1 叶文静,赵晓民,侯配强,等.老年大鼠组织mRNA分析中内参基因的选择[J].基础医学与临床,2009,29(1):82~84. 2 陈腾祥.内毒素休克小鼠肝脏核蛋白质组学研究[D].广州:第一军医大学,2007. 3 董晓丽,王加启,卜登攀,等.内参基因在实时定量PCR中应用的研究进展[J].中国畜牧兽医,2009,36(9):83~85. 4 Angus D C,Linde-Zwirble W T,Lidicker J,et al.Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care[J].Crit Care Med, 2001,29(7):1303~1310. 5 Cinar M U,Islam M A,Uddin M J,et al. Evaluation of suitable reference genes for gene expression studies in porcine alveolar macrophages in response to LPS and LTA[J].BMC Research Notes,2013,6:56. 6 De Boever S,Vangestel C,De Backer P,et al. Identification and validation of housekeeping genes as internal control for gene expression in an intravenous LPS inflammation model in chickens[J].Vet Immunol Immunopathol,2008,122(3~4):312~317. 7 Gachon C,Mingam A,Charrier B.Real-time PCR: What relevance to plant studies[J].Exp Bot,2004,55(402):1445~1454. 8 Huggett J,Dheda K,Bustin S,et al. Real-time RT-PCR normalisation:Strategies and considerations[J].Genes Immun, 2005(6):279~284. 9 Lossos I S, Czerwinski D K, Wechser M A, et al. Optimization of quantitative real-time RT-PCR parameters for the study of lymphoid malignancies[J].Leukemia, 2003,17(4):789~795. 10 Mamo S,Gal A B,Bodo S,et al. Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo[J].BMC Dev Biol,2007,7(14):24~34. 11 Radonic A,Thulke S,Mackay I M,et al. Guideline to reference gene selection for quantitative real-time PCR[J].Biochem Biophys Res Commun, 2004,23(313):856~862. 12 Radonic A, Thulke S, Bae H G,et al. Reference gene selection for quantitative real-time PCR analysis in virus infected cells: SARS corona virus, yellow fever virus, human Herpesvirus-6, camelpox virus and cytomegalo virus infections[J].Journal of Virology, 2005,2:7. 13 Sands K E,Bates D W,Lanken P N,et al. Epidemiology of sepsis syndrome in 8 academic medical centers[J].JAMA, 1997,16(278):234~240. 14 Solanas M,Moral R,Escrich E.Unsuitability of using ribosomal RNA as loading control for Northern blot analyses related to the imbalance between messenger and ribosomal RNA[J].Analytical Biochemistry, 2001,288(1):99~102. 15 Thellin O,Zorzi W,Lakaye B,et al. Housekeeping genes as internal standards: Use and limits[J].J Biotechnol,1999,75(3):291~295. 16 Udvardi M K,Czechowski T,Scheible W R.Eleven golden rules of quantitative RT-PCR[J].Plant Cell, 2008,20(7):1736~1737. 17 Vandesompele J,De Preter K,Pattyn F,et al. Accurate normalizaition of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes[J].Genome Biol, 2002,3(7):1~11. 18 Watson S, Mercier S,Bye C,et al. Determination of suitable housekeeping genes for normalisation of quantitative real-time PCR analysis of cells infected with human immunodeficiency virus and herpes viruses[J].Virol J,2007,4:130. 19 Willems E,Mateizel I,Kemp C,et al. Selection of reference genes in mouse embryos and in differentiating human and mouse ES cells[J].Int J Dev Biol, 2006,50(7):627~635. 20 Wong M L,MedranoJ F.Real-time PCR for mRNA quantitation[J].Biotechniques, 2005,39(1):75~85. 21 Yue H, Lei X W, Yang F L,et al. Reference gene selection for normalization of PCR analysis in chicken embryo fibroblast infected with H5N1 AIV[J].Virol Sin, 2010,25(6):425~431. |