Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Shinobu Yoshida"'
Autor:
Jun Kido, Shirou Matsumoto, Tetsuya Ito, Shinichi Hirose, Kaori Fukui, Kanako Kojima-Ishii, Yuichi Mushimoto, Shinobu Yoshida, Mika Ishige, Norio Sakai, Kimitoshi Nakamura
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 27, Iss , Pp 100724- (2021)
Urea cycle disorders (UCDs) are inherited metabolic diseases that lead to hyperammonemia. Severe hyperammonemia adversely affects the brain. Therefore, we conducted a nationwide study between January 2000 and March 2018 to understand the present stat
Externí odkaz:
https://doaj.org/article/1d109c7d81b5461b97f720590b122583
Autor:
Tatsuya Kawaguchi, Emma Tabe Eko Niba, Abdul Qawee Mahyoob Rani, Yoshiyuki Onishi, Makoto Koizumi, Hiroyuki Awano, Masaaki Matsumoto, Masashi Nagai, Shinobu Yoshida, Sachiko Sakakibara, Naoyuki Maeda, Osamu Sato, Hisahide Nishio, Masafumi Matsuo
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 6, p 1546 (2018)
Background: Dystrophin Dp71 is one of the isoforms produced by the DMD gene which is mutated in patients with Duchenne muscular dystrophy (DMD). Although Dp71 is expressed ubiquitously, it has not been detected in normal skeletal muscle. This study w
Externí odkaz:
https://doaj.org/article/904ff82e978341909303abe5fb3b17d4
Autor:
Kaori Fukui, Kanako Kojima-Ishii, Kimitoshi Nakamura, Shinichi Hirose, Shinobu Yoshida, Norio Sakai, Shirou Matsumoto, Mika Ishige, Tetsuya Ito, Yuichi Mushimoto, Jun Kido
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 27, Iss, Pp 100724-(2021)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Urea cycle disorders (UCDs) are inherited metabolic diseases that lead to hyperammonemia. Severe hyperammonemia adversely affects the brain. Therefore, we conducted a nationwide study between January 2000 and March 2018 to understand the present stat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a42433a11288de41b94f91a0e2acd8cb
http://www.sciencedirect.com/science/article/pii/S2214426921000185
http://www.sciencedirect.com/science/article/pii/S2214426921000185
Autor:
Yuko Katoh-Fukui, Atsushi Hattori, Marie Mitani, Shinobu Yoshida, Toshiaki Tanaka, Masanori Adachi, Akie Nakamura, Sumito Dateki, Hiroyuki Tanaka, Keisuke Nagasaki, Tsutomu Ogata, Erina Suzuki, Koji Muroya, Tsutomu Kamimaki, Kazuhiko Nakabayashi, Yoichi Matsubara, Kenichiro Hata, Keiko Matsubara, Satoshi Narumi, Maki Fukami, Shinobu Ida
Publikováno v:
Endocrine Journal. 64:947-954
Although mutations in ACAN, FGFR3, NPR2, and SHOX typically lead to skeletal dysplasia, and mutations in GHRHR, GH1, GHR, STAT5B, IGF1, IGFALS, and IGF1R usually underlie hormonal defects of the growth hormone (GH)-insulin-like growth factor 1 (IGF1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8792531bb5b285c5c37b3883a54bf1af
https://doi.org/10.1507/endocrj.ej17-0150
https://doi.org/10.1507/endocrj.ej17-0150
Autor:
Hiroaki Nagase, Shoichi Tokumoto, Azusa Maruyama, Ken Hayashi, Kazumoto Iijima, Hiroshi Yamaguchi, Hiroshi Kurosawa, Shinobu Yoshida, Toshikatsu Tanaka, Daisaku Toyoshima
Publikováno v:
Braindevelopment. 41(3)
Background Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is characterized by biphasic seizures and impaired consciousness. Takotsubo cardiomyopathy (TTC), which is typically triggered by psychological or physical stres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbc8e9290314b07304225b0a56fa47ca
