kanno hitoshi 菅野仁

… Alternative Names

KANNO Hitoshi 菅野仁

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Researcher Number	70221207
Other IDs
External Links
Affiliation (Current)	2025: 東京女子医科大学, 医学部, 特任教授
Affiliation (based on the past Project Information) *help	2022: 東京女子医科大学, 医学部, 特任教授 2013 – 2021: 東京女子医科大学, 医学部, 教授 2008 – 2013: 東京女子医科大学, 医学部, 准教授 2001 – 2006: Tokyo Women's Medical University, Department of Transfusion Medicine,. Associate Professor, 医学部, 助教授 1999 – 2000: 日本大学, 医学部, 専任講師 … More 1999 – 2000: 日本大学, 医学部, 講師 1999 – 2000: Tokyo Women's Medical University, Department of Biochemistry, Assistant Professor, 医学部・生化学教室, 講師 1998: Okinaka Memorial Inst.Med.Res.Research Fellow, 専任研究員 1997 – 1998: (財)冲中記念成人病研究所, 専任研究員 1996: 財団法人冲中記念成人病研究所, 専任研究員 1994 – 1995: (財)冲中記念成人病研究所, 専任研究員 1993: 財団法人冲中記念成人病研究所, 専任研究員 Less
Review Section/Research Field	Principal Investigator Pathological medical chemistry / Pediatrics / Pathological medical chemistry / Hematology Except Principal Investigator Hematology / Basic Section 52050:Embryonic medicine and pediatrics-related / Applied pharmacology / Hematology / Digestive surgery / Urology / Pediatrics
Keywords	Principal Investigator 溶血性貧血 / 赤血球 / ピルビン酸キナーゼ / 無効造血 / 赤血球酵素異常症 / 先天性溶血性貧血 / 解糖系 / 赤血球分化 / hemolytic anemia / フレンド細胞 … More / 遺伝子治療 / トランスジェニックマウス / モデルマウス / 代謝異常 / 細胞特異的発現 / 転写因子 / アイソザイム / 組織特異的発現 / ミトコンドリア / 疾患特異的iPS細胞 / オートファジー / 赤芽球分化 / iPS細胞 / ターゲット遺伝子シーケンスパネル / 次世代シークエンサー / 新生児溶血性貧血 / フローサイトメトリー / 赤血球浸透圧脆弱性 / 赤血球酵素 / 赤血球膜タンパク質 / 先天性赤血球形成異常性貧血 / 細胞周期 / 赤血球膜異常症 / 疾患遺伝子パネル / 次世代型シークエンサー / anti-oxidant / red cell life span / inborn error of metabolism / 酸化ストレス / 造血細胞コロニー解析 / 変異マウス / アンチオキシダント / 赤血球寿命 / 先天代謝異常症 / APOPTOSIS / ERYTHROCYTES / GLYCOLYSIS / PYRUVATE KINASE / MUTATION / HEMOLYTIC ANEMIA / RNAi / 遺伝性疾患 / Friend cells / disease model animals / reactive oxygen species / glycolysis / apoptosis / 活性酸素種 / アポトーシス / Erythroenzymopathies / Hemolytic anemia / Transcriptional regulation / Gene therapy / Transgenic mice / Metabolic disorder / Genetic disease / Glycolysis / 遺伝病 / 遺伝子変異 / 細胞特量的発現 / 転写調節 / 先天代謝異常 / 疾患モデルマウス / 微小血管障害 / IV型コラーゲン / 遺伝子検査 / 基底膜 / 全エクソーム解析 / 次世代型シーケンサー / 赤血球膜骨格蛋白 / 単一遺伝子病 / 貪食目印分子 / リン脂質 / 赤血球膜 / 単一遺伝子疾患 / 造血幹細胞移植 / 動物モデル / エンハンサー / プロモーター / 疾患モデル / 分化誘導 / 単一アミノ酸置換 / 調節遺伝子 / 劣性遺伝病 … More Except Principal Investigator 遺伝性非球状性溶血性貧血 / ピルビン酸キナーゼ異常症 / グルコース-6-リン酸脱水素酵素異常症 / 溶血性貧血 / ミスセンス変異 / 赤血球酵素異常症 / 遺伝子多型 / 赤血球 / neoadjuvant therapy / erythroenzymopathy / hereditary non-spherocytic hemolytic anemia / 感受性遺伝子 / 黄疸 / 超早産児 / 早産児 / 成人 / 新生児 / 臍帯血 / 遷延性重症黄疸 / UGT1A1 / DMET / バイオマーカー / CPT-11 / antioxidant / oxidative stress / single nucleotide polymorphisms (SNPs) / acute hemolysis / hemolytic anemia / α-hemoglobin stabilizing protein / 疾患感受性遺伝子 / アンチオキシダント / 酸化ストレス / 急性溶血発作 / α-ヘモグロビン安定化タンパク / ERYTHROCYTES / RETICULOCYTES / PYRIMIDINE / MUTATION / HEMOLYTIC ANEMIA / 変異酵素 / 免疫応答 / インフルエンザウイルス / トランスジェニックマウス / ピリミジン-5'-ヌクレオチダーゼ異常症 / ハプロタイプ / 遺伝子変異 / red cell deformability / pyruvate kinase deficiency / glucose-6-phosphate dehydrogenase deficiency / 塩基挿入 / 赤血球変形能 / 遺伝性非球状製溶血性貧血 / logistic regression / direct sequencing / immunohistochemical staining / treatment sensitivity / histopathologic effects / p53 gene / esophageal canoer / 術前治療 / 感受性 / 放射線療法 / 化学療法 / 化学放射線療法 / ロジスティック回帰分析 / ダイレクトシークエンス / 免疫組織染色 / 治療感受性 / 組織学的治療効果 / p53癌抑制遺伝子 / 食道癌 / missense mutation / intragenic deletion / enolase deficiency / hexokinase deficiency / フレームシフト変異 / スプライシング変異 / ピリミジン5′-ヌクレオチダーゼ異常症 / ヘキソキナーゼ異常症 / 遺伝子内欠失 / エノラーゼ異常症 / ヘキソナーゼ異常症 / がん免疫細胞療法 / 免疫細胞療法 / siRNA / レンチウイルスベクター / PK異常症 / 遺伝子治療 Less

Biochemical characteristics of erythrocytes in extremely preterm infants and identification of loci conferring susceptibility to prolonged severe hyperbilirubinemia
- Principal Investigator
  
  MORIOKA Ichiro
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Nihon University
Pathological analysis of congenital hemolytic anemia due to mitochondrial selective autophagy disorderPrincipal Investigator
- Principal Investigator
  
  KANNO HITOSHI
- Project Period (FY)
  2016 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Tokyo Women's Medical University
Identification of novel pathogenic genes for congenital hemolytic anemia and establishment of comprehensive gene testingPrincipal Investigator
- Principal Investigator
  
  KANNO HITOSHI
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Tokyo Women's Medical University
Comprehensive analysis of genetic polymorphisms and irinotecan-induced adverse events in Japanese gastrointestinal cancer patients: a DMET microarray profiling study
- Principal Investigator
  
  KURAMOCHI HIDEKAZU
- Project Period (FY)
  2013 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Applied pharmacology
- Research Institution
  Tokyo Women's Medical University
新規複合的アプローチによる腎細胞癌に対するγδ型Ｔ細胞傷害活性増強効果の検討
- Principal Investigator
  
  入部雄司
- Project Period (FY)
  2012 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Urology
- Research Institution
  Tokyo Women's Medical University
Development of novel gene therapy for congenital blood disorders using induced pluripotent stem cellsPrincipal Investigator
- Principal Investigator
  
  KANNO Hitoshi
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Hematology
- Research Institution
  Tokyo Women's Medical University
A novel gene therapy for pyruvate kinase deficiency.
- Principal Investigator
  
  UTSUGISAWA Taiju
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Tokyo Women's Medical University
Screening for causative genes in unknown hemolytic anemia
- Principal Investigator
  
  FUJII Hisaichi
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Hematology
- Research Institution
  Tokyo Women's Medical University
IDENTIFICATION OF THE CAUSATIVE GENES RESPONSIBLE FOR ERYTHROID APOPTOSIS INDUCED BY GLYCOLYTIC INHIBITIONPrincipal Investigator
- Principal Investigator
  
  KANNO HITOSHI
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  TOKYO WOMEN'S MEDICAL UNIVERSITY
MOLECULAR MECHANISMS OF ACCELERATED ERYTHROID APOPTOSIS DUE TO A GLYCOLYTIC ENZYME DEFECTPrincipal Investigator
- Principal Investigator
  
  KANNO Hitoshi
- Project Period (FY)
  2002 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  TOKYO WOMEN'S MEDICAL UNIVERSITY
MOLECULAR BASIS OF PYRIMIDINE 5'-NUCLEOTIDASE (P5N) DEFICIENCY AND FUNCTIONAL ANALYSIS OF P5N
- Principal Investigator
  
  FUJII Hisaichi
- Project Period (FY)
  2002 – 2003
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Hematology
- Research Institution
  TOKYO WOMEN'S MEDICAL UNIVERSITY
Diagnosis and molecular analysis of red cell enzyme anomalies and analysis of red cell deformabilities
- Principal Investigator
  
  HISAICHI |Fujii
- Project Period (FY)
  2000 – 2001
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Hematology
- Research Institution
  Tokyo Women 's Medical University
Physiological significance of pyruvate kinase isozymes in erythrocyte.Principal Investigator
- Principal Investigator
  
  KANNO Hitoshi
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  NIHON UNIVERSITY
Histopathologic Effects of Neoadjuvant Therapy for Esophageal Cancer and p53 status
- Principal Investigator
  
  KAJIYAMA Yoshiaki
- Project Period (FY)
  1999 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Digestive surgery
- Research Institution
  JUNTENDO UNIVERSITY
Molecular analysis of hereditary hemolytic anemia due to red cell enzyme anomalies
- Principal Investigator
  
  FUJII Hisaichi
- Project Period (FY)
  1998 – 1999
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Hematology
- Research Institution
  Tokyo Women's Medical University
Regulation of human pyruvate kinase gene in red cellsPrincipal Investigator
- Principal Investigator
  
  KANNO Hitoshi
- Project Period (FY)
  1997 – 1998
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Okinaka Memorial Institute for Medical Research
赤血球酵素異常症モデルマウスを用いた遺伝子治療の基礎的研究Principal Investigator
- Principal Investigator
  
  菅野仁
- Project Period (FY)
  1996
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Okinaka Memorial Institute for Medical Research
ピルビン酸キナーゼ異常症モデルマウスにおける遺伝性溶血性貧血の発症機構解明Principal Investigator
- Principal Investigator
  
  菅野仁
- Project Period (FY)
  1995
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Okinaka Memorial Institute for Medical Research
赤芽球分化に伴う赤血球型ピルビン酸キナーゼの発現とその転写制御Principal Investigator
- Principal Investigator
  
  菅野仁
- Project Period (FY)
  1994
- Research Category
  
  Grant-in-Aid for Scientific Research on Priority Areas
- Research Institution
  Okinaka Memorial Institute for Medical Research
トランスジェニックマウスを用いた赤芽球特異的遺伝子発現機構の解析Principal Investigator
- Principal Investigator
  
