Mizuta Ikuko 水田依久子

… Alternative Names

水田依久子ミズタイクコ

MIZUTA Ikuko 水田依久子

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Researcher Number	80397760
Other IDs
Affiliation (Current)	2025: 京都府立医科大学, 医学(系)研究科(研究院), 助教
Affiliation (based on the past Project Information) *help	2021 – 2023: 京都府立医科大学, 医学(系)研究科(研究院), 助教 2014 – 2019: 京都府立医科大学, 医学(系)研究科(研究院), 助教 2014: 京都府立医科大学, 大学院医学研究科・神経内科, 講師 2012 – 2013: 京都府立医科大学, 医学部附属病院, 研究員 2008: Osaka University, 医学部・附属病院, 医員 … More 2008: Osaka University, 医学部附属病院, 医員 2006 – 2007: Osaka University, Graduate School of Medicine, Research Fellow, 医学系研究科, 特別科学研究員 2005: 大阪大学, 医学系研究科, 助手 Less
Review Section/Research Field	Principal Investigator Neurology / Basic Section 52020:Neurology-related Except Principal Investigator Neurology
Keywords	Principal Investigator 脳小血管病 / 関連解析 / 疾患感受性遺伝子 / 一塩基多型 / パーキンソン病 / バイオバンク / NOTCH3バリアント / 大脳白質病変 / 一般集団 / NOTCH3 … More / 遺伝要因 / 白質病変 / 東北メディカル・メガバンク / association study / susceptibility gene / single nucleotide polymorphism / Parkinson's disease / 疾患モデル / 遺伝性脳小血管病 / Notch / ショウジョウバエ … More Except Principal Investigator 遺伝学 / 遺伝子 / 脳神経疾患 / 小血管病 / 遺伝性疾患 / エキソーム解析 / 脳白質疾患 / trasnendocytosis / Notch3 / 脳小血管病 / Notch / transendocytosis / NOTCH3 / 遺伝性脳小血管病 / CADASIL / 分子遺伝学 / 神経内科学 / トランスクリプトーム解析 / アストロサイト / GFAP / アレキサンダー病 Less

Cerebral white matter lesions and cerebral small vessel disease-related gene variants in the Japanese general populationPrincipal Investigator
- Principal Investigator
  
  水田依久子
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52020:Neurology-related
- Research Institution
  Kyoto Prefectural University of Medicine
Research on genetic pathomechanism of adult-onset white matter disease
- Principal Investigator
  
  Yoshida Tomokatsu
- Project Period (FY)
  2016 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Kyoto Prefectural University of Medicine
Pathomechanism of cerebral small vessel disease due to disturbance of transendocytosis
- Principal Investigator
  
  Mizuno Toshiki
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Kyoto Prefectural University of Medicine
Investigation of cerebral small vessel diseases using Notch3 transgenic DrosophilaPrincipal Investigator
- Principal Investigator
  
  Mizuta Ikuko
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Kyoto Prefectural University of Medicine
Research for drug effectiveness in Alexander disease model
- Principal Investigator
  
  YOSHIDA Tomokatsu
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Kyoto Prefectural University of Medicine
Analysis of SNPs susceptible to Parkinson's diseasePrincipal Investigator
- Principal Investigator
  
  MIZUTA Ikuko
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Osaka University
Identification of susceptibility genes for sporadic Parkinson's disease by genotyping multiple SNPsPrincipal Investigator
- Principal Investigator
  
  MIZUTA Ikuko
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Osaka University

All 2024 2020 2018 2017 2016 2015 2014 2013 2009 2008 2007 2006 Other

All Journal Article Presentation

[Journal Article] Progress to Clarify How NOTCH3 Mutations Lead to CADASIL, a Hereditary Cerebral Small Vessel Disease2024
- Author(s)
  Mizuta Ikuko、Nakao-Azuma Yumiko、Yoshida Hideki、Yamaguchi Masamitsu、Mizuno Toshiki
- Journal Title
  
  Biomolecules
  
  Volume: 14 Issue: 1 Pages: 127-127
- DOI
  10.3390/biom14010127
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07441
[Journal Article] Adult-onset leukoencephalopathy with homozygous LAMB1 missense mutation2020
- Author(s)
  Yasuda R, Yoshida T, Mizuta I, Watanabe M, Nakano M, Sato R, Tokuda Y, Omi N, Sakai N, Nakagawa M, Tashiro K, Mizuno T.
- Journal Title
  
