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A functional ARE has been identified upstream of the Notch1 major transcription start site.
Within the pectin clusters, a Crp family transcriptional regulator (Clocel_2253) was identified upstream of the hydrolase/isomerase pathway, and levels of this regulator were significantly increased.
For the carrier chromosomes, linkage drags were identified upstream and/or downstream of the donated target gene/QTL following transmission to the recipient genome.
Additionally, we identified upstream effectors that control Bmi-1 levels and function in chromatin modification.
A possible promoter was identified upstream of FTL_1432, but not anywhere else in the genetic sequence through FTL_1421.
In the three sequenced C. perfringens genomes [12], [23], VirR boxes have been identified upstream of several other genes, including genes encoding VR-RNA and α-clostripain.
In neuronal cell lines, HD transcription factors bind to TAAT motifs located within a regulatory region identified upstream of Npy [31].
A couple SRp40 binding sites were found within the EDB exon and the downstream intron, while PTB sites were identified upstream of the alternative exon.
After trypsin digestion, 13 peptides were identified upstream the formerly annotated starting M residue, confirming that the XopD protein sequence annotated in the public databases is not complete.
Two CAAT boxes were identified upstream of the TATA box.
σE2 promoter motifs were identified upstream of 40 asRNAs.
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