Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Yoshio, Yamakawa"'
Autor:
Fuyu Ito, Toshiaki Oharaseki, Daisuke Tsukui, Yoshitaka Kimura, Tamiko Yanagida, Fukuko Kishi, Yoshio Yamakawa, Yosuke Kameoka, Shoichi Suzuki, Kazuko Uno, Osamu Suzuki, Noriko N. Miura, Naohito Ohno, Kei Takahashi, Hajime Kono, Kazuo Suzuki
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 20, Iss 1, Pp 1-8 (2022)
Abstract Background Kawasaki disease (KD) is usually treated with high-dose intravenous immunoglobulin (IVIg) as severe infectious and other diseases. Due to issues that are associated with immunoglobulin preparation, such as the risk of possible con
Externí odkaz:
https://doaj.org/article/eeaaa3053cc34f258a82b5ce56632be9
Autor:
Ken'ichi Hagiwara, Yuko Sato, Yoshio Yamakawa, Hideyuki Hara, Minoru Tobiume, Yuko Okemoto-Nakamura, Tetsutaro Sata, Motohiro Horiuchi, Hiroaki Shibata, Fumiko Ono
Publikováno v:
PLoS ONE, Vol 14, Iss 5, p e0216807 (2019)
Classical- (C-) and atypical L-type bovine spongiform encephalopathy (BSE) prions cause different pathological phenotypes in cattle brains, and the disease-associated forms of each prion protein (PrPSc) has a dissimilar biochemical signature. Bovine
Externí odkaz:
https://doaj.org/article/50e3abb1243e4107a313e32e62fce864
Autor:
Yoshifumi Iwamaru, Morikazu Imamura, Yuichi Matsuura, Kentaro Masujin, Yoshihisa Shimizu, Yujing Shu, Megumi Kurachi, Kazuo Kasai, Yuichi Murayama, Shigeo Fukuda, Sadao Onoe, Ken’ichi Hagiwara, Yoshio Yamakawa, Tetsutaro Sata, Shirou Mohri, Hiroyuki Okada, Takashi Yokoyama
Publikováno v:
Emerging Infectious Diseases, Vol 16, Iss 7, Pp 1151-1154 (2010)
We recently reported the intraspecies transmission of L-type atypical bovine spongiform encephalopathy (BSE). To clarify the peripheral pathogenesis of L-type BSE, we studied prion distribution in nerve and lymphoid tissues obtained from experimental
Externí odkaz:
https://doaj.org/article/15df50730dd9426892ffbe78532a84e2
Efficacy of a recombinant single-chain fragment variable region, VasSF, as a new drug for vasculitis
Autor:
Yosuke, Kameoka, Fukuko, Kishi, Minako, Koura, Yoshio, Yamakawa, Rora, Nagasawa, Fuyu, Ito, Junichiro, Matsuda, Osamu, Suzuki, Toshinori, Nakayama, Kazuo, Suzuki
Publikováno v:
Drug Design, Development and Therapy
Yosuke Kameoka,1 Fukuko Kishi,1 Minako Koura,2 Yoshio Yamakawa,1 Rora Nagasawa,1 Fuyu Ito,3 Junichiro Matsuda,2 Osamu Suzuki,2 Toshinori Nakayama,4 Kazuo Suzuki1,3–5 1Department of Research and Development, A-CLIP Institute, Ltd., Chiba, Japan; 2La
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f10d219e2670995742bab8c261b5bf21
http://europepmc.org/articles/PMC6368128
http://europepmc.org/articles/PMC6368128
Autor:
Yuichi Murayama, Keiji Terao, Yoshio Yamakawa, Morikazu Imamura, Minoru Tobiume, Noriko Shimozaki, Hiroaki Shibata, Tetsutaro Sata, Kentaro Masujin, Fumiko Ono, Tomoaki Yamamura
Publikováno v:
Journal of General Virology. 95:2576-2588
Prion diseases are characterized by the prominent accumulation of the misfolded form of a normal cellular protein (PrPSc) in the central nervous system. The pathological features and biochemical properties of PrPScin macaque monkeys infected with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07a4a794901adaaadbaea8da2ca7c95e
