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基于应变模态的桥梁损伤识别方法研究进展
  • ISSN号:1671-2579
  • 期刊名称:《中外公路》
  • 时间:0
  • 分类:Q78[生物学—分子生物学] TS218[轻工技术与工程—粮食、油脂及植物蛋白工程;轻工技术与工程—食品科学与工程]
  • 作者机构:[1]Diabetes Center, Second Xiangya Hospital, and Institute of Metabolism and Endocrinology, Key Laboratory of Diabetes Immunology, Ministry of Education, Central South University, Changsha, Hunan 410011, China
  • 相关基金:This work was supported by grants from the National Natural Science Foundation of China (No. 81170725, 81070672, 81000316), the European Foundation for the Study of Diabetes (No. EFSD/CDS/Lilly-2010), the Key Project of Science and Technology Department of Hunan Province of China (No. 2010SK2007), Hunan Provincial Natural Science Foundation of China (No. 11JJ7005), the National Department Public Benefit (Health) Research Foundation of China (No. 201002002), Research Fund for the Doctoral Program of Higher Education of China (No. 200805331018). There are no financial/commercial conflicts of interests involving in this study.
中文摘要:

1 糖尿病( F1D )是的背景暴发性的类型复杂 disease.Microarray 分析被用来识别基因表示变化并且获得内在的 mechanisms.Methods Microarray 理解分析从六个 F1D 病人和六匹配的健康subjects.Real时间在外部血 mononuclear 房间上被执行聚合酶链反应被用来证实差别表示了 genes.NK 房间活动被识别的甲基 thiazoleterazolium assay.Results Microarray 分析检测

英文摘要:

Background Fulminant type 1 diabetes (F1D) is a complex disease. Microarray analysis was used to identify gene expression changes and obtain understanding of the underlying mechanisms. Methods Microarray analysis was performed on peripheral blood mononuclear cells from six F1D patients and six matched healthy subjects. Real-time polymerase chain reaction was used to verify the differentially expressed genes. NK cell activity was detected by methyl thiazoleterazolium assay. Results Microarray analysis identified 759 genes differing in expression between F1D patients and controls at a false discovery rate of 0.05. Expression of TLR9, ELF4 and ILIRAP were verified and consistent with changes in microarray results. NK cell activity was decreased in FID. With use of a knowledge base, differentially expressed genes could be placed within different pathways with predicted functions including interleukin-1, and tumor necrosis factor-a signaling. Conclusions These results identify several genes indicating possible mechanisms in FID. NK cell dysfunction resulting from changes in expression of TLR9, ELF4 and IL1RAP, and pathways of interleukin-1 and tumor necrosis factor-a sianalino miaht be involved in F1D throuoh inducino B-cell dysfunction.

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期刊信息
  • 《中外公路》
  • 中国科技核心期刊
  • 主管单位:长沙理工大学
  • 主办单位:长沙理工大学
  • 主编:刘玉兰
  • 地址:湖南省长沙市万家丽南路二段960号
  • 邮编:410004
  • 邮箱:zhongwaigonglu@163.com
  • 电话:0731-85258033
  • 国际标准刊号:ISSN:1671-2579
  • 国内统一刊号:ISSN:43-1363/U
  • 邮发代号:42-63
  • 获奖情况:
  • 交通部优秀科技期刊,湖南省优秀科技期刊,公路运输类中文核心期刊
  • 国内外数据库收录:
  • 中国中国科技核心期刊,中国北大核心期刊(2004版),中国北大核心期刊(2008版),中国北大核心期刊(2011版),中国北大核心期刊(2014版)
  • 被引量:15085