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Correlation study between the polymorphism of repetitive sequence in gene CAG of androgen receptor and the occurrence and progression of prostate cancer 被引量:1
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作者 Xiao-Lei Zhai Xiao-Wei Qu +1 位作者 Liang Guo Qian-He Ha 《Asian Pacific Journal of Tropical Medicine》 SCIE CAS 2014年第4期301-304,共4页
Objective:To explore the relation between the polymorphism of repetitive sequence in gene CAG of androgen receptor(AR)and the susceptibility and clinical stages as well as pathological grading of prostate cancer among... Objective:To explore the relation between the polymorphism of repetitive sequence in gene CAG of androgen receptor(AR)and the susceptibility and clinical stages as well as pathological grading of prostate cancer among Han population.Method:Sixty-eight cases with prostate cancer hospitalized in Urinary Surgery Department from Feb.2010 to Feb.2012 and 60 healthy cases were chosen as research subjects.Methods of PCR and direct sequencing were adopted to detect DNA sequence of AR gene and the length of repetitive sequence in CAG.Results:The lengths of repetitive sequence in CAG of patients with prostate cancer and healthy people were(22.3±4.6)and(23.0±4.9),respectively showing no statistical significance.Comparing length(repetitive sequence of CAG)>22,those with that<22 suffer a remarkably higher risk of prostate cancer(P<0.05).The number of repetitive sequence in CAG of patients at clinical stage C-D was less than that of patients at stage B,and the number of repetitive sequence in CAG of patients with poorly differentiated prostate cancer was also less than that of patients with moderately and highly differentiated prostate cancer.But there was no statistical significance int the difference(P>0.05);the proportion of patients with length<22 at clinical stage C-D was much larger than that of patients at clinical stage B(P<0.05),and as the aggravation of pathological grading,the proportion of patients with the length<22 was also remarkably increased and there was significant difference between patients with highly differentiated prostate cancer and those with poorly differentiated prostate cancer(P<0.05).Conclusions:There is correlation between the occurrence and development of prostate cancer in Han population and the polymorphism of repetitive sequence in gene CAG of androgen receptor.The less the number of repetitive sequence in CAG is,the higher the risk of prostate cancer will be and the more severe the clinical stage and pathological grading will be. 展开更多
关键词 PROSTATE cancer AnDROGEn receptor polymorphism of cag Gene
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Study on relationship between polymorphism of hAR gene (CAG)n micro-satellite and prostate cancer
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作者 王钢 王晓慧 +2 位作者 夏冰 陈光椿 卢建 《Journal of Medical Colleges of PLA(China)》 CAS 2002年第2期147-151,共5页
