REFERENCES
- Bond B. C., Virley D. J., Cairns N. J., Hunter A. J., Moore G. B., Moss S. J., Mudge A. W., Walsh F. S., Jazin E, Preece P. The quantification of gene expression in an animal model of brain ischaemia using TaqMan real-time RT-PCR. Brain Research Molecular Brain Research 2002; 106: 101–116, [PUBMED], [INFOTRIEVE], [CSA]
- Bustin S. A. Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays. Journal of Endocrinolology 2000; 25: 169–193, [CSA], [CROSSREF]
- Doroudi R, Gan L. M., Selin Sjogren L, Jern S. Effects of shear stress on eicosanoid gene expression and metabolite production in vascular endothelium as studied in a novel biomechanical perfusion model. Biochemical and Biophysical Research Communications 2000; 269: 257–264, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Ferre F., Marchese A, Pezzoli P, Buxton G. E., Boyer V. Quantitative PCR. An Overview of the Polymerase Chain Reaction. Birkhauser, Boston, MA 1994
- Gan L, Sjogren L. S., Doroudi R, Jern S. A new computerized biomechanical perfusion model for ex vivo study of fluid mechanical forces in intact conduit vessels. Journal of Vascular Research 1999; 36: 68–78, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Gibson U. E., Heid C. A., Williams P. M. A novel method for real time quantitative RT-PCR. Genome Research 1996; 6: 995–1001, [PUBMED], [INFOTRIEVE], [CSA]
- Gorzelniak K, Janke J, Engeli S, Sharma A. M. Validation of endogenous controls for gene expression studies in human adipocytes and preadipocytes. Hormone and Metabolic Research 2001; 33: 625–627, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Heid C. A., Stevens J, Livak K. J., Williams P. M. Real time quantitative PCR. Genome Research 1996; 6: 986–994, [PUBMED], [INFOTRIEVE], [CSA]
- Higuchi R, Fockler C, Dollinger G, Watson R. Kinetic PCR analysis: Real-time monitoring of DNA amplification reactions. Biotechnology New York 1993; 11: 1026–1030, [CSA]
- Karge W. H., 3rd, Schaefer E. J., Ordovas J. M. Quantification of mRNA by polymerase chain reaction (PCR) using an internal standard and a nonradioactive detection method. Methods in Molecular Biology 1998; 110: 43–61, [PUBMED], [INFOTRIEVE], [CSA]
- Livak K. J., Flood S. J., Marmaro J, Giusti W, Deetz K. Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. PCR Methods and Applications 1995; 4: 357–362, [PUBMED], [INFOTRIEVE], [CSA]
- Noonan K. E., Beck C, Holzmayer T. A., Chin J. E., Wunder J. S., Andrulis I. L., Gazdar A. F., Willman C. L., Griffith B, Von Hoff D. D., et al. Quantitative analysis of MDR1 (multidrug resistance) gene expression in human tumors by polymerase chain reaction. Proceedings of the National Academy of Sciences of the United States of America 1990; 87: 7160–7164, [PUBMED], [INFOTRIEVE], [CSA]
- Schmid H, Cohen C. D., Henger A, Irrgang S, Schlondorff D, Kretzler M. Validation of endogenous controls for gene expression analysis in microdissected human renal biopsies. Kidney International 2003; 64: 356–360, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Schmittgen T. D., Zakrajsek B. A. Effect of experimental treatment on housekeeping gene expression: Validation by real-time, quantitative RT-PCR. Journal of Biochemical and Biophysical Methods 2000; 46: 69–81, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Svensson P. A., Englund M. C., Markstrom E, Ohlsson B. G., Jernas M, Billig H, Torgerson J. S., Wiklund O, Carlsson L. M., Carlsson B. Copper induces the expression of cholesterogenic genes in human macrophages. Atherosclerosis 2003; 169: 71–76, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Thellin O, Zorzi W, Lakaye B, De Borman B, Coumans B, Hennen G, Grisar T, Igout A, Heinen E. Housekeeping genes as internal standards: Use and limits. Journal of Biotechnology 1999; 75: 291–295, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Tricarico C, Pinzani P, Bianchi S, Paglierani M, Distante V, Pazzagli M, Bustin S. A., Orlando C. Quantitative real-time reverse transcription polymerase chain reaction: Normalization to rRNA or single housekeeping genes is inappropriate for human tissue biopsies. Analytical Biochemistry 2002; 309: 293–300, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]
- Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A, Speleman F. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biology 2002; 3, RESEARCH0034[CSA], [CROSSREF]
- Zhong H, Simons J. W. Direct comparison of GAPDH, beta-actin, cyclophilin, and 28S rRNA as internal standards for quantifying RNA levels under hypoxia. Biochemical and Biophysical Research Communications 1999; 259: 523–526, [PUBMED], [INFOTRIEVE], [CSA], [CROSSREF]