Rchr
J-GLOBAL ID：201401068582609383
Update date: Mar. 14, 2024
Chonabayashi Kazuhisa
チョウナバヤシ カズヒサ | Chonabayashi Kazuhisa
Affiliation and department：
Research field (1)：
Hematology and oncology
Research theme for competitive and other funds (3)：
- 2021 - 2024 非定型3q26転座型骨髄性腫瘍のEVI1エピジェネティック制御機構解明と治療応用
- 2016 - 2019 Reprogramming technology revealed the genetic and functional diversity present in an individual myelodysplastic syndrome patient
- 2014 - 2016 Search for pathogenesis and novel therapeutics of acquired myelodysplastic syndromes using reprogramming technology
Papers (47)：
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Misato Nakanishi-Koakutsu, Kenji Miki, Yuki Naka, Masako Sasaki, Takayuki Wakimizu, Stephanie C Napier, Chikako Okubo, Megumi Narita, Misato Nishikawa, Reo Hata, et al. CD151 expression marks atrial- and ventricular- differentiation from human induced pluripotent stem cells. Communications biology. 2024. 7. 1. 231-231
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Yutaka Shimazu, Chisaki Mizumoto, Kazuhisa Chonabayashi, Yuta Hanyu, Junya Kanda, Akifumi Takaori-Kondo. Successful treatment with cyclosporine of pure red cell aplasia induced by obinutuzumab bendamustine therapy. Annals of hematology. 2023
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Jingshan Gao, Takeru Makiyama, Yuta Yamamoto, Takuya Kobayashi, Hisaaki Aoki, Thomas L Maurissen, Yimin Wuriyanghai, Asami Kashiwa, Tomohiko Imamura, Takanori Aizawa, et al. Novel Calmodulin Variant p.E46K Associated With Severe Catecholaminergic Polymorphic Ventricular Tachycardia Produces Robust Arrhythmogenicity in Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes. Circulation. Arrhythmia and electrophysiology. 2023. 16. 3. e011387
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奥田 瑠璃花, 越智 陽太郎, 蝶名林 和久, 眞田 昌, 半田 寛, 白石 友一, 千葉 滋, 石川 隆之, 大屋敷 一馬, 熱田 由子, et al. がん研究における女性研究者 不均衡転座der(1;7)(q10;p10)を有するMDSと関連疾患の特徴(Unbalanced translocation der(1;7)(q10;p10) as a distinct subtype in myelodysplastic syndromes). 日本癌学会総会記事. 2022. 81回. SS1-4
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Asami Kashiwa, Takeru Makiyama, Hirohiko Kohjitani, Thomas L Maurissen, Taisuke Ishikawa, Yuta Yamamoto, Yimin Wuriyanghai, Jingshan Gao, Hai Huang, Tomohiko Imamura, et al. Disrupted Cav1.2 Selectivity Causes Overlapping Long QT and Brugada Syndrome Phenotypes in CACNA1C-E1115K iPS Cell Model. Heart rhythm. 2022. 20. 1. 89-99
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MISC (48)：
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Rurika Okuda, Yasuhito Nannya, Yotaro Ochi, Kazuhisa Chonabayashi, Maria Creignou, Hideki Makishima, June Takeda, Ayana Kon, Satoru Miyano, Hiroshi Handa, et al. Distinct ethnic, clinical, and genetic characteristics of der(1;7) in myelodysplastic syndromes. CANCER SCIENCE. 2021. 112. 310-310
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中村桃子, 中村桃子, 蝶名林和久, 蝶名林和久, 森本有紀, 森本有紀, 越智陽太郎, 越智陽太郎, 南谷泰仁, 北脇年雄, et al. Elucidating the pathophysiology of AML with atypical 3q26 translocations using patient-derived iPSCs. 日本血液学会学術集会抄録(Web). 2021. 83rd
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奥田瑠璃花, 南谷泰人, 越智陽太郎, 蝶名林和久, 蝶名林和久, 牧島秀樹, 吉里哲一, 永田安伸, 竹田淳恵, 吉田健一, et al. ETNK1 mutations defines a subclass of der(1;7)(q10;p10) in myelodysplastic syndromes. 日本血液学会学術集会抄録(Web). 2021. 83rd
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奥田瑠璃花, 南谷泰仁, 越智陽太郎, 蝶名林和久, 蝶名林和久, 牧島秀樹, 永田安伸, 真田昌, 白石友一, 宮野悟, et al. ETNK1変異の有無を特徴とするder(1;7)(q10;p10)を伴う骨髄異形成症候群. 日本癌学会学術総会抄録集(Web). 2021. 80th
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奥田瑠璃花, 南谷泰仁, 越智陽太郎, 蝶名林和久, 蝶名林和久, 牧島秀樹, 吉里哲一, 永田安伸, 竹田淳恵, 吉田健一, et al. Der(1;7) 陽性骨髄異形成症候群における人種,臨床像,遺伝学的観点からみた特徴. 日本血液学会学術集会抄録(Web). 2020. 82nd
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