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α_(2B)肾上腺素受体遗传多态性的研究
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作者 宋小星 彭章龙 于布为 《国际麻醉学与复苏杂志》 CAS 2007年第5期434-437,共4页
目前,研究发现α_(2B)肾上腺素受体存在有插入/缺失型的遗传多态现象,缺失型α_(2B)肾上腺素受体由于激动剂促进其脱敏的机制完全丧失,故导致输入信号与受体反应之间的动力联系遭到破坏,进而使机体在临床表型上发生了一系列的改变,它与... 目前,研究发现α_(2B)肾上腺素受体存在有插入/缺失型的遗传多态现象,缺失型α_(2B)肾上腺素受体由于激动剂促进其脱敏的机制完全丧失,故导致输入信号与受体反应之间的动力联系遭到破坏,进而使机体在临床表型上发生了一系列的改变,它与疾病的发生和药物的效应均有密切联系。 展开更多
关键词 α2b肾上腺素受体 遗传多态性 DD基因型
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Lack of association between ADRA2B-4825 gene insertion/deletion poly- morphism and migraine in Chinese Han population
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作者 倪健强 贾莎莎 +4 位作者 刘民 陈守恭 姜玉婷 董万利 高玉振 《Neuroscience Bulletin》 SCIE CAS CSCD 2010年第4期322-326,共5页
Objective The present study aimed to estimate the association between susceptibility to migraine and the 12nucleotide insertion/deletion (indel) polymorphism in promoter region ofα 2B -adrenergic receptor gene (AD... Objective The present study aimed to estimate the association between susceptibility to migraine and the 12nucleotide insertion/deletion (indel) polymorphism in promoter region ofα 2B -adrenergic receptor gene (ADRA2B).Methods A case-control study was carried out in Chinese Han population,including 368 cases of migraine and 517 controls.Genomic DNA was extracted from blood samples,and DNA fragments containing the site of polymorphism were amplified by PCR.Data were adjusted for sex,age,migraine history and family history,and analyzed using a logistic regression model.Results There was no association between indel polymorphism and migraine,at either the allele or the genotype level.Conclusion These findings do not support a functional significance of ADRA2B indel polymorphism at position-4825 relative to the start codon in the far upstream region of the promoter in the present migraine subjects. 展开更多
关键词 MIGRAINE promoter ofα 2b -adrenergic receptor gene insertion/deletion polymorphism genetic association
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