Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Chiaki Taira"'
Autor:
Chiaki Taira, Masahiro Yoda, Yumiko Higuchi, Tomu Kamijo, Takahiro Kaido, Nobuo Okumura, Shinpei Arai
Publikováno v:
International Journal of Hematology. 114:325-333
We identified a patient with a novel heterozygous variant fibrinogen, γp.C352R (Niigata II; N-II), who had a bleeding episode and failed infertility treatment and was suspected to have hypodysfibrinogenemia based on low and discordant fibrinogen lev
Publikováno v:
Thrombosis Research. 196:152-158
Article
Thrombosis research. 196: 152-158. (2020)
Thrombosis research. 196: 152-158. (2020)
Publikováno v:
Thrombosis Research. 182:150-158
Article
Thrombosis research. 182: 150-158. (2019)
Thrombosis research. 182: 150-158. (2019)
Autor:
Masahiro, Yoda, Takahiro, Kaido, Tomu, Kamijo, Chiaki, Taira, Yumiko, Higuchi, Shinpei, Arai, Nobuo, Okumura
Publikováno v:
International journal of hematology. 114(3)
We identified a patient with a novel heterozygous variant fibrinogen, γp.C352R (Niigata II; N-II), who had a bleeding episode and failed infertility treatment and was suspected to have hypodysfibrinogenemia based on low and discordant fibrinogen lev
Autor:
Chiaki Taira, Masahiro Yoda, Shinpei Arai, Yumiko Higuchi, Tomu Kamijo, Takahiro Kaido, Nobuo Okumura
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 9422, p 9422 (2020)
International Journal of Molecular Sciences
Volume 21
Issue 24
International Journal of Molecular Sciences
Volume 21
Issue 24
We identified a novel heterozygous variant, B&beta
p.Pro234Leu (fibrinogen Tokorozawa), which was suspected to be associated with hypofibrinogenemia. Therefore, we analyzed the assembly and secretion of this fibrinogen using Chinese hamster ovar
p.Pro234Leu (fibrinogen Tokorozawa), which was suspected to be associated with hypofibrinogenemia. Therefore, we analyzed the assembly and secretion of this fibrinogen using Chinese hamster ovar
Publikováno v:
International journal of hematology. 112(3)
We identified two heterozygous dysfibrinogenemias, Bβp.Gly45Cys (Kyoto VII; K-VII) and Bβp.Arg74Cys (Iida II; I-II). The impairment of polymerization of Bβp.G45C has been well analyzed; however, that of Bβp.R74C has not. Thus, we compared fibrin
Autor:
Ryu Yanagisawa, Tomonari Shigemura, Miyuki Tanaka, Kenichi Koike, Kazuo Sakashita, Yozo Nakazawa, Daisuke Morita, Kentaro Yoshikawa, Shigetaka Shimodaira, Chiaki Taira, Shoji Saito, Saki Mukai, Kazuyuki Matsuda
Publikováno v:
Leukemialymphoma. 61(4)
Historically defined in the European Group for the Immunological Characterization of Leukemias (EGIL) [1], acute bilineal leukemia (ABLL) is characterized by 2 distinct blast populations (e.g. B/my...
Autor:
Chiaki Taira1 tairacha@shinshu-u.ac.jp, Kazuyuki Matsuda2 kmatsuda@shinshu-u.ac.jp, Shinpei Arai2 m061201h@shinshu-u.ac.jp, Mitsutoshi Sugano2 suga@shinshu-u.ac.jp, Takeshi Uehara3 tuehara@shinshu-u.ac.jp, Nobuo Okumura1 nobuoku@shinshu-u.ac.jp
Publikováno v:
International Journal of Molecular Sciences. Nov2017, Vol. 18 Issue 11, p2470. 10p.
Autor:
Takayuki Honda, Nobuo Okumura, Mitsutoshi Sugano, Kazuhiro Nagata, Shinpei Arai, Chiaki Taira
Publikováno v:
Thrombosis Research. 159:82-85
Article
THROMBOSIS RESEARCH.159:82-85(2017)
THROMBOSIS RESEARCH.159:82-85(2017)
Publikováno v:
International journal of laboratory hematologyREFERENCES. 42(2)
Introduction: Congenital fibrinogen disorders are classified as afibrinogenemia, hypofibrinogenemia, dysfibrinogenemia, and hypodysfibrinogenemia. However, difficulties are associated with discriminating between dysfibrinogenemia, hypofibrinogenemia,