟野宏之、酒井良忠、野津寛大、戸田達史
- Organizer
  日本筋学会
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] 新規細胞外小胞回収技術による福山型筋ジストロフィー特異的EV-microRNAの探索2022
- Author(s)
  舛田大樹、清水雄太、犬塚達俊、粟野宏之、戸田達史、池田真理子
- Organizer
  日本筋学会
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] 福山型筋ジストロフィーの根治療法の発見とiPS細胞を用いた疾患モデル化2022
- Author(s)
  池田真理子
- Organizer
  第7回日本筋学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] 福山型筋ジストロフィーの中枢神経系の疾患モデル構築と低分子化合物を用いたレスキュー2022
- Author(s)
  池田真理子
- Organizer
  CNS障害研究会
- Invited
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] 筋疾患と生殖医療の課題-単一遺伝性疾患に対する着床前診断～PGT-M の倫理審議会2022
- Author(s)
  池田真理子
- Organizer
  筋ジストロフィー研究班合同班会議
- Invited
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] 筋疾患と生殖医療の課題-単一遺伝性疾患に対する着床前診断～PGT-M の倫理審議会2022
- Author(s)
  池田　真理子
- Organizer
  筋ジストロフィー研究班合同班会議
- Invited
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] 単一遺伝性疾患に対する着床前遺伝学的検査の現状2022
- Author(s)
  池田真理子
- Organizer
  厚労省松村班班会議
- Invited
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] 神経・筋疾患の病態と新規治療開発2022
- Author(s)
  池田真理子
- Organizer
  神経病理学会
- Invited
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] Mutations in DNA ligase III cause mitochondrial neuro gastrointestinal encephalomyopathy,2021
- Author(s)
  池田　真理子
- Organizer
  ASHG 2021 American Society of Human Genetics
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] 福山型筋ジストロフィーの根治療法の発見とiPS細胞を用いた疾患モデル化2021
- Author(s)
  池田　真理子
- Organizer
  第7回日本筋学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] Mutations in LIG3 cause mitochondrial neurogastrointestinal encephalomyopathy by mtDNA depletion2021
- Author(s)
  池田真理子
- Organizer
  日本人類遺伝学会第66回大会第28回日本遺伝子診療学会大会合同開催
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] Restoration of the defect in radial glial fiber migration and cortical plate organization in a brain organoid model of Fukuyama muscular dystrophy2021
- Author(s)
  池田真理子
- Organizer
  ISSCR2021 International Society for Stem Cell Research (ISSCR)
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] 先天異常・遺伝：先天異常への基礎的アプローチ2021
- Author(s)
  池田　真理子
- Organizer
  第124回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07790
[Presentation] Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy2021
- Author(s)
  池田真理子
- Organizer
  WMS 2021 World Muscle Society
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] Mutations in DNA ligase III cause mitochondrial neuro gastrointestinal encephalomyopathy,2021
- Author(s)
  池田真理子
- Organizer
  ASHG 2021 American Society of Human Genetics
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] Mutations in LIG3 cause mitochondrial neurogastrointestinal encephalomyopathy by mtDNA depletion2021
- Author(s)
  池田真理子
- Organizer
  日本人類遺伝学会第66回大会第28回日本遺伝子診療学会大会合同開催
