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Several nucleotide polymorphisms in Rtcl, Rth3, Rum1, and Rul1 were significantly (P < 0.05) associated with seedling root traits in maize suggesting that all four tested genes are involved in the maize root development.
However, recent studies [9], [14] have detected significant positive selection on wx in Chinese waxy maize, suggesting that strong improvement might have acted on the mutation genotype to maintain the glutinous phenotype.
Both sites appear to be polymorphic in maize, suggesting that these Helitrons have been active recently.
For example, miR2019 was conserved in monocots such as wheat, Brachypodium distachyon, rice and maize, suggesting that it might be monocot-specific miRNA.
The eukaryotic DNA accumulation from the algal biomass was twice that from the maize, suggesting that the algal cell wall may be more resistant than that of the maize silage to microbial degradation.
Recently, methylation at CHHs in the close vicinity of genes was shown to positively correlate with gene expression in maize, suggesting that this methylation mark may be interlinked with gene expression [ 42].
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A recent study in rice and maize suggested that the majority of GBPs are involved in starch biosynthesis (Koziol et al. 2011).
The success application of MARB in maize suggests that this technology is applicable to any hybrid crop to breed new inbreds with improved hybrid performance but the same heterotic mode.
However, recent results in maize suggest that this may not be the case [ 14].
More CGI shores were methylated than CGIs in maize suggested that DNA methylation level was not positively correlated with CpG density.
The high similarities of protein sequences, conserved domains and three-dimensional models among OsHATs and their homologs in Arabidopsis and maize suggested that OsHATs have multiple functions.
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