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基因芯片检测HBV DNA聚合酶区基因多态性 被引量:1
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作者 孙承龙 王跃国 +4 位作者 王惠民 张冬雷 马达 赵建龙 吴月平 《交通医学》 2003年第6期618-620,共3页
目的 :建立基因芯片检测HBVDNA聚合酶区基因多态性。方法 :PCR扩增HBVDNAP区nt45 5~ 796片断 ,与预制的基因芯片杂交 ,运用激光共聚焦荧光检测系统扫描芯片分析基因突变类型。结果 :芯片检测HBVDNAP区变异具有较好的特异性和准确性 ;... 目的 :建立基因芯片检测HBVDNA聚合酶区基因多态性。方法 :PCR扩增HBVDNAP区nt45 5~ 796片断 ,与预制的基因芯片杂交 ,运用激光共聚焦荧光检测系统扫描芯片分析基因突变类型。结果 :芯片检测HBVDNAP区变异具有较好的特异性和准确性 ;初步应用显示 :慢性乙肝组nt5 2 8和nt5 5 2位点突变率分别为 8.6%和 9.6% ,而无症状肝炎组和重症肝炎组突变率均为 0 ;拉米夫定治疗组与非拉米夫定治疗组比较 ,nt5 2 8突变率分别为 10 .5 %和 8.1% ,nt5 5 2突变率分别为 15 .8%和 8.1%。结论 :HBVDNA聚合酶区基因多态性分布与病情轻重无关 ,而与病程慢性迁延有关 ;拉米夫定在耐药突变中发挥了重要作用 ;基因芯片检测乙肝患者耐药基因有其临床应用价值。 展开更多
关键词 基因芯片 HBV-DNA 聚合酶区 基因多态性 PCR 激光共聚焦荧光检测系统 耐药基因
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SARS冠状病毒RNA聚合酶编码区分析 被引量:3
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作者 芮伟 张其鹏 +4 位作者 石磊 卢铭 景霞 国强华 尚彤 《北京大学学报(医学版)》 CAS CSCD 北大核心 2003年第B05期137-138,共2页
关键词 SARS 冠状病毒 RNA 聚合编码分析
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庚型肝炎病毒NS3区聚合酶链反应临床RNA检测
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作者 赵清霞 许青田 +4 位作者 郝红梅 陈桂芬 杜绍财 季颖 陶其敏 《中国误诊学杂志》 CAS 2001年第11期1644-1645,共2页
关键词 庚型肝炎 诊断 病毒感染 治疗 NS3聚合链反应 RNA检测
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庚型肝炎病毒NS3区聚合酶链反应RNA检测
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作者 杨玉贵 许青田 杜绍财 《中国误诊学杂志》 CAS 2005年第9期1695-1696,共2页
关键词 肝炎 病毒性 人/诊断 聚合链反应 RNA 病毒/分析 NS3聚合链反应 庚型肝炎病毒 RNA检测 聚合链反应法 结果报告 HGV 逆转录
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非结核分枝杆菌菌种ITS-PCR测序鉴定法与表型鉴定法对比观察 被引量:4
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作者 桂静 王峰 李金莉 《检验医学》 CAS 2012年第11期908-912,共5页
目的评价16S~23S rRNA基因转录间隔区聚合酶链反应(ITS-PCR)在非结核分枝杆菌(NTM)菌种鉴定中的临床价值。方法采用ITS-PCR鉴定随机抽取的80株NTM,应用生长特性鉴定试验及鉴定性药物敏感性试验鉴定其表型特征,将3种鉴定方法所示结果进... 目的评价16S~23S rRNA基因转录间隔区聚合酶链反应(ITS-PCR)在非结核分枝杆菌(NTM)菌种鉴定中的临床价值。方法采用ITS-PCR鉴定随机抽取的80株NTM,应用生长特性鉴定试验及鉴定性药物敏感性试验鉴定其表型特征,将3种鉴定方法所示结果进行对比分析。结果 80株NTM中,鸟-胞分枝杆菌复合群(MAC)与脓肿分枝杆菌共占85%,运用ITS-PCR可将脓肿分枝杆菌、堪萨分枝杆菌、偶发分枝杆菌、苏尔加分枝杆菌准确鉴定,与生长特性鉴定试验及鉴定性药物敏感性试验结果基本符合;MAC采用3种方法鉴定其结果符合率存在偏差。结论 NTM ITS-PCR鉴定法与表型鉴定法相结合更适合临床应用。 展开更多
关键词 非结核分枝杆菌 基因转录间隔聚合链反应 生长特性鉴定试验 药物敏感性试验
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Mutation of DNA polymerase p in esophageal carcinoma of different regions 被引量:4
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作者 Guo-Qiang Zhao Tao Wang Qin Zhao Qin Zhao, Hong-Yan Yang, Xiao-Hui Tan, Zi-Ming Dong Hong-Yan Yang Xiao-Hui Tan Zi-Ming Dong 《World Journal of Gastroenterology》 SCIE CAS CSCD 2005年第30期4618-4622,共5页
AIM: To observe the variation of DNA polymerase β (polβ) in esophageal carcinoma. METHODS: Thirty specimens containing adjacent normal epithelial tissues were collected from patients in Linzhou region (a high r... AIM: To observe the variation of DNA polymerase β (polβ) in esophageal carcinoma. METHODS: Thirty specimens containing adjacent normal epithelial tissues were collected from patients in Linzhou region (a high risk area for esophageal squamous carcinoma) and 25 specimens were from a non-high risk area. Total RNA was extracted from the samples and reverse transcription polymerase chain reaction (RT-PCR) was performed. PCR products were cloned and sequenced to investigate the po1β gene with DNASIS and OMIGA. Statistical significance was evaluated using the X^2 test. RESULTS: High-inddence area group: Polβ gene variation was detected in 13 of 30 esophageal carcinoma tissue specimens, and only one variation was found in 30 corresponding adjacent normal tissue specimens. Non high-incidence area group: po1β gene variation was detected in 5 of 25 esophageal carcinoma tissue specimens, and no variation was found in 25 corresponding adjacent normal tissue specimens. The incidence of po1β gene variation observed in the high-incidence area group was significantly higher than in the non-high incidence area group. Two mutation hot spots (454-466 and 648-670 nt) and a 58 bp deletion (177-234 nt) were found. CONCLUSION: Variations of polβ perform different functions between the high-incidence areas and the other areas, and may play a more important role in the high-incidence areas. 展开更多
