KINOSHITA Koshi 木下耕史

Researcher Number	10585920
Affiliation (based on the past Project Information) *help	2012 – 2017: 富山大学, 大学院医学薬学研究部(医学), 助教 2013: 富山大学, 医学薬学研究部(医学), 助教
Review Section/Research Field	Principal Investigator General physiology / Circulatory organs internal medicine Except Principal Investigator Pediatrics / Legal medicine
Keywords	Principal Investigator LQT / 不整脈 / Yotiao/AKAP9 / LQT1 / Rab11 / KCNE1 / Yotiao / 膜移行 / KCNQ1 / IKsチャネル … More / パッチクランプ / イオンチャネル / 遺伝性心疾患 / 疾患モデル / 薬剤応答性 / 心筋誘導 / QT延長 / iPS細胞 … More Except Principal Investigator 遺伝子解析 / 心筋緻密化障害 / 心筋症 / cardiomyopathy / 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 / サルコメア遺伝子 / 遺伝子変異 / epilepsy / Epilepsy / Next-generation sequence / Channelopathy / Cardiomyopathy / Autopsy / Sudden unexplained death / 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 / チャネル異常症 / 心臓突然死 Less

Functional expression and characterization of cardiac IKs channelPrincipal Investigator
- Principal Investigator
  
  木下耕史
- Project Period (FY)
  2017
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  General physiology
- Research Institution
  University of Toyama
Comprehensive genetic analysis of sudden unexplained death syndrome cases using a next-generation sequencing
- 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
Uncovering the mechanism of LVNC; functional study of in vitro study using with iPSCs from the patient's blood sample
- Principal Investigator
  
  Hirono Keiichi
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  University of Toyama
Genetic background of sudden cardiac death in forensic autopsy cases.
- 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
Functional analysis and pharmacological testing of iPSc-derived cardiomyocyte as model for cardiac arrhythmiaPrincipal Investigator
- Principal Investigator
  
  KINOSHITA Koshi
- Project Period (FY)
  2012 – 2013
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Circulatory organs internal medicine
- Research Institution
  University of Toyama

