Hata Yukiko 畑由紀子

… Alternative Names

HATA Yukiko 畑由紀子

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Researcher Number	30311674
Other IDs	https://orcid.org/0000-0002-6441-3002
Affiliation (Current)	2025: 富山大学, 学術研究部医学系, 准教授
Affiliation (based on the past Project Information) *help	2019 – 2025: 富山大学, 学術研究部医学系, 准教授 2017 – 2018: 富山大学, 大学院医学薬学研究部(医学), 准教授 2012 – 2016: 富山大学, 大学院医学薬学研究部(医学), 助教 2011: 富山大学, 大学院・医学薬学研究部(医学), 助教 2009 – 2010: 富山大学, 大学院・医学薬学研究部, 助教 … More 2006: 富山大学, 教務職員 2006: University of Toyama, Department of Legal Medicine, Assistant, 大学院医学薬学研究部, 助教 2006: University of Toyama, Graduate School of Medicine and Pharmaceutical Science for Research, Teaching Associate, 大学院医学薬学研究部, 教務職員 2005: 富山大学, 医学部, 教務職員 1999 – 2004: 富山医科薬科大学, 医学部, 教務職員 2002: Toyama Medeical and Pharmaceutical University, Faculty of Medicine, Assistant, 医学部, 教務職員(研究職) Less
Review Section/Research Field	Principal Investigator Basic Section 58040:Forensics medicine-related / Legal medicine / Legal medicine Except Principal Investigator Legal medicine / Legal medicine / Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics / Sections That Are Subject to Joint Review: Basic Section90130:Medical systems-related , Basic Section90140:Medical technology assessment-related / Basic Section 90140:Medical technology assessment-related / Basic Section 90130:Medical systems-related
Keywords	Principal Investigator 次世代シーケンサー / エクソーム解析 / Autopsy / Sudden unexplained death / Alu配列 / 転写制御 / exome analysis / 法医学 / Exome analysis / Sudden death … More / Molecular Autopsy / 遺伝子変異 / 病理組織学的検索 / 突然死 / 代謝疾患 / 遺伝性心疾患 / てんかん / スプライシングアッセイ / 乳幼児・小児 / 原因不明の突然死 / Exome sequence / Infants and children / epilepsy / Epilepsy / Next-generation sequence / Channelopathy / Cardiomyopathy / transcription regulation / antisense RNA / human ABO gene / antisense遺伝子 / アンチセンスRNA / ABO式血液型遺伝子 / １塩基多型 / 遺伝子変異解析 / イオンチャンネル / 心臓性突然死 / イオンチャネル / 法医剖検 / 致死性不整脈遺伝子 / 法医剖検例 / 心筋症 / チャネル異常症 / 心臓突然死 / transmembrane domain / Golgi retention / glycosyltransferase / alternative transcription / ABO gene / MAR / ABO式血液型 … More Except Principal Investigator ABO式血液型遺伝子 / 転写制御 / プロモーター / N box / 転写 / transcription / DNAメチレーション / CpGアイランド / 遺伝子発現 / ABO式血液型 / 遺伝子解析 / 心筋緻密化障害 / 心筋症 / 法医解剖 / 神経変性疾患 / 神経病理 / 自殺 / ABO遺伝子 / 反復配列 / E box / ABO式血液型合成酵素 / DNA methylation / promoter assay / the human ABO blood group genes / サルコメア遺伝子 / 免疫染色 / レビー小体関連疾患 / 剖検脳研究 / 進行性核上性麻痺 / レビー小体病理 / 神経外傷 / てんかん / 頭部外傷 / 高齢者 / 気分障害 / 神経病理学 / 機能解析 / i PS細胞 / 突然死 / 心筋細胞 / 致死性不整脈 / 次世代シーケンサー / iPS細胞 / 遺伝子変異 / Lysozyme / Surfactant-associated protein C / Connective tissue growth factor / Galectin-3 / Myc / Gene expression / Hyperoxia exposure / Diffuse alveolar damage / 生体防禦 / 線維化 / ラット(Slc:Wistar / ハムスター(Slc:Syrian) / びまん性肺胞傷害 / 瀰漫性肺胞傷害 / 組織改築 / 免疫 / 肺胞中隔の線維化 / ST) / ラット(Slc : Wistar / ハムスター(Slc : Syrian) / 6J) / マウス(C57BL / 高濃度酸素曝露 / びまん性肺胞障害 / FUT2 gene / FUT1 gene / transcriptional regulation / bHLH factor / N-box / antisense RNA / human ABO gene / フコース転移酵素 / ABO遺伝子上流域 / N-box配列 / FUT2遺伝子 / FUT1遺伝子 / 転写調節 / bHLH因子 / Nbox / アンチセンスRNA / promoter / repression / ABO gene / Nボックス / 転写因子 / Alu / ABO antigens / LINE / alternative promoter usage / 細胞分化 / Alu配列 / ABO抗原 / 転写開始 / プロモーターアッセイ / CpG islands / Transcription / Fucosyltransferases / ABO glycosyltransferases / ABO blood group genes / Blood groups / DNAメチル化 / 5'RACE法 / 転写開始点 / H遺伝子 / FUT-2遺伝子 / 転写抑制因子 / フコシルトランスフェラーゼ / 血液型 / CpG island / 循環器 / 遺伝子 / サルコメア / 心筋発達 / 遺伝子異常 / 自律神経 / α-synuclein / a-synucleopathy / 心刺激伝導系 / 心臓性突然死 Less

原因不明の心臓突然死の診断，病態解明に向けた網羅的剖検研究Principal Investigator
- Principal Investigator
  
  畑由紀子
- Project Period (FY)
  2025 – 2027
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 58040:Forensics medicine-related
- Research Institution
  University of Toyama
法医剖検脳のリサーチリソース化とその特性を生かした多角的臨床病理研究
- Principal Investigator
  
  西田尚樹
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 90130:Medical systems-related
  Basic Section 90140:Medical technology assessment-related
  Sections That Are Subject to Joint Review: Basic Section90130:Medical systems-related , Basic Section90140:Medical technology assessment-related
- Research Institution
  University of Toyama
MYH7の多様性に着目した心筋緻密化障害の病態の解明
- Principal Investigator
  
  廣野恵一
- Project Period (FY)
  2022 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  University of Toyama
Comprehensive genetic and morphological analysis for sudden cardiac death autopsy casesPrincipal Investigator
- Principal Investigator
  
  Hata Yukiko
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 58040:Forensics medicine-related
- Research Institution
  University of Toyama
Pathophysiology of left ventricular noncompaction: focus on the importance of the downstream pathway of the transcription factor TBX5
- Principal Investigator
  
  Hirono Keiichi
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  University of Toyama
Investigating the Genetic Causes of Sudden Unexpected Death in infants and children.Principal Investigator
- Principal Investigator
  
  Hata Yukiko
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 58040:Forensics medicine-related
- Research Institution
  University of Toyama
Neuropathological analysis for aged suicide victims.
- Principal Investigator
  
  Nishida Naoki
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Legal medicine
- Research Institution
  University of Toyama
Comprehensive genetic analysis of sudden unexplained death syndrome cases using a next-generation sequencingPrincipal Investigator
- Principal Investigator
  
  Hata Yukiko
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Legal medicine
- Research Institution
  University of Toyama
Genetic analysis and pathological role in ventricular noncompaction associated with fatal arrhythmia
- Principal Investigator
  
  Ichida Fukiko
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  University of Toyama
Genetic background of sudden cardiac death in forensic autopsy cases.Principal Investigator
- Principal Investigator
  
  HATA Yukiko
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Legal medicine
- Research Institution
  University of Toyama
Genetic analysis of sarcmere in left ventricular noncompaction
- Principal Investigator
  
  ICHIDA Fukiko
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  University of Toyama
Significance ofα-synucleopathy in cardiac autonomic nervous system
- Principal Investigator
  
  NISHIDA Naoki
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Legal medicine
- Research Institution
  University of Toyama
Establishment of diffuse alveolar damage induced by hyperoxia exposure in mice and elucidation of its pathogenesis
- Principal Investigator
  
  SHIMADA Ichiroh
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Legal medicine
- Research Institution
  University of Toyama
Investigation of a novel transcription originated from the upstream region of the human ABO genePrincipal Investigator
- Principal Investigator
  
  HATA Yukiko
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Legal medicine
- Research Institution
  University of Toyama
Analysis of cooperative expression of the genes encoding glycosyltransferases involved in the histo-blood group ABH antigens.
- Principal Investigator
  
  TAKIZAWA Hisao
- Project Period (FY)
  2004 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Legal medicine
- Research Institution
  University of Toyama
  Toyama Medical and Pharmaceutical University
Transcriptional regulation of the human ABO histo-blood group genes is dependent on the negative regulation through the N box upstream of the proximal promoter
- Principal Investigator
  
  KOMINATO Yoshihiko
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Legal medicine
- Research Institution
  Gunma University
ABO血液型合成酵素の膜貫通ドメインの重要性とその変異に基づく血液型亜型の検索Principal Investigator
- Principal Investigator
  
  畑由紀子
- Project Period (FY)
  2002 – 2003
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Legal medicine
- Research Institution
  Toyama Medical and Pharmaceutical University
Progress in the biological science of ABO blood group system -a pioneer work in legal medicine-
- Principal Investigator
  
  TAKIZAWA Hisao
- Project Period (FY)
  2001 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Legal medicine
- Research Institution
  TOYAMA MEDICAL AND PHARMACEUTICAL UNIVERSITY
Analysis of transcriptional regulation of the human ABO genes during differentiation of erythroid lineage
- Principal Investigator
  
  KOMINATO Yoshihiko
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Legal medicine
- Research Institution
  TOYAMA MEDICAL AND PHARMACEUTICAL UNIVERSITY
ABO血液型遺伝子におけるAlu配列の転写調節機能についての検討Principal Investigator
- Principal Investigator
  
  畑由紀子
- Project Period (FY)
  2000 – 2001
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Legal medicine
- Research Institution
  Toyama Medical and Pharmaceutical University
Expression of human histo-blood group ABO genes is dependent upon DNA methylation of the promoter region
- Principal Investigator
  
  KOMINATO Yoshihiko
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Legal medicine
- Research Institution
  TOYAMA MEDICAL AND PHARMACEUTICAL UNIVERSITY

[Book] 病理と臨床【法医と病理の相互理解】法医解剖と病理2014
- Author(s)
  西田尚樹, 畑由紀子
- Publisher
  文光堂
- Data Source
  KAKENHI-PROJECT-24590852
[Journal Article] An autopsy case of infective aortic aneurysm with Pasteurella multocida infection: clinicopathological appearance and a review of literatures2023
- Author(s)
  Nomoto Kazuhiro、Hata Yukiko、Ichimata Shojiro、Mizuno Syu、Nishida Naoki
- Journal Title
  
  Annals of Clinical Microbiology and Antimicrobials
  
  Volume: 22 Issue: 1 Pages: 58-58
- DOI
  10.1186/s12941-023-00611-0
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K28447
[Journal Article] 10.3389/fped.2023.11952222023
- Author(s)
  Kawamura H, Ikawa M, Hirono K, Kimura J, Okuno T, Kawatani M, Inai K, Hata Y, Nishida N, Yoshida Y.
- Journal Title
  
  Front Pediatr.
  