  菅野仁
- Project Period (FY)
  1993
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Pathological medical chemistry
- Research Institution
  Okinaka Memorial Institute for Medical Research

[Book] 血液内科【貧血性疾患診療の進歩】先天性溶血性貧血の遺伝子診断2016
- Author(s)
  大賀正一, 山城安啓, 菅野仁
- Total Pages
  273
- Publisher
  科学評論社
- Data Source
  KAKENHI-PROJECT-16K10041
[Book] MedicalPractic 【貧血　実地医家に役立つ知識と診療の進めかた】セミナー臨床に役立つ知識と情報　溶血性貧血の鑑別診断の進め方2016
- Author(s)
  小倉浩美, 菅野仁
- Total Pages
  166
- Publisher
  文光堂
- Data Source
  KAKENHI-PROJECT-16K10041
[Book] 見過ごせないウイルス感染症ヒトパルボウイルスB192016
- Author(s)
  大賀正一,猪股裕紀洋,菅野仁,田村正徳,八重樫伸生
- Total Pages
  180
- Publisher
  メディカルレビュー社
- Data Source
  KAKENHI-PROJECT-16K10041
[Book] 小児内科　【血球の増加と減少】赤血球　貧血　遺伝性貧血2016
- Author(s)
  小倉浩美、菅野　仁
- Total Pages
  140
- Publisher
  東京医学社
- Data Source
  KAKENHI-PROJECT-16K10041
[Book] 第VIII章　2.先天性溶血性貧血、血液専門医テキスト改訂第二版2015
- Author(s)
  菅野　仁
- Total Pages
  604
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-25461609
[Book] 赤血球酵素活性、スタンダード検査血液学第3版2015
- Author(s)
  菅野　仁
- Total Pages
  496
- Publisher
  医歯薬出版
- Data Source
  KAKENHI-PROJECT-25461609
[Book] 溶血性貧血、こどもの病気遺伝について聞かれたら2015
- Author(s)
  菅野　仁
- Total Pages
  260
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-25461609
[Book] 溶血検査、最新ガイドライン準拠血液疾患診断・治療指針2015
- Author(s)
  菅野　仁
- Total Pages
  576
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-25461609
[Book] 診療の手引きと臨床データ集血液疾患診療ハンドブック改訂3版2015
- Author(s)
  菅野　仁、小倉浩美
- Total Pages
  592
- Publisher
  医薬ジャーナル社
- Data Source
  KAKENHI-PROJECT-25461609
[Book] 遺伝子医学MOOK 別冊いまさら聞けない「遺伝医学」2014
- Author(s)
  内山　智貴、菅野　仁
- Total Pages
  200
- Publisher
  メディカルドゥ
- Data Source
  KAKENHI-PROJECT-25461609
[Book] 【検査で切り込む溶血性貧血】非免疫性溶血性貧血を対象とした診断システムの構築2014
- Author(s)
  菅野　仁
- Total Pages
  400
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-25461609
[Book] ：XI-4-1リンパ球免疫療法－養子免疫療法を含む、新版日本輸血・細胞治療学会認定医制度指定カリキュラム2012
- Author(s)
  菅野仁
- Total Pages
  423
- Publisher
  日本輸血・細胞治療学会認定医制度指定カリキュラム委員会編
- Data Source
  KAKENHI-PROJECT-22591071
[Book] II-4-1 造血機構、新版日本輸血・細胞治療学会認定医制度指定カリキュラム、日本輸血・細胞治療学会認定医制度指定カリ2012
- Author(s)
  菅野仁
- Publisher
  キュラム委員会編
- Data Source
  KAKENHI-PROJECT-22591071
[Book] 院内・検査室における遺伝子情報の管理 Medical Technology2012
- Author(s)
  斎藤加代子、菅野仁、福島武春、川島眞
- Publisher
  医歯薬出版株式会社
- Data Source
  KAKENHI-PROJECT-22591071
[Book] XI-3-2腎移植、新版日本輸血・細胞治療学会認定医制度指定カリキュラム2012
- Author(s)
  菅野仁
- Total Pages
  423
- Publisher
  日本輸血・細胞治療学会認定医制度指定カリキュラム委員会編
- Data Source
  KAKENHI-PROJECT-22591071
[Book] XI-3-2 腎移植、新版日本輸血・細胞治療学会認定医制度指定カリキュラム、日本輸血・細胞治療学会認定医制度指定カリ2012
- Author(s)
  菅野仁
- Publisher
  キュラム委員会編
- Data Source
  KAKENHI-PROJECT-22591071
[Book] XI-4-1 リンパ球免疫療法-養子免疫療法を含む、新版日本輸血・細胞治療学会認定医制度指定カリキュラム、日本輸血・細胞治療学会認定医制度指定カ2012
- Author(s)
  菅野仁
- Publisher
  キュラム委員会編
- Data Source
  KAKENHI-PROJECT-22591071
[Book] ：VI-3-16腎疾患、新版日本輸血・細胞治療学会認定医制度指定カリキュラム2012
- Author(s)
  菅野仁
- Total Pages
  423
- Publisher
  日本輸血・細胞治療学会認定医制度指定カリキュラム委員会編
- Data Source
  KAKENHI-PROJECT-22591071
[Book] VI-3-16 腎疾患、新版日本輸血・細胞治療学会認定医制度指定カリキュラム、日本輸血・細胞治療学会認定医制度指定カリ2012
- Author(s)
  菅野仁
- Publisher
  キュラム委員会編
- Data Source
  KAKENHI-PROJECT-22591071
[Book] II-4-1造血機構、新版日本輸血・細胞治療学会認定医制度指定カリキュラム2012
- Author(s)
  菅野仁
- Total Pages
  423
- Publisher
  日本輸血・細胞治療学会認定医制度指定カリキュラム委員会編
- Data Source
  KAKENHI-PROJECT-22591071
[Book] 血液専門医テキスト(先天性溶血性貧血)2011
- Author(s)
  菅野仁
- Total Pages
  5
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-22591071
[Book] 先天性溶血性貧血血液専門医テキスト2011
- Author(s)
  菅野仁
- Publisher
  日本血液学会編
- Data Source
  KAKENHI-PROJECT-22591071
[Book] Genetic Errors Associated with Purine and Pyrimidine Metabolism in Humans : Diagnosis and Treatment2006
- Author(s)
  Hitoshi Kanno
- Publisher
  Biochemical and molecular basis of red blood cell pyrimidine 5'-nucleotidase deficiency
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591013
[Book] Genetic errors associated with purine and pyrimidine metabolism in humans : diagnosis and treatment2006
- Author(s)
  Kanno H
- Total Pages
  196
- Publisher
  Biochemical and molecular basis of red blood cell pyrimidine 5'-nucleotidase deficiency
- Data Source
  KAKENHI-PROJECT-17591013
[Journal Article] Variant spectrum of PIEZO1 and KCNN4 in Japanese patients with dehydrated hereditary stomatocytosis.2023
- Author(s)
  Nakahara E, Shimojima Yamamoto K, Ogura H, Aoki T , Utsugisawa T, Azuma K, Akagawa H, Watanabe K, Muraoka M, Nakamura F, Kamei M, Tatebayashi K, Shinozuka J, Yamane T, Hibino M, Katsura Y, Nakano-Akamatsu S, Kadowaki N, Maru Y, Etsuro Ito E, Ohga S, Yagasaki H, Morioka I, Yamamoto T and Kanno H.
- Journal Title
  
  Hum Genome Var
  
  Volume: 10 Issue: 1 Pages: 8-8
- DOI
  10.1038/s41439-023-00235-y
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19H03506, KAKENHI-PROJECT-20K08239, KAKENHI-PROJECT-23K21429, KAKENHI-PROJECT-21K07873
[Journal Article] Primrose syndrome associated with unclassified immunodeficiency and a novel ZBTB20 mutation.2020
- Author(s)
  Yamamoto-Shimojima K, Imaizumi T, Akagawa H, Kanno H, Yamamoto T.
- Journal Title
  
  Am J Med Genet A
  
  Volume: 182 Issue: 3 Pages: 521-526
- DOI
  10.1002/ajmg.a.61432
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07803, KAKENHI-PROJECT-17K18133, KAKENHI-PROJECT-17J40108, KAKENHI-PROJECT-16K10041
[Journal Article] Unexplained Late-Onset Hemolytic Jaundice Preceded by High Fetal Hemoglobin Level in an Extremely Low Birth Weight Infant2020
- Author(s)
  Kwon GoEun、Okahashi Aya、Nagano Nobuhiko、Nozaki Chihiro、Nakahara Erina、Fuwa Kazumasa、Yagasaki Hiroshi、Kanno Hitoshi、Morioka Ichiro
- Journal Title
  
  Clinical Laboratory
  
  Volume: 66 Issue: 01+02/2020
- DOI
  10.7754/clin.lab.2019.190625
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] KLF1 Mutation E325K Induces Cell-cycle Arrest in Erythroid Cells Differentiated from Congenital Dyserythropoietic Anemia (CDA) Patient-specific Induced Pluripotent Stem Cells.2019
- Author(s)
  Kohara H, Utsugisawa T, Sakamoto C, Hirose L, Ogawa Y, Ogura H, Sugawara A, Aoki T, Iwasaki T, Asai T, Doisaki S, Okuno Y, Muramatsu H, Abe T, Kurita R, Miyamoto S, Sakuma T, Shiba M, Yamamoto T, Ohga S, Yoshida K, Ogawa S, Ito E, Kojima S, Kanno H, Tani K.
- Journal Title
  
  Exp Hematol.
  
  Volume: 73 Pages: 25-37
- DOI
  10.1016/j.exphem.2019.03.001
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26221308, KAKENHI-PROJECT-17H01547, KAKENHI-PROJECT-19K16500, KAKENHI-PROJECT-19H05656, KAKENHI-PROJECT-16K10041, KAKENHI-PROJECT-16K19181
[Journal Article] 遺伝性メトヘモグロビン血症Ⅰ型の兄妹例2019
- Author(s)
  羽賀洋一、高橋浩之、三井一賢、中村俊紀、松岡正樹、小嶋靖子、小倉浩美、菅野仁、服部幸夫、小原明
- Journal Title
  
  日本小児科学会雑誌
  
  Volume: 123 Pages: 861-865
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] 特集　新生児黄疸を再び考える　各論　先天性溶血性疾患2019
- Author(s)
  小倉　浩美、菅野　仁
- Journal Title
  
  周産期医学
  
  Volume: 49 Pages: 211-216
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] Association between SLCO1B1 rs4149056 and tegafur?uracil-induced hepatic dysfunction in breast cancer2019
- Author(s)
  Kamio Hidenori、Uchiyama Toshitaka、Kanno Hitoshi、Onoe Yoshiko、Saito Kayoko、Kameoka Shingo、Kamio Takako、Okamoto Takahiro
- Journal Title
  