https://pubmed.ncbi.nlm.nih.gov/30327157
https://pubmed.ncbi.nlm.nih.gov/30327157
Autor:
Tomohiro Osugi, Kazuyoshi Tsutsui, Ganbat Gereltsetseg, Riyo Kinouchi, Toshiya Matsuzaki, Shinobu Yoshida, Masahiro Murakami, Takeshi Iwasa, Minoru Irahara
Publikováno v:
International Journal of Developmental Neuroscience. 30:31-37
The mammalian gonadotropin-inhibitory hormone (GnIH) ortholog RFamide-related peptide (RFRP) is considered to act on gonadotropin-releasing hormone (GnRH) neurons and on the pituitary to inhibit gonadotropin release and synthesis. To understand the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7309101187868732474b4e695c6a3a0
https://doi.org/10.1016/j.ijdevneu.2011.10.003
https://doi.org/10.1016/j.ijdevneu.2011.10.003
Autor:
Shinobu Yoshida, Satoshi Yamamoto, Takeshi Iwasa, Toshiyuki Yasui, Masahiro Murakami, Riyo Kinouchi, Minoru Irahara, Akira Kuwahara, Ganbat Gereltsetseg, Toshiya Matsuzaki
Publikováno v:
Endocrine Journal. 58:1003-1012
Kisspeptin, which is the product of the kiss1 gene and its receptor kiss1r, have emerged as the essential gatekeepers of reproduction. The present study used gonadally intact female rats to evaluate fasting-induced suppression of the KiSS-1 system of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f1f537f9cba32313554bdafc1afe6ef
https://doi.org/10.1507/endocrj.k11e-131
https://doi.org/10.1507/endocrj.k11e-131
Autor:
Minoru Irahara, Toshiyuki Yasui, Toshiya Matsuzaki, Akira Kuwahara, Masahiro Murakami, Shinobu Yoshida, Takeshi Iwasa, Riyo Kinouchi, Rie Ogata, Machiko Kiyokawa
Publikováno v:
The Journal of Medical Investigation. 58:11-18
Objectives : Reproductive functions are influenced by various feeding regula- tors. Orexin, which is one of orexinergic peptides, suppresses the pulsatile secretion of luteinizing hormone (LH) in bilaterally ovariectomized (OVX) rats. However, the me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5fceffe0b968e77f6480ac97020506c
https://doi.org/10.2152/jmi.58.11
https://doi.org/10.2152/jmi.58.11
Autor:
Shinobu, Yoshida
Publikováno v:
キリスト教学. 52:189-192
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::bd9d0e28eb7a3cdc5d80d8ef701a4ce6
http://id.nii.ac.jp/1062/00009708/
http://id.nii.ac.jp/1062/00009708/
Autor:
Hiroyuki Awano, Sachiko Sakakibara, Osamu Sato, Emma Tabe Eko Niba, Masashi Nagai, Yoshiyuki Onishi, Masaaki Matsumoto, Naoyuki Maeda, Abdul Qawee Mahyoob Rani, Hisahide Nishio, Makoto Koizumi, Tatsuya Kawaguchi, Shinobu Yoshida, Masafumi Matsuo
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 19; Issue 6; Pages: 1546
International Journal of Molecular Sciences, Vol 19, Iss 6, p 1546 (2018)
International Journal of Molecular Sciences; Volume 19; Issue 6; Pages: 1546
International Journal of Molecular Sciences, Vol 19, Iss 6, p 1546 (2018)
Background: Dystrophin Dp71 is one of the isoforms produced by the DMD gene which is mutated in patients with Duchenne muscular dystrophy (DMD). Although Dp71 is expressed ubiquitously, it has not been detected in normal skeletal muscle. This study w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91150dda70027f59185c51edf0a99181
http://www.lib.kobe-u.ac.jp/handle_kernel/90005080
http://www.lib.kobe-u.ac.jp/handle_kernel/90005080