Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Shogo Minami"'
Autor:
Terumasa Nakagawa, Akiko Shimasaki, Rei Miura, Hideki Inoue, Shogo Minami, Takehiro Ko, Yuichiro Izumi, Takashige Kuwabara, Masataka Adachi, Yukimasa Kohda, Masashi Mukoyama
Publikováno v:
Journal of Hypertension. 41:e444
Publikováno v:
MATERIALS TRANSACTIONS. 60:2016-2021
Publikováno v:
The Proceedings of Mechanical Engineering Congress, Japan. 2020:J01211
Publikováno v:
The Proceedings of Mechanical Engineering Congress, Japan. 2020:J01212
Publikováno v:
The Proceedings of The Computational Mechanics Conference. :021
Autor:
Chie Mori, Maho Ogoshi, Hideya Takahashi, Hirotaka Sakamoto, Daisuke Ojima, Shogo Minami, Tatsuya Sakamoto, Tsukasa Abe
Publikováno v:
Physiology & Behavior. 104:923-928
It has long been held that cortisol, a glucocorticoid in many vertebrates, carries out both glucocorticoid and mineralocorticoid actions in teleost fish. However, 11-deoxycorticosterone (DOC) has been identified as a specific endogenous ligand for th
Publikováno v:
2015 IEEE Energy Conversion Congress and Exposition (ECCE).
The miniaturization and high efficiency of permanent magnet synchronous motors (PMSMs) are desired in numerous applications. PMSMs have a number of design parameters in order to enable miniaturization and high efficiency. One such parameter is the ra
Autor:
Tomohiko Yamamura, Tomoko Horinouchi, Tomomi Adachi, Maki Terakawa, Yutaka Takaoka, Kohei Omachi, Minoru Takasato, Kiyosumi Takaishi, Takao Shoji, Yoshiyuki Onishi, Yoshito Kanazawa, Makoto Koizumi, Yasuko Tomono, Aki Sugano, Akemi Shono, Shogo Minamikawa, China Nagano, Nana Sakakibara, Shinya Ishiko, Yuya Aoto, Misato Kamura, Yutaka Harita, Kenichiro Miura, Shoichiro Kanda, Naoya Morisada, Rini Rossanti, Ming Juan Ye, Yoshimi Nozu, Masafumi Matsuo, Hirofumi Kai, Kazumoto Iijima, Kandai Nozu
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-8 (2020)
Alport syndrome is a progressive inherited nephritis accompanied by sensorineural loss of hearing and ocular abnormalities, for which there is currently no effective therapy. Here, the authors develop an exon-skipping therapy using an antisense-oligo
Externí odkaz:
https://doaj.org/article/165df2dbd3f44073aaae13fc966489b5
Autor:
Kei Nishiyama, Mari Kurokawa, Michiko Torio, Yasunari Sakai, Mitsuru Arima, Shoko Tsukamoto, Satoshi Obata, Shogo Minamikawa, Kandai Nozu, Noriyuki Kaku, Yoshihiko Maehara, Koh-Hei Sonoda, Tomoaki Taguchi, Shouichi Ohga
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Abstract Background Pierson syndrome (PS) is a rare autosomal recessive disorder, characterized by congenital nephrotic syndrome and microcoria. Advances in renal replacement therapies have extended the lifespan of patients, whereas the full clinical
Externí odkaz:
https://doaj.org/article/89410397a9ad484e82d6857e80d0f856
Autor:
Junya Fujimura, Kandai Nozu, Tomohiko Yamamura, Shogo Minamikawa, Keita Nakanishi, Tomoko Horinouchi, China Nagano, Nana Sakakibara, Koichi Nakanishi, Yuko Shima, Kenichi Miyako, Yoshimi Nozu, Naoya Morisada, Hiroaki Nagase, Takeshi Ninchoji, Hiroshi Kaito, Kazumoto Iijima
Publikováno v:
Kidney International Reports, Vol 4, Iss 1, Pp 119-125 (2019)
Introduction: Gitelman syndrome (GS) is a tubulopathy exhibited by salt loss. GS cases are most often diagnosed by chance blood test. Aside from that, some cases are also diagnosed from tetanic symptoms associated with hypokalemia and/or hypomagnesem
Externí odkaz:
https://doaj.org/article/1d6b1fae054a437ab716e908eaae2a63