  Pharmacogenomics
  
  Volume: 20 Issue: 5 Pages: 353-365
- DOI
  10.2217/pgs-2018-0100
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] Phase I study of cellular therapy using ex vivo expanded NK cell from autologous peripheral blood mononuclear cells combined with rituximab-containing chemotherapy for relapsed CD20-positive malignant lymphoma patients2019
- Author(s)
  Tanaka Junji、Tanaka Norina、Wang Yan-Hua、Mistuhashi Kenjiro、Ryuzaki Michiko、Iizuka Yuki、Watanabe Aya、Ishiyama Midori、Shinohara Akihito、Kazama Hiroshi、Hagiwara Shotaro、Yoshinaga Kentaro、Kougen Yumi、Kobayashi Hirohito、Kanno Hitoshi、Shiseki Masayuki
- Journal Title
  
  Haematologica
  
  Volume: 105 Issue: 4 Pages: e190-e193
- DOI
  10.3324/haematol.2019.226696
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] 血球酵素とその異常. 特集赤血球造血のメカニズムとその異常－最近の進歩―2018
- Author(s)
  小倉浩美、菅野仁
- Journal Title
  
  血液フロンティア
  
  Volume: 28 Pages: 1333-1341
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] SURVEY OF THE STATUS OF INTRAVENOUS IMMUNOGLOBULIN (IVIG) PRODUCTS: TRANSITION IN RECENT YEARS AT TOKYO WOMEN'S MEDICAL UNIVERSITY HOSPITAL2018
- Author(s)
  中林恭子, 松田和樹, 小林博人, 小野慎吾, 岩﨑拓也, 久保田友晶, 守屋友美, 緒方康貴, 及川美幸, 木下明美, 青木貴子, 千野峰子, 岡田真一, 高源ゆみ, 青木正弘, 岡本好雄, 今野マユミ, 槍澤大樹, 小倉浩美, 菅野仁
- Journal Title
  
  Japanese Journal of Transfusion and Cell Therapy
  
  Volume: 64 Issue: 1 Pages: 21-27
- DOI
  10.3925/jjtc.64.21
- NAID
  130006513931
- ISSN
  1881-3011, 1883-0625
- Language
  Japanese
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] HbA1cが偽低値をしめしたエノラーゼ、異常症合併2型糖尿病の1例2018
- Author(s)
  井島廣子、古賀正史、杉山正悟、小倉浩美、菅野仁、陣内秀昭
- Journal Title
  
  Diabetes Journal
  
  Volume: 46 Pages: 30-34
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome2018
- Author(s)
  Toki Tsutomu、Yoshida Kenichi、Wang RuNan、Okuno Yusuke、Kataoka Keisuke、Shiraishi Yuichi、Ohga Shouichi、Kuramitsu Madoka、Hamaguchi Isao、Ohara Akira、Kanno Hitoshi、Miyano Satoru、Kojima Seiji、Ishiguro Akira、Sugita Kanji、Kenmochi Naoya、Takahashi Satoru、Eto Koji、Ogawa Seishi、Ito Etsuro
- Journal Title
  
  The American Journal of Human Genetics
  
  Volume: 103 Issue: 3 Pages: 440-447
- DOI
  10.1016/j.ajhg.2018.07.020
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041, KAKENHI-PROJECT-17K10093, KAKENHI-PLANNED-15H05909, KAKENHI-PROJECT-26221308, KAKENHI-PROJECT-18H04039, KAKENHI-PROJECT-18K07868, KAKENHI-PROJECT-18H04164
[Journal Article] Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency2018
- Author(s)
  Paola Bianchi, Elisa Fermo, Bertil Glader, Hitoshi Kanno, Archana Agarwal, Wilma Barcellini, Stefan Eber, James D. Hoyer, David J. Kuter, Serge Pissard, Eduard van Beers, Patrick G. Gallagher, David C. Rees, Richard van Wijk
- Journal Title
  
  American Journal of Hematology
  
  Volume: 94 Issue: 1 Pages: 149-161
- DOI
  10.1002/ajh.25325
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] <b>In vitro enhancement of ATP in human erythrocytes from a healthy subject and two patients with thalassemia and hemoglobinopathy.</b>2018
- Author(s)
  Kamatani Naoyuki、Furihata Kenichi、Taniguchi Atsuo、Fukuuchi Tomoko、Yamaoka Noriko、Kaneko Kiyoko、Kanno Hitoshi
- Journal Title
  
  GOUT AND NUCLEIC ACID METABOLISM
  
  Volume: 42 Issue: 1 Pages: 59-64
- DOI
  10.6032/gnam.42.59
- NAID
  130007419211
- ISSN
  1344-9796, 2186-6368
- Year and Date
  2018-07-25
- Language
  English
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.2018
- Author(s)
  Sonoda M, Ishimura M, Ichimiya Y, Terashi E, Eguchi K, Sakai Y, Takada H, Hama A, Kanno H, Toki T, Ito E, Ohga S.
- Journal Title
  
  Int J Hematol.
  
  Volume: 印刷中 Issue: 2 Pages: 228-231
- DOI
  10.1007/s12185-018-2424-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26253061, KAKENHI-PROJECT-16K10041
[Journal Article] 新生児の遺伝性溶血性貧血～疾患概念の拡張～2018
- Author(s)
  大賀　正一、石村　匡崇、槍澤　大樹、菅野　仁
- Journal Title
  
  日本産婦人科・新生児血液学会誌
  
  Volume: 27 Pages: 41-47
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] Whole-exome analysis to detect congenital hemolytic anemia mimicking congenital dyserythropoietic anemia2018
- Author(s)
  Hamada Motoharu、Doisaki Sayoko、Okuno Yusuke、Muramatsu Hideki、Hama Asahito、Kawashima Nozomu、Narita Atsushi、Nishio Nobuhiro、Yoshida Kenichi、Kanno Hitoshi、Manabe Atsushi、Taga Takashi、Takahashi Yoshiyuki、Miyano Satoru、Ogawa Seishi、Kojima Seiji
- Journal Title
  
  International Journal of Hematology
  
  Volume: 108 Issue: 3 Pages: 306-311
- DOI
  10.1007/s12185-018-2482-7
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041, KAKENHI-PROJECT-18K12273, KAKENHI-PLANNED-15H05909, KAKENHI-PROJECT-26221308, KAKENHI-PROJECT-16K19311, KAKENHI-PROJECT-17K16248
[Journal Article] EFFICACY OF CELL-FREE AND CONCENTRATED ASCITES FOR AUTOLOGOUS ALBUMIN PRODUCTS2018
- Author(s)
  Utsugisawa Taiju、Kobayashi Ryosuke、Isoai Ayako、Onodera Hirokazu、Matsuno Yoshihiro、Kato Michio、Kanno Hitoshi
- Journal Title
  
  Japanese Journal of Transfusion and Cell Therapy
  
  Volume: 64 Issue: 5 Pages: 631-640
- DOI
  10.3925/jjtc.64.631
- NAID
  130007498542
- ISSN
  1881-3011, 1883-0625
- Year and Date
  2018-10-25
- Language
  Japanese
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia.2017
- Author(s)
  Ikeda F, Yoshida K, Toki T, Uechi T, Ishida S, Nakajima Y, Sasahara Y, Okuno Y, Kanezaki R, Terui K, Kamio T, Kobayashi A, Fujita T, Sato-Otsubo A, Shiraishi Y, Tanaka H, Chiba K, Muramatsu H, Kanno H, Ohga S, Ohara A, Kojima S, Kenmochi N, Miyano S, Ogawa S, Ito E.
- Journal Title
  
  Haematologica.
  
  Volume: - Issue: 3 Pages: e93-e96
- DOI
  10.3324/haematol.2016.153932
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PLANNED-15H05909, KAKENHI-PROJECT-26221308, KAKENHI-PROJECT-26253061, KAKENHI-PROJECT-25291003, KAKENHI-PROJECT-15K09656, KAKENHI-PROJECT-15K15367, KAKENHI-PROJECT-16K10041, KAKENHI-PROJECT-15K09647
[Journal Article] マイクロプレート法による赤血球浸透圧抵抗試験とeosin-5-maleimideを用いた赤血球膜band3定量法が診断に有用であった新生児期に重症黄疸を発症した赤血球膜蛋白異常症の1例2017
- Author(s)
  西本瑛里、西久保敏也、釜本智之、石原卓、山口直子、菅野　仁、高橋幸博
- Journal Title
  
  日本産婦人科・新生児血液学会誌
  
  Volume: 26 Pages: 71-76
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] Splenectomy resolves hemolytic anemia caused by adenylate kinase deficiency2017
- Author(s)
  Niizuma Hidetaka、Kanno Hitoshi、Sato Atsushi、Ogura Hiromi、Imaizumi Masue
- Journal Title
  
  Pediatr Int
  
  Volume: 59 Issue: 2 Pages: 228-230
- DOI
  10.1111/ped.13166
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing2017
- Author(s)
  Ichimura T, Yoshida K, Okuno Y, Yujiri T, Nagai K, Nishi M, Shiraishi Y, Ueno H, Toki T, Chiba K, Tanaka H, Muramatsu H, Hara T, Kanno H, Kojima S, Miyano S, Ito E, Ogawa S, Ohga S.
- Journal Title
  
  Int J Hematol.
  
  Volume: 105 Issue: 4 Pages: 515-520
- DOI
  10.1007/s12185-016-2151-7
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26253061, KAKENHI-PROJECT-26461421, KAKENHI-PROJECT-16K10041, KAKENHI-PROJECT-26221308, KAKENHI-PROJECT-15K09647
[Journal Article] Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes.2017
- Author(s)
  Muramatsu H, Okuno Y, Yoshida K, Shiraishi Y, Doisaki S, Narita A, Sakaguchi H, Kawashima N, Wang X, Xu Y, Chiba K, Tanaka H, Hama A, Sanada M, Takahashi Y, Kanno H, Yamaguchi H, Ohga S, Manabe A, Harigae H, Kunishima S, Ishii E, Kobayashi M, Koike K, Watanabe K, Ito E, Takata M, Yabe M, Ogawa S, Miyano S, Kojima S.
- Journal Title
  
  Genet Med.
  
  Volume: - Issue: 7 Pages: 796-802
- DOI
  10.1038/gim.2016.197
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PLANNED-15H05909, KAKENHI-PROJECT-26221308, KAKENHI-PROJECT-15H01738, KAKENHI-PROJECT-26253061, KAKENHI-PROJECT-26293225, KAKENHI-PROJECT-15K09647, KAKENHI-PROJECT-16K09832, KAKENHI-PROJECT-16K10041, KAKENHI-PROJECT-15H04874
[Journal Article] Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing2017
- Author(s)
  Ichimura T, Yoshida K, Okuno Y, Yujiri T, Nagai K, Nishi M, Shiraishi Y, Ueno H, Toki T, Chiba K, Tanaka H, Muramatsu H, Hara T, Kanno H, Kojima S, Miyano S, Ito E, Ogawa S, Ohga S
- Journal Title
  
  Int J Hematol.
  