关键词 DNA polymerase β Esophageal carcinoma Gene mutation
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Characterization of Bioaerosol Bacterial Communities During Hazy and Foggy Weather in Qingdao, China 被引量:2
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作者 QI Jianhua LI Mengzhe +1 位作者 ZHEN Yu WU Lijing 《Journal of Ocean University of China》 SCIE CAS CSCD 2018年第3期516-526,共11页
This study was conducted to evaluate the impact of hazy and foggy weather on the bacterial communities in bioaerosols, for which samples were collected from the Qingdao coastal region on sunny, foggy, and hazy days in... This study was conducted to evaluate the impact of hazy and foggy weather on the bacterial communities in bioaerosols, for which samples were collected from the Qingdao coastal region on sunny, foggy, and hazy days in January and March 2013. Bacterial community compositions were determined using polymerase chain reaction denaturing gradient gel electrophoresis(PCR-DGGE). The bacterial community diversity was found to be high on foggy and hazy days, and the dominant species differed during hazy weather. The Shannon-Wiener index revealed that the bacterial community diversity of coarse particles was higher than that of fine particles in the bioaerosols. The bacterial community diversity of fine particles significantly correlated with relative humidity(RH; r^2 = 0.986). The cluster analysis results indicated that the bacterial communities on sunny days differed from those on hazy and foggy days. Compared with sunny days, the bacterial communities in the fine particles during hazy weather exhibited greater changes than those in the coarse particles. Most of the sequenced bacteria were found to be closely affiliated with uncultured bacteria. During hazy weather, members of the classes Bacilli and Gammaproteobacteria(Pseudomonas and Acinetobacter) were dominant. The DGGE analysis revealed that Proteobacteria and Firmicutes were the predominant phyla, and their relative percentages to all the measured species changed significantly on hazy days, particularly in the fine particles. Haze and fog had a significant impact on the bacterial communities in bioaerosols, and the bacterial community diversity varied on different hazy days. 展开更多
关键词 bacterial community BIOAEROSOLS HAZE FOG Qingdao
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Association between gastric cancer and -1993 polymorphism of TBX21 gene 被引量:2
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作者 Le-Hui Zhang Qin Li +5 位作者 Peng Li Sheng-Tao Zhu Jing Wang Hong-Li Yang Chang-Qing Xu Xiu-Hua Guo 《World Journal of Gastroenterology》 SCIE CAS CSCD 2012年第10期1117-1122,共6页
