Literature DB >> 27098850

Molecular structural analysis of a novel and de-novo mutation in the SERPINC1 gene associated with type 1 antithrombin deficiency.

Tzu-Fei Wang1, Jennifer E Dawson2,3, Julie D Forman-Kay2,3, Walter H A Kahr3,4,5, Suzan Williams5, Anthony K Chan6, Riten Kumar7.   

Abstract

Entities:  

Keywords:  zzm321990SERPINC1zzm321990; antithrombin; molecular structure; thermodynamic stability; thrombophilia

Mesh：

Substances：

Year:  2016        PMID： 27098850     DOI： 10.1111/bjh.14090

Source DB:  PubMed          Journal:  Br J Haematol        ISSN： 0007-1048            Impact factor:   6.998


× No keyword cloud information.
  2 in total

1.  Gene analysis of inherited antithrombin deficiency and functional analysis of abnormal antithrombin protein (N87D).

Authors:  Sayaka Kamijima; Akiko Sekiya; Mao Takata; Haruka Nakano; Morika Murakami; Tomonori Nakazato; Hidesaku Asakura; Eriko Morishita
Journal:  Int J Hematol       Date:  2017-10-25       Impact factor: 2.490

2.  A case report of atrial fibrillation in a patient with heparin resistance associated with an antithrombin III deficiency successfully treated by radiofrequency catheter ablation using a direct thrombin inhibitor.

Authors:  Honsa Kang; Masao Takemoto; Kei-Ichiro Tayama; Ken-Ichi Kosuga
Journal:  Eur Heart J Case Rep       Date:  2019-01-09
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.