Nishigaki Yutaka 西垣裕

… Alternative Names

NISHIGAKI Yutaka 西垣裕

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Researcher Number	80296988
External Links
Affiliation (Current)	2025: 昭和大学, 医学部, 兼任講師
Affiliation (based on the past Project Information) *help	2011: 地方独立行政法人東京都健康長寿医療センター(東京都健康長寿医療センター研究所), 東京都健康長寿医療センター研究所, 研究員 2009 – 2010: 地方独立行政法人東京都健康長寿医療センター(東京都健康長寿医療センター研究所), 研究副部長 2009: 地方独立行政法人東京都健康長寿医療センター(東京都健康長寿医療センター研究所), 東京都健康長寿医療センター研究所, 研究副部長 2008: Tokyo Metropolitan Institute of Gerontology, 東京都老人総合研究所, 研究副部長 2007 – 2008: Tokyo Metropolitan Institute of Gerontology, 東京都老人総合研究所, 研究副部長 2006: (財)東京都高齢者研究・福祉振興財団, 東京都老人総合研究所, 研究副部長
Review Section/Research Field	Principal Investigator Human genetics Except Principal Investigator Human pathology / Applied health science
Keywords	Principal Investigator ゲノム定量 / 加齢 / ミトコンドリア / ゲノム Except Principal Investigator 網羅的解析 / Luminex / 剖検例 / パラフィン / 変異 / ミトコンドリアDNA … More / 遺伝子増幅 / ミトコンドリアゲノム多型 / 健康長寿 / 動脈硬化 / 脳梗塞 / 生活習慣病 / パラフィン包埋切片 / 病理解剖 / 身体活動 / 運動 / 大規模運動介入研究 / 筋力 / 脚伸展パワー / ハプログループ / 遺伝子多型 / ミトコンドリア Less

Development of mutation analysis system by multiplex PCR and suspension array for paraffin-embedded autopsy samples
- Principal Investigator
  
  HOSOYA Hiroko
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human pathology
- Research Institution
  Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology
大規模運動介入研究における運動の効果に及ぼす遺伝子多型の探索
- Principal Investigator
  
  福典之
- Project Period (FY)
  2008 – 2009
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Applied health science
- Research Institution
  Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology
  Tokyo Metropolitan Institute of Gerontology
Basic research for quantification of mitochondrial DNA copy number and mutations associated with agingPrincipal Investigator
- Principal Investigator
  
  NISHIGAKI Yutaka
- Project Period (FY)
  2006 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Human genetics
- Research Institution
  Tokyo Metropolitan Institute of Gerontology

All 2012 2011 2010 2009 2008 2007 2006 Other

All Journal Article Presentation Book

[Book] 老年医学update2007-082007
- Author(s)
  西垣裕
- Publisher
  メジカルビュー社
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Mitochondrial haplogroups A and M7a confer a genetic risk for coronary atherosclerosis in the Japanese elderly : An autopsy study of 1, 536 patients2011
- Author(s)
  Sawabe M, Tanaka M, Chida K, Arai T, Nishigaki Y, Fuku N, Mieno MN, Kuchiba A, Tanaka N
- Journal Title
  
  J Atheroscler Thromb
  
  Volume: 18(2) Issue: 3 Pages: 166-75
- DOI
  10.1002/ajpa.21561
- NAID
  130004444492
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590411, KAKENHI-PROJECT-22370088, KAKENHI-PROJECT-23247040, KAKENHI-PROJECT-23701014
[Journal Article] Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations2011
- Author(s)
  Yoshiji Yamada, Tamotsu Nishida, Sahoko Ichihara, Motoji Sawabe, Noriyuki Fuku, Yutaka Nishigaki, Yukitoshi Aoyagi, Masashi Tanaka, Yoshinori Fujiwara, Hiroto Yoshida, Shoji Shinkai, Kei Satoh, Kimihiko Kato, Tetsuo Fujimaki, Kiyoshi Yokoi, Mitsutoshi Oguri, Tetsuro Yoshida, Sachiro Watanabe, Yoshinori Nozawa, Aki Hasegawa, Toshio Kojima, Bok-Ghee Han, Younjin Ahn, Meehee Lee, Dong-Jik Shin, Jong Ho Lee, Yangsoo Jang
- Journal Title
  
