Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kohei Ohnuma"'
Autor:
Masakazu Kohda, Yoshimi Tokuzawa, Yoshihito Kishita, Hiromi Nyuzuki, Yohsuke Moriyama, Yosuke Mizuno, Tomoko Hirata, Yukiko Yatsuka, Yzumi Yamashita-Sugahara, Yutaka Nakachi, Hidemasa Kato, Akihiko Okuda, Shunsuke Tamaru, Nurun Nahar Borna, Kengo Banshoya, Toshiro Aigaki, Yukiko Sato-Miyata, Kohei Ohnuma, Tsutomu Suzuki, Asuteka Nagao, Hazuki Maehata, Fumihiko Matsuda, Koichiro Higasa, Masao Nagasaki, Jun Yasuda, Masayuki Yamamoto, Takuya Fushimi, Masaru Shimura, Keiko Kaiho-Ichimoto, Hiroko Harashima, Taro Yamazaki, Masato Mori, Kei Murayama, Akira Ohtake, Yasushi Okazaki
Publikováno v:
PLoS Genetics, Vol 12, Iss 1, p e1005679 (2016)
Mitochondrial disorders have the highest incidence among congenital metabolic disorders characterized by biochemical respiratory chain complex deficiencies. It occurs at a rate of 1 in 5,000 births, and has phenotypic and genetic heterogeneity. Mutat
Externí odkaz:
https://doaj.org/article/158105bef6724bed92af4dd632668bf3
Publikováno v:
Drug Testing and Analysis. 14:915-928
In the context of doping control, conventional direct chemical testing detects only a limited scope of target substances in equine biological samples. To expand the ability to detect doping agents and their detection windows, metabolomics has recentl
Autor:
Masakazu Kohda, Kohei Ohnuma, Yuta Ohtsu, Satomi Takeo, Tsunaki Asano, Yoshihito Kishita, Toshiro Aigaki, Yasushi Okazaki, Kei Murayama, Akira Ohtake, Yukiko Sato-Miyata, Hiromi Nyuzuki
Publikováno v:
FEBS Letters. 594:2168-2181
Tetratricopeptide repeat protein 37 (TTC37) is a causative gene of trichohepatoenteric syndrome (THES). However, little is known about the pathogenesis of this disease. Here, we characterize the phenotype of a Drosophila model in which ski3, a homolo
Autor:
Masaru Shimura, Hiromi Nyuzuki, Tsutomu Suzuki, Yoshihito Kishita, Kengo Banshoya, Keiko Kaiho-Ichimoto, Masato Mori, Jun Yasuda, Masao Nagasaki, Shunsuke Tamaru, Taro Yamazaki, Takuya Fushimi, Kei Murayama, Yutaka Nakachi, Toshiro Aigaki, Koichiro Higasa, Tomoko Hirata, Fumihiko Matsuda, Yohsuke Moriyama, Akira Ohtake, Masakazu Kohda, Yoshimi Tokuzawa, Akihiko Okuda, Yukiko Sato-Miyata, Yzumi Yamashita-Sugahara, Yosuke Mizuno, Yukiko Yatsuka, Kohei Ohnuma, Nurun Nahar Borna, Hiroko Harashima, Yasushi Okazaki, Masayuki Yamamoto, Hidemasa Kato, Asuteka Nagao, Hazuki Maehata
Publikováno v:
PLoS Genetics, Vol 12, Iss 1, p e1005679 (2016)
PLoS Genetics
PLoS Genetics
Mitochondrial disorders have the highest incidence among congenital metabolic disorders characterized by biochemical respiratory chain complex deficiencies. It occurs at a rate of 1 in 5,000 births, and has phenotypic and genetic heterogeneity. Mutat
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.