  Volume: 11 Pages: 1195222-1195222
- DOI
  10.3389/fped.2023.1195222
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K07932, KAKENHI-PROJECT-23K06924, KAKENHI-PROJECT-21K06967, KAKENHI-PROJECT-20H03908
[Journal Article] Comprehensive pathological and genetic investigation of three young adult myotonic dystrophy type 1 patients with sudden unexpected death.2023
- Author(s)
  Hata Y, Ichimata S, Yoshida K, Yamaguchi Y, Hirono K, Nishida N.
- Journal Title
  
  J Neurol
  
  Volume: 270 Issue: 11 Pages: 5380-5391
- DOI
  10.1007/s00415-023-11850-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22K07932, KAKENHI-PROJECT-21H03211, KAKENHI-PROJECT-23K28447
[Journal Article] G0S2 regulates innate immunity in Kawasaki disease via lncRNA HSD11B1-AS12022
- Author(s)
  Okabe Mako、Takarada Shinya、Miyao Nariaki、Nakaoka Hideyuki、Ibuki Keijiro、Ozawa Sayaka、Watanabe Kazuhiro、Tsuji Harue、Hashimoto Ikuo、Hatasaki Kiyoshi、Hayakawa Shotaro、Hamaguchi Yu、Hamada Michiaki、Ichida Fukiko、Hirono Keiichi
- Journal Title
  
  Pediatric Research
  
  Volume: 15 Issue: 2 Pages: 378-387
- DOI
  10.1038/s41390-022-01999-9
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16H05879, KAKENHI-PROJECT-17K20032, KAKENHI-PROJECT-22K07932, KAKENHI-PROJECT-18K07785
[Journal Article] An autopsy case of sudden unexpected death of a young adult with progressive intraventricular conduction delay2022
- Author(s)
  Hata Yukiko、Hachiwaka Ryotaro、Ichimata Shojiro、Yamaguchi Yoshiaki、Nishida Naoki
- Journal Title
  
  Pathology - Research and Practice
  
  Volume: 240 Pages: 154226-154226
- DOI
  10.1016/j.prp.2022.154226
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21H03211
[Journal Article] Clinicopathologic Appearance of Advanced Ketoacidosis With Basal Vacuolation in Renal Tubules2022
- Author(s)
  Ichimata Shojiro、Hata Yukiko、Nishida Naoki
- Journal Title
  
  Archives of Pathology & Laboratory Medicine
  
  Volume: 146 Issue: 9 Pages: 1102-1113
- DOI
  10.5858/arpa.2021-0226-oa
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21H03211
[Journal Article] Pathological and Comprehensive Genetic Investigation of Autopsy Cases of Idiopathic Bradyarrhythmia2022
- Author(s)
  Hata Yukiko、Ichimata Shojiro、Hirono Keiichi、Yamaguchi Yoshiaki、Oku Yuko、Ichida Fukiko、Nishida Naoki
- Journal Title
  
  Circ J
  
  Volume: 87 Issue: 1 Pages: 111-119
- DOI
  10.1253/circj.CJ-22-0397
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2022-12-23
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-22K07932, KAKENHI-PROJECT-18K07785
[Journal Article] An autopsy case of sudden unexpected death with Barlow's disease2022
- Author(s)
  Hata Yukiko、Tomita Naoko、Shibata Atsushi、Yokoyama Shigeki、Fukahara Kazuaki、Nishida Naoki
- Journal Title
  
  Cardiovascular Pathology
  
  Volume: 61 Pages: 107462-107462
- DOI
  10.1016/j.carpath.2022.107462
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21H03211
[Journal Article] A Novel NKX2-5 Variant in a Child with Left Ventricular Noncompaction, Atrial Septal Defect, Atrioventricular Conduction Disorder, and Syncope2022
- Author(s)
  Yamada Yuya、Yasuda Kazushi、Hata Yukiko、Nishida Naoki、Hirono Keiichi
- Journal Title
  
  Journal of Clinical Medicine
  
  Volume: 11 Issue: 11 Pages: 3171-3171
- DOI
  10.3390/jcm11113171
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22K07932
[Journal Article] Clinicopathological features of clinically undiagnosed sporadic transthyretin cardiac amyloidosis: a forensic autopsy-based series.2021
- Author(s)
  Ichimata S, Hata Y, Hirono K, Yamaguchi Y, Nishida N.
- Journal Title
  
  Amyloid
  
  Volume: 28 Issue: 2 Pages: 125-133
- DOI
  10.1080/13506129.2021.1882979
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-20K18979
[Journal Article] Electrocardiographic Diagnosis of Hypertrophic Cardiomyopathy in the Pre- and Post-Diagnostic Phases in Children and Adolescents2021
- Author(s)
  Yoshinaga M, Horigome H, Yasuda K, Kogaki S, Tateno S, Ohta K, Hirono K, Hosokawa S, Takechi F, Ishikawa Y, Hata T, Ichida F, Ohno S, Makita N, Horie M, Takahashi H, Nagashima M.
- Journal Title
  
  Circ J
  
  Volume: 86 Issue: 1 Pages: 118-127
- DOI
  10.1253/circj.CJ-21-0376
- NAID
  130008132672
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2021-12-24
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-21H02920, KAKENHI-PROJECT-18K02505, KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-21K07765
[Journal Article] A Case Report of a Rare Heterozygous Variant in the Desmin Gene Associated With Hypertrophic Cardiomyopathy and Complete Atrioventricular Block.2021
- Author(s)
  Oka H, Nakau K, Imanishi R, Furukawa T, Tanabe Y, Hirono K, Hata Y, Nishida N, Azuma H.
- Journal Title
  
  CJC Open.
  
  Volume: - Issue: 9 Pages: 1195-1198
- DOI
  10.1016/j.cjco.2021.05.003
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08295
[Journal Article] A burden of sarcomere gene variants in fetal-onset patients with left ventricular noncompaction2021
- Author(s)
  Hirono Keiichi、Hata Yukiko、Ozawa Sayaka Watanabe、Toda Takako、Momoi Nobuo、Fukuda Yutaka、Inuzuka Ryo、Nagamine Hiroki、Sakaguchi Heima、Kurosaki Kenichi、Okabe Mako、Takarada Shinya、Miyao Nariaki、Nakaoka Hideyuki、Ibuki Keijiro、Origasa Hideki、Bowles Neil E.、Nishida Naoki、Ichida Fukiko
- Journal Title
  
  International Journal of Cardiology
  
  Volume: 328 Pages: 122-129
- DOI
  10.1016/j.ijcard.2020.12.013
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-21H03211, KAKENHI-PROJECT-18K07785
[Journal Article] Increased Burden of Ion Channel Gene Variants Is Related to Distinct Phenotypes in Pediatric Patients With Left Ventricular Noncompaction2020
- Author(s)
  Hirono Keiichi、Hata Yukiko、Ichida Fukiko、et al
- Journal Title
  
  Circulation: Genomic and Precision Medicine
  
  Volume: 13 Issue: 4
- DOI
  10.1161/circgen.119.002940
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-19K08295
[Journal Article] Two autopsy cases of sudden unexpected death from Dravet syndrome with novel de novo SCN1A variants2020
- Author(s)
  Hata Yukiko、Oku Yuko、Taneichi Hiromichi、Tanaka Tomomi、Igarashi Noboru、Niida Yo、Nishida Naoki
- Journal Title
  
  Brain and Development
  
  Volume: 42 Issue: 2 Pages: 171-178
- DOI
  10.1016/j.braindev.2019.10.005
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K10480, KAKENHI-PROJECT-18K10119
[Journal Article] Left Ventricular Noncompaction and Congenital Heart Disease Increases the Risk of Congestive Heart Failure.2020
- Author(s)
  Hirono K, Hata Y, Miyao N, Okabe M, Takarada S, Nakaoka H, Ibuki K, Ozawa S, Yoshimura N, Nishida N, Ichida F, Lvnc Study Collaborators.
- Journal Title
  
  J Clin Med.
  
  Volume: 9 Issue: 3 Pages: 785-785
- DOI
  10.3390/jcm9030785
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-18K07785
[Journal Article] TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway2020
- Author(s)
  Miyao N., Hata Y., Izumi H., Nagaoka R., Oku Y., Takasaki I., Ishikawa T., Takarada S., Okabe M., Nakaoka H., Ibuki K., Ozawa S., Yoshida T., Hasegawa H., Makita N., Nishida N., Mori H., Ichida F., Hirono K.
- Journal Title
  
  PLOS ONE
  
  Volume: 15 Issue: 4 Pages: 0227393-0227393
- DOI
  10.1371/journal.pone.0227393
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-18KK0245, KAKENHI-PUBLICLY-19H04744, KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-18K15894, KAKENHI-PROJECT-18K07365, KAKENHI-PROJECT-20H03350
[Journal Article] A significance of school screening electrocardiogram in the patients with ventricular noncompaction.2020
- Author(s)
  Hirono K, Miyao N, Yoshinaga M, Nishihara E, Hata T, et al.
- Journal Title
  
  Heart Vessels
  
  Volume: 11 Issue: 7 Pages: 985-995
- DOI
  10.1007/s00380-020-01571-7
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K02505, KAKENHI-PROJECT-18K07813, KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-17H03589
[Journal Article] Cardiac Emerinopathy2020
- Author(s)
  Ishikawa Taisuke、Ichida Fukiko、Makita Naomasa　et al
- Journal Title
  
  Circulation: Arrhythmia and Electrophysiology
  
  Volume: 13 Issue: 10 Pages: 1165-1174
- DOI
  10.1161/circep.120.008712
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-19K21724, KAKENHI-PROJECT-18KK0245, KAKENHI-PROJECT-18H02808, KAKENHI-PROJECT-20H03591, KAKENHI-PROJECT-18K07850, KAKENHI-PROJECT-18K19550, KAKENHI-PROJECT-20K08416, KAKENHI-PROJECT-18H03083
[Journal Article] Efficacy of primary treatment with immunoglobulin plus ciclosporin for prevention of coronary artery abnormalities in patients with Kawasaki disease predicted to be at increased risk of non-response to intravenous immunoglobulin (KAICA): a randomised controlled, open-label, blinded-endpoints, phase 3 trial2019
- Author(s)
  Hamada H, Suzuki H, Onouchi Y, Ebata R, Terai M, Fuse S, Okajima Y, Kurotobi S, Hirai K, Soga T, Ishiguchi Y, et al.
- Journal Title
  
  Lancet.
  
  Volume: 393(10176): Issue: 10176 Pages: 1128-1137
- DOI
  10.1016/s0140-6736(18)32003-8
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K10072, KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-15K08815
[Journal Article] Clinicopathological and Genetic Profiles of Cases with Myocytes Disarray?Investigation for Establishing the Autopsy Diagnostic Criteria for Hypertrophic Cardiomyopathy2019
- Author(s)
  Hata Yukiko、Ichimata Shojiro、Yamaguchi Yoshiaki、Hirono Keiichi、Oku Yuko、Ichida Fukiko、Nishida Naoki
- Journal Title
  
  Journal of Clinical Medicine
  
  Volume: 8 Issue: 4 Pages: 463-463
- DOI
  10.3390/jcm8040463
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-18K10119, KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-17K09263
[Journal Article] An Autopsy Case of Preclinical/Early Clinical Pick Disease2019
- Author(s)
  Okada Keitaro、Hata Yukiko、Takayanagi Yoichiro、Takahashi Tsutomu、Takayanagi Isao、Nishida Naoki
- Journal Title
  
  Journal of Neuropathology & Experimental Neurology
  
  Volume: 78 Issue: 10 Pages: 971-974
- DOI
  10.1093/jnen/nlz077
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09263
[Journal Article] Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy2019
- Author(s)
  Hata Yukiko、Hirono Keiichi、Yamaguchi Yoshiaki、Ichida Fukiko、Oku Yuko、Nishida Naoki
- Journal Title
  
  Modern Pathology
  
  Volume: 32 Issue: 9 Pages: 1281-1290
- DOI
  10.1038/s41379-019-0274-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K10119, KAKENHI-PROJECT-19K08295, KAKENHI-PROJECT-17K09263
[Journal Article] Sudden unexpected death with rare compound heterozygous variants in PRICKLE12019
- Author(s)
  Hata Yukiko、Yoshida Koji、Nishida Naoki
- Journal Title
  
  neurogenetics
  
  Volume: 20 Issue: 1 Pages: 39-43
- DOI
  10.1007/s10048-018-0562-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09263
[Journal Article] Tau and Amyloid-β Pathology in Japanese Forensic Autopsy Series Under 40 Years of Age: Prevalence and Association with APOE Genotype and Suicide Risk2019
- Author(s)
  Yoshida Koji、Hata Yukiko、Ichimata Shojiro、Nishida Naoki
- Journal Title
  
  Journal of Alzheimer's Disease
  
  Volume: 72 Issue: 2 Pages: 641-652
- DOI
  10.3233/jad-190196
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09263
[Journal Article] Novel compound heterozygous TBX5 variants may induce hypoplastic left heart syndrome2019
- Author(s)
  Miyao Nariaki、Hirono Keiichi、Hata Yukiko、Yoshimura Naoki、Ichida Fukiko
- Journal Title
  
  Pediatrics International
  
  Volume: 61 Issue: 6 Pages: 607-609
- DOI
  10.1111/ped.13854
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K10726, KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-19K08295
[Journal Article] Fetal closed head injuries following maternal motor vehicle accident2018
- Author(s)
  Nishida Naoki、Ina Shihomi、Hata Yukiko、Nakanishi Yuko、Ishizawa Shin、Futatani Takeshi
- Journal Title
  
  Medicine
  
  Volume: 97 Issue: 44 Pages: e13133-e13133
- DOI
  10.1097/md.0000000000013133
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09263
[Journal Article] Sudden unexpected death with primary adrenal lymphoma2018
- Author(s)
  Hata Yukiko、Ishizawa Shin、Nishida Naoki
- Journal Title
  