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] Mutations in LIG3 cause mitochondrial neurogastrointestinal encephalomyopathy by mtDNA depletion2021
- Author(s)
  池田真理子
- Organizer
  第44回日本神経科学大会
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] Mutations in LIG3 cause mitochondrial neurogastrointestinal encephalomyopathy by mtDNA depletion2021
- Author(s)
  池田真理子
- Organizer
  第44回日本神経科学大会
- Data Source
  KAKENHI-PROJECT-21K19457
[Presentation] Restoration of the defect in radial glial fiber migration and cortical plate organization in a brain organoid model of Fukuyama muscular dystrophy2021
- Author(s)
  池田　真理子
- Organizer
  ISSCR2021 International Society for Stem Cell Research (ISSCR)
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] Biallelic variants in LIG3 cause a novel mitochondrial neurogastrointestinal encephalomyopathy2021
- Author(s)
  池田真理子
- Organizer
  WMS 2021 World Muscle Society
- Data Source
  KAKENHI-PROJECT-23K21430
[Presentation] 核酸を標的とした難治性神経・筋疾患の治療法開発・アンチセンス核酸を用いた福山型筋ジストロフィーに対する治療法開発2020
- Author(s)
  池田　真理子
- Organizer
  日本筋学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07790
[Presentation] A low molecular weight chemical compound restores glycosylation of alpha dystroglycan in Fukuyama muscular dystrophy,2020
- Author(s)
  池田　真理子
- Organizer
  ICMS Research Showcase
- Data Source
  KAKENHI-PROJECT-18K07790
[Presentation] 疾患iPSC/ゲノム編集ESCを用いた大脳三次元モデル作成2020
- Author(s)
  池田　真理子
- Organizer
  第6回藤田医科大学シーズニーズ研究発表会
- Data Source
  KAKENHI-PROJECT-18K07790
[Presentation] 福山型筋ジストロフィーに対する治療開発研究2020
- Author(s)
  池田　真理子
- Organizer
  第62回日本小児神経学会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07790
[Presentation] 福山型筋ジストロフィーの中枢治療2019
- Author(s)
  池田真理子
- Organizer
  日本小児科学会
- Data Source
  KAKENHI-PROJECT-18K07790
[Presentation] ‘Evaluating motor functions and biomarkers for Fukuyama muscular dystrophy.’2019
- Author(s)
  池田真理子
- Organizer
  欧州人類遺伝学会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07790
[Presentation] Severe mitochondrial neurogastrointestinal encephalomyopathy caused by DNA ligase enzyme deficiency2019
- Author(s)
  池田真理子
- Organizer
  日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-18K07790
[Presentation] 福山型筋ジストロフィーに対する治療法開発2019
- Author(s)
  池田真理子
- Organizer
  第46回日本脳科学会
- Invited
- Data Source
  KAKENHI-PROJECT-18K07790
[Presentation] Optimizing antisense oligonucleotides for the treatment of Fukuyama muscular dystrophy2019
- Author(s)
  Mariko Taniguchi-Ikeda
- Organizer
  World Muscle Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07790
[Presentation] アンチセンス核酸を用いた福山型筋ジストロフィーの治療法の開発2017
- Author(s)
  池田真理子
- Organizer
  Thermo Next Forum
- Invited
- Data Source
  KAKENHI-PROJECT-15K09621
[Presentation] 福山型筋ジストロフィーの核酸を用いた治療2017
- Author(s)
  池田真理子
- Organizer
  第23回日本遺伝子細胞治療学会
- Invited
- Data Source
  KAKENHI-PROJECT-15K09621
[Presentation] 希少遺伝性難病の出生前診断の現状2017
