Impact of hemostatic gene single point mutations in patients with non-diabetic coronary artery disease-Reference-Cited by-同舟云学术

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Impact of hemostatic gene single point mutations in patients with non-diabetic coronary artery disease

Published:2009-01-03 Issue:8 Volume:36 Page:2235-2243
ISSN:0301-4851
Container-title:Molecular Biology Reports
language:en
Short-container-title:Mol Biol Rep

Author:

Var Ahmet,Ütük Ozan,Akçalı Sinem,Şanlıdağ Tamer,Uyanık Bekir S.,Dinç Gönül

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s11033-008-9439-5.pdf

Reference54 articles.

1. Nordlie MA, Wold LE, Kloner RA (2005) Genetic contributors toward increased risk for ischemic heart disease. J Mol Cell Cardiol 39:667–679. doi: 10.1016/j.yjmcc.2005.06.006

2. Atherosclerosis, thrombosclerosis and vascular biology Italian study group (2003) No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age. Circulation 107:1117–1122. doi: 10.1161/01.CIR.0000051465.94572.D0

3. Pastinen T, Perola M, Niini P, Terwilliger J, Salomaa V, Vartiainen E, Peltonen L, Syvänen A (1998) Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population. Hum Mol Genet 7:1453–1462. doi: 10.1093/hmg/7.9.1453

4. Uitte de Willige S, de Visser MC, Houwing-Duistermaat JJ, Rosendaal FR, Vos HL, Bertina RM (2005) Genetic variation in the fibrinogen gamma gene increases the risk for deep venous thrombosis by reducing plasma fibrinogen gamma levels. Blood 106:4176–4183. doi: 10.1182/blood-2005-05-2180

5. Duga S, Asselta R, Santagostino E, Zeinali S, Simonic T, Malcovati M, Mannucci PM, Tenchini ML (2000) Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion. Blood 95:1336–1341

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2. Giresun İlinde FV, FXIII, ACE, ApoE Gen Varyantlarının Prevelansı ve Koroner Arter Hastalığı Profiline Etkilerinin Araştırılması;İstanbul Gelişim Üniversitesi Sağlık Bilimleri Dergisi;2019-12-31

3. Synergic predisposing effect of G894T (eNOS), 4G/5G (PAI) and T1131C (APOA5) polymorphisms to myocardial infarction;Gene Reports;2018-06

4. Association of FV G1691A Polymorphism but not A4070G With Coronary Artery Disease;Clinical and Applied Thrombosis/Hemostasis;2017-11-27

5. Features of coronary artery disease in patients with different genotypes of PAI-1 gene;Kazan medical journal;2017-04-15

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