ライフサイエンスコーパス: upstream stimulatory factor

1 in the presence of antibody specific for the upstream stimulatory factor.

2 the binding of Sp1, an Sp1-like protein, and upstream stimulatory factor.

3 existence of two E-like boxes known to bind upstream stimulatory factors.

4 ter is regulated by tandem E-boxes that bind upstream stimulatory factors.

5 which is highly similar in sequence to human upstream stimulatory factor 1 (hUSF1).

6 Upstream stimulatory factor 1 (USF 1), is a transcriptio

7 ors, revealed that the transcription factors upstream stimulatory factor 1 (USF-1) and USF-2 are indi

8 s interferon regulatory factor 1 (IRF-1) and upstream stimulatory factor 1 (USF-1) in gamma interfero

9 We previously demonstrated that upstream stimulatory factor 1 (USF1) and USF2 regulate t

10 sic helix-loop-helix leucine zipper proteins upstream stimulatory factor 1 (USF1) and USF2 were shown

11 tor (Inr) and a recognition site (E-box) for upstream stimulatory factor 1 (USF1), and to stimulate U

12 was found, whereas for rs8076131, changes in upstream stimulatory factor 1 and 2 transcription factor

13 ng the binding of transcription factor USF1 (upstream stimulatory factor 1).

14 Of these, upstream stimulatory factor 1, Runx1, and c-Myb appear n

15 EMSAs reveal that upstream stimulatory factor 1, Runx1, c-Myb, lymphoid en

16 p-helix leucine zipper transcription factors upstream stimulatory factors 1 and 2 (USF1 and USF2) did

17 1 as well as an E-box motif that is bound by upstream stimulatory factors 1 and 2 (USF1 and USF2).

18 , CaRE2, within BDNF promoter III that binds upstream stimulatory factors 1 and 2 (USF1/2) and show t

19 ologue-2 (Mash-2), which increases levels of upstream stimulatory factors 1 and 2 (USF1/2) and their

20 eriments demonstrated that overexpression of upstream stimulatory factors 1 and 2 increased cGMP-depe

21 te that two basic helix-loop-helix proteins, upstream stimulatory factors 1 and 2, are major proteins

22 strated that this region was occupied by the upstream stimulatory factors 1/2 (USF1/USF2), similar to

23 r binding the E-C4 element was identified as upstream stimulatory factor-1 (USF-1), a basic helix-loo

24 lucidation of a novel mechanism of action of upstream stimulatory factor-1 (USF-1), which involves it

25 s interactions of the basic helix-loop-helix upstream stimulatory factor-1 (USF1) with an E-box1-cont

26 Upstream stimulatory factor-1 acted to regulate alpha7 e

27 A site directly adjacent to the upstream stimulatory factor-1 binding site was shown to

28 -loop-helix-leucine-zip transcription factor upstream stimulatory factor 2 (USF2) is required for the

29 y identifies the human transcription factor, upstream stimulatory factor 2 (USF2), as a nuclear facto

30 ously determined that the regulatory factor, upstream stimulatory factor 2 (USF2), can stimulate tran

31 nism of transcriptional repression involving upstream stimulatory factor 2 (USF2), which inhibits lys

32 he DOR promoter contains an E-box that binds upstream stimulatory factor and is crucial for the DOR p

33 on assays indicated that members of both the upstream stimulatory factor and Sp families of transcrip

34 Cotransfection of the upstream stimulatory factor and various FAS promoter-luc

35 s and cotransfection experiments showed that upstream stimulatory factors and CCAAT/enhancer-binding

36 activating protein-2, nuclear factor 1, and upstream stimulatory factor, and together, they constitu

37 g luciferase reporter gene assays identified upstream stimulatory factors as the transcription factor

38 -2 gene in rat granulosa cells and binds the upstream stimulatory factor (as do E-box regions of othe

39 o binding studies suggest a function for the upstream stimulatory factor at both the -65 and -332 E-b

40 with 3-fold activation or repression and one upstream stimulatory factor binding site associated with

41 We reported that upstream stimulatory factor binding to the -65 E-box is

42 These results demonstrate that upstream stimulatory factor binding to the E-box at -65

43 In control cells, upstream stimulatory factor binding with the major late

44 promoter elements demonstrated a functional upstream stimulatory factor/E box in the TATA box-proxim

45 erved after deletion of the binding site for upstream stimulatory factor from the AdML promoter.

46 at -444 to -278 with an E-box at -332 where upstream stimulatory factor functions for maximal induct

47 the cell-specific enhancer, which binds the upstream stimulatory factor helix-loop-helix protein and

48 tivates the DOR promoter by synergizing with upstream stimulatory factor in specific DNA binding.

