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

1 to three families: jun, fos, and activating transcription factor (ATF).

2 (CRE)-binding protein (CREB) and activating transcription factor (ATF) 1 contributes to melanoma pro

3 taR-II promoter, and we demonstrate that the transcription factor ATF-1 binds to this site and strong

4 hat human histone acetyltransferase GCN5 and transcription factor ATF-1 can potentiate CFTR transcrip

5 producing E. coli mutant, including the bZip transcription factor atfs-1 (activating transcription fa

6 , a transcriptional response mediated by the transcription factor ATFS-1 that promotes the recovery a

7 s shown that the UPR(mt) is regulated by the transcription factor ATFS-1, which is regulated by organ

8 tochondrial protein import efficiency of the transcription factor ATFS-1, which mediates the mitochon

9 that: (i) PGN induced phosphorylation of the transcription factors ATF-1 and CREB; (ii) ATF-1 and CRE

10 Together, these studies suggest that the transcription factors ATF-1 and NF-Y play important role

11 ncluding c-Myc, Elk-1, c-Jun, and activating transcription factor (ATF) 2 was also differentially enh

12 anisomycin, a potent activator of activating transcription factor (ATF) 2, and c-Jun-NH(2)-kinase, in

13 exes with the AP-1 family members activating transcription factor (ATF) 2, ATF3, and ATF7.

14 otein (SMAD)-3 (nt -584 to -581), activating transcription factor (ATF)-2 (nt -571 to -568), IRF-7 (n

15 p38 target transcriptional factor activating transcription factor (ATF)-2 bound to the PTEN promoter,

16 nd CRE-binding protein (CREB) and activating transcription factor (ATF)-2 in vitro and was essential

17 tivation of p38 kinase substrate, activating transcription factor (ATF)-2.

18 ivity was enhanced by a wild-type activating transcription factor (ATF-2), whereas a phosphorylation-

19 t the basic leucine zipper domain (b-ZIP) of transcription factor ATF-2 (also called CRE-BP1) can int

20 The transcription factor ATF-2, a p38 MAPK substrate, is pho

21 aling p38 pathway, which may activate target transcription factor ATF-2, which in turn induces PTEN e

22 The transcription factor ATF-2, which is phosphorylated and

23 transcription through p38 and its downstream transcription factor ATF-2.

24 amily, as assessed by phosphorylation of the transcription factor ATF-2.

25 on TNF-alpha-induced phosphorylation of the transcription factor ATF-2.

26 and Jun kinases and increased p53 and other transcription factors (ATF-2, ELK-1, CREB, AP-1).

27 The transcription factors ATF-2 and c-Jun are important for

28 ation, we demonstrated that a heterodimer of transcription factors ATF-2 and c-JUN is constitutively

29 ed protein kinases as well as the downstream transcription factors ATF-2 and c-Jun.

30 hibiting p38SAPK prevented activation of the transcription factors ATF-2 and CREB and significantly r

31 increase in the phosphorylated forms of the transcription factors ATF-2 and Elk-1.

32 ulate signal transduction pathways involving transcription factors ATF-2 and Jun repress apoCIII prom

33 (MAP) kinase activity and the binding of the transcription factors ATF-2 and Jun to the TNF-alpha cAM

34 The transcription factors ATF-2, c-jun, Egr-1, and Sp1 are a

35 In virus-infected cells the transcription factors ATF-2, c-Jun, interferon regulator

36 tains several putative binding sites for the transcription factors ATF-2, Ets-1, Egr-1 and SP1/SP3.

37 s assembly of an enhanceosome containing the transcription factors ATF-2/c-Jun, IRF-3/IRF-7, NF-kappa

38 transcription and reduced expression of the transcription factors, ATF-2 and c-Jun, which normally b

39 antly inhibited the expression of activating transcription factor (ATF) 3, a member of the ATF/cyclic

40 Activating transcription factor (ATF)3 regulates the expression of

41 es the first in vivo evidence for activating transcription factor (ATF)-3 binding to the proximal ASN

42 of the transcriptional repressor activating transcription factor (ATF-3) in a STAT1-dependent manner

43 t two-hybrid assay, we identified activating transcription factor (ATF) 4 as a potential Nrf2-interac

44 e identified basic leucine zipper activating transcription factor (ATF) 4 as one of the HRG-inducible

45 tor 2, and increased synthesis of activating transcription factor (ATF) 4 by a translational control

46 CHOP as an interacting partner of activating transcription factor (ATF) 4 in a yeast two-hybrid scree

47 Activating transcription factor (ATF) 4 is a ubiquitous basic leuci

48 2alpha (eIF2alpha)-like ER kinase/activation transcription factor (ATF) 4 pathway.