Objective: To study the relationship between the polymorphic (CAG)n micro-satellite of human androgen receptor (hAR) gene and prostate cancer (PCa). Methods: The number of (CAG)n repeats in 107 normal males were measu... Objective: To study the relationship between the polymorphic (CAG)n micro-satellite of human androgen receptor (hAR) gene and prostate cancer (PCa). Methods: The number of (CAG)n repeats in 107 normal males were measured by a two-step [α-32P]-dCTP incorporated asymmetric polymeric chain reaction (PCR), and the (CAG)n repeats of both malignant and nonmalignant prostate cells in fixed paraffin-embedded tissue (PET) specimen from 36 case of PCa were determined by sequence analysis. Results: The repeats of polymorphic (CAG) n among normal men ranged from 11 to 29, and the most frequent repeat was 22(18. 69%), with 23(14. 02%), 24(10. 28%) and 21(10. 28%) being less frequent. The (CAG)n repeats of malignant prostate cells equaled to that of nonmalignant adjacent prostate tissue cells from the same PET specimen in all 36 PCa, and the (CAG)n repeats in 36 PCa which ranged from 16 to 22 were shorter than that in normal males significantly (P<0. 05), while no significant difference in (CAG)n repeats among various grade of tumor's differentiation (well-differentiated, intermediate-differentiated and poor-differentiated) was found (P>0. 05). Conclusion; The present study suggest that short hAR gene (CAG)n micro-satellite might be associated with the occurrence of PCa, but not with the differentiation of PCa. 展开更多
关键词 androgen receptor (cag)n micro-satellite polymorphism prostate cancer
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Polymorphism of N-acetyltransferase 2 (NAT2) Gene Polymorphism in Shanghai population: Occupational and Non-occupational Bladder Cancer Patient Groups 被引量:13
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作者 QING-WENMA GUO-FANGLIN +4 位作者 JI-GANGCHEN CUI-QINGXIANG WEI-CHAOGUO KLAUSGOLKA JIAN-HUASHEN 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2004年第3期291-298,共8页
Objective Arylamine N-acetyltransferases (NATs) are involved in the detoxification of aromatic amines and hydrazine. In order to explore the possible association of NAT2 polymorphism with bladder cancer risk in benzi... Objective Arylamine N-acetyltransferases (NATs) are involved in the detoxification of aromatic amines and hydrazine. In order to explore the possible association of NAT2 polymorphism with bladder cancer risk in benzidine exposed or non-exposed Chinese individuals, healthy subjects, subjects with bladder cancer of a former benzidine exposed cohort in Shanghai dyestuff industry and a group of bladder cancer patients without known occupational exposure to aromatic amines were genotyped for NAT2 gene polymorphism. Methods NAT2 genotyping was performed with a set of RFLP procedures at seven major polymorphic loci of gene coding area: G191A, C282T, T341C, C481T, G590A, A803G and G857A. Results The wild allele NAT2 *4 was the most prevalent allele (59%) in healthy individuals. The alleles NAT2*6A and NAT2*7B were also frequently observed (21% and 17%, respectively). In contrast to Caucasians, the percentage of slow acetylators was lower (12% in Chinese vs. 58% in Caucasians, P<0.001). No relevant differences were observed for homogenous rapid, heterogeneous rapid/slow and homogeneous slow acetylation genotypes between the healthy subjects and both groups of bladder cancer patients. Conclusion The present work did not support the association of slow acetylating genotypes of NAT2 gene with elevated risk of bladder cancer in Chinese whereas it was documented as an important genetically determined risk factor in Caucasians. Different mechanisms might play a role in individual susceptibility to bladder cancer related with aromatic amine exposure in various races or ethnic groups. 展开更多
关键词 BEnZIDInE Occupational exposure n-Acetyltransferase 2 polymorphism Bladder cancer Dyestuff industry
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Effect of variable number of tandem repeats polymorphism in the human dopamine transporter gene on conflict information processing according to event-related potential
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作者 Chunyu Han Yuping Wang +1 位作者 Xin Wang Ying Liu 《Neural Regeneration Research》 SCIE CAS CSCD 2010年第15期1196-1200,共5页
The dopamine transporter (DAT) is responsible for dopamine reuptake from the synaptic cleft. A variable number of tandem repeats polymorphism in the DAT gene is related to DAT availability and has been associated wi... The dopamine transporter (DAT) is responsible for dopamine reuptake from the synaptic cleft. A variable number of tandem repeats polymorphism in the DAT gene is related to DAT availability and has been associated with cognition. With the advantage of high-time resolution, event-related potential is an important method to study the time course of human information processing. Previous results have suggested that dopamine exhibits a close relationship with conflicting information processing. Therefore, the present study assumed that conflicting information processing could be influenced by DAT variable number of tandem repeats polymorphism. To confirm this, the present study analyzed the influence of DAT genotypes on N270, which is presumed to reflect neural activity of conflict information processing in young healthy adults. A S1-S2 matching task was performed in healthy adults with 10/10 genotype (n = 14) and 10/9 genotypes (n = 14), respectively, when event-related potentials were recorded. Results demonstrated that subjects with the 10/10 genotype exhibited shorter N270 latency and quicker reaction times compared with subjects with the 10/9 genotype. There were no differences in N270 amplitude between the two genotypes. These results suggested that 10/10 genotype subjects more efficiently processed conflict information. 展开更多
关键词 event-related potentials dopamine transporter gene polymorphism n270 P300 COGnITIOn nerve electrophysiology neural regeneration
