188 related articles for article (PubMed ID: 33776563)
21. Association between genetic polymorphisms in fibrinogen genes and bleeding risk in patients treated with direct oral anticoagulants.
Choi KH; Yee J; Song TJ; Park J; Gwak HS
Ann Acad Med Singap; 2023 Jul; 52(7):340-347. PubMed ID: 38904499
[TBL] [Abstract][Full Text] [Related]
22. Modulation of the risk of coronary sclerosis/myocardial infarction by the interaction between factor XIII subunit A Val34Leu polymorphism and fibrinogen concentration in the high risk Hungarian population.
Bereczky Z; Balogh E; Katona E; Pocsai Z; Czuriga I; Széles G; Kárpáti L; Adány R; Edes I; Muszbek L
Thromb Res; 2007; 120(4):567-73. PubMed ID: 17250879
[TBL] [Abstract][Full Text] [Related]
23. alpha-fibrinogen Thr312Ala polymorphism and venous thromboembolism.
Carter AM; Catto AJ; Kohler HP; Ariëns RA; Stickland MH; Grant PJ
Blood; 2000 Aug; 96(3):1177-9. PubMed ID: 10910940
[TBL] [Abstract][Full Text] [Related]
24. Role of blood coagulation factor XIII in patients with acute pulmonary embolism. Correlation of factor XIII antigen levels with pulmonary occlusion rate, fibrinogen, D-dimer, and clot firmness.
Kucher N; Schroeder V; Kohler HP
Thromb Haemost; 2003 Sep; 90(3):434-8. PubMed ID: 12958612
[TBL] [Abstract][Full Text] [Related]
25. The association of alpha-fibrinogen Thr312Ala polymorphism and venous thromboembolism in the LITE study.
Rasmussen-Torvik LJ; Cushman M; Tsai MY; Zhang Y; Heckbert SR; Rosamond WD; Folsom AR
Thromb Res; 2007; 121(1):1-7. PubMed ID: 17433418
[TBL] [Abstract][Full Text] [Related]
26. Monocyte chemoattractant protein-1 gene (MCP-1) polymorphisms are associated with risk of premature coronary artery disease in Mexican patients from the Genetics of Atherosclerotic Disease (GEA) study.
Angeles-Martínez J; Posadas-Sánchez R; Álvarez-León E; Villarreal-Molina T; Cardoso-Saldaña G; Fragoso JM; Juárez-Rojas JG; Medina-Urrutia A; Posadas-Romero C; Vargas-Alarcón G
Immunol Lett; 2015 Oct; 167(2):125-30. PubMed ID: 26277553
[TBL] [Abstract][Full Text] [Related]
27. Genetic polymorphisms influencing total and γ' fibrinogen levels and fibrin clot properties in Africans.
Kotzé RC; Nienaber-Rousseau C; De Lange Z; De Maat MP; Hoekstra T; Pieters M
Br J Haematol; 2015 Jan; 168(1):102-12. PubMed ID: 25156046
[TBL] [Abstract][Full Text] [Related]
28. A Case-Control Study of the Association of the Polymorphisms of MTHFR and APOE with Risk Factors and the Severity of Coronary Artery Disease.
Long Y; Zhao XT; Liu C; Sun YY; Ma YT; Liu XY; Liu JX
Cardiology; 2019; 142(3):149-157. PubMed ID: 31163415
[TBL] [Abstract][Full Text] [Related]
29. Haplotype-based association of four lymphotoxin-alpha gene polymorphisms with the risk of coronary artery disease in Han Chinese.
Liu Y; Sheng H; Lu L; Wu Z; Chen Q; Xiao H; Jin W
Tohoku J Exp Med; 2011 Jun; 224(2):119-25. PubMed ID: 21628868
[TBL] [Abstract][Full Text] [Related]
30. Coagulation factor XIII-A Val34Leu polymorphism and the risk of coronary artery disease and myocardial infarction in a Chinese Han population.
