127 related articles for article (PubMed ID: 22311493)
21. ATP-binding cassette transporter A1 gene I823M polymorphism affects plasma high-density lipoprotein cholesterol level and modifies the effect of low high-density lipoprotein cholesterol on the risk of coronary artery disease.
Tsai CT; Hwang JJ; Chiang FT; Tseng CD; Lin JL; Tseng YZ; Lai LP
Cardiology; 2007; 107(4):321-8. PubMed ID: 17268197
[TBL] [Abstract][Full Text] [Related]
22. Effect of fenofibrate therapy and ABCA1 polymorphisms on high-density lipoprotein subclasses in the Genetics of Lipid Lowering Drugs and Diet Network.
Tsai MY; Ordovas JM; Li N; Straka RJ; Hanson NQ; Arends VL; Arnett D
Mol Genet Metab; 2010 Jun; 100(2):118-22. PubMed ID: 20346718
[TBL] [Abstract][Full Text] [Related]
23. [Effect of transcription activity regulated by VNTR-ZNF and -14C/T variants in the promoter region of ATP-binding cassette transporter 1 in HepG2 cells].
Gao S; Zhao L; Zhang Y; Mao Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):633-6. PubMed ID: 27577210
[TBL] [Abstract][Full Text] [Related]
24. Associations of the ATP-binding cassette transporter A1 R219K polymorphism with HDL-C level and coronary artery disease risk: a meta-analysis.
Ma XY; Liu JP; Song ZY
Atherosclerosis; 2011 Apr; 215(2):428-34. PubMed ID: 21310416
[TBL] [Abstract][Full Text] [Related]
25. Genetic variants in ABCA1 promoter affect transcription activity and plasma HDL level in pigs.
Dang XY; Chu WW; Shi HC; Yu SG; Han HY; Gu SH; Chen J
Gene; 2015 Jan; 555(2):414-20. PubMed ID: 25445391
[TBL] [Abstract][Full Text] [Related]
26. Novel rare mutations and promoter haplotypes in ABCA1 contribute to low-HDL-C levels.
Slatter TL; Jones GT; Williams MJ; van Rij AM; McCormick SP
Clin Genet; 2008 Feb; 73(2):179-84. PubMed ID: 18199144
[TBL] [Abstract][Full Text] [Related]
27. ABCA1 single nucleotide polymorphisms on high-density lipoprotein-cholesterol and overweight: the D.E.S.I.R. study.
Porchay I; Péan F; Bellili N; Royer B; Cogneau J; Chesnier MC; Caradec A; Tichet J; Balkau B; Marre M; Fumeron F
Obesity (Silver Spring); 2006 Nov; 14(11):1874-9. PubMed ID: 17135600
[TBL] [Abstract][Full Text] [Related]
28. Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population.
Frikke-Schmidt R; Nordestgaard BG; Jensen GB; Tybjaerg-Hansen A
J Clin Invest; 2004 Nov; 114(9):1343-53. PubMed ID: 15520867
[TBL] [Abstract][Full Text] [Related]
29. Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients.
Kyriakou T; Pontefract DE; Viturro E; Hodgkinson CP; Laxton RC; Bogari N; Cooper G; Davies M; Giblett J; Day IN; Simpson IA; Albrecht C; Ye S
Hum Mol Genet; 2007 Jun; 16(12):1412-22. PubMed ID: 17412755
[TBL] [Abstract][Full Text] [Related]
30. Association of HDL deficiency with a novel mutation in the ABCA1 gene.
Denk GU; Aslanidis C; Schmitz G; Parhofer KG; Pusl T
Exp Clin Endocrinol Diabetes; 2011 Jan; 119(1):53-5. PubMed ID: 20533173
[TBL] [Abstract][Full Text] [Related]
