Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Yohsuke Moriyama"'
Autor:
Naoki Urakawa, Satoru Nakamura, Mariko Kishimoto, Yohsuke Moriyama, Shigeyuki Kawano, Tetsuya Higashiyama, Narie Sasaki
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-10 (2022)
Abstract The maternal/uniparental inheritance of mitochondria is controlled by the selective elimination of paternal/uniparental mitochondria and digestion of their mitochondrial DNA (mtDNA). In isogamy, the selective digestion of mtDNA in uniparenta
Externí odkaz:
https://doaj.org/article/ba329efa94ce48bb95965b0bcf89262e
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
Cellular senescence, irreversible cell cycle arrest, is induced by various triggers including telomere shortening, oncogene activation, and DNA damage. Senescent cells exhibit the senescence-associated secretory phenotype (SASP), a pathological featu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a0f8d19f93938bc8fe187f58889cbcd
https://doi.org/10.1101/2022.06.27.497690
https://doi.org/10.1101/2022.06.27.497690
Autor:
Keiko Kono, Makoto Nakanishi, Yoshikazu Johmura, Tetsuya Higashiyama, Yoshikatsu Sato, Shinju Sugiyama, Hiroshi Takase, Hunter Barbee, Koutarou Nishimura, Yatzu Chiu, Nurhanani Binti Razali, Yumiko Masukagami, Yohsuke Moriyama, Kojiro Suda
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6063a3ac2e6e014aa2a771280dc1e2f3
https://doi.org/10.15252/rc.2022362089
https://doi.org/10.15252/rc.2022362089
Autor:
Naoki, Urakawa, Satoru, Nakamura, Mariko, Kishimoto, Yohsuke, Moriyama, Shigeyuki, Kawano, Tetsuya, Higashiyama, Narie, Sasaki
Publikováno v:
Scientific reports. 12(1)
The maternal/uniparental inheritance of mitochondria is controlled by the selective elimination of paternal/uniparental mitochondria and digestion of their mitochondrial DNA (mtDNA). In isogamy, the selective digestion of mtDNA in uniparental mitocho
Autor:
Kojiro Suda, Yohsuke Moriyama, Yumiko Masukagami, Nurhanani Binti Razali, Yatzu Chiu, Koutarou Nishimura, Hunter Barbee, Hiroshi Takase, Shinju Sugiyama, Yoshikatsu Sato, Tetsuya Higashiyama, Yoshikazu Johmura, Makoto Nakanishi, Keiko Kono
Plasma membrane damage (PMD) occurs in all cell types due to environmental perturbation and cell-autonomous activities. However, cellular outcomes of PMD remain largely unknown except for recovery or death. Here, using budding yeast and normal human
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a49f7b4a08a45d2d656772c5ba4a5279
https://doi.org/10.1101/2021.03.26.437120
https://doi.org/10.1101/2021.03.26.437120
Autor:
Mikiko Morita, Yuka Aoyama, Kazuhisa Akiba, Tomohiro Hori, Kei Murayama, Yukihiro Hasegawa, Yohsuke Moriyama, Toshiyuki Fukao, Rik K. Wierenga, Akira Ohtake, Nobuteru Usuda, Nobuki Kuwayama, Takashi Hashimoto, Yuki Hasegawa, Yosuke Shigematsu, Rajaram Venkatesan, Masahiro Goto
Publikováno v:
Journal of Human Genetics. 59:609-614
2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (2M3HBD) deficiency (HSD10 disease) is a rare inborn error of metabolism, and30 cases have been reported worldwide. This disorder is typically characterized by progressive neurodegenerative disease from 6 t
Autor:
Yohsuke Moriyama, Yoshimi Tokuzawa, Nana Matoba, Taro Yamazaki, Masato Mori, Yutaka Nakachi, Kei Murayama, Masakazu Kohda, Yosuke Mizuno, Keisuke Hattori, Yasunori Fujita, Shunsuke Tamaru, Yasushi Okazaki, Natsumi Uehara, Masashi Tanaka, Masafumi Ito, Akira Ohtake, Takanori Yamagata, Ken-ichi Nibu, Hiroko Harashima, Tetsuro Sakai, Jun-Ichi Hayashi
Publikováno v:
Annals of Clinical and Translational Neurology
Objective Mitochondrial respiratory chain disorder (MRCD) is an intractable disease of infants with variable clinical symptoms. Our goal was to identify the causative mutations in MRCD patients. Methods The subjects were 90 children diagnosed with MR
Autor:
Kei Murayama, Yzumi Yamashita, Taro Yamazaki, Masato Mori, Yumi Mizuno, Shunsuke Tamaru, Yutaka Nakachi, Hiroko Harashima, Yohsuke Moriyama, Hidemasa Kato, Akira Ohtake, Masakazu Kohda, Yoshimi Tokuzawa, Yoshihito Kishita, Yasushi Okazaki
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1840(4):1355-1359
Mitochondrial disorders have the highest incidence among congenital metabolic diseases, and are thought to occur at a rate of 1 in 5000 births. About 25% of the diseases diagnosed as mitochondrial disorders in the field of pediatrics have mitochondri
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