Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Midori Shimanuki"'
Autor:
Kenta Wada, Yoshibumi Matsushima, Tomoki Tada, Sayaka Hasegawa, Yo Obara, Yasuhiro Yoshizawa, Gou Takahashi, Hiroshi Hiai, Midori Shimanuki, Sari Suzuki, Junichi Saitou, Naoki Yamamoto, Masumi Ichikawa, Kei Watanabe, Yoshiaki Kikkawa
Publikováno v:
PLoS ONE, Vol 9, Iss 10, p e111432 (2014)
Microphthalmia is a severe ocular disorder, and this condition is typically caused by mutations in transcription factors that are involved in eye development. Mice carrying mutations in these transcription factors would be useful tools for defining t
Externí odkaz:
https://doaj.org/article/06646f858edb4fc3a91f62cd2ce2d139
Autor:
Seiya Yamayoshi, Choji Taya, Kum Thong Wong, Yuko Sato, Midori Shimanuki, Hiroshi Shitara, Satoshi Koike, Noriyo Nagata, Ken Fujii, Kien Chai Ong
Publikováno v:
Proceedings of the National Academy of Sciences. 110:14753-14758
Enterovirus 71 (EV71) typically causes mild hand-foot-and-mouth disease in children, but it can also cause severe neurological disease. Recently, epidemic outbreaks of EV71 with significant mortality have been reported in the Asia-Pacific region, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc0a9d85ea7537d3c987e6765b63870b
https://doi.org/10.1073/pnas.1217563110
https://doi.org/10.1073/pnas.1217563110
Autor:
Satoshi Nishiyama, Hiromichi Yonekawa, Hiroshi Shitara, Kazuto Nakada, Tomio Ono, Junya Yamaguchi, Midori Shimanuki, Jun-Ichi Hayashi, Akitsugu Sato
Publikováno v:
Transgenic Research. 21:439-447
Mitochondria are essential for many cellular functions such as oxidative phosphorylation and calcium homeostasis; consequently, mitochondrial dysfunction could cause many diseases, including neurological disorders. Recently, mitochondrial dynamics, s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb7bc8a3e8a83d59a30e7bcb4001172f
https://doi.org/10.1007/s11248-011-9539-1
https://doi.org/10.1007/s11248-011-9539-1
Publikováno v:
Experimental Animals. 59:99-103
The most common approach to analyzing the static morphology of mitochondria involves staining by antibodies or fluorescent dyes specific for mitochondrial components. In this study, we present a new approach using transgenic (Tg) mice, mtGFP-Tg mice,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f024999bf53f98f1ba634e035002dfb
https://doi.org/10.1538/expanim.59.99
https://doi.org/10.1538/expanim.59.99
Autor:
Masaaki Komatsu, Shigeto Sato, Keiko Saisho, Yu-shin Sou, Mayumi Kimura, Kei Okatsu, Noriyuki Matsuda, Midori Shimanuki, Hiroshi Shitara, Nobutaka Hattori, Kazuto Nakada, Keiji Tanaka
Publikováno v:
Genes to Cells.
PINK1 and Parkin were first identified as the causal genes responsible for familial forms of early-onset Parkinson’s disease (PD), a prevalent neurodegenerative disorder. PINK1 encodes a mitochondrial serine/threonine protein kinase, whereas Parkin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfee54f7e959392878a5d4fbd5793593
https://doi.org/10.1111/j.1365-2443.2010.01426.x
https://doi.org/10.1111/j.1365-2443.2010.01426.x
Autor:
Tomoki Tada, Yasuhiro Yoshizawa, Sayaka Hasegawa, Kei Watanabe, Hiroshi Hiai, Yoshiaki Kikkawa, Masumi Ichikawa, Gou Takahashi, Yoshibumi Matsushima, Sari Suzuki, Junichi Saitou, Kenta Wada, Midori Shimanuki, Naoki Yamamoto, Yo Obara
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 10, p e111432 (2014)
PLoS ONE, Vol 9, Iss 10, p e111432 (2014)
Microphthalmia is a severe ocular disorder, and this condition is typically caused by mutations in transcription factors that are involved in eye development. Mice carrying mutations in these transcription factors would be useful tools for defining t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d7087c94abfcc349f2f1f596f2b45ef
https://doi.org/10.1371/journal.pone.0111432
https://doi.org/10.1371/journal.pone.0111432
Autor:
Wada, Kenta1,2, Matsushima, Yoshibumi2,3, Tada, Tomoki1, Hasegawa, Sayaka1, Obara, Yo2,4, Yoshizawa, Yasuhiro1, Takahashi, Gou1, Hiai, Hiroshi5, Shimanuki, Midori6, Suzuki, Sari1,2, Saitou, Junichi2,4, Yamamoto, Naoki7, Ichikawa, Masumi6, Watanabe, Kei2,4, Kikkawa, Yoshiaki2 kikkawa-ys@igakuken.or.jp
Publikováno v:
PLoS ONE. Oct2014, Vol. 9 Issue 10, p1-11. 11p.
Autor:
Fujii, Ken, Nagata, Noriyo, Sato, Yuko, Kien Chai Ong, Kum Thong Wong, Yamayoshi, Seiya, Shimanuki, Midori, Shitara, Hiroshi, Taya, Choji, Koike, Satoshi
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 9/3/2013, Vol. 110 Issue 36, p14753-14758, 6p
Autor:
Yamaguchi, Junya, Nishiyama, Satoshi, Shimanuki, Midori, Ono, Tomio, Sato, Akitsugu, Nakada, Kazuto, Hayashi, Jun-Ichi, Yonekawa, Hiromichi, Shitara, Hiroshi
Publikováno v:
Transgenic Research; Apr2012, Vol. 21 Issue 2, p439-447, 9p