Zobrazeno 1 - 10
of 233
pro vyhledávání: '"Mitsuyoshi Suzuki"'
Autor:
Susumu Yamazaki, Masaki Shimizu, Ayane Yakabe, Eisuke Inage, Keisuke Jimbo, Mitsuyoshi Suzuki, Futaba Miyaoka, Shuya Kaneko, Hitoshi Irabu, Asami Shimbo, Yoshiyuki Ohtomo, Masaaki Mori, Tomohiro Morio, Toshiaki Shimizu
Publikováno v:
Immunological Medicine, Vol 47, Iss 2, Pp 110-117 (2024)
AbstractAlthough the clinical efficacy of tofacitinib has been reported in adult patients with anti-melanoma differentiation-associated gene 5 (MDA5) antibody-positive (Ab+) dermatomyositis, data on its use in refractory juvenile dermatomyositis (JDM
Externí odkaz:
https://doaj.org/article/9f9970c3b01e4b01ab486a325509d0ab
Autor:
Hiroki Kondou, Satoshi Nakano, Tadahaya Mizuno, Kazuhiko Bessho, Yasuhiro Hasegawa, Atsuko Nakazawa, Ken Tanikawa, Yoshihiro Azuma, Tatsuya Okamoto, Ayano Inui, Kazuo Imagawa, Mureo Kasahara, Yoh Zen, Mitsuyoshi Suzuki, Hisamitsu Hayashi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background Progressive familial intrahepatic cholestasis type 2 (PFIC2) is an ultra-rare disease caused by mutations in the ABCB11 gene. This study aimed to understand the course of PFIC2 during the native liver period. Methods From November
Externí odkaz:
https://doaj.org/article/a61c9bf2045b487ab9f244d1259d0b5f
Autor:
Masahiro Takeda, Hajime Takei, Mitsuyoshi Suzuki, Takafumi Tsukui, Koichi Tsuboi, Hiroko Watayo, Takanori Ochi, Hiroyuki Koga, Hiroshi Nittono, Atsuyuki Yamataka
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract Bile acids have received increasing attention as a marker of the long-term prognosis and a potential therapeutic target in patients with biliary atresia, which is a progressive disease of the hepatobiliary system. A detailed analysis of seru
Externí odkaz:
https://doaj.org/article/423dd75d73734d9195dc325379ffb119
Autor:
Ryutaro Tamura, Yusuke Sabu, Tadahaya Mizuno, Seiya Mizuno, Satoshi Nakano, Mitsuyoshi Suzuki, Daiki Abukawa, Shunsaku Kaji, Yoshihiro Azuma, Ayano Inui, Tatsuya Okamoto, Seiichi Shimizu, Akinari Fukuda, Seisuke Sakamoto, Mureo Kasahara, Satoru Takahashi, Hiroyuki Kusuhara, Yoh Zen, Tomohiro Ando, Hisamitsu Hayashi
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract Choline is an essential nutrient, and its deficiency causes steatohepatitis. Dietary phosphatidylcholine (PC) is digested into lysoPC (LPC), glycerophosphocholine, and choline in the intestinal lumen and is the primary source of systemic cho
Externí odkaz:
https://doaj.org/article/6e3497d067f34e50bfe570fb76233f5d
Autor:
Hiroshi Nittono, Mitsuyoshi Suzuki, Hiromi Suzuki, Satoru Sugimoto, Jun Mori, Rieko Sakamoto, Yugo Takaki, Hisamitsu Hayashi, Hajime Takei, Akihiko Kimura
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
Inborn errors of bile acid metabolism (IEBAM) cause cholestasis during the neonatal period, and 8 types of IEBAM have been reported to date. IEBAM accounts for approximately 2% of cases of cholestasis of unknown cause. As only 10 patients have been i
Externí odkaz:
https://doaj.org/article/042438bd43724392be42c9a47166f6fd
Autor:
Kei Minowa, Daniel Rodriguez-Agudo, Mitsuyoshi Suzuki, Yamato Muto, Saeko Hirai, Yaping Wang, Lianyong Su, Huiping Zhou, Qun Chen, Edward J. Lesnefsky, Kuniko Mitamura, Shigeo Ikegawa, Hajime Takei, Hiroshi Nittono, Michael Fuchs, William M. Pandak, Genta Kakiyama
Publikováno v:
Journal of Lipid Research, Vol 64, Iss 5, Pp 100363- (2023)
CYP7B1 catalyzes mitochondria-derived cholesterol metabolites such as (25R)26-hydroxycholesterol (26HC) and 3β-hydroxy-5-cholesten-(25R)26-oic acid (3βHCA) and facilitates their conversion to bile acids. Disruption of 26HC/3βHCA metabolism in the
Externí odkaz:
https://doaj.org/article/ad9e745a75d64f8194bdbfb5527e40ba
Autor:
Hitoshi Tajiri, Mitsuyoshi Suzuki, Kazuhiko Bessho, Yoshinori Ito, Jun Murakami, Reiko Hatori, Tomoko Takano, Yoko Miyoshi, Stephen Brooks
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-7 (2022)
Abstract At present, noninvasive fibrosis markers are not available for the assessment of liver fibrosis in children with chronic hepatitis C. Sixty-three children with chronic hepatitis C were included. Changes in Wisteria floribunda agglutinin-posi
Externí odkaz:
https://doaj.org/article/a1fc05e0794a4d109234d92493d9acdb
Publikováno v:
Pediatrics and Neonatology, Vol 63, Iss 3, Pp 262-268 (2022)
Background: The diagnosis of Yersinia enterocolitica (Ye) enteritis is not easy because detection from stool culture is more difficult for Ye than for other bacterial enteritides. The establishment of characteristic ultrasonographic findings for Ye e
Externí odkaz:
https://doaj.org/article/b9407f9a1f7c4f06b86296e002806707
Autor:
Shigetaka Fukuda, Mitsuyoshi Suzuki, Kei Minowa, Hiroyuki Koga, Atsuyuki Yamataka, Toshiaki Shimizu
Publikováno v:
Children, Vol 10, Iss 5, p 900 (2023)
Pancreatic neuroendocrine tumors (PNETs) are relatively rare, especially in the pediatric age group. This report describes a pediatric case of acute pancreatitis secondary to stenosis of the main pancreatic duct due to a PNET. The patient was a boy,
Externí odkaz:
https://doaj.org/article/87a865b00fc447a983eaace0aa750d6d
Autor:
Hajime Takei, Seiko Narushima, Mitsuyoshi Suzuki, Genta Kakiyama, Takahiro Sasaki, Tsuyoshi Murai, Yuichiro Yamashiro, Hiroshi Nittono
Publikováno v:
Journal of Lipid Research, Vol 63, Iss 10, Pp 100275- (2022)
Although most bile acids (BAs) in feces are present in noncovalent forms that can be extracted with ethanol, non-negligible amounts of saponifiable BAs are also present. It is a major concern that such saponifiable BAs are routinely omitted from feca
Externí odkaz:
https://doaj.org/article/532be0ea86c34217bacd055e6322d0b7