Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Toju Tanaka"'
Autor:
Yoshiki Fujii, Takeshi Tsugawa, Yuya Fukuda, Shuhei Adachi, Saho Honjo, Yusuke Akane, Kenji Kondo, Yoshiyuki Sakai, Toju Tanaka, Toshiya Sato, Yoshihito Higasidate, Noriaki Kubo, Toshihiko Mori, Shinsuke Kato, Ryo Hamada, Masayoshi Kikuchi, Yasuo Tahara, Kazushige Nagai, Toshio Ohara, Masaki Yoshida, Shuji Nakata, Atsuko Noguchi, Wakako Kikuchi, Hiromichi Hamada, Shoko Tokutake-Hirose, Makoto Fujimori, Masamichi Muramatsu
Publikováno v:
Frontiers in Microbiology, Vol 15 (2024)
In the 2010s, several unusual rotavirus strains emerged, causing epidemics worldwide. This study reports a comprehensive molecular epidemiological study of rotaviruses in Japan based on full-genome analysis. From 2014 to 2019, a total of 489 rotaviru
Externí odkaz:
https://doaj.org/article/7ee01ff0a4ae47e7aa634340d86adc51
Publikováno v:
International Journal of Neonatal Screening, Vol 4, Iss 1, p 5 (2018)
Citrullinemia is the earliest identifiable biochemical abnormality in neonates with intrahepatic cholestasis due to a citrin deficiency (NICCD) and it has been included in newborn screening panels using tandem mass spectrometry. However, only one neo
Externí odkaz:
https://doaj.org/article/2e956df21c4041689bab57316a2bd2a8
Autor:
Yuya Fukuda, Atsuo Togashi, Satoshi Hirakawa, Masaki Yamamoto, Shinobu Fukumura, Tomohiro Nawa, Saho Honjo, Jun Kunizaki, Kouhei Nishino, Toju Tanaka, Toshitaka Kizawa, Dai Yamamoto, Ryoh Takeuchi, Yuta Sasaoka, Masayoshi Kikuchi, Takuro Ito, Kazushige Nagai, Hirofumi Asakura, Katsumasa Kudou, Masaki Yoshida
Publikováno v:
Pediatric Infectious Disease Journal; Sep2023, Vol. 42 Issue 9, p766-773, 8p
Autor:
Jun Kunizaki, Yoshiyuki Sakai, Dai Yamamoto, Yuya Fukuda, Ryo Hamada, Yukihiko Kawasaki, Hirofumi Asakura, Satoshi Hirakawa, Masayoshi Kikuchi, Tomohiro Nawa, Takeshi Tsugawa, Akira Ishii, Toshitaka Kizawa, Yoshinobu Nagaoka, Masaki Yoshida, Rina Tanaka, Toju Tanaka, Atsuo Togashi, Kazushige Nagai, Junya Iida, Ryoh Takeuchi
Publikováno v:
Journal of Infection and Chemotherapy
Introduction The epidemic of coronavirus disease 2019 (COVID-19) rapidly spread worldwide, and the various infection control measures have a significant influence on the spread of many infectious diseases. However, there have been no multicenter stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59332ca135c49ae1baeb3ec628bf0af7
http://europepmc.org/articles/PMC8332734
http://europepmc.org/articles/PMC8332734
Autor:
Hiroaki Nagase, Hikaru Kitahara, Takeshi Ninchoji, Yoshinori Araki, Ryojiro Tanaka, Toru Igarashi, Shinya Ishiko, Kazumoto Iijima, Kandai Nozu, Eri Okada, Koji Nagatani, Naoya Morisada, Kumiko Jinnouchi, Nana Sakakibara, Takeshi Ijuin, Shogo Minamikawa, Taro Okada, China Nagano, Toju Tanaka, Mari S Harada, Takeshi Matsuyama, Tomoko Horinouchi, Rini Rossanti, Yasufumi Ohtsuka, Koichi Kamei, Yuya Aoto, Shun-ichi Nakamura, Hiroyuki Awano, Masafumi Oka, Tomohiko Yamamura
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 37(2)
