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中国蒙古族人MBL基因启动子区SNP的研究 被引量:5
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作者 吕成伟 陈政良 +3 位作者 王方勇 钟成全 张丽芸 卢晓 《免疫学杂志》 CAS CSCD 北大核心 2004年第2期91-94,共4页
目的 研究中国蒙古族人群甘露聚糖结合凝集素 (MBL)基因启动子区单核苷酸多态性 (SNP)。方法 抽提人外周血白细胞基因组DNA ,建立SSP PCR及分子灯塔实时荧光PCR技术 ,检测MBL基因启动子区SNP位点 - 5 5 0 (G C ,称H L等位基因 )、- 2 ... 目的 研究中国蒙古族人群甘露聚糖结合凝集素 (MBL)基因启动子区单核苷酸多态性 (SNP)。方法 抽提人外周血白细胞基因组DNA ,建立SSP PCR及分子灯塔实时荧光PCR技术 ,检测MBL基因启动子区SNP位点 - 5 5 0 (G C ,称H L等位基因 )、- 2 2 0 (G C ,X Y等位基因 )和 +4(C T ,P Q等位基因 ) ,分析其单倍型及基因型频率。结果 从 82人中检出等位基因型LYP LYP 4例 (4 .9% ) ,HYP LYQ 5例 (6 .1% ) ,LYP LYQ 35例 (4 2 .9% ) ,LXP LXP 1例 (1.2 % ) ,LYQ LYQ 11例 (13.4 % ) ,LXP LYQ 14例 (17.1% ) ,HYP LYP 2例 (2 .4 % ) ,HYP LXP 1例 (1.2 % ) ,HYP HYP 9例 (11.0 % )。结论 中国蒙古族人群MBL基因启动子区SNP等位基因型以LYP LYQ、LXP LYQ、LYQ LYQ和HYP 展开更多
关键词 启动子区 甘露聚糖结合凝集素 单核苷酸多态性 序列特异性引物一多聚酶链反应 多聚酶链反应-分子灯塔实时分析
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广东地区汉族人MBL基因启动子区SNP的研究 被引量:5
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作者 吕成伟 陈政良 +1 位作者 刁志宏 王方勇 《第一军医大学学报》 CSCD 北大核心 2003年第11期1165-1168,共4页
目的研究广东汉族人群甘露聚糖结合凝集素(MBL) 基因启动子单核苷酸多态性(SNP) 。方法抽提人外周血白细胞基因组DNA,建立SSP-PCR及分子灯塔实时荧光PCR技术,检测MBL基因启动子区SNP位点-550(G/C,称H/L等位基因) 、-220(G/C,X/Y等位基... 目的研究广东汉族人群甘露聚糖结合凝集素(MBL) 基因启动子单核苷酸多态性(SNP) 。方法抽提人外周血白细胞基因组DNA,建立SSP-PCR及分子灯塔实时荧光PCR技术,检测MBL基因启动子区SNP位点-550(G/C,称H/L等位基因) 、-220(G/C,X/Y等位基因) 和+4(C/T,P/Q等位基因),分析其单倍型及基因型频率。结果从167人中检出等位基因型LYP/LYP 10例(5.9%)、HYP/LYQ 7例(4.2%)、LYP/LYQ 94例(56.3%)、LXP/LXP 6例(3.6%)、LYQ/LYQ 4例(2.4%)、LXP/LYQ 29例(17.4%)、HYP/LYP 3例(1.8%)、HYP/LXP 2例(1.2%)、HYP/HYP 12例(7.2%)。结论广东地区汉族人群MBL基因启动子区SNP等位基因型以LYP/LYQ和LXP/LYQ为主。 展开更多
关键词 广东地区 汉族 MBL 基因启动子区 SNP 甘露聚糖结合凝集素
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分子信标的原理、应用及其研究进展 被引量:7
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作者 周海清 沈鹤柏 +1 位作者 陈新斌 巢强国 《光谱实验室》 CAS CSCD 2004年第3期417-422,共6页
分子信标是一种设计巧妙的新型荧光标记核酸探针。特殊的发夹结构使分子信标具有很强的特异性识别靶标序列的能力 ,目前已成为分子生物学和生物技术中一种强有力的研究工具。本文介绍了分子信标的原理及其在 PCR、核酸序列的分析、活细... 分子信标是一种设计巧妙的新型荧光标记核酸探针。特殊的发夹结构使分子信标具有很强的特异性识别靶标序列的能力 ,目前已成为分子生物学和生物技术中一种强有力的研究工具。本文介绍了分子信标的原理及其在 PCR、核酸序列的分析、活细胞内核酸的动态检测、蛋白质 (酶 )与核酸的相互作用等方面的应用和研究进展。 展开更多
关键词 分子信标 荧光核酸探针 荧光共振能量转移 聚合酶链反应 核酸分析
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Expression signatures of long non-coding RNA and mRNA in human traumatic brain injury 被引量:8
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作者 Li-Xiang Yang Li-Kun Yang +3 位作者 Jie Zhu Jun-Hui Chen Yu-Hai Wang Kun Xiong 《Neural Regeneration Research》 SCIE CAS CSCD 2019年第4期632-641,共10页
Long non-coding RNAs(lncRNAs) play a key role in craniocerebral disease, although their expression profiles in human traumatic brain injury are still unclear. In this regard, in this study, we examined brain injury ti... Long non-coding RNAs(lncRNAs) play a key role in craniocerebral disease, although their expression profiles in human traumatic brain injury are still unclear. In this regard, in this study, we examined brain injury tissue from three patients of the 101 st Hospital of the People's Liberation Army, China(specifically, a 36-year-old male, a 52-year-old female, and a 49-year-old female), who were diagnosed with traumatic brain injury and underwent brain contusion removal surgery. Tissue surrounding the brain contusion in the three patients was used as control tissue to observe expression characteristics of lncRNAs and mRNAs in human traumatic brain injury tissue. Volcano plot filtering identified 99 lncRNAs and 63 mRNAs differentially expressed in frontotemporal tissue of the two groups(P < 0.05, fold change > 1.2). Microarray analysis showed that 43 lncRNAs were up-regulated and 56 lncRNAs were down-regulated. Meanwhile, 59 mRNAs were up-regulated and 4 mRNAs were down-regulated. Gene Ontology(GO) and Kyoto Encyclopedia of Genes and Genomes(KEGG) analyses revealed 27 signaling pathways associated with target genes and, in particular, legionellosis and influenza A signaling pathways. Subsequently, a lncRNA-gene network was generated, which showed an absolute correlation coefficient value > 0.99 for 12 lncRNA-mRNA pairs. Finally, quantitative real-time polymerase chain reaction confirmed different expression of the five most up-regulated mRNAs within the two groups, which was consistent with the microarray results. In summary, our results show that expression profiles of mRNAs and lncRNAs are significantly different between human traumatic brain injury tissue and surrounding tissue, providing novel insight regarding lncRNAs' involvement in human traumatic brain injury. All participants provided informed consent. This research was registered in the Chinese Clinical Trial Registry(registration number: ChiCTR-TCC-13004002) and the protocol version number is 1.0. 展开更多