  Neurology Genetics
  
  Volume: -
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K09698
[Journal Article] New diagnostic criteria for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukocencephalopathy in Japan.2017
- Author(s)
  Mizuta I, Hosomi-Watanabe A, Koizumi T, Mukai M, Hamano A, Tomii Y, Kondo M, Nakagawa M, Tomimoto H, Hirano T, Uchino M, Onodera O, Mizuno T
- Journal Title
  
  J Neurol Sci
  
  Volume: 381 Pages: 62-67
- DOI
  10.1016/j.jns.2017.08.009
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09731, KAKENHI-PROJECT-15H05293, KAKENHI-PROJECT-26461276
[Journal Article] CADASILの臨床像と遺伝子異常2017
- Author(s)
  渡邉明子, 水田依久子, 水野敏樹
- Journal Title
  
  神経内科
  
  Volume: 87 Pages: 630-637
- Data Source
  KAKENHI-PROJECT-26461276
[Journal Article] CADASIL Presenting as Acute Bilateral Multiple Subcortical Infarcts without a Characteristic Temporal Pole or Any External Capsule Lesions2016
- Author(s)
  Takashi Ando, Yoji Goto, Kazuo Mano, Akihiko Ueda, Yukio Ando, Ikuko Mizuta and Toshiki Mizuno
- Journal Title
  
  Intern. Med.
  
  Volume: 55 Issue: 19 Pages: 2873-2876
- DOI
  10.2169/internalmedicine.55.7123
- NAID
  130005605891
- ISSN
  0918-2918, 1349-7235
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26461276
[Journal Article] Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL.2016
- Author(s)
  Nozaki H, Kato T, Nihonmatsu M, Saito Y, Mizuta I, Noda T, Koike R, Miyazaki K, Kaito M, Ito S, Makino M, Koyama A, Shiga A, Uemura M, Sekine Y, Murakami A, Moritani S, Hara K, Yokoseki A, Kuwano R, Endo N, Momotsu T, Yoshida M, Nishizawa M, Mizuno T, Onodera O
- Journal Title
  
  Neurology
  
  Volume: 86 Issue: 21 Pages: 1-10
- DOI
  10.1212/wnl.0000000000002694
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461276, KAKENHI-PLANNED-26117006, KAKENHI-PROJECT-16H02656
[Journal Article] A Japanese CADASIL kindred with a novel two-base NOTCH3 mutation.2016
- Author(s)
  Suda, Satoshi; Okubo, Seiji; Ueda, Masayuki; Sowa, Kota; Abe, Arata; Aoki, Junya; Muraga, Kanako; Suzuki, Kentaro; Sakamoto, Yuki; Mizuta, Ikuko; Mizuno, Toshiki; Kimura, Kazumi.
- Journal Title
  
  Eur J Neurol
  
  Volume: 23 Issue: 5 Pages: 32-34
- DOI
  10.1111/ene.12977
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461276
[Journal Article] Characteristic abnormal signals in medulla oblongata-“eye spot” sign: four cases of elderly-onset Alexander disease.2015
- Author(s)
  Yoshida T, Mizuta I, Saito K, Kimura Y, Park K, Ito Y, Haji S, Nakagawa M, Mizuno T.
- Journal Title
  
  Neurology clinical practice
  
  Volume: - Issue: 3 Pages: 259-262
- DOI
  10.1212/cpj.0000000000000124
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-24591273, KAKENHI-PROJECT-24659433
[Journal Article] Effects of a polymorphism in the GFAP promoter on age of onset and ambulatory disability in late-onset Alexander disease.2013
- Author(s)
  Yoshida T, Mizuta I, Saito K, et al.
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 58 Issue: 9 Pages: 635-638
- DOI
  10.1038/jhg.2013.83
- NAID
  10031195302
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591273, KAKENHI-PROJECT-24659433
[Journal Article] Mutations for Gaucer disease confer highsusceptibility to Parkinson disease2009
- Author(s)
  Mitsui J, Mizuta I, Toyoda A, Ashida R, Takahashi Y, Goto J, Fukuda Y, Date H, Iwata A, Yamamoto M, Hattori N, Murata M, Toda T, Tsuji S.
- Journal Title
  
  Arch Neurol 66
  
  Pages: 571-576
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590990
[Journal Article] N LRRK2 P755L variant in sporadic Parkinson's disease2008
- Author(s)
  Tomiyama H, Mizuta I, Li Y, Funayama M, Yoshino H, Li L, Murata M, Yamamoto M, Kubo SI, Mizuno Y, Toda T, Hattori
- Journal Title
  
