Takuwa Ayako

Research theme for competitive and other funds (1)：

2018 - 2022 Search for novel mutation of inherited cardiovascular disease with combination of RNA-seq and WES

Papers (11)：

Ryuya Edahiro, Yuya Shirai, Yusuke Takeshima, Shuhei Sakakibara, Yuta Yamaguchi, Teruaki Murakami, Takayoshi Morita, Yasuhiro Kato, Yu-Chen Liu, Daisuke Motooka, et al. Single-cell analyses and host genetics highlight the role of innate immune cells in COVID-19 severity. Nature genetics. 2023. 55. 5. 753-767
Jun-Ya Kaimori, Yamato Kikkawa, Daisuke Motooka, Tomoko Namba-Hamano, Ayako Takuwa, Atsuko Imai-Okazaki, Kaori Kobayashi, Arisa Tanigawa, Yuko Kotani, Yoshihiro Uno, et al. A heterozygous LAMA5 variant may contribute to slowly progressive, vinculin-enhanced familial FSGS and pulmonary defects. JCI Insight. 2022
Hideyuki Hakui, Hidetaka Kioka, Yohei Miyashita, Shunsuke Nishimura, Ken Matsuoka, Hisakazu Kato, Osamu Tsukamoto, Yuki Kuramoto, Ayako Takuwa, Yusuke Takahashi, et al. Loss-of-function mutations in the co-chaperone protein BAG5 cause dilated cardiomyopathy requiring heart transplantation. Science translational medicine. 2022. 14. 628. eabf3274
Haruki Shinomiya, Hisakazu Kato, Yuki Kuramoto, Nozomi Watanabe, Toshihiro Tsuruda, Tadaaki Arimura, Yohei Miyashita, Yoshiki Miyasaka, Tomoji Mashimo, Ayako Takuwa, et al. Aberrant accumulation of TMEM43 accompanied by perturbed transmural gene expression in arrhythmogenic cardiomyopathy. FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 2021. 35. 11. e21994
Jun-Ya Kaimori, Tatsuhiko Mori, Tomoko Namba-Hamano, Takeshi Morimoto, Ayako Takuwa, Daisuke Motooka, Atsuko Okazaki, Kaori Kobayashi, Yuta Asahina, Sachio Kajimoto, et al. Cyclosporine A Treatment of Proteinuria in a New Case of MAFB-Associated Glomerulopathy without Extrarenal Involvement: A Case Report. Nephron. 2021. 145. 4. 445-450

ｍore...

MISC (3)：

朝野仁裕, 宮下洋平, 多久和綾子, 木岡秀隆, 四宮春輝, 伯井秀行, 宮脇大, 大谷朋仁, 坂田泰史. 心不全病態の層別化における疾患ゲノム解析の役割. 日本心不全学会学術集会プログラム・抄録集. 2018. 22nd
朝野仁裕, 木岡秀隆, 宮下洋平, 多久和綾子, 高島成二, 坂田泰史. 希少循環器疾患におけるゲノム解析による遺伝子診断. 日本心不全学会学術集会プログラム・抄録集. 2018. 22nd
多久和綾子, 川上知紗, 木岡秀隆, 山田憲明, 宮下洋平, 四宮春輝, 伯井秀行, 世良英子, 大谷朋仁, 山口修, et al. 心筋症のエクソーム解析による原因変異探索. 生命科学系学会合同年次大会. 2017. 2017年度. [3P-0731]

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