Quest for Genes and Mechanisms Linking the Human Chromosome 9p21.3 Locus to Cardiovascular Disease

被引：5
作者：
Hamsten, Anders [1 ]
Eriksson, Per
机构：
[1] Karolinska Inst, Karolinska Univ Hosp, Ctr Mol Med, Atherosclerosis Res Unit,Dept Med Solna, S-17176 Stockholm, Sweden
来源：
CIRCULATION | 2012年 / 126卷 / 15期
关键词：
Editorials; atherosclerosis; cardiovascular diseases; polymorphism; single nucleotide; CORONARY-ARTERY-DISEASE; ATHEROSCLEROSIS; ANRIL; SUSCEPTIBILITY; IDENTIFICATION; ASSOCIATION; DELETION;
D O I：
10.1161/CIRCULATIONAHA.112.136556
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
[No abstract available]
引用
收藏
页码：1815 / 1817
页数：3
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  • [1] Association of genetic variation on chromosome 9p21.3 and arterial stiffness
    Bjorck, H. M.
    Lanne, T.
    Alehagen, U.
    Persson, K.
    Rundkvist, L.
    Hamsten, A.
    Dahlstrom, U.
    Eriksson, P.
    [J]. JOURNAL OF INTERNAL MEDICINE, 2009, 265 (03) : 373 - 381
  • [2] Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p
    Broadbent, Helen M.
    Peden, John F.
    Lorkowski, Stefan
    Goel, Anuj
    Ongen, Halit
    Green, Fiona
    Clarke, Robert
    Collins, Rory
    Franzosi, Maria Grazia
    Tognoni, Gianni
    Seedorf, Udo
    Rust, Stephan
    Eriksson, Per
    Hamsten, Anders
    Farrall, Martin
    Watkins, Hugh
    [J]. HUMAN MOLECULAR GENETICS, 2008, 17 (06) : 806 - 814
  • [3] Expression of Linear and Novel Circular Forms of an INK4/ARF-Associated Non-Coding RNA Correlates with Atherosclerosis Risk
    Burd, Christin E.
    Jeck, William R.
    Liu, Yan
    Sanoff, Hanna K.
    Wang, Zefeng
    Sharpless, Norman E.
    [J]. PLOS GENETICS, 2010, 6 (12) : 1 - 15
  • [4] Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression
    Cunnington, Michael S.
    Koref, Mauro Santibanez
    Mayosi, Bongani M.
    Burn, John
    Keavney, Bernard
    [J]. PLOS GENETICS, 2010, 6 (04):
  • [5] Relationship between CAD Risk Genotype in the Chromosome 9p21 Locus and Gene Expression. Identification of Eight New ANRIL Splice Variants
    Folkersen, Lasse
    Kyriakou, Theodosios
    Goel, Anuj
    Peden, John
    Malarstig, Anders
    Paulsson-Berne, Gabrielle
    Hamsten, Anders
    Franco-Cereceda, Anders
    Gabrielsen, Anders
    Eriksson, Per
    Watkins, Hugh
    [J]. PLOS ONE, 2009, 4 (11):
  • [6] p19ARF Deficiency Reduces Macrophage and Vascular Smooth Muscle Cell Apoptosis and Aggravates Atherosclerosis
    Gonzalez-Navarro, Herminia
    Abu Nabah, Yafa Naim
    Vinue, Angela
    Andres-Manzano, Maria J.
    Collado, Manuel
    Serrano, Manuel
    Andres, Vicente
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2010, 55 (20) : 2258 - 2268
  • [7] 9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response
    Harismendy, Olivier
    Notani, Dimple
    Song, Xiaoyuan
    Rahim, Nazli G.
    Tanasa, Bogdan
    Heintzman, Nathaniel
    Ren, Bing
    Fu, Xiang-Dong
    Topol, Eric J.
    Rosenfeld, Michael G.
    Frazer, Kelly A.
    [J]. NATURE, 2011, 470 (7333) : 264 - +
  • [8] Recent Studies of the Human Chromosome 9p21 Locus, Which Is Associated With Atherosclerosis in Human Populations
    Holdt, Lesca M.
    Teupser, Daniel
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2012, 32 (02) : 196 - 206
  • [9] Expression of Chr9p21 genes CDKN2B (p15INK4b), CDKN2A (p16INK4a, p14ARF) and MTAP in human atherosclerotic plaque
    Holdt, Lesca Miriam
    Sass, Kristina
    Gaebel, Gabor
    Bergert, Hendrik
    Thiery, Joachim
    Teupser, Daniel
    [J]. ATHEROSCLEROSIS, 2011, 214 (02) : 264 - 270
  • [10] Functional Analysis of the Chromosome 9p21.3 Coronary Artery Disease Risk Locus
    Jarinova, Olga
    Stewart, Alexandre F. R.
    Roberts, Robert
    Wells, George
    Lau, Paulina
    Naing, Thet
    Buerki, Christine
    McLean, Bradley W.
    Cook, Richard C.
    Parker, Joel S.
    McPherson, Ruth
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2009, 29 (10) : 1671 - U670
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