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家族性肾阳虚的基因功能富集分析
引用本文:刘 明,丁维俊,蔡 欣,张天娥,李炜弘,王米渠.家族性肾阳虚的基因功能富集分析[J].中国生物化学与分子生物学报,2009,25(8):747-752.
作者姓名:刘 明  丁维俊  蔡 欣  张天娥  李炜弘  王米渠
作者单位:(1)四川大学华西医院生物治疗国家重点实验室,信号转导及分子靶向治疗研究室,成都610041;2)成都中医药大学,成都610075;3)成都铁路中心医院内分泌科,成都610081)
摘    要:在临床调查中筛选出一个典型肾阳虚证家系,选取典型肾阳虚证患者3例及家系内正常人3例进行表达谱芯片试验.芯片分析结果显示,肾阳虚证者表达上调基因106条,下调基因16条.通过基因功能分类及深入的基因功能富集分析发现,肾阳虚证与GnRH信号通路及氧化磷酸化密切相关(P≤005),从而为肾阳虚证本质的研究提供了新的思路,但具体的机制有待深入研究.

关 键 词:肾阳虚证  基因功能富集分析  家系  氧化磷酸化  GnRH信号通路  
收稿时间:2009-2-18

Gene Function Enrichment Analysis of a Pedigree with Typical Kidney-Yang Deficiency Syndrome
LIU Ming,DING Wei-Jun,CAI Xin,ZHANG Tian-E,LI Wei-Hong,WANG Mi-Qu

.Gene Function Enrichment Analysis of a Pedigree with Typical Kidney-Yang Deficiency Syndrome[J].Chinese Journal of Biochemistry and Molecular Biology,2009,25(8):747-752.
Authors:LIU Ming  DING Wei-Jun  CAI Xin  ZHANG Tian-E  LI Wei-Hong  WANG Mi-Qu

Institution:(1)Laboratory of Signal Transduction &; Molecular Targeting Therapy, State Key Laboratory of Biotherapy, West China Hospital,Sichuan University, Chengdu 610041, China;2) Chengdu University of TCM, Chengdu 610075, China;3) Department of Endocrine, Chengdu Railway Center Hospital, Chengdu 610081, China)
Abstract:A typical deficiency-cold syndrome pedigree were analyzed based on clinical investigation, and microarrays were made to examine expression profile of kidney-yang deficiency syndrome. Compared with normal members in the family, members with kidney-yang deficiency syndrome showed that there were 106 genes up-regulated and 16 down-regulated by at least 1.5 fold. Gene classification and gene function enrichment analysis of differentially expressed genes indicated that kidney-yang deficiency syndrome was closely associated with GnRH signaling pathway and oxidative phosphorylation (P≤005), but the exact mechanisms keeps unknown.
Keywords:kidney-yang deficiency syndrome  gene function enrichment analysis  pedigree  oxidative phosphorylation  GnRH signaling pathway
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