  Legal Medicine
  
  Volume: 35 Pages: 25-28
- DOI
  10.1016/j.legalmed.2018.09.001
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09263
[Journal Article] Autopsy of an Elderly Man With Incidentally Diagnosed TDP-43 Proteinopathy2018
- Author(s)
  Hata Yukiko、Yoshida Koji、Nishida Naoki
- Journal Title
  
  Alzheimer Disease & Associated Disorders
  
  Volume: 32 Issue: 2 Pages: 158-161
- DOI
  10.1097/wad.0000000000000234
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09263
[Journal Article] Sarcomere gene variants act as a genetic trigger underlying the development of left ventricular noncompaction2018
- Author(s)
  Takasaki Asami、Hirono Keiichi、Hata Yukiko、Wang Ce、Takeda Masafumi、Yamashita Jun K、Chang Bo、Nakaoka Hideyuki、Okabe Mako、Miyao Nariaki、Saito Kazuyoshi、Ibuki Keijiro、Ozawa Sayaka、Sekine Michikazu、Yoshimura Naoki、Nishida Naoki、Bowles Neil E.、Ichida Fukiko
- Journal Title
  
  Pediatric Research
  
  Volume: 84 Issue: 5 Pages: 733-742
- DOI
  10.1038/s41390-018-0162-1
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-18K10119, KAKENHI-PROJECT-18H04048
[Journal Article] Clinical and Echocardiographic Impact of Tafazzin Variants on Dilated Cardiomyopathy Phenotype in Left Ventricular Non-Compaction Patients in Early Infancy2018
- Author(s)
  Hirono K、Hata Y、Nakazawa M、Momoi N、Tsuji T、Matsuoka T、Ayusawa M、Abe Y、Hayashi T、Tsujii N、Abe T、Sakaguchi H、Wang C、Takasaki A、Takarada S、Okabe M、Miyao N、Nakaoka H、Ibuki K、Saito K、Ozawa S、Nishida N、Bowles N E.、Ichida F
- Journal Title
  
  Circ J
  
  Volume: 82 Issue: 10 Pages: 2609-2618
- DOI
  10.1253/circj.CJ-18-0470
- NAID
  130007487877
- ISSN
  1346-9843, 1347-4820
- Year and Date
  2018-09-25
- Language
  English
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07785, KAKENHI-PROJECT-18K10119
[Journal Article] Argyrophilic grain disease in a 46-year-old male suicide victim2017
- Author(s)
  Yoshida Koji、Hata Yukiko、Kinoshita Koshi、Nishida Naoki
- Journal Title
  
  Journal of the Neurological Sciences
  
  Volume: 380 Pages: 223-225
- DOI
  10.1016/j.jns.2017.07.043
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09263, KAKENHI-PROJECT-15K08867
[Journal Article] A Case of Sudden Unexpected Death with the Presence of Multiple Myocardial Bridges2017
- Author(s)
  Nishida Naoki
- Journal Title
  
  International Journal of Clinical Cardiology
  
  Volume: 4 Issue: 2 Pages: 099-099
- DOI
  10.23937/2378-2951/1410099
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09263, KAKENHI-PROJECT-15K08867
[Journal Article] An Autopsy Case of Sudden Unexpected Death of a Young Adult in a Hot Bath: Molecular Analysis Using Next-Generation DNA Sequencing2017
- Author(s)
  Hata Yukiko、Kinoshita Koshi、Nishida Naoki
- Journal Title
  
  Clinical Medicine Insights: Case Reports
  
  Volume: 10 Pages: 1-6
- DOI
  10.1177/1179547617702884
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17K09263, KAKENHI-PROJECT-15K08867
[Journal Article] Sudden unexpected death in early Parkinson's disease: neurogenic or cardiac death?2017
- Author(s)
  Nishida Naoki、Yoshida Koji、Hata Yukiko
- Journal Title
  
  Cardiovascular Pathology
  
  Volume: 30 Pages: 19-22
- DOI
  10.1016/j.carpath.2017.06.001
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09263, KAKENHI-PROJECT-15K08867
[Journal Article] Incipient progressive supranuclear palsy is more common than expected and may comprise clinicopathological subtypes: a forensic autopsy series2017
- Author(s)
  Yoshida Koji、Hata Yukiko、Kinoshita Koshi、Takashima Shutaro、Tanaka Kortaro、Nishida Naoki
- Journal Title
  
  Acta Neuropathologica
  
  Volume: 133 Issue: 5 Pages: 809-823
- DOI
  10.1007/s00401-016-1665-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09263, KAKENHI-PROJECT-15K08867
[Journal Article] A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular Noncompaction.2017
- Author(s)
  Wang C, Hata Y, Hirono K, Takasaki A, Ozawa SW, Nakaoka H, Saito K, Miyao N, Okabe M, Ibuki K, Nishida N, Origasa H, Yu X, Bowles NE, Ichida F; for LVNC Study Collaborators.
- Journal Title
  
  J Am Heart Assoc.
  
  Volume: 6 Issue: 9
- DOI
  10.1161/jaha.117.006210
- NAID
  120006772542
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10139, KAKENHI-PROJECT-15K09685
[Journal Article] Intramyocardial bronchogenic cyst: histological appearance and a review of the literature2017
- Author(s)
  Nishida Naoki、Hata Yukiko、Nomoto Kazuhiro
- Journal Title
  
  Cardiovascular Pathology
  
  Volume: 28 Pages: 64-67
- DOI
  10.1016/j.carpath.2017.03.005
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K09263, KAKENHI-PROJECT-15K08867
[Journal Article] Epilepsy-related sudden unexpected death: targeted molecular analysis of inherited heart disease genes using next-generation DNA sequencing2017
- Author(s)
  Hata Yukiko、Yoshida Koji、Kinoshita Koshi、Nishida Naoki
- Journal Title
  
  Brain Pathology
  
  Volume: 27 Issue: 3 Pages: 292-304
- DOI
  10.1111/bpa.12390
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K08867
[Journal Article] Latent pathogenicity of the G38S polymorphism of KCNE1 K+ channel modulator.2017
- Author(s)
  2)Yamaguchi Y, Mizumaki K, Hata Y, Sakamoto T, Nakatani Y, Kataoka N, Ichida F, Inoue H, Nishida N.
- Journal Title
  
  Heart Vessels
  
  Volume: 32 Issue: 2 Pages: 186-192
- DOI
  10.1007/s00380-016-0859-1
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15K09685, KAKENHI-PROJECT-15K08867
[Journal Article] Postmortem genetic analysis of sudden unexplained death syndrome under 50 years of age: A next-generation sequencing study.2016
- Author(s)
  Hata Y, Kinoshita K, Mizumaki K, Yamaguchi Y, Hirono K, Ichida F, Takasaki A, Mori H, Nishida N.
- Journal Title
  
  Heart Rhythm.
  
  Volume: 13 Issue: 7 Pages: 1544-1551
- DOI
  10.1016/j.hrthm.2016.03.038
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K08867, KAKENHI-PROJECT-15K09686
[Journal Article] Pseudoaneurysmal defect of mitral-aortic intervalvular fibrosa is likely to be a cerebral embolic source. An autopsy study in remote period from the stroke.2016
- Author(s)
  Nishida N, Hata Y, Kinoshita K, Nonomura M.
- Journal Title
  
  Pathol Int
  
  Volume: 66 Issue: 8 Pages: 472-474
- DOI
  10.1111/pin.12421
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K08867
[Journal Article] Abnormal repolarization dynamics in a patient with KCNE1(G38S) who presented with torsades de pointes.2016
- Author(s)
  Yamaguchi Y, Mizumaki K, Hata Y, Inoue H.
- Journal Title
  
  J Electrocardiol
  
  Volume: 49 Issue: 1 Pages: 94-98
- DOI
  10.1016/j.jelectrocard.2015.10.002
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-24591040, KAKENHI-PROJECT-15K08867
[Journal Article] Left ventricular non-compaction revealed by aortic regurgitation due to Kawasaki disease in a boy with LDB3 mutation.2016
- Author(s)
  Hachiya A, Motoki N, Akazawa Y, Matsuzaki S, Hirono K, Hata Y, Nishida N, Ichida F, Koike K.
- Journal Title
  
  Pediatr Int
  
  Volume: 58 Issue: 8 Pages: 797-800
- DOI
  10.1111/ped.12983
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K08867
[Journal Article] Anomalous origin of the right coronary artery evaluated with multidetector computed tomography and its clinical relevance.2016
- Author(s)
  Hirono K, Hata Y, Miyao N, Nakaoka H, Saito K, Ibuki K, Watanabe K, Ozawa S, Higuma T, Yoshimura N, Nishida N, Ichida F
- Journal Title
  
  J Cardiol
  
  Volume: 68 Issue: 3 Pages: 196-201
- DOI
  10.1016/j.jjcc.2015.12.010
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K19604, KAKENHI-PROJECT-15K08867, KAKENHI-PROJECT-15K09686
[Journal Article] Anomalous origin of the right coronary artery from the left coronary sinus with an intramural course: comparison between sudden-death and non-sudden-death cases.2015
- Author(s)
  Hata Y, Kinoshita K, Kudo K, Ikeda N, Nishida N
- Journal Title
  
  Cardiovasc Pathol.
  
  Volume: 24 Issue: 3 Pages: 154-159
- DOI
  10.1016/j.carpath.2014.11.004
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K08867, KAKENHI-PROJECT-25460870
[Journal Article] A novel MYH7 gene mutation in a fetus with left ventricular noncompaction.2015
- Author(s)
  Nomura Y, Momoi N, Hirono K, Hata Y, Takasaki A, Nishida N, Ichida F.
- Journal Title
  
  Can J Cardiol.
  
  Volume: 1 Issue: 1 Pages: 1-3
- DOI
  10.1016/j.cjca.2014.11.012
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-24591571, KAKENHI-PROJECT-25860848, KAKENHI-PROJECT-15K08867, KAKENHI-PROJECT-15K09685
[Journal Article] An autopsy case of pneumococcal Waterhouse-Friderichsen syndrome with possible functional asplenia/hyposplenia.2015
- Author(s)
  Hata Y, Chiba T, Ohtani M, Ishizawa S, Nishida N.
- Journal Title
  
  Int J Clin Exp Pathol.
  
  Volume: 8 Pages: 7518-7525
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K08867
[Journal Article] A novel ACTC1 gene mutation in a young boy with left ventricular noncompaction and arrhythmias.2015
- Author(s)
  Yoshida Y, Keiichi Hirono, Kae Nakamura, Tsugutoshi Suzuki, Yukiko Hata, Naoki Nishida
- Journal Title
  
  Heart Rhythm Case Report
  
  Volume: 1 Issue: 1 Pages: 0-0
- DOI
  10.1016/j.hrcr.2015.11.008
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-15K09685, KAKENHI-PROJECT-25860848, KAKENHI-PROJECT-15K08867
[Journal Article] The Susceptibilities of Human Ether-à-Go-Go-Related Gene Channel with the G487R Mutation to Arrhythmogenic Factors2015
- Author(s)
  Hisajima N, Hata Y, Kinoshita K, Fukushima T, Nishida N, Kano M, Tabata T.
- Journal Title
  
  Biological and Pharmaceutical Bulletin
  
  Volume: 38 Issue: 5 Pages: 781-784
- DOI
  10.1248/bpb.b14-00630
- NAID
  130005068093
- ISSN
  0918-6158, 1347-5215
- URL
  https://pure.teikyo.jp/en/publications/67a7ba40-42e9-4e71-937c-ca38e15e1a37
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K08867, KAKENHI-PROJECT-26430012
[Journal Article] Identification and characterization of a novel genetic mutation with prolonged QT syndrome in an unexplained postoperative death2014
- Author(s)
  Yukiko Hata, Hisashi Mori, Ayumi Tanaka, Yosuke Fujita, Takeshi Shimomura, Toshihide Tabata, Koshi Kinoshita, Yoshiaki Yamaguchi, Fukiko Ichida, Yoshihiko Kominato, Noriaki Ikeda, Naoki Nishida
- Journal Title
  
  International Journal of Legal Medicine
  
  Volume: 128 Issue: 1 Pages: 105-115
- DOI
  10.1007/s00414-013-0853-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23500384, KAKENHI-PROJECT-24590852, KAKENHI-PROJECT-24591571, KAKENHI-PROJECT-24790745
[Journal Article] Glycine/Serine polymorphism at position 38 influences KCNE1 subunit's modulatory actions on rapid and slow delayed rectifier K+ currents.2014
- Author(s)
  Yamaguchi Y, Nishide K, Kato M, Hata Y, Mizumaki K, Kinoshita K, Nonobe Y, Tabata T, Sakamoto T, Kataoka N, Nakatani Y, Ichida F, Mori H, Fukurotani K, Inoue H, Nishida N.
- Journal Title
  
  Circ J.
  