- Author(s)
  池田真理子
- Organizer
  第41回日本遺伝カウンセリング学会
- Invited
- Data Source
  KAKENHI-PROJECT-15K09621
[Presentation] 核酸医薬を用いた福山型筋ジストロフィーの治療2017
- Author(s)
  池田真理子
- Organizer
  日本DDS学会第33回大会
- Invited
- Data Source
  KAKENHI-PROJECT-15K09621
[Presentation] 希少遺伝性難病の出生前診断の現状2017
- Author(s)
  池田真理子
- Organizer
  周産期シンポジウム
- Invited
- Data Source
  KAKENHI-PROJECT-15K09621
[Presentation] 間質性肺炎を発症したエンテロウイルスD68感染症の1例2016
- Author(s)
  松本真明、粟野宏之、荻美貴、冨岡和美、運崎愛、西山将広、豊嶋大作、池田真理子、石田明人、永瀬裕朗、森岡一朗、飯島一誠
- Organizer
  第30回日本小児救急医学会
- Place of Presentation
  仙台
- Year and Date
  2016-07-01
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] Advantage of next generation sequencing in molecular diagnosis in DMD -mutation screening with long preserved dried umbilical cord and detection of mosaicism-.2016
- Author(s)
  Taniguchi-Ikeda M, Unzaki A, Takeshima Y, Lee T, Awano H, Yagi M, Kurahashi H, Morioka I, Toda T, Matsuo M, Iijima K
- Organizer
  13th International Congress of Human Genetics
- Place of Presentation
  Kyoto, Japan
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] 福山型筋ジストロフィーのアンチセンス治療2016
- Author(s)
  池田真理子
- Organizer
  第58回日本小児神経学会
- Place of Presentation
  東京
- Year and Date
  2016-06-04
- Invited
- Data Source
  KAKENHI-PROJECT-15K09621
[Presentation] Evaluating motor functions and biomarkers for Fukuyama type congenital muscular dystrophy.2016
- Author(s)
  池田真理子
- Organizer
  American Society of Human Genetics
- Place of Presentation
  バンクーバー　カナダ
- Year and Date
  2016-10-21
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09621
[Presentation] 診断に難渋したtranscriptomopathyの3例2016
- Author(s)
  運﨑　愛、池田真理子、稲垣秀人、上田雅章、森貞直哉、岡本伸彦、森岡一朗、戸田達史、倉橋浩樹、飯島一誠
- Organizer
  第119回日本小児科学会
- Place of Presentation
  札幌
- Year and Date
  2016-05-13
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] 1次小児救急施設の2歳以下の感染性胃腸炎の受診児と重症児数：ウイルス流行時期での比較2016
- Author(s)
  神吉直宙、西山将広、岩谷壮太、池田真理子、石橋和人、飯島一誠、石田明人、森岡一朗
- Organizer
  第30回日本小児救急医学会
- Place of Presentation
  仙台
- Year and Date
  2016-07-01
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] A pediatric patient with interstitial pneumonia due to enterovirus D68.2016
- Author(s)
  Matsumoto M, Awano H, Ogi M, Tomioka K, Unzaki A, Nishiyama M, Toyoshima D, Taniguchi-Ikeda M, Ishida A, Nagase H, Morioka I, Iijima K
- Organizer
  12nd Congress of Asian Society for Pediatric Research
- Place of Presentation
  Bangkok, Thailand
- Year and Date
  2016-11-10
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] Advantage of next generation sequencing in molecular diagnosis in DMD - mutation screening with long preserved dried umbilical cord and detection of mosaicism-2016
- Author(s)
  Unzaki A, Taniguchi-Ikeda M, Takeshima Y, Lee T, Awano H, Yagi M, Kurahashi H, Morioka I, Toda T, Matsuo M, Iijima K
- Organizer
  the 13th International Congress of Human Genetics
