Kiyota Kyoko

Research field (1)： Fetal medicine/Pediatrics

Research keywords (2)： SLE , PIK3CD

Research theme for competitive and other funds (3)：

2021 - 2025 新規PIK3CD遺伝子変異によるSLE発症機構を解明する
2021 - 2024 ゼブラフィッシュを用いた遠位尿細管アシドーシスに伴う難聴発症のメカニズム解明
2019 - 2021 Elucidation of the molecular mechanism of SLE onset due to a novel mutation in the PIK3CD gene

Papers (4)：

Yuka Kimura, Kyoko Kiyota, Mayo Ikeuchi, Kazuhito Sekiguchi, Kenji Ihara. Rituximab-induced serum sickness in a girl with nephrotic syndrome. CEN case reports. 2022. 11. 4. 506-510
Masanori Inoue, Hiroaki Miyahara, Hiroshi Shiraishi, Nobuyuki Shimizu, Mika Tsumori, Kyoko Kiyota, Miwako Maeda, Ryohei Umeda, Tohru Ishitani, Reiko Hanada, et al. Leucyl-tRNA synthetase deficiency systemically induces excessive autophagy in zebrafish. Scientific reports. 2021. 11. 1. 8392-8392
Kyoko Kiyota, Koh-Ichiro Yoshiura, Ryoko Houbara, Hiroaki Miyahara, Seigo Korematsu, Kenji Ihara. Auto-immune disorders in a child with PIK3CD variant and 22q13 deletion. European journal of medical genetics. 2018. 61. 10. 631-633
Kazuhito Sekiguchi, Tomoki Maeda, So-ichi Suenobu, Nobutaka Kunisaki, Miki Shimizu, Kyoko Kiyota, Yo-suke Handa, Kensuke Akiyoshi, Seigo Korematsu, Yoko Aoki, et al. A transient myelodysplastic/myeloproliferative neoplasm in a patient with cardio-facio-cutaneous syndrome and a germline BRAF mutation. American journal of medical genetics. Part A. 2013. 161A. 10. 2600-3

MISC (1)：

池内真代, 清田今日子, 木村裕香, 石和翔, 小宅桃子, 松田史佳, 糸永知代, 前田美和子, 井原健二. 2型糖尿病発症前から蛋白尿を認めた新規WFS1遺伝子バリアントを有する一例. 日本小児腎臓病学会雑誌. 2022. 35. 1. 46-46

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