  J Hum Genet 53
  
  Pages: 1012-1015
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590990
[Journal Article] Calbindin 1, fibroblast growth factor 20, and α-synuclein in sporadic Parkinson's disease.2008
- Author(s)
  Mizuta I, Tsunoda T, Satake W, et al.
- Journal Title
  
  Human Genetics 124
  
  Pages: 89-94
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590990
[Journal Article] Calbindin 1, fibroblast growth factor 20, and α-synuclein in sporadic Parkinson's disease2008
- Author(s)
  Mizuta I, Tsunoda T, Satake W, Nakabayashi Y, Watanabe M, Takeda A, Hasegawa K, Nakashima K, Yamamoto M, Hattori N, Murata M, Toda T.
- Journal Title
  
  Hum Genet 124
  
  Pages: 89-94
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590990
[Journal Article] LRRK2 P755L variant in sporadic Parkinson's disease.2008
- Author(s)
  Tomiyama H, Mizuta I, Li Y, et al.
- Journal Title
  
  Journal of Human Genetics 53
  
  Pages: 1012-1015
- NAID
  10025584966
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19590990
[Journal Article] 孤発性パーキンソン病のメカニズム2008
- Author(s)
  水田依久子、戸田達史
- Journal Title
  
  成人病と生活習慣病(東京医学社) 38
  
  Pages: 887-892
- Data Source
  KAKENHI-PROJECT-19590990
[Journal Article] Fibroblast growth factor 20 gene and Parkinson' s disease in the Japanese population2007
- Author(s)
  Wataru Satake, Ikuko Mizuta, Satoko Suzuki et al.
- Journal Title
  
  NeuroReport (In press)
- Data Source
  KAKENHI-PROJECT-17590874
[Journal Article] PARK1, PARK4 (α-synuclein)2007
- Author(s)
  水田依久子, 戸田達史
- Journal Title
  
  Clinical Neuroscience 25巻1号
  
  Pages: 72-73
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590874
[Journal Article] Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population2007
- Author(s)
  Wataru Satake, Ikuko Mizuta, Satoko Suzuki et al.
- Journal Title
  
  NeuroReport (In press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590874
[Journal Article] Multiple candidate gene analysis identifies α-synuclein as a susceptibility gene for sporadic Parkinson's disease2006
- Author(s)
  Ikuko Mizuta, Wataru Sarake, Yuko Nakabayashi et al.
- Journal Title
  
  Human Molecular Genetics 15
  
  Pages: 1151-1158
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590874
[Journal Article] Multiple candidate gene analysis identifies α-synuclein as a susceptibility gene for sporadic Parkinson's disease2006
- Author(s)
  Ikuko Mizuta, Wataru Sarake, Yuko Nakabayashi et al.
- Journal Title
  
  Human Molecular Genetics Vol.15, No.7
  
  Pages: 1151-1158
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590874
[Journal Article] Multiple candidate gene analysis identifies α-synuclein as a susceptibility gene for sporadic Parkinson' s disease2006
- Author(s)
  Ikuko Mizuta, Wataru Sarake, Yuko Nakabayashi et al.
- Journal Title
  
  Human Molecular Genetics Vol. 15, No. 7
  
  Pages: 1151-1158
- Data Source
  KAKENHI-PROJECT-17590874
[Journal Article] 21個の候補遺伝子関連解析の結果、α-synucleinが孤発性パーキンソン病の疾患感受性遺伝子であることが確実となった2006
- Author(s)
  水田依久子, 戸田達史
- Journal Title
  
  PD Today 15巻8号
  
  Pages: 17-17
- Data Source
  KAKENHI-PROJECT-17590874
[Journal Article] Multiple candidate gene analysis identifies α-synuclein as a susceptibility gene for sporadic Parkinson's disease2006
- Author(s)
  Ikuko Mizuta et al.
- Journal Title
  
  Human Molecular Genetics (In press)
- Data Source
  KAKENHI-PROJECT-17590874
[Journal Article] 121個の候補遺伝子関連解析の結果、α-synucleinが孤発性パーキンソン病の疾患感受性遺伝子であることが確実となった2006
- Author(s)
  水田依久子, 戸田達史
- Journal Title
  
