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Primers and probes specific for HSV and VZV genes were combined and optimized in a multiplex PCR.
The differential expressed genes were combined with published gene lists to obtain the BR-regulated genes by microarrays were and listed in Supplementary Data 3 and 4. The Split Luciferase Complementation Assays were performed as described50.
Surprisingly, when the tRNA-AT and VAIα genes were combined in the same vector (DC-AT-VAIα), an enhancement of viral replication was noticed.
The resulting promoter-engineered isoprenoid genes were combined by serial P1 transductions into a host strain harboring a reporter plasmid containing β-carotene biosynthesis genes allowing a visual screen for yellow color indicative of β-carotene accumulation.
The optimal genes were combined with the overexpression of phosphoenolpyruvate carboxylase, developing a full biosynthetic pathway capable of producing a titer of 4.7 g/L DPA directly from glucose.
Combined genotype data on SNPs on eight other candidate genes were combined with our IL-3 results, to estimate relationships between pairs of loci and RA, by maximum-likelihood analysis.
When these genes were combined into a single survival score, the median survival for patients with a favorable versus unfavorable score was 65 versus 29 months (P < 0.0001, hazard ratio = 0.4221).
PubMed IDs (PMIDs) corresponding to homologous genes were combined.
A Dunnett's T3 multiple comparison test was used to investigate the time effect after these two genes were combined (Fig. 3d).
On one hand, a great reduction of risk was detected when rare alleles at SLC45A2 and SILV/CDK2 genes were combined (OR = 0.31; p = 0.0001).
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When all genes are combined, the relationship between conservation of gene expression and morphological similarity is partially masked by housekeeping genes and genes with diverged expression.
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