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趋化因子受体CCR2b基因G190A多态性与脑梗死关系的研究 被引量:2
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作者 陈施艳 吴秀丽 +1 位作者 张志坚 林红 《中风与神经疾病杂志》 CAS CSCD 北大核心 2009年第6期645-648,共4页
目的探讨趋化因子受体CCR2b基因G190A多态性与中国福建地区汉族人群脑梗死(cerebral infarction,CI)的关系。方法采用聚合酶链反应-限制性片段长度多态性(polymerase chain reaction-restriction frag-ment length polymorphism,PCR-RF... 目的探讨趋化因子受体CCR2b基因G190A多态性与中国福建地区汉族人群脑梗死(cerebral infarction,CI)的关系。方法采用聚合酶链反应-限制性片段长度多态性(polymerase chain reaction-restriction frag-ment length polymorphism,PCR-RFLP)和DNA序列测定法检测200例CI及200名健康对照者趋化因子受体CCR2b基因G190A多态性分布,对两组之间的基因型频率和等位基因频率进行比较。结果CI组趋化因子受体CCR2b基因G190A多态位点的基因型和等位基因频率分布与对照组比较差异有统计学意义(P<0.05)。脑梗死组GG、GA、AA基因型频率分别为83.5%、15.0%、1.5%;G、A等位基因频率分别为91.0%、9.0%。正常对照组GG、GA、AA基因型频率分别为73.0%、22.5%、4.5%;G、A等位基因频率分别为84.3%、15.7%。脑梗死组GG基因型和G等位基因频率高于对照组(P<0.05)。结论趋化因子受体CCR2b基因G190A多态性与脑梗死的发病具有相关性,G等位基因可能是中国福建地区汉族人群脑梗死发病的遗传易感基因。 展开更多
关键词 趋化因子受体 脑梗死 基因多态性
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Antagonistic effects of extracts from Artemisia rupetris L. and Leontopodium leontopodioides to CC chemokine receptor 2b(CCR2b)
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作者 YU Qin-Wei HU Jie +7 位作者 WANG Hao CHEN Xin ZHAO Fang GAO Peng YANG Qiu-Bin SUN Dan-Dan ZHANG Lu-Yong YAN Ming 《Chinese Journal of Natural Medicines》 SCIE CAS CSCD 2016年第5期363-369,共7页
The present study was designed to establish a suitable assay to explore CCR2 b receptor antagonists from the natural products of Artemisia rupetris and Leontopodium leontopodioides. An aequorin assay was developed as ... The present study was designed to establish a suitable assay to explore CCR2 b receptor antagonists from the natural products of Artemisia rupetris and Leontopodium leontopodioides. An aequorin assay was developed as a cell-based assay suitable for 384-well microplate and used for screening CCR2 b receptor antagonists from natural products. Through establishing suitable conditions, the assay was shown to be suitable for screening of CCR2 b receptor antagonists. Seven compounds were identified in preliminary screening. Five of them showed evident dose-response relationship in secondary screening. The structure–activity relationship study suggested that 7-position hydroxyl group of flavonoids was necessary, a polar group should be introduced on the 3-position, and the substituents on 2-position benzene ring of flavonoids have little influence on the potentency of the inhibition activity on CCR2 b receptor. The ortho-position dihydroxyl structure in quinic acid compounds may be important. In conclusion, Compounds HR-1, 5, 7, and AR-20, 35 showed activity as antagonist of CCR2 b receptor, which shed lights on the development of novel drugs as CCR2 b receptor antagonists for preventing inflammation related diseases. 展开更多
关键词 ccr2b antagonist Inflammation Aequorin assay Artemisia rupetris Leontopodium leontopodioides
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中国汉族人HIV-1辅助受体等相关基因CCR5、CCR2b、CXCR4和SDF1编码区SNP位点调查
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作者 刘明旭 洪卫国 +4 位作者 王福生 王波 金磊 雷周云 侯静 《传染病信息》 2003年第1期21-26,共6页