Background Although Lowe syndrome and Dent disease-2 are caused by Oculocerebrorenal syndrome of Lowe (OCRL) mutations, their clinical severities differ substantially and their molecular mechanisms remain unclear. Truncating mutations in OCRL exons 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05ad5b6640f41e611604a6ae5e3331c1
https://pubmed.ncbi.nlm.nih.gov/34586410
https://pubmed.ncbi.nlm.nih.gov/34586410
Publikováno v:
Journal of mucopolysaccharidosis and rare disease. 2:19-22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d43bb82094dbc9affd618684d292ade2
https://doi.org/10.19125/jmrd.2016.2.1.19
https://doi.org/10.19125/jmrd.2016.2.1.19
Publikováno v:
Molecular Genetics and Metabolism. 110:460-464
Methionine adenosyltransferase I/III deficiency (MAT I/III deficiency) is an inborn error of metabolism that results in isolated persistent hypermethioninemia. Definitive diagnosis is now possible by molecular analyses of the MAT1A gene. Based on new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a254b874607fa6addc85976d386ebcf
https://doi.org/10.1016/j.ymgme.2013.10.013
https://doi.org/10.1016/j.ymgme.2013.10.013
Autor:
Toju Tanaka, Isaku Omori, Kiyoshi Kikuchi, Masaru Miura, Hiroshi Kawame, Erika Okano, Kenji Ihara, Johji Inazawa, Toshihiro Ohura, Yoichi Matsubara, Hiroyo Mabe, Akira Ohtake, Shin Nabatame, Kenji Kurosawa, Hironao Numabe, Kyoko Watanabe, Seiji Mizuno, Tetsuya Niihori, Hirofumi Ohashi, Yoko Aoki, Yoshikazu Kuroki, Shinichi Niijima, Nobuhiko Okamoto, Hiroshi Arai
Publikováno v:
Journal of Human Genetics. 56:707-715
Costello syndrome (CS) is a congenital disease that is characterized by a distinctive facial appearance, failure to thrive, mental retardation and cardiomyopathy. In 2005, we discovered that heterozygous germline mutations in HRAS caused CS. Several
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9fc9aeb1143f53a79764a5fe3ebaf13
https://doi.org/10.1038/jhg.2011.85
https://doi.org/10.1038/jhg.2011.85
Autor:
Toju Tanaka, Toshiyuki Fukao, Reiko Horikawa, Seiji Yamaguchi, Naomi Kondo, Masaki Takayanagi, Yasuhiro Naiki
Publikováno v:
Molecular Genetics and Metabolism. 100:339-344
Mitochondrial acetoacetyl-CoA thiolase (T2) deficiency is an inherited disorder affecting isoleucine catabolism and ketone body metabolism. A Japanese female developed a severe ketoacidotic attack at the age of 7 months. Urinary organic acid analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2382f99c59e39c992770cb591c19373f
https://doi.org/10.1016/j.ymgme.2010.03.012
https://doi.org/10.1016/j.ymgme.2010.03.012
Autor:
Tadao Orii, Torayuki Okuyama, Yasuyuki Suzuki, Hiroyuki Ida, Toju Tanaka, Yoshikatsu Eto, Gerald F. Cox, Akemi Tanaka
Publikováno v:
Molecular Genetics and Metabolism. 99:18-25
This open-label clinical study enrolled 10 adults with attenuated Mucopolysaccharidosis II and advanced disease under the direction of the Japan Society for Research on Mucopolysaccharidosis Disorders prior to regulatory approval of idursulfase in Ja
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b6f89c78b9df26ee29d225b5cd33597
https://doi.org/10.1016/j.ymgme.2009.08.006
https://doi.org/10.1016/j.ymgme.2009.08.006