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首页> 外文期刊>Clinical Biochemistry >Clinical application of cytokine-related gene polymorphism analysis using a newly developed DNA chip in critically ill patients.
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Clinical application of cytokine-related gene polymorphism analysis using a newly developed DNA chip in critically ill patients.

机译:使用新开发的DNA芯片在重症患者中进行细胞因子相关基因多态性分析的临床应用。

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摘要

OBJECTIVES: To investigate the usefulness of analysis of single nucleotide polymorphism (SNP) using a newly developed DNA chip assay involving single base extension(SBE) and subsequent hybridization in cytokine-related genes in critical care patients. DESIGN AND METHODS: Genotyping was performed in 76 ICU patients admitted to the ICU. First, the DNA samples from 58 patients were subjected to PCR and SBE conditioning for DNA. Second, another 18 patients were subjected to genotyping for SNPs in IL-6 -596G/A, -572C/G, -174G/C, TNF-alpha -308G/A, -238G/A, IL-1beta -511C/T and -31T/C by both TaqMan and DNA chip method, and by DNA direct sequencing prospectively. RESULTS: First, PCR and SBE condition were established with initial sample sets, which were consistent with results by TaqMan method. Second, no difference was observed between two assay methods in prospective validation set. CONCLUSIONS: The genotyping assay using the new chip was developed and its usefulness was confirmed.
机译:目的:研究使用新开发的涉及单碱基延伸(SBE)和随后在重症监护患者中与细胞因子相关基因杂交的DNA芯片测定法分析单核苷酸多态性(SNP)的有用性。设计与方法:对76例入ICU的ICU患者进行基因分型。首先,对58例患者的DNA样本进行PCR和SBE调节以检测DNA。其次,对18例患者的IL-6 -596G / A,-572C / G,-174G / C,TNF-alpha -308G / A,-238G / A,IL-1beta -511C / T中的SNP进行基因分型TaqMan法和DNA芯片法同时检测-31T / C和DNA直接测序。结果:首先,用初始样品组建立了PCR和SBE条件,这与TaqMan方法的结果一致。第二,在前瞻性验证集中的两种测定方法之间未观察到差异。结论:开发了使用新芯片的基因分型方法,并证实了其有用性。

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