These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

289 related articles for article (PubMed ID: 15520867)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Genotypic variation in ATP-binding cassette transporter-1 (ABCA1) as contributors to the high and low high-density lipoprotein-cholesterol (HDL-C) phenotype.
    Mantaring M; Rhyne J; Ho Hong S; Miller M
    Transl Res; 2007 Apr; 149(4):205-10. PubMed ID: 17383594
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Common polymorphisms of ATP binding cassette transporter A1, including a functional promoter polymorphism, associated with plasma high density lipoprotein cholesterol levels in Turks.
    Hodoğlugil U; Williamson DW; Huang Y; Mahley RW
    Atherosclerosis; 2005 Dec; 183(2):199-212. PubMed ID: 15935359
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Screening for functional sequence variations and mutations in ABCA1.
    Probst MC; Thumann H; Aslanidis C; Langmann T; Buechler C; Patsch W; Baralle FE; Dallinga-Thie GM; Geisel J; Keller C; Menys VC; Schmitz G
    Atherosclerosis; 2004 Aug; 175(2):269-79. PubMed ID: 15262183
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Do DNA sequence variants in ABCA1 contribute to HDL cholesterol levels in the general population?
    Pajukanta P
    J Clin Invest; 2004 Nov; 114(9):1244-7. PubMed ID: 15520856
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic variation in the ABCA1 gene, HDL cholesterol, and risk of ischemic heart disease in the general population.
    Frikke-Schmidt R
    Atherosclerosis; 2010 Feb; 208(2):305-16. PubMed ID: 19596329
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A promoter variant of the ATP-binding cassette transporter A1 gene alters the HDL cholesterol level in the general Japanese population.
    Shioji K; Nishioka J; Naraba H; Kokubo Y; Mannami T; Inamoto N; Kamide K; Takiuchi S; Yoshii M; Miwa Y; Kawano Y; Miyata T; Miyazaki S; Goto Y; Nonogi H; Tago N; Iwai N
    J Hum Genet; 2004; 49(3):141-147. PubMed ID: 14986172
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Genetic variation in ABCA1 predicts ischemic heart disease in the general population.
    Frikke-Schmidt R; Nordestgaard BG; Jensen GB; Steffensen R; Tybjaerg-Hansen A
    Arterioscler Thromb Vasc Biol; 2008 Jan; 28(1):180-6. PubMed ID: 17951323
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Novel polypyrimidine variation (IVS46: del T -39...-46) in ABCA1 causes exon skipping and contributes to HDL cholesterol deficiency in a family with premature coronary disease.
    Hong SH; Rhyne J; Miller M
    Circ Res; 2003 Nov; 93(10):1006-12. PubMed ID: 14576201
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tangier disease caused by compound heterozygosity for ABCA1 mutations R282X and Y1532C.
    Cameron J; Ranheim T; Halvorsen B; Kulseth MA; Leren TP; Berge KE
    Atherosclerosis; 2010 Mar; 209(1):163-6. PubMed ID: 19765707
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Relationships between common polymorphisms of adenosine triphosphate-binding cassette transporter A1 and high-density lipoprotein cholesterol and coronary heart disease in a population with type 2 diabetes mellitus.
    Porchay-Baldérelli I; Péan F; Emery N; Maimaitiming S; Bellili N; Travert F; Mohammedi K; Roussel R; Marre M; Fumeron F;
    Metabolism; 2009 Jan; 58(1):74-9. PubMed ID: 19059534
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. ATP-binding cassette transporter A1 locus is not a major determinant of HDL-C levels in a population at high risk for coronary heart disease.
    Kakko S; Kelloniemi J; von Rohr P; Hoeschele I; Tamminen M; Brousseau ME; Kesäniemi YA; Savolainen MJ
    Atherosclerosis; 2003 Feb; 166(2):285-90. PubMed ID: 12535741
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol.
    Candini C; Schimmel AW; Peter J; Bochem AE; Holleboom AG; Vergeer M; Dullaart RP; Dallinga-Thie GM; Hovingh GK; Khoo KL; Fasano T; Bocchi L; Calandra S; Kuivenhoven JA; Motazacker MM
    Atherosclerosis; 2010 Dec; 213(2):492-8. PubMed ID: 20880529
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The effects of ABCG5/G8 polymorphisms on HDL-cholesterol concentrations depend on ABCA1 genetic variants in the Boston Puerto Rican Health Study.
    Junyent M; Tucker KL; Smith CE; Lane JM; Mattei J; Lai CQ; Parnell LD; Ordovas JM
    Nutr Metab Cardiovasc Dis; 2010 Oct; 20(8):558-66. PubMed ID: 19692220
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.