A complex genomic abnormality found in a patient with antithrombin deficiency and autoimmune disease-like symptoms-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

A complex genomic abnormality found in a patient with antithrombin deficiency and autoimmune disease-like symptoms

Published:2014-06-03 Issue:2 Volume:100 Page:200-205
ISSN:0925-5710
Container-title:International Journal of Hematology
language:en
Short-container-title:Int J Hematol

Author:

Kato Io,Takagi Yuki,Ando Yumi,Nakamura Yuki,Murata Moe,Takagi Akira,Murate Takashi,Matsushita Tadashi,Nakashima Tadaaki,Kojima Tetsuhito

Publisher

Springer Science and Business Media LLC

Subject

Hematology

Link

http://link.springer.com/content/pdf/10.1007/s12185-014-1596-9.pdf

Reference19 articles.

1. Rosenberg RD. Biochemistry of heparin antithrombin interactions, and the physiologic role of this natural anticoagulant mechanism. Am J Med. 1989;87:2S–9S.

2. Cooper PC, Coath F, Daly ME, Makris M. The phenotypic and genetic assessment of antithrombin deficiency. Int J Lab Hematol. 2011;33:227–37.

3. Egeberg O. Inherited antithrombin deficiency causing thrombophilia. Thromb Diath Haemorrh. 1965;13:516–30.

4. Patnaik MM, Moll S. Inherited antithrombin deficiency: a review. Haemophilia. 2008;14:1229–39.

5. Ishiguro K, Kojima T, Kadomatsu K, Nakayama Y, Takagi A, Suzuki M, et al. Complete antithrombin deficiency in mice results in embryonic lethality. J Clin Invest. 2000;106:873–8.

Cited by 15 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. Long-range and real-time PCR identification of a large SERPINC1 deletion in a patient with antithrombin deficiency;International Journal of Hematology;2024-05-27

2. Regulation of inflammatory diseases via the control of mRNA decay;Inflammation and Regeneration;2024-03-15

3. Regulation of non-coding RNA promoters;Bidirectional Gene Promoters;2023

4. Roquin-dependent gene regulation in immune-mediated diseases and future therapies;International Immunology;2022-12-16

5. Long-Read Sequencing Identifies the First Retrotransposon Insertion and Resolves Structural Variants Causing Antithrombin Deficiency;Thrombosis and Haemostasis;2022-06-28

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3