  Volume: 105 Pages: 515-520
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] 貧血学-最新の診断・治療動向-V溶血性貧血　赤血球酵素異常症・不安定ヘモグロビン症2017
- Author(s)
  小倉　浩美、菅野　仁
- Journal Title
  
  日本臨床
  
  Volume: 75 Pages: 472-477
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] Discrimination of Diamond-Blackfan anemia from parvovirus B19 infection by RBC glutathione2017
- Author(s)
  Noguchi Jun、Kanno Hitoshi、Chiba Yuta、Ito Etsuro、Ishiguro Akira
- Journal Title
  
  Pediatrics International
  
  Volume: 59 Issue: 7 Pages: 838-840
- DOI
  10.1111/ped.13284
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K10041, KAKENHI-PROJECT-26253061
[Journal Article] A novel PGK1 mutation associated with neurological dysfunction and the absence of episodes of hemolytic anemia or myoglobinuria2017
- Author(s)
  Matsumaru S, Oguni H, Ogura H, Shimojima K, Nagata S, Kanno H, Yamamoto T
- Journal Title
  
  Intractable Rare Diseases Research
  
  Volume: 6 Issue: 2 Pages: 132-136
- DOI
  10.5582/irdr.2017.01020
- NAID
  130005695959
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K10041, KAKENHI-PROJECT-17K18133, KAKENHI-PROJECT-17J40108
[Journal Article] Early-onset parkinsonism in a pedigree with phosphoglycerate kinase deficiency and a heterozygous carrier: do PGK-1 mutation contribute to vulnerability to parkinsonism?2017
- Author(s)
  Satoshi Sakaue, Takashi Kasai, Ikuko Mizuta, Masaya Suematsu, Shinya Osone, Yumiko Azuma, Toshihiko Imamura, Takahiko Tokuda, Hitoshi Kanno, Omar M.A. El-Agnaf, Masafumi Morimoto, Masanori Nakagawa, Hajime Hosoi and Toshiki Mizuno
- Journal Title
  
  NPJ Parkinsons Disease
  
  Volume: 31
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] 循環系の基礎と臨床（２）血管新生2017
- Author(s)
  槍澤　大樹、菅野　仁
- Journal Title
  
  東京女子医科大学雑誌
  
  Volume: 87 Pages: 5-12
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] Successful long-term management with low-dose prednisolone in an adult patient with Diamond-Blackfan anemia2017
- Author(s)
  小笠原壽恵、川内喜代隆、森直樹、佐倉宏、加藤文代、菅野仁、伊藤悦朗
- Journal Title
  
  Rinsho Ketsueki
  
  Volume: 58 Issue: 8 Pages: 917-921
- DOI
  10.11406/rinketsu.58.917
- NAID
  130006067981
- ISSN
  0485-1439, 1882-0824
- Language
  Japanese
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] Worldwide study of hematopoietic allogeneic stem cell transplantation in pyruvate kinase deficiency2017
- Author(s)
  van Straaten Stephanie、Bierings Marc、Bianchi Paola、Smiers Frans、Raymakers Reinier、Yanez Lucrecia、Sevilla Julian、van Solinge Wouter、Segovia Jose Carlos、van Wijk Richard
- Journal Title
  
  Haematologica
  
  Volume: 103 Issue: 2 Pages: e82-e86
- DOI
  10.3324/haematol.2017.177857
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan.2016
- Author(s)
  Ikeda F, Toki T, Kanezaki R, Terui K, Yoshida K, Kanno H, Ohga S, Ohara A, Kojima S, Ogawa S, Ito E.
- Journal Title
  
  Int J Hematol.
  
  Volume: 103 Issue: 1 Pages: 112-114
- DOI
  10.1007/s12185-015-1891-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26253061, KAKENHI-PROJECT-25461609, KAKENHI-PLANNED-15H05909, KAKENHI-PROJECT-26221308, KAKENHI-PROJECT-16K10041
[Journal Article] ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia2016
- Author(s)
  Arashiki N, Takakuwa Y, Mohandas N, Hale J, Yoshida K, Ogura H, Utsugisawa T, Ohga S, Miyano S, Ogawa S, Kojima S, Kanno H
- Journal Title
  
  Haematologica
  
  Volume: 101 Pages: 559-565
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Journal Article] Erythrocyte glutathione is a novel biomarker of Diamond-Blackfan anemia2016
- Author(s)
  Utsugisawa T, Uchiyama T, Toki T, Ogura H, Aoki T, Hamaguchi I, Ishiguro A, Ohara A, Kojima S, Ohga S, Ito E, Kanno H
- Journal Title
  
  Blood Cells, Molecules and Diseases
  
  Volume: 59 Pages: 31-36
- DOI
  10.1016/j.bcmd.2016.03.007
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-25461609, KAKENHI-PROJECT-26253061, KAKENHI-PROJECT-16K10041
[Journal Article] PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.2016
- Author(s)
  Imashuku S, Muramatsu H, Sugihara T, Okuno Y, Wang X, Yoshida K, Kato A, Tatsumi Y, Hattori A, Kita S, Oe K, Sueyoshi A, Usui T, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ogawa S, Kojima S, Kanno H
- Journal Title
  
  Int J Hematol
  
  Volume: 印刷中 Issue: 1 Pages: 125-129
- DOI
  10.1007/s12185-016-1970-x
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25461609, KAKENHI-PLANNED-15H05909, KAKENHI-PROJECT-26221308, KAKENHI-PROJECT-26461392, KAKENHI-PROJECT-16K10041
[Journal Article] ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia.2016
- Author(s)
  Nobuto Arashiki, Yuichi Takakuwa, Hitoshi Kanno
- Journal Title
  
  Haematologica
  
  Volume: 印刷中 Issue: 5 Pages: 559-565
- DOI
  10.3324/haematol.2016.142273
- Peer Reviewed / Acknowledgement Compliant / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25460375, KAKENHI-PROJECT-25461609, KAKENHI-PLANNED-15H05909, KAKENHI-PROJECT-26221308
[Journal Article] Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.2015
- Author(s)
  Wang R, Yoshida K, Toki T, Sawada T, Uechi T, Okuno Y, Sato-Otsubo A, Kudo K, Kamimaki I, Kanezaki R, Shiraishi Y, Chiba K, Tanaka H, Terui K, Sato T, Iribe Y, Ohga S, Kuramitsu M, Hamaguchi I, Ohara A, Hara J, et al.
- Journal Title
  
  British Journal of Haematology
  
  Volume: 168 Issue: 6 Pages: 854-864
- DOI
  10.1111/bjh.13229
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24591556, KAKENHI-PROJECT-25291003, KAKENHI-PROJECT-25461601, KAKENHI-PROJECT-25461609, KAKENHI-PROJECT-25860798, KAKENHI-PROJECT-26253061
[Journal Article] Glucose-6-phosphate dehydrogenase deficiency in Japan2015
- Author(s)
  Kanno H, Ogura H.
- Journal Title
  
  Rinsho Ketsueki
  
  Volume: 56 Issue: 7 Pages: 771-777
- DOI
  10.11406/rinketsu.56.771
- NAID
  130005093113
- ISSN
  0485-1439, 1882-0824
- Language
  Japanese
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-25461609
[Journal Article] 非免疫性溶血性貧血を対象とした診断システムの構築2014
- Author(s)
  菅野　仁
- Journal Title
  
  臨床検査
  
  Volume: 58 Pages: 327-335
- Data Source
  KAKENHI-PROJECT-25461609
[Journal Article] Human parvovirus B19-induced aplastic crisis in an adult patient with hereditary spherocytosis: a case report and review of the literature.2014
- Author(s)
  Kobayashi Y, Hatta Y, Ishiwatari Y, Kanno H, Takei M.
- Journal Title
  
  BMC Res Notes
  
  Volume: 7 Issue: 1 Pages: 137-137
- DOI
  10.1186/1756-0500-7-137
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25461609
[Journal Article] Deficiency of Nicotinamide Mononucleotide Adenylyltransferase 3 (Nmnat3) Causes Hemolytic Anemia by Altering the Glycolytic Flow in Mature Erythrocytes.2014
- Author(s)
  Hikosaka K, Ikutani M, Shito M, Kazuma K, Gulshan M, Nagai Y, Takatsu K, Konno K, Tobe K, Kanno H, Nakagawa T.
- Journal Title
  
  J Biol Chem
  
  Volume: 印刷中
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461609
[Journal Article] ABO血液型不適合腎移植におけるアルブミン製剤の必要性2014
- Author(s)
  守屋　友美、岡本好雄、小林博人、松田和樹、久保田友晶、緒方康貴、及川美幸、李舞香、木下明美、青木貴子、千野峰子、岡田真一、高源ゆみ、青木正弘、中林恭子、今野マユミ、槍澤大樹、小倉浩美、菅野　仁
- Journal Title
  
  日本輸血細胞治療学会誌
  
  Volume: 60 Pages: 521-526
- NAID
  130004688193
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461609
[Journal Article] Deficiency of nicotinamide mononucleotide adenylyltransferase 3 (nmnat3) causes Hemolytic anemia by altering the glycolytic flow in mature erythrocytes.2014
- Author(s)
  Hikosaka K., Ikutani M., Shito M., Kazuma K., Gulshan M., Nagai Y., Takatsu K., Konno K., Tobe K., Kanno H., Nakagawa T.
- Journal Title
  
  Journal of Biological Chemistry
  
  Volume: 289 Issue: 21 Pages: 14796-14811
- DOI
  10.1074/jbc.m114.554378
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390119, KAKENHI-PROJECT-24590577, KAKENHI-PUBLICLY-25126707, KAKENHI-PROJECT-25461609, KAKENHI-PROJECT-26461327
[Journal Article] 先天性溶血性貧血の病型および鑑別診断法の進歩と今後の課題2014
- Author(s)
  菅野　仁
- Journal Title
  
  日本小児血液・がん学会
  
  Volume: 51 Pages: 446-451
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461609
[Journal Article] Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression.2014
- Author(s)
  Viprakasit V, Ekwattanakit S, Riolueang S, Chalaow N, Fisher C, Lower K, Kanno H, Tachavanich K, Bejrachandra S, Saipin J, Juntharaniyom M, Sanpakit K, Tanphaichitr VS, Songdej D, Babbs C, Gibbons RJ, Philipsen S, Higgs DR.
- Journal Title
  
  Blood
  
  Volume: 123 Issue: 10 Pages: 1596-1596
- DOI
  10.1182/blood-2013-09-526087
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461609
[Journal Article] Enhanced expression of myogenic differentiation factors and skeletal muscle proteins in human amnion-derived cells via the forced expression of MYOD12013
- Author(s)
  Akizawa Y, Kanno H, Kawamichi Y, Matsuda Y, Ohta H, Fujii H, Matsui H, Saito K
- Journal Title
  
  Brain Dev
  
  Volume: 35 Pages: 349-355
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger.2013
- Author(s)
  Tsuzuki S, Akahira-Azuma M, Kaneshige M, Shoya K, Hosokawa S, Kanno H, Matsushita T.
- Journal Title
  
  Springerplus
  
  Volume: 2 Issue: 1 Pages: 434-434
- DOI
  10.1186/2193-1801-2-434
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461609
[Journal Article] Enhanced expression of myogenic differentiation factors and skeltal muscle proteins in human amnion-derived cells via the forced expression of MYOD1.2013
- Author(s)
  Yoshika Akizawa
- Journal Title
  
  Brain＆Development
  
  Volume: 35 Issue: 4 Pages: 349-355
- DOI
  10.1016/j.braindev.2012.05.012
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071, KAKENHI-PROJECT-25461609
[Journal Article] Pyruvate supplementation enhances vascular endothelial growth factor production of bone marrow-derived mononuclear cells2012
- Author(s)
  Kanno H, Iribe Y, Aoki T, Ogura H, Fujii H
- Journal Title
  
