Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Masako Kurihara"'
Autor:
Hiroko Iida, Kunnika Kuaha, Suthat Fucharoen, Masako Kurihara, Chayanon Peerapittayamongkol, Worawan Chumpia, Pantep Angchaisuksiri, Naotaka Hamasaki, Sumiko Inoue, Nantarat Komanasin, Yui Wada, Koichiro Muta
Publikováno v:
Blood Coagulation & Fibrinolysis. 17:13-18
Protein C (PC) and protein S (PS) play key roles in an anticoagulant pathway in order to control the haemostatic system. We identified single nucleotide polymorphisms (SNPs) and/or haplotypes in the promotor and exons of the whole PC and PS genes and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fe8d9632bebb5383632d03dadcccba6
https://doi.org/10.1097/01.mbc.0000198051.27387.a3
https://doi.org/10.1097/01.mbc.0000198051.27387.a3
Autor:
Naotaka Hamasaki, Hiroko Iida, Sumiko Inoue, Sachiko Kinoshita, Masako Kurihara, Yui Wada, Kumiko Watanabe, Dongchon Kang, Hiroko Tsuda
Publikováno v:
Clinical Biochemistry. 38:908-915
Objectives: Coagulation factor V Leiden has not been detected in Japanese patients suffering from thrombosis. Hitherto, the constitutional background of Japanese thrombotic patients has never been systematically examined. We have performed a systemat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13ddffe84cf3b7902ac00c749cc9ae38
https://doi.org/10.1016/j.clinbiochem.2005.05.006
https://doi.org/10.1016/j.clinbiochem.2005.05.006
Autor:
Miyuki Ono, Sumiko Inoue, Hiroko Iida, Naotaka Hamasaki, Machiko Wakiyama, Kumiko Watanabe, Yui Wada, Sachiko Kinoshita, Masako Kurihara
Publikováno v:
Thrombosis Research. 115:351-358
We investigated the molecular basis of reduced functional levels of antithrombin (AT) in two individuals suffering from thromboembolic events. In each case direct sequencing of amplified DNA revealed 13,260-13,262 del in one patient and 2511C>A in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::809bd6dd8a7ceea8d7252c6df0a68fcf
https://doi.org/10.1016/j.thromres.2004.08.025
https://doi.org/10.1016/j.thromres.2004.08.025
Autor:
Yui Wada, Worawan Chumpia, Dongchon Kang, Sachiko Kinoshita, Sumiko Inoue, Michiyo Urata, Hiroko Iida, Masako Kurihara, Hiroko Tsuda, Tomomi Fujii, Naotaka Hamasaki, Miyuki Ono
Publikováno v:
Japanese Journal of Thrombosis and Hemostasis. 16:641-649
プロテインS活性低下を示した血栓症患者に見出された変異型分子2種類（Thr37MetおよびCys206Phe）をhuman embryo kidney 293（HEK293）細胞に安定発現させ，細胞培養上清中のプロテインS活性と蛋白
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e591991809f920bc46d12ef10d43f25a
https://doi.org/10.2491/jjsth.16.641
https://doi.org/10.2491/jjsth.16.641
Autor:
Sachiko Kinoshita, Atsushi Shibuya, Eiichi Ishii, Kumiko Watanabe, Sumiko Inoue, Hiroko Iida, Naotaka Hamasaki, Kenji Muraoka, Machiko Wakiyama, Masafumi Zaitsu, Masako Kurihara, Yui Wada, Miyuki Ono
Publikováno v:
British Journal of Haematology. 120:101-108
Afibrinogenaemia usually induces a bleeding tendency during infancy, whereas protein C deficiency increases susceptibility to thrombosis in children or adolescence. Mutations of these genes have been, therefore, established as independent risk factor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7cb69d346b413e0229f9a842feb6f5f9
https://doi.org/10.1046/j.1365-2141.2003.03985.x
https://doi.org/10.1046/j.1365-2141.2003.03985.x
Autor:
Eiichi Ishii, Naotaka Hamasaki, Mutsuko Nakahara, Hiroko Iida, Kenji Ihara, Machiko Wakiyama, Michiyo Urata, Sachiko Kinoshita, Takeshi Kai, Kumiko Watanabe, Masako Kurihara
Publikováno v:
Thrombosis and Haemostasis. 84:49-53
SummaryCongenital afibrinogenemia due to a novel homozygous nonsense mutation of the fibrinogen γ-chain gene, fibrinogen Hakata, was found in an 18-year-old Japanese girl who had received supplemental fibrinogen therapy since she was 4 months old. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::232689719233e1008b543002f6e6e381
https://doi.org/10.1055/s-0037-1613966
https://doi.org/10.1055/s-0037-1613966
Autor:
Yuzo, Kayamori, Akiyoshi, Fujishima, Nozomi, Noda, Masako, Kurihara, Toshiharu, Tsutsui, Tomomi, Mochimaru, Yohko, Ikematsu, Nobuhisa, Monji, Takuya, Ishigaki, Kanae, Aoki, Sayaka, Ushinohama, Shoko, Nishioka, Sadaomi, Egashira, Dongchon, Kang
Publikováno v:
Rinsho byori. The Japanese journal of clinical pathology. 58(8)
With the increasing need for medical laboratory data, the importance of the medical laboratory in medical care has grown exponentially. Therefore, it is necessary that the medical laboratory provide the doctor and the patient receiving medical care w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::42b6fd1cf41053c70e80df348865a44a
https://pubmed.ncbi.nlm.nih.gov/20860179
https://pubmed.ncbi.nlm.nih.gov/20860179
Autor:
Hiroko Iida, Mitsuko Toyofuku, Sachiko Kinoshita, Yui Wada, Masako Kurihara, Naotaka Hamasaki, Minako Kawamura, Yuzou Kayamori
Publikováno v:
Clinical chemistry and laboratory medicine. 42(1)
Allowable imprecision and bias reference limits for laboratory data can be calculated based on measurements of biological variation. Although biological variation of clinical chemical data has been reported from many laboratories, there have been few
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb2e94f38b40d2e117aa1fc20c7930c3
https://pubmed.ncbi.nlm.nih.gov/15061385
https://pubmed.ncbi.nlm.nih.gov/15061385
Autor:
Kazuhiko Yoshimura, Hiroyoshi Yamada, Satoshi Yamazaki, Hiroshi Nomura, Mie Hayashida, Naotaka Hamasaki, Masako Kurihara, Keishi Kubo, Kunio Momose, Osamu Kitahara
Publikováno v:
Internal medicine (Tokyo, Japan). 42(3)
A young man with repetitive deep venous thrombosis of the legs and the inferior vena cava, and his family were eventually diagnosed by means of molecular genetic analysis as having both hereditary protein C and protein S deficiency. There have been a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c5752d6fc2dbd107cd3e2ad304330ac
https://pubmed.ncbi.nlm.nih.gov/12705793
https://pubmed.ncbi.nlm.nih.gov/12705793
Autor:
Kumiko, Watanabe, Atsushi, Shibuya, Eiichi, Ishii, Masako, Kurihara, Sumiko, Inoue, Miyuki, Ono, Yui, Wada, Machiko, Wakiyama, Masafumi, Zaitsu, Hiroko, Iida, Kenji, Muraoka, Sachiko, Kinoshita, Naotaka, Hamasaki
Publikováno v:
British journal of haematology. 120(1)
Afibrinogenaemia usually induces a bleeding tendency during infancy, whereas protein C deficiency increases susceptibility to thrombosis in children or adolescence. Mutations of these genes have been, therefore, established as independent risk factor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eb615b947d4151a3cfee90711e7db7c4
https://pubmed.ncbi.nlm.nih.gov/12492584
https://pubmed.ncbi.nlm.nih.gov/12492584