- Place of Presentation
  Kyoto, Japan
- Year and Date
  2016-04-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] 1次小児救急施設の2歳以下の感染性胃腸炎の受診児と重症児数：2011～2014年の変遷2016
- Author(s)
  神吉直宙、西山将広、岩谷壮太、池田真理子、石橋和人、飯島一誠、石田明人、森岡一朗
- Organizer
  第30回日本小児救急医学会
- Place of Presentation
  仙台
- Year and Date
  2016-07-01
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] 症候性てんかんと新生児期に重篤な心機能障害を認めた兄弟例2016
- Author(s)
  長坂美和子、池田真理子、稲垣秀人、大内雄矢、西山将広、粟野宏之、永瀬裕朗、森岡一朗、戸田達史、倉橋浩樹、飯島一誠
- Organizer
  第39回日本小児遺伝学会
- Place of Presentation
  東京
- Year and Date
  2016-12-09
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] Evaluating biomarkers and natural history of Fukuyama Congenital Muscular Dystrophy2016
- Author(s)
  池田真理子
- Organizer
  International Congress of Human Genetics
- Place of Presentation
  京都
- Year and Date
  2016-04-04
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09621
[Presentation] Countermeasures against congenital toxoplasmosis and cytomegalovirus infection led by the research team under the supervision of the Ministry of Health, Labor and Welfare in Japan.2016
- Author(s)
  Fujii T, Ikeda T, Inoue N, Kanayama N, Kawana T, Kimura H, Kobayashi Y, Koyano S, Masuzaki H, Matsuyama H, Minematsu T, Morioka I, Moriuchi H, Oka A, Saito S, Samejima H, Suzutani T, Yamada H, Yoshikawa T
- Organizer
  CMV Public Health & Policy Conference
- Place of Presentation
  Austin, Texas, USA
- Year and Date
  2016-09-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] Changes in patients with acute gastroenteritis after voluntary introduction of rotavirus vaccine in a Japanese children’s primary emergency medical center.2016
- Author(s)
  Kamiyoshi N, Iwatani S, Nishiyama M, Yamamura T, Minamikawa S, Taniguchi-Ikeda M, Ishibashi K, Iijima K, Ishida A, Morioka I
- Organizer
  12nd Congress of Asian Society for Pediatric Research
- Place of Presentation
  Bangkok, Thailand
- Year and Date
  2016-11-10
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] Comprehensive analysis of serum cytokines/chemokines in febrile children with primary human herpes virus-6B infection.2016
- Author(s)
  Morioka I, Nagasaka M, Kawabata A, Yamagishi Y, Iwatani S, Taniguchi-Ikeda M, Ishida A, Iijima K, Mori Y
- Organizer
  12nd Congress of Asian Society for Pediatric Research
- Place of Presentation
  Bangkok, Thailand
- Year and Date
  2016-11-10
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] transcriptomopathyの2例2015
- Author(s)
  運崎　愛、池田真理子、上田雅章、森貞直哉、岡本伸彦、森岡一朗、戸田達史、飯島一誠
- Organizer
  第266回日本小児科学会兵庫県地方会
- Place of Presentation
  姫路
- Year and Date
  2015-09-26
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] Antisense oligonucleotide therapy for Fukuyama type congenital muscular dystrophy2015
- Author(s)
  池田真理子、戸田達史
- Organizer
  Neuroscience Network in Kobe
