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Genetika ; 49(6): 783-7, 2013 Jun.
Article in Russian | MEDLINE | ID: mdl-24450202

ABSTRACT

Single-nucleotide polymorphisms (SNPs) in the 9p21.3 locus have recently been demonstrated to be strongly associated with the risk of developing human atherosclerotic lesions. However, the pathophysiology of this locus is insufficiently studied. Here, the methylation profile of the nearest mapped genes for cyclin-dependent kinase inhibitors CDKN2A (p16(INK4a), p14(ARF)) and CDKN2B (p15(LNK4b)) in the tissues of the carotid artery in patients with atherosclerosis was evaluated for the first time. Aberrant DNA methylation of the analyzed loci was not established in either the atherosclerotic plaques and in the tissues from the macroscopically unchanged previa vascular wall in the same patients.


Subject(s)
Atherosclerosis/genetics , Cyclin-Dependent Kinase Inhibitor p15/genetics , Cyclin-Dependent Kinase Inhibitor p16/genetics , DNA Methylation , Genetic Loci , Tumor Suppressor Protein p14ARF/genetics , Aged , Atherosclerosis/metabolism , Carotid Arteries/metabolism , Case-Control Studies , Cyclin-Dependent Kinase Inhibitor p15/metabolism , Cyclin-Dependent Kinase Inhibitor p16/metabolism , Humans , Male , Middle Aged , Tumor Suppressor Protein p14ARF/metabolism
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