Accumulation of mitochondrial DNA with a point mutation in tRNALeu(UUR) gene induces brain dysfunction in mice
Ishikawa, Kaori, Miyata, Daiki, Hattori, Satoko, Tani, Haruna, Kuriyama, Takayoshi, Wei, Fan-Yan, Miyakawa, Tsuyoshi, Nakada, Kazuto
Published in Pharmacological research (01.10.2024)
Published in Pharmacological research (01.10.2024)
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Aberrant RNA processing contributes to the pathogenesis of mitochondrial diseases in trans-mitochondrial mouse model carrying mitochondrial tRNALeu(UUR) with a pathogenic A2748G mutation
Tani, Haruna, Ishikawa, Kaori, Tamashiro, Hiroaki, Ogasawara, Emi, Yasukawa, Takehiro, Matsuda, Shigeru, Shimizu, Akinori, Kang, Dongchon, Hayashi, Jun-Ichi, Wei, Fan-Yan, Nakada, Kazuto
Published in Nucleic acids research (09.09.2022)
Published in Nucleic acids research (09.09.2022)
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Journal Article
Accumulation of mitochondrial DNA with a point mutation in tRNA gene induces brain dysfunction in mice
Ishikawa, Kaori, Miyata, Daiki, Hattori, Satoko, Tani, Haruna, Kuriyama, Takayoshi, Wei, Fan-Yan, Miyakawa, Tsuyoshi, Nakada, Kazuto
Published in Pharmacological research (01.10.2024)
Published in Pharmacological research (01.10.2024)
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Pathological mutations promote proteolysis of mitochondrial tRNA-specific 2-thiouridylase 1 (MTU1) via mitochondrial caseinolytic peptidase (CLPP)
Ahmad, Raja Norazireen Raja, Zhang, Long-Teng, Morita, Rikuri, Tani, Haruna, Wu, Yong, Chujo, Takeshi, Ogawa, Akiko, Harada, Ryuhei, Shigeta, Yasuteru, Tomizawa, Kazuhito, Wei, Fan-Yan
Published in Nucleic acids research (09.02.2024)
Published in Nucleic acids research (09.02.2024)
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Journal Article
Mice deficient in the Shmt2 gene have mitochondrial respiration defects and are embryonic lethal
Tani, Haruna, Ohnishi, Sakiko, Shitara, Hiroshi, Mito, Takayuki, Yamaguchi, Midori, Yonekawa, Hiromichi, Hashizume, Osamu, Ishikawa, Kaori, Nakada, Kazuto, Hayashi, Jun-Ichi
Published in Scientific reports (11.01.2018)
Published in Scientific reports (11.01.2018)
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Journal Article
Accumulation of mitochondrial DNA with a point mutation in tRNA Leu(UUR) gene induces brain dysfunction in mice
Ishikawa, Kaori, Miyata, Daiki, Hattori, Satoko, Tani, Haruna, Kuriyama, Takayoshi, Wei, Fan-Yan, Miyakawa, Tsuyoshi, Nakada, Kazuto
Published in Pharmacological research (01.10.2024)
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Published in Pharmacological research (01.10.2024)
Journal Article
Acquired Expression of Mutant Mitofusin 2 Causes Progressive Neurodegeneration and Abnormal Behavior
Ishikawa, Kaori, Yamamoto, Satoshi, Hattori, Satoko, Nishimura, Naoya, Tani, Haruna, Mito, Takayuki, Matsumoto, Hirokazu, Miyakawa, Tsuyoshi, Nakada, Kazuto
Published in The Journal of neuroscience (27.02.2019)
Published in The Journal of neuroscience (27.02.2019)
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Journal Article
Disruption of the mouse Shmt2 gene confers embryonic anaemia via foetal liver-specific metabolomic disorders
Tani, Haruna, Mito, Takayuki, Velagapudi, Vidya, Ishikawa, Kaori, Umehara, Moe, Nakada, Kazuto, Suomalainen, Anu, Hayashi, Jun-Ichi
Published in Scientific reports (05.11.2019)
Published in Scientific reports (05.11.2019)
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Cytoplasmic transfer of heritable elements other than mtDNA from SAMP1 mice into mouse tumor cells suppresses their ability to form tumors in C57BL6 mice
Shimizu, Akinori, Tani, Haruna, Takibuchi, Gaku, Ishikawa, Kaori, Sakurazawa, Ryota, Inoue, Takafumi, Hashimoto, Tetsuo, Nakada, Kazuto, Takenaga, Keizo, Hayashi, Jun-Ichi
Published in Biochemical and biophysical research communications (04.11.2017)
Published in Biochemical and biophysical research communications (04.11.2017)
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