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1 rect interactions with the VEGF gene and the Sp1 transcription factor.
2 R3, which inhibited nuclear transport of the Sp1 transcription factor.
3 hCtr1 mRNA level, which is regulated by the Sp1 transcription factor.
4 onsive DNA-protein complex that contains the Sp1 transcription factor.
5 elates with increased phosphorylation of the Sp1 transcription factor.
6 onsive DNA-protein complex that contains the Sp1 transcription factor.
7 es and by antibody supershifts, contains the Sp1 transcription factor.
8 te is dependent on two binding sites for the Sp1 transcription factor.
9 criptional activity, most likely through the Sp1 transcription factor.
10 uction are clusters of binding sites for the Sp1 transcription factor.
11 the core of the recognition sequence of the SP1 transcription factor.
12 do not bind known receptors but do bind the SP1 transcription factor.
13 contain overlapping sites for the EGR-1 and Sp1 transcription factors.
14 ene expression is mediated by both Egr-1 and Sp1 transcription factors.
15 effect was shown to be mediated by C/EBP and Sp1 transcription factors.
16 pression is developmentally regulated by the Sp1 transcription factor, a member of the Kruppel-like f
19 ement from bases 35-67 that appeared to bind Sp1 transcription factor and cause a shift to higher mol
20 r, leading to a decreased nuclear content of Sp1 transcription factor and the rapid downregulation of
21 e element-binding protein (CREB), Egr-1, and Sp1 transcription factors and that CREB-binding protein
23 n of GC-rich sequences capable of binding to Sp1 transcription factors as necessary elements for the
25 00 bp of upstream sequence), has 17 putative SP1 transcription factor binding sites and no TATA or CA
26 he region from -91 to +103 bp, where several Sp1 transcription factor binding sites are localized.
28 6 gene was found to contain seven functional Sp1 transcription factor binding sites that each bind Sp
29 4) have previously been reported to modulate Sp1 transcription factor binding to the promoter of the
30 t is interesting that a minimum of two viral Sp1 transcription factor-binding sites are retained and
33 From these results, we conclude that the Sp1 transcription factor exhibits enhanced binding to pr
34 amines disrupted the DNA binding activity of Sp1 transcription factor family members to an ERalpha mi
35 eled consensus oligonucleotides for AP-1 and Sp1 transcription factors in the presence and absence of
36 e present study, we examined the role of SP3/SP1 transcription factors in the regulation of the Col10
37 o sequence motifs known to interact with the Sp1 transcription factor mark promoters of more hypometh
38 romatin immunoprecipitation assays show that Sp1 transcription factor mediated Ad-MMP-2-Si-CM-stimula
39 to the Pkc1-dependent specificity protein-1 (Sp1) transcription factors of metazoans, was identified
40 l collagen genes, suggest that the family of Sp1 transcription factors play a role in physiological a
44 ctional evidence that Specificity protein 1 (Sp1) transcription factor plays a pivotal role in the tr
45 ootprinting assays correlate to suggest that Sp1 transcription factor(s) bind at several sites upstre
48 and that both LF Sp1 binding sites bind the Sp1 transcription factor specifically in myeloid cells.
49 Here we show that the Caenorhabditis elegans Sp1 transcription factor SPTF-3 specifies the programmed
50 significant reduction in DNA binding of the Sp1 transcription factor to the ATM promoter, and quanti
52 ET-743 did not affect the binding of CBF or Sp1 transcription factors to their cognate COL1A1 elemen
54 oth the glucocorticoid receptor (GR) and the Sp1 transcription factor were required for dexamethasone
55 tumor cells markedly induced the activity of Sp1 transcription factor, which plays a key role in the
56 hift assays confirmed the interaction of the SP1 transcription factor with the proximal promoter regi
57 nteractions of the nuclear factor kappaB and Sp1 transcription factors with the immunoglobulin heavy
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