- Place of Presentation
  神戸大学
- Year and Date
  2015-02-06
- Invited
- Data Source
  KAKENHI-PROJECT-24591510
[Presentation] GPI欠損症に対し出生前診断を行った１家系2015
- Author(s)
  運崎愛、中川卓、池田　真理子、岡本伸彦、村上良子、森岡一朗、戸田達史、飯島一誠
- Organizer
  第38回日本小児遺伝学会
- Place of Presentation
  横浜
- Year and Date
  2015-07-25
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] 福山型先天性筋ジストロフィーにおけるバイオマーカーの検索2015
- Author(s)
  池田真理子，運崎　愛，粟野宏之，李　知子，竹島泰弘，小林千浩*，森岡一朗，飯島一誠，戸田達史*
- Organizer
  日本人類遺伝学会
- Place of Presentation
  東京　日本
- Year and Date
  2015-10-14
- Data Source
  KAKENHI-PROJECT-15K09621
[Presentation] 福山型先天性ジストロフィーのアンチセンス治療における至適薬剤の選択2015
- Author(s)
  池田真理子，佐藤洋平，岩山達志，増田博文，小林千浩*，森岡一朗，飯島一誠，戸田達史*
- Organizer
  日本小児科学会学術集会
- Place of Presentation
  大阪　日本
- Year and Date
  2015-04-17
- Data Source
  KAKENHI-PROJECT-15K09621
[Presentation] 福山型先天性筋ジストロフィーのアンチセンス治療における至適薬剤の選択2015
- Author(s)
  池田真理子、佐藤洋平、若山達志、増田博文、小林千浩、森岡一朗、飯島一誠、戸田達史
- Organizer
  日本小児科学会
- Place of Presentation
  国際会議場　大阪
- Year and Date
  2015-04-17
- Data Source
  KAKENHI-PROJECT-24591510
[Presentation] 福山型先天性筋ジストロフィーにおける血清中miRNAの発現解析2015
- Author(s)
  池田真理子,小林千浩*,李　知子,竹島泰弘,森岡一朗,飯島一誠,戸田達史*
- Organizer
  日本小児神経学会
- Place of Presentation
  大阪　日本
- Year and Date
  2015-05-28
- Data Source
  KAKENHI-PROJECT-15K09621
[Presentation] 次子の出生前診断を契機に確定診断に至った先天性GPI欠損症の孤発例2015
- Author(s)
  運崎　愛、池田真理子、中川　卓、西山将広、豊嶋大作、森貞直哉、岡本伸彦、倉橋浩樹、村上良子、森岡一朗、戸田達史、飯島一誠
- Organizer
  第60回日本人類遺伝学会
- Place of Presentation
  東京
- Year and Date
  2015-10-15
- Data Source
  KAKENHI-PROJECT-26461632
[Presentation] 福山型先天性筋ジストロフィーのアンチセンス治療における至適薬剤の選択2014
- Author(s)
  池田真理子、佐藤洋平、若山達志、増田博文、小林千浩、森岡一朗、飯島一誠、戸田達史
- Organizer
  日本人類遺伝学会
- Place of Presentation
  タワーホール舟橋　東京
- Year and Date
  2014-11-20
- Data Source
  KAKENHI-PROJECT-24591510
[Presentation] 福山型先天性筋ジストロフィーのアンチセンス治療における至適薬剤の選択2014
- Author(s)
  池田真理子、佐藤洋平、若山達志、増田博文、小林千浩、森岡一朗、飯島一誠、戸田達史
- Organizer
  小児神経学会
- Place of Presentation
  アクトシティー　浜松
- Year and Date
  2014-05-31
- Data Source
  KAKENHI-PROJECT-24591510
[Presentation] 福山型先天性筋ジストロフィーのアンチセンス治療における至適薬剤の選択2014
- Author(s)
  池田真理子、佐藤洋平、若山達志、増田博文、小林千浩、森岡一朗、飯島一誠、戸田達史
- Organizer
  日本小児遺伝学会
- Place of Presentation
  名古屋市立大学　愛知県
- Year and Date
  2014-04-10
- Data Source
  KAKENHI-PROJECT-24591510
[Presentation] Pathogenic exon-trapping by SVA retrotransposon and therapeutic rescue by antisense oligonucleotides in Fukuyama muscular dystrophy2012
- Author(s)
  池田(谷口)真理子・小林千浩・戸田達史
- Organizer
  日仏国際交流シンポジウム
- Place of Presentation
  大阪・大阪大学
- Year and Date
  2012-02-10
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] 福山型筋ジストロフィーのSVA挿入によるスプライシング異常とレスキュー2012
- Author(s)
  谷口(池田)真理子、小林千浩、金川基、游智傑、小田哲也、久我敦、倉橋浩樹、武田伸一、竹島泰弘、飯島一誠、戸田達史
- Organizer
  第110回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] RNA-based mechanism and therapy for muscular dystrophy.2012
- Author(s)
