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Aph1a deletion by GFP- ires-Cre expression did not alter spine formation as compared to control neurons expressing GFP, suggesting that Aph1a has a redundant function in spine formation in vitro when Aph1bc is present.
Importantly, reduction of Eto2 and Rybp expression did not alter blood lineage specification assayed by blast colony assays (Fig. 7h).
Osteocalcin and Cbfa1 mRNA expression did not alter in the presence of Dex and RA at these time points.
Forced huTIMP-3 expression did not alter endogenous muTIMP-3 expression (Figure S1B).
Other early hematopoietic and/or endothelial-associated genes that Lhx2 expression did not alter were CD41, CD34 and CD44.
Interestingly, mitochondrial targeted catalase expression did not alter the contractile profile in the isolated extensor digitorum longus (EDL) muscle.
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First, VP088 expression does not alter the cellular property including an ES cell phenotype, self-renewal, pluripotency gene expression, SGIV susceptibility and host cell response to SGIV infection at molecular and cellular (flow cytometry) levels.
Similar values were obtained in GFP-HX1 (8.3% and 66.1%) and 88GFP-HX1 cells (8.6% and 65.4%) (Fig. 4), which indicates that the VP88GFP expression does not alter the cell death profile and pathways.
The B7RP-1+/+ and B7RP-1+/− T cells had similar ICOS surface expression levels; indicating that unlike ICOS expression, reduced B7RP-1 expression does not alter ICOS expression on T cells (Fig. 5B).
A number of studies involving GFP-labeled strains of bacteria have revealed that GFP expression does not alter the biochemical, morphological, or survival characteristics of the labeled bacteria; however, only limited data regarding the effects of GFP expression on microbial growth are provided in these studies [11], [12].
Genetic reduction of arrestin-1 or GRK1 expression does not alter S → A responses.
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