49 nslation of a "master regulator," activating transcription factor (ATF) 4, and ultimately, to regulat

50 s of phosphorylated eIF2alpha and activating transcription factor (ATF) 4, which is essential for Fgf

51 N gene expression, interacts with activating transcription factor (ATF)4, a key component of the inte

52 d the CRE as a complex containing activating transcription factor (ATF)-4 and CCAAT enhancer-binding

53 -regulates the translation and expression of transcription factor ATF-4.

54 response, resulting in the induction of the transcription factor ATF-4.

55 eased by the ER stress modulator, activating transcription factor (ATF)6, which can induce genes that

56 -regulated oxidative stress pathways and the transcription factors ATF (activating transcription fact

57 vegetalizing (beta-catenin) and animalizing transcription factor (ATF) activities and their region o

58 ding sites for sequence-dependent activating transcription factor (ATF)-adenosine 3',5'-monophosphate

59 liberate NF-kappaB also activate activating transcription factor (ATF) and activator protein 1 (AP-1

60 p1, glucocorticoid receptor (GR), activating transcription factor (ATF) and cAMP response element-bin

61 by using a library of zinc finger artificial transcription factors (ATFs) and functional screening of

62 Artificial transcription factors (ATFs) and genomic nucleases based

63 Bacterial allosteric transcription factors (aTFs) are a major class of regula

64 ulatory proteins (DRPs), in which artificial transcription factors (ATFs) are fused to cell-penetrati

65 Artificial transcription factors (ATFs) are potent synthetic biolog

66 Artificial transcription factors (ATFs) are precision-tailored mole

67 nd a region containing a consensus activated transcription factor (ATF) binding site.

68 In this paper, we identified an activating transcription factor (ATF)/cAMP-responsive element-bindi

69 l as transcription from the C/EBP-activating transcription factor (ATF) composite motif in the GADD15

70 The structure of this artificial transcription factor (ATF) consists of three parts: (i)

71 Two activating transcription factor (ATF)/CREB family members, CREB-1 a

72 heart and somites via one or more activating transcription factor (ATF)/cyclic AMP response element b

73 get for binding of members of the activating transcription factor (ATF)/cyclic AMP response element b

74 downstream of a binding site for activating transcription factor (ATF)/cyclic AMP response element b

75 downstream components, including activating transcription factor (ATF)/cyclic AMP-responsive element

76 role of different members of the activating transcription factor (ATF) family in survival of diffuse

77 s are dimers of JUN, FOS, MAF and activating transcription factor (ATF) family proteins characterized

78 transcription factor of the CREB/activating transcription factor (ATF) family, increases in expressi

79 g proteins include members of the activating transcription factor (ATF) family.

80 Although the name Activating Transcription Factor (ATF) implies that they are transcr

81 ger synthetic zinc finger protein artificial transcription factors (ATFs) in an epidermoid squamous c

82 osarcoma (c-Maf), Bcl6, basic leucine zipper transcription factor ATF-like (Batf), and IL-21, and STA

83 Here, we show that the basic leucine zipper transcription factor ATF-like, Batf is important for IL-

84 Mice without the basic leucine zipper transcription factor, ATF-like (BATF) gene (Batf(-/-)) l

85 The AP-1 factor basic leucine zipper transcription factor, ATF-like (BATF) is important for C

86 ogram includes upregulation of basic leucine transcription factor, ATF-like (BATF), a transcription f

87 Bcl6 target genes Batf (basic leucine zipper transcription factor, ATF-like) and Bcl6, in part throug

88 related inversely BATF (basic leucine zipper transcription factor, ATF-like) and IRF4 (interferon-reg

89 report here that BATF (basic leucine zipper transcription factor, ATF-like), an AP-1 protein family

90 We have constructed artificial transcription factors (ATFs) made of six zinc-finger (ZF

91 e basic leucine zipper containing activating transcription factors (ATFs) modulates the expression of

92 tains a sequence homologous to an activating transcription factor (ATF) motif, and ATF-1 is a major c

93 relate Tax activation of the CREB/activating transcription factor (ATF) or NFkappaB/Rel transcription

94 se element binding protein (CREB)/activating transcription factor (ATF) site overlapping a CpG island

95 y appeared to be mediated via the activating transcription factor (ATF) site, because mutation of thi

96 to its cAMP-response element (CRE)/activated transcription factor (ATF) site.

97 te is adjacent to identified CREB/activating transcription factor (ATF) sites, present in the Igamma1

98 We engineered two artificial transcription factors (ATFs) that contain Cys(2)His(2) z

99 rch tools and therapeutic agents, artificial transcription factors (ATFs) that up-regulate transcript

100 d a sequence-specific zinc finger artificial transcription factor (ATF) to up-regulate the Maspin pro