115 related articles for article (PubMed ID: 31173806)
21. Serum PCSK9 levels, but not PCSK9 polymorphisms, are associated with CAD risk and lipid profiles in southern Chinese Han population.
Cai G; Yu L; Huang Z; Li L; Fu X
Lipids Health Dis; 2018 Sep; 17(1):213. PubMed ID: 30205809
[TBL] [Abstract][Full Text] [Related]
22. Association Study of rs1333040 and rs1004638 Polymorphisms in the 9p21 Locus with Coronary Artery Disease in Southwest of Iran.
Golabgir Khademi K; Foroughmand AM; Galehdari H; Yazdankhah S; Pourmahdi Borujeni M; Shahbazi Z; Dinarvand P
Iran Biomed J; 2016; 20(2):122-7. PubMed ID: 26597055
[TBL] [Abstract][Full Text] [Related]
23. CDKN2BAS gene polymorphisms and the risk of intracranial aneurysm in the Chinese population.
Chen Y; Li G; Fan H; Guo S; Li R; Yin J; Zhang X; Li X; He X; Duan C
BMC Neurol; 2017 Dec; 17(1):214. PubMed ID: 29228923
[TBL] [Abstract][Full Text] [Related]
24. The association of cholesterol absorption gene Numb polymorphism with Coronary Artery Disease among Han Chinese and Uighur Chinese in Xinjiang, China.
Abudoukelimu M; Fu ZY; Maimaiti A; Ma YT; Abudu M; Zhu Q; Adi D; Yang YN; Li XM; Xie X; Liu F; Chen BD
Lipids Health Dis; 2015 Sep; 14():120. PubMed ID: 26415596
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. LncRNA CDKN2BAS rs2157719 genetic variant contributes to medulloblastoma predisposition.
Chen YD; Zhang N; Qiu XG; Yuan J; Yang M
J Gene Med; 2018 Jan; 20(1):. PubMed ID: 29314442
[TBL] [Abstract][Full Text] [Related]
27. The rs2070895 (-250G/A) Single Nucleotide Polymorphism in Hepatic Lipase (HL) Gene and the Risk of Coronary Artery Disease in North Indian Population: A Case-Control Study.
Verma P; Verma DK; Sethi R; Singh S; Krishna A
J Clin Diagn Res; 2016 Aug; 10(8):GC01-6. PubMed ID: 27656463
[TBL] [Abstract][Full Text] [Related]
28. Association of two Common Single Nucleotide Polymorphisms (+45T/G and +276G/T) of ADIPOQ Gene with Coronary Artery Disease in Type 2 Diabetic Patients.
Mohammadzadeh G; Ghaffari MA; Heibar H; Bazyar M
Iran Biomed J; 2016 Jul; 20(3):152-60. PubMed ID: 26781170
[TBL] [Abstract][Full Text] [Related]
29. Association between the XKR6 rs7819412 SNP and serum lipid levels and the risk of coronary artery disease and ischemic stroke.
Zheng PF; Yin RX; Deng GX; Guan YZ; Wei BL; Liu CX
BMC Cardiovasc Disord; 2019 Aug; 19(1):202. PubMed ID: 31429711
[TBL] [Abstract][Full Text] [Related]
30. 9p21.3 coronary artery disease risk locus and interferon alpha 21: Association study in an Asian Indian population.
Kalpana B; Murthy DK; Balakrishna N
Indian Heart J; 2019; 71(6):476-480. PubMed ID: 32248921
[TBL] [Abstract][Full Text] [Related]
31. Incidence of MicroR-4513C/T Gene Variability in Coronary Artery Disease - A Case-Control Study.
Mir R; Jha CK; Elfaki I; Javid J; Rehman S; Khullar N; Banu S; Chahal SMS
Endocr Metab Immune Disord Drug Targets; 2019; 19(8):1216-1223. PubMed ID: 31038082
[TBL] [Abstract][Full Text] [Related]
32. Glutathione S-transferase P1 gene polymorphisms and susceptibility to coronary artery disease in a subgroup of north Indian population.
Bhat MA; Gandhi G
J Genet; 2017 Dec; 96(6):927-932. PubMed ID: 29321351
[TBL] [Abstract][Full Text] [Related]
33. Association of KALRN, ADIPOQ, and FTO gene polymorphism in type 2 diabetic patients with coronary artery disease: possible predisposing markers.
Mofarrah M; Ziaee S; Pilehvar-Soltanahmadi Y; Zarghami F; Boroumand M; Zarghami N
Coron Artery Dis; 2016 Sep; 27(6):490-6. PubMed ID: 27218147
[TBL] [Abstract][Full Text] [Related]
34. Associations between low serum levels of ANRIL and some common gene SNPs in Iranian patients with premature coronary artery disease.
Taheri Bajgan E; Zahedmehr A; Shakerian F; Maleki M; Bakhshandeh H; Mowla SJ; Malakootian M
Sci Rep; 2024 Jan; 14(1):1244. PubMed ID: 38218954
[TBL] [Abstract][Full Text] [Related]
35. Association of the rs1870634 Variant in Long Intergenic Non-protein Coding RNA 841 with Coronary Artery Disease: A GWAS-Replication Study in an Iranian Population.
Tarighi S; Alipoor B; Zare A; Ghaedi H; Shanaki M
Biochem Genet; 2018 Oct; 56(5):522-532. PubMed ID: 29654577
[TBL] [Abstract][Full Text] [Related]
36. Single nucleotide polymorphisms in long noncoding RNA, ANRIL, are not associated with severe periodontitis but with adverse cardiovascular events among patients with cardiovascular disease.
Schulz S; Seitter L; Werdan K; Hofmann B; Schaller HG; Schlitt A; Reichert S
J Periodontal Res; 2018 Oct; 53(5):714-720. PubMed ID: 29732560
[TBL] [Abstract][Full Text] [Related]
37. Polymorphisms of TGFβ-1 and TGFBR2 in relation to coronary artery disease in a Chinese population.
Yang M; Zhu M; Tang L; Zhu H; Lu Y; Xu B; Jiang J; Chen X
Clin Biochem; 2016 Aug; 49(12):873-8. PubMed ID: 27234600
[TBL] [Abstract][Full Text] [Related]
38. Impact of polymorphism rs7041 and rs4588 of Vitamin D Binding Protein on the extent of coronary artery disease.
Daffara V; Verdoia M; Rolla R; Nardin M; Marino P; Bellomo G; Carriero A; De Luca G;
Nutr Metab Cardiovasc Dis; 2017 Sep; 27(9):775-783. PubMed ID: 28779988
[TBL] [Abstract][Full Text] [Related]
39. Analysis of GLT6D1 and CDKN2BAS gene polymorphisms in Brazilian patients with advanced periodontitis.
Rodrigues RS; Rêgo R; Caminaga RMS; Goveia JM; Silveira VRS
Braz Oral Res; 2022; 36():e077. PubMed ID: 35703703
[TBL] [Abstract][Full Text] [Related]
40. The association of functional polymorphisms in genes encoding growth factors for endothelial cells and smooth muscle cells with the severity of coronary artery disease.
Osadnik T; Strzelczyk JK; Lekston A; Reguła R; Bujak K; Fronczek M; Gawlita M; Gonera M; Wasilewski J; Szyguła-Jurkiewicz B; Gierlotka M; Gąsior M
BMC Cardiovasc Disord; 2016 Nov; 16(1):218. PubMed ID: 27835972
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]