  Atherosclerosis
  
  Volume: 215 Issue: 1 Pages: 145-152
- DOI
  10.1016/j.atherosclerosis.2010.12.005
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590411, KAKENHI-PROJECT-21590912
[Journal Article] Extensive and Rapid Screening for Major Mitochondrial DNA Point Mutations in Patients with Hereditary Hearing Loss2010
- Author(s)
  Kato T, Nishigaki Y, Noguchi Y, Ueno H, Hosoya H, Ito T, Kimura Y, Kitamura K, Tanaka M
- Journal Title
  
  J Hum Genet 55
  
  Pages: 147-154
- NAID
  10030733907
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590411
[Journal Article] Pyruvate therapy for Leigh syndrome due to cytochrome c oxidase deficiency2010
- Author(s)
  Komaki H, Nishigaki Y, Fuku N, Hosoya H, Murayama K, Ohtake A, Goto Y, Wakamoto H, Koga Y, Tanaka M
- Journal Title
  
  Biochim Biophys Acta
  
  Volume: 1800 Pages: 313-315
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590411
[Journal Article] Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations2010
- Author(s)
  Nishigaki Y, Ueno H, Coku J, Koga Y, Fujii T, Sahashi K, Nakano K, Yoneda M, Nonaka M, Tang L, Liou CW, Paquis-Flucklinger V, Harigaya Y, Ibi T, Goto Y, Hosoya H, DiMauro S, Hirano M, Tanaka M
- Journal Title
  
  Mitochondrion
  
  Volume: 10 Issue: 3 Pages: 300-308
- DOI
  10.1016/j.mito.2010.01.003
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590411
[Journal Article] Pyruvate therapy for Leigh syndrome due to cytochrome c oxidase deficiency2010
- Author(s)
  Komaki H, Nishigaki Y, Fuku N, Hosoya H, Murayama K, Ohtake A, Goto YI, Wakamoto H, Koga Y, Tanaka M
- Journal Title
  
  Biochim Biophys Acta 1800
  
  Pages: 313-315
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20650113
[Journal Article] Mitochondrial haplogroups associated with lifestyle-related diseases and longevity in the Japanese population2010
- Author(s)
  Nishigaki Y., et al.
- Journal Title
  
  Geriatr Gerontol Int
  
  Volume: 10Suppl 1
- NAID
  10027274092
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590411
[Journal Article] Mitochondrial haplogroups associated with lifestyle-related diseases and longevity in the Japanese population2010
- Author(s)
  Yutaka Nishigaki, Noriyuki Fuku, Masashi Tanaka
- Journal Title
  
  Geriatr Gerontol Int
  
  Volume: 10 Issue: s1 Pages: 221-235
- DOI
  10.1111/j.1447-0594.2010.00599.x
- NAID
  10027274092
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590411
[Journal Article] Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss2010
- Author(s)
  Kato T, Nishigaki Y, Noguchi Y, Ueno H, Hosoya H, Ito T, Kimura Y, Kitamura K, Tanaka M
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Issue: 3 Pages: 147-154
- DOI
  10.1038/jhg.2009.143
- NAID
  10030733907
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21590411
[Journal Article] Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.2009
- Author(s)
  Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Nozawa Y, Yamada Y.
- Journal Title
  
  Int J Mol Med 24
  
  Pages: 233-246
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Analysis of mitochondrial DNA variants in Japanese patients with schizophrenia2009
- Author(s)
  Ueno H, Nishigaki Y, Kong QP, Fuku N, Kojima S, Iwata N, Ozaki N, Tanaka M
- Journal Title
  
  Mitochondrion 9
  
  Pages: 385-393
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20650113
[Journal Article] Association of candidate gene polymorphisms with chronic kidney disease in Japanese individuals with hypertension.2009
- Author(s)
  Yoshida T, Kato K, Yokoi K, Watanabe S, Metoki N, Satoh K, Aoyagi Y, Nishigaki Y, Nozawa Y, Yamada Y.
- Journal Title
  
