Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Ryoji Fujiki"'
Autor:
Norikazu Yogi, Genki Usui, Keisuke Matsusaka, Masaki Fukuyo, Ryoji Fujiki, Motoaki Seki, Shigetsugu Takano, Hiroyuki Abe, Teppei Morikawa, Tetsuo Ushiku, Masayuki Ohtsuka, Atsushi Kaneda
Publikováno v:
Cancer Medicine, Vol 12, Iss 2, Pp 1122-1136 (2023)
Abstract Infection with certain viruses is an important cause of cancer. The Pan‐Cancer Analysis of Whole Genomes (PCAWG) Consortium recently analyzed the whole‐genome sequencing (WGS) data from 2656 cases across 21 cancer types, and indicated th
Externí odkaz:
https://doaj.org/article/eef0e6833b7a4b999cf1edde36f2c194
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 26, Iss , Pp 100702- (2021)
Background: Glycogen storage disease type 0a (GSD 0a), caused by GYS2 mutations, has a broad phenotypic spectrum, mostly associated with hypoglycemia. This disease has been characterized by the inability to store glycogen in the liver, leading to no
Externí odkaz:
https://doaj.org/article/d8d85e0b907349dc87ecee49437a455f
Autor:
Masato Mima, Atsushi Okabe, Takayuki Hoshii, Takuya Nakagawa, Tomoya Kurokawa, Satoru Kondo, Harue Mizokami, Masaki Fukuyo, Ryoji Fujiki, Bahityar Rahmutulla, Tomokazu Yoshizaki, Toyoyuki Hanazawa, Kiyoshi Misawa, Atsushi Kaneda
Publikováno v:
International Journal of Cancer. 152:1847-1862
Autor:
Norikazu Yogi, Genki Usui, Keisuke Matsusaka, Masaki Fukuyo, Ryoji Fujiki, Motoaki Seki, Shigetsugu Takano, Hiroyuki Abe, Teppei Morikawa, Tetsuo Ushiku, Masayuki Ohtsuka, Atsushi Kaneda
Publikováno v:
Cancer medicineREFERENCES.
Infection with certain viruses is an important cause of cancer. The Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium recently analyzed the whole-genome sequencing (WGS) data from 2656 cases across 21 cancer types, and indicated that Epstein-Ba
Autor:
Daichi Yamasoba, Izumi Kimura, Hesham Nasser, Yuhei Morioka, Naganori Nao, Jumpei Ito, Keiya Uriu, Masumi Tsuda, Jiri Zahradnik, Kotaro Shirakawa, Rigel Suzuki, Mai Kishimoto, Yusuke Kosugi, Kouji Kobiyama, Teppei Hara, Mako Toyoda, Yuri L. Tanaka, Erika P. Butlertanaka, Ryo Shimizu, Hayato Ito, Lei Wang, Yoshitaka Oda, Yasuko Orba, Michihito Sasaki, Kayoko Nagata, Kumiko Yoshimatsu, Hiroyuki Asakura, Mami Nagashima, Kenji Sadamasu, Kazuhisa Yoshimura, Jin Kuramochi, Motoaki Seki, Ryoji Fujiki, Atsushi Kaneda, Tadanaga Shimada, Taka-aki Nakada, Seiichiro Sakao, Takuji Suzuki, Takamasa Ueno, Akifumi Takaori-Kondo, Ken J. Ishii, Gideon Schreiber, Hirofumi Sawa, Akatsuki Saito, Takashi Irie, Shinya Tanaka, Keita Matsuno, Takasuke Fukuhara, Terumasa Ikeda, Kei Sato
Publikováno v:
Cell. 185(12)
Soon after the emergence and global spread of the SARS-CoV-2 Omicron lineage BA.1, another Omicron lineage, BA.2, began outcompeting BA.1. The results of statistical analysis showed that the effective reproduction number of BA.2 is 1.4-fold higher th
Autor:
Tatsuo Fuchigami, Maki Furukawa, Koji Hashimoto, Toshiyuki Fukao, Nobuyuki Ishige, Mika Ishige, Ryoji Fujiki, Ichiro Morioka, Yasuji Inamo, Hideo Sasai, Erika Ogawa, Hironori Kobayashi
Publikováno v:
Journal of Infection and Chemotherapy. 25:913-916
Rotavirus infection is a major cause of gastroenteritis, which occurs mainly in children. Liver dysfunction due to rotavirus gastroenteritis has been reported; however, acute hepatitis due to this disease is very rare. We present a rare case in which
Autor:
Harumi Yamada, Hideyuki Takeshima, Ryoji Fujiki, Satoshi Yamashita, Shigeki Sekine, Takayuki Ando, Naoko Hattori, Atsushi Okabe, Takaki Yoshikawa, Kazutaka Obama, Hitoshi Katai, Atsushi Kaneda, Toshikazu Ushijima
Publikováno v:
Cancer Letters. 532:215587
The CpG island methylator phenotype (CIMP) is associated with prognosis and drug sensitivity in multiple cancer types. In gastric cancer, the CIMP is closely associated with Epstein-Barr virus (EBV) infection and AT-rich interactive domain 1A (ARID1A
Autor:
Toshiyuki Fukao, Osamu Ohara, Mitsuru Kubota, Mina Nakama, Yuki Hasegawa, Torayuki Okuyama, Hideo Sasai, Ryoji Fujiki
Publikováno v:
Human Genome Variation, Vol 7, Iss 1, Pp 1-4 (2020)
Human Genome Variation
Human Genome Variation
We encountered a patient with mitochondrial trifunctional protein deficiency in whom the corresponding mutations were not identified by a DNA panel for newborn screening for targeted diseases. After diagnosis confirmation by an enzyme assay and immun
Autor:
Maeda Akiko, Osamu Ohara, Tomoaki Tanaka, Akiko Yoshida, Tomohiko Ichikawa, Kazuyuki Matsushita, Takayuki Morisaki, Makoto Ikeda, Motio Nishimura, Yue Yao, Hiroko Morisaki, Ryoji Fujiki
Publikováno v:
The Journal of Molecular Diagnostics. 20:572-582
There is significant debate within the diagnostics community regarding the accuracy of variant identification by next-generation sequencing and the necessity of confirmatory testing of detected variants. Because the quality threshold to discriminate
Autor:
Yasuhiko, Ago, Hiroki, Otsuka, Hideo, Sasai, Elsayed, Abdelkreem, Mina, Nakama, Yuka, Aoyama, Hideki, Matsumoto, Ryoji, Fujiki, Osamu, Ohara, Kazumasa, Akiyama, Kaori, Fukui, Yoriko, Watanabe, Yoko, Nakajima, Hidenori, Ohnishi, Tetsuya, Ito, Toshiyuki, Fukao
Publikováno v:
Experimental and Therapeutic Medicine
Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase (HMGCS2) deficiency is a metabolic disorder caused by mutations in the HMGCS2 gene. The present study describes the identification of four cases of HMGCS2 deficiency in Japan. Hepatomegaly and sev