AIM: To investigate the association between the polymorphism of TBX21 gene and the risk of gastric cancer in a Chinese population. METHODS: The -1993 polymorphism located in TBX21 gene promoter region was identified b... AIM: To investigate the association between the polymorphism of TBX21 gene and the risk of gastric cancer in a Chinese population. METHODS: The -1993 polymorphism located in TBX21 gene promoter region was identified by polymerase chain reactionrestriction fragment length polymorphism (PCR-RFLP) method. The risk between TBX21 gene genotype and gastric cancer was determined by multivariate logistic regression analysis in 220 gastric cancer patients and 262 cancer-free controls matched by age, sex and ethnicity. RESULTS: Compared with the TBX21 -1993TT genotype, the -1993CC genotype exhibited a significantly elevated risk for gastric cancer [Odds ratio (OR) = 3.42, 95% confidence interval (CI): 1.41-8.31]. The relation-ship between the -1993 polymorphic genotype and the invasive status such as lymph node and distant metastasis was found among the gastric cancer patients (OR = 4.02, 95% CI: 1.87-8.66; OR = 7.02, 95% CI: 3.44-14.34, respectively). CONCLUSION: TBX21 -1993 polymorphism might contribute to the risk of gastric cancer, especially to the distant metastasis. 展开更多
关键词 TBX21 gene Gastric cancer POLYMORPHISM Genetic susceptibility Association analysis
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Rapid Identification of Pathogenic Bacteria by means of TwoConservative Gene Loci′ Specific PCR-CE-RFLP
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作者 高鹏 张卓然 +13 位作者 徐维家 安万新 张晓慧 戴兵 范艳萍 王运铎 李萍 温杰 于卫健Dalian Red Cross Blood Center Dalian 116001 China 高向仪 谢凡迪 王永海 《Journal of Microbiology and Immunology》 2003年第1期38-43,共6页
To establish a rapid identification method for common pathogenic bacteria on the basis of molecular biology and to construct a preliminary Polymerase Chain Reaction-Capillary Electrophoresis - Restriction Fragment Len... To establish a rapid identification method for common pathogenic bacteria on the basis of molecular biology and to construct a preliminary Polymerase Chain Reaction-Capillary Electrophoresis - Restriction Fragment Length Polymorphism (PCR-CE-RFLP) database of bacteria isolated from clinical specimens frequently, 183 strains collected from clinical samples belonging to 12 genera and 19 species whose biochemical characterizations corresponded to the typical ones were examined. The genomic DNAs were amplified by two pairs of fluorescence labeled primers aiming at 16S rRNA gene and 16S-23S rRNA spacer region gene respectively at the same time. PCR products were then digested by restriction endonuclease HaeⅢ incompletely before taking capillary electrophoresis. The results with the PCR-CE-RFLP patterns of 16S rRNA genes were just alike within some genera, but when it comes to 16S-23S rRNA spacer region genes, each bacterium showed a unique pattern, which can be distinguished from each other easily. It seems that PCR-CE-RFLP patterns of 16S rRNA gene could only be used to classify the bacteria into family level, whereas the data of 16S-23S rRNA spacer region gene could be utilized to identify the whole microorganisms as precisely as the species level. In spite of the data of the spacer region gene alone can be sufficiently to verify the whole bacteria, we insist that the 16S rRNA gene could be of some assistant in case that there should be lots of families of bacteria, in which some similar ones, with the same RFLP data of 16S-23S rRNA spacer region gene, may coexist. This study proves that the utility of PCR-CE-RFLP is a convenient, rapid method to identify pathogenic bacteria, and is also a quick diagnosis measure for application to clinical use. 展开更多
关键词 S rRNA gene 16S-23S rRNA gene spacer region Polymerase chain reaction Pathogenic bacteria RFLP
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2017年安庆市急性胃肠炎暴发疫情病原体诺如病毒的鉴定及基因特征分析 被引量:6