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更年期后女性代谢综合征患者AR基因(CAG)n多态性的研究 被引量:2
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作者 郭志琴 李小鹰 +4 位作者 曹剑 刘建伟 朱冰坡 丁宇 石海燕 《中国医药导刊》 2008年第2期264-267,共4页
目的:研究更年期后女性代谢综合征患者雄激素受体基因(CAG)n重复序列多态性。方法:使用DNA测序方法对150例更年期后健康女性和代谢综合征患者AR基因外显子1 NH2端转录调节区内(CAG)n重复序列长度进行测定。结果:1.健康女性AR基因(CAG)n... 目的:研究更年期后女性代谢综合征患者雄激素受体基因(CAG)n重复序列多态性。方法:使用DNA测序方法对150例更年期后健康女性和代谢综合征患者AR基因外显子1 NH2端转录调节区内(CAG)n重复序列长度进行测定。结果:1.健康女性AR基因(CAG)n重复数最短为18,最长为34,平均值为23.34±2.44;2.代谢综合征女性AR基因(CAG)n重复数最短为8,最长为29,重复数平均值为22.29±2.82;3.代谢综合征组(CAG)n重复数与健康女性组之间(CAG)n重复序列多态性有差异(P=0.030)。结论:1.更年期后女性AR基因(CAG)n重复序列长度存在多态性;2.更年期后女性代谢综合征组AR基因外显子INH2转录调节区(CAG)n的重复数小于健康对照组。 展开更多
关键词 雄激素受体基因 (cag)n重复序列多态 更年期后女性 代谢综合征
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中国北方汉族男性雄激素受体基因(CAG)n多态分布及其与低氧训练效果的关联性研究 被引量:1
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作者 王海燕 胡扬 +4 位作者 郝鑫 许春艳 李燕春 衣龙彦 聂晶 《中国运动医学杂志》 CAS CSCD 北大核心 2010年第2期128-132,共5页
目的:探讨雄激素受体(AR)基因外显子1中(CAG)n多态在中国北方汉族男性中的分布特征及其与低氧训练后VO2max变化的关联性。方法:65名中国北方汉族健康青年男性进行为期30天HiHiLo(常压低氧)训练,晚上居住房间氧浓度为14.3-14.8... 目的:探讨雄激素受体(AR)基因外显子1中(CAG)n多态在中国北方汉族男性中的分布特征及其与低氧训练后VO2max变化的关联性。方法:65名中国北方汉族健康青年男性进行为期30天HiHiLo(常压低氧)训练,晚上居住房间氧浓度为14.3-14.8%(模拟海拔2800-3000米),每周进行3次75%常氧VO2max的低氧训练,训练环境氧浓度约15.4%(模拟海拔约2500米)。实验前后测试体重和VO2max等指标,采用GeneScan和测序方法分析AR(CAG)n多态的等位基因(基因型)。结果:(1)共观察到(CAG)12、(CAG)16-28、(CAG)30共15种重复次数的等位基因(基因型),其中22次重复等位基因分布频率最高;(2)当分别以21和22次重复为分割点划分基因型时,短链组体重基础值均显著低于长链组;(3)当分别以21和22次重复为分割点划分基因型时,低氧训练后短链基因型携带者ΔVO2max和ΔrVO2max均显著高于长链组(P〈0.01)。结论:中国北方汉族男性AR基因(CAG)n多态与HiHiLo(常压低氧)训练效果之间存在关联,重复次数较少基因型携带者的低氧训练敏感性较好。 展开更多
关键词 雄激素受体(AR) (cag)n多态 低氧暴露和低氧训练
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雄激素受体基因CAG、GGN重复片段多态性与指长比(2D∶4D)的关联性 被引量:1
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作者 张钏 陆宏 +5 位作者 郝胜菊 闫有圣 党洁 郑雷 张庆华 霍正浩 《解剖学报》 CAS CSCD 北大核心 2016年第3期409-414,共6页
目的探讨雄激素受体(AR)基因CAG、GGN重复片段多态性与指长比之间的关联性。方法研究对象来自宁夏医科大学2011级健康学生共685例,男性294例,平均年龄(20.02±1.28)岁,女性391例,平均年龄(19.25±1.55)岁。用ABI 3730XL测序仪测... 目的探讨雄激素受体(AR)基因CAG、GGN重复片段多态性与指长比之间的关联性。方法研究对象来自宁夏医科大学2011级健康学生共685例,男性294例,平均年龄(20.02±1.28)岁,女性391例,平均年龄(19.25±1.55)岁。用ABI 3730XL测序仪测定AR基因的(CAG)n及(GGN)n重复数目,照片打好点后用电子游标卡尺对指长比进行测定。2D∶4D经均值±2标准差筛选,用独立样本t检验检测2D∶4D在男性与女性个体中的分布差异。用四分位法筛选出较低(Q1)与较高(Q3)2D∶4D。用相关分析检验AR基因中CAG和GGN两个多态性位点与2D∶4D的关联性。结果女性右手、左手及左右手平均2D∶4D均高于男性(P<0.05,P<0.01,P<0.01),但DR-L2D∶4D的分布差异无统计学意义(P>0.05)。AR CAG/GGN重复多态性与男性右手及左手2D∶4D无关联性(P>0.05),但CAG重复多态性与Q1 DR-L及Q3平均2D∶4D存在关联性(r=0.280,P<0.05,r=0.274,P<0.05)。女性较短CAG等位基因与Q3平均2D∶4D存在关联性(r=0.337,P<0.05),女性较长CAG等位基因与Q3右手及DR-L2D∶4D存在关联性(r=0.238,P<0.05;r=0.175,P<0.05),女性平均CAG等位基因与Q3平均2D∶4D存在关联性(r=0.236,P<0.05)。女性较长GGN等位基因与女性右手2D∶4D存在关联性(r=0.204,P<0.05),女性平均GGN等位基因与Q3平均2D∶4D存在关联性(r=0.225,P<0.05)。结论 AR基因CAG与GGN重复片段多态性可能与指长比存在关联性,联合运用四分位法与相关分析可能是揭示AR多态性与指长比关联性的一种更好的方法。 展开更多
关键词 雄激素受体基因 2D∶4D cag重复多态性 GGn重复多态性 四分位法
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中国北方汉族男性雄激素受体基因(CAG)n多态与低氧训练后心功能变化的关联性
