Zobrazeno 1 - 10
of 196
pro vyhledávání: '"Yoshihide Sunada"'
Autor:
Hidekazu Tomimoto, Takayuki Kondo, Yoshihide Sunada, Hidehiro Ishikawa, Akihiro Shindo, Yuishin Izumi, Haruhiko Banno, Satoshi Morita, Koji Fujita, Ryosuke Takahashi, Haruhisa Inoue, Takakuni Maki, Toshifumi Watanabe, Kenji Ishii, Manabu Ikeda, Taro Okunomiya, Yoko Amino, Kayoko Endo, Akiyoshi Nakakura, Akemi Kinoshita, Harue Tada, Ken Yasuda, Yosuke Taruno, Takashi Suehiro, Kohji Mori, Kazutomi Kanemaru, Kazue Shigenobu, Yumiko Kutoku, Shinobu Kawakatsu, Shunji Shiota, Osamu Uchikawa
Publikováno v:
BMJ Open, Vol 11, Iss 6 (2021)
Introduction Alzheimer’s disease (AD) is one of the most common causes of dementia. Pathogenic variants in the presenilin 1 (PSEN1) gene are the most frequent cause of early-onset AD. Medications for patients with AD bearing PSEN1 mutation (PSEN1-A
Externí odkaz:
https://doaj.org/article/5a95f19b8f854322a9c17d2f1445538b
Autor:
José Andrés González Coraspe, Joachim Weis, Mary E. Anderson, Ute Münchberg, Kristina Lorenz, Stephan Buchkremer, Stephanie Carr, René Peiman Zahedi, Eva Brauers, Hannah Michels, Yoshihide Sunada, Hanns Lochmüller, Kevin P. Campbell, Erik Freier, Denisa Hathazi, Andreas Roos
Publikováno v:
Skeletal Muscle, Vol 8, Iss 1, Pp 1-19 (2018)
Abstract Background Caveolin-3 (CAV3) is a muscle-specific protein localized to the sarcolemma. It was suggested that CAV3 is involved in the connection between the extracellular matrix (ECM) and the cytoskeleton. Caveolinopathies often go along with
Externí odkaz:
https://doaj.org/article/6d998471d66f4de781e502ffc59dcddf
Autor:
Shoji Hemmi, Katsumi Kurokawa, Taiji Nagai, Akio Asano, Toshio Okamoto, Tatsufumi Murakami, Masahito Mihara, Yoshihide Sunada
Publikováno v:
Clinical Neurophysiology Practice, Vol 3, Iss , Pp 54-58 (2018)
Objective: We investigated how the active electrode placement site influences compound muscle action potential (CMAP) configuration of the upper trapezius muscle (TM). Methods: A nerve conduction study of the accessory nerve was performed, and the CM
Externí odkaz:
https://doaj.org/article/7038ef8dcc3647d69205854a19daae12
Autor:
Yutaka Ohsawa, Kentaro Takayama, Shin-ichiro Nishimatsu, Tadashi Okada, Masahiro Fujino, Yuta Fukai, Tatsufumi Murakami, Hiroki Hagiwara, Fumiko Itoh, Kunihiro Tsuchida, Yoshio Hayashi, Yoshihide Sunada
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0133713 (2015)
Myostatin, a muscle-specific transforming growth factor-β (TGF-β), negatively regulates skeletal muscle mass. The N-terminal prodomain of myostatin noncovalently binds to and suppresses the C-terminal mature domain (ligand) as an inactive circulati
Externí odkaz:
https://doaj.org/article/d84e91bda6ef4f7da64228030dc9be37
Autor:
Emi Kawakami, Nobuhiko Kawai, Nao Kinouchi, Hiroyo Mori, Yutaka Ohsawa, Naozumi Ishimaru, Yoshihide Sunada, Sumihare Noji, Eiji Tanaka
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e64719 (2013)
BACKGROUND: Growing evidence suggests that small-interfering RNA (siRNA) can promote gene silencing in mammalian cells without induction of interferon synthesis or nonspecific gene suppression. Recently, a number of highly specific siRNAs targeted ag
Externí odkaz:
https://doaj.org/article/8bad8563df844614b27e72a3f27467b0
Autor:
Yuan-Zong Song, Zhan-Hui Zhang, Wei-Xia Lin, Xin-Jing Zhao, Mei Deng, Yan-Li Ma, Li Guo, Feng-Ping Chen, Xiao-Ling Long, Xiang-Ling He, Yoshihide Sunada, Shun Soneda, Akiko Nakatomi, Sumito Dateki, Lock-Hock Ngu, Keiko Kobayashi, Takeyori Saheki
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e74544 (2013)
BACKGROUND: The human SLC25A13 gene encodes citrin, the liver-type mitochondrial aspartate/glutamate carrier isoform 2 (AGC2), and SLC25A13 mutations cause citrin deficiency (CD), a disease entity that encompasses different age-dependant clinical phe
Externí odkaz:
https://doaj.org/article/df48e85b90484940ac751d1a7a24c7cd
Autor:
Yutaka Ohsawa, Hideaki Ohtsubo, Asami Munekane, Kohei Ohkubo, Tatsufumi Murakami, Masahiro Fujino, Shin-ichiro Nishimatsu, Hiroki Hagiwara, Hirotake Nishimura, Ryuki Kaneko, Takahiro Suzuki, Ryuichi Tatsumi, Wataru Mizunoya, Atsushi Hinohara, Masao Fukunaga, Yoshihide Sunada
Publikováno v:
The American Journal of Pathology. 193:591-607
Autor:
Keiro Shirotani, Kaori Watanabe, Daisuke Hatta, Yumiko Kutoku, Yutaka Ohsawa, Yoshihide Sunada, Takayuki Kondo, Haruhisa Inoue, Nobuhisa Iwata
Publikováno v:
Genes to Cells. 28:319-325
Autor:
Ichizo Nishino, Tokiko Fukuda, Yutaka Ohsawa, Shin-ichiro Nishimatsu, Yoshihiko Saito, Hirotake Nishimura, Asami Munekane, Yoshihide Sunada, Hideo Sugie
Publikováno v:
Internal Medicine. 61:1241-1245
Muscle phosphorylase b kinase (PHK) deficiency is a rare mild metabolic disorder caused by mutations of the PHKA1 gene encoding the αM subunit of PHK. A 16-year-old boy experienced myalgia during the maximal multistage 20-m shuttle run test targetin
Autor:
Yutaka Ohsawa, Hideaki Ohtsubo, Yoshihiko Saito, Shin-ichiro Nishimatsu, Hiroki Hagiwara, Tatsufumi Murakami, Ichizo Nishino, Yoshihide Sunada
Publikováno v:
Biochemical and biophysical research communications. 628
Mutations of the caveolin 3 gene cause autosomal dominant limb-girdle muscular dystrophy (LGMD)1C. In mice, overexpression of mutant caveolin 3 leads to loss of caveolin 3 and results in myofiber hypotrophy in association with activation of neuronal