Kanezaki Rika 金崎里香

… Alternative Names

KANEZAKI RIKA 金崎里香

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Researcher Number	60722882
Other IDs
Affiliation (Current)	2025: 弘前大学, 医学研究科, 助教
Affiliation (based on the past Project Information) *help	2016 – 2024: 弘前大学, 医学研究科, 助教 2014 – 2015: 弘前大学, 医学(系)研究科(研究院), 助教
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Pediatrics Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / Medium-sized Section 52:General internal medicine and related fields / Pediatrics
Keywords	Principal Investigator 白血病 / 転写因子 / ダウン症関連白血病 / 急性巨核芽球性白血病 / ダウン症 / コヒーシン Except Principal Investigator ダウン症候群 / GATA1 / 急性巨核芽球性白血病 / TAM … More / MYC / p53 / MDM2 / Diamond-Blackfan貧血 / 分子標的療法 / CDKN2A / RUNX1 / 骨髄性白血病 / 赤血球分化 / ダウン症関連急性巨核芽球性白血病 / 赤血球造血 / 腫瘍抑制因子 / 血球分化 / ダウン症候群に伴う骨髄性白血病 / IRX1 / 造血不全モデルマウス / 難病プラットフォーム / リボソーム / 悪性腫瘍 / 急性巨核芽性白血病 / 付加的遺伝子異常 / MYC/E2F経路 / リボゾーム蛋白遺伝子 / RNA-seq / マウス胎仔線維芽細胞 / 造血不全 / リボゾームタンパク / リボゾーム / リボゾーム蛋白 / 巨核球系分化 / 巨核球造血 / ダウン症 / EZH2 / CTCF / コヒーシン / 白血病 Less

Understanding of the molecular mechanisms of myeloid leukemia associated with Down syndrome and developing molecular target therapy
- Principal Investigator
  
  伊藤悦朗
- Project Period (FY)
  2024 – 2027
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hirosaki University
Analysis of the function of the long non-coding RNA PVT1 in Down syndrome-associated leukemia.Principal Investigator
- Principal Investigator
  
  金崎里香
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hirosaki University
Diamond-Blackfan貧血に合併する悪性腫瘍発症機構の解明
- Principal Investigator
  
  神尾卓哉
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Jikei University School of Medicine
  Hirosaki University
Elucidation of the function of transcription factor, IRX1, in erythropoesis
- Principal Investigator
  
  Sato Tomohiko
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hirosaki University
Clarification of the mechanism of multistep leukemogenesis of acute megakaryoblastic leukemia associated with Down syndrome and development of the molecular targeted therapy
- Principal Investigator
  
  伊藤悦朗
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hirosaki University
Analysis of transcriptional dysregulation mechanisms in Down syndrome-related LeukemiaPrincipal Investigator
- Principal Investigator
  
  Kanezaki Rika
- 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
  Hirosaki University
Functional analysis of a transcription factor, IRX1, in megakaryocyte differentiation
- Principal Investigator
  
  Sato Tomohiko
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hirosaki University
Elucidation of etiology in Diamond-Blackfan anemia focusing on the ribosomal protein genes abnormality
- Principal Investigator
  
  KAMIO TAKUYA
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Hirosaki University
Multistep molecular mechanisms for acute megakaryoblastic leukemia in Down syndrome
- Principal Investigator
  
  Ito Etsuro
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Review Section
  
  Medium-sized Section 52:General internal medicine and related fields
- Research Institution
  Hirosaki University
Molecular pathogenesis of leukemia by the GATA1 gene mutationPrincipal Investigator
- Principal Investigator
  
  Kanezaki Rika
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Hirosaki University
The multistep molecular mechanism of acute megakaryoblastic leukemia in Down syndrome
- Principal Investigator
  
  Ito Etsuro
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Pediatrics
- Research Institution
  Hirosaki University
Elucidation of molecular mechanism of leukemogenesis with GATA1 and cohesin gene mutationsPrincipal Investigator
- Principal Investigator
  
  KANEZAKI RIKA
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Hirosaki University

All 2024 2022 2020 2019 2018 2017 2016 2015 2014 Other

All Journal Article Presentation

[Journal Article] Antileukemic effect of azacitidine, a DNA methyltransferase inhibitor, on cell lines of myeloid leukemia associated with Down syndrome2024
- Author(s)
  Tanaka Tatsuhiko、Kudo Ko、Kanezaki Rika、Yuzawa Kentaro、Toki Tsutomu、Okuse Ryo、Kobayashi Akie、Sato Tomohiko、Kamio Takuya、Terui Kiminori、Ito Etsuro
- Journal Title
  