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作者 王海燕 胡扬 +4 位作者 许春艳 郝鑫 衣龙彦 聂晶 李燕春 《中国运动医学杂志》 CAS CSCD 北大核心 2011年第9期793-800,共8页
目的:探讨雄激素受体(AR)基因外显子1中(CAG)n多态与中国北方汉族男性心功能对低氧训练应答的关联性。方法:58名中国北方汉族健康青年男性进行为期30天的HiHiLo(常压低氧)训练,晚上居住房间的氧浓度为14.8~14.3%(模拟海拔约2800~3000... 目的:探讨雄激素受体(AR)基因外显子1中(CAG)n多态与中国北方汉族男性心功能对低氧训练应答的关联性。方法:58名中国北方汉族健康青年男性进行为期30天的HiHiLo(常压低氧)训练,晚上居住房间的氧浓度为14.8~14.3%(模拟海拔约2800~3000米);每周进行3次、每次30分钟的低氧训练,训练强度为常氧75%VO2max强度,训练环境氧浓度15.4%~14.8%(模拟海拔约2500~2800米);每周进行5次、每次90分钟常氧环境下的专项训练。分别于低氧训练前和低氧训练后使用超声心动仪测试安静时,50W、100W、150W递增负荷运动,以及运动后恢复期的心功能。使用GeneScan和测序方法分析AR(CAG)n多态性。结果:(1)短链重复组(≤21和≤22)身高和低氧训练前体重基础值分别显著低于长链组(>21和>22);(2)≤22次重复组低氧训练前安静时、三种负荷和恢复时的每搏输出量基础值均显著低于>22组;(3)与低氧训练前相比,低氧训练后各基因型组安静、运动和恢复时的心率均显著下降,但是仅两个短链组每分输出量和心指数呈现显著性降低;(4)除≤21组50W和≤22组150W外,低氧训练后短链重复组安静和运动时ΔCI下降幅度均显著大于长链组。结论:AR基因(CAG)n多态与中国北方汉族男性心功能对模拟常压低氧环境下HiHiLo训练的应答可能存在关联性。 展开更多
关键词 雄激素受体(AR) (cag)n多态 低氧训练 心功能
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健康更年期后女性AR基因(CAG)n多态性的调查
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作者 郭志琴 李小鹰 +1 位作者 曹剑 叶玲 《中国分子心脏病学杂志》 CAS 2008年第2期99-102,共4页
目的研究健康更年期后女性雄激素受体基因(CAG)n重复序列多态性。方法使用DNA测序方法对60例更年期后健康女性AR基因外显子1 NH2端转录调节区内(CAG)n重复序列长度进行测定。结果(1)健康更年期后女性AR基因(cAG)n重复数最短为18,最长为... 目的研究健康更年期后女性雄激素受体基因(CAG)n重复序列多态性。方法使用DNA测序方法对60例更年期后健康女性AR基因外显子1 NH2端转录调节区内(CAG)n重复序列长度进行测定。结果(1)健康更年期后女性AR基因(cAG)n重复数最短为18,最长为34,平均值为23.34±2.44;(2)更年期后女性(CAG)n重复序列多态性与育龄妇女有差异(P>0.05)。结论(1)健康更年期后女性AR基因(CAG)n重复序列长度存在多态性;(2)健康更年期后女性AR基因(CAG)n的重复数大于育龄期女性。 展开更多
关键词 雄激素受体基因 (cag)n重复序列多态 更年期后女性
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雄激素受体基因CAG、GGN重复片段多态性与身体质量指数/腰臀比的关联性
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作者 张钏 陆宏 +5 位作者 裴利国 郝胜菊 闫有圣 郑雷 党洁 霍正浩 《解剖学报》 CAS CSCD 北大核心 2016年第4期534-538,共5页
目的探讨雄激素受体基因CAG、GGN重复片段多态性与身体质量指数(BMI)、腰臀比(WHR)之间的关联性。方法研究对象来自宁夏医科大学2011级健康学生共654例,男性280例,女性374例,平均年龄(20.35±1.24)岁。用ABI 3730XL测序仪测定AR基因... 目的探讨雄激素受体基因CAG、GGN重复片段多态性与身体质量指数(BMI)、腰臀比(WHR)之间的关联性。方法研究对象来自宁夏医科大学2011级健康学生共654例,男性280例,女性374例,平均年龄(20.35±1.24)岁。用ABI 3730XL测序仪测定AR基因的(CAG)n及(GGN)n重复数目,直接测量法测得身高、体重、腰围与臀围。结果 BMI与WHR的分布存在性别差异。较长GGN等位基因与女性BMI呈正相关(P<0.05),AR基因的(CAG)n与女性BMI无相关性(P>0.05);男性AR基因的(CAG)n及(GGN)n与BMI及WHR无相关性(P>0.05)。结论 BMI与WHR在不同性别间的分布存在差异性;较长GGN等位基因与女性BMI存在关联性。 展开更多
关键词 身体质量指数 腰臀比 cag重复多态性 GGn重复多态性 直接测量法
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北京万寿路地区319例男性AR基因(CAG)n重复序列多态的研究
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作者 楚新梅 李小鹰 +2 位作者 梁春红 叶玲 刘建伟 《中国分子心脏病学杂志》 CAS 2006年第1期27-29,共3页
目的研究自然人群中老年男性雄激素受体(AR)基因CAG重复序列多态。方法使用DNA测序方法对319例老年男性AR基因外显子1 NH2端转录调节区内CAG重复序列长度进行测定。结果男性雄激素受体基因CAG重复数最短为8,最长为35。CAG重复数平均值为... 目的研究自然人群中老年男性雄激素受体(AR)基因CAG重复序列多态。方法使用DNA测序方法对319例老年男性AR基因外显子1 NH2端转录调节区内CAG重复序列长度进行测定。结果男性雄激素受体基因CAG重复数最短为8,最长为35。CAG重复数平均值为(22.70 ±3.66)。CAG重复数分布频率最多的为21(13.8%),22(15.7%),23(13.5%)和24(10.3%),共占 53.3%。结论自然人群中老年男性雄激素受体基因CAG重复序列呈现多态性,多数集中在21- 24,为进一步研究AR基因变异与疾病的关系提供依据。 展开更多
关键词 雄激素受体基因 cag重复序列多态 男性
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雄激素受体基因(CAG)n微卫星多态性与疾病易感性 被引量:3
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作者 王钢 《国外医学(生理病理科学与临床分册)》 2002年第6期612-615,共4页
