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[文献書誌] Iida h.Ishi E, Nakahara M, Urata M, Wakiyama K, Kurihara M, Watanabe K, Kai T, Kinoshita S, Hamasaki N: "A Case of Congenital Afibrinogenemia : Fibrinogen Hakata, a Novel Nonsense Mutation of the Fibrinogen γ-Chain Gene"Thrombosis Haemostasis. 84(1). 49-53 (2000)
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[文献書誌] Nakahara M, Iida H, Urata M, Fujise M, Wakiyama M, Kinoshita S, Tsuda H, Okamura T, Yao K, Yao T, Hamasaki N: "A Novel Splice Acceptor Site Mutation of Protein S Gene in Affected Individuals with Type I Protein S Deficiency : Allelic Exclusion of the Mutant Gene"Thromosis Research. 101. 387-393 (2001)
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[文献書誌] Iida h, Nakahara M, Komori K, Fujise M, Wakiyama M, Urata M, Kinoshita S, Tsuda H, Sugimachi K, Hamasaki N: "Failure in the Detection of Aberrant mRNA from the Heterozygotic Splice Site Mutant Allele for Protein S in a Patient with Protein S Deficiency"Thromosis Research. 102. 187-196 (2001)
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[文献書誌] Oka, T., Murata, Y., Namba, M., Yoshimizu, T., Takao Toyomura, T., Yamamoto, A., Ge-Hong Sun-Wada, Hamasaki, N., Wada, Y., Futai, M: "a4, a Unique Kidney-specific Isoform of Mouse Vacuolar H^+-ATPase Subunit α"J. Biological Chemistry. 276(43). 40050-40054 (2001)
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[文献書誌] Heinzmann A, (32 authers) Hamasaki N(28th): "Genetic variants of IL-13 signalling and human asthma and atopy"Human Molelcular Genetics. 9(4). 549-559 (2000)
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[文献書誌] Ota K, Sakaguchi M, Hamasaki N, Mihara K.: "Membrane integration of the second transmembrane segment of band 3 requires closely apposed preceding signal-anchor sequence"J. Biological Chemistry. 275(38). 29743-29748 (2000)