  Experimental Hematology
  
  Volume: 132 Pages: 104179-104179
- DOI
  10.1016/j.exphem.2024.104179
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07790, KAKENHI-PROJECT-23K21429
[Journal Article] Landscape of driver mutations and their clinical effects on Down syndrome-related myeloid neoplasms2024
- Author(s)
  Sato Tomohiko、Yoshida Kenichi、...、Matsuo Hidemasa、...、Ito Etsuro
- Journal Title
  
  Blood
  
  Volume: - Issue: 25 Pages: 2627-2643
- DOI
  10.1182/blood.2023022247
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-22K08475, KAKENHI-PROJECT-22K08508, KAKENHI-PROJECT-23K07847, KAKENHI-PROJECT-21K07766, KAKENHI-PROJECT-21K07790, KAKENHI-PROJECT-22K16320
[Journal Article] Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia2022
- Author(s)
  Kobayashi Akie、Ohtaka Ryusei、Toki Tsutomu、Hara Junichi、Muramatsu Hideki、Kanezaki Rika、Takahashi Yuka、Sato Tomohiko、Kamio Takuya、Kudo Ko、Sasaki Shinya、Yoshida Taro、Utsugisawa Taiju、Kanno Hitoshi、Yoshida Kenichi、Nannya Yasuhito、Takahashi Yoshiyuki、Kojima Seiji、Miyano Satoru、Terui Kiminori、et al.
- Journal Title
  
  eJHaem
  
  Volume: 3 Issue: 1 Pages: 163-167
- DOI
  10.1002/jha2.374
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07790, KAKENHI-PROJECT-23K21429
[Journal Article] Mechanism of KIT gene regulation by GATA1 lacking the N-terminal domain in Down syndrome-related myeloid disorders2022
- Author(s)
  Kanezaki Rika、Toki Tsutomu、Terui Kiminori、Sato Tomohiko、Kobayashi Akie、Kudo Ko、Kamio Takuya、Sasaki Shinya、Kawaguchi Koji、Watanabe Kenichiro、Ito Etsuro
- Journal Title
  
  Scientific Reports
  
  Volume: 12 Issue: 1 Pages: 20587-20587
- DOI
  10.1038/s41598-022-25046-z
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07790, KAKENHI-PROJECT-23K21429
[Journal Article] Childhood acute myeloid leukemia with 5q deletion and HNRNPH1-MLLT10 fusion: the first case report2022
- Author(s)
  Kudo Ko、Kubota Yasuo、Toki Tsutomu、Kanezaki Rika、Kobayashi Akie、Sato Tomohiko、Kamio Takuya、Sasaki Shinya、Shiba Norio、Tomizawa Daisuke、Adachi Souichi、Yoshida Kenichi、Ogawa Seishi、Seki Masafumi、Takita Junko、Ito Etsuro、Terui Kiminori
- Journal Title
  
  Blood Advances
  
  Volume: 6 Issue: 10 Pages: 3162-3166
- DOI
  10.1182/bloodadvances.2021006383
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19H05656, KAKENHI-PROJECT-20H00528, KAKENHI-PROJECT-21K07813, KAKENHI-PROJECT-21K19405, KAKENHI-PROJECT-23K21429
[Journal Article] BRAFV600E-positive cells as molecular markers of bone marrow disease in pediatric Langerhans cell histiocytosis.2022
- Author(s)
  Ko Kudo, Tsutomu Toki, Rika Kanezaki, and Etsuro Ito
- Journal Title
  
  Haematologica
  
  Volume: epub ahead Issue: 7 Pages: 000-000
- DOI
  10.3324/haematol.2021.279857
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07813, KAKENHI-PROJECT-21K06909, KAKENHI-PROJECT-21K06938, KAKENHI-PROJECT-20K07442, KAKENHI-PROJECT-23K21429, KAKENHI-PROJECT-23K24297
[Journal Article] Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 212020
- Author(s)
  Yuzawa Kentaro、Terui Kiminori、Toki Tsutomu、Kanezaki Rika、Kobayashi Akie、Sato Tomohiko、Kamio Takuya、Kudo Ko、Sasaki Shinya、Endo Mikiya、Ozono Shuichi、Nomura Keiko、Ito Etsuro
- Journal Title
  
