Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Yaeko, Ichikawa"'
Autor:
Yasuo Terao, Motoyasu Honma, Yuki Asahara, Shin-ichi Tokushige, Toshiaki Furubayashi, Tai Miyazaki, Satomi Inomata-Terada, Ayumi Uchibori, Shinji Miyagawa, Yaeko Ichikawa, Atsuro Chiba, Yoshikazu Ugawa, Masahiko Suzuki
Publikováno v:
Frontiers in Neuroscience, Vol 15 (2021)
Although animal studies and studies on Parkinson’s disease (PD) suggest that dopamine deficiency slows the pace of the internal clock, which is corrected by dopaminergic medication, timing deficits in parkinsonism remain to be characterized with di
Externí odkaz:
https://doaj.org/article/df846a331552405b8bd00e38cc56d859
Autor:
Yasuo Nakahara, Jun Mitsui, Hidetoshi Date, Kristine Joyce Porto, Yasuhiro Hayashi, Atsushi Yamashita, Yoshio Kusakabe, Takashi Matsukawa, Hiroyuki Ishiura, Tsutomu Yasuda, Atsushi Iwata, Jun Goto, Yaeko Ichikawa, Yoshio Momose, Yuji Takahashi, Tatsushi Toda, Rikifumi Ohta, Jun Yoshimura, Shinichi Morishita, Emil K Gustavsson, Darren Christy, Melissa Maczis, Matthew J. Farrer, Han-Joon Kim, Sung-Sup Park, Beomseok Jeon, Jin Zhang, Weihong Gu, Sonja W. Scholz, Andrew B. Singleton, Henry Houlden, Ichiro Yabe, Hidenao Sasaki, Masaaki Matsushima, Hiroshi Takashima, Akio Kikuchi, Masashi Aoki, Kenju Hara, Akiyoshi Kakita, Mitsunori Yamada, Hitoshi Takahashi, Osamu Onodera, Masatoyo Nishizawa, Hirohisa Watanabe, Mizuki Ito, Gen Sobue, Kinya Ishikawa, Hidehiro Mizusawa, Kazuaki Kanai, Satoshi Kuwabara, Kimihito Arai, Shigeru Koyano, Yoshiyuki Kuroiwa, Kazuko Hasegawa, Tatsuhiko Yuasa, Kenichi Yasui, Kenji Nakashima, Hijiri Ito, Yuishin Izumi, Ryuji Kaji, Takeo Kato, Susumu Kusunoki, Yasushi Osaki, Masahiro Horiuchi, Ken Yamamoto, Mihoko Shimada, Taku Miyagawa, Yosuke Kawai, Nao Nishida, Katsushi Tokunaga, Alexandra Dürr, Alexis Brice, Alessandro Filla, Thomas Klockgether, Ullrich Wüllner, Caroline M. Tanner, Walter A. Kukull, Virginia M.-Y. Lee, Eliezer Masliah, Phillip A. Low, Paola Sandroni, Laurie Ozelius, Tatiana Foroud, Shoji Tsuji
To elucidate the molecular basis of multiple system atrophy (MSA), a neurodegenerative disease, we conducted a genome-wide association study (GWAS) in a Japanese MSA case/control series followed by replication studies in Japanese, Korean, Chinese, Eu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0ca23eb995d2b34d1429411448aeb26
https://doi.org/10.1101/2023.05.02.23289328
https://doi.org/10.1101/2023.05.02.23289328
Autor:
Shoji Tsuji, Tatsuo Mano, Toshihiro Hayashi, Hiroyuki Ishiura, Shotaro Karino, Yaeko Ichikawa, Yu Nagashima, Jun Goto, Yuji Takahashi, Takashi Matsukawa, Takashi Kanbayashi, Jun Shimizu, Jun Ichi Kira, Junko Kanda Kikuchi
Publikováno v:
Journal of Molecular Neuroscience. 71:1796-1801
The phenotypes of patients with disease-associated variants in DNMT1 have been classified into two syndromes: hereditary sensory and autonomic neuropathy type 1E (HSAN1E, MIM614116, https://www.omim.org/ ) and autosomal dominant cerebellar ataxia, de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e58f02440e7f80069f06e01e5f471bb5
https://doi.org/10.1007/s12031-020-01784-5
https://doi.org/10.1007/s12031-020-01784-5
Autor:
Rie Kunitomo, Masanori Nakajima, Hikaru Kukimoto, Ai Takemori, Yoshinori Komagata, Satoshi Kobayashi, Ayumi Uchibori, Sachiko Shimoda, Shinya Kaname, Lee Heryong, Atsuro Chiba, Ayako Miyamoto, Eriko Nakajima, Miho Karube, Yaeko Ichikawa
Publikováno v:
Nihon Toseki Igakkai Zasshi. 53:553-558
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b28ce8d1ab29288cc99abe4566ca16b
https://doi.org/10.4009/jsdt.53.553
https://doi.org/10.4009/jsdt.53.553
Autor:
M. Asem Almansour, Takuya Sasaki, Yusuke Sugiyama, Takashi Matsukawa, Jun Mitsui, Yoshio Sakiyama, Ryo Ohtomo, Katsuhisa Ogata, Mizuho Kawai, Wei Qu, Gaku Ohtomo, Shoji Tsuji, Jun Yoshimura, Yasuo Harigaya, Makiko Taira, Ai Huey Tan, Ichizo Nishino, Masaki Tanaka, Yoshihiko Nakazato, Yutaka Kohno, Tatsushi Toda, Satoru Morimoto, Hiroyuki Ishiura, Hisatomo Kowa, Yasushi Shiio, Yuko Saito, Aki Mitsue, Akihiko Mitsutake, Koichiro Doi, Junko Kanda Kikuchi, Hiroyuki Hatsuta, Yuji Takahashi, Shota Shibata, Yuta Suzuki, Shigeo Murayama, Shen-Yang Lim, Yasuo Terao, Atsushi Iwata, Tatsuo Mano, Hidetoshi Date, Yuichiro Shirota, Akitoshi Takeda, Yumi Umeda-Kameyama, Masashi Hamada, Jun Shimizu, Yaeko Ichikawa, Jun Goto, Miho Matsukawa, Jun Shinmi, Shinichi Morishita
Publikováno v:
Nature Genetics. 51:1222-1232
Noncoding repeat expansions cause various neuromuscular diseases, including myotonic dystrophies, fragile X tremor/ataxia syndrome, some spinocerebellar ataxias, amyotrophic lateral sclerosis and benign adult familial myoclonic epilepsies. Inspired b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fabbca88fccb4f7916d5eafc2c7dbef
https://doi.org/10.1038/s41588-019-0458-z
https://doi.org/10.1038/s41588-019-0458-z
Autor:
Shinji Miyagawa, Tai Miyazaki, Yasuo Terao, Atsuro Chiba, Shin-ichi Tokushige, Ayumi Uchibori, Yaeko Ichikawa, Toshiaki Furubayashi, Satomi Inomata-Terada, Masahiko Suzuki, Yuki Asahara, Yoshikazu Ugawa, Motoyasu Honma
Publikováno v:
Frontiers in Neuroscience
Frontiers in Neuroscience, Vol 15 (2021)
Frontiers in Neuroscience, Vol 15 (2021)
Although animal studies and studies on Parkinson’s disease (PD) suggest that dopamine deficiency slows the pace of the internal clock, which is corrected by dopaminergic medication, timing deficits in parkinsonism remain to be characterized with di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::503c346500cd6eed63c42eabf8bee2d2
https://doi.org/10.3389/fnins.2021.648814
https://doi.org/10.3389/fnins.2021.648814
Autor:
Junko Kanda, Kikuchi, Yu, Nagashima, Tatsuo, Mano, Hiroyuki, Ishiura, Toshihiro, Hayashi, Jun, Shimizu, Takashi, Matsukawa, Yaeko, Ichikawa, Yuji, Takahashi, Shotaro, Karino, Takashi, Kanbayashi, Junichi, Kira, Jun, Goto, Shoji, Tsuji
Publikováno v:
Journal of molecular neuroscience : MN. 71(9)
The phenotypes of patients with disease-associated variants in DNMT1 have been classified into two syndromes: hereditary sensory and autonomic neuropathy type 1E (HSAN1E, MIM614116, https://www.omim.org/ ) and autosomal dominant cerebellar ataxia, de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da8e94ae799804b4d6476db87b1941ae
https://pubmed.ncbi.nlm.nih.gov/33433851
https://pubmed.ncbi.nlm.nih.gov/33433851
Autor:
Shoji Tsuji, Jun Goto, Chizuko Oishi, Atsuro Chiba, Masaki Tanaka, Yaeko Ichikawa, Eriko Kurita, Masanori Nakajima