关键词 nerve REGENERATION HUMAN TRAUMATIC brain injuries long noncoding RNA messenger RNA GO analysis real-time quantitative polymerase chain reaction biomarkers microarray analysis biological processes medical informatics neural REGENERATION
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Correlation between mitochondrial TRAP-1 expression and lymph node metastasis in colorectal cancer 被引量:13
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作者 Jing-Yan Gao Bao-Rong Song +1 位作者 Jun-Jie Peng Yuan-Ming Lu 《World Journal of Gastroenterology》 SCIE CAS CSCD 2012年第41期5965-5971,共7页
AIM: To evaluate the effect of mitochondrial tumor ne- crosis factor receptor-associated protein-1 (TRAP-l) on the lymph node metastasis (LNM) in Chinese colorectal cancer (CRC) patients, and develop potential ... AIM: To evaluate the effect of mitochondrial tumor ne- crosis factor receptor-associated protein-1 (TRAP-l) on the lymph node metastasis (LNM) in Chinese colorectal cancer (CRC) patients, and develop potential LNM- associated biomarkers for CRC using quantitative real- time polymerase chain reaction (RT-PCR) analysis. METHODS: Differences in mitochondrial TRAP-1 gene expression between primary CRC with LNM (LNM CRC) and without LNM (non-LNM CRC) were assessed in 96 Chinese colorectal carcinoma samples using quantita- tive RT-PCR analysis, Western blotting, and confirmed with immunohistochemical assay. The relationship between clinicopathological parameters and potential diaclnostic biomarkers was also examined.RESULTS: TRAP-1 was significantly upregulated in LNM CRC compared with non-LNM CRC, which was confirmed by RT-PCR, Western blotting and immuno- histochemical assay. The expression of TRAP-1 in two different metastatic potential human colorectal cancer cell lines, LoVo and HT29, was analyzed with Western blotting. The expression level of TRAP-1 was dramati- cally higher in LoVo than in HT29. Overexpression of TRAP-1 was significantly associated with LNM (90.2% in LNM group vs 22% in non-LNM group, P 〈 0.001), the advanced tumor node metastasis stage (89.1% in LNM group vs 26.9% in non-LNM group, P 〈 0.001), the increased 5-year recurrence rate (82.7% in LNM group vs 22.6% in non-LNM group, P 〈 0.001) and the decreased 5-year overall survival rate (48.4% in LNM vs 83.2% in non-LNM group, P 〈 0.001). Univariate and multivariate analyses indicated that TRAP-1 expression was an independent prognostic factor for recurrence and survival of CRC patients (Hazard ratio of 2.445 in recurrence, P = 0.017; 2.867 in survival, P = 0.028). CONCLUSION: Mitochondria TRAP-1 affects the lymph node metastasis in CRC, and may be a potential bio- marker for LNM and a prognostic factor in CRC. Over- expression of TRAP-1 is a predictive factor for the poor outcome of colorectal cancer patients. 2012 Baishideng. All rights reserved 展开更多
关键词 Colorectal cancer Lymph node metastasis PROGNOSIS Quantitative real-time polymerase chain reaction analysis Hsp90 family Mitochondria tumor necrosis factor receptor-associated protein-1
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Use of blood-based biomarkers for early diagnosis and surveillance of colorectal cancer 被引量:11
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作者 Ganepola AP Ganepola Joel Nizin +1 位作者 John R Rutledge David H Chang 《World Journal of Gastrointestinal Oncology》 SCIE CAS 2014年第4期83-97,共15页