  Hypertens Res 32
  
  Pages: 411-418
- NAID
  10026122841
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] 蛍光ビーズアレイを用いたミトコンドリアDNAの網羅的迅速解析法2009
- Author(s)
  西垣裕、上野仁美、細矢博子、福典之、田中雅嗣
- Journal Title
  
  基礎老化研究 33
  
  Pages: 23-26
- NAID
  10024808387
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Macrophages that survive hyperoxia exposure have higher superoxide dismutase activities in their mitochondria2009
- Author(s)
  Kokubo K, Soeda S, Shinbo T, Hirose M, Fuku N, Nishigaki Y, Tanaka M, Kobayashi H.
- Journal Title
  
  Adv Exp Med Biol 662
  
  Pages: 662-663
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20650113
[Journal Article] Association of gene polymorphisms with chronic kidney disease in high-risk or low-risk subjects defined by conventional risk factors2009
- Author(s)
  Yoshida T, Kato K, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Nozawa Y, Yamada Y.
- Journal Title
  
  Int J Mol Med 23
  
  Pages: 785-792
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Mitochondrial haplogroup N9a confers resistance against metabolic syndrome and type 2 diabetes mellitus in Asian individuals2009
- Author(s)
  Fuku N, Nishigaki Y, Tanaka M
- Journal Title
  
  Asia-Pacific J Endocrinol 1
  
  Pages: 65-73
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20650113
[Journal Article] Association of genetic vriants with myocardial infarction in Japanese individuals with chronic kidney disease.2009
- Author(s)
  Fujimaki T, Kato K, Yoshida T, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Tanaka M, Nozawa Y, Kimura G, Yamada Y.
- Journal Title
  
  Thromb Haemost 101
  
  Pages: 963-968
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Association of genetic variants with chronic kidney disease in Japanese individuals with type 2 diabetes mellitus.2009
- Author(s)
  Yoshida T, Kato K, Yokoi K, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Suzuki T, Nozawa Y, Yamada Y.
- Journal Title
  
  Int J Mol Med 23
  
  Pages: 529-537
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] その他の寿命関連遺伝子-ミトコンドリア遺伝子.アンチエイジング医学-基礎・臨床研究の進歩-2009
- Author(s)
  西垣裕、田中雅嗣
- Journal Title
  
  日本臨床 67
  
  Pages: 1299-1305
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] 第5章神経の変性・老化とミトコンドリア2009
- Author(s)
  西垣裕、田中雅嗣
- Journal Title
  
  脳内老化制御とバイオマーカー
  
  Pages: 65-76
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Association of a polymorphism of apolipoprotein E gene with chronic kidney disease in Japanese individuals with metabolic syndrome.2009
- Author(s)
  Yoshida T, Kato K, Fujimaki T, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Tanaka M, Nozawa Y, Yamada Y.
- Journal Title
  
  Genomics 93
  
  Pages: 221-226
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] ミトコンドリアDNAと寿命, 遺伝子変異蓄積とポリプラズミーのメカニズム, Mitochondrial DNA and longevity: Polyplasmy and accumulation of mtDNA mutation2008
- Author(s)
  西垣裕、田中雅嗣
- Journal Title
  
  医学のあゆみ 227
  
  Pages: 567-572
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] ミトコンドリアDNAと寿命, 遺伝子変異蓄積とポリプラズミーのメカニズム2008
- Author(s)
  西垣裕
- Journal Title
  
  医学のあゆみ 227
  
  Pages: 567-572
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Functionally Dominant Mitochondrial DNA Mutation2008
- Author(s)
  Sacconi S, Salviati L, Nishigaki Y, 以下省略12.
- Journal Title
  
  Hum Mol Genet 17
  
  Pages: 1814-20
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] 「Industry News」蛍光ビーズアレイを用いたミトコンドリアDNA網羅的迅速解析法の有用性2008
- Author(s)
  阿部由紀子、西垣裕
- Journal Title
  