All 2017 2016 2015 2014 2013 2012 Other

All Journal Article Presentation Other

[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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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
[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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] 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] Targeted Next-generation Sequencing for Postmortem Molecular Analysis of Sudden Cardiac Death.2015
- Author(s)
  Yukiko Hata, Koshi Kinoshita, Fukiko Ichida, Keiich Hirono, Hisashi Mori, Naoki Nishida
- 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-25860848
[Presentation] C-terminal helix D of KCNQ1 contributes to normal IKs channelfunction.2014
- Author(s)
  Takuto Komatsu, Koshi Kinoshita, Katsuya Kimoto, Yukiko Hata, Kei Aonuma, Eikichi Tsushima, Kohki Nishide, Nozomi Hisajima, Hiroyuki Takahashi, Kenkichi Fukurotani, Naoki Nishida, Toshihide Tabata
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島
- Year and Date
  2014-03-17
- Data Source
  KAKENHI-PROJECT-24790745
[Presentation] KCNQ1C末端のhelix Dは正常なIKsチャネル機能に寄与する2014
- Author(s)
  小松卓人、木下耕史、木本克哉、畑由紀子、青沼慶、津島永吉、西出康貴、久嶋希望、高橋宏幸、袋谷賢吉、西田尚樹、田端俊英
- Organizer
  第91回日本生理学会大会
- Place of Presentation
  鹿児島大学郡元キャンパス
- Data Source
  KAKENHI-PROJECT-24790745
[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] Functional Characterization of KCNQ1 Channel Subunit with an A590T Mutation.2013
- Author(s)
  Koshi Kinoshita, Takuto Komatsu, Katsuya Kimoto, Kohki Nishide, Toshihide Tabata, Fukiko Ichida, Yoshiaki Yamaguchi, Kunihiro Nishida, Hiroshi Inoue, Yukiko Hata, Naoki Nishida
- Organizer
  Basic Cardiovascular Sciences 2013
- Place of Presentation
  Paris Las Vegas, Las Vegas, Nevada
- Data Source
  KAKENHI-PROJECT-24790745
[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] Abnormal modulation of hERG and KCNQ1 channels.2013
- Author(s)
  Kohki Nishide, Mario Kato, Yoshiaki Yamaguchi, Koshi Kinoshita, Akira Fujita, Yuki Nonobe, Yukiko Hata, Koichi Mizumaki, Hiroshi Inoue, Naoki Nishida, Toshihide Tabata
- Organizer
  第90回日本生理学会大会
- Place of Presentation
  東京
- Year and Date
  2013-03-27
- Data Source
  KAKENHI-PROJECT-24790745
[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] Functional Characterization of KCNQ1 Channel Subunit with an A590T mutation.2013
- Author(s)
  Koshi Kinoshita, Takuto Komatsu, Katsuya Kimoto, Kohki Nishide, Toshihide Tabata, Fukiko Ichida, Yoshiaki Yamaguchi, Kunihiro Nishida, Hiroshi Inoue, Yukiko Hata, Naoki Nishida
- Organizer
  Basic Cardiovascular Sciences (BCVS)
- Place of Presentation
  Las Vegas
- Year and Date
  2013-07-22
- Data Source
  KAKENHI-PROJECT-24790745
[Presentation] 遅延整流性カリウム・チャネル・サブユニット新規変異体KCNQ1(Y461X)の機能解析2013
- Author(s)
  木本　克哉, 西出　康貴, 木下　耕史, 野々部　雄樹, 藤田　陽, 山口　由明, 畑　由紀子, 水牧　功一, 井上　博, 西田　尚樹, 田端　俊英
- Organizer
  第90回日本生理学会大会
- Place of Presentation
  タワーホール船堀
- Data Source
  KAKENHI-PROJECT-24790745
[Presentation] Characterization of a New Mutant KCNQ1 Channel Subunit with aC-TerminalTruncation.2013
- Author(s)
  Katsuya Kimoto, Kohki Nishide, Koshi Kinoshita, Yuki Nonobe, Akira Fujita, Yoshiaki Yamaguchi, Yukiko Hata, Koichi Mizumaki, Hiroshi Inoue, Naoki Nishida, Toshihide Tabata
- Organizer
  第90回日本生理学会大会
- Place of Presentation
  東京
- Year and Date
  2013-03-27
- Data Source
  KAKENHI-PROJECT-24790745
[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] KCNE1サブユニットのG38S変異がもたらすhERGおよびKCNQ1チャネルに対する変調作用の変化2013
- Author(s)
  西出　康貴, 加藤　真理夫, 山口　由明, 木下　耕史, 藤田　陽, 野々部　雄樹, 畑　由紀子, 水牧　功一, 井上　博, 西田　尚樹, 田端　俊英
- Organizer
  第90回日本生理学会大会
- Place of Presentation
  タワーホール船堀
- Data Source
  KAKENHI-PROJECT-24790745
[Presentation] Characterization of KCNQ1 (Kv7.1, IKs) channel subunit with an A590Tmutation.2013
- Author(s)
  Koshi Kinoshita, Toshihide Tabata, Fukiko Ichida, Yoshiaki Yamaguchi, Kunihiro Nishida, Hiroshi Inoue, Yukiko Hata, Naoki Nishida
- Organizer
  第77回日本循環器学会学術総会
- Place of Presentation
  横浜
- Year and Date
  2013-03-15
- Data Source
  KAKENHI-PROJECT-24790745
[Presentation] Characterization of KCNQ1 (KV7.1, IKs) Channel Subunit with an A590T Mutation2013
- Author(s)
  Koshi Kinoshita, Toshihide Tabata, Fukiko Ichida, Yoshiaki Yamaguchi, Kunihiro Nishida, Hiroshi Inoue, Yukiko Hata, Naoki Nishida
- Organizer
  第77回日本循環器学会
- Place of Presentation
  パシフィコ横浜
- Data Source
  KAKENHI-PROJECT-24790745
[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] 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] 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. HATA Yukiko (30311674)

# of Collaborated Projects: 3 results

# of Collaborated Products: 33 results
2. NISHIDA Naoki (10315088)

# of Collaborated Projects: 3 results

# of Collaborated Products: 33 results
3. MORI Hisashi (00239617)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
4. Ichida Fukiko (30223100)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
5. Hirono Keiichi (80456384)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
6. 小澤綾佳 (40596540)

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 1 results

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

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results

KINOSHITA Koshi 木下 耕史

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Functional expression and characterization of cardiac IKs channelPrincipal Investigator

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

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Genetic analysis and pathological role in ventricular noncompaction associated with fatal arrhythmia

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Uncovering the mechanism of LVNC; functional study of in vitro study using with iPSCs from the patient's blood sample

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Genetic background of sudden cardiac death in forensic autopsy cases.

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Functional analysis and pharmacological testing of iPSc-derived cardiomyocyte as model for cardiac arrhythmiaPrincipal Investigator

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[Journal Article] Argyrophilic grain disease in a 46-year-old male suicide victim2017

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[Journal Article] An Autopsy Case of Sudden Unexpected Death of a Young Adult in a Hot Bath: Molecular Analysis Using Next-Generation DNA Sequencing2017

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[Journal Article] Epilepsy-related sudden unexpected death: targeted molecular analysis of inherited heart disease genes using next-generation DNA sequencing2017

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[Journal Article] Incipient progressive supranuclear palsy is more common than expected and may comprise clinicopathological subtypes: a forensic autopsy series2017

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[Journal Article] Postmortem genetic analysis of sudden unexplained death syndrome under 50 years of age: A next-generation sequencing study.2016

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[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

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[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

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[Journal Article] The Susceptibilities of Human Ether-à-Go-Go-Related Gene Channel with the G487R Mutation to Arrhythmogenic Factors2015

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NAID

KINOSHITA Koshi 木下耕史

[Journal Article] Glycine/Serine Polymorphism at Position 38 Influences KCNE1 Subunit’s Modulatory Actions on Rapid and Slow Delayed Rectifier K<sup>+</sup> Currents2014