  Pediatric Blood & Cancer
  
  Volume: 67 Issue: 4
- DOI
  10.1002/pbc.28188
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18H04039, KAKENHI-PROJECT-18K07782, KAKENHI-PROJECT-18K07810
[Journal Article] Reduced-intensity conditioning is effective for hematopoietic stem cell transplantation in young pediatric patients with Diamond?Blackfan anemia2020
- Author(s)
  Koyamaishi Shun、Ogawa Seishi et al.
- Journal Title
  
  Bone Marrow Transplantation
  
  Volume: 56 Issue: 5 Pages: 1013-1020
- DOI
  10.1038/s41409-020-01056-1
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19H05656, KAKENHI-PROJECT-18H04039, KAKENHI-PROJECT-18K07868, KAKENHI-PROJECT-23K21429
[Journal Article] ダウン症関連巨核芽球性白血病発症の分子機構2019
- Author(s)
  金崎　里香
- Journal Title
  
  BIO Clinica
  
  Volume: 34 Pages: 1344-1350
- Data Source
  KAKENHI-PROJECT-17K10094
[Journal Article] TAMおよびDS-AMKL発症の分子機構2019
- Author(s)
  金崎　里香
- Journal Title
  
  BIO Clinica
  
  Volume: 34 Pages: 642-647
- Data Source
  KAKENHI-PROJECT-17K10094
[Journal Article] Highly sensitive detection of GATA1 mutations in patients with myeloid leukemia associated with Down syndrome by combining Sanger and targeted next generation sequencing.2019
- Author(s)
  Terui K, Toki T, Taga T, Iwamoto S, Miyamura T, Hasegawa D, Moritake H, Hama A, Nakashima K, Kanezaki R, Kudo K, Saito AM, Horibe K, Adachi S, Tomizawa D, Ito E.
- Journal Title
  
  Genes Chromosomes Cancer.
  
  Volume: - Issue: 3 Pages: 160-167
- DOI
  10.1002/gcc.22816
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18H04039, KAKENHI-PROJECT-17H04110
[Journal Article] Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation.2018
- Author(s)
  Kudo K, Ueno H, Sato T, Kubo K, Kanezaki R, Kobayashi A, Kamio T, Sasaki S, Terui K, Kurose A, Yoshida K, Shiozawa Y, Toki T, Ogawa S, Ito E.
- Journal Title
  
  Genes Chromosomes Cancer.
  
  Volume: 57 Issue: 12 Pages: 665-669
- DOI
  10.1002/gcc.22676
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18H04039
[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] 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] 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] 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] ダウン症候群に伴うTAM発症の分子機構2015
- Author(s)
  照井君典, 金崎里香, 土岐力, 伊藤悦朗
- Journal Title
  
  日本産婦人科・新生児血液学会誌
  
  Volume: 25 Pages: 49-54
- Data Source
  KAKENHI-PROJECT-26461559
[Journal Article] Gene alterations involving the CRLF2-JAK pathway and recurrent gene deletions in Down syndrome-associated acute lymphoblastic leukemia in Japan.2014
- Author(s)
  Hanada I, Terui K, Ikeda F, Toki T, Kanezaki R, Sato T, Kamio T, Kudo K, Sasaki S, Takahashi Y, Hayashi Y, Inukai T, Kojima S, Koike K, Kosaka Y, Kobayashi M, Imaizumi M, Mitsui T, Hori H, Hara J, Horibe K, Nagai J, Goto H, Ito E.
- Journal Title
  
  Genes Chromosomes Cancer
  
  Volume: 53 Issue: 11 Pages: 902-910
- DOI
  10.1002/gcc.22201
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-24390268, KAKENHI-PROJECT-24591539, KAKENHI-PROJECT-25461611, KAKENHI-PROJECT-25670482, KAKENHI-PROJECT-26253061, KAKENHI-PROJECT-26461560, KAKENHI-PROJECT-26461598, KAKENHI-PROJECT-26461599
[Journal Article] 非ダウン症小児急性巨核芽球性白血病にみとめられた新規GATA1インフレーム変異2014
- Author(s)
  王汝南, 金崎里香, 土岐力, 照井君典, 佐々木伸也, 工藤耕, 神尾卓哉, 佐藤知彦, 池田史圭, 荒木亮, 落合英俊, 伊藤悦朗
- Journal Title
  