  Volume: 78 Pages: 610-618
- NAID
  130003391006
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591571
[Journal Article] High takeoff of the left main coronary artery at autopsy after sudden unexpected death in a male.2014
- Author(s)
  Nishida N, Hata Y, Kinoshita K.
- Journal Title
  
  Pathology
  
  Volume: 46 Issue: 4 Pages: 361-364
- DOI
  10.1097/pat.0000000000000099
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-24590852
[Journal Article] A590T mutation in KCNQ1 C-terminal helix D decreases IKs channel trafficking and function but not Yotiao interaction.2014
- Author(s)
  Kinoshita K, Komatsu T, Nishide K, Hata Y, Hisajima N, Takahashi H, Kimoto K, Aonuma K, Tushima E, Tabata T, Yoshida T, Mori H, Nishida K, Yamaguchi Y, Ichida F, Fukurotani K, Inoue H, Nishida N.
- Journal Title
  
  J Mol Cell Cardiol
  
  Volume: 72 Pages: 273-280
- DOI
  10.1016/j.yjmcc.2014.03.019
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24590852, KAKENHI-PROJECT-24591040, KAKENHI-PROJECT-24591571, KAKENHI-PROJECT-24790745, KAKENHI-PUBLICLY-25110708, KAKENHI-PROJECT-25293057, KAKENHI-PROJECT-26430012, KAKENHI-PROJECT-26640038
[Journal Article] An autopsy case of infantile-onset vanishing white matter disease related to an EIF2B2 mutation (V85E) in a hemizygous region.2014
- Author(s)
  Hata Y, Kinoshita K, Miya K, Hirono K, Ichida F, Yoshida K, Nishida N.
- Journal Title
  
  Int J Clin Exp Pathol.
  
  Volume: 7 Pages: 3355-62
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591571
[Journal Article] Familial Ebstein's anomaly, left ventricular noncompaction, and ventricular septal defect associated with an MYH7 mutation.2014
- Author(s)
  Hirono K, Hata Y, Ibuki K, Yoshimura N.
- Journal Title
  
  J Thorac Cardiovasc Surg
  
  Volume: 148 Issue: 5 Pages: 223-226
- DOI
  10.1016/j.jtcvs.2014.08.049
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24590852, KAKENHI-PROJECT-25860848
[Journal Article] Modification of KCNH2-encoded cardiac potassium channels by KCNE1 polymorphism.2014
- Author(s)
  Tabata T, Yamaguchi Y, Hata Y, Ichida F, Mori H.
- Journal Title
  
  Circ J
  
  Volume: 78 Pages: 2331-2331
- Data Source
  KAKENHI-PROJECT-24590852
[Journal Article] Glycine/Serine Polymorphism at Position 38 Influences KCNE1 Subunit’s Modulatory Actions on Rapid and Slow Delayed Rectifier K<sup>+</sup> Currents2014
- Author(s)
  Yoshiaki Yamaguchi, Kohki Nishide, Mario Kato, Yukiko Hata, Koichi Mizumaki, Koshi Kinoshita, Yuki Nonobe, Toshihide Tabata, Tamotsu Sakamoto, Naoya Kataoka, Yosuke Nakatani, Fukiko Ichida, Hisashi Mori, Kenkichi Fukurotani, Hiroshi Inoue, MD, Naoki Nishida
- Journal Title
  
  Circ J
  
  Volume: 78 Issue: 3 Pages: 610-618
- DOI
  10.1253/circj.CJ-13-1126
- NAID
  130003391006
- ISSN
  1346-9843, 1347-4820
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23500384, KAKENHI-PROJECT-24590852, KAKENHI-PROJECT-24591040, KAKENHI-PROJECT-24790745
[Journal Article] 14-3-3ε gene variants in a Japanese patient with left ventricular noncompaction and hypoplasia of the corpus callosum.2013
- Author(s)
  Chang B, Gorbea C, Lezin G, Li L, Shan L, Sakai N, Kogaki S, Otomo T, Okinaga T, Hamaoka A, Yu X, Hata Y, Nishida N, Yost HJ, Bowles NE, Brunelli L, Ichida F.
- Journal Title
  
  Gene
  
  Volume: 515 Issue: 1 Pages: 173-180
- DOI
  10.1016/j.gene.2012.12.049
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24590852, KAKENHI-PROJECT-24591571
[Journal Article] Characterization of a novel mutant KCNQ1 channel subunit lacking a large part of the C-terminal domain2013
- Author(s)
  Katsuya Kimoto, Koshi Kinoshita, Tomoki Yokoyama, Yukiko Hata, Takuto Komatsu, Eikichi Tsushima, Kohki Nishide, Yoshiaki Yamaguchi, Koichi Mizumaki, Toshihide Tabata, Hiroshi Inoue, Naoki Nishida, Kenkichi Fukurotani
- Journal Title
  
  Biochemical and Biophysical Research Communications
  
  Volume: 440 Issue: 2 Pages: 283-288
- DOI
  10.1016/j.bbrc.2013.09.075
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23500384, KAKENHI-PROJECT-24590852, KAKENHI-PROJECT-24591040, KAKENHI-PROJECT-24790745
[Journal Article] Outcomes of ChildhoodPulmonary Arterial Hypertension in BMPR2 and ALK1 Mutation Carriers.2012
- Author(s)
  Chida A, Shintani M, Nakanishi T and et al.
- Journal Title
  
  Am J Cardiol.
  
  Volume: 110 Issue: 4 Pages: 586-593
- DOI
  10.1016/j.amjcard.2012.04.035
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22390213, KAKENHI-PROJECT-24591571, KAKENHI-PROJECT-24591599
[Journal Article] Surgical repair of left ventricular noncompaction in a patient with a novel mutation of the myosin heavy chain 7 gene.2012
- Author(s)
  Uchiyama T, Yoshimura K, Kaneko K, Nemoto S, Ichida F, Hata Y, Nishida N.
- Journal Title
  
  Tohoku J. Exp.
  
  Volume: 228 Pages: 301-304
- NAID
  10031135554
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24591571
[Journal Article] Surgical repair of left ventricular noncompaction in a patient with a novel mutation of the myosin heavy chain 7 gene.2012
- Author(s)
  Uchiyama T., Yoshimura K., Kaneko K., Nemoto S., Ichida F., Hata Y., Nishida N.
- Journal Title
  
  Tohoku J Exp Med
  
  Volume: 228 Pages: 301-314
- NAID
  10031135554
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24590852
[Journal Article] A novel missense mutation causing a G487R substitution in the S2-S3 loop of human ether-a-go-go-related gene channel2012
- Author(s)
  Kinoshita K, Yamaguchi Y, Nishide K, Kimoto K, Nonobe Y, Fujita A, Asano K, Tabata T, Mori H, Inoue H, Hata Y, Fukurotani K, Nishida N
- Journal Title
  
  J Cardiovasc Electrophysiol
  
  Volume: 23 Issue: 11 Pages: 1246-1253
- DOI
  10.1111/j.1540-8167.2012.02383.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23500384, KAKENHI-PROJECT-24590852, KAKENHI-PROJECT-24790745
[Journal Article] Identification and characterization of a novel antisense RNA transcribed from the opposite strand of the human blood group ABO gene.2007
- Author(s)
  Hata Y, Kominato Y, Takizawa H
- Journal Title
  
  Transfusion (in press)
- Data Source
  KAKENHI-PROJECT-17590575
[Journal Article] Identification and characterization of a novel antisense RNA transcribed from the opposite strand of the human blood group ABO gene.2007
- Author(s)
  Hata Y, Kominato Y, Takizawa H.
- Journal Title
  
  TRANSFUSION (in press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590575
[Journal Article] Identification and characterization of a novel antisense RNA transcribed from the opposite strand of the human group ABO gene.2007
- Author(s)
  Hata Y, Kominato Y, Takizawa H.
- Journal Title
  
  TRANSFUSION (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590575
[Journal Article] Identification and characterization of a novel antisense RNA transcribed from the opposite strand of the human blood group ABO gene.2007
- Author(s)
  Hata Y, Kominato Y, Takizawa H
- Journal Title
  
  TRANSFUSION (in press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] Identification and characterization of a novel antisense RNA transcribed from the opposite strand of the human group ABO gene.2007
- Author(s)
  Hata Y, Kominato Y, Takizawa H.
- Journal Title
  
  TRANSFUSION (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] Demonstration of A antigen and A allele of ABO histo-blood group in nail in a case with the absence of A antigen and anti-A antibody in blood.2005
- Author(s)
  Michino J, Hata Y, Matsui K, Takizawa H, Kominato Y at el.
- Journal Title
  
  LEGAL MEDICINE 7
  
  Pages: 194-197
- NAID
  10027261079
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590575
[Journal Article] Demonstration of A antigen and A allele of ABO histo-blood group in nail in a case with the absence of A antigen and anti-A antibody in blood.2005
- Author(s)
  Michino J, Hata Y, Matsui K, Takizawa H, Kominato Y. et al.
- Journal Title
  
  LEGAL MEDICINE 7
  
  Pages: 194-197
- NAID
  10027261079
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590575
[Journal Article] Regulation of ABO gene expression.2005
- Author(s)
  Kominato Y, Hata Y, Takizawa H.
- Journal Title
  
  Legal Medicine 7
  
  Pages: 263-265
- NAID
  10027261433
- Data Source
  KAKENHI-PROJECT-17590575
[Journal Article] Demonstration of A antigen and A allele of ABO histo-blood group in nail in a case with the absence of A antigen and anti-A antibody in blood2005
- Author(s)
  Michino J, Hata Y, Matsui K, Takizawa H, Kominato Y. et al.
- Journal Title
  
  LEGAL MEDICINE (in press)
- NAID
  10027261079
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] Regulation of ABO gene expression.2005
- Author(s)
  Kominato Y, Hata Y, Takizawa H
- Journal Title
  
  LEGAL MEDICINE 7
  
  Pages: 263-265
- NAID
  10027261433
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] Regulation of ABO gene expression.2005
- Author(s)
  Kominato Y, Hata Y, Takizawa H.
- Journal Title
  
  LEGAL MEDICINE 7
  
  Pages: 263-265
- NAID
  10027261433
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17590575
[Journal Article] Demonstration of A antigen and A allele of ABO histo-blood group in nail in a case with the absence of A antigen and anti-A antibody in blood.2005
- Author(s)
  Michino J, Hata Y, Matsui K, Takizawa H, Kominato Y. et al.
- Journal Title
  
  Legal Medicine 7
  
  Pages: 194-197
- NAID
  10027261079
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] Regulation of ABO gene expression2005
- Author(s)
  Kominato Y, Hata Y, Takizawa H.
- Journal Title
  
  LEGAL MEDICINE (in press)
- NAID
  10027261433
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] Regulation of ABO gene expression2005
- Author(s)
  Kominato Y, Hata Y, Takizawa H.
- Journal Title
  
  LEGAL MEDICINE 7
  
  Pages: 263-265
- NAID
  10027261433
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17590575
[Journal Article] Demonstration of A antigen and A allele of ABO histo-blood group in nail in a case with the absence of A antigen and anti-A antibody in blood.2005
- Author(s)
  Michino J, Hata Y, Matsui K, Takizawa H, Kominato Y. et al.
- Journal Title
  
  LEGAL MEDICINE 7
  
  Pages: 194-197
- NAID
  10027261079
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] Demonstration of A antigen and A allele of ABO histo-blood group in nail in a case with the absence of A antigen and anti-A antibody in blood.2005
- Author(s)
  Michino J, Hata Y, Matsui K, Takizawa H, Kominato Y at el.
- Journal Title
  
  LEGAL MEDICINE 7
  
  Pages: 194-197
- NAID
  10027261079
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] Regulation of ABO gene expression.2005
- Author(s)
  Kominato Y, Hata Y, Takizawa H.
- Journal Title
  
  Legal Medicine 7
  
  Pages: 263-265
- NAID
  10027261433
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] Regulation of ABO gene expression.2005
- Author(s)
  Kominato Y, Hata Y, Takizawa H.
- Journal Title
  
  LEGAL MEDICINE 7
  
  Pages: 263-265
- NAID
  10027261433
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] Transcriptional regulation of the human ABO histo-blood group gene is dependent upon N box in the upstream of the proximal promoter.2004
- Author(s)
  Kominato Y, Hata Y, Takizawa H, Tsukada J, Nakajima T, Kaneko Y, Kishi K.
- Journal Title
  
  TRANSFUSION 44
  
  Pages: 1741-1749
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] Transcriptional regulation of the human ABO histo-blood group gene is dependent upon N box in the upstream of the proximal promoter.2004
- Author(s)
  Kominato Y, Hata Y, Takizawa H, Tsukada J, Nakajima T, Kaneko Y, Kishi K
- Journal Title
  
