2005
DOI: 10.1016/s0076-6879(05)96033-3
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Determination of Nitric Oxide–Donor Effects on Tissue Gene Expression In Vivo Using Low‐Density Gene Arrays

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Cited by 3 publications
(2 citation statements)
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“…TaqMan Arrays (TAs) have recently been introduced as a novel approach to measure gene expression. They combine the high sensitivity provided by the real time quantitative reverse-transcription polymerase chain reaction (qRT-PCR) with the ability to simultaneously assay RNA expression levels of up to 384 target genes in a single sample [ 1 , 2 ]. However, an accurate quantification with this approach could be limited by the low sample amount commonly encountered in clinical research.…”
Section: Introductionmentioning
confidence: 99%
“…TaqMan Arrays (TAs) have recently been introduced as a novel approach to measure gene expression. They combine the high sensitivity provided by the real time quantitative reverse-transcription polymerase chain reaction (qRT-PCR) with the ability to simultaneously assay RNA expression levels of up to 384 target genes in a single sample [ 1 , 2 ]. However, an accurate quantification with this approach could be limited by the low sample amount commonly encountered in clinical research.…”
Section: Introductionmentioning
confidence: 99%
“…If a twofold change was used as a threshold criterion, the results would indicate alteration in the expression of 65 and 23 genes, respectively, in mouse liver and lungs. Using more rigorous statistical approaches (Tran et al 2005), we found six specific genes to be significantly up-regulated, viz., those encoding VEGF and VEGFD in the lung, and FGF1, FGF4 (fibroblast growth factor 1 and 4, respectively), Hsp70 (heat shock 70-kDa protein 4), and PF4 (platelet factor 4) in the liver. Marginally stimulated genes in the liver were those encoding HO-1 (heme oxygenase-1) and Smad7.…”
Section: In Vivo Regulation Of Vegf Gene and Protein Expression By Inmentioning
confidence: 99%