  Medical Science Digest 34
  
  Pages: 361-365
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Mitochondrial DNA Haplogroup D4a is a Marker for Extreme Longevity in Japan.2008
- Author(s)
  Bilal E, Rabadan R, Alexe G, Fuku N, Ueno H, Nishigaki Y, Fujita Y, Ito M, Arai Y, Hirose N, Ruckenstein A, Bhanot G, Tanaka M.
- Journal Title
  
  PLoS ONE 3
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] ミトコンドリアと酸化ストレス、アポトーシス2008
- Author(s)
  西垣裕
- Journal Title
  
  Medical Science Digest 34
  
  Pages: 339-342
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] ミトコンドリアと酸化ストレス、アポトーシス2008
- Author(s)
  西垣裕、福典之、田中雅嗣
- Journal Title
  
  Medical Science Digest 34
  
  Pages: 339-342
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] 蛍光ビーズアレイを用いたミトコンドリアDNAの網羅的迅速解析法2008
- Author(s)
  西垣裕
- Journal Title
  
  基礎老化研究 33
  
  Pages: 23-26
- NAID
  10024808387
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Enrichment of longevity phenotype in mtDNA haplogroups D4b2b, D4a, and D5 in the Japanese population.2007
- Author(s)
  Alexe G, Fuku N, Bilal E, Ueno H, Nishigaki Y, Fujita Y, Ito M, Arai Y, Hirose N, Bhanot G, Tanaka M.
- Journal Title
  
  Hum Genet 121
  
  Pages: 347-356
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Letter to the Editor, Therapeutic potential of pyruvate therapy for mitochondrial diseases.2007
- Author(s)
  Tanaka M, Nishigaki Y, Ibi T, Sahashi K. Koga Y.
- Journal Title
  
  Mitochondrion 7
  
  Pages: 399-401
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] ミトコンドリア心筋症(Mitochondrlal cardiomyopathy)-診断と治療戦略-2007
- Author(s)
  西垣裕
- Journal Title
  
  分子心血管病 8
  
  Pages: 119-129
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] ミトコンドリア機能異常と老年病(総説)2007
- Author(s)
  西垣裕、福典之、田中雅嗣
- Journal Title
  
  老年医学update 2007-08, メジカルビュー社
  
  Pages: 154-163
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Mitochondrial haplogroup A is a genetic riskfactor for atherothrombotic cerebral infarction in Japanese females.2007
- Author(s)
  Nishigaki Y, Yamada Y, Fuku N, Matsuo H, Segawa T, Watanabe S, Kato K, Yokoi K, Yamaguchi S, Nozawa Y, Tanaka M.
- Journal Title
  
  Mitochondrion 7
  
  Pages: 72-79
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Mitochondrial haplogroup A is a genetic risk factor for artherothrombotic cerebral infarction in Japanese females.2007
- Author(s)
  Nishigaki Y
- Journal Title
  
  Mitochondrion 7・1
  
  Pages: 72-79
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males.2007
- Author(s)
  Nishigaki Y, Yamada Y, Fuku N, Matsuo H, Segawa T, Watanabe S, Kato K, Yokoi K, Yamaguchi S, Nozawa Y, Tanaka M.
- Journal Title
  
  Hum Genet 120
  
  Pages: 827-836
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Mitochondrial haplogroup N9a confers resistance against type 2 diabetes in Asians.2007
- Author(s)
  Fuku N, Park KS, Yamada Y, Nishigaki Y, Cho YM, Matsuo H, Segawa T, Watanabe S, Kato K, Yokoi K, Nozawa Y, Lee HK, Tanaka M.
- Journal Title
  
  Am J Hum Genet 80
  
  Pages: 407415-407415
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Mitochondrial haplogroup N9b is protective against myocardial infarction in Japanese males.2007
- Author(s)
  Nishigaki Y
- Journal Title
  
  Hum Genet 120・6
  
  Pages: 827-836
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Women with mitochondrial haplogroup N9a are protected against metabolic syndrome.2007
- Author(s)
  Tanaka M, Fuku N, Nishigaki Y, Matsuo H, Segawa T, Watanabe S, Kato K, Yokoi K, Yamaguchi S, Nozawa Y, Yamada Y.
- Journal Title
  