  TRANSFUSION 44
  
  Pages: 1741-1749
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] A case of postoperative hemorrhage after a hysterectomy in which a bleeding point of the left uterine artery was identified by postmortem angiography2004
- Author(s)
  Kominato Y, Fujikura T, Hata Y, Matsui K, Takizawa H.
- Journal Title
  
  Legal Med 6(3)
  
  Pages: 187-189
- NAID
  10020570705
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590575
[Journal Article] Transcriptional regulation of the human ABO histo-blood group genes in dependent on the N box upstream of the proximal promoter2004
- Author(s)
  Kominato Y, Hata Y, Matsui K, Takizawa H, Tsukada J, Nakajima T, Kaneko Y, Kishi K.
- Journal Title
  
  Transfusion 44
  
  Pages: 1741-1749
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590575
[Journal Article] A case of postoperative hemorrhage after a hysterectomy in which a bleeding point of the left uterine artery was identified by postmortem angiography.2004
- Author(s)
  Kominato Y, Fujikura T, Hata Y, Matsui K, Takizawa H.
- Journal Title
  
  Legal Medicine 6
  
  Pages: 187-189
- NAID
  10020570705
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590575
[Journal Article] Transcritional regulation of the human ABO histo-blood group genes is dependent upon N box in the upstream of the proximal promoter2004
- Author(s)
  Kominato Y, Hata Y, Takizawa H, Tsukada J, Nakajima T, Kaneko Y, Kishi K.
- Journal Title
  
  TRANSFUSION 44
  
  Pages: 1741-1749
- Data Source
  KAKENHI-PROJECT-16390192
[Journal Article] A case of acute subdural hematoma not accompanied by brain injury2004
- Author(s)
  Kominato Y, Matsui K, Hata Y, Matsui K, Kuwayama N, Ishizawa S, Takizawa H.
- Journal Title
  
  Legal Med 6(4)
  
  Pages: 256-260
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590575
[Journal Article] Transcriptional regulation of the human ABO histo-blood group genes is dependent on the N box upstream of the proximal promoter2004
- Author(s)
  Kominato Y, Hata Y, Matsui K, Takizawa H, Tsukada J, Nakajima T, Kaneko Y, Kishi K.
- Journal Title
  
  Transfusion 44(12)
  
  Pages: 1741-1749
- NAID
  10015685731
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590575
[Journal Article] A case of acute subdural hematoma not accompanied by brain injury2004
- Author(s)
  Kominato Y, Matsui K, Hata Y, Matsui K, Kuwayama N, Ishizawa S, Takizawa H.
- Journal Title
  
  Legal Medicine 6
  
  Pages: 256-260
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590575
[Journal Article] Transcription starting from an alternative promoter leads to the expression of the human ABO histo-blood group antigen.2003
- Author(s)
  Hata Y, Kominato Y, Takizawa H, Tabata S, Michino J, Nishino K, Yasuhara H, Yamamoto F
- Journal Title
  
  Transfusion 43
  
  Pages: 656-662
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590575
[Journal Article] A novel missence mutation causing a G487R substitution in the S2-S3 loop of human ether-a-go-go-related gene channel
- Author(s)
  Kinoshita K, Yamaguchi Y, Nishide K, Kimoto K, Nonobe Y, Fujita A, Asano K, Tabata T, Mori H, Inoue H, Hata Y, Nishida N
- Journal Title
  
  J Cardiovasc Electrophysiol
  
  Volume: (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590734
[Journal Article] Identification and characterization of a novel antisense RNA transcribed from the opposite strand of the human blood group ABO gene.
- Author(s)
  Hata Y, Kominato Y, Takizawa H
- Journal Title
  