  PD Today 15巻8号
  
  Pages: 17-17
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590874
[Journal Article] Fibroblast growth factor 20 gene and Parkinson' s disease in the Japanese population
- Author(s)
  Wataru Satake, Ikuko Mizuta, Satoko Suzuki et al.
- Journal Title
  
  Neuro Report (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590874
[Presentation] 晩期発症型アレキサンダー病の発症年齢に関連する遺伝的変異の検討.2018
- Author(s)
  安田怜，吉田誠克，中野正和，佐藤隆一，足立博子，徳田雄市，水田依久子，齋藤光象，松浦　潤，中川正法，田代啓，水野敏樹．
- Organizer
  第59回日本神経学会学術大会．
- Data Source
  KAKENHI-PROJECT-16K09698
[Presentation] Endothelin1による白質脳症の機序2017
- Author(s)
  水野敏樹水田依久子、渡邊明子、向井麻央、小泉崇
- Organizer
  第36回日本認知症学会学術集会
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461276
[Presentation] NEW DIAGNOSTIC CRITERIA FOR CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOCENCEPHALOPATHY IN JAPAN2017
- Author(s)
  T. MizunoI. Mizuta 　A. Watanabe-Hosomi 　T. Koizumi 　M. Mukai 　A. Hamano Y. Tomii 　M. Kondo 　M. Nakagawa 　T. Hirano 　M. Uchino 　O. Onodera H. Tomimoto
- Organizer
  World Congress of Neurology 2107
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461276
[Presentation] キメラNOTCH3導入ショウジョウバエを用いた遺伝性脳小血管病CADASIL病態解明へのアプローチ2017
- Author(s)
  水田依久子, 東裕美子, 吉田英樹, 山口政光, 水野敏樹
- Organizer
  2017年度生命科学系学会合同年次大会
- Data Source
  KAKENHI-PROJECT-26461296
[Presentation] Strategy to elucidate pathogenesis of CADASIL using transgenic Drosophila models of human NOTCH32016
- Author(s)
  Ikuko Mizuta, Yumiko Azuma, Narumi Toda, Hideki Yoshida, Masamitsu Yamaguchi, Toshiki Mizuno
- Organizer
  第39回日本分子生物学会年会
- Place of Presentation
  パシフィコ横浜
- Year and Date
  2016-12-01
- Data Source
  KAKENHI-PROJECT-26461296
[Presentation] 日本人に即したCADASILスケール作成およびその有効性の検討．2016
- Author(s)
  小泉崇　向井麻央，濱野愛，渡邊明子，水田依久子，水野敏樹．
- Organizer
  第7回日本脳血管・認知症学会学術大会
- Place of Presentation
  金沢
- Data Source
  KAKENHI-PROJECT-26461276
[Presentation] A case report of heterozygous Pro285Leu HTRA1 mutation2016
- Author(s)
  T Mizuno , I Mizuta, M Makino, H Nozaki, T Kato, O Onodera
- Organizer
  The 8th Vas-Cog World Conference
- Place of Presentation
  Amsterdam, Netherland
- Year and Date
  2016-10-13
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461276
[Presentation] Strategy to elucidate pathogenesis of CADASIL using transgenic Drosophila models of human NOTCH32016
- Author(s)
  Ikuko Mizuta, Yumiko Azuma, Narumi Toda, Hideki Yoshida, Masamitsu Yamaguchi, Toshiki Mizuno
- Organizer
  第57回日本神経学会学術大会
- Place of Presentation
  神戸
- Year and Date
  2016-05-19
- Data Source
  KAKENHI-PROJECT-26461296
[Presentation] A Case Report of CADASIL with a Homozygous NOTCH3 Mutation Arg544Cys2015
- Author(s)
  Mao Mukai, Daisuke N,Yukie Kushimura,Yu-ichi Noto, Tomoyuki Ohara, Ikuko Mizuta, Toshiki Mizuno.
- Organizer
  The 7th Vas-Cog World Conference
- Place of Presentation
  Tokyo
- Year and Date
  2015-09-16
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461276
[Presentation] Consideration of Issues Related to Pre-and Post-Genetic Test for CADASIL2015
- Author(s)
  Ikuko Mizuta, Mao Mukai, Akiko Watanabe, Ai Hamano, Tomoyuki Ohara, Tomokatsu Yoshida, Toshiki Mizuno
- Organizer
  The 7th Vas-Cog World Conference
- Place of Presentation
  Tokyo
- Year and Date
  2015-09-16
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461276
[Presentation] Validation of Japanese Diagnostic Criteria for Cerebral Autosomal Dominant Arteriopathy with Subcorical Infarcts and Leukocencephalopathy2015
- Author(s)
  Toshiki Mizuno, Ikuko Mizuta, Akiko Watanabe, Ai Hamano, Mao Mukai, Masaki Kondo, Masanori Nakagawa, Hidekazu Tomimoto, Makoto Uchino, Osamu Onodera.
- Organizer
  The 7th Vas-Cog World Conference
- Place of Presentation
  Tokyo
- Year and Date
  2015-09-16
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461276
[Presentation] 延髄前部のMRI異常信号は成人期発症アレキサンダー病の特徴的な所見である2014
- Author(s)
  吉田誠克，水田依久子，斉藤光象，中川正法, 木村康義，朴貴瑛，伊藤康男,椎裕章，高橋義秋，井手俊宏，土師正太郎，水野敏樹．
