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We examined whether expression of the O-antigen biosynthetic genes were altered when the host strain C6706lacZ was grown in the presence of 50% vol:vol spent medium from E. coli DH5α cultures expressing cloned CAI-1 or AI-2 by monitoring the expression of a number of such genes.
We therefore investigated the role of cGMP in the cross-talk between different hormonal signalling pathways by monitoring the expression of PDF1.2 and ERF1, which are related to the jasmonic acid (JA -dependent and ethylene-dependent pathways, respectively.
These results correlated with the Stat1-driven gene expression as assessed by monitoring the expression of Stat1-mediated IFN-inducible 6-16 mRNA.
Such arrays offer a powerful approach for monitoring the expression of thousands of genes simultaneously and provide access for techniques designed to assess patterns or "fingerprints" of gene expression that may ultimately be used as signatures of response to therapeutic intervention.
An experiment was designed to validate these arrays by monitoring the expression profiles of known genes following the addition of 1% (w/v) glucose to wild-type A. nidulans cultures grown to mid-exponential phase in Vogel's minimal medium with ethanol as the sole carbon source.
These techniques are extensively used for monitoring the expression of transgenes, tumour growth and metastasis, infections and gene therapy assessments.
Normally, monitoring the expression profile of a gene encoding of an industrially important product of microbial origin is a subject of a prime importance in the agenda of commercialized bio-processing.
Consequently, recent focus has shifted to monitoring the expression of prostate-specific membrane antigen (PSMA), in which elevated levels have been histologically correlated with PCa tumor progression [17], androgen independence [18], and metastasis [19].
Studies in the rat model of myocardial infarct have shown that monitoring the expression of αvβ3 integrin by molecular imaging provides valuable prognostic information about myocardial repair after infarct [5 8].
Similar(2)
The recombination was confirmed using R26RYFP indicator allele and monitoring the expression of yellow fluorescent protein in the AP at P14.
By monitoring the expression of nucleolin mRNA, and by measuring the level of nucleolin protein recovered from the surface and nucleus of cells, here we show that the presence of nucleolin at the cell surface is dependent on the constant induction of nucleolin mRNA.
More suggestions(15)
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