  Transfusion (in press)
- Data Source
  KAKENHI-PROJECT-16390192
[Presentation] Pathological and comprehensive genetic investigation of autopsy cases of idiopathic bradyarrhythmia.2024
- Author(s)
  Hata Y, Ichimata S, Hirono K, Yamaguchi Y, Oku Y, Ichida F, Nishida N.
- Organizer
  第88回日本循環器学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-21H03211
[Presentation] 筋強直性ジストロフィーI型突然死剖検例の病理、遺伝子学的背景2023
- Author(s)
  畑由紀子, 一萬田正二郎, 西田尚樹
- Organizer
  第112回日本病理学会総会
- Data Source
  KAKENHI-PROJECT-23K28447
[Presentation] 進行性心室内伝導遅延を呈した若年者突然死の1剖検例.2023
- Author(s)
  畑由紀子，一萬田正二郎，西田尚樹.
- Organizer
  第１０７次日本法医学会学術全国集会
- Data Source
  KAKENHI-PROJECT-21H03211
[Presentation] グラニュリン遺伝子変異に伴う多系統の神経変性疾患関連蛋白の蓄積を認めた早期発症型認知症の一剖検例2023
- Author(s)
  田中遼, 一萬田正二郎, 畑由紀子, 西田尚樹
- Organizer
  第49回臨床神経病理懇話会
- Data Source
  KAKENHI-PROJECT-23K28447
[Presentation] 24.A distinct genotype and phenotypes in pediatric patients with biventricular noncompaction.2023
- Author(s)
  Hirono K, Hata Y, Tsuboi K, Takarada S, Okabe M, Nakaoka H, Ozawa S, Nishida N, Ichida F.
- Organizer
  ASHG 2023
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K07932
[Presentation] 晩期発症小脳変性症の1例2023
- Author(s)
  小川京香, 畑由紀子, 一萬田正二郎, 西田尚樹
- Organizer
  第112回日本病理学会総会
- Data Source
  KAKENHI-PROJECT-23K28447
[Presentation] 19.A distinct genotype and phenotypes in pediatric patients with biventricular noncompaction.2023
- Author(s)
  Hirono K, Hata Y, Tsuboi K, Takarada S, Okabe M, Nakaoka H, Ozawa S, Nishida N, Ichida F.
- Organizer
  Human Genetics Asia 2023
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K07932
[Presentation] 筋強直性筋ジストロフィーI型突然死剖検例の病理および遺伝子学的背景.2023
- Author(s)
  畑由紀子，一萬田正二郎，西田尚樹.
- Organizer
  第１１２回日本病理学会総会
- Data Source
  KAKENHI-PROJECT-21H03211
[Presentation] PSEN1_p.L392Vの2剖検例2023
- Author(s)
  西田尚樹, 畑由紀子, 一萬田正二郎, 吉田幸司
- Organizer
  第64回日本神経病理学会総会学術研究会
- Data Source
  KAKENHI-PROJECT-23K28447
[Presentation] Barlow症候群による心臓突然死の一剖検例2022
- Author(s)
  畑由紀子，一萬田正二郎，西田尚樹
- Organizer
  第44回第69回日本法医学会学術中部近畿地方集会
- Data Source
  KAKENHI-PROJECT-21H03211
[Presentation] Pathological and comprehensive genetic investigation of autopsy cases of idiopathic bradyarrhythmia2022
- Author(s)
  畑由紀子, 一萬田正二郎, 廣野恵一, 山口由明, 市田蕗子, 西田尚樹
- Organizer
  第68回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-21H03211
[Presentation] 右室心筋緻密化障害の臨床像2022
- Author(s)
  廣野恵一, 坪井香緒里, 寳田真也, 岡部真子, 宮尾成明, 仲岡英幸, 伊吹圭二郎, 小澤綾佳, 畑由紀子, 西田尚樹, 市田蕗子
- Organizer
  第58回日本小児循環器学会総会・学術集会
- Data Source
  KAKENHI-PROJECT-22K07932
[Presentation] てんかんの病理と遺伝子検索2022
- Author(s)
  西田尚樹, 畑由紀子
- Organizer
  第5回法医分子病理研究会
- Invited
- Data Source
  KAKENHI-PROJECT-21H03211
[Presentation] Pathological and Comprehensive Genetic Investigation for Autopsy Cases with Advanced Bradyarrhythmia.2021
- Author(s)
  畑由紀子，一萬田正二郎，西田尚樹.
- Organizer
  第85回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-21H03211
[Presentation] Genotype-Phenotype correlation for children with left ventricular noncompaction and congenital heart disease2021
- Author(s)
  Keiichi Hirono, Yukiko Hata, Nariaki Miyao, Mako Okabe, Shinya Takarada, Hideyuki Nakaoka, Keijiro Ibuki, Sayaka Ozawa, Naoki Yoshimura, Naoki Nishida, Fukiko Ichida, and LVNC study collaborators
- Organizer
  第85回日本循環器学会
- Data Source
  KAKENHI-PROJECT-19K08295
[Presentation] Emery-Dreifuss型筋ジストロフィーⅤによる心臓突然死と考えられた一剖検例．2021
- Author(s)
  八若遼太朗，畑由紀子，一萬田正二郎，西田尚樹．
- Organizer
  第110回日本病理学会総会
- Data Source
  KAKENHI-PROJECT-21H03211
[Presentation] Two autopsy cases of sudden unexpected death from Dravet syndrome with novel de novo SCN1A variants.2020
- Author(s)
  西田尚樹，畑由紀子，一萬田正二郎．
- Organizer
  第109回日本病理学会総会オンライン総会
- Data Source
  KAKENHI-PROJECT-18K10119
[Presentation] 原因不明の突然死症例に認めたスプライス変異のmini-gene assayを用いた機能解析．2020
- Author(s)
  畑由紀子，一萬田正二郎，西田尚樹
- Organizer
  第104次日本法医学会学術全国集会
- Data Source
  KAKENHI-PROJECT-18K10119
[Presentation] 神経疾患を伴う小児焼死剖検例．2020
- Author(s)
  西田尚樹，畑由紀子，一萬田正二郎．
- Organizer
  第42回日本法医学会学術中部地方会
- Data Source
  KAKENHI-PROJECT-18K10119
[Presentation] Dravet syndromeの2剖検例2019
- Author(s)
  西田尚樹，畑由紀子，種市尋宙，田中朋美，廣野恵一，五十嵐登，新井田要
- Organizer
  第39回北陸臨床遺伝研究会
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] Titin遺伝子のsplice site variantを認めた若年者突然死の1剖検例．2019
- Author(s)
  西田尚樹，畑由紀子，一萬田正二郎．
- Organizer
  第108回日本病理学会総会
- Data Source
  KAKENHI-PROJECT-18K10119
[Presentation] Two autopsy cases of sudden unexpected death with Dravet syndrome related to novel de novo SCN1A variants.2019
- Author(s)
  西田尚樹，畑由紀子，一萬田正二郎．
- Organizer
  第60回日本神経病理学会総会学術研究会
- Data Source
  KAKENHI-PROJECT-18K10119
[Presentation] A distinct phenotype of fetal patients with left ventricular noncompaction in a large cohort in Japan.2019
- Author(s)
  Hirono K, Hata Y, Takarada S, Okabe M, Miyao N, Nakaoka H, Ibuki K, Ozawa S, Nishida N, Ichida F.
- Organizer
  ESC congress 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08295
[Presentation] Two autopsy cases of sudden unexpected death with Dravet syndrome related to novel de novo SCN1A variants.2019
- Author(s)
  西田尚樹，畑由紀子，一萬田正二郎
- Organizer
  第60回日本神経病理学会総会学術研究会
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] Titin遺伝子のsplice site variantを認めた若年者突然死の1剖検例．2019
- Author(s)
  西田尚樹，畑由紀子，一萬田正二郎
- Organizer
  第108回日本病理学会総会
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] Sudden unexpected death with rare compound heterozygous variants in PRICKLE1.2019
- Author(s)
  畑由紀子，一萬田正二郎，小野塚昇，西田尚樹
- Organizer
  第103次日本法医学会学術全国集会
- Data Source
  KAKENHI-PROJECT-18K10119
[Presentation] 心筋内微小炎症細胞湿潤巣は遺伝性心筋症の初期病変である．2019
- Author(s)
  畑由紀子，廣野恵一，山口由明，市田蕗子，奥祐子，一萬田正二郎，西田尚樹．
- Organizer
  第108回日本病理学会総会
- Data Source
  KAKENHI-PROJECT-18K10119
[Presentation] Non-ischemic minimal lesions in the heart may predict to have early inherited cardiomyopathy with arrhythmogenic potential.2018
- Author(s)
  Hata Y, Yamaguchi Y, Hirono K, Ichida F, Nishida N.
- Organizer
  第65回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-18K10119
[Presentation] 心臓突然死のmolecular aotopsy2018
- Author(s)
  西田尚樹，畑由紀子
- Organizer
  第66回日本心臓病学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18K10119
[Presentation] An autopsy case of incipient Pick's disease with long standinghistory of schizopherenia2018
- Author(s)
  Okada K, Hata Y, Yoshida K, Takahashi T, Takayanagi Y, Nishida N
- Organizer
  19th International Congress of Neurupathology; Tokyo
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] Non-ischemic minimal lesions in the heart may predict to have cardiomyopathy-related genetic variants.2018
- Author(s)
  Hata Y, Nishida N, Hirono K, Yamaguchi Y, Ichida F.
- Organizer
  24th Congress of the International Academy of Legal Medicine (IALM)
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K10119
[Presentation] Early tau pathology in young Japanese forensic autopsy series: Frequency and association with APOE genotype and suicidal risk.2018
- Author(s)
  Yoshida K, Hata Y, Terasawa H, Shimizu H, Uehara T, Nakatsuji Y, Kita Y, Nishida N
- Organizer
  19th International Congress of Neurupathology; Tokyo
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] Autopsy of an Elderly Man With Incidentally Diagnosed TDP-43 Proteinopathy2018
- Author(s)
  Hata Y, Yoshida K, Nishida N
- Organizer
  19th International Congress of Neurupathology; Tokyo
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] 認知症関連病理を有した50才以下自殺剖検例．2017
- Author(s)
  西田尚樹，畑由紀子，木下耕史．
- Organizer
  第39回日本法医学会学術中部地方集会；2017 Oct 14；岐阜．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] 法医解剖における進行性核上性麻痺の臨床病理.2017
- Author(s)
  西田尚樹，畑由紀子，吉田幸司
- Organizer
  第101次日本法医学会学術全国集会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 若年者冠状動脈硬化症の臨床病理学的特徴2017
- Author(s)
  西田尚樹，畑由紀子，木下耕史．
- Organizer
  第106回日本病理学会総会；2017 Apr 27-29；東京．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] 交通事故に関連した緊急帝王切開にて出生後，死亡した胎児剖検例．2017
- Author(s)
  西田尚樹，畑由紀子．
- Organizer
  第24回東北神経病理研究会；2017 Oct 7；仙台．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] Lewy body diseaseの発生，進展様式に関する病理学的検討．2017
- Author(s)
  水野将治，畑由紀子，吉田幸司，西田尚樹
- Organizer
  第106回日本病理学会総会；2017 Apr 27-29；東京．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] 若年者冠状動脈硬化症の臨床病理学的特徴2017
- Author(s)
  西田尚樹，畑由紀子，木下耕史．
- Organizer
  第106回日本病理学会総会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 若年者の早期アルツハイマー病変についての検討：法医解剖症例における自殺との関連性．2017
- Author(s)
  吉田幸司，畑由紀子，木下耕史，中辻裕司，西田尚樹
- Organizer
  第58回日本神経病理学会総会学術研究会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 心臓突然死症例のmolecular autopsy．2017
- Author(s)
  畑由紀子，西田尚樹
- Organizer
  第101次日本法医学会学術全国集会
- Invited
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 40才未満冠状動脈硬化症剖検例の検討．2017
- Author(s)
  西田尚樹，畑由紀子．
- Organizer
  第65回日本心臓病学会学術集会 ;2017 Sep 29- Oct 1; 大阪．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] 次世代シーケンサーを用いた心臓突然死症例の遺伝子解析.2017
- Author(s)
  畑由紀子，西田尚樹．
- Organizer
  NGS現場の会・第5回研究会；2017 May 22-24；仙台．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] Phenotype-Genotype correlations in the fetal patients with left ventricular noncompaction.2017
- Author(s)
  Hirono K, Hata Y, Ozawa S, Wang C, Toda T, Momoi N, Inuzuka R, Hiroki N, Sakaguchi H, Kurosaki K, Okabe M, Miyao N, Nakaoka H, Ibuki K, Saito K, Nishida N, Ichida F.
- Organizer
  The 13th Japan-China-Korea Pediatric Heart Forum with Asian Pacific Symposium
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 次世代シーケンサーを用いた心臓突然死症例の遺伝子解析2017
- Author(s)
  畑由紀子，西田尚樹
- Organizer
  NGS現場の会・第5回研究会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 法医解剖における進行性核上性麻痺の臨床病理．2017
- Author(s)
  西田尚樹，畑由紀子，吉田幸司．
- Organizer
  第101次日本法医学会学術全国集会；2017 Jun 7-9；岐阜．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] 連続法医解剖例を用いたLewy body diseaseの早期病変，進展様式に関する研究．2017
- Author(s)
  水野将治，畑由紀子，吉田幸司，西田尚樹
- Organizer
  第58回日本神経病理学会総会学術研究会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 病早期と考えられる進行性核上性麻痺（PSP）の一剖検例．2017
- Author(s)
  西田尚樹，畑由紀子，吉田幸司．
- Organizer
  第45回臨床神経病理懇話会；2017 Nov 4-5；米子．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] 病早期と考えられる進行性核上性麻痺（PSP）の一剖検例．2017
- Author(s)
  西田尚樹，畑由紀子，吉田幸司
- Organizer
  第45回臨床神経病理懇話会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 連続法医解剖例を用いたLewy body diseaseの早期病変，進展様式に関する研究．2017
- Author(s)
  水野将治，畑由紀子，吉田幸司，西田尚樹．
- Organizer
  第58回日本神経病理学会総会学術研究会；2017 Jun 1-3；東京．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] Postmortem genetic analysis for sudden unexpected death - the current status and future perspectives-2017
- Author(s)
  畑由紀子，木下耕史，西田尚樹
- Organizer
  第81回日本循環器学会学術集会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] Postmortem genetic analysis for sudden unexpected death -the current status and future perspectives-2017
- Author(s)
  畑由紀子，木下耕史，西田尚樹
- Organizer
  第81回日本循環器学会学術集会；2017 Mar 17-19；金沢．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] Sudden unexpected death in parkinson’s disease: neurogenic or cardiac death ?2017
- Author(s)
  Nishida N, Hata Y, Yoshida K.
- Organizer
  第64回日本不整脈心電学会学術大会；2017 Sep 14-17；横浜．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] 40才未満冠状動脈硬化症剖検例の検討．2017
- Author(s)
  西田尚樹，畑由紀子
- Organizer
  第65回日本心臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 広範なtau pathologyを伴った陳旧性多発脳梗塞の1剖検例．2017
- Author(s)
  西田尚樹，畑由紀子，吉田幸司
- Organizer
  第24回東北神経病理研究会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] A novel MYH7 and CD36 gene variants in a fetus with left ventricular noncompaction; crosstalk between beta myosin heavy chain and fatty acid translocase deteriorates heart failure after surgical intervention.2017
- Author(s)
  廣野恵一，酒井武彦，小澤綾佳，畑由紀子，西田直徳，岡部真子，宮尾成明，齋藤和由，芳村直樹，西田尚樹，市田蕗子
- Organizer
  日本人類遺伝学会第62回大会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] Phenotype-Genotype correlations in the fetal patients with left ventricular noncompaction.2017
- Author(s)
  Hirono K, Hata Y, Ozawa S, Wang C, Toda T, Momoi N, Inuzuka R, Hiroki N, Sakaguchi H, Kurosaki K, Okabe M, Miyao N, Nakaoka H, Ibuki K, Saito K, Nishida N, Ichida F.
- Organizer
  The 13th Japan-China-Korea Pediatric Heart Forum with Asian Pacific Symposium; 2017 July 9; Hamamatsu
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] 心臓突然死症例のmolecular autopsy．2017
- Author(s)
  畑由紀子，西田尚樹．
- Organizer
  第101次日本法医学会学術全国集会；2017 Jun 7-9；岐阜．
- Invited
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] 高度の嗜銀顆粒病変を主体とするtauopathyの1例．2017
- Author(s)
  西田尚樹，畑由紀子，吉田幸司．
- Organizer
  第9回日本神経病理学会東海・北陸地方会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 認知症関連病理を有した50才以下自殺剖検例．2017
- Author(s)
  西田尚樹，畑由紀子，木下耕史
- Organizer
  第39回日本法医学会学術中部地方集会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 若年者の早期アルツハイマー病変についての検討：法医解剖症例における自殺との関連性．2017
- Author(s)
  吉田幸司，畑由紀子，木下耕史，中辻裕司，西田尚樹．
- Organizer
  第58回日本神経病理学会総会学術研究会；2017 Jun 1-3；東京．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] MYH7遺伝子変異とCD36遺伝子変異が見いだされた心筋緻密化障害の一例．2017
- Author(s)
  廣野恵一，酒井武彦，小澤綾佳，畑由紀子，西田直徳，岡部真子，宮尾成明，齋藤和由，芳村直樹，西田尚樹，市田蕗子
- Organizer
  第26回日本小児心筋疾患学会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] Sudden unexpected death in parkinson’s disease: neurogenic or cardiac death ?2017
- Author(s)
  Nishida N, Hata Y, Yoshida K.
- Organizer
  第64回日本不整脈心電学会学術大会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 交通事故に関連した緊急帝王切開にて出生後，死亡した胎児剖検例．2017
- Author(s)
  西田尚樹，畑由紀子．
- Organizer
  第24回東北神経病理研究会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 高度の嗜銀顆粒病変を主体とするtauopathyの1例．2017
- Author(s)
  西田尚樹，畑由紀子，吉田幸司．
- Organizer
  第9回日本神経病理学会東海・北陸地方会；2017 Sep 9；名古屋．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] 広範なtau pathologyを伴った陳旧性多発脳梗塞の1剖検例．2017
- Author(s)
  西田尚樹，畑由紀子，吉田幸司．
- Organizer
  第24回東北神経病理研究会；2017 Oct 7；仙台．
- Data Source
  KAKENHI-PROJECT-17K09263
[Presentation] Lewy body diseaseの発生，進展様式に関する病理学的検討2017
- Author(s)
  水野将治，畑由紀子，吉田幸司，西田尚樹
- Organizer
  第106回日本病理学会総会
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] Clinical features and prognosis of pediatic patients with left ventricular noncompaction.2016
- Author(s)
  Hirono K, Takasaki A, Hata Y, Okabe M, Nakaoka H, Ibuki K, Ozawa S, Nishida N, Ichida F.
- Organizer
  European society for cardiology congress 2016
- Place of Presentation
  Rome
- Year and Date
  2016-08-26
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] てんかん関連急死例に対する次世代型シーケンサーを用いた心疾患関連遺伝子検索．2016
- Author(s)
  西田尚樹，畑由紀子，吉田幸司，木下耕史．
- Organizer
  第57回日本神経病理学会総会学術研究会
- Place of Presentation
  弘前
- Year and Date
  2016-06-01
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] Postmortem genetic analysis of sudden unexplained death syndrome under 50 years of age : a next-generation sequencing study.2016
- Author(s)
  Hata Y, Kinoshita K, Mizumaki K, Yamaguchi Y, Misaki T, Nishida N.
- Organizer
  第63回日本不整脈心電学会学術大会
- Place of Presentation
  札幌
- Year and Date
  2016-07-14
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] β-blockerの過剰服用が疑われた1剖検例．2016
- Author(s)
  19) 西田尚樹，畑由紀子，木下耕史
- Organizer
  第38回日本法医学会学術中部地方集会
- Place of Presentation
  福井
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 産褥期に発症した心不全で明らかになった，左室心筋緻密化障害の一例．2016
- Author(s)
  木下聡，島袋祐士，平辻知也，知念清治，廣野恵一，市田蕗子，畑由紀子，西田尚樹．
- Organizer
  第120回日本循環器学会九州地方会
- Place of Presentation
  大分
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] SCN5A(R1193Q)変異が引き起こすNa+チャネル電流の温度依存的変化に対する影響．2016
- Author(s)
  木下耕史，中田崇仁，田端俊英，畑由紀子，西田尚樹
- Organizer
  第100次日本法医学会学術全国集会
- Place of Presentation
  東京
- Year and Date
  2016-06-15
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 遺伝子解析で診断した特発性心筋症の早期像を呈していると考えられた2剖検例．2016
- Author(s)
  畑由紀子，木下耕史，西田尚樹．
- Organizer
  第105回日本病理学会総会
- Place of Presentation
  仙台
- Year and Date
  2016-05-12
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 若年性左室心筋緻密化障害におけるサルコメア遺伝子異常とその臨床的意義.2015
- Author(s)
  高崎麻美, 廣野恵一, 畑由紀子，仲岡英幸，伊吹圭二郎，小澤綾佳，西田尚樹，芳村直樹，関根道和，市田蕗子
- Organizer
  第1回日本心筋症研究会
- Place of Presentation
  東京
- Year and Date
  2015-07-04
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] TAZ遺伝子変異を伴う左室心筋緻密化障害における臨床遺伝学的検討.2015
- Author(s)
  廣野恵一，畑由紀子，宮尾成明，高崎麻美，仲岡英幸，伊吹圭二郎，小澤綾佳，西田尚樹，市田蕗子
- Organizer
  第1回日本心筋症研究会
- Place of Presentation
  東京
- Year and Date
  2015-07-04
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] A novel ACTC1 gene mutation in a young boy with left ventricular noncompaction and lethal ventricular arrhythmias.2015
- Author(s)
  Yoshida Y, Yoshida S, Suzuki T, Nakamura Y, Hata Y, Nishida N.
