ライフサイエンスコーパス: Sp1 transcription factor

1 R3, which inhibited nuclear transport of the Sp1 transcription factor.

2 hCtr1 mRNA level, which is regulated by the Sp1 transcription factor.

3 onsive DNA-protein complex that contains the Sp1 transcription factor.

4 elates with increased phosphorylation of the Sp1 transcription factor.

5 rect interactions with the VEGF gene and 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 tein kinase B/mTOR signaling pathway and the SP1 transcription factor.

14 contain overlapping sites for the EGR-1 and Sp1 transcription factors.

15 ene expression is mediated by both Egr-1 and Sp1 transcription factors.

16 effect was shown to be mediated by C/EBP and Sp1 transcription factors.

17 pression is developmentally regulated by the Sp1 transcription factor, a member of the Kruppel-like f

18 in part be explained by decreased c-Myc and Sp1 transcription factor activities.

19 These data suggest that the Sp1 transcription factor acts as a platform for recruitm

20 ement from bases 35-67 that appeared to bind Sp1 transcription factor and cause a shift to higher mol

21 r, leading to a decreased nuclear content of Sp1 transcription factor and the rapid downregulation of

22 e element-binding protein (CREB), Egr-1, and Sp1 transcription factors and that CREB-binding protein

23 This circuitry uses Sp1 transcription factor as a copper sensor in modulatin

24 n of GC-rich sequences capable of binding to Sp1 transcription factors as necessary elements for the

25 increased LncRNA MALAT1 levels by increasing Sp1 transcription factor binding at its promoter.

26 One of the sequences identified is the Sp1 transcription factor binding site.

27 00 bp of upstream sequence), has 17 putative SP1 transcription factor binding sites and no TATA or CA

28 he region from -91 to +103 bp, where several Sp1 transcription factor binding sites are localized.

29 The proximal promoter contains multiple Sp1 transcription factor binding sites but lacks a conse

30 6 gene was found to contain seven functional Sp1 transcription factor binding sites that each bind Sp

31 4) have previously been reported to modulate Sp1 transcription factor binding to the promoter of the

32 t is interesting that a minimum of two viral Sp1 transcription factor-binding sites are retained and

33 This region contains five Sp1 transcription factor-binding sites.

34 Sp1 transcription factor controls a pleiotropic group of

35 From these results, we conclude that the Sp1 transcription factor exhibits enhanced binding to pr

36 amines disrupted the DNA binding activity of Sp1 transcription factor family members to an ERalpha mi

37 eled consensus oligonucleotides for AP-1 and Sp1 transcription factors in the presence and absence of

38 e present study, we examined the role of SP3/SP1 transcription factors in the regulation of the Col10

39 o sequence motifs known to interact with the Sp1 transcription factor mark promoters of more hypometh

40 romatin immunoprecipitation assays show that Sp1 transcription factor mediated Ad-MMP-2-Si-CM-stimula

41 to the Pkc1-dependent specificity protein-1 (Sp1) transcription factors of metazoans, was identified

42 l collagen genes, suggest that the family of Sp1 transcription factors play a role in physiological a

43 The Sp1 transcription factor plays a crucial role in COL1A1

44 The Sp1 transcription factor plays an important role in medi

45 These results imply that the Sp1 transcription factor plays an important role in the

46 ctional evidence that Specificity protein 1 (Sp1) transcription factor plays a pivotal role in the tr

47 ootprinting assays correlate to suggest that Sp1 transcription factor(s) bind at several sites upstre

48 Here we demonstrate that Sp1 transcription factor(s) play a role in transcription

49 sid p7 protein (NCp7-F2) and finger 3 of the Sp1 transcription factor (Sp1-F3).

50 and that both LF Sp1 binding sites bind the Sp1 transcription factor specifically in myeloid cells.

51 Here we show that the Caenorhabditis elegans Sp1 transcription factor SPTF-3 specifies the programmed

52 significant reduction in DNA binding of the Sp1 transcription factor to the ATM promoter, and quanti

53 Binding of Sp1 transcription factors to the occluded promoter was r

54 ET-743 did not affect the binding of CBF or Sp1 transcription factors to their cognate COL1A1 elemen

55 We also found that the quantity of Sp1 transcription factor was lower in MCF7/Adr than in M

56 oth the glucocorticoid receptor (GR) and the Sp1 transcription factor were required for dexamethasone

57 tumor cells markedly induced the activity of Sp1 transcription factor, which plays a key role in the

58 hift assays confirmed the interaction of the SP1 transcription factor with the proximal promoter regi

59 nteractions of the nuclear factor kappaB and Sp1 transcription factors with the immunoglobulin heavy