Guodong Jin ; Beili Feng ; Peng Chen ; Oushan Tang ; Jian Wang ; Ji Ma ; Yuping Shi ; Geng Xu
Clin Appl Thromb Hemost; 2011 Apr; 17(2):208-13. PubMed ID: 20211923
[TBL] [Abstract][Full Text] [Related]
31. Association of genetic variants of hemostatic genes with myocardial infarction in Egyptian patients.
El-Fattah AAA; Sadik NAH; Sedrak H; Battah A; Nabil M
Gene; 2018 Jan; 641():212-219. PubMed ID: 29054763
[TBL] [Abstract][Full Text] [Related]
32. The prevalence of C807T mutation of glycoprotein Ia gene among young male survivors of myocardial infarction: a relation with coronary angiography results.
Lewandowski K; Swierczyńska A; Kwaśnikowski P; Elikowski W; Rzeźniczak M
Kardiol Pol; 2005 Aug; 63(2):107-13; discussion114. PubMed ID: 16136407
[TBL] [Abstract][Full Text] [Related]
33. RRM1, RRM2 and ERCC2 Gene Polymorphisms in Coronary Artery Disease.
Altinkilic EM; Isbir S; Gormus U; Yilmaz SG; Dalan AB; Duman S; Isbir T
In Vivo; 2016 09-10; 30(5):611-5. PubMed ID: 27566080
[TBL] [Abstract][Full Text] [Related]
34. Activity and levels of factor XIII in a Venezuelan admixed population: association with rs5985 (Val35Leu) and STR F13A01 polymorphisms.
Vívenes M; Castro de Guerra D; Rodríguez-Larralde A; Arocha-Piñango CL; Guerrero B
Thromb Res; 2012 Nov; 130(5):729-34. PubMed ID: 22909824
[TBL] [Abstract][Full Text] [Related]
35. Beta-fibrinogen gene-455 G/A polymorphism and fibrinogen levels. Risk factors for coronary artery disease in subjects with NIDDM.
Carter AM; Mansfield MW; Stickland MH; Grant PJ
Diabetes Care; 1996 Nov; 19(11):1265-8. PubMed ID: 8908392
[TBL] [Abstract][Full Text] [Related]
36. Factor VII R353Q (rs6046), FGA A6534G (rs6050), and FGG C10034T (rs2066865) Gene Polymorphisms and Risk of Recurrent Pregnancy Loss in Iranian Women.
Kavosh Z; Mohammadzadeh Z; Alizadeh S; Sharifi MJ; Hajizadeh S; Choobineh H; Omidkhoda A
Indian J Hematol Blood Transfus; 2024 Apr; 40(2):297-302. PubMed ID: 38708173
[TBL] [Abstract][Full Text] [Related]
37. Elevated plasma fibrinogen gamma' concentration is associated with myocardial infarction: effects of variation in fibrinogen genes and environmental factors.
Mannila MN; Lovely RS; Kazmierczak SC; Eriksson P; Samnegård A; Farrell DH; Hamsten A; Silveira A
J Thromb Haemost; 2007 Apr; 5(4):766-73. PubMed ID: 17263791
[TBL] [Abstract][Full Text] [Related]
38. The T-786C endothelial nitric oxide synthase genotype is a novel risk factor for coronary artery disease in Caucasian patients of the GENICA study.
Rossi GP; Cesari M; Zanchetta M; Colonna S; Maiolino G; Pedon L; Cavallin M; Maiolino P; Pessina AC
J Am Coll Cardiol; 2003 Mar; 41(6):930-7. PubMed ID: 12651036
[TBL] [Abstract][Full Text] [Related]
39. Fibrinogen Aα Thr312Ala polymorphism specifically contributes to chronic thromboembolic pulmonary hypertension by increasing fibrin resistance.
Li JF; Lin Y; Yang YH; Gan HL; Liang Y; Liu J; Yang SQ; Zhang WJ; Cui N; Zhao L; Zhai ZG; Wang J; Wang C
PLoS One; 2013; 8(7):e69635. PubMed ID: 23894515
[TBL] [Abstract][Full Text] [Related]
40. The differential effects of age on the association of KLOTHO gene polymorphisms with coronary artery disease.
Rhee EJ; Oh KW; Lee WY; Kim SY; Jung CH; Kim BJ; Sung KC; Kim BS; Kang JH; Lee MH; Kim SW; Park JR
Metabolism; 2006 Oct; 55(10):1344-51. PubMed ID: 16979405
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