  Jpn J Transf Cell Ther
  
  Volume: 58 Pages: 26-32
- NAID
  10030760776
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] An SNP in CYP39A1 is associated with severe neutropenia induced by docetaxel2012
- Author(s)
  Uchiyama T, Kanno H, Ishitani K, Fujii H, Ohta H, Matsui H, Kamatani N, Saito K
- Journal Title
  
  Cancer Chemother Pharmacol
  
  Volume: 69 Pages: 1617-1624
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] PYRUVATE SUPPLEMENTATION ENHANCES VASCULAR ENDOTHELIAL GROWTH FACTOR PRODUCTION BY BONE MARROW-DERIVED MONONUCLEAR CELLS2012
- Author(s)
  Hitoshi Kanno
- Journal Title
  
  Japanese Journal of Transfusion and Cell Therapy
  
  Volume: 58 Issue: 1 Pages: 26-32
- DOI
  10.3925/jjtc.58.26
- NAID
  130004542654
- ISSN
  1881-3011, 1883-0625
- Language
  Japanese
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] Pyruvate supplementation enhanced vascular endothelial growth factor production by bone marrow-derived mononuclear cells2012
- Author(s)
  Kanno H, Iribe T, Aoki T, Ogura H, FujiiH.
- Journal Title
  
  Japanese Journal of Transfusion and Cell Therapy
  
  Volume: 58 Pages: 26-32
- NAID
  10030760776
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] High-dose chemotherapy followed by autologous and allogeneic peripheral blood stem cell transplantation for recurrent disseminated trilateral retinoblastoma2011
- Author(s)
  Tsuruta T, Aihara Y, Kanno H, Kiyotani C, Maebayashi K, Sakauchi M, Osawa M, Fujii H, Kubo O, Okada Y
- Journal Title
  
  Childs Nerv Syst
  
  Volume: 27 Pages: 1019-1024
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] Extensive gene deletions in Japanese patients with Diamond-Blackfan anemia2011
- Author(s)
  Kuramitsu M, Matsubara A, Morio T, Takagi M, Toki T, Terui K, RuNan W, Kanno H, Ohga S, Ohara A, Kitoh T, Sugita K, Kudo K, Matsubayashi T, Mizue N, Ozeki M, Masumi A, Momose H, Takizawa K, Mizukami T, Yamaguchi K, Ogawa S, Ito E, Hamaguchi I
- Journal Title
  
  Blood
  
  Volume: (in press) Issue: 10 Pages: 2376-84
- DOI
  10.1182/blood-2011-07-368662
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21591388, KAKENHI-PROJECT-22591071, KAKENHI-PROJECT-22790922, KAKENHI-PROJECT-23390266, KAKENHI-PROJECT-23791093, KAKENHI-PROJECT-23791162, KAKENHI-PUBLICLY-23118501
[Journal Article] Shared molecular targets in pediatric gliomas and ependymomas2011
- Author(s)
  Tsuruta T, Aihara Y, Kanno H, Funase M,Murayama T, Osawa M, Fujii H, Kubo O, Okada Y.
- Journal Title
  
  Pediatr Blood Cancer
  
  Volume: 57 Pages: 1117-1123
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] Shared molecular targets in pediatric gliomas and ependymomas2011
- Author(s)
  Tsuruta T, Aihara Y, Kanno H, Funase M, et al
- Journal Title
  
  Pediatr Blood Cancer
  
  Volume: 57 Issue: 7 Pages: 1117-23
- DOI
  10.1002/pbc.23009
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] 小児科領域における研究と治療の進歩-遺伝子医療2011
- Author(s)
  斎藤加代子、松尾真理、菅野仁、浦野真理、相楽有規子
- Journal Title
  
  東京女子医科大学雑誌
  
  Volume: 81 Pages: 349-355
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] High-dose chemotherapy followed by autologous and allogenic peripheral blood stem cell transplantation for recurrent disseminated trilateral retinoblastoma2011
- Author(s)
  Tsuruta T, Aihara Y, Kanno H, Kiyotani C, et al
- Journal Title
  
  Childs Nerv Syst
  
  Volume: 27 Issue: 6 Pages: 1019-24
- DOI
  10.1007/s00381-011-1419-8
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] 遺伝情報管理の現状と展望電子カルテによる遺伝子情報管理の実際.2010
- Author(s)
  菅野仁、斎藤加代子
- Journal Title
  
  日本遺伝カウンセリング学会誌
  
  Volume: 31 Pages: 127-129
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] 遺伝子情報管理の現状と展望遺伝子検査結果の電子化2010
- Author(s)
  福島武春、斎藤加代子、菅野仁、川島眞、肝付浩一郎
- Journal Title
  
  日本遺伝カウンセリング学会誌
  
  Volume: 31 Pages: 131-135
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] Double high-dose chemotherapy followed by autologous peripheral blood stem cell transplantation for primary disseminated medulloblastoma:a report of 3 cases2010
- Author(s)
  Aihara Y, Tsuruta T, Kawamata T, Kanno H, Maebayashi K, Wada E, Osawa M, Fujii H,Kubo O, Hori T.
- Journal Title
  
  J Pediatr Hematol Oncol
  
  Volume: 32
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591071
[Journal Article] Transgenic rescue of hemolytic anemia due to red blood cell pyruvate kinase deficiency2007
- Author(s)
  Hitoshi Kanno et al.
- Journal Title
  
  Haematologica (in press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591013
[Journal Article] Transgenic rescue of hemolytic anemia due to red blood cell pyruvatekinase deficiency2007
- Author(s)
  Kanno H, et al.
- Journal Title
  
  Haematologica (in press)
- Data Source
  KAKENHI-PROJECT-17591013
[Journal Article] 寿命を終えた赤血球の処理機構-赤血球膜に出現する貪食目印分子に関する最近の知見-2007
- Author(s)
  菅野仁, 藤井寿一
- Journal Title
  
  Membrane 31・3(in press)
- NAID
  130005077797
- Data Source
  KAKENHI-PROJECT-17591013
[Journal Article] 寿命を終えた赤血球の処理機構~赤血球膜に出現する貪食目印分子に関する最近の知見~2007
- Author(s)
  菅野仁, 藤井寿一
- Journal Title
  
  Membrane 31・3(in press)
- NAID
  130005077797
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591013
[Journal Article] Biochemical and molecular basis of red blood cell pyrimidine5'-nucleotidase deficiency2006
- Author(s)
  Hitoshi Kanno
- Journal Title
  
  Genetic Errors Associated with Purine and Pyrimidine Metabolism in Humans : Diagnosis and Treatment
  
  Pages: 143-154
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-17591013
[Journal Article] 細胞療法・再生医療と中央部門のかかわり2006
- Author(s)
  菅野仁
- Journal Title
  
  日本アフェレシス学会雑誌 25・3
  
  Pages: 226-232
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-17591013
[Journal Article] Ineffective erythropoiesis in mutant mice with deficient pyruvate kinase activity.2005
- Author(s)
  Aizawa, S., Harada, T., Kanbe, E., Tsuboi, I., Aisaki, K., Fujii, H., Kanno, H.
- Journal Title
  
  Exp Hematol 33
  
  Pages: 1292-1298
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590254
[Journal Article] Ineffective erythropoiesis in mutant mice with deficient pyruvate kinase activity.2005
- Author(s)
  Aizawa S, Harada T, Kanbe E, Tsuboi I, Aisaki K, Fujii H, Kanno H
- Journal Title
  
  Exp.Hematol. 33(11)
  
  Pages: 1292-1298
- Data Source
  KAKENHI-PROJECT-17591013
[Journal Article] Cyclic polylactate inhibited growth of cloned leukemic cells through reducing glycolytic enzyme activities.2005
- Author(s)
  Harada, T., Nagasu, M., Tsuboi, I., Koshinaga, M., Kanno.H., Aizawa, S.
- Journal Title
  
  Oncol Rep 14
  
  Pages: 501-505
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590254
[Journal Article] A novel homozygous mutation of PKLR gene in a pyruvate-kinase-deficient Korean family.2005
- Author(s)
  Park-Hah JO, Kanno H, Kim WD, Fujii H
- Journal Title
  
  Acta Haematol. 113(3)
  
  Pages: 208-211
- Data Source
  KAKENHI-PROJECT-16590254
[Journal Article] Ineffective erythropoiesis in mutant mice with deficient pyruvate kinase activity.2005
- Author(s)
  Aizawa S, Harada T, Kanbe E, Tsuboi I, Aisaki K, Fujii H, Kanno H
- Journal Title
  
  Exp.Hematol. 33(11)
  
  Pages: 1292-1298
- Data Source
  KAKENHI-PROJECT-16590254
[Journal Article] A novel homozygous mutation of PKLR gene in a pyruvate-kinase-deficient Korean family.2005
- Author(s)
  Park-Hah JO, Kanno H, Kim WD, Fujii H
- Journal Title
  
  Acta Haematol. 113(3)
  
  Pages: 208-211
- Data Source
  KAKENHI-PROJECT-17591013
[Journal Article] A novel homozygous mutation of PKLR gene in a pyruvate-kinase-deficient Korean family.2005
- Author(s)
  Park-Hah, J.O., Kanno, H., Kim, W.D., Fujii, H.
- Journal Title
  
  Acta Haematol 113
  
  Pages: 208-211
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590254
[Journal Article] Molecular basis of Japanese variants of pyrimidine 5'-nucleotidase deficiency.2004
- Author(s)
  Kanno H, et al.
- Journal Title
  
  British Journal of Haematology 126
  
  Pages: 265-271
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590254
[Journal Article] Molecular basis of Japanese variants of pyrimidine 5'-nucleotidase deficiency2004
- Author(s)
  Hitoshi Kanno
- Journal Title
  
  British Journal of Haematology 126
  
  Pages: 265-271
- Data Source
  KAKENHI-PROJECT-16590254
[Journal Article] Molecular basis of Japanese variants of pyrimidine 5'-nucleotidase deficiency.2004
- Author(s)
  Kanno, H., Takizawa, T., Miwa, S., Fujii, H.
- Journal Title
  
  Brit J Haematol 126
  
  Pages: 265-271
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590254
[Journal Article] Gelatinase expression in ocular surface disorders.2004
- Author(s)
  Sakimoto, T., Shoji, J., Kanno, H., Sawa, M.
- Journal Title
  
  Jpn J Ophthalmol 48
  
  Pages: 12-22
- NAID
  10012208686
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590254
[Journal Article] Histopathological study of lattice corneal dystrophy with L 527 R mutation of transforming growth factor-beta induced gene.2004
- Author(s)
  Nakagawa, E., Sakimoto, T., Inada, N., Shoji, J., Sawa, M., Kanno, H., Nakagawa, S.
- Journal Title
  
