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作 者:林大东[1] 毕新岭[1] 朱克军[2] 缪明永[2] 米庆胜[1] 顾军[1]
机构地区:[1]第二军医大学附属长海医院皮肤科,上海200433 [2]第二军医大学生物化学与分子生物学教研室
出 处:《中华皮肤科杂志》2005年第3期151-153,共3页Chinese Journal of Dermatology
基 金:国家自然科学基金资助项目(30271197)
摘 要:目的探讨血小板活化因子乙酰水解酶(PAF-AH)在银屑病发病机制中的作用。方法等位基因特异性聚合酶链反应技术分析银屑病患者及健康对照者PAF-AH基因Val279Phe位点的多态性,并对含有突变等位基因的多态性片段进行DNA测序分析。采用PAF-AH活性检测试剂盒测定血浆PAF-AH的活性。结果所有研究对象中发现3例Val279Phe突变型杂合子,未发现突变型纯合子;银屑病组的突变等位基因频率与健康对照组差异无统计学意义(P>0.1);银屑病患者血浆PAF-AH活性低于健康献血者,两组比较差异有统计学意义(P<0.01)。结论本研究结果提示PAF-AH基因的Val279Phe突变与银屑病无明显的相关关系,可能不是银屑病患者血浆PAF-AH活性降低的主要原因。Objective To investigate the association of Val279Phe missense mutation in the PAF-AH gene with genetic susceptibility to psoriasis vulgaris, and the role of single nucleotide polymorphisms of PAF-AH gene in the pathogenesis of psoriasis. Methods Genomic DNA was analyzed by the allele specific polymerase chain reaction for the Val279Phe mutation in patients with psoriasis and the healthy controls matched in age and sex. DNA sequencing was used to detect the PCR products with the mutant allele gene. Plasma PAF-AH activity was tested by PAF-AH assay kit. Results The prevalence of the mutation and the frequency of the mutation in the patients with psoriasis was not significantly different from those in the healthy controls (P > 0.1). Plasma PAF-AH activity in the patients with psoriasis was significantly lower than that in the healthy controls(P < 0.01). Conclusions The results suggest that Val279Phe missense mutation in the PAF-AH gene has no significant relationship with psoriasis. It may not be a genetic risk factor for psoriasis in the Chinese patients. But it can result in significant deficiency of plasma PAF-AH activity.
关 键 词:银屑病 PAF 血小板活化因子乙酰水解酶 患者 血浆 突变型 健康 AH 片段 测试
分 类 号:R758.63[医药卫生—皮肤病学与性病学] R541.75[医药卫生—临床医学]
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