Rchr
J-GLOBAL ID:201901010925546071   Update date: Oct. 27, 2021

Borna Nurun Nahar

Borna Nurun Nahar
Affiliation and department:
Job title: Postdoctoral Researcher
Research field  (1): Genomics
Research keywords  (4): Drug delivery ,  Genome Editing ,  Functional Genomics ,  Mitochondrial Disorders
Research theme for competitive and other funds  (2):
  • 2017 - 2019 Research fellowship
  • 2014 - 2017 Research fellowship
Papers (8):
  • Nurun Nahar Borna, Yoshihito Kishita, Norio Sakai, Yusuke Hamada, Koji Kamagata, Masakazu Kohda, Akira Ohtake, Kei Murayama, Yasushi Okazaki. Leigh Syndrome Due to NDUFV1 Mutations Initially Presenting as LBSL. Genes. 2020. 11. 11. 1325
  • Nurun Nahar Borna, Yoshihito Kishita, Jiro Abe, Takuro Furukawa, Minako Ogawa-Tominaga, Takuya Fushimi, Atsuko Imai-Okazaki, Atsuhito Takeda, Akira Ohtake, Kei Murayama, et al. NAD(P)HX dehydratase protein-truncating mutations are associated with neurodevelopmental disorder exacerbated by acute illness. Brain : a journal of neurology. 2020. 143. 7. e54
  • Matsunaga Ayako, Sugiyama Yohei, Borna Nurun Nahar, Kishita Yoshihito, Shimura Masaru, Hisatomi Yuichiro, Fushimi Takuya, Okazaki Yasushi, Ohtake Akira, Murayama Kei. ミトコンドリア性リボソームタンパク質PTCD3の変異はリー症候群の新規の原因である(Mitochondrial ribosomal protein PTCD3 mutations are novel cause of Leigh syndrome). 日本先天代謝異常学会雑誌. 2019. 35. 165-165
  • Nurun Nahar Borna, Yoshihito Kishita, Masakazu Kohda, Sze Chern Lim, Masaru Shimura, Yibo Wu, Kaoru Mogushi, Yukiko Yatsuka, Hiroko Harashima, Yuichiro Hisatomi, et al. Mitochondrial ribosomal protein PTCD3 mutations cause oxidative phosphorylation defects with Leigh syndrome. Neurogenetics. 2019. 20. 1. 9-25
  • Borna Nurun Nahar, Kishita Yoshihito, Ishikawa Kaori, Nakada Kazuto, Kohda Masakazu, Nasu Takashi, Takeda Atsuhito, Murayama Kei, Ohtake Akira, Okazaki Yasushi. Tazの新規変異は心筋症を引き起こさずにミトコンドリア呼吸鎖障害を誘導する(A novel mutation in TAZ causes mitochondrial respiratory chain disorder without cardiomyopathy). 日本先天代謝異常学会雑誌. 2017. 33. 213-213
more...
MISC (1):
  • 神田将和, 徳澤佳美, 木下善仁, 森山陽介, 森山陽介, 水野洋介, 平田智子, 八塚由紀子, 菅原泉, 仲地豊, et al. ミトコンドリア呼吸鎖複合体異常症のゲノム解析と新規原因遺伝子の発見. 日本人類遺伝学会大会プログラム・抄録集. 2015. 60th. 228
Lectures and oral presentations  (3):
  • Participiant
    (Intractable disease symposium, Nagoya 2019)
  • Poster Presentation
    (The 59th Annual Meeting of the Japanese Society for Inherited Metabolic Diseases and The 15th Asian Symposium of Inherited Metabolic Diseases 2017)
  • Poster Presentation
    (The 13th Conference of Asian Society for Mitochondrial Research and Medicine [ASMRM] and The 16th Conference of Japanese Society of Mitochondrial Research and Medicine [J-mit] 2016)
Education (3):
  • 2015 - 2019 Juntendo University PhD
  • 2010 - 2014 Bangabandhu Sheikh Mujib Medical University, Bangladesh MD
  • 2000 - 2005 Chittagong Medical College, Bangladesh MBBS
Work history (2):
  • 2014/05 - 2015/03 Saitama Medical University Functional Genomics and Systems Medicine Research Fellow
  • 2007 - 2010 BIRDEM, Bangladesh Chronic Kidney Disease Project Research officer
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