Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Takahito Ino"'
Publikováno v:
Sensors, Vol 24, Iss 19, p 6416 (2024)
In this paper, we introduce a security approach for on-device learning Edge AIs designed to detect abnormal conditions in factory machines. Since Edge AIs are easily accessible by an attacker physically, there are security risks due to physical attac
Externí odkaz:
https://doaj.org/article/b3a87a7e1d1b42eebb99e62186603b25
Publikováno v:
Journal of Signal Processing (1342-6230); Jul2024, Vol. 28 Issue 4, p107-110, 4p
Autor:
Yusuke Hattori, Takaaki Sawada, Jun Kido, Keishin Sugawara, Shinichiro Yoshida, Shirou Matsumoto, Takahito Inoue, Shinichi Hirose, Kimitoshi Nakamura
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 37, Iss , Pp 101003- (2023)
Mucopolysaccharidosis II (MPS II) is an X-linked, recessive, inborn metabolic disorder caused by defects in iduronate-2-sulfatase (IDS). The age at onset, disease severity, and rate of progression vary significantly among patients. This disease is cl
Externí odkaz:
https://doaj.org/article/642c5eeae3634f7fa2a355daad47e2e0
Publikováno v:
Journal of the American College of Emergency Physicians Open, Vol 4, Iss 3, Pp n/a-n/a (2023)
Externí odkaz:
https://doaj.org/article/80ce08f469cf4b13b737f95f1ac33795
Autor:
Takaaki Sawada, Jun Kido, Keishin Sugawara, Ken Momosaki, Shinichiro Yoshida, Kanako Kojima-Ishii, Takahito Inoue, Shirou Matsumoto, Fumio Endo, Shouichi Ohga, Shinichi Hirose, Kimitoshi Nakamura
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-14 (2021)
Abstract Background Pompe disease is an autosomal recessive inherited metabolic disorder caused by a deficiency of the acid α-glucosidase (GAA). Pompe disease manifests as an accumulation of lysosomal glycogen in the skeletal and heart muscle. We co
Externí odkaz:
https://doaj.org/article/5bcc5203a9df4ca3a5d7188233c212fb
Autor:
Takaaki Sawada, Jun Kido, Keishin Sugawara, Shinichiro Yoshida, Shirou Matsumoto, Tomoyuki Shimazu, Yuki Matsushita, Takahito Inoue, Shinichi Hirose, Fumio Endo, Kimitoshi Nakamura
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 31, Iss , Pp 100850- (2022)
Gaucher disease (GD) is an autosomal recessive inborn metabolic disorder caused by a glucocerebrosidase (GCase) defect. GD is classified into three main types depending on accompanying neurological symptoms. Enzyme replacement therapy and substrate r
Externí odkaz:
https://doaj.org/article/8b268ceb9fbe409a863a9ad2cc28d5c3
Autor:
Takaaki Sawada, Jun Kido, Shinichiro Yoshida, Keishin Sugawara, Ken Momosaki, Takahito Inoue, Go Tajima, Hirotake Sawada, Shirou Mastumoto, Fumio Endo, Shinichi Hirose, Kimitoshi Nakamura
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 22, Iss , Pp - (2020)
Newborn screening (NBS) for Fabry disease (FD) is the best way to detect FD early prior to presentation of symptoms and is currently implemented in Taiwan and several states such as Illinois, Missouri, and Tennessee in the United States of America. I
Externí odkaz:
https://doaj.org/article/83888c1f15a64980a61065ec7cb18971
Publikováno v:
Asia-Pacific Journal of Sports Medicine, Arthroscopy, Rehabilitation and Technology, Vol 1, Iss 1, Pp 31-37 (2014)
No standard surgical procedure for medial patellofemoral ligament (MPFL) reconstruction exists. The purpose of this study was to evaluate the clinical effectiveness and limitation of the reconstructions of the MPFL in single patellar and femoral bone
Externí odkaz:
https://doaj.org/article/f12f107c1f90495991a8374a0191637a
Autor:
Daisaku Toyoshima, Kenji Mandai, Tomohiko Maruo, Irwan Supriyanto, Hideru Togashi, Takahito Inoue, Masahiro Mori, Yoshimi Takai
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e89763 (2014)
The formation and remodeling of mossy fiber-CA3 pyramidal cell synapses in the stratum lucidum of the hippocampus are implicated in the cellular basis of learning and memory. Afadin and its binding cell adhesion molecules, nectin-1 and nectin-3, toge
Externí odkaz:
https://doaj.org/article/3d5db2a9240b42999de4577783731600