  弘前医学
  
  Volume: 65 Pages: 227-237
- NAID
  110009838312
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26461559
[Presentation] BRAFV600E-POSITIVE PRECURSORS AS MOLECULAR MARKERS OF BONE MARROW INVOLVEMENT IN PEDIATRIC LANGERHANS CELL HISTIOCYTOSIS.2019
- Author(s)
  Ko Kudo, Rika Kanezaki, Masaru Imamura, Chihaya Imai, Masahiro Irie, Yoji Sasahara, Kumiko Ando, Harumi Kakuda, Takehiko Doi, Hiroshi Kawaguchi, Kazuko Kudo, Hirokazu Kanegane, Tsutomu Toki, and Etsuro Ito.
- Organizer
  35th Annual Meeting of the Histiocyte Society
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18H04039
[Presentation] ダウン症児に発症する巨核芽球性白血病におけるエピゲノム異常2018
- Author(s)
  渡辺　亮、才田　聡、中村　正裕、土岐　力、金崎　里香、照井　君典、渡邉　健一郎、伊藤　悦朗
- Organizer
  第80回日本血液学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18H04039
[Presentation] ダウン症関連骨髄疾患におけるGATA1によるKIT遺伝子発現の制御機構2018
- Author(s)
  金崎里香, 土岐力, 照井君典, 佐々木伸也, 工藤耕, 神尾卓哉, 佐藤知彦, 小林明恵, 伊藤悦朗
- Organizer
  第80回日本血液学会学術集会
- Data Source
  KAKENHI-PROJECT-17K10094
[Presentation] Dysregulation of the KIT gene expression by GATA1s in Down syndrome related myeloid disorders.2016
- Author(s)
  金崎里香, 土岐力, 照井君典, 佐々木伸也, 工藤耕, 神尾卓哉, 佐藤知彦, 池田史圭, 伊藤悦朗
- 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）
- Year and Date
  2016-10-13
- Data Source
  KAKENHI-PROJECT-26461559
[Presentation] In-frame deletion of GATA1 in pediatric acute megakaryoblastic leukemia without Down syndrome.
- Author(s)
  金崎里香, 王汝南, 土岐力, 照井君典, 佐々木伸也, 工藤耕, 神尾卓哉, 池田史圭, 伊藤悦朗
- Organizer
  第76回日本血液学会学術集会
- Place of Presentation
  大阪国際会議場（大阪府大阪市）
- Year and Date
  2014-10-31 – 2014-11-02
- Data Source
  KAKENHI-PROJECT-26461559

1. TOKI Tsutomu (50195731)

# of Collaborated Projects: 9 results

# of Collaborated Products: 14 results
2. Ito Etsuro (20168339)

# of Collaborated Projects: 5 results

# of Collaborated Products: 10 results
3. Sato Tomohiko (70587005)

# of Collaborated Projects: 4 results

# of Collaborated Products: 0 results
4. 照井君典 (00333740)

# of Collaborated Projects: 4 results

# of Collaborated Products: 8 results
5. 工藤耕 (20455728)

# of Collaborated Projects: 3 results

# of Collaborated Products: 5 results
6. KAMIO TAKUYA (50587011)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
7. 林泰秀

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

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

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
11. 佐藤悠佑

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
12. 松尾英将

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
13. 菅野仁

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Kanezaki Rika 金崎 里香

KANEZAKI RIKA 金崎 里香

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Analysis of the function of the long non-coding RNA PVT1 in Down syndrome-associated leukemia.Principal Investigator

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Analysis of transcriptional dysregulation mechanisms in Down syndrome-related LeukemiaPrincipal Investigator

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Molecular pathogenesis of leukemia by the GATA1 gene mutationPrincipal Investigator

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Elucidation of molecular mechanism of leukemogenesis with GATA1 and cohesin gene mutationsPrincipal Investigator

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[Journal Article] Antileukemic effect of azacitidine, a DNA methyltransferase inhibitor, on cell lines of myeloid leukemia associated with Down syndrome2024

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[Journal Article] Landscape of driver mutations and their clinical effects on Down syndrome-related myeloid neoplasms2024

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[Journal Article] Dyserythropoietic anaemia with an intronic GATA1 splicing mutation in patients suspected to have Diamond‐Blackfan anaemia2022

Kanezaki Rika 金崎里香

KANEZAKI RIKA 金崎里香