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J-GLOBAL ID：202002273842229031   Reference number：20A0656467

Heterozygous variant fibrinogen γA289V (Kanazawa III) was confirmed as hypodysfibrinogenemia by plasma and recombinant fibrinogens

ヘテロ接合変異型フィブリノーゲンγA289V(金沢III)は血漿および組換えフィブリノゲンによる低フィブリノーゲン血症として確認される【JST・京大機械翻訳】

Author (6)： Kaido Takahiro (Department of Clinical Laboratory Investigation, Graduate School of Medicine, Shinshu University, Matsumoto, Japan) ,  Yoda Masahiro (Department of Clinical Laboratory Investigation, Graduate School of Medicine, Shinshu University, Matsumoto, Japan) ,  Kamijo Tomu (Department of Clinical Laboratory Investigation, Graduate School of Medicine, Shinshu University, Matsumoto, Japan) ,  Taira Chiaki (Department of Clinical Laboratory Investigation, Graduate School of Medicine, Shinshu University, Matsumoto, Japan) ,  Higuchi Yumiko (Department of Clinical Laboratory Investigation, Graduate School of Medicine, Shinshu University, Matsumoto, Japan) ,  Okumura Nobuo (Department of Clinical Laboratory Investigation, Graduate School of Medicine, Shinshu University, Matsumoto, Japan)
Material： International Journal of Laboratory Hematology  (Int J Lab Hematol)
Volume： 42  Issue： 2  Page： 190-197  Publication year： 2020 
JST Material Number： T0133A  ISSN： 1751-5521  Document type： Article
Article type： 原著論文  Country of issue： United States (USA)  Language： ENGLISH (EN)

Abstract/Point： INTRODUCTION: Congenital fibri...

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Thesaurus term： fibrin ,  wild type ,  mutation ,  interaction ,  site-directed mutagenesis ,  transfection ,  CHO cell ,  mutagen ,  *plasma(blood) ,  vector(genetics) ,  hemolysis ,  catalyst ,  *fibrinogen ,  *heterojunction ,  polymerization

Author keywords (5)： “D:D” interaction ,  dysfibrinogenemia ,  fibrinogen ,  hypodysfibrinogenemia ,  γ-module

JST classification (2)： Congenital diseases,deformities in general.  (GD03010V) ,  Hematologic diseases  (GK03000F)

Terms in the title (8)： ヘテロ接合 ,  変異型 ,  フィブリノーゲン ,  金沢 ,  血漿 ,  組換え ,  フィブリノゲン ,  低フィブリノーゲン血症