Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Yasushi Kogo"'
Autor:
Jun Watanabe, Yasumasa Mitani, Yuki Kawai, Takeshi Kikuchi, Yasushi Kogo, Atsuko Oguchi-Katayama, Hajime Kanamori, Kengo Usui, Masayoshi Itoh, Paul E. Cizdziel, Alexander Lezhava, Kenji Tatsumi, Yasushi Ichikawa, Shinji Togo, Hiroshi Shimada, Yoshihide Hayashizaki
Publikováno v:
BioTechniques, Vol 43, Iss 4, Pp 479-484 (2007)
A key feature of the smart amplification process version 2 (SMAP-2) is the ability to suppress mismatch amplification by using a unique asymmetric primer design and Thermus aquaticus MutS (Taq MutS). However, we report here that use of SMAP-2 for pol
Externí odkaz:
https://doaj.org/article/bae6626065e1408e86499c5b5adcd25f
Autor:
Yuki Kawai, Yasumasa Kimura, Alexander Lezhava, Hajime Kanamori, Kengo Usui, Takeshi Hanami, Takahiro Soma, Jean-Étienne Morlighem, Satomi Saga, Yuri Ishizu, Shintaro Aoki, Ryuta Endo, Atsuko Oguchi-Katayama, Yasushi Kogo, Yasumasa Mitani, Takefumi Ishidao, Chiharu Kawakami, Hideshi Kurata, Yumiko Furuya, Takayuki Saito, Norio Okazaki, Masatsugu Chikahira, Eiji Hayashi, Sei-ichi Tsuruoka, Tokumichi Toguchi, Yoshitomo Saito, Toshiaki Ban, Shinyu Izumi, Hideko Uryu, Koichiro Kudo, Yuko Sakai-Tagawa, Yoshihiro Kawaoka, Aizan Hirai, Yoshihide Hayashizaki, Toshihisa Ishikawa
Publikováno v:
PLoS ONE, Vol 7, Iss 1, p e30236 (2012)
BACKGROUND: In 2009, a pandemic (pdm) influenza A(H1N1) virus infection quickly circulated globally resulting in about 18,000 deaths around the world. In Japan, infected patients accounted for 16% of the total population. The possibility of human-to-
Externí odkaz:
https://doaj.org/article/df211cf300504e4b8e83db32fa137197
Autor:
Hiroshi Shimada, Yoshihide Hayashizaki, Noburou Ogawa, Alexander Lezhava, Paul E. Cizdziel, Syuji Uno, Takahiro Arakawa, Chiaki Kato, Takeshi Kikuchi, Yasushi Kogo, Yuki Kawai, Toru Miyagi, Shinji Togo, Yasushi Ichikawa, Nobuyoshi Momiyama, Kenji Tatsumi, Yasumasa Mitani, Hideki Takakura, Kanako Hoshi
Supplementary Figures S1-S2 from Rapid Detection of Epidermal Growth Factor Receptor Mutations in Lung Cancer by the SMart-Amplification Process
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48e50cabb54c86a9687f51f02011b34e
https://doi.org/10.1158/1078-0432.22440267.v1
https://doi.org/10.1158/1078-0432.22440267.v1
Autor:
Hiroshi Shimada, Yoshihide Hayashizaki, Noburou Ogawa, Alexander Lezhava, Paul E. Cizdziel, Syuji Uno, Takahiro Arakawa, Chiaki Kato, Takeshi Kikuchi, Yasushi Kogo, Yuki Kawai, Toru Miyagi, Shinji Togo, Yasushi Ichikawa, Nobuyoshi Momiyama, Kenji Tatsumi, Yasumasa Mitani, Hideki Takakura, Kanako Hoshi
Purpose: A positive response to gefitinib in non–small cell lung cancer (NSCLC) has been correlated to mutations in epidermal growth factor receptor (EGFR) gene. Previous reports have been based mainly on diagnostic screening by sequencing. However
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75585a98f8d44f9d39094e1721a8f3cc
https://doi.org/10.1158/1078-0432.c.6517620
https://doi.org/10.1158/1078-0432.c.6517620
Autor:
