Naruto Takuya

ナルトタクヤ | Naruto Takuya

Affiliation and department：

Research field (1)： Molecular biology

Research theme for competitive and other funds (10)：

2022 - 2025 Pathological analysis of malignant rhabdoid tumor by utilizing the human disease model library
2022 - 2025 Establishment of biomarkers and elucidation of pathophysiology for coronary artery lesions of Kawasaki disease
2018 - 2020 塩基変異の引き起こすエクソンスキップを分子機構の解明と治療法の開発
2015 - 2018 CRLF2高発現を示す小児B細胞型急性リンパ球性白血病発症の分子機構の解明
2014 - 2017 Genetic and genomic analysis on the patients with multiple congenital anomalies

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Papers (106)：

Yukiko Kuroda, Takuya Naruto, Kenji Kurosawa. Subtle phenotypes of Mowat-Wilson syndrome in a patient with a novel ZEB2 C-ZF domain variant. American journal of medical genetics. Part A. 2024. e63822
Yukiko Kuroda, Takeshi Uehara, Yumi Enomoto, Takuya Naruto, Nozomi Matsumura, Kenji Kurosawa. GPC4 truncating variant associated with Keipert syndrome and lacrimal punctal agenesis. American journal of medical genetics. Part A. 2024. e63799
Yasuhiro Hirano, Yukiko Kuroda, Yumi Enomoto, Takuya Naruto, Koji Muroya, Kenji Kurosawa. Noonan syndrome-like phenotype associated with an ERF frameshift variant. American journal of medical genetics. Part A. 2024. e63652
Yukiko Kuroda, Takuya Naruto, Yu Tsuyusaki, Ayumi Kato, Noriko Aida, Kenji Kurosawa. Role of TOE1 variants at the nuclear localization motif in pontocerebellar hypoplasia 7. Journal of human genetics. 2024
Yukiko Kuroda, Yoko Saito, Yumi Enomoto, Takuya Naruto, Kenji Kurosawa. A novel ACTB variant in an atypical case of Baraitser-Winter syndrome with cerebellar hypoplasia and diaphragmatic hernia. Clinical dysmorphology. 2024. 33. 2. 75-78

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MISC (16)：

Akira Nishimura, Kazuaki Yokoyama, Chika Yamagishi, Toshihiko Imamura, Takuya Naruto, Tomohiro Morio, Yukie Tanaka, Akinori Kanai, Hirotaka Matsui, Naoko Higuchi, et al. Comprehensive Genetic Analysis Revealed Myeloid/Natural Killer (NK) Cell Precursor Acute Leukemia As a Novel Distinctive Leukemia Entity. BLOOD. 2020. 136
Akira Nishimura, Kazuaki Yokoyama, Chika Yamagishi, Takuya Naruto, Tomohiro Morio, Akinori Kanai, Hirotaka Matsui, Naoko Higuchi, Akiko Takada, Haruna Okuno, et al. Clinical Feature and Genetic Alterations in Myeloid/Natural Killer (NK) Cell Precursor Acute Leukemia and Myeloid/NK Cell Acute Leukemia. BLOOD. 2018. 132
湊川真理, 横井貴之, 榎本友美, 井田一美, 鶴崎美徳, 原田法彰, 成戸卓也, 黒澤健司. TBL1XR1遺伝子に新規変異を認めた知的障害、自閉スペクトラム症および特異顔貌を示す1症例(A novel mutation of TBL1XR1 in individual with autism spectrum disorder and facial dysmorphism). 脳と発達. 2017. 49. Suppl. S425-S425
成戸卓也, 梶浦耕一郎, 増田清士, 近藤知也, 丹黒章, 井本逸勢. 肺腺癌の早期からDNAメチル化により高頻度に発現抑制を受ける新規癌抑制遺伝子候補TSLAC1の同定. 日本癌学会総会記事. 2016. 75回. P-3040
小野朱美, 伊藤弘道, 阿部容子, 森達夫, 東田好広, 早渕康信, 成戸卓也, 井本逸勢, 香美祥二. 重症蒼白型の憤怒痙攣に対してレベチラセタムが奏効した1p36欠失症候群の1女児例. 脳と発達. 2016. 48. Suppl. S418-S418

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