Gly197Arg mutation in protein C causes recurrent thrombosis in a heterozygous carrier-Reference-Cited by-同舟云学术

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Gly197Arg mutation in protein C causes recurrent thrombosis in a heterozygous carrier

Published:2020-04-09 Issue:5 Volume:18 Page:1141-1153
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

Lu Yeling¹²,Giri Hemant²,Villoutreix Bruno O.³,Ding Qiulan¹,Wang Xuefeng¹,Rezaie Alireza R.²⁴^ORCID

Affiliation:

1. Department of Laboratory Medicine Ruijin Hospital Shanghai Jiaotong University School of Medicine Shanghai China

2. Cardiovascular Biology Research Program Oklahoma Medical Research Foundation Oklahoma City OK, USA

3. University of Lille Inserm Institut Pasteur de Lille U1177 ‐ Drugs and Molecules for Living Systems Lille France

4. Department of Biochemistry and Molecular Biology University of Oklahoma Health Sciences Center Oklahoma City OK, USA

Funder

National Heart, Lung, and Blood Institute

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jth.14777

Reference37 articles.

1. Molecular Events that Control the Protein C Anticoagulant Pathway

2. Regulation of blood coagulation by the protein C system

3. Characterization of a cDNA coding for human protein C.

4. Structure-function relationships of epidermal growth factor modules in vitamin K-dependent clotting factors

5. The 2.8 A crystal structure of Gla-domainless activated protein C.

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Met343Val mutation disrupts the shuttling of Trp380 leading to a low-activity conformer of activated protein C and causes thrombosis;Journal of Thrombosis and Haemostasis;2024-08

2. Mutation Ter462GlnextTer17 introduces a tail to C-terminus of protein C and causes venous thrombosis;Thrombosis Research;2024-08

3. Analysis of four hereditary protein C deficiencies associated with vascular thromboembolism;Annals of Hematology;2024-03-04

4. Analysis of Four Hereditary Protein C Deficiencies Associated with Vascular Thromboembolism;2023-12-19

5. Ser252Asn Mutation Introduces a New N-Linked Glycosylation Site and Causes Type IIb Protein C Deficiency;Thrombosis and Haemostasis;2023-11-27

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