Yoko Edahiro, Soji Morishita, Misa Imai, Marito Araki, Hajime Yasuda, Akimichi Ohsaka, Yasushi Kogo, Masayoshi Itoh, Yoshihide Hayashizaki, Hideya Kawaji, Masafumi Ito, Norio Komatsu, Satoshi Tsuneda, Saya Yamawaki
Publikováno v:
Cancer Science
Discrimination of Philadelphia‐negative myeloproliferative neoplasms (Ph‐MPNs) from reactive hypercytosis and myelofibrosis requires a constellation of testing including driver mutation analysis and bone marrow biopsies. We searched for a biomark
Autor:
Emi Yamano, Haruhiko Koseki, Yasushi Kogo, Hirohiko Kuratsune, Yasuhito Nakatomi, Hiroshi Ohno, Yasuyoshi Watanabe, Yuuri Tsuboi, Masayoshi Itoh, Sanae Fukuda, Yoshihide Hayashizaki, Toshimori Kitami, Masaki Suimye Morioka, Yosky Kataoka, Harukazu Suzuki, Jun Kikuchi, Hideya Kawaji, Kouzi Yamaguti, Tamotsu Kato, Kei Mizuno
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a complex and debilitating disease with no molecular diagnostics and no treatment options. To identify potential markers of this illness, we profiled 48 patients and 52 controls for stand
Autor:
T Ohtsu, Hideya Kawaji, Kengo Usui, Y Ueno, Emiko Yoshida, Yasushi Kogo, Masayoshi Itoh, Yasuhisa Terao, Yasuhiko Ito, T Kato, M Ozawa, S Nojiri, H Kato
Publikováno v:
ePoster.
Introduction/Background Lymphadenectomy in endometrial cancer should be considered depending on individual patients owing to its postoperative risks such as lymphedema. Although assessment of lymph node metastasis provides crucial information for app
Autor:
Hideya Kawaji, Soji Morishita, Yasushi Kogo, Akimichi Ohsaka, Yoko Edahiro, Marito Araki, Yoshihide Hayashizaki, Hajime Yasuda, Misa Imai, Satoshi Tsuneda, Norio Komatsu, Saya Yamawaki, Masayoshi Itoh
Publikováno v:
Blood. 136:41-41
Discrimination of Philadelphia-negative myeloproliferative neoplasms (Ph-MPNs) from reactive hypercytosis and myelofibrosis is imperative because treatment strategies differ greatly, and an exhaustive search for the underlying cause becomes mandatory
Autor:
Ryuya Horiuchi, Alexander Lezhava, Yasushi Kogo, Yukiyoshi Fujita, Mia Wadelius, Koujirou Yamamoto, Lena Ekström, Kyoko Obayashi, Atsuko Oguchi-Katayama, Paul E. Cizdziel, Cristine Skogastierna, Masahiko Kurabayashi, Hugo Kohnke, Tohru Aomori, Katsunori Nakamura, Yoshihide Hayashizaki, Yasumasa Mitani, Yuki Kawai, Takefumi Ishidao, Anders Rane, Masami Murakami
Publikováno v:
Clinical Chemistry. 55:804-812
Background: Polymorphisms of the CYP2C9 (cytochrome P450, family 2, subfamily C, polypeptide 9) gene (CYP2C9*2, CYP2C9*3) and the VKORC1 (vitamin K epoxide reductase complex, subunit 1) gene (−1639G>A) greatly impact the maintenance dose for the dr
Autor:
Ai Kaiho, Takeshi Kikuchi, Kengo Usui, Paul E. Cizdziel, Hideki Takakura, Yasushi Kogo, Yoshihide Hayashizaki, Yuki Kawai, Kanako Hoshi, Masayoshi Itoh, Hajime Kanamori, Yasumasa Mitani
Publikováno v:
Biologicals. 36:234-238
In a previous study, a single nucleotide polymorphism (SNP) diagnostic system named the SMart Amplification Process version 2 (SMAP 2) was reported, which enabled rapid gene diagnostics from crude samples such as whole blood. The asymmetric primer de