  戸田達史, 池田真理子, 小林千浩
- Organizer
  第35回日本分子生物学会年会
- Place of Presentation
  福岡国際会議場・マリンメッセ福岡
- Invited
- Data Source
  KAKENHI-PROJECT-23249049
[Presentation] SVA型レトロトランスポゾンによる病的エクソントラッピングとアンチセンス核酸を用いた福山型筋ジストロフィーの治療2012
- Author(s)
  池田真理子
- Organizer
  分子生物学学会
- Place of Presentation
  福岡
- Invited
- Data Source
  KAKENHI-PROJECT-24591510
[Presentation] 福山型筋ジストロフィーのスプライシング異常の発見とアンチセンス治療法に関する研究2012
- Author(s)
  池田真理子
- Organizer
  日本人類遺伝学会
- Place of Presentation
  東京
- Invited
- Data Source
  KAKENHI-PROJECT-24591510
[Presentation] 福山型筋ジストロフィーのSVA挿入によるスプライシング異常とレスキュー2012
- Author(s)
  池田真理子，小林千浩，金川　基，遊　智傑，小田哲也，久我　敦，倉橋浩樹,　武田伸一，戸田達史
- Organizer
  日本小児科学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-24591510
[Presentation] Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy2012
- Author(s)
  池田真理子, 竹島泰弘, 戸田達史
- Organizer
  日本小児神経学会
- Place of Presentation
  北海道
- Data Source
  KAKENHI-PROJECT-24591510
[Presentation] 福山型筋ジストロフィーのSVA挿入によるスプライシング異常とレスキュー2012
- Author(s)
  谷口(池田)真理子、竹島泰弘、戸田達史
- Organizer
  第54回日本小児神経学会学術集会
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] SVAレトロトランスポゾンによる病的エクソントラッピングと福山型筋ジストロフィーにおけるレスキュー2011
- Author(s)
  谷口(池田)真理子
- Organizer
  日本人類遺伝学会第56回大会
- Place of Presentation
  幕張メッセ(千葉)
- Year and Date
  2011-11-12
- Data Source
  KAKENHI-PROJECT-23249049
[Presentation] 福山型筋ジストロフィーにおけるSVAレトロトランスポゾン挿入による病的エクソントラッピングとアンチセンスオリゴヌクレオチドにおけるレスキュー2011
- Author(s)
  谷口(池田)真理子, 小林千浩, 金川基, 遊智傑, 小田哲也, 久我敦, 倉橋浩樹, 横田俊文, 武田伸一, 戸田達史
- Organizer
  第56回日本人類遺伝学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] 福山型筋ジストロフィーにおけるSVAレトロトランスポゾン挿入による病的exon-trappingとアンチセンスオリゴヌクレオチドによるレスキュー2011
- Author(s)
  谷口(池田)真理子, 小林千浩、金川基、Chih Chieh Yu、小田哲也、久我敦、横田俊文、倉橋浩樹、武田伸一、戸田達史
- Organizer
  日本人類遺伝学会
- Place of Presentation
  千葉幕張
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] Pathogenic exon trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy2011
- Author(s)
  Mariko Taniguchi-Ikeda ; Kazuhiro Kobayashi ; Motoi Kanagawa ; Chih-chieh Yu ; Hasan O. Akman ; Salvatore DiMauro ; Toshifumi Yokota ; Shin´ichi Takeda ; Tatsushi Toda
- Organizer
  World Muscle Society 2011 16th International congress
- Place of Presentation
  Almancil
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] 福山型筋ジストロフィーにおけるSVAレトロトランスポゾン挿入による病的exon-trappingとアンチセンスオリゴヌクレオチドによるレスキュー2011
- Author(s)
  谷口(池田)真理子、小林千浩、金川基、Chih Chieh Yu、小田哲也、久我敦、横田俊文、倉橋浩樹、武田伸一、戸田達史
- Organizer
  西野班班会議
- Place of Presentation
  JA共済ビルカンファレンスホール(東京都)
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy2011
- Author(s)
  Taniguchi-Ikeda M., Kobayashi K., Kanagawa M., Yu CC., Mori K., Oda T., Kuga A., Kurahashi H., Akman HO., DiMauro S., Kaji R., Yokota T., Takeda S., Toda T.
- Organizer
  世界筋学会
- Place of Presentation
  ポルトガルアルガルベ
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy2011
- Author(s)