- Organizer
  第30回日本不整脈学会学術大会・第32回日本心電学会学術集会合同学術大会
- Place of Presentation
  京都
- Year and Date
  2015-07-28
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] Targeted Next-generation Sequencing for Postmortem Molecular Analysis of Sudden Cardiac Death.2015
- Author(s)
  Hata Y, Kinoshita K, Ichida F, Hirono K, Mori H, Nishida N.
- Organizer
  第79回日本循環器学会学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-04-24
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 若年性左室心筋緻密化障害におけるサルコメア遺伝子異常とその臨床的意義.2015
- Author(s)
  12)高崎麻美、廣野恵一、畑由紀子、仲岡英幸、伊吹圭二郎、小澤綾佳、西田尚樹、芳村直樹、関根道和、市田蕗子
- Organizer
  第1回日本心筋症研究会
- Place of Presentation
  東京
- Year and Date
  2015-07-04
- Data Source
  KAKENHI-PROJECT-15K09685
[Presentation] 胎児期・新生児期発症の左室心筋緻密化障害における臨床遺伝学的検討2015
- Author(s)
  廣野恵一, 畑由紀子, 宮尾成明, 仲岡英幸, 高崎麻美, 伊吹圭二郎, 小澤綾佳, 西田尚樹, 市田蕗子.
- Organizer
  第51回日本小児循環器学会総会・学術集会
- Place of Presentation
  東京
- Year and Date
  2015-07-16
- Data Source
  KAKENHI-PROJECT-15K09685
[Presentation] 家族歴による早期遺伝子診断と介入を行ないえたBarth症候群の乳児例2015
- Author(s)
  趙　麻未, 鮎沢　衛, 加藤雅崇, 渡邊拓史, 小森暁子, 阿部百合子, 神保詩乃, 神山　浩, 高橋昌里, 廣野恵一, 市田蕗子, 畑由紀子, 西田尚樹
- Organizer
  第51回日本小児循環器学会総会・学術集会
- Place of Presentation
  東京
- Year and Date
  2015-07-16
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] Sarcomere gene mutations in the patients with left ventricular noncompaction.2015
- Author(s)
  Hirono K, Takasaki A, Hata Y, Nakaoka H, Ibuki K, Ozawa S, Sekine M, Yoshimura N, Nishida N, Ichida F.
- Organizer
  第79回日本循環器学会学術集会
- Place of Presentation
  大阪
- Year and Date
  2015-04-24
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 心臓特異的転写因子TBX5に遺伝子変異を認めた心臓突然死の2剖検例．2015
- Author(s)
  畑由紀子，木下耕史，西田尚樹．
- Organizer
  第37回日本法医学会学術中部地方集会
- Place of Presentation
  甲府
- Year and Date
  2015-10-16
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] Electrophysiological characterization of a novel SCN5A mutant identified in a Brugada syndrome patient.2015
- Author(s)
  Takahashi H, Kinoshita K, Hata Y, Yoshida S, Fujita H, Murai K, Yamaguchi Y, Mizumaki K, Inoue H, Nishida N, Tabata T.
- Organizer
  第120回日本解剖学会総会･全国学術集会・第92回日本生理学会大会
- Place of Presentation
  神戸
- Year and Date
  2015-05-21
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] TAZ遺伝子変異を伴う左室心筋緻密化障害における臨床遺伝学的検討.2015
- Author(s)
  11)廣野恵一、畑由紀子、宮尾成明、高崎麻美、仲岡英幸、伊吹圭二郎、小澤綾佳、西田尚樹、市田蕗子.
- Organizer
  第1回日本心筋症研究会、
- Place of Presentation
  東京
- Year and Date
  2015-07-04
- Data Source
  KAKENHI-PROJECT-15K09685
[Presentation] 胎児期・新生児期発症の左室心筋緻密化障害における臨床遺伝学的検討.2015
- Author(s)
  廣野恵一, 畑由紀子, 宮尾成明, 仲岡英幸, 高崎麻美, 伊吹圭二郎, 小澤綾佳, 西田尚樹, 市田蕗子
- Organizer
  第51回日本小児循環器学会総会・学術集会
- Place of Presentation
  東京
- Year and Date
  2015-07-16
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] 入浴中の急死例における次世代シーケンサーを用いた遺伝子解析2015
- Author(s)
  畑由紀子，木下耕史，西田尚樹
- Organizer
  第99次日本法医学会学術全国集会
- Place of Presentation
  高知
- Year and Date
  2015-06-10
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] ジストロフィン（DMD）遺伝子のミスセンス変異を認めた若年性心臓突然死症例．2015
- Author(s)
  畑由紀子，水牧功一，城宝秀司，市田蕗子，西田尚樹
- Organizer
  第63回日本心臓病学会学術集会
- Place of Presentation
  横浜
- Year and Date
  2015-09-18
- Data Source
  KAKENHI-PROJECT-15K08867
[Presentation] Sarcomere gene mutations in the patients with left ventricular noncompaction2015
- Author(s)
  10)Keiichi Hirono, Asami Takasaki, Yukiko Hata, Hideyuki Nakaoka, Keijiro Ibuki, Sayaka Ozawa, Michikazu Sekine, Naoki Yoshimura, Naoki Nishida, and Fukiko Ichida
- Organizer
  第79回日本循環器学会
- Place of Presentation
  大阪
- Year and Date
  2015-04-25
- Data Source
  KAKENHI-PROJECT-15K09685
[Presentation] 新生児期に心不全にて発症しサルコメア遺伝子の二重変異異常を認めた左室心筋緻密化障害の一例.2014
- Author(s)
  廣野恵一，仲岡英幸，伊吹圭二郎，小澤綾佳，市田蕗子，畑由紀子，西田尚樹，小垣滋豊，福嶌教偉.
- Organizer
  第311回日本小児科学会北陸地方会
- Place of Presentation
  福井
- Year and Date
  2014-06-08
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] 次世代シークエンサーを用いた心臓性突然死症例の遺伝子解析.2014
- Author(s)
  畑由紀子，木下耕史，西田尚樹
- Organizer
  第36回日本法医学会学術中部地方集会
- Place of Presentation
  愛知
- Year and Date
  2014-10-18
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] 家族歴による早期診断と遺伝子解析を行ないえたBarth症候群の乳児例.2014
- Author(s)
  趙麻未，鮎沢衛，加藤雅崇，渡邉拓史，小森暁子，阿部百合子，神保詩乃，神山浩，廣野恵一，市田蕗子，畑由紀子，西田尚樹．
- Organizer
  第23回日本小児心筋疾患学会
- Place of Presentation
  東京
- Year and Date
  2014-10-11
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] Functional Characterization of KCNQ1 Channel Subunit with an A590T Mutation.2013
- Author(s)
  Kinoshita K, Komatsu T, Kimoto K, Nishide K, Tabata F, Ichda F, Yamaguchi Y, Nishida K, Inoue H, Hata Y, Nishida N
- Organizer
  Basic Cardiovascular Sciences 2013
- Place of Presentation
  Las Vegas
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] Optimal timing of initial treatment in severe Kawasaki disease: A sub-analysis of the RAISE study.2013
- Author(s)
  6. Ikeda K, Saji T, Kobayashi T, Yahata T, Okamoto A, Arakawa H, Kato T, Hara T, Ogawa S, Miura M, Nomura , Fuse S, Ichida F, Ayusawa M, Abe J, Morikawa A, Hamaoka K.
- Organizer
  47th Annual Meeting of AEPC
- Place of Presentation
  London, 英国
- Data Source
  KAKENHI-PROJECT-24591571
[Presentation] Vanishing white matter disease (VWMD)の1剖検例2013
- Author(s)
  畑由紀子、木下耕史、西田尚樹
- Organizer
  第102回日本病理学会総会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] 突然死した筋強直性ジストロフィー症の1剖検例2013
- Author(s)
  畑由紀子、木下耕史、西田尚樹
- Organizer
  第97次日本法医学会学術全国集会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] 遺伝子検査でKCNE1遺伝子にD85N SNPを有するQT延長症候群例におけるQT/RR関係，T-Wave peak-to-end/RR関係の解析2012
- Author(s)
  山口由明，水牧功一，西田邦洋，坂本　有，片岡直也，木下耕史，畑由紀子，市田蕗子，西田尚樹，井上　博
- Organizer
  第29回日本心電学会学術集会
- Place of Presentation
  千葉
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] Abnormal repolarization dynamics in Patients with G38S single nucleotide polymorphism of KCNE1 Gene.2012
- Author(s)
  Yamaguchi Y., Mizumaki K., Nishida K., Iwamoto J., Nakatani Y., Kataoka N., Hata Y., Ichida F., Nishida N., Inoue H.
- Organizer
  Heart Rhythm Society
- Place of Presentation
  Boston USA
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] 心臓性突然死症例において認められたHERG遺伝子の新規M579fs＋75Mフレームシフト変異の機能解析2012
- Author(s)
  畑由紀子，森　寿，田中亜由美，田端俊英，下村岳司，藤田洋介，木下耕史，山口由明，水牧功一，井上　博，西田尚樹
- Organizer
  第60回日本心臓病学会学術集会
- Place of Presentation
  金沢
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] Genetic Basis Of Left Ventricular Noncompaction2011
- Author(s)
  Ichida F, Hata Y, Chang B, Ozawa S, Saito K, Ibuki K, Watanabe K, Hirono H, Nishida N, Bowles NE, Miyawaki T
- Organizer
  The 84^<th> Scientific sessions of AHA 2011
- Place of Presentation
  Orlando
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] PSP-perkinsonismの2剖検例2011
- Author(s)
  中川貴美子,畑由紀子,西田尚樹
- Organizer
  第100回日本病理学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] Pathologically proven corticobasal degenerationと考えられた1例2011
- Author(s)
  西田尚樹,畑由紀子,木下耕史
- Organizer
  第52回神経病理学会総会学術研究会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 未治療の進行胃癌に合併したペラグラ脳症の一剖検例2011
- Author(s)
  竹内結,畑由紀子,西田尚樹
- Organizer
  第100回日本病理学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] ビタミン欠乏を伴っていたと考えられる未治療進行胃癌の一剖検例2011
- Author(s)
  西田尚樹,畑由紀子,木下耕史
- Organizer
  第3回日本神経病理学会東海・北陸地方会
- Place of Presentation
  愛知
- Year and Date
  2011-09-10
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 複数のchannel異常と心肥大を認めた心臓性突然死の一例2011
- Author(s)
  畑由紀子,木下耕史,西田尚樹
- Organizer
  第95次日本法医学会学術全国集会
- Place of Presentation
  福島
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] パーキンソン病患者の転倒死亡事故の1例2011
- Author(s)
  井上哲,畑由紀子,西田尚樹
- Organizer
  第100回日本病理学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 突然死の家族歴を有し早期再分極とQT延長症候群が混在したSCN5A遺伝子異常の1家系2011
- Author(s)
  山口由明,水牧功一,西田邦洋,岩本譲太郎,中谷洋介,片岡直也,坂本有,井上博,畑由紀子,西田尚樹
- Organizer
  第24回心臓性急死研究会
- Place of Presentation
  品川
- Year and Date
  2011-12-17
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] Genetic Basis of Left Ventricular Noncompaction2011
- Author(s)
  Ichida F, Hata Y, Chang B, Ozawa S, Saito K, Ibuki K, Watanabe K, Nishida N
- Organizer
  ESC Congress 2011
- Place of Presentation
  Paris
- Year and Date
  2011-08-28
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 病原性大腸菌O111感染後に発症した急性脳症2011
- Author(s)
  西田尚樹,畑由紀子,木下耕史
- Organizer
  第18回東北神経病理研究会
- Place of Presentation
  秋田
- Year and Date
  2011-10-29
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] パーキンソン病患者の転倒死亡事故の1例2011
- Author(s)
  井上哲, 畑由紀子, 西田尚樹
- Organizer
  第100回日本病理学会総会
- Place of Presentation
  東京
- Year and Date
  2011-04-30
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] K channel異常を認めた若年者の心臓性突然死の一例2011
- Author(s)
  畑由紀子, 木下耕史, 西田尚樹
- Organizer
  第100回日本病理学会総会
- Place of Presentation
  東京
- Year and Date
  2011-04-30
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] Pathologically proven corticobasal degenerationと考えられた1例2011
- Author(s)
  西田尚樹, 畑由紀子, 木下耕史
- Organizer
  第52回日本神経病理学会総会
- Place of Presentation
  京都
- Year and Date
  2011-06-02
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] ビタミン欠乏を伴っていたと考えられる未治療進行胃癌の一剖検例2011
- Author(s)
  西田尚樹, 畑由紀子, 木下耕史
- Organizer
  第3回日本神経病理学会東海・北陸地方会
- Place of Presentation
  東京
- Year and Date
  2011-09-11
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 先天性QT延長症候群LQT1とLQT2における心拍依存性のQT間隔とT波高の変動の検討2011
- Author(s)
  山口由明,水牧功一,西田邦洋,井上博,齋藤和由,伊吹圭二郎,小澤綾佳,渡辺一洋,市田蕗子,畑由紀子,西田尚樹
- Organizer
  第47回日本小児循環器学会
- Place of Presentation
  福岡
- Year and Date
  2011-07-07
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] Identification and characterization of a novel mutation M579fs+75X in HERG2011
- Author(s)
  Hata Y, Mori H, Tanaka A, Fujita Y, Shimomura T, Tabata T, Kinoshita K, Nishida N
- Organizer
  The 4th Asia Pacific Heart Rhythm Society Scientific Session(APHRS 2011)
- Place of Presentation
  Fukuoka
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] Diffuse neurofibrillary tangle with calcificationと考えられた1剖検例2011
- Author(s)
  西田尚樹,畑由紀子
- Organizer
  第100回日本病理学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] K channel異常を認めた若年者の心臓性突然死の一例2011
- Author(s)
  畑由紀子,木下耕史,西田尚樹
- Organizer
  第100回日本病理学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] Diffuse neurofibrillary tangle with calcificationと考えられた1剖検例2011
- Author(s)
  西田尚樹, 畑由紀子
- Organizer
  第100回日本病理学会総会
- Place of Presentation
  東京
- Year and Date
  2011-04-28
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 未治療の進行胃癌に合併したペラグラ脳症の一剖検例2011
- Author(s)
  竹内結, 畑由紀子, 西田尚樹
- Organizer
  第100回日本病理学会総会
- Place of Presentation
  東京
- Year and Date
  2011-04-30
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] アルコール性中枢神経障害を背景とした焼死の1例2011
- Author(s)
  西田尚樹,畑由紀子,木下耕史
- Organizer
  第95次日本法医学会学術全国集会
- Place of Presentation
  福島
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] PSP-perkinsonismの2剖検例2011
- Author(s)
  中川貴美子, 畑由紀子, 西田尚樹
- Organizer
  第100回日本病理学会総会
- Place of Presentation
  東京
- Year and Date
  2011-04-30
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 起始部の異常走行を伴う右冠状動脈左冠状動脈洞起始の2例2010
- Author(s)
  西田尚樹, 畑由紀子
- Organizer
  第136回東海・第121回北陸合同地方会
- Place of Presentation
  金沢エクセルホテル東急(石川県)
- Year and Date
  2010-11-07
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 起始部の異常走行を伴う右冠状動脈左冠状動脈洞起始の2例2010
- Author(s)
  西田尚樹,畑由紀子
- Organizer
  第136回東海・第121回北陸合同地方会
- Place of Presentation
  石川
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 神経疾患を背景因子に有すると考えられた高齢者の自殺例2010
- Author(s)
  西田尚樹,畑由紀子,大谷真紀,千葉孝,吉岡尚文
- Organizer
  第94次日本法医学会学術全国集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 神経変性疾患を背景とした高齢者転倒死亡事故の一例2010
- Author(s)
  畑由紀子,木下耕史,西田尚樹
- Organizer
  第32回日本法医学会学術中部地方集会
- Place of Presentation
  富山
- Year and Date
  2010-10-23
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] NFT predominant form of dementia of Alzheimer typeと考えられた1例2010
- Author(s)
  西田尚樹,畑由紀子
- Organizer
  第99回日本病理学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] Na channel異常を認めた若年者突然死の一例2010
- Author(s)
  畑由紀子,西田尚樹,木下耕史
- Organizer
  第94次日本法医学会学術全国集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 非定型的な病変分布を認めた高齢者PSPの一例2010
- Author(s)
  西田尚樹,畑由紀子,木下耕史
- Organizer
  第17回東北神経病理研究会
- Place of Presentation
  宮城
- Year and Date
  2010-11-13
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 神経疾患を背景因子に有すると考えられた高齢者の自殺例2010
- Author(s)
  西田尚樹, 畑由紀子
- Organizer
  第94次日本法医学会学術全国集会
- Place of Presentation
  タワーホール船堀(東京都)
- Year and Date
  2010-06-24
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 起始部の大動脈壁内走行を伴う右冠状動脈左冠状動脈洞起始の2例2010
- Author(s)
  中曽根泰人,畑由紀子,西田尚樹
- Organizer
  第99回日本病理学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 神経変性疾患を背景とした高齢者転倒死亡事故の一例2010
- Author(s)
  畑由紀子, 西田尚樹
- Organizer
  第32回日本法医学会学術中部地方集会
- Place of Presentation
  県民会館(富山県)
- Year and Date
  2010-10-23
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] NFT predominant form of dementia of Alzheimer typeと考えられた1例2010
- Author(s)
  西田尚樹, 畑由紀子
- Organizer
  第99回日本病理学会総会
- Place of Presentation
  京王プラザホテル(東京都)
- Year and Date
  2010-04-28
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] Na channel異常を認めた若年者突然死の一例2010
- Author(s)
  畑由紀子, 西田尚樹
- Organizer
  第94次日本法医学会学術全国集会
- Place of Presentation
  タワーホール船堀(東京都)
- Year and Date
  2010-06-24
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 非定型的な病変分布を認めた高齢者PSPの一例2010
- Author(s)
  西田尚樹, 畑由紀子
- Organizer
  第17回東北神経病理研究会
- Place of Presentation
  東北大学(宮城県)
- Year and Date
  2010-11-13
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] Dementia with Lewy bodies(DLB)と考えられた1例2010
- Author(s)
  守吉秀行,畑由紀子,西田尚樹
- Organizer
  第99回日本病理学会総会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 中心性橋髄鞘崩壊症の一例2009
- Author(s)
  西田尚樹, 畑由紀子
- Organizer
  第93次日本法医学会学術全国集会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 外傷受傷後に急死したと考えられる一例2009
- Author(s)
  西田尚樹, 畑由紀子
- Organizer
  第31回日本法医学会学術中部地方集会
- Place of Presentation
  浜松
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 認知症発症後2年で死亡した1例2009
- Author(s)
  西田尚樹,畑由紀子
- Organizer
  第16回日本神経病理学会東北地方会
- Place of Presentation
  山形
- Year and Date
  2009-11-21
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] 躁鬱病の経過中に認知症を発症した1剖検例2009
- Author(s)
  西田尚樹,畑由紀子
- Organizer
  第16回日本神経病理学会東北地方会
- Place of Presentation
  山形
- Year and Date
  2009-11-21
- Data Source
  KAKENHI-PROJECT-21590734
[Presentation] Sarcomere gene mutations in left ventricular noncompaction.
- Author(s)
  Takasaki A, Hata Y, Hirono K, Nakaoka H, Ibuki K, Ozawa S, Yoshimura N, Nishida N, Ichida F.
- Organizer
  The 87th Scientific sessions of AHA 2014
- Place of Presentation
  Chicago
- Year and Date
  2014-11-15 – 2014-11-19
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] Sarcomere gene mutations in left ventricular noncompaction.
- Author(s)
  12.Asami Takasaki, Yukiko Hata, Keiichi Hirono, Hideyuki Nakaoka, Keijiro Ibuki, Sayaka Ozawa, Naoki Yoshimura, Naoki Nishida, Fukiko Ichida.
- Organizer
  The 87th Scientific sessions of AHA 2014
- Place of Presentation
  Chicago,
- Year and Date
  2014-11-15 – 2014-11-19
- Data Source
  KAKENHI-PROJECT-24591571
[Presentation] 胎児期に心不全を契機に発見されたMYH7遺伝子変異を有する左室心筋緻密化障害の一例．
- Author(s)
  廣野恵一，野村泰久，畑由紀子，仲岡英幸，伊吹圭二郎，小澤綾佳，桃井伸緒，西田尚樹，市田蕗子，足立雄一
- Organizer
  第50回日本小児循環器学会
- Place of Presentation
  岡山
- Year and Date
  2014-07-03 – 2014-07-05
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] Postmortem molecular analysis of long QT syndrome-associated genes for sudden cardiac death in 2 to 50 year olds.
- Author(s)
  Hata Y, Kinoshita K, Yamaguchi Y, Hirono K, Ichida F, Nishida N.
- Organizer
  The 9th International Symposium on Advances in Legal Medicine
- Place of Presentation
  Fukuoka
- Year and Date
  2014-06-16 – 2014-06-20
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] 左冠状動脈口のvery high take-offによる突然死と考えられた1例
- Author(s)
  西田尚樹、畑由紀子、木下耕史
- Organizer
  日本循環器学会第142回東海・第127回北陸合同地方会
- Place of Presentation
  金沢
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] A case of sudden cardiac death with a G487R mutation in the hERG channel.
- Author(s)
  Kinoshita K, Nishide K, Kimoto K, Tabata T, Hata Y, Nishida N.
- Organizer
  The 9th International Symposium on Advances in Legal Medicine
- Place of Presentation
  Fukuoka
- Year and Date
  2014-06-16 – 2014-06-20
- Data Source
  KAKENHI-PROJECT-24590852
[Presentation] 法医剖検例における心臓性突然死の遺伝子検索
- Author(s)
  畑由紀子、木下耕史、西田尚樹
- Organizer
  富山大学学術交流会
- Place of Presentation
  富山
- Data Source
  KAKENHI-PROJECT-24590852
[]
[]

