Characterization of molecular defect of 13387-9delG mutated antithrombin in inherited type I antithrombin deficiency-Reference-Cited by-同舟云学术

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Characterization of molecular defect of 13387-9delG mutated antithrombin in inherited type I antithrombin deficiency

Published:2005-03 Issue:2 Volume:16 Page:149-155
ISSN:0957-5235
Container-title:Blood Coagulation & Fibrinolysis
language:en
Short-container-title:

Author:

Wang Wen-Bin,Fu Qi-Hua,Ding Qiu-Lan,Zhou Rong-Fu,Wu Wen-Man,Hu Yi-Qun,Wang Xue-Feng,Yan Li-Xing,Wang Zhen-Yi,Wang Hong-Li

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hematology,General Medicine

Reference23 articles.

1. Heparin binding domain of human antithrombin III inferred from the sequential reduction of its three disulfide linkages. An efficient method for structural analysis of partially reduced proteins;Sun;J Biol Chem,1989

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

3. Antithrombin III deficiency;Beresford;Blood Rev,1988

4. Antithrombin and its inherited deficiency states;van Boven;Semin Hematol,1997

5. Antithrombin mutation database: 2nd (1997) update. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis;Lane;Thromb Haemost,1997

Cited by 8 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. Clinical and Molecular Characterization of Nine Novel Antithrombin Mutations;International Journal of Molecular Sciences;2024-03-01

2. Identification and characterization of two SERPINC1 mutations causing congenital antithrombin deficiency;Thrombosis Journal;2023-01-09

3. Genetic Analysis of a Pedigree With Antithrombin and Prothrombin Compound Mutations and Antithrombin Heterozygotes;Frontiers in Genetics;2022-04-04

4. Novel SERPINC1 missense mutation (Cys462Tyr) causes disruption of the 279Cys-462Cys disulfide bond and leads to type Ⅰ hereditary antithrombin deficiency;Clinical Biochemistry;2020-11

5. Clinical Manifestation and Mutation Spectrum of 53 Unrelated Pedigrees with Protein S Deficiency in China;Thrombosis and Haemostasis;2019-01-22

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