Zobrazeno 1 - 10
of 154
pro vyhledávání: '"Osamu Sakamoto"'
Autor:
Hiroyasu Takei, Tomoko Nakada, lat Wai Leong, Atsuki Ito, Kakeru Hanada, Hinako Maeda, Muhammad Shan Sohail, Kazuhiko Tomiyasu, Osamu Sakamoto, Norihiko Naono, Masateru Taniguchi
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)
Abstract Emerging infectious diseases, cancer, and other diseases are quickly tested mainly via immune reactions based on specific molecular recognition between antigens and antibodies. By changing the diameter of solid-state pores, biomolecules of v
Externí odkaz:
https://doaj.org/article/e7e488587b0d4ec78c93a58dbc51f83e
Autor:
Ayumi Morimura, Masateru Taniguchi, Hiroyasu Takei, Osamu Sakamoto, Norihiko Naono, Yukihiro Akeda, Daisuke Onozuka, Jumpei Yoshimura, Kazunori Tomono, Satoshi Kutsuna, Shigeto Hamaguchi
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract Methods for identifying bacterial pathogens are broadly categorised into conventional culture-based microbiology, nucleic acid-based tests, and mass spectrometry. The conventional method requires several days to isolate and identify bacteria
Externí odkaz:
https://doaj.org/article/49fdfb0eac0e46149c103b62703054c5
Autor:
Masateru Taniguchi, Shohei Minami, Chikako Ono, Rina Hamajima, Ayumi Morimura, Shigeto Hamaguchi, Yukihiro Akeda, Yuta Kanai, Takeshi Kobayashi, Wataru Kamitani, Yutaka Terada, Koichiro Suzuki, Nobuaki Hatori, Yoshiaki Yamagishi, Nobuei Washizu, Hiroyasu Takei, Osamu Sakamoto, Norihiko Naono, Kenji Tatematsu, Takashi Washio, Yoshiharu Matsuura, Kazunori Tomono
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-8 (2021)
Rapid, accurate and specific point-of-care diagnostics can help manage and contain fast-spreading infections. Here, the authors present a nanopore-based system that uses artificial intelligence to discriminate between four coronaviruses in saliva, wi
Externí odkaz:
https://doaj.org/article/7cfcb758d04548a9925462a3e647155b
Publikováno v:
BMC Pediatrics, Vol 20, Iss 1, Pp 1-4 (2020)
Abstract Background Citrin deficiency (CD) is a recessive metabolic disease caused by biallelic pathogenic variants in SLC25A13. Although previous studies have reported ketosis in CD, it was observed at the time of euglycemia or mild hypoglycemia. Bl
Externí odkaz:
https://doaj.org/article/8a7c74260a1a4ab1950ac92cb7ca17fe
Autor:
Shunsuke Mori, Yukinori Koga, Kazuyoshi Nakamura, Sayuri Hirooka, Takako Matsuoka, Hideshi Uramoto, Osamu Sakamoto, Yukitaka Ueki
Publikováno v:
PLoS ONE, Vol 15, Iss 12, p e0243110 (2020)
ObjectiveThe aim of this study was to compare long-term mortality following diagnosis of pulmonary nontuberculous mycobacterial (NTM) disease between patients with and without rheumatoid arthritis (RA) and to evaluate predictive factors for death out
Externí odkaz:
https://doaj.org/article/0cfe863fc98d4042b5169f4ff41e66bc
Autor:
Yasutsugu Chinen, Sadao Nakamura, Kunihito Tamashiro, Osamu Sakamoto, Kyoko Tashiro, Takahiro Inokuchi, Koichi Nakanishi
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 11, Iss C, Pp 2-5 (2017)
Isovaleric acidemia (IVA) is an organic acid disease caused by a deficiency of isovaleryl-CoA dehydrogenase. Deficiency of this enzyme leads to accumulation of organic acids, such as isovalerylcarnitine and isovalerylglycine. The proposed IVA treatme
Externí odkaz:
https://doaj.org/article/fc626dc59ca3444bb33f9ceec1caea5b
Publikováno v:
Case Reports in Infectious Diseases, Vol 2017 (2017)
Kocuria kristinae is a catalase-positive, coagulase-negative, Gram-positive coccus found in the environment and in normal skin and mucosa in humans; however, it is rarely isolated from clinical specimens and is considered a nonpathogenic bacterium. W
Externí odkaz:
https://doaj.org/article/6acf934ad64441c3b9e99574f6a095a6
Publikováno v:
Acta Dermato-Venereologica, Vol 98, Iss 8, Pp 805-806 (2018)
Externí odkaz:
https://doaj.org/article/3cca4c9aa2234bc289ae5cc9eadf843a
Autor:
Mohammad Al-Haggar, Osamu Sakamoto, Ali Shaltout, Amany El-Hawary, Yahya Wahba, Dina Abdel-Hadi
Publikováno v:
Case Reports in Nephrology, Vol 2011 (2011)
Background. Fanconi-Bickel syndrome (FBS) is an autosomal recessive disorder caused by defects in facilitative glucose transporter 2 (GLUT2 or SLC2A2) gene mapped on chromosome 3q26.1-26.3, that codes for the glucose transporter protein 2. Methods. T
Externí odkaz:
https://doaj.org/article/4bc57789affa4e5baf01cf2c625eb082
Publikováno v:
The Journal of Physical Chemistry C. 126:12197-12209
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::280e21b366c27b518b63061701be516a
https://doi.org/10.1021/acs.jpcc.2c02674
https://doi.org/10.1021/acs.jpcc.2c02674