A novel Ala275Val mutation in factor X gene influences its structural compatibility and impairs intracellular trafficking and coagulant activity-Reference-Cited by-同舟云学术

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A novel Ala275Val mutation in factor X gene influences its structural compatibility and impairs intracellular trafficking and coagulant activity

Published:2016-02 Issue: Volume:138 Page:108-113
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Sun Nannan,Chen Yongheng,Peng Hongling,Luo Yujiao,Zhang Guangsen

Funder

National Natural Science Foundation, PR China

Famous Clinical Doctors in Xiang-Ya Medical College of Central South University

Publisher

Elsevier BV

Subject

Hematology

Reference27 articles.

1. Factor X deficiency;Menegatti;Semin. Thromb. Hemost.,2009

2. Coagulant protein of Russell's viper venom;Furie;Methods Enzymol.,1976

3. Gene for human factor X: a blood coagulation factor whose gene organization is essentially identical with that of factor IX and protein C;Leytus;Biochemistry,1986

4. Structure-function relationships of epidermal growth factor modules in vitamin K-dependent clotting factors;Stenflo;Blood,1991

5. Comparative modeling methods: application to the family of the mammalian serine proteases;Greer;Proteins,1990

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1. Molecular basis of rare congenital bleeding disorders;Blood Reviews;2023-05

2. Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiency;Blood Reviews;2021-11

3. Molecular mechanism of a novel Ser362Asn mutation causing inherited FX deficiency in a Chinese family;International Journal of Hematology;2020-04-13

4. Rare bleeding disorders and advances in gene therapy;Blood Coagulation & Fibrinolysis;2019-12

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