  Diabetes 56
  
  Pages: 518-521
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] ミトコンドリア機能異常と老年病2006
- Author(s)
  西垣裕
- Journal Title
  
  日本老年医学会雑誌 43・3
  
  Pages: 274-282
- NAID
  10018178336
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] 老化に関連するミトコンドリアゲノム多型2006
- Author(s)
  西垣裕
- Journal Title
  
  日本農芸化学会会誌・化学と生物 44・10
  
  Pages: 674-680
- NAID
  10018252487
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Association of genetic variants with chronic kidney disease in Japanese individuals.
- Author(s)
  Yoshida T, Kato K, Fujimaki T, Yokoi K, Oguri M, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Tanaka M, Nozawa Y, Kimura G, Yamada Y.
- Journal Title
  
  Clin J Am Soc Nephrol (印刷中)
  
  Pages: 0-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Association of polymorphisms of THBS2 and HSPA8 with hypertension in Japanese individuals with chronic kidney disease.
- Author(s)
  Oguri M, Kato K, Yokoi K, Watanabe S, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Yoshida H, Nozawa Y, Yamada Y.
- Journal Title
  
  Mol Med Rep (印刷中)
  
  Pages: 0-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Association of genetic variants with myocardial infarction in Japanese individuals with metabolic syndrome
- Author(s)
  Oguri M, Kato K, Yokoi K, Itoh T, Metoki N, Yoshida H, Satoh K, Aoyagi Y, Nishigaki Y, Tanaka M, Nozawa Y, Yamada Y.
- Journal Title
  
  Atherosclerosis (印刷中)
  
  Pages: 0-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Analysis of mitochondrial DNA variants in Japanese patients with schizophrenia.
- Author(s)
  Ueno H, Nishigaki Y, Kong QP, Fuku N, Kojima S, Iwata N, Ozaki N, Tanaka M.
- Journal Title
  
  Mitochondrion (印刷中)
  
  Pages: 0-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590317
[Journal Article] Mitochondrial haplogroups associated with lifestyle-related diseases and longevity in the Japanese population. In: Gerontology and Geriatrics Science: Gene to Longevity, Takubo K, Maruyama N (eds)
- Author(s)
  Nishigaki Y, Fuku N, Tanaka M.
- Journal Title
  
  Wiley-Blackwell, Hoboken, NJ (印刷中)
  