- Organizer
  第５５回日本神経学会総会学術大会
- Place of Presentation
  福岡国際会議場
- Year and Date
  2014-05-22
- Data Source
  KAKENHI-PROJECT-24591273
[Presentation] CADASILのNOTCH3遺伝子変異分布と臨床像との関連性について2014
- Author(s)
  水田依久子，渡邉明子，濱野愛，中川正法，水野敏樹．
- Organizer
  第5回日本血管性認知障害研究会
- Place of Presentation
  京都
- Year and Date
  2014-08-23
- Data Source
  KAKENHI-PROJECT-26461276
[Presentation] パーキンソン病感受性遺伝子の同定および統計学的相互作用解析2008
- Author(s)
  水田依久子、佐竹渉、角田達彦、渡邊雅彦、武田篤、長谷川一子、中島健二、山本光利、服部信孝、村田美穂、戸田達史
- Organizer
  第49回日本神経学会総会
- Place of Presentation
  横浜パシフィコ横浜
- Year and Date
  2008-05-17
- Data Source
  KAKENHI-PROJECT-19590990
[Presentation] Genome-wide association study of Parkinson's disease by 550K SNP Array.2008
- Author(s)
  Satake W, Nakabayashi Y, Mizuta I, et al.
- Organizer
  The American Society of Human Genetics 58^<th>Annual Meeting
- Place of Presentation
  Philadelphia, Pennsylvania, USA
- Year and Date
  2008-11-14
- Data Source
  KAKENHI-PROJECT-19590990
[Presentation] Toda Genome-wide association study of Parkinson's disease by550K SNP Array2008
- Author(s)
  W. Satake, Y. Nakabayashi, I. Mizuta, T. Kawaguchi, T. Tsunoda, M. Kubo, S. Sakoda, M. Yamamoto, N. Hattori, M. Murata, Y. Nakamura, T. Gasser, A.B. Singleton, T.
- Organizer
  The American Society of Human Genetics 58th Annual Meeting
- Place of Presentation
  Philadelphia, Pennsylvania, USA
- Year and Date
  2008-11-14
- Data Source
  KAKENHI-PROJECT-19590990
[Presentation] Multiple candidate gene analysis identifiesCALB1(calbindin1) as a susceptibility gene for sporadic Parkinson's disease2007
- Author(s)
  I. Mizuta, W. Satake, T. Tsunoda, M.Watanabe, A. Takeda, K. Hasegawa, M.Yamamoto, N. Hattori, M. Murata, T. Toda
- Organizer
  The American Society of Human Genetics 57th Annual Meeting October 26^<th>
- Place of Presentation
  San Diego Convention Center,San Diego, USA
- Year and Date
  2007-10-26
- Data Source
  KAKENHI-PROJECT-19590990
[Presentation] 多数の候補遺伝子アプローチによるパーキンソン病感受性遺伝子calbindin1の同定2007
- Author(s)
  水田依久子、佐竹渉、角田達彦、長谷川一子、渡邊雅彦、武田篤、服部信孝、山本光利、村田美穂、戸田達史
- Organizer
  日本人類遺伝学会第52回大会
- Place of Presentation
  東京京王プラザホテル
- Year and Date
  2007-09-14
- Data Source
  KAKENHI-PROJECT-19590990
[Presentation] Multiple candidate gene analysis identifies CALB1(calbindin1) as a susceptibility gene for sporadic Parkinson's disease2007
- Author(s)
  I. Mizuta, W. Satake, T. Tsunoda, M. Watanabe, A. Takeda, K. Hasegawa, M. Yamamoto, N. Hattori, M. Murata, T. Toda
- Organizer
  The American Society of Human Genetics 57th Annual Meeting
- Place of Presentation
  San Diego Convention Center, San Diego, USA
- Year and Date
  2007-10-26
- Data Source
  KAKENHI-PROJECT-19590990
[Presentation] Association between FGF20 and Parkinson's disease and Genome-wide association study using 27,158 microsatellite by The Japanese PD Susceptibility Gene Consortium2007
- Author(s)
  W. Satake, I. Mizuta, Y. Hirota, A. Oka, M.Watanabe, A. Takeda, K. Hasegawa, S. Sakoda,M. Yamamoto, N. Hattori, M. Murata, H. Inoko,T. Toda
- Organizer
  The American Society of Human Genetics 57th Annual Meeting October 26^<th>
- Place of Presentation
  San Diego Convention Center, San Diego, USA
- Year and Date
  2007-10-26
- Data Source
  KAKENHI-PROJECT-19590990
[Presentation] 多数の候補遺伝子アプローチによるパーキンソン病感受性遺伝子calbindin1の同定日本人類遺伝学会2007
- Author(s)
  水田依久子、佐竹渉、角田達彦、長谷川一子、渡邊雅彦、武田篤、服部信孝、山本光利、村田美穂、戸田達史
- Organizer
  第52回大会
- Place of Presentation
  東京京王プラザホテル
- Year and Date
  2007-09-14
- Data Source
  KAKENHI-PROJECT-19590990
[Presentation] アレキサンダー病の臨床診断指針に対する有用性の検討．
- Author(s)
  吉田誠克，水田依久子，斉藤光象，中川正法．
- Organizer
  第54回日本神経学会学術大会．
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24591273
[Presentation] 塩酸ロメリジンによるCADASIL患者における脳梗塞発症に対する予防効果
- Author(s)
  水野敏樹，濱野　愛，渡邉明子，水田依久子，近藤正樹，中川正法
- Organizer
  第32回日本神経治療学会総会．2014年11月20-22日；東京
- Place of Presentation
  東京
- Year and Date
  2014-11-20 – 2014-11-22
- Data Source
  KAKENHI-PROJECT-26461276

