Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Minato Yamashita"'
Autor:
Tomohiro Umeda, Tetsuya Kimura, Kayo Yoshida, Keizo Takao, Yuki Fujita, Shogo Matsuyama, Ayumi Sakai, Minato Yamashita, Yuki Yamashita, Kiyouhisa Ohnishi, Mamiko Suzuki, Hiroshi Takuma, Tsuyoshi Miyakawa, Akihiko Takashima, Takashi Morita, Hiroshi Mori, Takami Tomiyama
Publikováno v:
Acta Neuropathologica Communications, Vol 5, Iss 1, Pp 1-15 (2017)
Abstract The E693Δ (Osaka) mutation in APP is linked to familial Alzheimer’s disease. While this mutation accelerates amyloid β (Aβ) oligomerization, only patient homozygotes suffer from dementia, implying that this mutation is recessive and cau
Externí odkaz:
https://doaj.org/article/22482dc3cde0468b9c8450aa2fae8a6a
Publikováno v:
Analytical chemistry. 94(32)
Extracellular vesicles (EVs) are essential intercellular communication tools, but the regulatory mechanisms governing heterogeneous EV secretion are still unclear due to the lack of methods for precise analysis. Monitoring the dynamics of secretion f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0860db598d4140ff2d8b8a8e1cd59501
https://pubmed.ncbi.nlm.nih.gov/35797226
https://pubmed.ncbi.nlm.nih.gov/35797226
Autor:
Mineyuki Mizuguchi, Ayumi Sakai, Kenjiro Ono, Minato Yamashita, Hiroshi Mori, Takami Tomiyama, Masahito Yamada, Tomohiro Umeda, William L. Klein
Publikováno v:
Brain. 139(5):1568-1586
Amyloid-β, tau, and α-synuclein, or more specifically their soluble oligomers, are the aetiologic molecules in Alzheimer's disease, tauopathies, and α-synucleinopathies, respectively. These proteins have been shown to interact to accelerate each o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e192a85d7db2cbc1cef720d5c8460dcd
https://dlisv03.media.osaka-cu.ac.jp/il/meta_pub/G0000438repository_00068950-139-5-1568
https://dlisv03.media.osaka-cu.ac.jp/il/meta_pub/G0000438repository_00068950-139-5-1568
Autor:
Akihiko Takashima, Takashi Morita, Hiroshi Takuma, Kiyouhisa Ohnishi, Tomohiro Umeda, Keizo Takao, Yuki Yamashita, Kayo Yoshida, Takami Tomiyama, Mamiko Suzuki, Shogo Matsuyama, Ayumi Sakai, Tsuyoshi Miyakawa, Hiroshi Mori, Yuki Fujita, Minato Yamashita, Tetsuya Kimura
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 5, Iss 1, Pp 1-15 (2017)
Acta Neuropathologica Communications, Vol 5, Iss 1, Pp 1-15 (2017)
The E693Δ (Osaka) mutation in APP is linked to familial Alzheimer’s disease. While this mutation accelerates amyloid β (Aβ) oligomerization, only patient homozygotes suffer from dementia, implying that this mutation is recessive and causes loss-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::830cbec50ca1bd3709409292f1975e9e
http://europepmc.org/articles/PMC5537936
http://europepmc.org/articles/PMC5537936
Autor:
Koichi Nakajima, Takami Tomiyama, Hiroshi Mori, Tomohiro Umeda, Minato Yamashita, Elisa M. Ramser, Michael A. Silverman
Publikováno v:
Acta Neuropathologica Communications
Introduction: Synaptic dysfunction and intracellular transport defects are early events in Alzheimer's disease (AD). Extracellular amyloid β (Aβ) oligomers cause spine alterations and impede the transport of proteins and organelles such as brain-de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d00e60456641add11af82cc6e56714ab
https://dlisv03.media.osaka-cu.ac.jp/il/meta_pub/G0000438repository_20515960-3-51
https://dlisv03.media.osaka-cu.ac.jp/il/meta_pub/G0000438repository_20515960-3-51
Autor:
Tomohiro Umeda, Ono, Kenjiro, Ayumi Sakai, Minato Yamashita, Mineyuki Mizuguchi, Klein, William L., Masahito Yamada, Hiroshi Mori, Takami Tomiyama, Umeda, Tomohiro, Sakai, Ayumi, Yamashita, Minato, Mizuguchi, Mineyuki, Yamada, Masahito, Mori, Hiroshi, Tomiyama, Takami
Publikováno v:
Brain: A Journal of Neurology; 5/1/2016, Vol. 139 Issue 5, p1568-1586, 19p
Autor:
Tomohiro Umeda, Ramser, Elisa M., Minato Yamashita, Koichi Nakajima, Hiroshi Mori, Silverman, Michael A., Takami Tomiyama
Publikováno v:
Acta Neuropathologica Communications; Aug2015, Vol. 3 Issue 1, p1-15, 15p