https://doi.org/10.1099/vir.0.066225-0
https://doi.org/10.1099/vir.0.066225-0
Autor:
Takashi Yokoyama, Yoshio Yamakawa, Shirou Mohri, Tetsuyuki Kitamoto, Yukiko Ishikawa, Yuichi Matsuura, Ken'ichi Hagiwara, Tetsutaro Sata, Robert A. Somerville
Publikováno v:
Open Journal of Veterinary Medicine. :79-85
The rapid detection of infectivity of several agents that cause Creutzfeldt-Jakob disease has previously been achieved by assaying for deposits of abnormal prion protein (PrPSc) in follicular dendritic cells in the spleens of transgenic mice carrying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aee87c56a29635e7504959c41871b7e7
https://doi.org/10.4236/ojvm.2013.31013
https://doi.org/10.4236/ojvm.2013.31013
Publikováno v:
Journal of Comparative Pathology. 144:269-276
This study reports the experimental transmission of bovine spongiform encephalopathy (BSE) to guinea pigs and describes the cerebellar lesions in these animals. Guinea pigs were inoculated intracerebrally with 10% brain homogenates from BSE-affected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5be983279042918dfd5d1ed448fb5a7a
https://doi.org/10.1016/j.jcpa.2010.10.004
https://doi.org/10.1016/j.jcpa.2010.10.004
Autor:
Fumiko, Ono, Naomi, Tase, Asuka, Kurosawa, Akio, Hiyaoka, Atsushi, Ohyama, Yukio, Tezuka, Naomi, Wada, Yuko, Sato, Minoru, Tobiume, Ken'ichi, Hagiwara, Yoshio, Yamakawa, Keiji, Terao, Tetsutaro, Sata
Publikováno v:
Japanese Journal of Infectious Diseases. 64:81-84
A low molecular weight type of atypical bovine spongiform encephalopathy (L-BSE) was transmitted to two cynomolgus macaques by intracerebral inoculation of a brain homogenate of cattle with atypical BSE detected in Japan. They developed neurological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3207c01dfcd1537eb82a6e64d1bae546
https://doi.org/10.7883/yoken.64.81
https://doi.org/10.7883/yoken.64.81
Autor:
Yujing Shu, Tetsutaro Sata, Sadao Onoe, Kentaro Masujin, Shirou Mohri, Yoshifumi Iwamaru, Ken'ichi Hagiwara, Takashi Yokoyama, Shigeo Fukuda, Yuichi Matsuura, Yuichi Murayama, Kazuo Kasai, Yoshio Yamakawa, Yoshihisa Shimizu, Hiroyuki Okada, Morikazu Imamura, Megumi Kurachi
Publikováno v:
Emerging Infectious Diseases
Emerging Infectious Diseases, Vol 16, Iss 7, Pp 1151-1154 (2010)
Emerging Infectious Diseases, Vol 16, Iss 7, Pp 1151-1154 (2010)
We recently reported the intraspecies transmission of L-type atypical bovine spongiform encephalopathy (BSE). To clarify the peripheral pathogenesis of L-type BSE, we studied prion distribution in nerve and lymphoid tissues obtained from experimental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb37de677ce5b91887af9e63d431a93e
https://doi.org/10.3201/eid1607.091882
https://doi.org/10.3201/eid1607.091882
Publikováno v:
Uirusu. 59:155-166
Transmissible spongiform encephalopathies, or prion diseases, are fatal neurodegenerative disorders. In aetiological viewpoint, human prion diseases are classified into 1) sporadic Creutzfeldt-Jakob disease (CJD) which comprises 80-90% of the total p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ccb21061f4009ff5986ff0aab76bd43f
https://doi.org/10.2222/jsv.59.155
https://doi.org/10.2222/jsv.59.155