雄激素受体 (AR)基因第一外显子中含有遗传多态性的 (CAG)n微卫星序列 ,此序列编码AR转录激活区中的多聚谷氨酰胺片段。近年来研究相继证实 ,AR中的多聚谷氨酰胺重复数与其转录活性负相关 ,并进而发现该微卫星多态性与前列腺癌、延髓脊... 雄激素受体 (AR)基因第一外显子中含有遗传多态性的 (CAG)n微卫星序列 ,此序列编码AR转录激活区中的多聚谷氨酰胺片段。近年来研究相继证实 ,AR中的多聚谷氨酰胺重复数与其转录活性负相关 ,并进而发现该微卫星多态性与前列腺癌、延髓脊髓性肌萎缩、雄激素不敏感综合征、乳腺癌、子宫内膜癌及卵巢癌等多种疾病的发生、发展密切相关。 展开更多
关键词 受体 雄激素 (cag)n微卫星 基因多态性 易感性
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家族性亨廷顿病临床和(CAG)n多态性分析
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作者 初海鹰 王剑锋 +1 位作者 杨佩满 黄尚志 《中国优生与遗传杂志》 2003年第6期23-24,共2页
关键词 家族性亨廷顿病 常染色体显性遗传 (cag)n基因 基因多态性 临床特点
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雄激素受体基因(CAG)n多态性对多囊卵巢综合征形成的影响 被引量:4
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作者 董文娇 王玉霞 杨海婷 《国际生殖健康/计划生育杂志》 CAS 2017年第1期70-73,共4页
雄激素受体基因位于染色体Xq11-12上,其第一外显子存在CAG的重复序列,该重复序列(CAG)n在不同种族、地域中存在多态性。雄激素受体基因(CAG)n的长度或重复次数与多囊卵巢综合征(PCOS)患者雄激素受体(AR)活性呈负相关,与雄激素水平呈正相... 雄激素受体基因位于染色体Xq11-12上,其第一外显子存在CAG的重复序列,该重复序列(CAG)n在不同种族、地域中存在多态性。雄激素受体基因(CAG)n的长度或重复次数与多囊卵巢综合征(PCOS)患者雄激素受体(AR)活性呈负相关,与雄激素水平呈正相关,且(CAG)n多态性影响PCOS相关特征,如胰岛素抵抗、痤疮及多毛的形成,而短的或重复次数少的(CAG)n可能增加PCOS患者的易感性。但是X染色体失活可以调节AR的效应,如果考虑X染色体失活对AR的影响,则长的或重复次数多的(CAG)n能增加PCOS的患病风险。综述雄激素受体基因(CAG)n多态性对PCOS形成的影响。 展开更多
关键词 多囊卵巢综合征 受体 雄激素 多态性 限制性片段长度 雄激素受体基因 (cag)n多态性
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两个亨廷顿舞蹈病家系IT15基因(CAG)n检测 被引量:2
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作者 高歌 陈晓蕾 +4 位作者 付汪星 张桐 朱揆 邹顺鸿 陈辉 《郑州大学学报(医学版)》 CAS 北大核心 2010年第6期936-939,共4页
目的:检测两个亨廷顿舞蹈病(HD)家系的IT15基因CAG重复序列[(CAG)n]。方法:采用PCR和测序分析方法检测两个家系28名成员(A家系为已确诊HD家系,B家系为疑似HD家系)和两名正常对照IT15基因的(CAG)n。结果:两名正常对照IT15基因的CAG拷贝... 目的:检测两个亨廷顿舞蹈病(HD)家系的IT15基因CAG重复序列[(CAG)n]。方法:采用PCR和测序分析方法检测两个家系28名成员(A家系为已确诊HD家系,B家系为疑似HD家系)和两名正常对照IT15基因的(CAG)n。结果:两名正常对照IT15基因的CAG拷贝数分别为17、18;A家系中患者CAG拷贝数大于50;B家系中患者CAG拷贝数为40~50。B家系通过基因检测确诊为HD家系,并检出一名症状前患者。结论:IT15基因(CAG)n检测是诊断HD简便、快捷和有效的方法。 展开更多
关键词 亨廷顿舞蹈病 IT15基因 cag重复序列
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In vitro effect of amoxicillin and clarithromycin on the 3' region of cagA gene in Helicobacter pylori isolates 被引量:5
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作者 Javier Andrés Bustamante-Rengifo Andrés Januer Matta +1 位作者 Alvaro Pazos Luis Eduardo Bravo 《World Journal of Gastroenterology》 SCIE CAS 2013年第36期6044-6054,共11页
AIM:To evaluate the in vitro effect of amoxicillin and clarithromycin on the cag pathogenicity island(cag PAI).METHODS:One hundred and forty-nine clinical isolates of Helicobacter pylori(H.pylori)cultured from gastric... AIM:To evaluate the in vitro effect of amoxicillin and clarithromycin on the cag pathogenicity island(cag PAI).METHODS:One hundred and forty-nine clinical isolates of Helicobacter pylori(H.pylori)cultured from gastric biopsies from 206 Colombian patients with dyspeptic symptoms from a high-risk area for gastric cancer were included as study material.Antimicrobial susceptibility was determined by the agar dilution method.Resistant isolates at baseline and in amoxicillin and clarithromycin serial dilutions