Kanezaki Rika

カネザキリカ | Kanezaki Rika

Affiliation and department：

Research field (1)： Fetal medicine/Pediatrics

Research theme for competitive and other funds (14)：

2021 - 2025 Clarification of the mechanism of multistep leukemogenesis of acute megakaryoblastic leukemia associated with Down syndrome and development of the molecular targeted therapy
2021 - 2024 赤血球分化における転写因子IRX1の機能の解明
2021 - 2024 Diamond-Blackfan貧血に合併する悪性腫瘍発症機構の解明
2020 - 2023 Mechanism of Transcriptional Dysregulation in Down Syndrome-Related Leukemia
2022 - ダウン症関連白血病の迅速診断法の開発

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Papers (45)：

Tomohiko Sato, Kenichi Yoshida, Tsutomu Toki, Rika Kanezaki, Kiminori Terui, Ryunosuke Saiki, Masami Ojima, Yotaro Ochi, Seiya Mizuno, Masaharu Yoshihara, et al. Landscape of driver mutations and their clinical effects on Down syndrome-related myeloid neoplasms. Blood Journal. 2024
Rika Kanezaki, Tsutomu Toki, Kiminori Terui, Tomohiko Sato, Akie Kobayashi, Ko Kudo, Takuya Kamio, Shinya Sasaki, Koji Kawaguchi, Kenichiro Watanabe, et al. Mechanism of KIT gene regulation by GATA1 lacking the N-terminal domain in Down syndrome-related myeloid disorders. Scientific reports. 2022. 12. 1. 20587-20587
Ko Kudo, Yasuo Kubota, Tsutomu Toki, Rika Kanezaki, Akie Kobayashi, Tomohiko Sato, Takuya Kamio, Shinya Sasaki, Norio Shiba, Daisuke Tomizawa, et al. Childhood acute myeloid leukemia with 5q deletion and HNRNPH1-MLLT10 fusion: the first case report. Blood advances. 2022. 6. 10. 3162-3166
Ko Kudo, Tsutomu Toki, Rika Kanezaki, Tatsuhiko Tanaka, Takuya Kamio, Tomohiko Sato, Shinya Sasaki, Masaru Imamura, Chihaya Imai, Kumiko Ando, et al. BRAFV600E-positive cells as molecular markers of bone marrow disease in pediatric Langerhans cell histiocytosis. Haematologica. 2022
Karasawa Takao, Hashimoto Shun, Sato Riko, Fujita Masashi, Aizawa Tomomi, Tsugawa Koji, Toki Tsutomu, Kanezaki Rika, Sato Tomohiko, Kudo Ko, et al. Erythromelalgia presenting as recurrent purpura and hypogammaglobulinemia: A case report. Hirosaki Medical Journal. 2022. 72. 1-4. 80-83

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MISC (36)：

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
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
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. 1. 163-167
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. ダイアモンドブラックファン貧血に対する骨髄非破壊的前処置を用いた同種造血細胞幹移植の有用性. 日本血液学会学術集会抄録(Web). 2020. 82nd
金崎里香. TAMおよびDS-AMKL発症の分子機構. BIO Clinica. 2019. 34. 6. 642-647

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