Early screening for colorectal cancer(CRC) holds the key to combat and control the increasing global burden of CRC morbidity and mortality. However, the current available screening modalities are severely inadequate b... Early screening for colorectal cancer(CRC) holds the key to combat and control the increasing global burden of CRC morbidity and mortality. However, the current available screening modalities are severely inadequate because of their high cost and cumbersome preparatory procedures that ultimately lead to a low participation rate. People simply do not like to have colonoscopies. It would be ideal, therefore, to develop an alternative modality based on blood biomarkers as the first line screening test. This will allow for the differentiation of the general population from high risk individuals. Colonoscopy would then become the secondary test, to further screen the high risk segment of the population. This will encourage participation and therefore help to reach the goal of early detection and thereby reduce the anticipated increasing global CRC incidence rate. A blood-based screening test is anappealing alternative as it is non-invasive and poses minimal risk to patients. It is easy to perform, can be repeated at shorter intervals, and therefore would likely lead to a much higher participation rate. This review surveys various blood-based test strategies currently under investigation, discusses the potency of what is available, and assesses how new technology may contribute to future test design. 展开更多
关键词 Colorectal neoplasms Early detection of cancer Colonoscopy Biological markers BLOOD Messenger RNA MicroRNA Long NON-CODING RNA DNA methylation Microsatellite instability Loss of HETEROZYGOSITY High-throughput NUCLEOTIDE sequencing Mass spectrometry real-time polymerase chain reaction Microarray analysis
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Atypical chemokine receptor CCRL2 is overexpressed in prostate cancer cells 被引量:1
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作者 Niradiz Reyes Ines Benedetti +2 位作者 Juan Rebollo Oscar Correa Jan Geliebter 《The Journal of Biomedical Research》 CAS CSCD 2019年第1期17-23,共7页
Atypical chemokine receptors have recently emerged as important molecular players in health and diseases; they affect chemokine availability and function and impact a multitude of pathophysiological events, including ... Atypical chemokine receptors have recently emerged as important molecular players in health and diseases; they affect chemokine availability and function and impact a multitude of pathophysiological events, including the tumorigenesis process. This family of atypical receptors comprises five members: ACKR1/DARC, ACKR2/D6,ACKR3/CXCR7, ACKR4/CCRL1, and ACKR5/CCRL2. This work evaluated the differential expression of these receptors in prostate cancer using quantitative PCR. Further evaluation of CCRL2 at the protein level confirmed its overexpression in a metastatic cell line and in malignant prostatic tissues from patients. CCRL2, a presumed member of the atypical chemokine receptor family, plays a key role in lung dendritic cell trafficking to peripheral lymph nodes.Recent studies have reported the expression of CCRL2 in different human cancer cell lines and tissues. However, its function and expression in prostate cancer has not been previously addressed. 展开更多
关键词 CHEMOKINE RECEPTOR PROSTATIC NEOPLASMS CCRL2 RECEPTOR real-time polymerase chain reaction tissue array analysis
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分子信标熔解曲线法分析SLC11A1基因插入/缺失多态性
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作者 朱玉梅 刘小立 +3 位作者 龚春梅 莫俊銮 谭春燕 周继昌 《中国卫生检验杂志》 CAS 2015年第13期2167-2170,共4页
目的针对溶质转运蛋白家族11成员1蛋白(SLC11A1)基因插入/缺失多态性位点rs17235416,建立基于荧光定量PCR(q PCR)的分子信标熔解曲线法对其进行基因分型。方法针对该位点设计特异性的引物和分子信标探针,联合应用非对称q PCR、分子信标... 目的针对溶质转运蛋白家族11成员1蛋白(SLC11A1)基因插入/缺失多态性位点rs17235416,建立基于荧光定量PCR(q PCR)的分子信标熔解曲线法对其进行基因分型。方法针对该位点设计特异性的引物和分子信标探针,联合应用非对称q PCR、分子信标探针和熔解曲线分析等技术建立分子信标熔解曲线法进行基因分型。对210份全血样本提取DNA后,用上述方法和改进的PCR-RFLP法对该位点进行检测和分型,并以测序法验证。结果 210份样本的基因型TGTG+/+、TGTG-/-和TGTG+/-分布频率分别为69.5%、4.8%和25.7%。分子信标熔解曲线法和PCR-RFLP法的分型结果与测序结果完全一致。结论国内外首次成功建立分子信标熔解曲线法检测SLC11A1基因rs17235416位点;该方法在大人群样本检测中具有简便、快速、准确等优点。 展开更多
关键词 溶质转运蛋白家族11成员1蛋白 插入/缺失多态性 分子信标 熔解曲线分析 聚合酶链反应-限制性片段长度多态性
