Unraveling von Willebrand factor deficiency.
作者信息
Hayward Catherine P M
机构信息
McMaster University.
出版信息
Blood. 2021 Jun 10;137(23):3160-3161. doi: 10.1182/blood.2021010942.
Abstract
摘要
相似文献
1
Unraveling von Willebrand factor deficiency.解析血管性血友病因子缺乏症
Blood. 2021 Jun 10;137(23):3160-3161. doi: 10.1182/blood.2021010942.
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Factor VIII/von Willebrand factor binding to von Willebrand's disease platelets.因子VIII/血管性血友病因子与血管性血友病血小板的结合。
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Variants of von Willebrand's disease.血管性血友病的变异型
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Rapid assay for von Willebrand factor activity using formalin-fixed platelets and microtitration technic.使用福尔马林固定血小板和微量滴定技术快速检测血管性血友病因子活性
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Role of the von Willebrand factor in atherogenesis.血管性血友病因子在动脉粥样硬化形成中的作用。
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The varieties of von Willebrand's disease.血管性血友病的类型。
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本文引用的文献
1
ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease.ASH ISTH NHF 2021 指南：关于血管性血友病的诊断。
Blood Adv. 2021 Jan 12;5(1):280-300. doi: 10.1182/bloodadvances.2020003265.
2
von Willebrand factor antigen levels are associated with burden of rare nonsynonymous variants in the VWF gene.血管性血友病因子抗原水平与 VWF 基因中罕见非同义变异的负担有关。
Blood. 2021 Jun 10;137(23):3277-3283. doi: 10.1182/blood.2020009999.
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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls.20791 例 2 型糖尿病病例和 24440 例对照的外显子组测序。
Nature. 2019 Jun;570(7759):71-76. doi: 10.1038/s41586-019-1231-2. Epub 2019 May 22.
4
Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.全基因组关联跨种族荟萃分析鉴定出调控凝血因子 VIII 和血管性血友病因子血浆水平的新关联。
Circulation. 2019 Jan 29;139(5):620-635. doi: 10.1161/CIRCULATIONAHA.118.034532.
5
Genetic regulation of plasma von Willebrand factor levels in health and disease.遗传调控健康和疾病状态下的血浆血管性血友病因子水平。
J Thromb Haemost. 2018 Dec;16(12):2375-2390. doi: 10.1111/jth.14304. Epub 2018 Oct 30.
6
Comorbidities associated with higher von Willebrand factor (VWF) levels may explain the age-related increase of VWF in von Willebrand disease.与较高 von Willebrand 因子 (VWF) 水平相关的合并症可能解释了 von Willebrand 病中 VWF 随年龄增长而增加的原因。
Br J Haematol. 2018 Jul;182(1):93-105. doi: 10.1111/bjh.15277. Epub 2018 May 16.
7
Novel insights into the clinical phenotype and pathophysiology underlying low VWF levels.对低血管性血友病因子（VWF）水平潜在的临床表型和病理生理学的新见解。
Blood. 2017 Nov 23;130(21):2344-2353. doi: 10.1182/blood-2017-05-786699. Epub 2017 Sep 15.
8
Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.非裔美国人常见和罕见血管性血友病因子 (VWF) 编码变异体、VWF 水平和因子 VIII 水平：美国国立卫生研究院外显子组测序计划。
Blood. 2013 Jul 25;122(4):590-7. doi: 10.1182/blood-2013-02-485094. Epub 2013 May 20.
9
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants.对 6515 个外显子组的分析揭示了大多数人类蛋白质编码变异的近期起源。
Nature. 2013 Jan 10;493(7431):216-20. doi: 10.1038/nature11690. Epub 2012 Nov 28.
10
Evolution and functional impact of rare coding variation from deep sequencing of human exomes.人类外显子组深度测序中罕见编码变异的进化和功能影响。
Science. 2012 Jul 6;337(6090):64-9. doi: 10.1126/science.1219240. Epub 2012 May 17.
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