49 Moreover, an E box (-185 to -180) that binds upstream stimulatory factor is essential for the dor pro

50 ich binds the basic helix-loop-helix protein upstream stimulatory factor, is required for PIGR promot

51 e BRCA2 promoter by inhibiting binding of an upstream stimulatory factor protein complex to the promo

52 esis of the E-boxes abolished the binding of upstream stimulatory factor proteins and decreased the a

53 ted with Sp1/Sp3 and USF1/USF2 (where USF is upstream stimulatory factor), respectively, were require

54 Mutation of the 3' upstream stimulatory factor site did not affect promoter

55 thermore, we have demonstrated that Ik-2 and upstream stimulatory factor synergize in trans-activatin

56 Binding of upstream stimulatory factors to the -65 E-box is functio

57 that two cellular transcription factors, an upstream stimulatory factor USF, and a member of the E2F

58 show that FIRE3 (-68/-58) binds not only the upstream stimulatory factors USF-1/USF-2 but also the CC

59 , we now demonstrate that two such proteins, upstream stimulatory factor (USF) 1 and 2, readily assoc

60 Previous in vitro studies demonstrated that upstream stimulatory factor (USF) 1 and USF2 bind to the

61 we showed that the E-box specifically binds upstream stimulatory factor (Usf) 1 and Usf2, which are

62 ansactivators specificity factor 1 (Sp1) and upstream stimulatory factor (USF) and an open reading fr

63 Upstream stimulatory factor (USF) and CCAAT enhancer bin

64 (FAS), we examined the relationship between upstream stimulatory factor (USF) and SREBP-1c, two tran

65 has been shown to bind transcription factor upstream stimulatory factor (USF) and to contribute to e

66 cipitation assay, we show that Myc, Max, and upstream stimulatory factor (USF) bind to the chromosoma

67 ur finding that the depolarization-sensitive upstream stimulatory factor (USF) binds to a composite C

68 (COUP-TF) binds specifically to AF3 and that upstream stimulatory factor (USF) binds to an E-box moti

69 ch members of the nuclear factor 1 (NF1) and upstream stimulatory factor (USF) families bind to and r

70 We show here that the protein levels of upstream stimulatory factor (USF) increase during differ

71 Upstream stimulatory factor (USF) is a bHLH-ZIP protein

72 Here we report the binding of the upstream stimulatory factor (USF) to an E-box motif imme

73 on -226 to -194 of the ADH promoter, whereas upstream stimulatory factor (USF) was shown previously t

74 Indeed, the upstream stimulatory factor (USF), a ubiquitous basic/he

75 ding activator proteins 1 and 4, CAAT, GATA, upstream stimulatory factor (USF), estrogen receptor (ER

76 The roles of the bHLH-Zip protein, upstream stimulatory factor (USF), in mouse metallothion

77 H complex as a heterodimer of the ubiquitous upstream stimulatory factor (USF)-1 and USF-2 proteins.

78 primed 5'Dbeta2 promoter requires binding of upstream stimulatory factor (USF)-1 to a noncanonical E-

79 PUFA had no effect on the nuclear content of upstream stimulatory factor (USF)-1.

80 sequences contain putative binding sites for upstream stimulatory factor (USF)-1/-2.

81 l signaling and OPN promoter activity via an upstream stimulatory factor (USF)-activated cognate inhi

82 nsactivators, specificity factor 1 (Sp1) and upstream stimulatory factor (USF).

83 ion of binding of the basic helix-loop-helix upstream stimulatory factor (USF).

84 Gel-shift assays show that upstream stimulatory factor (USF)1 and USF2 preferential

85 The gene encoding the transcription factor upstream stimulatory factor (USF)1 influences susceptibi

86 unctional consequences of binding of Myc and upstream stimulatory factor (USF)1 to endogenous cellula

87 and gel mobility supershift assays identify upstream stimulatory factor (USF; USF1:USF2) and activat

88 Previously, we showed that upstream stimulatory factors (USF) 1 and 2 are implicate

89 r proteins binding to the 12-bp sequence are upstream stimulatory factors (USF) 1 and 2.

90 In this study, we investigated the role of upstream stimulatory factors (USF) in the regulation of

91 ne analysis, with evidence of recruitment of upstream stimulatory factors (USF) transcription factors

92 Mobility shift assays demonstrated that upstream stimulatory factors (USF) USF-1 and USF-2 bind

93 iched (BETA2:E47) and generally distributed (upstream stimulatory factor [USF]) protein-DNA complexes

94 ion site in a protein complex containing the upstream stimulatory factor (USF1).

95 These elements bind the upstream stimulatory factors (USF1 and USF2), which acti

96 Upstream stimulatory factors (USF1/USF2) were shown to b

97 Element F can be recognized partially by upstream stimulatory factors, USF1 and/or USF2.

98 Gel mobility shift assays identified the upstream stimulatory factors (USFs) as a major E-box-bin

99 mal promoter region from -71 to -50 and that upstream stimulatory factors (USFs), including USF1 and

100 a consensus E-box (CACGTG) was shown to bind upstream stimulatory factor using nuclear extracts from

101 Using EMSA, the upstream stimulatory factor was shown to be a component

102 The bHLHZip protein USF (Upstream Stimulatory factor) was identified as a Stra13

103 racteristics of the helix-loop-helix protein upstream stimulatory factor, whereas a factor binding th