Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Ryuta, Tanaka"'
Autor:
Hiroshi Sakuma, Jun-ichi Takanashi, Kazuhiro Muramatsu, Hidehito Kondo, Takashi Shiihara, Motomasa Suzuki, Kazuo Okanari, Mariko Kasai, Osamu Mitani, Tomoyuki Nakazawa, Taku Omata, Konomi Shimoda, Yuichi Abe, Yoshihiro Maegaki, Kei Murayama, Yuka Murofushi, Hiroaki Nagase, Akihisa Okumura, Yasunari Sakai, Hiroko Tada, Masashi Mizuguchi, Japanese Pediatric Neuro-COVID-19 Study Group, Tsuyoshi Matsuoka, Hiroshi Oakada, Tatsuharu Sato, Kenjiro Kikuchi, Satoshi Akamine, Nanako Kawata, Shinichiro Morichi, Hideyuki Iwayama, Ryuta Tanaka, Yoshiyuki Hanaoka, Yuki Minamisawa, Tatsuya Ema, Mitsuo Motobayashi, Tomoshiro Ito, Fumikazu Sano
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
Background and objectivesTo clarify whether severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection cause acute encephalopathy in children and which are the most common syndromes that cause them and what are the outcomes.MethodsA natio
Externí odkaz:
https://doaj.org/article/d27b86d3fea846ce99dd9d7559309e79
Autor:
Kazushi Aoto, Mitsuhiro Kato, Tenpei Akita, Mitsuko Nakashima, Hiroki Mutoh, Noriyuki Akasaka, Jun Tohyama, Yoshiko Nomura, Kyoko Hoshino, Yasuhiko Ago, Ryuta Tanaka, Orna Epstein, Revital Ben-Haim, Eli Heyman, Takehiro Miyazaki, Hazrat Belal, Shuji Takabayashi, Chihiro Ohba, Atsushi Takata, Takeshi Mizuguchi, Satoko Miyatake, Noriko Miyake, Atsuo Fukuda, Naomichi Matsumoto, Hirotomo Saitsu
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
A member of the vacuolar H+-ATPase family, ATP6V0A1 is involved in lysosomal activity. Here, the authors report that ATP6V0A1 variants identified in individuals with developmental and epileptic encephalopathy are associated with impairment of lysosom
Externí odkaz:
https://doaj.org/article/7bc108343b5a4de8a62d1fd709f2183f
Autor:
Shingo Numoto, Hirokazu Kurahashi, Atsushi Sato, Masaya Kubota, Takashi Shiihara, Tohru Okanishi, Ryuta Tanaka, Ichiro Kuki, Tetsuhiro Fukuyama, Mitsuru Kashiwagi, Mitsuru Ikeno, Kazuo Kubota, Manami Akasaka, Masakazu Mimaki, Akihisa Okumura
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-9 (2021)
Abstract Objective We examined the clinical manifestations of acute encephalopathy (AE) and identify risk factors for AE in children with tuberous sclerosis complex (TSC). Methods The clinical data of 11 children with clinically diagnosed TSC associa
Externí odkaz:
https://doaj.org/article/1355176fa3e24f4c807cd92d8458cae2
Publikováno v:
Plant Production Science, Vol 21, Iss 4, Pp 407-412 (2018)
Abscisic acid (ABA) is a key factor regulating starch biosynthesis genes and is involved in assimilate partitioning to individual spikelets. The objective of this study was to clarify the effects of high temperature and shading during grain filling o
Externí odkaz:
https://doaj.org/article/d1232797c4834dc39420a6372e545548
Autor:
Shuji Katsuki, Shogo Hayashi, Ryuta Tanaka, Daisuke Kiyoshima, Ning Qu, Kaori Suyama, Kou Sakabe
Publikováno v:
Applied Sciences, Vol 11, Iss 19, p 9262 (2021)
In the literature, the passive movement of the biceps brachii during shoulder motion is unclear. This study investigated the passive movement of the long head (LHBB) and short head (SHBB) of the biceps brachii during shoulder rotation. We included 18
Externí odkaz:
https://doaj.org/article/2b6cffb7cda9474693c4b79917b6c8d2
Autor:
Shuji Takabayashi, Hiroki Mutoh, Naomichi Matsumoto, Mitsuhiro Kato, Takeshi Mizuguchi, Mitsuko Nakashima, Yasuhiko Ago, Revital Ben-Haim, Kazushi Aoto, Atsuo Fukuda, Kyoko Hoshino, Hirotomo Saitsu, Noriyuki Akasaka, Yoshiko Nomura, Noriko Miyake, Eli Heyman, Atsushi Takata, Hazrat Belal, Orna Epstein, Tenpei Akita, Takehiro Miyazaki, Jun Tohyama, Satoko Miyatake, Chihiro Ohba, Ryuta Tanaka
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-17 (2021)
Vacuolar H+-ATPases (V-ATPases) transport protons across cellular membranes to acidify various organelles. ATP6V0A1 encodes the a1-subunit of the V0 domain of V-ATPases, which is strongly expressed in neurons. However, its role in brain development i
Autor:
Saki Saeki, Hisato Suzuki, Hiroshi Shiraku, Kenjiro Kosaki, Ryuta Tanaka, Yuichi Ueno, Maiko Hatano, Tatsuyuki Ohto, Mai Tanaka, Hiroko Fukushima, Yu Kanai, Takashi Enokizono, Toshiki Takenouchi, Kazuo Imagawa, Tomoko Uehara, Hidetoshi Takada, Mitsuhiro Kato
Publikováno v:
American Journal of Medical Genetics Part A. 185:1113-1119
Cortical dysplasia, complex, with other brain malformations 3 (CDCBM3) is a rare autosomal dominant syndrome caused by Kinesin family Member 2A (KIF2A) gene mutation. Patients with CDCBM3 exhibit posterior dominant agyria/pachygyria with severe motor
Publikováno v:
Nihon Kikai Gakkai ronbunshu, Vol 82, Iss 835, Pp 15-00406-15-00406 (2016)
The aim of this research is to construct a topology optimization method for the design of micropumps driven by induced-charge electro-osmosis. Micropumps are one of the most important components in micro-fluid devices such as μ-TAS (Micro Total Anal
Externí odkaz:
https://doaj.org/article/d02ee5522f854d719fa9cc234df9ab38
Autor:
Ryuta Tanaka, Shogo Hayashi, Kou Sakabe, Daisuke Kiyoshima, Ning Qu, Shuji Katsuki, Kaori Suyama
Publikováno v:
Applied Sciences, Vol 11, Iss 9262, p 9262 (2021)
Applied Sciences
Volume 11
Issue 19
Applied Sciences
Volume 11
Issue 19
In the literature, the passive movement of the biceps brachii during shoulder motion is unclear. This study investigated the passive movement of the long head (LHBB) and short head (SHBB) of the biceps brachii during shoulder rotation. We included 18
Publikováno v:
Building Simulation Conference Proceedings.