Publikováno v:
Human Genome Variation
Human Genome Variation, Vol 6, Iss 1, Pp 1-4 (2019)
Human Genome Variation, Vol 6, Iss 1, Pp 1-4 (2019)
Idiopathic basal ganglia calcification-1 (IBGC1) is an autosomal dominant disorder characterized by calcification in the basal ganglia, which can manifest a range of neuropsychiatric symptoms, including parkinsonism. We herein describe a 64-year-old
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dde96e0d0ba2c244854997ccf28e03c1
http://europepmc.org/articles/PMC6804589
http://europepmc.org/articles/PMC6804589
Autor:
Shoji Tsuji, Hiroyuki Ishiura, Yuji Takahashi, Jun Goto, Jun Mitsui, Yaeko Ichikawa, Masashi Hamada, Jun Shimizu, Takashi Matsukawa, Hiroya Naruse, Tatsushi Toda
Publikováno v:
Internal Medicine
Friedreich ataxia (FRDA) is an autosomal recessive spinocerebellar ataxia caused by mutations of FXN. Hypotonus and hyporeflexia of the lower extremities are observed in most FRDA patients. Patients with hyperreflexia, called Friedreich ataxia with r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4067a97bcb7da38153977811a68ea5d7
https://pubmed.ncbi.nlm.nih.gov/31178521
https://pubmed.ncbi.nlm.nih.gov/31178521
Autor:
Shigeru Koyano, Masatoyo Nishizawa, Masashi Aoki, Ryuji Kaji, Paola Sandroni, Yasuo Nakahara, Eliezer Masliah, Yuishin Izumi, Sid Gilman, Akio Kikuchi, Masaaki Matsushima, Susumu Kusunoki, Hiroyuki Ishiura, Yaeko Ichikawa, Miho Murata, Mizuki Ito, Tatsuhiko Yuasa, Takeo Kato, Takamichi Hattori, Ullrich Wüllner, Mitsunori Yamada, Atsushi Iwata, Kenju Hara, Caroline M. Tanner, Alexis Brice, Laurie J. Ozelius, Yoshiyuki Kuroiwa, Kazuaki Kanai, Walter A. Kukull, Garth A. Nicholson, Alexandra Durr, Kinya Ishikawa, Tomoyoshi Kondo, Jun Mitsui, Hidenao Sasaki, Hidehiro Mizusawa, Akiyoshi Kakita, Kenji Nakashima, Phillip A. Low, Masahiro Horiuchi, Thomas Klockgether, Shoji Tsuji, Jun Goto, Satoshi Kuwabara, Ichiro Yabe, John Q. Trojanowski, Shigeo Murayama, Hidetoshi Date, Alessandro Filla, Mathew B. Stern, Hiroshi Takashima, Tsutomu Yasuda, Tatiana Foroud, Yuji Takahashi, Hitoshi Takahashi, Gen Sobue, Yasushi Osaki, Osamu Onodera, Nobutaka Hattori, Tatsushi Toda, Virginia M.-Y. Lee, Kazuko Hasegawa, Kimihito Arai, Takashi Matsukawa, Hirohisa Watanabe, Yoshio Momose, Mitsutoshi Yamamoto, Kenichi Yasui, Wataru Satake, Budrul Ahsan, Hijiri Ito
Publikováno v:
Annals of Clinical and Translational Neurology 2(4), 417-426 (2015). doi:10.1002/acn3.185
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Wiley, 2015, 2 (4), pp.417-426 ⟨10.1002/acn3.185⟩
Annals of Clinical and Translational Neurology, 2015, 2 (4), pp.417-426 ⟨10.1002/acn3.185⟩
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Wiley, 2015, 2 (4), pp.417-426 ⟨10.1002/acn3.185⟩
Annals of Clinical and Translational Neurology, 2015, 2 (4), pp.417-426 ⟨10.1002/acn3.185⟩
International audience; Objective : Glucocerebrosidase gene (GBA) variants that cause Gaucher disease are associated with Parkinson disease (PD) and dementia with Lewy bodies (DLB). To investigate the role of GBA variants in multiple system atrophy (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e586c67e40726301ea115b0caa95d74b
https://doi.org/10.1002/acn3.185
https://doi.org/10.1002/acn3.185