  Nippon Ganka Gakkai Zasshi 108
  
  Pages: 118-123
- NAID
  10016999648
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590254
[Presentation] Significance of comprehensive genetic testing in the diagnosis of congenital hemolytic anemia2021
- Author(s)
  中原衣里菜, 山本圭子, 青木貴子, 小倉浩美, 槍澤大樹, 森岡一朗, 山本俊至, 菅野仁
- Organizer
  日本人類遺伝学会第66回大会
- Data Source
  KAKENHI-PROJECT-20K08239
[Presentation] 新生児溶血性疾患の迅速な鑑別診断法～定量的赤血球浸透圧脆弱性検査法の確立～2021
- Author(s)
  中原衣里菜, 菅野仁, 山本俊至, 谷ヶ崎博, 森岡一朗
- Organizer
  第124回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08239
[Presentation] 臍帯血赤血球を用いた赤血球膜異常症のスクリーニング法2021
- Author(s)
  中原衣里菜, 菅野仁, 山本俊至, 谷ヶ崎博, 森岡一朗
- Organizer
  第83回日本血液学会学術集会
- Data Source
  KAKENHI-PROJECT-20K08239
[Presentation] Donath-Landsteiner抗体検出により早期診断と安全な寒冷暴露制限解除ができたPCHの一例2020
- Author(s)
  中原衣里菜，藤田　浩，中原美千代，源川　結，伊東正剛，吉橋知邦，三澤正弘，菅野　仁，谷ヶ崎　博，森岡一朗
- Organizer
  第68回日本輸血・細胞治療学会学術総会
- Data Source
  KAKENHI-PROJECT-20K08239
[Presentation] 当院の心臓血管外科手術における回収式自己血の実施状況2019
- Author(s)
  及川美幸、中林恭子、岡本好雄、槍澤大樹、小林博人、菅野　仁
- Organizer
  第67回日本輸血・細胞治療学会学術総会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] Differential Diagnosis Of Congenital Hemolytic Anemia Of Neonates And Infants In Japan2019
- Author(s)
  Hiromi Ogura, Taiju Utsugisawa, Takako Aoki, Akemi Kinoshita, Yoshio Okamoto, Takahiro Kawasaki, Toshiyuki Yamamoto, Hitoshi Kanno
- Organizer
  European Hematology Association
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 移植後微小残存病変に対するエロツズマブ併用体外増幅NK細胞輸注療法第一例目の報告2019
- Author(s)
  萩原將太郎, 王艶華, 小林博人, 加藤豊, 飯塚有希, 田中紀奈, 町島智人, 石山みどり, 吉永健太郎, 志関雅幸, 菅野仁, 田中淳司
- Organizer
  第44回日本骨髄腫学会学術集会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 2歳以降に輸血依存性になった赤芽球癆2019
- Author(s)
  金子裕貴, 鶴田敏久, 杉本圭, 平澤恭子, 菅野仁, 永田智
- Organizer
  第122回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] Ex-Vivo Expanded NK Cell Therapy Combined with Elotuzumab for MRD after Autologous Stem Cell Transplantation: A Phase I/ II Clinical Trial in Progress.2019
- Author(s)
  HAGIWARA Shotaro, WANG Yan-Hua, KOBAYASHI Hirohito, KATO Yutaka, TANAKA Norina, IIZUKA Yuki, WATANABE Aya, ISHIYAMA Midori, SHINOHARA Akihito, KAZAMA Hiroshi, YOSHINAGA Kentaro, SHISEKI Masayuki, KANNO Hitoshi, TANAKA Junji
- Organizer
  61st ASH Annual Meeting & Expositon
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 先天性溶血性貧血関連遺伝子パネルを用いた新生児溶血性疾患の病因解析2019
- Author(s)
  青木　貴子、小倉　浩美、槍澤　大樹、山本　俊至、中原　衣里菜、谷ケ崎　博、森岡　一朗、菅野　仁
- Organizer
  第64回日本人類遺伝学会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 先天性溶血性貧血～新生児期における鑑別診断の重要性2019
- Author(s)
  菅野　仁
- Organizer
  第125回東京新生児研究会
- Invited
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] A Global Longitudinal Observational Study Of Patients With Pyruvate Kinase Deficiency2019
- Author(s)
  Paola Bianchi, Bertil Glader, Rachael F. Grace, Hitoshi Kanno, D. Mark Layton, Eduard J. van Beers, Joan-Lluis Vives Corrons, Lei Hua, Bryan Jones
- Organizer
  American Society of Pediatric Hematology/Oncology Conference
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 重症心不全に対する再生医療等製品「ハートシート」の院内調整の問題点2019
- Author(s)
  高源ゆみ, 岡田真一, 稲田紹子, 岡本好雄, 小林博人, 菅野　仁
- Organizer
  第67回日本輸血・細胞治療学会学術総会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 濾過濃縮後腹水における抗A,抗B抗体価について2019
- Author(s)
  岡本好雄, 中林恭子, 及川美幸, 千野峰子, 岡田真一, 木下明美, 守屋友美, 久保田友晶, 松田和樹, 今野マユミ, 槍澤大樹, 小林博人, 菅野　仁
- Organizer
  第67回日本輸血・細胞治療学会学術総会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] パルスオキシメーターにて酸素飽和度異常低値を示した不安定ヘモグロビン症の2例2019
- Author(s)
  豊間優里子, 鶴田敏久, 谷諭美, 金子裕貴, 花谷あき, 千葉幸英, 中舘尚也, 山城安啓, 服部幸夫, 菅野仁, 永田智
- Organizer
  第122回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] A case of hereditary spherocytosis with ANK1 mutation and SLC4A1 variant with persistent severe anemia2019
- Author(s)
  Akira Nishimura, Yuichi Miyakawa, Miki Murakoshi, Asami Shimbo, Rika Ishiguro, Michiko Kajiwara, Atsushi Shibuya, Hiromi Ogura, Hitoshi Kanno, Katsuyoshi Koh, Yoshihiro Minosaki, Masato Nishioka, Masayuki Shimohira
- Organizer
  第61回小児血液・がん学会学術集会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] Meta-Analysis Using Data Of Red Blood Cel Enzyme Assay And Proteome In Patients With Diamond-Blackfan Anemia.2019
- Author(s)
  Taiju Utsugisawa, Toshitaka Uchiyama, Takako Aoki, Akemi kinoshita, Yoshio Okamoto, Takahiro Kawakami, Hiromi Ogura, Tsutomu Toki, Toshiyuki Yamamoto, Akira Ohara, Shouichi Ohga, Etsuro Ito, Hitoshi Kanno.
- Organizer
  European Hematology Association
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 輸血を必要とする疾患の理解と輸血の実際2019
- Author(s)
  菅野　仁
- Organizer
  第2回関東甲信越ブロック医薬情報担当者研修会
- Invited
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 腹水由来γδ型T細胞を用いた癌免疫細胞療法の開発2018
- Author(s)
  小林博人、阿部結貴、槍澤大樹、菅野仁
- Organizer
  第39回日本アフェレシス学会学術大会
- Invited
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 健常人とサラセミア、異常ヘモグロビン血症患者から得た赤血球におけるATP増強2018
- Author(s)
  鎌谷直之、降旗謙一、谷口敦夫、福内友子、山岡法子、金子希代子、菅野仁
- Organizer
  日本人類遺伝学会第63回大会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 自己活性化γδ型T細胞を用いたがん免疫療法の臨床研究支援2018
- Author(s)
  高源ゆみ、稲田紹子、木下明美、小林博人、菅野仁
- Organizer
  第66回日本輸血・細胞治療学会総会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] Pyruvate kinase deficiency in Japan: A Summary of clinical feature, laboratory data and enzymatic diagnosis2018
- Author(s)
  Taiju Utsugisawa, Toshiyuki Yamamoto, Hiromi Ogura, Takako Aoki, Yoshio Okamoto, Takahiro Kawakami, Shouichi Ohga, Akira Ohara, Etsuro Ito, Hitoshi Kanno.
- Organizer
  The European Hematology Association
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 先天性溶血性貧血の疫学と病型診断2018
- Author(s)
  菅野仁
- Organizer
  第17回日本新生児黄疸管理研究会
- Invited
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 遺伝子パネルシークエンスにより脱水型遺伝性有口赤血球(DHSt)と診断し得た一例2018
- Author(s)
  青木貴子、小倉浩美、槍澤大樹、山根孝久、山本俊至、菅野仁
- Organizer
  日本人類遺伝学会第63回大会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] アンケート調査からみた日本のガンマグロブリン製剤使用実態2018
- Author(s)
  菅野仁、岡本好雄
- Organizer
  第66回日本輸血・細胞治療学会総会
- Invited
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 胸水・腹水濾過濃縮静注法における遊離ヘモグロビン検査の重要性2018
- Author(s)
  千野峰子、小野慎吾、松田和樹、久保田友晶、守谷友美、及川美幸、木下明美、岡田真一、青木正弘、中林恭子、岡本好雄、今野マユミ、槍澤大樹、小林博人、菅野仁
- Organizer
  第66回日本輸血・細胞治療学会総会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 当院における血液製剤使用状況の実態に関する解析2018
- Author(s)
  中林恭子、岡本好雄、槍澤大樹、菅野仁
- Organizer
  第66回日本輸血・細胞治療学会総会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 健常人とサラセミア、異常ヘモグロビン血症患者から得た赤血球におけるイノシンによるATP増強2018
- Author(s)
  鎌谷直之、降旗謙一、谷口敦夫、福内友子、山岡法子、金子希代子、菅野仁
- Organizer
  日本痛風・核酸代謝学会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 液製剤使用実態調査で明らかになった血漿分画製剤の使用状況について2018
- Author(s)
  菅野仁
- Organizer
  第66回日本輸血・細胞治療学会総会
- Invited
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] アンケート調査から見た輸血後感染症検査の実施状況2018
- Author(s)
  菅野仁、岡本好雄
- Organizer
  第66回日本輸血・細胞治療学会総会
- Invited
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 先天性溶血性貧血の秒型診断と治療～最近のトピックス2018
- Author(s)
  菅野仁
- Organizer
  第4回北陸小児血液研究会
- Invited
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 乳児期の一過性溶血性貧血を呈するinfantile pyknocytosisの臨床像と検査所見2018
- Author(s)
  小倉浩美、青木貴子、槍澤大樹、岡本好雄、川上高弘、山本俊至、大賀正一、伊藤悦朗、菅野仁
- Organizer
  第80回日本血液学会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 血液製剤使用実態調査から分かること2018
- Author(s)
  菅野仁
- Organizer
  第66回日本輸血・細胞治療学会総会
- Invited
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 新生児に重症黄疸と溶血性貧血を来した一例2018
- Author(s)
  平形絢子、佐藤実紅、春日夏那子、橋本真理、田中健佑、水野隆久、河野美幸、須永康夫、田代雅彦、小倉浩美、菅野仁
- Organizer
  日本小児科学会群馬地方会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 先天性溶血性貧血診断における網羅的遺伝子検査の有用性2018
- Author(s)
  槍澤大樹、青木貴子、小倉浩美、岡本好雄、川上高弘、山根孝久、山本俊至、菅野仁
- Organizer
  第80回日本血液学会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 冷蔵保存腹水によるCARTの安全性と有効性2018
- Author(s)
  岡本好雄、槍澤大樹、中林恭子、千野峰子、守屋友美、松田和樹、小林博人、菅野仁
- Organizer
  第39回日本アフェレシス学会学術大会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] The Flow Cytometric Osmotic Fragility Test is an Effective Screening Test for Red Cell Membrane Disorders, Including Dehydrated Hereditary Stomatocytosis2017
- Author(s)
  Takuya Iwasaki, Taiju Utsugisawa, Hiromi Ogura, Takako Aoki, Akemi Kinoshita, Yasutaka Ogata, Yoshio Okamoto, Takahiro Kawakami, Hitoshi Kanno
- Organizer
  International Sciety for Laboratory Hematology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 腹水濾過時に得られる単核球を利用したγδ型T細胞療法の開発2017
- Author(s)
  高源　ゆみ、木下　明美、小林　博人、菅野　仁
- Organizer
  第65回　日本輸血・細胞治療学会総会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] ABO同型クリオプレシピテート供給体制の是非に関する考察2017
- Author(s)
  小野　慎吾、及川　美幸、中林　恭子、岡本　好雄、菅野　仁
- Organizer
  第65回　日本輸血・細胞治療学会総会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 低温保存腹水を用いた腹水濾過濃縮再静注法(CART)の有用性の検討2017
- Author(s)
  槍澤　大樹、中林　恭子、松田　和樹、守屋　友美、千野　峰子、岡本　好雄、菅野　仁
- Organizer
  第65回　日本輸血・細胞治療学会総会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] Heterogeneous KCNN4 or PIEZO1 gene mutation cause dehydrated hereditary Stomatocytosis in Japan2017
- Author(s)
  槍澤大樹、小倉浩美、岩﨑拓也、青木貴子、岡本好雄、川上高弘、菅野　仁.
- Organizer
  第79回日本血液学会学術集会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] AG-348,a pyruvate kinase activator,for pyruvate kinase deficiency:Results the drive PK study2017
- Author(s)
  Hitoshi Kanno、Rachael F.Grace, D.Mark Layton, Frederic Galacteros, D.Holmes Morton, Kevin H.M.Kuo, Sujit Sheth, Janet L.Kwiatkowski, Bruce Silver, Charles Kung, Marvin Cohen, Hua Yang, Penelope A. Kosinski, Lei Hua, Ann J. Barbier, Bertil Glader
- Organizer
  第79回日本血液学会学術集会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 高張アルブミン製剤適正使用の推進2017
- Author(s)
  守屋　友美、小野　慎吾、小林　博人、菅野　仁
- Organizer
  第65回　日本輸血・細胞治療学会総会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 系統的検査による先天性溶血性貧血80症例の病型診断2017
- Author(s)
  小倉浩美、槍澤大樹、岩﨑拓也、青木貴子、岡本好雄、川上高弘、菅野　仁
- Organizer
  第79回日本血液学会学術集会
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] A patient with hereditary Pyropoikilocytosis caused by a combination of a novel in-frame deletion and a common functional but non-pathogenic allele,αLELY,in SPTA12017
- Author(s)
  Tomoko Goto, Takao Togawa, Tsuyoshi Ito, Masanori Kouwaki, Hiromi Ogura, Hitoshi Kanno, Shinji Saitoh, Norihisa Koyama
- Organizer
  American Society of Human Genetics
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] Congenital hemolytic anemia due to red cell enzymopathies.2016
- Author(s)
  Kanno H, Utsugisawa T, Ogura H
- Organizer
  The 5th TSH International Symposium, Red Cell Disorders.: From Bench to Bedside
- Place of Presentation
  Bangkok, Thailand
- Year and Date
  2016-05-20
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] The Novel missense Mutation of GATA1 Caused red Cell Adenosine Deaminase Overproduction Associated with Congenital Hemolytic Anemia2016
