Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Kazuki Ohuchi"'
Autor:
Sora Sakamoto, Yuichi Riku, Teiko Komori Nomura, Akio Kimura, Naoki Yamahara, Kazuki Ohuchi, Mari Yoshida, Yasushi Iwasaki, Takayoshi Shimohata, Masatoshi Inden, Ryo Honda
Publikováno v:
Translational Neurodegeneration, Vol 13, Iss 1, Pp 1-5 (2024)
Externí odkaz:
https://doaj.org/article/553156f79250496cbe86aea492066627
Autor:
Ayaka Fujimaki, Kazuki Ohuchi, Shinnosuke Takizawa, Takanori Murakami, Hisaka Kurita, Isao Hozumi, Xiaopeng Wen, Yoshihisa Kitamura, Zhiliang Wu, Yoichi Maekawa, Masatoshi Inden
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract Parkinson’s disease (PD) is a neurodegenerative disorder characterized by the loss of dopaminergic neurons in the substantia nigra. The pathological hallmark of PD is the appearance of intraneuronal cytoplasmic α-synuclein (α-Syn) aggreg
Externí odkaz:
https://doaj.org/article/23e27bfe83714e1d87896050c05584de
Publikováno v:
Energy Reports, Vol 9, Iss , Pp 557-567 (2023)
Numerous distributed generators (DGs), which often include renewable energy sources, are connected to modern power grids through grid-connected inverters. Conventional linear model approximation methods may not be sufficient to accurately analyze the
Externí odkaz:
https://doaj.org/article/8cc9ce5a0cee4848b29da5207993c1b9
Publikováno v:
Energy Reports, Vol 8, Iss , Pp 1073-1084 (2022)
The use of renewable energy to realize decarbonization is rapidly increasing, and considerable research is being performed to achieve highly efficient high-voltage direct current (HVDC) transmission for offshore wind power generation over long distan
Externí odkaz:
https://doaj.org/article/0733ffb96a1741aa9e103510688bf0d3
Autor:
Tsubasa Kameyama, Kazuki Ohuchi, Michinori Funato, Shiori Ando, Satoshi Inagaki, Arisu Sato, Junko Seki, Chizuru Kawase, Kazuhiro Tsuruma, Ichizo Nishino, Shinsuke Nakamura, Masamitsu Shimazawa, Takashi Saito, Shin’ichi Takeda, Hideo Kaneko, Hideaki Hara
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
Duchenne muscular dystrophy (DMD) is a recessive X-linked form of muscular dystrophy characterized by progressive muscle degeneration. This disease is caused by the mutation or deletion of the dystrophin gene. Currently, there are no effective treatm
Externí odkaz:
https://doaj.org/article/0fb712442bbb401bb9f0fa17e684523c
Autor:
Masatoshi Inden, Yuna Kimura, Kazuya Nishii, Tomohiko Masaka, Naoko Takase, Mai Tsutsui, Kazuki Ohuchi, Hisaka Kurita, Isao Hozumi
Publikováno v:
Biochemical and Biophysical Research Communications. 640:21-25
Primary brain calcification (PBC), also known as idiopathic basal ganglia calcification (IBGC), primary familial brain calcification (PFBC) and so on, is a rare intractable disease characterized by abnormal mineral deposits, including mostly calcium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44c073512173b69ae72bca51c270f588
https://doi.org/10.1016/j.bbrc.2022.11.106
https://doi.org/10.1016/j.bbrc.2022.11.106
Publikováno v:
Energy Reports, Vol 8, Iss, Pp 1073-1084 (2022)
The use of renewable energy to realize decarbonization is rapidly increasing, and considerable research is being performed to achieve highly efficient high-voltage direct current (HVDC) transmission for offshore wind power generation over long distan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22d5fcac4d43e247fe35ccfde6a64b76
http://www.sciencedirect.com/science/article/pii/S2352484721011963
http://www.sciencedirect.com/science/article/pii/S2352484721011963
Publikováno v:
IEEJ Journal of Industry Applications.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c384db3928e402a36048231647f44346
https://doi.org/10.1541/ieejjia.22007710
https://doi.org/10.1541/ieejjia.22007710
Autor:
Kazuki Ohuchi, Michinori Funato, Hideo Kaneko, Arisu Sato, Chizuru Kawase, Satoshi Inagaki, Hideaki Hara, Shiori Ando, Shinsuke Nakamura, Junko Seki, Masamitsu Shimazawa
Publikováno v:
NeuroReport. 30:350-357
Survival motor neuron (SMN) deficiency indicates that various cellular processes are impaired in spinal muscular atrophy (SMA). Previous reports have shown that SMN deficiency causes motor neuron degeneration, whereas the numbers of astrocytes and mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c160d577ab580fb2d4ae3b7b14fea2c
https://doi.org/10.1097/wnr.0000000000001206
https://doi.org/10.1097/wnr.0000000000001206
Autor:
Hideaki Hara, Hideo Kaneko, Toshio Saito, Chizuru Kawase, Arisu Sato, Shinsuke Nakamura, Kazuki Ohuchi, Junko Seki, Shiori Ando, Hisahide Nishio, Satoshi Inagaki, Yuta Yoshino, Michinori Funato, Masamitsu Shimazawa
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Scientific Reports
Scientific Reports
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder characterized by the degeneration of spinal motor neurons and muscle atrophy. The disease is mainly caused by low level of the survival motor neuron (SMN) protein, which i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::626f3401089be995df8a33533b137d8a
http://link.springer.com/article/10.1038/s41598-019-39788-w
http://link.springer.com/article/10.1038/s41598-019-39788-w