31. A novel haplotype in ABCA1 gene effects plasma HDL-C concentration.
Saleheen D; Khanum S; Haider SR; Nazir A; Ahmad U; Khalid H; Hussain I; Shuja F; Shahid K; Habib A; Frossard PM
Int J Cardiol; 2007 Jan; 115(1):7-13. PubMed ID: 16806540
[TBL] [Abstract][Full Text] [Related]
32. Common and rare ABCA1 variants affecting plasma HDL cholesterol.
Wang J; Burnett JR; Near S; Young K; Zinman B; Hanley AJ; Connelly PW; Harris SB; Hegele RA
Arterioscler Thromb Vasc Biol; 2000 Aug; 20(8):1983-9. PubMed ID: 10938021
[TBL] [Abstract][Full Text] [Related]
33. Promoter haplotype of a new ABCA1 mutant influences expression of familial hypoalphalipoproteinemia.
Slatter TL; Williams MJ; Frikke-Schmidt R; Tybjaerg-Hansen A; Morison IM; McCormick SP
Atherosclerosis; 2006 Aug; 187(2):393-400. PubMed ID: 16225879
[TBL] [Abstract][Full Text] [Related]
34. R219K polymorphism of ATP binding cassette transporter A1 related with low HDL in overweight/obese Thai males.
Kitjaroentham A; Hananantachai H; Tungtrongchitr A; Pooudong S; Tungtrongchitr R
Arch Med Res; 2007 Nov; 38(8):834-8. PubMed ID: 17923263
[TBL] [Abstract][Full Text] [Related]
35. Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease.
Clee SM; Zwinderman AH; Engert JC; Zwarts KY; Molhuizen HO; Roomp K; Jukema JW; van Wijland M; van Dam M; Hudson TJ; Brooks-Wilson A; Genest J; Kastelein JJ; Hayden MR
Circulation; 2001 Mar; 103(9):1198-205. PubMed ID: 11238261
[TBL] [Abstract][Full Text] [Related]
36. ATP-binding cassette transporter A1 gene polymorphisms and serum lipid levels in young Greek nurses.
Kolovou V; Kolovou G; Marvaki A; Karakosta A; Vasilopoulos G; Kalogiani A; Degiannis D; Marvaki C; Demopoulos CA
Lipids Health Dis; 2011 Apr; 10():56. PubMed ID: 21489276
[TBL] [Abstract][Full Text] [Related]
37. Genotypic effect of the -565C>T polymorphism in the ABCA1 gene promoter on ABCA1 expression and severity of atherosclerosis.
Kyriakou T; Hodgkinson C; Pontefract DE; Iyengar S; Howell WM; Wong YK; Eriksson P; Ye S
Arterioscler Thromb Vasc Biol; 2005 Feb; 25(2):418-23. PubMed ID: 15528481
[TBL] [Abstract][Full Text] [Related]
38. Association between the ABCA1-565C/T gene promoter polymorphism and coronary heart disease severity and cholesterol efflux in the Chinese Han population.
Qi LP; Chen LF; Dang AM; Li LY; Fang Q; Yan XW
Genet Test Mol Biomarkers; 2015 Jul; 19(7):347-52. PubMed ID: 26090796
[TBL] [Abstract][Full Text] [Related]
39. HDL particle size is a critical determinant of ABCA1-mediated macrophage cellular cholesterol export.
Du XM; Kim MJ; Hou L; Le Goff W; Chapman MJ; Van Eck M; Curtiss LK; Burnett JR; Cartland SP; Quinn CM; Kockx M; Kontush A; Rye KA; Kritharides L; Jessup W
Circ Res; 2015 Mar; 116(7):1133-42. PubMed ID: 25589556
[TBL] [Abstract][Full Text] [Related]
40. Increase in HDL-C concentration by a dietary portfolio with soy protein and soluble fiber is associated with the presence of the ABCA1R230C variant in hyperlipidemic Mexican subjects.
Guevara-Cruz M; Tovar AR; Larrieta E; Canizales-Quinteros S; Torres N
Mol Genet Metab; 2010; 101(2-3):268-72. PubMed ID: 20797885
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
