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The expression of the dhaD gene was evaluated via qRT-PCR.
A polymorphism within the intron 8 of the DAT1 gene was evaluated in 27 healthy men.
The expression of each gene was evaluated in other skin diseases and compared to its expression in normal skin.
The expression level of characteristic osteogenic gene was evaluated using Reverse Transcription Polymerase Chain Reaction (RT-PCR).
The transcript expression level of the α-glucosidase III gene was evaluated by RT-PCR on total RNA extractions from eggs, larvae, pupae, and foraging imagoes.
Seven days after transfecting the plasmid or chemically modified sgRNA/Cas9n mRNA into the Jurkat-KI-R5 cells, the disruption of the CCR5 gene was evaluated by flow cytometry.
mRNA expression of each mutant gene was evaluated by real-time qPCR of cDNA product.
The mRNA level of crmA gene was evaluated using conventional PCR assay.
The classification power for each gene was evaluated using the bootstrap re-sampling method [29] coupled with two-tailed t-statistics.
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PvuII and XbaI polymorphisms in ERα gene were evaluated in genomic DNA by using the polymerase chain reaction (PCR).
Meanwhile, the linkage disequilibrium (LD) regions of 15 SNPs within the CTLA4 gene were evaluated using the Haploview program [30].
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