A novel frameshift mutation in the fibrinogen gamma C terminal region, FGG c. 1169_1170 del AT, leading to hypofibrinogenemia THROMBOSIS RESEARCH,159:82-85 2017(Nov.) Author:Nagata, Kazuhiro; Arai, Shinpei; Sugano, Mitsutoshi; Taira, Chiaki; Okumura, Nobuo; Honda, Takayuki;
A Novel Mutation in the Fibrinogen B Chain (c.490G > A; End of Exon 3) Causes a Splicing Abnormality and Ultimately Leads to Congenital Hypofibrinogenemia INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,18(11) 2017(Nov.) Author:Taira, Chiaki; Matsuda, Kazuyuki; Arai, Shinpei; Sugano, Mitsutoshi; Uehara, Takeshi; Okumura, Nobuo;
The fibrous form of intracellular inclusion bodies in recombinant variant fibrinogen-producing cells is specific to the hepatic fibrinogen storage disease-inducible variant fibrinogen INTERNATIONAL JOURNAL OF HEMATOLOGY,105(6):758-768 2017(Jun.) Author:Arai, Shinpei; Ogiwara, Naoko; Mukai, Saki; Takezawa, Yuka; Sugano, Mitsutoshi; Honda, Takayuki; Okumura, Nobuo;
講演・口頭発表等 Novel approach for the phenotypes of congenital fibrinogen disorders using alternative fibrinogen value, |min1|c, obtained from clot waveform analysis The 17th Congress of Asian Society of Clinical Pathology and Laboratory Medicine (ASCPaLM) 2022(Oct.) Presenter:Arai, Shinpei; kamijo, Tomu; Kaido, Takahiro; Shinohara, sho; Suzuki, Takeshi; Arai, Nobuo; Uehara Takeshi; Okumura, Nobuo