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To predict whether GPCRs in hES or hiPS cells are expressed, sufficiently above background we compared expression in these cells to other tissues.
We compared expression in heads in either male or female flies over-expressing one of the FruM isoforms, as compared to wild type adult male or female heads, respectively.
Because of very low numbers of individuals homozygous for the minor allele, we compared expression in individuals homozygous for the major allele with that of individuals with one or two copies of the minor allele.
We compared expression in 6 tissues between non-blood-fed females and males (Fig. 8a f).
We compared expression in cardiac tissue from the CAG-TAG1 founder (F0), F1, F2 and F3 adult male mice.
To verify that BP and BEL1 are regulated by endogenous JAG, we compared expression in WT and jag-2 young floral buds with RNA in situ hybridization.
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Venezuelan equine encephalitis virus replicon particles (VRP) were engineered to express different forms of SIV Gag to compare expression in vitro, formation of intra- and extracellular structures and induction of humoral and cellular immunity in mice.
The expression of a number of specific individual genes involved in the immune response to LPS was investigated further to compare expression in different cell types.
Gene Set Enrichment Analysis (GSEA)[4] was used to compare expression in groups of genes (gene-sets), between different tissues or between different comparison groups within the same tissue.
For this study SAM was first used to measure the significance of differential gene expression for each gene by comparing expression in the sporozoite, RAS, 24 hour liver stage or 48 hr liver stage to expression in the blood stage.
We desired to compare expression in the wild-type F. heterosporum with expression in an eqx knockout strain.
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