Iwate Medical University · Graduate School of Medicine / Department of Medicine / Faculty of Medicine

Research keywordshemostasis on endothelial cell・血管内皮細胞・血栓止血・血小板

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• StyI polymorphism at nucleotide 1610 in the human platelet glycoprotein Ib alpha gene.
• G-->A transition at nucleotide 2110 in the human platelet glycoprotein (GP) IX gene resulting in Ala139(ACC)-->Thr(GCC) substitution.
• 先天性血液凝固第Ⅶ因子欠乏症患者に認められたヘテロ接合体変異(p.Arg337Cys)と遺伝子多型性(p.Arg413Gln)のハプロタイプ解析
• Severe bleeding tendency in a patient with Bernard-Soulier syndrome associated with a homozygous single base pair deletion in the gene coding for the human platelet glycoprotein Ibalpha.

• 先天性凝固因子欠乏症の分子病態
• regulation of hemostasis and fiblinolysis on vascular endothelial cell
• 血管内皮細胞における凝固線溶因子の発現調節
• 先天性血小板機能異常症の分子病態

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