  Pages: 0-0
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] Comprehensive Mitochondrial Haplogroup Analysis System Based On Suspension-Array Technology Using DNA From Formalin-Fixed Paraffin-Embedded Autopsy Tissues2012
- Author(s)
  Yutaka Nishigaki, Hiroko Hosoya, Makiko Naka-Mieno, Tomio Arai, Motoji Sawabe, Masashi Tanaka
- Organizer
  American Academy of Neurology 2012
- Place of Presentation
  アメリカ・ニューオリンズ
- Year and Date
  2012-04-26
- Data Source
  KAKENHI-PROJECT-21590411
[Presentation] Comprehensive Mitochondrial Haplogroup Analysis System Based On Suspension-Array Technology Using DNA From Formalin-Fixed Paraffin-Embedded Autopsy TissuesComprehensive Mitochondrial Haplogroup Analysis System Based On Suspension-Array Technology Using DNA From Formalin-Fixed Paraffin-Embedded Autopsy Tissues2012
- Author(s)
  Yutaka Nishigaki, Hiroko Hosoya, Makiko Naka-Mieno, Tomio Arai, Motoji Sawabe, Masashi Tanaka
- Organizer
  American Academy of Neurology 2012
- Place of Presentation
  アメリカ・ニューオリンズ
- Year and Date
  2012-04-26
- Data Source
  KAKENHI-PROJECT-21590411
[Presentation] The establishment of an expanded simultaneous swift diagnosing system for mitochondrial DNA pathological mutations2009
- Author(s)
  Nishigaki Y, Hosoya H, Fuku N, DiMauro S, Hirano M, Tanaka M
- Organizer
  61st Annual Meeting of the American Academy of Neurology
- Place of Presentation
  Seattle, U.S.A.
- Data Source
  KAKENHI-PROJECT-21590411
[Presentation] Mitochondrial haplogroups associated with elite Japanese athlete status2009
- Author(s)
  Mikami E, Fuku N, Kawahara T, Takahashi H, Ohiwa N, Nishigaki Y, Higuchi M, Tanaka M
- Organizer
  14th International Conference Biochemistry of Exercise
- Place of Presentation
  Guelph, Canada
- Data Source
  KAKENHI-PROJECT-20650113
[Presentation] The establishment of an expanded simultaneous swift diagnosing system for mitochondrial DNA pathological mutations.2009
- Author(s)
  Nishigaki Y
- Organizer
  61st Annual Meeting of the American Academy of Neurology
- Place of Presentation
  Seattle, U.S.A.
- Year and Date
  2009-04-25
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] Mitochondrial DNA haplogroup D4a is a marker for extreme longevity in Japan2009
- Author(s)
  Fuku N, Bilal E, Nishigaki Y, Bhanot G, Tanaka M
- Organizer
  14th International Conference Biochemistry of Exercise
- Place of Presentation
  Guelph, Canada
- Data Source
  KAKENHI-PROJECT-20650113
[Presentation] Mitochondrial Haplogroup for Successful Ageing2008
- Author(s)
  Fuku N, Alexe G, Ueno H, Nishigaki Y, et al
- Organizer
  ACSM's 55th Annual Meeting
- Place of Presentation
  アメリカ・インディアナポリス
- Year and Date
  2008-05-28
- Data Source
  KAKENHI-PROJECT-20650113
[Presentation] A novel comprehensive diagnosing system for mitochondrial DNA mutations using suspension array technology2008
- Author(s)
  Yutaka Nishigaki
- Organizer
  60 Annual Meeting of the American Academy of Neurology
- Place of Presentation
  Chicago, U. S. A
- Year and Date
  2008-04-15
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] ミトコンドリア病の網羅的かつ迅速診断を目的とした蛍光ビーズアレイ・システムの構築2008
- Author(s)
  西垣裕
- Organizer
  第31回日本分子生物学会年会・第81回日本生化学会大会合同大会
- Place of Presentation
  神戸
- Year and Date
  2008-12-09
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] 蛍光ビーズ多重解析システムを用いたミトコンドリア病病因変異の迅速・網羅的検出法の確立2008
- Author(s)
  西垣裕
- Organizer
  日本人類遺伝学会第53回大会
- Place of Presentation
  東京
- Year and Date
  2008-09-28
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] A novel comprehensive diagnosing system for mitochondrial DNA mutations using suspension array technology.2008
- Author(s)
  Nishigaki Y
- Organizer
  60th Annual Meeting of the American Academy of Neurology
- Place of Presentation
  Chicago, U.S.A.
- Year and Date
  2008-04-12
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] A new comprehensive diagnosing system for mitochondria DNA mutations using suspension array technology2008
- Author(s)
  Yutaka Nishigaki
- Organizer
  5th Meeting of Asian Society for Mitochondrial Research and Medicine (ASMRM)
- Place of Presentation
  中国天津市
- Year and Date
  2008-11-09
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] A new comprehensive diagnosing system for mitochondrial DNA mutations using fluorescent beads2008
- Author(s)
  Yutaka Nishigaki
- Organizer
  The 7th European Meeting on Mitochondrial Pathology (Euromit 7)
- Place of Presentation
  Stockholm, スウェーデン
- Year and Date
  2008-06-12
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] A new comprehensive diagnosing system for mitochondrial DNA mutations using suspension array technology.2008
- Author(s)
  Nishigaki Y
- Organizer
  5th Meeting of Asian Society for Mitochondrial Research and Medicine (ASMRM)
