Research keywords (4)：
Drug delivery
, Genome Editing
, Functional Genomics
, Mitochondrial Disorders
Research theme for competitive and other funds (3)：
2019 - 2021 Novel mitochondrial ribosomal genes are associated with mitochondrial disorders
2017 - 2019 Research fellowship
2014 - 2017 Research fellowship
Papers (9)：
Nurun Nahar Borna, Yoshihito Kishita, Masaru Shimura, Kei Murayama, Akira Ohtake, Yasushi Okazaki. Identification of a novel MT-ND3 variant and restoring mitochondrial function by allotopic expression of MT-ND3 gene. Mitochondrion. 2024. 101858-101858
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
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 Intractable Disease Research Center PhD
2010 - 2014 Bangabandhu Sheikh Mujib Medical University, Bangladesh Medical virology MD
2000 - 2005 Chittagong Medical College, Bangladesh Medical Doctor MBBS
Work history (2)：
2014/05 - 2015/03 Saitama Medical University Functional Genomics and Systems Medicine Research Fellow
