Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Natsue Omi"'
Autor:
Yasuo Takashima, Tohru Inaba, Tasuku Matsuyama, Kengo Yoshii, Masami Tanaka, Kazumichi Matsumoto, Kazuki Sudo, Yuichi Tokuda, Natsue Omi, Masakazu Nakano, Takaaki Nakaya, Naohisa Fujita, Chie Sotozono, Teiji Sawa, Kei Tashiro, Bon Ohta
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
In this study, we analyzed a relatively large subset of proteins, including 109 kinds of blood-circulating cytokines, and precisely described a cytokine storm in the expression level and the range of fluctuations during hospitalization for COVID-19.
Externí odkaz:
https://doaj.org/article/1395283332bd45c981215ae38b44b441
Autor:
Masakazu Nakano, Yoko Ikeda, Yuichi Tokuda, Masahiro Fuwa, Natsue Omi, Morio Ueno, Kojiro Imai, Hiroko Adachi, Masaaki Kageyama, Kazuhiko Mori, Shigeru Kinoshita, Kei Tashiro
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e33389 (2012)
BACKGROUND: To date, only a small portion of the genetic variation for primary open-angle glaucoma (POAG), the major type of glaucoma, has been elucidated. METHODS AND PRINCIPAL FINDINGS: We examined our two data sets of the genome-wide association s
Externí odkaz:
https://doaj.org/article/1f44411c63504bb6bb56f3ef07af379a
Autor:
Yoko Ikeda, Kazuhiko Mori, Yuko Maruyama, Morio Ueno, Kengo Yoshii, Yuji Yamamoto, Kojiro Imai, Natsue Omi, Ryuichi Sato, Fumiko Sato, Masakazu Nakano, Junji Hamuro, Kei Tashiro, Chie Sotozono, Shigeru Kinoshita
Publikováno v:
Journal of glaucoma.
We propose a new classification model to serve as a control for future genomic studies of glaucoma by distinguishing normal subjects maintaining non-glaucoma status for 10 years using the vertical cup-to-disc ratio.This study aimed to develop a class
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df9e3135b751db63b05ef46b0e305ef1
https://pubmed.ncbi.nlm.nih.gov/36001508
https://pubmed.ncbi.nlm.nih.gov/36001508
Autor:
Toshihide Yamasaki, Kengo Yoshii, Natsue Omi, Kojiro Imai, Yoko Ikeda, Yuji Yamamoto, Kei Tashiro, Kazuhiko Mori, Masakazu Nakano, Fumiko Sato, Yuko Maruyama, Ryuichi Sato, Chie Sotozono, Morio Ueno, Shigeru Kinoshita
Publikováno v:
American journal of ophthalmology. 234
To investigate the trend of seasonal variation of intraocular pressure (IOP) in patients with normal-tension glaucoma over a 20-year period by retrospectively analyzing the Kyoto Prefectural University of Medicine Glaucoma Registry database as real-w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77fe1bfcc11a6d5c26a4b66de73b79fa
https://pubmed.ncbi.nlm.nih.gov/34648775
https://pubmed.ncbi.nlm.nih.gov/34648775
Autor:
Rei, Yasuda, Tomokatsu, Yoshida, Ikuko, Mizuta, Masashi, Watanabe, Masakazu, Nakano, Ryuichi, Sato, Yuichi, Tokuda, Natsue, Omi, Norio, Sakai, Masanori, Nakagawa, Kei, Tashiro, Toshiki, Mizuno
Publikováno v:
Neurology: Genetics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2201d82c4c7f1df771a81c5c80db4e5c
https://pubmed.ncbi.nlm.nih.gov/32548278
https://pubmed.ncbi.nlm.nih.gov/32548278
Autor:
Norio Sakai, Natsue Omi, Rei Yasuda, Masanori Nakagawa, Tomokatsu Yoshida, Ryuichi Sato, Masashi Watanabe, Toshiki Mizuno, Masakazu Nakano, Kei Tashiro, Yuichi Tokuda, Ikuko Mizuta
Publikováno v:
Neurology Genetics. 6:e442
LAMB1 encodes laminin subunit beta 1, a constituent of the extracellular matrix glycoprotein of basement membranes.1 Mutations of LAMB1 have been reported in patients with congenital or infantile- to childhood-onset leukoencephalopathy and severe dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f17ab23c70d03edb98c2466f0bbba65e
https://doi.org/10.1212/nxg.0000000000000442
https://doi.org/10.1212/nxg.0000000000000442
Autor:
Yoko Ikeda, Natsue Omi, Yuichi Tokuda, Kei Tashiro, Kazuhiko Mori, Shigeru Kinoshita, Chie Sotozono, Masakazu Nakano, Morio Ueno
Publikováno v:
Scientific Reports
Lymphoblastoid cell lines (LCLs) transformed by Epstein-Barr virus (EBV) serve as an unlimited resource of human genomic DNA. The protocol that is widely used to establish LCLs involves peripheral blood mononuclear cell isolation by density gradient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::213610bccc7e4e7c28412cb4cd8a1658
https://pubmed.ncbi.nlm.nih.gov/28272413
https://pubmed.ncbi.nlm.nih.gov/28272413
Autor:
Ryosuke Matsui, Kei Tashiro, Masami Tanaka, Akihiko Okamoto, Junya Toguchida, Hua Han, Mahito Miyamae, Natsue Omi, Masaya Ikegawa
Publikováno v:
Developmental Dynamics. 237:2506-2517
Secreted Frizzled-related protein 2 (Sfrp2) or Stromal Cell Derived Factor-5 (SDF-5) is highly expressed in the developing limbs. Here we showed the single Sfrp2 inactivation in mice resulted in syndactyly and preaxial synpolydactyly, predominantly i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f02ccc2d3f7ecbd97e7871e86afee645
https://doi.org/10.1002/dvdy.21655
https://doi.org/10.1002/dvdy.21655
Autor:
Jun Kawai, Shuichi Yamada, Natsue Omi, Etsuko Kiyokawa, Yun Wang, Kazumi Yamada, Yoshibumi Matsushima, Kazuo Kinoshita, Hiroshi Hiai, Masanori Suzuki, Michiyuki Matsuda, Yoshihide Hayashizaki
Publikováno v:
Experimental Eye Research. 86:828-834
Rupture of lens cataract (RLC) in the mouse is a spontaneous mutation inherited by a single autosomal recessive gene mapped on chromosome 14. Fine mapping of the mutant locus revealed a nucleotide deletion of 27-bp at the end of 15th exon of Dock5 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a0385c744455a84b5ae88f9b65d8191
https://doi.org/10.1016/j.exer.2008.02.011
https://doi.org/10.1016/j.exer.2008.02.011
Autor:
Kojiro Imai, Natsue Omi, Masaaki Kageyama, Hiroko Adachi, Ryuichi Sato, Yoko Ikeda, Kei Tashiro, Morio Ueno, Yuichi Tokuda, Masakazu Nakano, Shigeru Kinoshita, Masahiro Fuwa, Kazuhiko Mori
Publikováno v:
Scientific Reports
The common variants in lysyl oxidase-like 1 gene (LOXL1) are associated with exfoliation glaucoma (XFG) patients developed through exfoliation syndrome (XFS). However, the risk allele of a variant in LOXL1 has been found to be inverted between Asian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af6fc4c9c6e9ef55889aba203b2ccaeb
https://doi.org/10.1038/srep05340
https://doi.org/10.1038/srep05340