  谷口(池田)真理子、小林千浩、金川基、Chih Chieh Yu、小田哲也、久我敦、横田俊文、倉橋浩樹、武田伸一、戸田達史
- Organizer
  筋ジストロフィー治療研究会
- Place of Presentation
  熊本・天草
- Year and Date
  2011-11-06
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] 福山型先天性筋ジストロフィーはスプライシング病である2010
- Author(s)
  谷口真理子、小林千浩、金川基、戸田達史
- Organizer
  筋ジストロフィー総合班会議
- Place of Presentation
  東京
- Year and Date
  2010-01-15
- Data Source
  KAKENHI-PROJECT-20790725
[Presentation] 福山型筋ジストロフィーはスプライシング異常症である2010
- Author(s)
  谷口真理子
- Organizer
  日本小児神経学会
- Place of Presentation
  福岡国際会議場(福岡県)
- Year and Date
  2010-05-21
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] 福山型筋ジストロフィーはスプライシング異常症である2010
- Author(s)
  谷口真理子
- Organizer
  日本人類遺伝学会
- Place of Presentation
  ソニックシティーホール(さいたま県)
- Year and Date
  2010-10-30
- Data Source
  KAKENHI-PROJECT-22790980
[Presentation] Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.2009
- Author(s)
  Mariko Taniguchi
- Organizer
  The 15^<th> World Muscle Society
- Place of Presentation
  ジュネーブ、スイス
- Data Source
  KAKENHI-PROJECT-20790725
[Presentation] Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycano pathy2009
- Author(s)
  Taniguchi, M., Kanagawa, M., (4), Campbell, K.P., Toda, T.
- Organizer
  The American Society of Human Genetics
- Place of Presentation
  Hawaii, USA
- Data Source
  KAKENHI-PROJECT-20790725
[Presentation] 福山型先天性筋ジストロフィーはスプライシング病である2009
- Author(s)
  谷口真理子、小林千浩、金川基、戸田達史
- Organizer
  砂田班班会議
- Place of Presentation
  東京、日本
- Data Source
  KAKENHI-PROJECT-20790725
[Presentation] Residual laminin -binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy2009
- Author(s)
  Taniguchi, M., Kanagawa, M., (3) Kobayashi, K., Campbell, K.P., Toda, T.
- Organizer
  20th Glycobiology Joint Meeting
- Place of Presentation
  Koln, Germany
- Data Source
  KAKENHI-PROJECT-20790725
[Presentation] Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.2009
- Author(s)
  Mariko Taniguchi
- Organizer
  米国人類遺伝学会
- Place of Presentation
  ハワイ、アメリカ合衆国
- Data Source
  KAKENHI-PROJECT-20790725
[Presentation] Residual laminin-binding activity and enhanceddystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy2009
- Author(s)
  Taniguchi, M., Kanagawa, M., Miyagoe-Suzuki, Y., Takeda, S., Endo, T., Kobayashi, K., Campbell, K.P., Toda, T.
- Organizer
  The 15th World Muscle Society Genova
- Place of Presentation
  Switzerand
- Data Source
  KAKENHI-PROJECT-20790725
[Presentation] A single nucleotide polymorphism in the NKG2D gene is associated with clinical outcome of congenital cytomegalovirus infection at birth
- Author(s)
  Taniguchi R, Koyano S, Suzutani T, Goishi K, Ito Y, Morioka I, Nakamura H, Yamada H, Oka A, Inoue N.
- Organizer
  39th Annual International Herpesvirus Workshop
- Place of Presentation
  Kobe, Japan
- Year and Date
  2014-07-19 – 2014-07-23
- Data Source
  KAKENHI-PROJECT-26461632
[]