目的调查中国汉族人群中HIV-1感染相关基因CCR5、CCR2b、CXCR4及SDF1编码区的基因多态性特点,为我国的艾滋病防治提供基础数据。方法 CCR5用2对引物进行PCR扩增,用PCR产物做模板直接测序。CCR2b编码区经PCR扩增后,用测序引物逐段分别测... 目的调查中国汉族人群中HIV-1感染相关基因CCR5、CCR2b、CXCR4及SDF1编码区的基因多态性特点,为我国的艾滋病防治提供基础数据。方法 CCR5用2对引物进行PCR扩增,用PCR产物做模板直接测序。CCR2b编码区经PCR扩增后,用测序引物逐段分别测序。CXCR4(cDNA编号AF147204)编码区用2对引物进行PCR扩增,然后测序。SDF1编码区用4对引物进行PCR扩增,然后分别测序。样本总数为45例,测序结果用DNAstar综合分析,寻找和鉴定SNP位点。结果 CCR5基因编码区共发现6个SNP位点,4个引起氨基酸改变,1个单碱基缺失,引起移码突变和翻译提前终止。184A→G、503G→T、668G→A、999G→T等位基因频率分别为1.1%、21.1%、8.9%和10.0%。CCR2b编码区共发现8个SNP位点,6个错义突变,即43位G→C、190位G→A、260位C→A、302位C→A、315位G→C、433位G→A,突变频率分别为:30.0%、27.8%、32.2%、5.6%、10.0%和3.3%。CXCR4编码区共发现7个SNP位点,3个错义突变即38位C→T、90位A→T、712位A→C,1个终止突变:106位G→T,基因突变频率分别为:4.4%、4.4%、10.0%和3.3%。在SDF1编码区发现1个错义SNP位点:192位G→T,突变频率为8.9%;1例单碱基缺失:100位T缺失(100△T),引起34位氨基酸移码突变。结论中国汉族人HIV-1相关基因编码区有自己的多态性特点。4个HIV-1相关基因编码区共找到22个SNP位点,17个为首次报道;2个单碱基缺失均导致移码突变和翻译提前终止,1个已经报道。它们对HIV-1感染和艾滋病病程的影响值得进一步研究。 展开更多
关键词 中国 汉族人 HIV-1 辅助受体 相关基因 CCR5 ccr2b CXCR4 SDF1 编码区 艾滋病 基因多态性
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Characterization of CCR5Δ32、CCR2b-641、CX3CR1-2491280M and SDF1-3'A Allelic Polymorphisms in the Chinese Uygur Population
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作者 刘明旭 王福生 +6 位作者 金磊 洪卫国 雷周云 张冰 候静 张战平 唐纯军 《Chinese Journal of Sexually Transmitted Infections》 2002年第2期7-11,共5页
Objective: Allelic polymorphisms of CCR5△32CCR2b-64I,CX3CR1-2491280M and SDF1-3'A associatedwith HIV-1 infection and disease progression wereinvestigated in indigenous Uygur populations from theXinjiang Uygur Aut... Objective: Allelic polymorphisms of CCR5△32CCR2b-64I,CX3CR1-2491280M and SDF1-3'A associatedwith HIV-1 infection and disease progression wereinvestigated in indigenous Uygur populations from theXinjiang Uygur Autonomous Region of China. Methods: The study population comprised 316 healthyUygur subjects with an age range of 1-80 years old, fromwhom whole peripheral blood samples were collected andnone were HIV-1 seropositive. Genomic DNA samples werepurified using a Qiagen Blood Kit. Genotyping of theaforementioned four alleles was performed using PCR orPCR/RFLP assay, and further confirmed by direct DNAsequencing. Results: The allelic frequencies in Chinese Uygurpopulation were as follows: 3.48% for CCR5△32; 19.45% forCCR2b-64I; 13.8% for CX3CR1-2491280M haplotype, and20.41% for SDF1-3'A. Mutant allele distributions amongUygur populations were in accordance with theHardy-Weinberg equilibrium. No statistical difference wasfound between the frequency of the three HIV coreceptors andtheir respective ligand genes. Conclusion: The frequency of SDF1-3'A andCX3CR1-2491280M haplotypes in these Uygur populationswas similar to that of Caucasian people, while the frequency ofthe CCR2b-64I haplotype more closely matched the HanChinese. The frequency of CCR5△A32 in Uygur populationswas between Caucasian and Hall frequencies, the more closelymatching the frequency in Medi-Asia people. No geneticlinkage between any two of the three HIV coreceptor geneswas found, but obvious genetic linkages existed betweenCX3CR1-249I and CX3CR1-280M,with even higher linkagedegrees than Caucasian people. 展开更多
关键词 HIV-1 coreceptor Allelic polymorphism Gene mutation PCR-RFLP
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