Zobrazeno 1 - 10
of 131
pro vyhledávání: '"Naoko MATSUI"'
Autor:
Kota KISHISHITA, Tomohiro NAKAMURA, Marino MIZUTANI, Toshia FUJISATO, Takeshi HASHIMOTO, Naoko MATSUI, Hiroko MARUKI-UCHIDA, Naoki IEMOTO, Sho YOKOYAMA
Publikováno v:
Journal of Biomechanical Science and Engineering, Vol 18, Iss 4, Pp 23-00396-23-00396 (2023)
Atrophy is characterized by muscle weakness and reduced mobility and results from inactivity, aging, cancer cachexia, and excessive glucocorticoid use. Skeletal muscle is essential for locomotion and energy production and accounts for a significant p
Externí odkaz:
https://doaj.org/article/234f0ddc0b3141a09e9bbd9884251541
Autor:
Yosuke Yamada, Djeda Belharazem-Vitacolonnna, Hanibal Bohnenberger, Christel Weiß, Naoko Matsui, Mark Kriegsmann, Katharina Kriegsmann, Peter Sinn, Katja Simon-Keller, Gerhard Hamilton, Thomas Graeter, Gerhard Preissler, German Ott, Sebastian Schölch, Naoki Nakajima, Akihiko Yoshizawa, Hironori Haga, Hiroshi Date, Roman K. Thomas, Iacopo Petrini, Giuseppe Giaccone, Philipp Ströbel, Alexander Marx
Publikováno v:
Cell Death and Disease, Vol 13, Iss 11, Pp 1-11 (2022)
Abstract Tuft cells are chemosensory epithelial cells in the respiratory tract and several other organs. Recent studies revealed tuft cell-like gene expression signatures in some pulmonary adenocarcinomas, squamous cell carcinomas (SQCC), small cell
Externí odkaz:
https://doaj.org/article/aaade6c0d522458ea3d812565b5a42cc
Autor:
Naoki Suzuki, Madoka Mori-Yoshimura, Satoshi Yamashita, Satoshi Nakano, Ken-ya Murata, Megumi Mori, Yukie Inamori, Naoko Matsui, En Kimura, Hirofumi Kusaka, Tomoyoshi Kondo, Hidefumi Ito, Itsuro Higuchi, Akihiro Hashiguchi, Hiroyuki Nodera, Ryuji Kaji, Maki Tateyama, Rumiko Izumi, Hiroya Ono, Masaaki Kato, Hitoshi Warita, Toshiaki Takahashi, Ichizo Nishino, Masashi Aoki
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Background Sporadic inclusion body myositis (sIBM) is the most prevalent muscle disease in elderly people, affecting the daily activities. sIBM is progressive with unknown cause and without effective treatment. In 2015, sIBM was classified a
Externí odkaz:
https://doaj.org/article/d90db870023f4f18ac3c75896e30fe96
Autor:
Mitsuteru Yoshida, Kazuya Kondo, Naoko Matsui, Yuishinn Izumi, Yoshimi Bando, Michihiro Yokoishi, Kouichirou Kajiura, Akira Tangoku
Publikováno v:
PLoS ONE, Vol 15, Iss 10, p e0239756 (2020)
BackgroundIt is popularly believed that myasthenia gravis (MG) patients show acetylcholine receptor antibody (AChRAb) production associated with the thymus (germinal centers, approximately 80%). It has been suggested that thymectomy can remove the ar
Externí odkaz:
https://doaj.org/article/61467a6945c94d3fb90daa9d1c9ab61d
Autor:
Frederick M. Tomlin, Ulla I. M. Gerling-Driessen, Yi-Chang Liu, Ryan A. Flynn, Janakiram R. Vangala, Christian S. Lentz, Sandra Clauder-Muenster, Petra Jakob, William F. Mueller, Diana Ordoñez-Rueda, Malte Paulsen, Naoko Matsui, Deirdre Foley, Agnes Rafalko, Tadashi Suzuki, Matthew Bogyo, Lars M. Steinmetz, Senthil K. Radhakrishnan, Carolyn R. Bertozzi
Publikováno v:
ACS Central Science, Vol 3, Iss 11, Pp 1143-1155 (2017)
Externí odkaz:
https://doaj.org/article/deaad0a3f1e64ba9ac1a503375d3faa2
Autor:
Naoki Suzuki, Madoka Mori-Yoshimura, Satoshi Yamashita, Satoshi Nakano, Ken-ya Murata, Yukie Inamori, Naoko Matsui, En Kimura, Hirofumi Kusaka, Tomoyoshi Kondo, Itsuro Higuchi, Ryuji Kaji, Maki Tateyama, Rumiko Izumi, Hiroya Ono, Masaaki Kato, Hitoshi Warita, Toshiaki Takahashi, Ichizo Nishino, Masashi Aoki
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 11, Iss 1, Pp 1-7 (2016)
Abstract Background Sporadic inclusion body myositis (sIBM) is the most prevalent acquired muscle disease in the elderly. sIBM is an intractable and progressive disease of unknown cause and without effective treatment. The etiology of sIBM is still u
Externí odkaz:
https://doaj.org/article/ccf1c87722e743dcae8206450e0f9648
Autor:
Waka Sakai, Naoko Matsui, Mitsuyo Ishida, Takahiro Furukawa, Yoshimichi Miyazaki, Koji Fujita, Ryosuke Miyamoto, Nobuaki Yamamoto, Wataru Sako, Kenta Sato, Kazuya Kondo, Yoshihiko Nishida, Takao Mitsui, Yuishin Izumi, Ryuji Kaji
Publikováno v:
eNeurologicalSci, Vol 2, Iss C, Pp 17-20 (2016)
Objective: The continuous increase in the number of patients presenting with late-onset myasthenia gravis (LOMG) underscores the need for a better understanding of the clinical course and the establishment of an optimal therapeutic strategy. We aimed
Externí odkaz:
https://doaj.org/article/e5ca09d9a4ea43fe9277010f1022eb6f
Autor:
Hiroki Yamazaki, Naoko Matsui, Naoko Takamatsu, Takeshi Yoshida, Koji Fukushima, Tadayuki Takata, Yusuke Osaki, Keiko Tanaka, Yoshiaki Kubo, Yuishin Izumi
Publikováno v:
Neuromuscular Disorders. 32:590-593
Autor:
Naoko Matsui, Mika Takahara, Hiroki Yamazaki, Naoko Takamatsu, Yusuke Osaki, Ryuji Kaji, Ichizo Nishino, Satoshi Yamashita, Yuishin Izumi
Publikováno v:
Neurology and Clinical Neuroscience. 11:46-48
Autor:
Yu Hiramatsu, Yuji Okamoto, Akiko Yoshimura, Jun-Hui Yuan, Masahiro Ando, Yujiro Higuchi, Akihiro Hashiguchi, Eiji Matsuura, Fumihito Nozaki, Tomohiro Kumada, Kei Murayama, Mikiya Suzuki, Yuki Yamamoto, Naoko Matsui, Yoshimichi Miyazaki, Masamitsu Yamaguchi, Youji Suzuki, Jun Mitsui, Hiroyuki Ishiura, Masaki Tanaka, Shinichi Morishita, Ichizo Nishino, Shoji Tsuji, Hiroshi Takashima
Publikováno v:
Journal of Neurology. 269:4129-4140
Mitochondrial disorders are a group of clinically and genetically heterogeneous multisystem disorders and peripheral neuropathy is frequently described in the context of mutations in mitochondrial-related nuclear genes. This study aimed to identify t