1. Mizuno Toshiki (30264782)

# of Collaborated Projects: 4 results

# of Collaborated Products: 18 results
2. YOSHIDA Tomokatsu (90457987)

# of Collaborated Projects: 2 results

# of Collaborated Products: 6 results
3. TODA Tatsushi (30262025)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
4. 田中雅樹 (80264753)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 大原亮 (80636986)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
6. 山口政光 (00182460)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
7. 渡辺明子 (90828881)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. 佐々木真理 (80205864)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. 布施昇男 (10302134)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. Mukai Mao

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
11. HIRANO Teruyuki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Mizuta Ikuko 水田 依久子

水田 依久子 ミズタ イクコ

MIZUTA Ikuko 水田 依久子

Research Projects

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Co-Researchers

Cerebral white matter lesions and cerebral small vessel disease-related gene variants in the Japanese general populationPrincipal Investigator

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Research on genetic pathomechanism of adult-onset white matter disease

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Pathomechanism of cerebral small vessel disease due to disturbance of transendocytosis

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Investigation of cerebral small vessel diseases using Notch3 transgenic DrosophilaPrincipal Investigator

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Research for drug effectiveness in Alexander disease model

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Analysis of SNPs susceptible to Parkinson's diseasePrincipal Investigator

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Identification of susceptibility genes for sporadic Parkinson's disease by genotyping multiple SNPsPrincipal Investigator

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[Journal Article] Progress to Clarify How NOTCH3 Mutations Lead to CADASIL, a Hereditary Cerebral Small Vessel Disease2024

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[Journal Article] Adult-onset leukoencephalopathy with homozygous LAMB1 missense mutation2020

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[Journal Article] New diagnostic criteria for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukocencephalopathy in Japan.2017

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[Journal Article] CADASILの臨床像と遺伝子異常2017

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[Journal Article] CADASIL Presenting as Acute Bilateral Multiple Subcortical Infarcts without a Characteristic Temporal Pole or Any External Capsule Lesions2016

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[Journal Article] Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL.2016

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[Journal Article] A Japanese CADASIL kindred with a novel two-base NOTCH3 mutation.2016

Mizuta Ikuko 水田依久子

水田依久子ミズタイクコ

MIZUTA Ikuko 水田依久子