A novel variant fibrinogen, AαE11del, demonstrating the importance of AαE11 residue in thrombin binding von Kaido, Takahiro, Yoda, Masahiro, Kamijo, Tomu, Arai, Shinpei, Yamauchi, Kazuyoshi, Okumura, Nobuo

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Citrullinated fibrinogen-SAAs complex causes vascular metastagenesis von Han, Yibing, Tomita, Takeshi, Kato, Masayoshi, Ashihara, Norihiro, Higuchi, Yumiko, Matoba, Hisanori, Wang, Weiyi, Hayashi, Hikaru, Itoh, Yuji, Takahashi, Satoshi, Kurita, Hiroshi, Nakayama, Jun, Okumura, Nobuo, Hiratsuka, Sachie

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A Novel Amino Acid Substitution, Fibrinogen Bβp.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion von Kaido, Takahiro, Yoda, Masahiro, Kamijo, Tomu, Arai, Shinpei, Taira, Chiaki, Higuchi, Yumiko, Okumura, Nobuo

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Rapid single nucleotide polymorphism based method for hematopoietic chimerism analysis and monitoring using high-speed droplet allele-specific PCR and allele-specific quantitative... von Taira, Chiaki, Matsuda, Kazuyuki, Yamaguchi, Akemi, Uehara, Masayuki, Sugano, Mitsutoshi, Okumura, Nobuo, Honda, Takayuki

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Congenital Hypofibrinogenemia in a Neonate with a Novel Mutation in the FGB Gene von Shinozuka, Jun, Okumura, Nobuo, Nagasawa, Mayumi, Nishikado, Motokazu, Kadowaki, Sayaka, Katsuda, Itsuro, Imashuku, Shinsaku

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The fibrous form of intracellular inclusion bodies in recombinant variant fibrinogen-producing cells is specific to the hepatic fibrinogen storage disease-inducible variant fibrino... von Arai, Shinpei, Ogiwara, Naoko, Mukai, Saki, Takezawa, Yuka, Sugano, Mitsutoshi, Honda, Takayuki, Okumura, Nobuo

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γ375W fibrinogen-synthesizing CHO cells indicate the accumulation of variant fibrinogen within endoplasmic reticulum von Kobayashi, Tamaki, Arai, Shinpei, Ogiwara, Naoko, Takezawa, Yuka, Nanya, Mai, Terasawa, Fumiko, Okumura, Nobuo

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Citrullinated fibrinogen shows defects in FPA and FPB release and fibrin polymerization catalyzed by thrombin von Okumura, Nobuo, Haneishi, Ayumi, Terasawa, Fumiko

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Familial discrepancy of clinical outcomes associated with fibrinogen Dorfen: A case of huge genital hematoma after episiotomy von Kagami, Kyosuke, Yamazaki, Rena, Minami, Tetsuya, Okumura, Nobuo, Morishita, Eriko, Fujiwara, Hiroshi

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Lateral medullary syndrome in a boy with hereditary dysfibrinogenemia von Kibe, Tetsuya, Ikeya, Manae, Yokochi, Kenji, Okumura, Nobuo

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Spontaneous regression of the inhibitor against the coagulation factor XIII A subunit in acquired factor XIII deficiency von Ishida, Fumihiro, Okubo, Kentaro, Ito, Toshiro, Okumura, Nobuo, Souri, Masayoshi, Ichinose, Akitada

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In vitro transcription of compound heterozygous hypofibrinogenemia Matsumoto IX; first identification of FGB IVS6 deletion of 4 nucleotides and FGG IVS3-2A > G causing abnormal RNA... von Terasawa, Fumiko, Kamijyo, Yuka, Fujihara, Noriko, Yamauchi, Kazuyoshi, Kumagai, Toshiko, Honda, Takayuki, Shigematsu, Satoshi, Okumura, Nobuo

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Molecular analysis of afibrinogenemic mutations caused by a homozygous FGA1238 bp deletion, and a compound heterozygous FGA1238 bp deletion and novel FGA c.54+3A>C substitution von Takezawa, Yuka, Terasawa, Fumiko, Matsuda, Kazuyuki, Sugano, Mitsutoshi, Tanaka, Aiko, Fujiwara, Mitsuhiro, Kainuma, Keigo, Okumura, Nobuo

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γD318Y fibrinogen shows no fibrin polymerization due to defective “A-a” and “B-b” interactions, whereas that of γK321E fibrinogen is nearly normal von Kamijo, Tomu, Mukai, Saki, Taira, Chiaki, Higuchi, Yumiko, Okumura, Nobuo

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Genetic analyses of novel compound heterozygous hypodysfibrinogenemia, Tsukuba I: FGG c.1129 + 62_65 del AATA and FGG c.1299 + 4 del A von Mukai, Saki, Nagata, Kazuhiro, Ikeda, Minami, Arai, Shinpei, Sugano, Mitsutoshi, Honda, Takayuki, Okumura, Nobuo

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Fibrinogen Otsu I:A γ Asn319,Asp320 deletion dysfibrinogen identified in an asymptomatic pregnant woman von Terasawa, Fumiko, Hogan, Kelly A., Kani, Satomi, Hirose, Masaya, Eguchi, Yutaka, Noda, Yoichi, Hongo, Minoru, Okumura, Nobuo

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In vitro expression demonstrates impaired secretion of the γAsn319, Asp320 deletion variant fibrinogen von Kani, Satomi, Terasawa, Fumiko, Lord, Susan T., Tozuka, Minoru, Ota, Hiroyoshi, Okumura, Nobuo, Katsuyama, Tsutomu

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Screening Method for Hepatic Fibrinogen Storage Disease Associated with Congenital Hypofibrinogenemia von Arai, Shinpei, Mukai, Saki, Takezawa, Yuka, Sugano, Mitsutoshi, Honda, Takayuki, Ishida, Fumihiro, Okumura, Nobuo

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Congenital dysfibrinogenemia in a Japanese family with fibrinogen Naples (BβAla68Thr) manifesting as superior sagittal sinus thrombosis von Yoshida, Satoru, Kibe, Tetsuya, Matsubara, Risa, Koizumi, Shin-ichiro, Nara, Kenji, Amano, Koji, Okumura, Nobuo

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Fibrinopeptide A release is necessary for effective B:b interactions in polymerisation of variant fibrinogens with impaired A:a interactions von Soya, Keisuke, Terasawa, Fumiko, Okumura, Nobuo

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