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This study described a novel application of the ant algorithm in predicting a role of each of the random DNA sequences as a transcription-factor binding motif in human chondrogenesis.
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Here, we investigated the nucleosome occupancy profiles around computationally inferred binding sites, based on 519 TF binding motifs, in human GM12878 and K562 cells.
The simple computational approach taken to identify the location of this methylation-dependent and novel DNA-binding motif in human gene promoters identified 274 genes potentially regulated by overcoming epigenetic silencing during the viral replicative cycle.
DGF with deep sequencing has been implemented to uncover cell-specific TF binding motifs in humans, yielding expansive knowledge on regulatory circuits and the role of TF binding in relation to chromatin structure, gene expression, and cellular differentiation [ 19, 78].
Zinc fingers are the most abundant DNA-binding motifs in humans.
Then, we quantified the overall loss or gain of binding motifs in the human lineage using a novel statistical test for regulatory divergence (Kostka et al., in preparation).
Here, we identify 129 potential DNA binding motifs in the human malaria parasite's genome, most of them being novel.
Our modelling data indicated the C terminal region of RIG-I/MDA5 proteins across vertebrates possessed a conserved C4 type zinc finger nucleotide binding motif, in agreement with the studies in humans where a putative domain distantly related to the C4 type zinc finger protein was shown to bind to viral nucleotide PAMPs [ 12].
Mutation of the Creb- but not the Klf-binding motif in the human and mouse Mmp9 and MMP9 promoter significantly decreased activity (Fig. 4D; supplementary material Fig. S10).
This suggests that differences in the mouse and human PDX1 cistrome contribute to the differential expression of genes between mouse and human beta cells, as is illustrated by the Sytl4 gene, which is uniquely expressed in mouse beta cells and is associated with a strong mouse-specific PDX1 ChIP-Seq peak that overlies a consensus Pdx1 binding motif in the mouse that is absent from human.
As in case of humans and yeast, the primary sequence of NgoL reveals the presence of a conserved metal binding motif in the C-terminal domain.
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