were subjected to genotyping(cagA,vacA alleles s and m),Glu-Pro-Ile-Tyr-Ala(EPIYA)polymerase chain reaction and random amplified polymorphic DNA(RAPD).Images of the RAPD amplicons were analyzed by Gel-Pro Analyzer 4.5program.Cluster analyses was done using SPSS 15.0statistical package,where each of the fingerprint bands were denoted as variables.Dendrograms were designed by following Ward’s clustering method and the estimation of distances between each pair of H.pylori isolates was calculated with the squared Euclidean distance.RESULTS:Resistance rates were 4%for amoxicillin and 2.7%for clarithromycin with 2%double resistances.Genotyping evidenced a high prevalence of the genotype cagA-positive/vacA s1m1.The 3’region of cagA gene was successfully amplified in 92.3%(12/13)of the baseline resistant isolates and in 60%(36/60)of the resistant isolates growing in antibiotic dilutions.Upon observing the distribution of the number of EPIYA repetitions in each dilution with respect to baseline isolates,it was found that in 61.5%(8/13)of the baseline isolates,a change in the number of EPIYA repetitions lowered antibiotic pressure.The gain and loss of EPIYA motifs resulted in a diversity of H.pylori subclones after bacterial adjustment to changing conditions product of antibiotic pressure.RAPD PCR evidenced the close clonal relationship between baseline isolates and isolates growing in antibiotic dilutions.CONCLUSION:Antibiotic pressure does not induce loss of the cag pathogenicity island,but it can leadin most cases-to genetic rearrangements within the3’region cagA of the founding bacteria that can affect the level of tyrosine phosphorylation impacting on its cellular effects and lead to divergence of cagA-positive subclones. 展开更多
关键词 HELICOBACTER PYLORI Antimicrobial susceptibility cag pathogenicity island cagA 3’region Random amplified polymorphIC DnA-polymerase chain reaction
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CYP2C19基因多态性、血清NT-proBNP水平与急性脑梗死静脉溶栓预后不良的关系 被引量:1
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作者 钱倩 张静 +2 位作者 张欣 邢晓明 边伟林 《山东医药》 CAS 2024年第4期13-17,共5页
目的探讨CYP2C19基因多态性、血清N末端B型脑利钠肽前体(NT-proBNP)水平与急性脑梗死(ACI)患者静脉溶栓预后不良的关系。方法选择210例ACI患者,均行阿替普酶静脉溶栓治疗,治疗90 d后根据改良Rankin量表(mRS)评分将患者分为预后不良组(mR... 目的探讨CYP2C19基因多态性、血清N末端B型脑利钠肽前体(NT-proBNP)水平与急性脑梗死(ACI)患者静脉溶栓预后不良的关系。方法选择210例ACI患者,均行阿替普酶静脉溶栓治疗,治疗90 d后根据改良Rankin量表(mRS)评分将患者分为预后不良组(mRS评分≥3分)52例、预后良好组(mRS评分<3分)158例。治疗前采用实时荧光定量PCR法检测CYP2C19基因多态性,时间分辨荧光免疫层析法检测血清NT-proBNP。用Pearson或Spearman分析CYP2C19基因多态性、血清NT-proBNP水平与mRS评分的相关性;用多因素Logistic回归分析ACI患者静脉溶栓预后的影响因素;用受试者工作特征曲线分析CYP2C19基因多态性、血清NT-proBNP水平对ACI患者静脉溶栓预后不良的预测价值。结果预后不良组年龄、高血压比例、糖尿病比例、入院美国国立卫生研究所脑卒中(NIHSS)评分、空腹血糖水平高于预后良好组(P均<0.05)。预后不良组和预后良好组CYP2C19基因多态性比较差异有统计学意义(P<0.05),预后不良组血清NT-proBNP水平高于预后良好组(P<0.05)。ACI患者CYP2C19基因多态性(r_(s)=0.362)、血清NT-proBNP水平(r=0.426)与mRS评分均呈正相关(P均<0.05)。高NIHSS评分、CYP2C19基因慢代谢型、高血清NT-proBNP水平是ACI患者预后不良的危险因素(P均<0.05)。CYP2C19基因多态性、血清NT-proBNP水平单独及联合预测ACI患者静脉溶栓预后的曲线下面积分别为0.752、0.786、0.861,二者联合预测的曲线下面积高于单独预测(P均<0.05)。结论CYP2C19基因多态性和高水平NT-proBNP是ACI患者静脉溶栓预后不良的危险因素,二者联合对不良预后有较高的预测价值。 展开更多
