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Thus, these eight peptides containing epitopic core sequences may act as probable vaccine candidates and they may be considered for the development of epitope-based vaccines for melioidosis.
Analyses of small vertebrate introns suggest that GGG-containing sequences may act as intronic splicing enhancers in small introns [28].
Interestingly, a recent analysis of the D. discoideum kinome identified a number of kinases that, based on their primary sequences, may act as tyrosine kinases [18].
First, centromere sequences may act as selfish elements in the asymmetric meioses of female plants and animals [ 1, 8].
These sequences may act as transcriptional enhancers (e.g. Muller et al. [ 42]), although other experiments will be needed to prove it.
Increasing reports indicate that the nondominantly expressed miRNA sequences may act as potential regulatory molecules with unexpectedly abundant expression levels [ 16– 16].
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GP XX suggested that a consensus SNP -2081 sequence may act as a co-repressor for SNP -2604.
Although we cannot assume that the putative stem-loop structures found within the pmpFE operon sequence may act as classic rho-independent type transcriptional terminators [49], the possibility of hairpin formation (a common phenomenon in mRNA, mainly on large transcripts) cannot be ignored nor can its hypothetical processing role in mRNA degradation and maturation be discounted.
Hence the isoforms lacking the sequence may act differently compared to the isoforms containing the TAD/NES.
Therefore, these conserved regions in the 5′-flanking sequence may act as a promoter for the spatio-temporal expression of MYH14, and the regulatory sequences are conserved in medaka miR-499 despite the loss of the MYH14 gene.
A similar splice variant of ErbB3 encoding most of the extracellular region followed by intron-encoded sequence may act as an inhibitor of cell growth by binding ligand to form nonproductive ligand receptor complexes (Lee et al, 2001).
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