1. KEIKO Ishigaki (10366304)

# of Collaborated Projects: 4 results

# of Collaborated Products: 1 results
2. KOBAYASHI Kazuhiro (90324780)

# of Collaborated Projects: 3 results

# of Collaborated Products: 16 results
3. Nagasaka Miwako (70723998)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
4. TATSUSHI Toda (30262025)

# of Collaborated Projects: 1 results

# of Collaborated Products: 11 results
5. KANAGAWA Motoi (00448044)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
6. MORIOKA Ichiro (80437467)

# of Collaborated Projects: 1 results

# of Collaborated Products: 19 results
7. MORI Yasuko (50343257)

# of Collaborated Projects: 1 results

# of Collaborated Products: 20 results
8. DEGUCHI Masashi (50403291)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. HARADA Risa (30736864)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
10. YOSHIDA Masaru (00419475)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. TAKAO Keizo (80420397)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. NEGISHI Youichi (50286978)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. 竹島泰弘 (40281141)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
14. 竹内敦子 (80154970)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. 加藤武馬 (20387690)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. 粟野宏之 (30437470)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. 斉藤史明 (40286993)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. 青井貴之 (00546997)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
19. 丸山達生 (30346811)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
20. 青井三千代 (90432327)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. 中嶋和紀 (10442998)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
22. 芳本玲 (70595652)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
23. KOYANAGI Michiyo

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
24. SAKAGUCHI Hirofumi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
25. 倉橋浩樹

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. 李知子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
27. 野津寛大

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
28. 庄野朱美

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
29. 飯島一誠

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
30. 西山将広

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
31. 位田隆一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
32. 手塚裕之

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
33. 上山健彦

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
34. 山本哲志

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Mariko Taniguchi-Ikeda 池田 真理子 (谷口 真理子)

Taniguchi-Ikeda Mariko 池田 真理子

谷口真理子

谷口

TANIGUCHI-IKEDA Mariko 池田 真理子(谷口真理子)

IKEDA Mariko 池田 真理子

TANIGUCHI Mariko 谷口 真理子

池田 真理子(谷口真理子) イケダ マリコ

Research Projects

Research Products

Co-Researchers

深部イントロン変異をもつ福山型筋ジストロフィー（FCMD）に対する新規治療法の開発Principal Investigator

Principal Investigator

Project Period (FY)

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Establishing Diagnostic Methods and Elucidating the Pathogenesis of Fukuyama Congenital Muscular Dystrophy Using Long-Read Sequencers

Principal Investigator

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Review Section

Research Institution

Splicing switch therapy for FCMD by utilizing genome editor systemPrincipal Investigator

Principal Investigator

Project Period (FY)

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Review Section

Research Institution

Homeostasis of alpha dystroglycan glycosylation in Fukuyama congenital muscular dystrophyPrincipal Investigator

Principal Investigator

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Review Section

Research Institution

Central Nervous System Involvement of Fukuyama type muscular dystrophyPrincipal Investigator

Principal Investigator

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Review Section

Research Institution

Basic research aimed at developing a prostanoid synthetase inhibitor for patients with Fukuyama congenital muscular dystrophy

Principal Investigator

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Research Institution

Research on Fukuyama musucular dystrophy towards clincal trial using antisense oligonucleotidsPrincipal Investigator

Principal Investigator

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Pathogenic microorganism identification in neonatal infectious diseases by a meta-genomic analysis using the next generation sequencer

Principal Investigator

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Research Institution

Antisense oligonucleotide therapy for Fukuyama type congenital muscular dystrophyPrincipal Investigator

Principal Investigator

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Research Institution

Molecular targeting therapy and pathomechanism for Fukuyama muscular dystrophy and related disorders

Principal Investigator

Project Period (FY)

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Research Institution

Establishment of radical therapy for Fukuyama Muscular DystrophyPrincipal Investigator

Principal Investigator

Project Period (FY)

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Research Field

Research Institution

New pathomechanism and the application of the treatment for Fukuyama-type congenital muscular dystrophyPrincipal Investigator

Principal Investigator

Project Period (FY)

Mariko Taniguchi-Ikeda 池田真理子 (谷口真理子)

Taniguchi-Ikeda Mariko 池田真理子

TANIGUCHI-IKEDA Mariko 池田真理子(谷口真理子)

IKEDA Mariko 池田真理子

TANIGUCHI Mariko 谷口真理子

池田真理子(谷口真理子) イケダマリコ

[Book] 【小児科医が知っておくべき筋疾患診療:遺伝学的理解と治療の最新事情】代表的筋疾患　その他の先天性筋ジストロフィー(解説)2023

[Book] 小児疾患診療のための病態生理３　福山型筋ジストロフィー2016

[Book] 症候群ハンドブック福山型筋ジストロフィー2011