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作者 刘敏鸿 金爱武 +3 位作者 曹孟婵 史永林 李贤相 徐四清 《中国病原生物学杂志》 CSCD 北大核心 2018年第9期1006-1009,共4页
目的对安徽省安庆市2017年2-3月间发生的10起急性胃肠炎暴发疫情病原诺和病毒进行鉴定及基因分型。方法采集聚集性和暴发疫情中有胃肠炎症状者的肛拭子标本,采用实时荧光定量RT-PCR检测诺如病毒(NoV)核酸,使用RT-PCR对核酸阳性标本扩增... 目的对安徽省安庆市2017年2-3月间发生的10起急性胃肠炎暴发疫情病原诺和病毒进行鉴定及基因分型。方法采集聚集性和暴发疫情中有胃肠炎症状者的肛拭子标本,采用实时荧光定量RT-PCR检测诺如病毒(NoV)核酸,使用RT-PCR对核酸阳性标本扩增NoV衣壳区-聚合酶区,选取27份琼脂糖电泳条带清晰的阳性标本进行基因测序及型别鉴定,并与国内外参考株序列构建进化树,进行遗传进化分析。结果 10起胃肠炎暴发疫情中共采集103份肛拭子标本,实时荧光定量RT-PCR检测诺如病毒核酸阳性41份,且均为GII型,阳性率为39.81%。选取27份阳性标本测序,其中20份测序成功,进化分析显示19条序列为NoV GII.P16/GII.2,1条序列为NoV GII.P17/GII.17。结论诺如病毒GII.P16/GII.2是安庆市2017年2-3月份急性胃肠炎暴发疫情的主要病原体。 展开更多
关键词 诺如病毒 RT-PCR 衣壳-聚合酶区 进化分析
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诺如病毒基因分型研究进展 被引量:22
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作者 沈玲羽 姜博 +3 位作者 严寒秋 李伟红 高志勇 王全意 《中华流行病学杂志》 CAS CSCD 北大核心 2020年第11期1927-1932,共6页
诺如病毒是引起急性胃肠炎的主要病原体之一,极易突变和重组,型别众多。研究早期采用VP1区氨基酸序列对诺如病毒进行分型及鉴定。由于处在或接近聚合酶和衣壳区的重叠区为重组发生的热点区域,因此国际上提出使用聚合酶和衣壳区的双区域... 诺如病毒是引起急性胃肠炎的主要病原体之一,极易突变和重组,型别众多。研究早期采用VP1区氨基酸序列对诺如病毒进行分型及鉴定。由于处在或接近聚合酶和衣壳区的重叠区为重组发生的热点区域,因此国际上提出使用聚合酶和衣壳区的双区域分型系统。目前基于2 s标准的双区域分型方法,聚合酶区可分为10个基因组及76种基因型,包括2个暂定基因组及16种暂定基因型,VP1可分为12个基因组及53种基因型,包括2个暂定基因组及5种暂定基因型。暂定基因组和基因型有待进一步型别鉴定和基因组划分。本文对诺如病毒分子特征、不同分型方法的原理、序列扩增方法、在线分型工具及最新的基因分型研究进展进行综述。 展开更多
关键词 诺如病毒 基因分型 聚合酶区 衣壳
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Microbial and hydrodynamic properties of aerobic granules in a sequencing batch reactor treating landfill leachate
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作者 Yan-jie WEI Min JI +1 位作者 Guo-yi LI Fei-fei QIN 《Journal of Zhejiang University-Science A(Applied Physics & Engineering)》 SCIE EI CAS CSCD 2012年第3期219-229,共11页
A sequencing batch reactor (SBR) seeded with activated sludge was established for landfill leachate treatment. Small bio-aggregates began to appear after 40-d operation, and gradually changed to mature aerobic granu... A sequencing batch reactor (SBR) seeded with activated sludge was established for landfill leachate treatment. Small bio-aggregates began to appear after 40-d operation, and gradually changed to mature aerobic granules, with a mean size of 0.36-0.60 ram. Their sludge volume index at 5 min (SVI5 rain), mixed liquor volatile suspended solids (MLVSS), and wet density were around 35 ml/g, 3.4 g/L, and 1.062 g/cm3, respectively. The settling velocities of the granules in distilled water ranged from 0.3 to 1.3 cm/s, which were faster than those in landfill leachate with a salt content of 1.4% (w/v), and also slightly faster than those predicted by Stokes' law for porous but impermeable particles. Microbial community evolution during the granulation process and stages under different nitrogen loading rates (NLRs) were monitored and analyzed by polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE), cloning, and sequencing of 16S ribosomal RNA (rRNA) fragments. Results revealed that some primary and dominant communities in inoculating activated sludge died out gradually; while a few common bacteria, inhabiting soils, municipal wastewater, or activated sludge systems, dominated in the SBR system throughout. In addition, some other dominant species, associated with the aerobic granulation process, were thought to play a significant role in the formation and growth of aerobic granular sludge. During the stable operation time under low NLR, a few species were present in abundance, and may have been responsible for the high organic removal efficiency at this time. 展开更多
关键词 Aerobic granules Microbial community Polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) Landfill leachate
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