- Place of Presentation
  Tianjin, China.
- Year and Date
  2008-11-09
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] A new comprehensive diagnosing system for mitochondrial DNA mutations using fluorescent beads.2008
- Author(s)
  Nishigaki Y
- Organizer
  The 7th European Meeting on Mitochondrial Pathology (Euromit 7)
- Place of Presentation
  Stockholm, Sweden.
- Year and Date
  2008-06-11
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] 厚生労働省精神・神経疾患研究委託費「筋ジストロフィーに関連する疾患の病態解明と治療法の開発に関する研究」2008
- Author(s)
  西垣裕
- Organizer
  砂田班班会議「蛍光ビーズ多重解析システムを用いたミトコンドリアゲノム病因変異の迅速かつ網羅的診断法の確立」
- Place of Presentation
  東京
- Year and Date
  2008-12-14
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] ミトコンドリア病の網羅的かつ迅速診断を目的とした蛍光ビーズアレイ・システムの構築2008
- Author(s)
  西垣裕
- Organizer
  第31回日本分子生物学会年会・第81回日本生化学会大会
- Place of Presentation
  兵庫県神戸市
- Year and Date
  2008-12-09
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] 生活習慣病に関連するミトコンドリアハプログループの検索を目的としたミトコンドリアゲノム一塩基多型網羅的・迅速解析系の確立.2007
- Author(s)
  西垣裕
- Organizer
  日本人類遺伝学会第52回大会
- Place of Presentation
  東京
- Year and Date
  2007-09-12
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] ミトコンドリアゲノム多型研究の生活習慣病一次予防への活用-ミトコンドリアゲノム一塩基多型網羅的・迅速解析系の確立-2007
- Author(s)
  西垣裕
- Organizer
  花王健康科学研究会第4回研究成果報告会
- Place of Presentation
  東京
- Year and Date
  2007-12-08
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] 蛍光ビーズアレイを用いたミトコンドリア病病因変異の網羅的迅速診断システムの構築2007
- Author(s)
  西垣裕
- Organizer
  日本ミトコンドリア学会第7回年会
- Place of Presentation
  鹿児島
- Year and Date
  2007-12-20
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] 蛍光ビーズアレイを用いたミトコンドリア病病因変異の網羅的迅速診断システムの構築2007
- Author(s)
  西垣裕
- Organizer
  日本ミトコンドリア学会第7回年会
- Place of Presentation
  鹿児島県鹿児島市
- Year and Date
  2007-12-21
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] Ageing and mitochondrial neurogastrointestinal encephalomyopathy(MNGIE):an autosomal recessive mitochondrial disorder.2007
- Author(s)
  Yutaka Nishigaki
- Organizer
  The 8th Asia/Oceania Regional Congress of Gerontology and Geriatrics,.
- Place of Presentation
  Beijing,China
- Year and Date
  2007-10-23
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] Ageing and an autosomal recessive mitochondrial disorder: mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).2007
- Author(s)
  西垣裕
- Organizer
  日本基礎老化学会第30回年会
- Place of Presentation
  札幌
- Year and Date
  2007-06-21
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] 厚生労働省精神・神経疾患研究委託費「筋ジストロフィーに関連する疾患の病態解明と治療法の開発に関する研究」2007
- Author(s)
  西垣裕
- Organizer
  清水班班会議「蛍光ビーズ多重解析システムを用いたミトコンドリアゲノム病因変異の迅速かつ網羅的診断法の確立」
- Place of Presentation
  東京
- Year and Date
  2007-12-07
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] 生活習慣病に関連するミトコンドリアハプログループの検索を目的としたミトコンドリアゲノム-塩基多型網羅的・迅速解析系の確立.2007
- Author(s)
  西垣裕
- Organizer
  日本人類遺伝学会第52回大会
- Place of Presentation
  東京
- Year and Date
  2007-09-14
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] Ageing and an autosomal recessive mitochondrial disorder:mitochondrial neurogastrointestinal encephalomyopathy(MNGIE).2007
- Author(s)
  西垣裕
- Organizer
  日本基礎老化学会第30回年会
- Place of Presentation
  北海道札幌市
- Year and Date
  2007-06-21
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] ミトコンドリア病の主要病因変異における網羅的迅速診断法の構築と検討2007
- Author(s)
  西垣裕
- Organizer
  日本ミトコンドリア学会第8回年会
- Place of Presentation
  東京
- Year and Date
  2007-12-18
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] Women with mitochondrial haplogroup A are susceptible to atherothrombotic cerebral infarction.2007
- Author(s)
  Nishigaki Y
- Organizer
  59th Annual Meeting of the American Academy of Neurology
- Place of Presentation
  Boston, U.S.A.
- Year and Date
  2007-04-28
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] Ageing and mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): an autosomal recessive mitochondrial disorder.2007
- Author(s)
  Nishigaki Y
- Organizer
  The 8th Asia/Oceania Regional Congress of Gerontology and Geriatrics
- Place of Presentation
  Beijing, China.
- Year and Date
  2007-10-22
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] Women with mitochondriaI haplogroup A are susceptible to atherothrombotic cerebral infarction.2007
- Author(s)
  Yutaka Nishigaki
- Organizer
  59th Annual Meeting of the American Academy of Neurology,
- Place of Presentation
  Boston,U.S.A
- Year and Date
  2007-05-02
- Data Source
  KAKENHI-PROJECT-18590317
[Presentation] Mitochondrial haplogroups are associated with atherosclerosis-related diseases in Japanese.2007
- Author(s)
  Nishigaki Y
- Organizer
  4th ASMRM (Asian Society for Mitochondrial Research and Medicine), Mitochondria
- Place of Presentation
  Seoul, South Korea.
- Year and Date
  2007-02-04
- Data Source
  KAKENHI-PROJECT-18590317

