Genetic variants and expression study ofFOXP3gene in acute coronary syndrome in Iranian patients-Reference-Cited by-同舟云学术

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Genetic variants and expression study ofFOXP3gene in acute coronary syndrome in Iranian patients

Published:2016-02-29 Issue:3 Volume:34 Page:158-162
ISSN:0263-6484
Container-title:Cell Biochemistry and Function
language:en
Short-container-title:Cell Biochem Funct

Author:

Gholami Milad¹,Esfandiary Ali¹,Vatanparast Masoumeh²,Mirfakhraie Reza¹,Hosseini Mir Mohsen³,Ghafouri-Fard Soudeh¹

Affiliation:

1. Department of Medical Genetics; School of Medicine; Shahid Beheshti University of Medical Sciences; Tehran Iran

2. Cardiovascular Research Center; Shahid Beheshti University of Medical Sciences; Tehran Iran

3. Department of Microbiology; Faculty of Basic and Medical Science; Islamic Azad University, Zanjan Branch; Zanjan Iran

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,General Medicine,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/cbf.3174/fullpdf

Reference22 articles.

1. Heart disease and stroke statistics-2015 update: a report from the American Heart Association;Mozaffarian;Circulation,2015

2. Ambrose JA Singh M Pathophysiology of coronary artery disease leading to acute coronary syndromes 2015 7 08

3. ESC guidelines for the management of acute coronary syndromes in patients presenting without persistent ST-segment elevation: task force for the management of acute coronary syndromes in patients presenting without persistent ST-segment elevation of the European Society of Cardiology (ESC);Roffi;Eur Heart J,2016

4. The Th17/Treg imbalance in patients with acute coronary syndrome;Cheng;Clin Immunol,2008

5. Methylation of FOXP3 in regulatory T cells is related to the severity of coronary artery disease;Jia;Atherosclerosis,2013

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