Subtypes of SERPINC1 mutations and the thrombotic phenotype of inherited antithrombin deficient individuals in Chinese Han population-Reference-Cited by-同舟云学术

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Subtypes of SERPINC1 mutations and the thrombotic phenotype of inherited antithrombin deficient individuals in Chinese Han population

Published:2016-11 Issue: Volume:62 Page:38-41
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Wang Dong,Cui Guanglin,Hu Senlin,Wang Dao Wen

Funder

National Natural Science Foundation of China

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference26 articles.

1. Antithrombin: the principal inhibitor of thrombin;Olds;Semin. Thromb. Hemost.,1994

2. Molecular genetics of human antithrombin deficiency;Perry;Hum. Mutat.,1996

3. Assignment of the human antithrombin III structural gene to chromosome 1q23–25;Bock;Cytogenet. Cell Genet.,1985

4. Regulation of thrombin activity by antithrombin and heparin;Olson;Semin. Thromb. Hemost.,1994

5. The anticoagulant activation of antithrombin by heparin;Jin;Proc. Natl. Acad. Sci. U. S. A.,1997

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1. Investigation of the Differences in Antithrombin to Heparin Binding among Antithrombin Budapest 3, Basel, and Padua Mutations by Biochemical and In Silico Methods;Biomolecules;2021-04-08

2. A Translational Model for Venous Thromboembolism: MicroRNA Expression in Hibernating Black Bears;Journal of Surgical Research;2021-01

3. Type II antithrombin deficiency caused by a novel missense mutation (p.Leu417Gln) in a Chinese family;Blood Coagulation & Fibrinolysis;2021-01

4. A novel mutation of SERPINC1 in a patient presenting as recurrent cerebral sinus venous and portal vein thrombosis;Blood Coagulation & Fibrinolysis;2020-04

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