Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tomoki Togashi"'
Autor:
Tomoki Togashi, Nemekhbayar Baatartsogt, Yasumitsu Nagao, Yuji Kashiwakura, Morisada Hayakawa, Nobuhiko Kamoshita, Takafumi Hiramoto, Takayuki Fujiwara, Eriko Morishita, Osamu Nureki, Tsukasa Ohmori
Protein C (PC) is a plasma anticoagulant encoded byPROC; mutation in bothPROCalleles results in neonatal purpura fulminans—a fatal systemic thrombotic disorder. In the present study, we aimed to develop a genome editing treatment to cure congenital
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e772340ccd6dbbefffcaa2cf0cc07c96
https://doi.org/10.1101/2023.02.26.530058
https://doi.org/10.1101/2023.02.26.530058
Autor:
Yuta Imai, Satomi Nagaya, Yuhei Araiso, Makiko Meguro-Horike, Tomoki Togashi, Kensho Ohmori, Yuka Makita, Eiichi Sato, Toshiaki Yujiri, Yuta Nagamori, Shin-ichi Horike, Atsushi Watanabe, Eriko Morishita
Publikováno v:
International journal of hematology.
Hereditary antithrombin (AT) deficiency is an autosomal dominant inherited thrombophilia. In three pedigrees of hereditary type I AT deficiency, we identified novel variants c.126delC (p.Lys43Serfs
Autor:
Hidesaku Asakura, Yuta Imai, Tomoki Togashi, Makiko Meguro-Horike, Keiji Nogami, Shin-ichi Horike, Satomi Nagaya, Kana Kuzasa, Eriko Morishita, Masayuki Nagasawa, Akiko Sekiya
Publikováno v:
International Journal of Hematology. 111:51-56
Congenital factor X (FX) deficiency is a rare bleeding disorder with an incidence of one in one million. The proband, a 2-year-old girl, exhibited easy bruising and a history of umbilical cord bleeding at birth. Prothrombin time ( 40 s) and activated
Autor:
Eriko Morishita, Koichi Yamaguchi, Sayaka Sugihara, Atsushi Watanabe, Kotaro Mori, Kana Kuzasa, Shin-ichi Horike, Tatsuo Ichinohe, Makiko Meguro-Horike, Tomoki Togashi, Yuta Imai, Hidesaku Asakura, Satomi Nagaya, Yuhei Araiso
Publikováno v:
Thrombosis research. 188