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These results demonstrate that the proximal CRX binding element present in the human and mouse Nxnl1 upstream regions is necessary for their promoter activity.
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To assess whether the EMT-inducing transcription factors can directly bind to the consensus binding elements present in the promoters of ABC transporters, we undertook a chromatin immunoprecipitation (ChIP) assay with MCF7 cells transiently transfected with pCDNA3-Flag-Twist construct.
Methylation of cytosine in CpG islands is associated with transcriptional repression by impeding the binding of transcription factors to cis-DNA binding elements present in the promoter regions of genes [ 80].
It is clear that the increasing number of DRE binding elements present in the most highly expressed Cold/Dehydration responsive genes (XERO2, RD29A and ERD10) is related to their transcriptional efficiency independently of light (Table 2, Figure 8).
These transcription factors activate EMT by binding to elements present in the promoter regions of a number of epithelial-specific genes including the E-cadherin promoter, thus suppressing synthesis of this cell-cell adhesion protein [ 7, 45- 47].
Promoter region analysis of genes that are up-regulated in human ER-negative breast tumors with high NOS2 expression revealed that the Ets-binding sequence is the only common promoter element present in all of these genes, indicating that Ets-1 is the key transcriptional factor down-stream of oncogenic NOS2-signaling.
A previous report stated that a Smad binding element is present in the murine gastrin promoter near its transcription start site [15].
List each element present in the molecule.
EPO synthesis is primarily stimulated by hypoxia at the transcriptional level by HIF binding to HRE elements present in the EPO gene (reviewed in [ 57]).
Secondly, we used EMSA to determine Sp1 binding to cis-elements present in the HS site that were shown to have enhancer activity.
These transcription factors activate EMT by binding to E-box elements present in the E-cadherin promoter, thereby suppressing the synthesis of this cell-cell adhesion protein [ 20, 21].
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