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Chin. med. j ; Chin. med. j;(24): 166-170, 2003.
Artigo em Inglês | WPRIM | ID: wpr-356842

RESUMO

<p><b>OBJECTIVE</b>To clone the full-length cDNA of a gene responsible for vascular smooth muscle cell (v-SMC) proliferation in atherogenesis, and study its function.</p><p><b>METHODS</b>Oxidized low density lipoprotein (ox-LDL) at optimal concentration was used as the stimulant to induce v-SMC proliferation in culture medium. A cDNA subtractive library of v-SMC proliferation specific to ox-LDL stimulation was established using subtractive hybridization technique. Methods, including blotting, Northern hybridization and gene sequencing, were used to clone new gene fragments. By using full-length cDNA screening and protein expression techniques, one full-length cDNA was cloned and its function was studied.</p><p><b>RESULTS</b>One full-length cDNA was cloned. The new gene (Genbank AF 174647) expressed a 44 kDa protein, which might be associated with the activity of ox-LDL.</p><p><b>CONCLUSION</b>The new gene cloned may be associated with SMC proliferation in atherogenesis.</p>


Assuntos
Humanos , Sequência de Aminoácidos , Arteriosclerose , Genética , Sequência de Bases , Northern Blotting , Divisão Celular , Células Cultivadas , Clonagem Molecular , Biblioteca Gênica , Lipoproteínas LDL , Farmacologia , Dados de Sequência Molecular , Músculo Liso Vascular , Biologia Celular , Hibridização de Ácido Nucleico
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