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Genetika ; 49(6): 783-7, 2013 Jun.
Artigo em Russo | MEDLINE | ID: mdl-24450202

RESUMO

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.


Assuntos
Aterosclerose/genética , Inibidor de Quinase Dependente de Ciclina p15/genética , Inibidor p16 de Quinase Dependente de Ciclina/genética , Metilação de DNA , Loci Gênicos , Proteína Supressora de Tumor p14ARF/genética , Idoso , Aterosclerose/metabolismo , Artérias Carótidas/metabolismo , Estudos de Casos e Controles , Inibidor de Quinase Dependente de Ciclina p15/metabolismo , Inibidor p16 de Quinase Dependente de Ciclina/metabolismo , Humanos , Masculino , Pessoa de Meia-Idade , Proteína Supressora de Tumor p14ARF/metabolismo
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