Rchr
J-GLOBAL ID：201801017805669533
Update date: Mar. 30, 2024
(Unregistered) (Unregistered)
イトウ エツロウ | (Unregistered) (Unregistered)
Affiliation and department：
Research field (1)：
Fetal medicine/Pediatrics
Research theme for competitive and other funds (31)：
- 2021 - 2025 Clarification of the mechanism of multistep leukemogenesis of acute megakaryoblastic leukemia associated with Down syndrome and development of the molecular targeted therapy
- 2018 - 2021 Multistep molecular mechanisms for acute megakaryoblastic leukemia in Down syndrome
- 2014 - 2018 The multistep molecular mechanism of acute megakaryoblastic leukemia in Down syndrome
- 2015 - 2017 Development of an epoch-making method for identification of Down syndrome patients with TAM who will subsequently develop acute megakaryoblastic leukemia
- 2014 - 2017 Elucidation of molecular mechanism of leukemogenesis with GATA1 and cohesin gene mutations
- 2014 - 2017 a novel adoptive T cell therapy exerting ADCC for pediatric cancer
- 2014 - 2016 Pathogenetic and therapeutic studies of myeloid leukemia with Down syndrome using xenograft model
- 2011 - 2014 Molecular basis of myeloid leukemogenesis
- 2011 - 2014 The study on the mechanisms of leukemogenesis caused by qualitative and quantitative abnormalities of GATA1 transcription factor
- 2011 - 2013 ダウン症候群に伴う急性巨核球性白血病の多段階発症の分子機構
- 2010 - 2012 Development of molecular targeted therapy of bone marrow fibrosis with BACH1 transgenic mice
- 2008 - 2010 The molecular mechanisms of transient leukemia by GATA1 mutation and development of molecular target therapy
- 2005 - 2009 Molecular mechanisms of multi-step leukemogenesis in Down syndrome
- 2005 - 2007 The molecular mechanisms of leukmogenesis by GATA1
- 2005 - 2006 The differential regulation of target genes by transcription factor BACH 1 in erythroid and megakaryocytic cells.
- 2004 - 2004 BACH1転写因子活性化を利用した小児白血病の治療法の開発
- 2004 - 2004 ダウン症候群に伴う急性巨核球性白血病の転写因子による発症機構
- 2003 - 2004 Functional analysis of transcription factor BACH1 on thrombopiesis and megakaryocyte diffrentiation
- 2002 - 2004 Identification of the causative genes fox Down syndrome associated acute megakaryocytic leukemia
- 2003 - 2003 BACH2転写因子活性化を利用したフィラデルフィア染色体陽性白血病の治療法の開発
- 2001 - 2002 Study of the function and target genes of BACH transcripton factors.
- 2001 - 2001 Bach転写因子群による発がんの分子機構
- 2000 - 2001 Study for the mechanism of lymphocyte development by Bach2 transcription factor and clinical analysis of Bach2 gene
- 2000 - 2000 Bach転写因子群による発がんの分子機構
- 1999 - 1999 Bach転写因子群による発がんの分子機構
- 1998 - 1999 Study for the mechanism of lymphocyte development by NF-E2 transcription factors and clinical analysis of NF-E2 gene.
- 1997 - 1999 Analysis of expression of transcription factors during erythroid development of hematpoietic stem.
- 1997 - 1997 NF-E2関連蛋白による赤血球造血の分子機構
- 1996 - 1997 Megakaryocytic differentiation of hematopoietic stem cell by NF-E2 transcription factors.
- 1995 - 1996 Analysis of expression of lineage-specific transcription factors during stem cell differentiation in aplastic anemia.
- 1994 - 1995 New classification of infantile leukemia using lineage-specific transcription
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Papers (189)：
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山本 洋平, 山本 達也, 土岐 力, 奥瀬 諒, 伊東 竜也, 梅津 英典, 工藤 耕, 伊藤 悦朗, 照井 君典, 品川 友江, et al. 次世代シークエンサーを用いた結節性硬化症の遺伝学的検討. 日本小児科学会雑誌. 2023. 127. 4. 664-664
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工藤 耕, 土岐 力, 金崎 里香, 小林 明恵, 佐藤 知彦, 神尾 卓哉, 佐々木 伸也, 今村 勝, 今井 千速, 安藤 久美子, et al. BRAFV600E-positive precursors as molecular markers of bone marrow disease in LCH(和訳中). 日本血液学会学術集会. 2021. 83回. OS2-2
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伊東 竜也, 浅利 有紗, 八木 弘子, 山本 達也, 伊藤 悦朗. 可逆性脳血管攣縮症候群を合併したIgA血管炎の1例. 日本小児科学会雑誌. 2021. 125. 2. 340-340
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山本 達也, 浅利 有紗, 伊東 竜也, 伊藤 悦朗. 頭部MRI Arterial spin labeling(ASL)灌流画像が診断に有用であった可逆性脳血管攣縮症候群の1例. 脳と発達. 2020. 52. Suppl. S373-S373
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山本 達也, 浅利 有紗, 伊東 竜也, 伊藤 悦朗. 頭部MRI Arterial spin labeling(ASL)灌流画像が診断に有用であった可逆性脳血管攣縮症候群の1例. 脳と発達. 2020. 52. Suppl. S373-S373
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MISC (243)：
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板倉陽介, 安積昌平, 川口晃司, 高地貴行, 小倉妙美, 堀越泰雄, 工藤耕, 照井君典, 伊藤悦朗, 渡邉健一郎. Refractory Langerhans cell histiocytosis treated with cord blood transplantation and BRAF inhibitor. 日本造血・免疫細胞療法学会総会プログラム・抄録集. 2022. 44th
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工藤 耕, 土岐 力, 金崎 里香, 小林 明恵, 佐藤 知彦, 神尾 卓哉, 佐々木 伸也, 今村 勝, 今井 千速, 安藤 久美子, et al. 小児ランゲルハンス組織球症の骨髄病変におけるBRAFV600E変異(BRAFV600E-positive precursors as molecular markers of bone marrow disease in LCH). 日本血液学会学術集会. 2021. 83回. OS2-2
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高橋佑果, 工藤耕, 小林明恵, 佐藤知彦, 神尾卓哉, 佐々木伸也, 浅野研一郎, 小川薫, 黒瀬顕, 照井君典, et al. Recurrent isolated osseous medulloblastoma with MYCN amplification and 17p deletion. 日本小児科学会雑誌. 2021. 125. 2
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神尾卓哉, 小山石隼, 小林明恵, 佐藤知彦, 工藤耕, 佐々木伸也, 金崎里香, 長谷川大一郎, 村松秀城, 高橋義行, et al. Reduced-intensity conditioning is effective for HSCT in patients with Diamond-Blackfan Anemia. 日本造血細胞移植学会総会プログラム・抄録集. 2021. 43rd
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小林明恵, 大高龍星, 土岐力, 金崎里香, 高橋佑果, 佐藤知彦, 神尾卓哉, 工藤耕, 佐々木伸也, 村松秀城, et al. Dyserythropoietic anemia with an intronic GATA1 splicing mutation in patients suspected to have DBA. 日本血液学会学術集会抄録(Web). 2021. 83rd
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