- Author(s)
  Taiju Utsugisawa, Hiromi Ogura,Toshiyuki Yamamoto,Takako Aoki,Takuya Iwasaki,Yumiko Ondo,Takahiro Kawakami, Shinichiro Nakagawa, Shuichi Ozono, Hiroko Inada, Hitoshi Kanno
- Organizer
  American Society of Hematology, 58th Annual Meeting ＆Exposition
- Place of Presentation
  San Diego（America)
- Year and Date
  2016-12-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] HbA1cが偽性低値を示したエノラーゼ異常症の1例2016
- Author(s)
  井島廣子, 古賀正史, 中村倫子, 松下文美, 坂本英美, 岩崎剛, 松本理恵, 陣内冨男, 梶原敬三, 稗島州雄, 杉山正悟, 小倉浩美, 菅野仁, 陣内秀昭
- Organizer
  第59回日本糖尿病学会年次学術集会
- Place of Presentation
  国立京都国際会館（京都）
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] Next generation sequencing in diagnosis of congenital hemolytic anemia.2016
- Author(s)
  Kanno H, Utsugisawa T, Ogura H
- Organizer
  The 5th TSH International Symposium, Red Cell Disorders.: From Bench to Bedside
- Place of Presentation
  Bangkok, Thailand
- Year and Date
  2016-05-21
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] Generation and Fanctional Analysis of Congenital Dyserythropoietic Anemia(CDA) Patient-Specific Induced Pluripotent Stem Cells2016
- Author(s)
  Hiroshi Kohara, Hiromi Ogura, Takako Aoki, Chika Sakamoto, Yoshie Ogawa, Shohei Miyamoto, Hitoshi Kanno, Kenzaburo Tani
- Organizer
  American Society of Hematology, 58th Annual Meeting ＆Exposition
- Place of Presentation
  San Diego（America)
- Year and Date
  2016-12-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 先天性溶血性貧血の診断におけるターゲットシークエンシングの有用性2016
- Author(s)
  岩﨑　拓也、山本　俊至、村松　秀城、奥野友介、佐藤　裕子、三井　哲夫、小野田　正志、矢野　未央、小松　博史、坂本　謙一、青木　貴子、岡本　好雄、槍澤　大樹、小倉浩美、小島　勢二、菅野　仁
- Organizer
  第78回日本血液学会学術集会
- Place of Presentation
  パシフィコ横浜（神奈川県）
- Data Source
  KAKENHI-PROJECT-16K10041
[Presentation] 診断に苦慮したグルコース-6-リン酸脱水素酵素(G6PD)異常症の女児例2015
- Author(s)
  宇佐美郁哉、窪田博仁、毎原敏郎、菅野仁
- Organizer
  日本小児科学会
- Place of Presentation
  大阪国際会議場（大阪府大阪市）
- Year and Date
  2015-04-17
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] COL4A1 is a Novel Causative Gene Responsible for Congenital Hemolytic Anemia, Representing Characteristic Clinical Course in Infants2015
- Author(s)
  小倉浩美、大賀正一、青木貴子、槍澤大樹、高橋秀弘、岩井朝幸、渡邉健一郎、奥野友介、吉田健一、宮野悟、小川誠司、小島勢二、菅野仁
- Organizer
  The American Society of Hematology
- Place of Presentation
  オーランド（アメリカ）
- Year and Date
  2015-12-05
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] Significance of gene analysis in a patient with hemolytic anemia in the adulthood2015
- Author(s)
  小倉浩美、大賀正一、青木貴子、槍澤大樹、高橋秀弘、岩井朝幸、濱端隆行、渡邉健一郎、常松健一郎、奥野友介、村松秀城、吉田健一、宮野悟、小川誠司、小島勢二、菅野仁
- Organizer
  日本血液学会
- Place of Presentation
  石川県立音楽堂（石川県金沢市）
- Year and Date
  2015-10-17
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] ATP11C Encodes a Major Flippase in Human Erythrocyte and Its Genetic Defect Causes Congenital Non-Spherocytic Hemolytic Anemia2015
- Author(s)
  新敷信人、高桑雄一、小倉浩美、槍澤大樹、宮野悟、小川誠司、小島勢二、大賀正一、Narla Mohandas、菅野仁
- Organizer
  The American Society of Hematology
- Place of Presentation
  オーランド（アメリカ）
- Year and Date
  2015-12-05
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] 先天性貧血症の鑑別診断における次世代シークエンスの有用性2015
- Author(s)
  青木貴子、岩﨑拓也、小倉浩美、浅井隆善、土居崎小夜子、奥野友介、村松秀城、大賀正一、小川誠司、小島勢二、菅野仁
- Organizer
  日本人類遺伝学会
- Place of Presentation
  京王プラザホテル（東京都新宿区）
- Year and Date
  2015-10-16
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] 病因未確定の先天性溶血性貧血に対する全エクソーム解析2014
- Author(s)
  青木　貴子、市東　正幸、小倉　浩美、高橋　秀弘、岩井　朝幸、濱端　隆行、渡邉　健一郎、常松　健一郎、奥野　友介、村松　秀城、吉田　健一、宮野　悟、大賀　正一、小川　誠司、小島　勢二、菅野　仁
- Organizer
  日本人類遺伝学会
- Place of Presentation
  タワーホール船堀（東京都江戸川区）
- Year and Date
  2014-11-19
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] 非溶血性輸血副作用発生状況と副作用報告回収改善への取り組み2014
- Author(s)
  久保田　友晶、松田和樹、守屋友美、及川美幸、李舞香、木下明美、千野峰子、岡田真一、高源ゆみ、青木正弘、中林恭子、岡本好雄、今野マユミ、槍澤大樹、小林博人、小倉浩美、菅野　仁
- Organizer
  日本輸血細胞治療学会
- Place of Presentation
  奈良県文化会館・奈良県新公会堂・東大寺総合文化センター（奈良県）
- Year and Date
  2014-05-15
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] クリオプレシピテート製剤の院内調製と心臓血管外科手術への応用2014
- Author(s)
  岡本　好雄、松田和樹、久保田友晶、守屋友美、及川美幸、李舞香、木下明美、千野峰子、岡田真一、高源ゆみ、青木正弘、中林恭子、今野マユミ、槍澤大樹、小林博人、小倉浩美、菅野　仁
- Organizer
  日本輸血細胞治療学会
- Place of Presentation
  奈良県文化会館・奈良県新公会堂・東大寺総合文化センター（奈良県）
- Year and Date
  2014-05-16
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] 安全なCARTの運用と適応拡大への新たな試み2014
- Author(s)
  槍澤　大樹、松田和樹、久保田友晶、守屋友美、及川美幸、李舞香、木下明美、千野峰子、岡田真一、高源ゆみ、青木正弘、中林恭子、今野マユミ、槍澤大樹、小林博人、小倉浩美、菅野　仁
- Organizer
  日本輸血細胞治療学会
- Place of Presentation
  奈良県文化会館・奈良県新公会堂・東大寺総合文化センター（奈良県）
- Year and Date
  2014-05-16
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] Diamond-Blackfan貧血(DBA)母子の診断における全エクソーム解析2014
- Author(s)
  市村　卓也、尻俊昭、下村麻衣子、永井功造、西眞範、吉田健一、小川誠司、奥野友介、村松秀城、小島勢二、菅野仁、伊藤悦朗、大賀正一
- Organizer
  日本血液学会
- Place of Presentation
  大阪国際会議場（大阪府）
- Year and Date
  2014-10-30
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] 新生児・乳児期に発症する先天性溶血性貧血の病因と診断2014
- Author(s)
  菅野　仁
- Organizer
  日本産婦人科・新生児血液学会
- Place of Presentation
  ワークピア横浜（横浜市中区）
- Year and Date
  2014-06-13
- Invited
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] 原因不明先天性溶血性貧血症例の全エクソーム解析による膜骨格蛋白遺伝子変異の同定2014
- Author(s)
  市東　正幸、青木貴子、槍澤大樹、小倉浩美、大賀正一、岩井朝幸、末延聡一、伊藤悦朗、奥野友介、小島勢二、小川誠司、菅野　仁
- Organizer
  日本血液学会
- Place of Presentation
  大阪国際会議場（大阪府）
- Year and Date
  2014-10-31
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] 当院における静注用免疫グロブリン(IVIG)の使用状況について2014
- Author(s)
  松田　和樹、久保田友晶、守屋友美、及川美幸、李舞香、木下明美、千野峰子、岡田真一、高源ゆみ、青木正弘、中林恭子、岡本好雄、今野マユミ、槍澤大樹、小林博人、小倉浩美、菅野　仁
- Organizer
  日本輸血細胞治療学会
- Place of Presentation
  奈良県文化会館・奈良県新公会堂・東大寺総合文化センター（奈良県）
- Year and Date
  2014-05-16
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] わが国におけるG6PD異常症の現状2014
- Author(s)
  菅野　仁、青木貴子、市東正幸、槍澤大樹、小倉浩美
- Organizer
  日本血液学会
- Place of Presentation
  大阪国際会議場（大阪府）
- Year and Date
  2014-10-31
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] Elevated red cell reduced glutathione is a novel biomaker of Diamond-Blackfan anemia2014
- Author(s)
  Utsugisawa T,Uchiyama T,Ogura H,Aoki T,Ohara A,Ishiguro A,Kojima S,Ohga S,Ito E,Kanno H
- Organizer
  ASH Annual Meeting＆Exposition
- Place of Presentation
  San Francisco
- Year and Date
  2014-12-07
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] アスコルビン酸とリボフラビンとの併用療法が有効であった遺伝性メトヘモグロビン血症.2013
- Author(s)
  2) 羽賀洋一、三井一賢、小嶋靖子、佐藤真理、松裏裕行、関根孝司、舘野昭彦、菅野仁、小原明、佐地勉.
- Organizer
  第116回日本小児科学会学術集会
- Place of Presentation
  広島
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] 先天性溶血性貧血およびダイアモンド・ブラックファン貧血の診断法の進歩2013
- Author(s)
  菅野　仁
- Organizer
  第55回日本小児血液・がん学会学術集会
- Place of Presentation
  福岡
- Invited
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] 心不全を伴う危急的貧血で発症したDiamond-Blackfan貧血の乳児例.2013
- Author(s)
  1) 古賀木綿子、野口磨依子、大園秀一、中川慎一郎、上田耕一郎、稲田浩子、松石豊次郎、財津亜友子、横地一興、大賀正一、菅野仁, 伊藤悦朗
- Organizer
  第116回日本小児科学会学術集会
- Place of Presentation
  広島
- Data Source
  KAKENHI-PROJECT-25461609
[Presentation] 適正使用評価方法の問題点と血液製剤使用量を減少させるための方策. シンポジウム2「輸血医療 Pros and Cons」 III. 輸血管理料2012
- Author(s)
  菅野仁
- Organizer
  第19回日本輸血・細胞治療学会秋季シンポジウム
- Place of Presentation
  岡山コンベンションセンター
- Year and Date
  2012-11-16
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] 適正使用評価方法の問題点と血液製剤使用量を減少させるための方策2012
- Author(s)
  菅野仁
- Organizer
  第19回日本輸血・細胞治療学会秋季シンポジウム
- Place of Presentation
  岡山コンベンションセンター
- Invited
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] 遺伝子情報管理:薬理遺伝学を含むゲノム診療体制の実際2012
- Author(s)
  菅野仁
- Organizer
  第19回日本遺伝子診療学会シンポジウム
- Year and Date
  2012-07-27
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] 濾過濃縮後腹水の安全性と有効性～血漿分画製剤としての視点から2012
- Author(s)
  菅野仁
- Organizer
  第33回日本アフェレシス学会学術大会
- Place of Presentation
  長崎ハウステンボス
- Invited
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] 遺伝子情報管理：薬理遺伝学を含むゲノム診療体制の実際2012
- Author(s)
  菅野仁
- Organizer
  第19回日本遺伝子診療学会シンポジウム
- Place of Presentation
  三井ガーデンホテル千葉
- Invited
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] CART ろ過濃縮後保存の新技術について2012
- Author(s)
  菅野仁
- Organizer
  第7回 CART 研究会特別講演I、第17回日本緩和医療学会学術大会
- Year and Date
  2012-06-22
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] 濾過濃縮後腹水の安全性と有効性～血漿分画製剤としての視点から2012
- Author(s)
  菅野仁
- Organizer
  第33回日本アフェレシス学会学術大会ランチョンセミナー2
- Place of Presentation
  長崎ハウステンボス
- Year and Date
  2012-11-09
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] PGx 検査はどこまで医療に浸透したか～がん PGx の現状と本学会が果たすべき役割～2012
- Author(s)
  菅野仁
- Organizer
  日本人類遺伝学会第57回大会シンポジウム
- Year and Date
  2012-10-25
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] CARTろ過濃縮後保存の新技術について2012
- Author(s)
  菅野仁
- Organizer
  第17回日本緩和医療学会学術大会
- Place of Presentation
  神戸国際展示場
- Invited
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] PGx検査はどこまで医療に浸透したか～がんPGxの現状と本学会が果たすべき役割2012
- Author(s)
  菅野仁
- Organizer
  日本人類遺伝学会第57回大会
- Place of Presentation
  新宿京王プラザホテル
- Invited
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] ダイアモンド・ブラックファン貧血の新規バイオマーカー同定2011
- Author(s)
  菅野仁
- Organizer
  第73回日本血液学会学術集会
- Place of Presentation
  名古屋国際会議場
- Year and Date
  2011-10-14
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] 先天性溶血性貧血2011
- Author(s)
  菅野仁
- Organizer
  第56回日本未熟児新生児学会
- Year and Date
  2011-11-15
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] 先天性溶血性貧血2011
- Author(s)
  菅野仁
- Organizer
  第56回日本未熟児新生児学会学術集会
- Place of Presentation
  東京国際フォーラム(招待講演)
- Year and Date
  2011-11-15
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] 免疫寛容導入療法におけるドナー、レシピエント細胞キメリズム解析2010
- Author(s)
  菅野仁, 槍澤大樹, 小倉浩美, 濱田貴子, 藤井寿一
- Organizer
  第58回日本輸血・細胞治療学会総会
- Year and Date
  2010-05-30
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] がん治療におけるPGx 検査と電子カルテによる遺伝子情報管理2010
- Author(s)
  菅野仁、斎藤加代子
- Organizer
  第8回全国遺伝子医療部門連絡会議
- Year and Date
  2010-10-30
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] Diamond Blackfan 貧血に関する新規の病因候補遺伝子同定2010
- Author(s)
  菅野仁、山本俊至, 大賀正一, 立石浩, 濱田貴子 , 槍澤大樹 , 小倉浩美 , 藤井寿一
- Organizer
  第72回日本血液学会総会
- Year and Date
  2010-09-25
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] 電子カルテによる遺伝子情報管理の実際2010
- Author(s)
  菅野仁、斎藤加代子
- Organizer
  第34回日本遺伝カウンセリング学会学術集会シンポジウム2
- Year and Date
  2010-05-29
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] Diamond Blackfan貧血に関する新規の病因候補遺伝子同定2010
- Author(s)
  菅野仁
- Organizer
  第72回日本血液学会学術集会
- Place of Presentation
  パシフィコ横浜
- Year and Date
  2010-09-25
- Data Source
  KAKENHI-PROJECT-22591071
[Presentation] 薬物トランスポーター遺伝子多型を用いた薬理遺伝学的検査～ドセタキセル投与における好中球減少症予測2010
- Author(s)
  菅野仁、石谷健、相崎潤子、濱田貴子、内山智貴、浦野真理、近藤恵里、松井英雄、藤井寿一、太田博明、斎藤加代子
- Organizer
  第17回日本遺伝子診療学会大会
- Year and Date
  2010-08-07
- Data Source
  KAKENHI-PROJECT-22591071

