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The abovementioned primers amplified all NBPF transcripts, but the constitutional translocation disrupted only the NBPF1 gene, so we also determined the expression profile of this gene specifically.
To correlate MLV integration with the expression level of the target genes, we determined the expression profile of T cells activated with the same procedure used for transduction (mock-transduced) on Affymetrix HG-U133 plus 2.0 microarrays, run in triplicate.
To evaluate the level and fate of hESC upon differentiation induced by NaB, we determined the expression profile of 83 hESC and liver markers using a homemade cDNA macroarray.
After we determined the expression profile for HID13 and verified expression levels by QPCR for representative (up-, down, and unchanged) genes we also checked the expression of those and other genes in matched quantities of mRNA from other HI strains we had isolated to verify that the effects were not HID13-specific.
We determined the expression profile of CtT37L in Cx. tarsalis by reverse transcriptase PCR.
Here, we determined the expression profile of microRNAs (miRNAs) in the nucleus accumbens (NAc) of rats treated with alcohol.
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To directly address this question, we substituted the bacterial plasmid DNA with various lengths of extragenic spacer DNAs between the 5′ and 3′ ends of the transgene expression cassette and determined the expression profiles using two different reporter expression cassettes.
We determined the expression profiles in skeletal muscle from people with type 2 diabetes, first degree relatives, and healthy control individuals by microarray experiments.
To further evaluate the significance of RASSF9 gene expression for normal mouse development, we determined the expression profiles of RASSF9 gene in various organs of WT mice at one or two weeks old.
Using the RNA-Seq data we determined the expression profiles of all 1,294 genes putatively under positive selection.
We first determined the expression profiles of sRNAs during eight distinct stages of early zebrafish development by sRNA-seq technology.
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