1. TANAKA Masashi (60155166)

# of Collaborated Projects: 3 results

# of Collaborated Products: 35 results
2. FUKU Noriyuki (40392526)

# of Collaborated Projects: 3 results

# of Collaborated Products: 23 results
3. HOSOYA Hiroko (00158841)

# of Collaborated Projects: 1 results

# of Collaborated Products: 7 results

Nishigaki Yutaka 西垣 裕

NISHIGAKI Yutaka 西垣 裕

Research Projects

Research Products

Co-Researchers

Development of mutation analysis system by multiplex PCR and suspension array for paraffin-embedded autopsy samples

Principal Investigator

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Research Institution

大規模運動介入研究における運動の効果に及ぼす遺伝子多型の探索

Principal Investigator

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Research Institution

Basic research for quantification of mitochondrial DNA copy number and mutations associated with agingPrincipal Investigator

Principal Investigator

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[Book] 老年医学update2007-082007

Author(s)

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[Journal Article] Mitochondrial haplogroups A and M7a confer a genetic risk for coronary atherosclerosis in the Japanese elderly : An autopsy study of 1, 536 patients2011

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DOI

NAID

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[Journal Article] Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations2011

Author(s)

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DOI

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[Journal Article] Extensive and Rapid Screening for Major Mitochondrial DNA Point Mutations in Patients with Hereditary Hearing Loss2010

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NAID

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[Journal Article] Pyruvate therapy for Leigh syndrome due to cytochrome c oxidase deficiency2010

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[Journal Article] Extensive screening system using suspension array technology to detect mitochondrial DNA point mutations2010

Author(s)

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DOI

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[Journal Article] Pyruvate therapy for Leigh syndrome due to cytochrome c oxidase deficiency2010

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[Journal Article] Mitochondrial haplogroups associated with lifestyle-related diseases and longevity in the Japanese population2010

Author(s)

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NAID

Data Source

[Journal Article] Mitochondrial haplogroups associated with lifestyle-related diseases and longevity in the Japanese population2010

Author(s)

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DOI

NAID

Data Source

[Journal Article] Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss2010

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NAID

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[Journal Article] Association of genetic variants with chronic kidney disease in individuals with different lipid profiles.2009

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[Journal Article] Analysis of mitochondrial DNA variants in Japanese patients with schizophrenia2009

Author(s)

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Nishigaki Yutaka 西垣裕

NISHIGAKI Yutaka 西垣裕