Mito-mice∆ and mitochondrial DNA mutator mice as models of human osteoporosis caused not by aging but by hyperparathyroidism

por Mito, Takayuki, Tani, Haruna, Suzuki, Michiko, Ishikawa, Kaori, Nakada, Kazuto, Hayashi, Jun-Ichi
Publicado 2018

Disruption of the mouse Shmt2 gene confers embryonic anaemia via foetal liver-specific metabolomic disorders

por Tani, Haruna, Mito, Takayuki, Velagapudi, Vidya, Ishikawa, Kaori, Umehara, Moe, Nakada, Kazuto, Suomalainen, Anu, Hayashi, Jun-Ichi
Publicado 2019

Mice deficient in the Shmt2 gene have mitochondrial respiration defects and are embryonic lethal

por Tani, Haruna, Ohnishi, Sakiko, Shitara, Hiroshi, Mito, Takayuki, Yamaguchi, Midori, Yonekawa, Hiromichi, Hashizume, Osamu, Ishikawa, Kaori, Nakada, Kazuto, Hayashi, Jun-Ichi
Publicado 2018

Aberrant RNA processing contributes to the pathogenesis of mitochondrial diseases in trans-mitochondrial mouse model carrying mitochondrial tRNA(Leu(UUR)) with a pathogenic A2748G...

por Tani, Haruna, Ishikawa, Kaori, Tamashiro, Hiroaki, Ogasawara, Emi, Yasukawa, Takehiro, Matsuda, Shigeru, Shimizu, Akinori, Kang, Dongchon, Hayashi, Jun-Ichi, Wei, Fan-Yan, Nakada, Kazuto
Publicado 2022