首页> 外文OA文献 >Type 2M von Willebrand Disease: F606I and I662F Mutations in the Glycoprotein Ib Binding Domain Selectively Impair Ristocetin- but not Botrocetin-Mediated Binding of von Willebrand Factor to Platelets

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Type 2M von Willebrand Disease: F606I and I662F Mutations in the Glycoprotein Ib Binding Domain Selectively Impair Ristocetin- but not Botrocetin-Mediated Binding of von Willebrand Factor to Platelets

机译：2M von Willebrand疾病：F606i和糖蛋白Ib结合结构域的F606i和I662F突变选择性地损害ristocetin-但不是雌激素介导的von Willebrand因子对血小板的结合

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Cheryl A. Hillery; David J. Mancuso; J. Evan Sadler; Jay W. Ponder; Mary A. Jozwiak; Pamela A. Christopherson; Joan Cox Gill; J. Paul Scott; Robert R. Montgomery;
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1. N1421K mutation in the glycoprotein Ib binding domain impairs ristocetin- and botrocetin-mediated binding of von Willebrand factor to platelets. [J] . Lanke E, Kristoffersson AC, Isaksson C, European Journal of Haematology . 2008,第5期

机译：糖蛋白Ib结合域中的N1421K突变削弱了ristocetin和Botrocetin介导的von Willebrand因子与血小板的结合。
2. The interaction of von Willebrand factor-A1 domain with collagen: mutation G1324S (type 2M von Willebrand disease) impairs the conformational change in A1 domain induced by collagen. [J] . Morales LD, Martin C, Cruz MA Journal of thrombosis and haemostasis: JTH . 2006,第2期

机译：von Willebrand因子-A1结构域与胶原蛋白的相互作用：突变G1324S（2M型von Willebrand疾病）损害了胶原蛋白诱导的A1结构域的构象变化。
3. Visualizing the von Willebrand factor/glycoprotein Ib-IX axis with a platelet-type von Willebrand disease mutation [J] . GuerreroJ.A., KyeiM., RussellS., Blood: The Journal of the American Society of Hematology . 2009,第27期

机译：用血小板型von Willebrand疾病突变可视化von Willebrand因子/糖蛋白Ib-IX轴
4. Surface Dependent Expression of Platelet GPIb Binding Domain Within Human von Willebrand Factor Studied by Atomic Force Microscopy [C] . Inkyung Kang, Madhusudan Raghavachari, Roger E. Marchant Annual meeting of the Society For Biomaterials . 2002

机译：原子力显微镜研究人von Willebrand因子中血小板GPIb结合域的表面依赖性表达
5. Understanding the Regulation of the Shear-Enhanced Binding of the Platelet Protein GPIbalpha and the A1 Domain of von Willebrand Factor. [D] . Penkala, Rebecca A. 2010

机译：了解血小板蛋白GPIbalpha和von Willebrand因子的A1结构域的剪切结合的调节。
6. von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib. [O] . I Rabinowitz, E A Tuley, D J Mancuso, 1992

机译：von Willebrand疾病B型：错义突变选择性消除了ristocetin诱导的von Willebrand因子与血小板糖蛋白Ib的结合。
7. von Willebrand disease type B: a missense mutation selectively abolishes ristocetin-induced von Willebrand factor binding to platelet glycoprotein Ib. [O] . Rabinowitz, I, Tuley, E A, Mancuso, D J, 1992

机译：von Willebrand疾病B型：错义突变选择性消除了ristocetin诱导的von Willebrand因子与血小板糖蛋白Ib的结合。

Type 2M von Willebrand Disease: F606I and I662F Mutations in the Glycoprotein Ib Binding Domain Selectively Impair Ristocetin- but not Botrocetin-Mediated Binding of von Willebrand Factor to Platelets

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