Rchr
J-GLOBAL ID:201601010534000137   Update date: Oct. 21, 2021

Kishita Yoshihito

キシタ ヨシヒト | Kishita Yoshihito
Affiliation and department:
Homepage URL  (1): https://kishitalab.com/
Research field  (3): Molecular biology ,  Fetal medicine/Pediatrics ,  Genomics
Research keywords  (3): 人類遺伝学 ,  分子生物学 ,  ミトコンドリア
Research theme for competitive and other funds  (7):
  • 2020 - 2022 The relationship between iron homeostasis and pathogenesis
  • 2019 - 2022 Comprehensive analysis of of aberrant gene expression in mitochondrial disorders
  • 2018 - 2019 高難度ゲノム領域での構造異常に着目したゲノム解析手法の開発と遺伝性疾患の解明
  • 2016 - 2019 Elucidation of the molecular pathogenesis of mitochondrial disease
  • 2017 - クリステ形成異常とミトコンドリアDNA枯渇症候群の関連
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Papers (40):
  • Tomohiro Ebihara, Taro Nagatomo, Yohei Sugiyama, Tomoko Tsuruoka, Yoshiteru Osone, Masaru Shimura, Makiko Tajika, Tetsuro Matsuhashi, Keiko Ichimoto, Ayako Matsunaga, et al. Neonatal-onset mitochondrial disease: clinical features, molecular diagnosis and prognosis. Archives of disease in childhood. Fetal and neonatal edition. 2021
  • Yoshihito Kishita, Masaru Shimura, Masakazu Kohda, Takuya Fushimi, Kazuhiro R Nitta, Yukiko Yatsuka, Akira Ohtake, Kei Murayama, Yasushi Okazaki. Genome sequencing and RNA-seq analyses of mitochondrial complex I deficiency revealed Alu insertion-mediated deletion in NDUFV2. Human mutation. 2021
  • Shintaro Kinoshita, Miki Ando, Jun Ando, Midori Ishii, Yoshiki Furukawa, Osamu Tomita, Yoko Azusawa, Shuichi Shirane, Yoshihito Kishita, Yukiko Yatsuka, et al. Trigenic ADH5/ALDH2/ADGRV1 mutations in myelodysplasia with Usher syndrome. Heliyon. 2021. 7. 8. e07804
  • Atsuko Imai-Okazaki, Ayako Matsunaga, Yukiko Yatsuka, Kazuhiro R Nitta, Yoshihito Kishita, Ayumu Sugiura, Yohei Sugiyama, Takuya Fushimi, Masaru Shimura, Keiko Ichimoto, et al. Long-term prognosis and genetic background of cardiomyopathy in 223 pediatric mitochondrial disease patients. International journal of cardiology. 2021
  • Yoshihito Kishita, Kaori Ishikawa, Kazuto Nakada, Jun-Ichi Hayashi, Takuya Fushimi, Masaru Shimura, Masakazu Kohda, Akira Ohtake, Kei Murayama, Yasushi Okazaki. A high mutation load of m.14597A>G in MT-ND6 causes Leigh syndrome. Scientific reports. 2021. 11. 1. 11123-11123
more...
MISC (55):
Education (1):
  • - 2012 Tokyo Metropolitan University Department of Biological Sciences
Professional career (1):
  • 博士(理学) (首都大学東京)
Work history (7):
  • 2020/04 - 現在 Juntendo University Graduate School of Medicine
  • 2020/04 - 現在 Kindai University Graduate School of Medicine
  • 2019/01 - 現在 Saitama Medical University Faculty of Medicine Pediatrics
  • 2012/04 - 現在 Tokyo Metropolitan University
  • 2017/05 - 2020/03 Juntendo University Graduate School of Medicine
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Awards (1):
  • 2008 - 日本基礎老化学会 日本基礎老化学会奨励賞
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