1. FUJII Hisaichi (70107762)

# of Collaborated Projects: 8 results

# of Collaborated Products: 14 results
2. MIWA Shiro (40034954)

# of Collaborated Projects: 5 results

# of Collaborated Products: 0 results
3. KOIZUMI Tsutomu (40126579)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
4. UTSUGISAWA Taiju (30337133)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
5. AIZAWA Shin (30202443)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
6. NOGUCHI Tamio (70135721)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. NAKAGAWA Shigeki (40059465)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. OYAIZU Naoki (00282773)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. KAJIYAMA Yoshiaki (70241239)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. TSURUMARU Masahiko (70155448)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. TAKIZAWA Takenori (40192158)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. AISAKI KEN-ICHI (40322086)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
13. KURAMOCHI HIDEKAZU (30287362)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. MORIOKA Ichiro (80437467)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
15. 谷憲三朗 (00183864)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
16. 入部雄司 (20348618)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. 小林博人 (80318047)

# of Collaborated Projects: 1 results

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18. 小原洋志 (40528733)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
19. 林和彦 (10208613)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
20. 中島豪 (80338996)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
21. 谷ヶ崎博 (90378141)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
22. NAGAI Yoshinori

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
23. IKUTANI Masashi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
24. ARASHIKI Nobuto

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
25. 小川誠司

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
26. 江藤浩之

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
27. 佐藤悠佑

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
28. 大賀正一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
29. 伊藤悦朗

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
30. 照井君典

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
31. 金崎里香

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
32. 土岐力

# of Collaborated Projects: 0 results

# of Collaborated Products: 3 results
33. 丸義朗

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
34. 上地珠代

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
35. 高津聖志

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
36. 高桑雄一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
37. 山本俊至

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

kanno hitoshi 菅野 仁

KANNO Hitoshi 菅野 仁

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Pathological analysis of congenital hemolytic anemia due to mitochondrial selective autophagy disorderPrincipal Investigator

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Identification of novel pathogenic genes for congenital hemolytic anemia and establishment of comprehensive gene testingPrincipal Investigator

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Development of novel gene therapy for congenital blood disorders using induced pluripotent stem cellsPrincipal Investigator

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IDENTIFICATION OF THE CAUSATIVE GENES RESPONSIBLE FOR ERYTHROID APOPTOSIS INDUCED BY GLYCOLYTIC INHIBITIONPrincipal Investigator

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MOLECULAR MECHANISMS OF ACCELERATED ERYTHROID APOPTOSIS DUE TO A GLYCOLYTIC ENZYME DEFECTPrincipal Investigator

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Physiological significance of pyruvate kinase isozymes in erythrocyte.Principal Investigator

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kanno hitoshi 菅野仁

KANNO Hitoshi 菅野仁

[Book] 血液内科【貧血性疾患診療の進歩】先天性溶血性貧血の遺伝子診断2016

[Book] MedicalPractic 【貧血　実地医家に役立つ知識と診療の進めかた】セミナー臨床に役立つ知識と情報　溶血性貧血の鑑別診断の進め方2016

[Book] 小児内科　【血球の増加と減少】赤血球　貧血　遺伝性貧血2016

[Book] 第VIII章　2.先天性溶血性貧血、血液専門医テキスト改訂第二版2015