Zobrazeno 1 - 10
of 86
pro vyhledávání: '"Yukiko Matsuda"'
Publikováno v:
Eng, Vol 4, Iss 4, Pp 2542-2552 (2023)
Background: Oral frailty is associated with systemic frailty. The vertical position of the hyoid bone is important when considering the risk of dysphagia. However, dentists usually do not focus on this position. Purpose: To create an AI model for det
Externí odkaz:
https://doaj.org/article/d45d1c3e7b444cb48002202681802dc0
Autor:
Kengo Yoshida, Yasunari Satoh, Arikuni Uchimura, Munechika Misumi, Seishi Kyoizumi, Masataka Taga, Yukiko Matsuda, Asao Noda, Yoichiro Kusunoki
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Clonal hematopoiesis (CH) is prevalent in the elderly and associates with hematologic malignancy and cardiovascular disease. Although the risk of developing these diseases increases with radiation doses in atomic-bomb survivors, the causal r
Externí odkaz:
https://doaj.org/article/71030037e2b94d7f88d9a49cc0a30d48
Autor:
Naoyuki Hara, Hiroyuki Morino, Yukiko Matsuda, Kenichi Satoh, Kouichi Hashimoto, Hirofumi Maruyama, Hideshi Kawakami
Publikováno v:
Molecular Brain, Vol 13, Iss 1, Pp 1-7 (2020)
Abstract Spinocerebellar ataxia (SCA) 42 is caused by a mutation in CACNA1G, which encodes the low voltage-gated calcium channel CaV3.1 (T-type). Patients with SCA42 exhibit a pure form of cerebellar ataxia. We encountered a patient with the p.Arg171
Externí odkaz:
https://doaj.org/article/e8ef198876784ec3b67003af4f4fe37a
Autor:
Kodai Kume, Hiroyuki Morino, Ryosuke Miyamoto, Yukiko Matsuda, Ryosuke Ohsawa, Yuhei Kanaya, Yui Tada, Takashi Kurashige, Hideshi Kawakami
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-4 (2020)
Abstract Background The TWNK gene encodes the twinkle protein, which is a mitochondrial helicase for DNA replication. The dominant TWNK variants cause progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3, while
Externí odkaz:
https://doaj.org/article/22f05a9c7cd84ecea5a2659576d84a38
Autor:
Yukiko Matsuda, Arikuni Uchimura, Yasunari Satoh, Naohiro Kato, Masaaki Toshishige, Junko Kajimura, Kanya Hamasaki, Kengo Yoshida, Tomonori Hayashi, Asao Noda, Osamu Tanabe
Publikováno v:
Proceedings of the National Academy of Sciences. 120
Spectra and frequencies of spontaneous and X-ray-induced somatic mutations were revealed with mouse long-term hematopoietic stem cells (LT-HSCs) by whole-genome sequencing of clonal cell populations propagated in vitro from single isolated LT-HSCs. S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::561566728d470bc08c604707ec8544aa
https://doi.org/10.1073/pnas.2216550120
https://doi.org/10.1073/pnas.2216550120
Publikováno v:
The Showa University Journal of Medical Sciences. 33:74-81
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0bc19618ef040339fe04cc0d7d2aee1
https://doi.org/10.15369/sujms.33.74
https://doi.org/10.15369/sujms.33.74
Publikováno v:
International Journal of Environmental Research and Public Health; Volume 19; Issue 8; Pages: 4529
Background: Dysphagia relates to quality of life; this disorder is related to the difficulties of dental treatment. Purpose: To detect radiographic signs of dysphagia by using panoramic radiograph with an AI system. Methods: Seventy-seven patients wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8c4ed2974ada37d7f1444f8b2d0d452
Autor:
Kouichi Hashimoto, Yukiko Matsuda, Manabu Abe, Hiroyuki Morino, Kenji Sakimura, Miwako Yamasaki, Hideshi Kawakami, Masahiko Watanabe, Toshinori Matsuoka
Publikováno v:
The Journal of Physiology. 599:547-569
Key points Some ion channels are known to behave as inductors and make up the parallel resonant circuit in the plasma membrane of neurons, which enables neurons to respond to current inputs with a specific frequency (so-called 'resonant properties').
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9650a6b67fcbceba780202f9a6540aba
https://doi.org/10.1113/jp280342
https://doi.org/10.1113/jp280342
Autor:
Hiroyuki Morino, Yukiko Matsuda, Hirofumi Maruyama, Hideshi Kawakami, Naoyuki Hara, Kenichi Satoh, Kouichi Hashimoto
Publikováno v:
Molecular Brain, Vol 13, Iss 1, Pp 1-7 (2020)
Molecular Brain
Molecular Brain
Spinocerebellar ataxia (SCA) 42 is caused by a mutation in CACNA1G, which encodes the low voltage-gated calcium channel CaV3.1 (T-type). Patients with SCA42 exhibit a pure form of cerebellar ataxia. We encountered a patient with the p.Arg1715His muta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d56bed92b1af3e11e8daf6642a39e4f1
http://link.springer.com/article/10.1186/s13041-020-00700-7
http://link.springer.com/article/10.1186/s13041-020-00700-7
Autor:
Ryosuke Ohsawa, Yui Tada, Tadayuki Takata, Hiroyuki Morino, Kodai Kume, Takashi Kurashige, Yukiko Matsuda, Hideshi Kawakami
Publikováno v:
Journal of Human Genetics. 65:917-920
Primary familial brain calcification (PFBC) is a hereditary neurological disorder characterized by idiopathic calcification of the bilateral basal ganglia and other areas of the brain. MYORG has been identified as the first causative gene of autosoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e911705a149a3d6b5ab18723a4940728
https://doi.org/10.1038/s10038-020-0779-x
https://doi.org/10.1038/s10038-020-0779-x