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Monitoring Soil Microbial Activities in Different Cropping Systems Using Combined Methods 被引量:2
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作者 YUAN Zhimin LIU Haijun +3 位作者 HAN Jun SUN Jingjing WU Xiaoying YAO Jun 《Pedosphere》 SCIE CAS CSCD 2017年第1期138-146,共9页
Cropping activities may affect soil microbial activities and biomass,which would affect C and N cycling in soil and thus the crop yields and quality.In the present study,a combination of microcalorimetric,enzyme activ... Cropping activities may affect soil microbial activities and biomass,which would affect C and N cycling in soil and thus the crop yields and quality.In the present study,a combination of microcalorimetric,enzyme activity(sucrase,urease,catalase,and fluorescein diacetate hydrolysis),and real-time polymerase chain reaction(RT-PCR) analyses was used to investigate microbial status of farmland soils,collected from 5 different sites in Huazhong Agriculture University,China.Our results showed that among the 5sites,both positive and negative impacts of cropping activities on soil microbial activity were observed.Enzyme activity analysis showed that cropping activities reduced soil sucrase and urease activities,which would influence the C and N cycles in soil.Much more attentions should be given to microbial status affected by cropping activities in future.According to the correlation analysis,fluorescein diacetate hydrolysis showed a significantly(P < 0.05) negative correlation with the time to reach the maximum power output(R ——0.898),but a significantly(P < 0.05) positive correlation with bacterial gene copy number(R = 0.817).Soil catalase activity also showed a significantly(P < 0.05) positive correlation with bacterial gene copy number(R = 0.965).Using combined methods would provide virtual information of soil microbial status. 展开更多
关键词 cropping activity enzyme activity fluorescein diacetate hydrolysis microbial biomass microealorimetric analysis real-time polymerase chain reaction
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Bacterial community composition and abundance in leachate of semi-aerobic and anaerobic landfills 被引量:2
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作者 Wei Zhang Bo Yue +3 位作者 Qi Wang Zechun Huang Qifei Huang Zengqiang Zhang 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2011年第11期1770-1777,共8页
The abundance and phylogenetic composition of bacterial community in leachate of semi-aerobic and anaerobic landfill were compared through real-time polymerase chain reaction and denaturing gradient gel electrophoresi... The abundance and phylogenetic composition of bacterial community in leachate of semi-aerobic and anaerobic landfill were compared through real-time polymerase chain reaction and denaturing gradient gel electrophoresis. In semi-aerobic landfill scenario, the bacterial 16S rRNA copy numbers in leachate had no significant reduction from initial stage to stable period. In the scenario of anaerobic landfill, the largest bacterial 16S rRNA gene copy number was found in leachate at initial stage, but it reduced significantly at stable period. Moreover, methane-oxidizing bacteria population in stable period was lower than that in initial period in both two landfill processes. However, semi-aerobic landfill leachate had more methanotrophic bacteria populations than that in the anaerobic one. Furthermore, according to the sequences and phylogenetic analysis, obvious difference could be detected in bacterial community composition in different scenarios. Proteobacteria and bacteroidetes took up a dominantly higher proportion in semi-aerobic landfill leachate. To summarize up, different landfill methods and its landfill ages had crucial impacts on bacterial abundance and composition in leachate of semi-aerobic and anaerobic landfills. 展开更多
关键词 real-time polymerase chain reaction denaturing gradient gel electrophoresis bacterial 16S rRNA gene methane-oxidizing bacteria phylogenetic analysis
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