关键词 急性脑梗死 静脉溶栓 CYP2C19基因多态性 n末端B型脑利钠肽前体
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Predicting Physical Properties of Tetragonal,Monoclinic and Orthorhombic M_3N_4(M=C,Si,Sn) Polymorphs via First-Principles Calculations
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作者 仓玉萍 连帅彬 +1 位作者 杨慧明 陈东 《Chinese Physics Letters》 SCIE CAS CSCD 2016年第6期90-94,共5页
The recently discovered tetragonal, monoclinie and orthorhombic polymorphs of M3N4 (M=C, Si, Sn) are in- vestigated by using first-principles calculations. A set of anisotropic elastic quantities, i.e., the bulk and... The recently discovered tetragonal, monoclinie and orthorhombic polymorphs of M3N4 (M=C, Si, Sn) are in- vestigated by using first-principles calculations. A set of anisotropic elastic quantities, i.e., the bulk and shear moduli, Young's modulus, Poisson ratio, H/G ratio and rickets hardness of M3N4 (M=C, Si, Sn) are predicted. The quasi-harmonic Debye model, assuming that the solids are isotopic, may lead to large errors for the non-cubic crystals. The thermal effects are obtained by the traditional quasi-harmonic approach. The dependences of heat capacity, thermal expansion coefficient and Debye temperature on temperature and pressure are systematically discussed in the pressure range of 0 IOGPa and in the temperature range of 0-1100 K. More importantly, o- C3N4 is a negative thermal expansion material. Our results may have important consequences in shaping the understanding of the fundamental properties of these binary nitrides. 展开更多
关键词 SI M=C Si Sn on of Predicting Physical Properties of Tetragonal Monoclinic and Orthorhombic M3n4 M polymorphs via First-Principles Calculations that in is
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PIG3启动子结合元件(TGYCC)n与肿瘤易感性的研究进展
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作者 陈凤霞 浦飞飞 《数理医药学杂志》 CAS 2024年第3期217-221,共5页
PIG3是受p53调控的下游靶基因,通过参与合成活性氧及对氧化应激的调控参与细胞凋亡过程。PIG3的启动子区有一段串联重复序列(TGYCC)n(Y=C或T),其转录调控与这段五核苷酸重复序列密切相关。本文对(TGYCC)n这段串联重复序列在PIG3转录调... PIG3是受p53调控的下游靶基因,通过参与合成活性氧及对氧化应激的调控参与细胞凋亡过程。PIG3的启动子区有一段串联重复序列(TGYCC)n(Y=C或T),其转录调控与这段五核苷酸重复序列密切相关。本文对(TGYCC)n这段串联重复序列在PIG3转录调控中的作用进行综述,探讨其多态性与肿瘤易感性的关系。 展开更多
关键词 PIG3 (TGYCC)n P53 PHB1/PHB2 转录调控 多态性
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新疆结核病患者N-乙酰基转移酶2基因分型特征分析
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作者 黄旭林 李树涛 《新疆医学》 2024年第5期527-529,540,共4页
目的研究新疆结核病患者N-乙酰基转移酶2基因(NAT2)多态性分布特点。方法纳入诊断为肺结核的132例患者为研究对象,应用多通道荧光定量分析仪测定NAT2基因多态性。所获取的数据采用χ^(2)检验,比较各组间基因型分布差异,以P<0.05为差... 目的研究新疆结核病患者N-乙酰基转移酶2基因(NAT2)多态性分布特点。方法纳入诊断为肺结核的132例患者为研究对象,应用多通道荧光定量分析仪测定NAT2基因多态性。所获取的数据采用χ^(2)检验,比较各组间基因型分布差异,以P<0.05为差异有统计学意义。结果132名患者中快乙酰化型患者为32人(24.2%),中间乙酰化型患者为66人(50%),慢乙酰化型患者为34人(25.8%),男性与女性患者间、老年与非老年患者间、北疆与南疆患者间乙酰化型的NAT2基因多态性存在一定差异,但均不具有统计学意义(P>0.05)。结论我区结核病患者NAT2基因多态性以中间乙酰化型为主,NAT2基因多态性在不同性别、年龄段及地区的结核患者中的分布无显著差异。 展开更多
关键词 结核病 n-乙酰基转移酶2 基因多态性 异烟肼
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