1. NISHIDA Naoki (10315088)

# of Collaborated Projects: 11 results

# of Collaborated Products: 187 results
2. KOMINATO Yoshihiko (30205512)

# of Collaborated Projects: 6 results

# of Collaborated Products: 29 results
3. TAKIZAWA Hisao (90171579)

# of Collaborated Projects: 5 results

# of Collaborated Products: 22 results
4. OZAWA Sayaka (40596540)

# of Collaborated Projects: 4 results

# of Collaborated Products: 13 results
5. Hirono Keiichi (80456384)

# of Collaborated Projects: 4 results

# of Collaborated Products: 22 results
6. KINOSHITA Koshi (10585920)

# of Collaborated Projects: 3 results

# of Collaborated Products: 30 results
7. MORI Hisashi (00239617)

# of Collaborated Projects: 3 results

# of Collaborated Products: 7 results
8. ICHIDA Fukiko (30223100)

# of Collaborated Projects: 3 results

# of Collaborated Products: 20 results
9. 長谷川英之 (00344698)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
10. 伊吹圭二郎 (20566096)

# of Collaborated Projects: 2 results

# of Collaborated Products: 6 results
11. SAITO Kazuyoshi (30566097)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
12. KIMURA Hiroshi (20112039)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. SOEJIMA Mikiko (80279140)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. KODA Yoshiro (90231307)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. SHIMADA Ichiroh (20272908)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. 高崎麻美 (80749739)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
17. 高崎一朗 (00397176)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. 長岡亮 (60781648)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
19. 一萬田正二郎 (60849355)

# of Collaborated Projects: 1 results

# of Collaborated Products: 9 results
20. 中川崇 (40610374)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. 田端俊英

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
22. 鈴木啓之

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
23. 水牧功一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
24. 種市尋宙

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
25. 浜田道昭

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. 蒔田直昌

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
27. 畑忠善

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
28. 芳村直樹

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
29. 青木正哉

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Hata Yukiko 畑 由紀子

HATA Yukiko 畑 由紀子

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原因不明の心臓突然死の診断，病態解明に向けた網羅的剖検研究Principal Investigator

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Comprehensive genetic and morphological analysis for sudden cardiac death autopsy casesPrincipal Investigator

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Investigating the Genetic Causes of Sudden Unexpected Death in infants and children.Principal Investigator

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Comprehensive genetic analysis of sudden unexplained death syndrome cases using a next-generation sequencingPrincipal Investigator

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Genetic background of sudden cardiac death in forensic autopsy cases.Principal Investigator

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Investigation of a novel transcription originated from the upstream region of the human ABO genePrincipal Investigator

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Hata Yukiko 畑由紀子

HATA Yukiko 畑由紀子

[Book] 病理と臨床【法医と病理の相互理解】法医解剖と病理2014