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

1 pression profile of genes controlled by this GATA transcription factor.

2 rotein is an apparent zinc finger-containing GATA transcription factor.

3 ine-1-phosphate lyase gene is regulated by a GATA transcription factor.

4 ion of cell type-specific gene expression by GATA transcription factors.

5 evealed potential binding sites for bHLH and GATA transcription factors.

6 ivated in the Drosophila fat body by Rel and GATA transcription factors.

7 ting the cardiogenesis-promoting function of GATA transcription factors.

8 binding sites for AP-1, NF-kappaB, Ets, and GATA transcription factors.

9 gh functional and physical interactions with GATA transcription factors.

10 including a sequential cascade of redundant GATA transcription factors.

11 ed by the coordinate action of NF-kappaB and GATA transcription factors.

12 ity of endogenous globin genes to respond to GATA transcription factors.

13 angements, and suggests a novel function for GATA transcription factors.

14 two conserved consensus sites for binding of GATA transcription factors.

15 rol of cardiac and neural gene expression by GATA transcription factors.

16 GATA transcription factors 2 and 3 could be involved in

17 ced into consensus binding sites for AP-1 or GATA transcription factors abolished the pressure overlo

18 The friend of GATA (FOG)-1 protein regulates GATA transcription factor activity in several stages of

19 es (twist, snailA, snailB, forkhead, mef2, a GATA transcription factor and a LIM transcription factor

20 of distribution is, thus far, unique to the GATA transcription factors and suggests a protein-protei

21 e mechanism responsible for the silencing of GATA transcription factors and the subsequent loss of a

22 PU.1 and GATA transcription factors appear to antagonize each oth

23 Additionally, GATA transcription factors appeared to bind rs8023462 on

24 pancy determined by ChIP-seq, recruitment by GATA transcription factors appears to be a stronger dete

25 In this study, we show that Gata transcription factors are expressed in the lateral

26 Mammalian GATA transcription factors are expressed in various tiss

27 GATA transcription factors are implicated in establishin

28 GATA transcription factors are important regulators of b

29 GATA transcription factors are important regulators of t

30 GATA transcription factors are required for crypt cell p

31 GATA transcription factors are required for the differen

32 t the GATA motif is required in cis and that GATA transcription factors are required in trans for exp

33 ters as a coactivator of the global nitrogen GATA transcription factor AreA.

34 Our findings uncover a novel role for GATA transcription factors as repressors of hedgehog sig

35 Thus, we identified the ZML2 and ZML1 GATA transcription factors as two essential components o

36 GATA transcription factors bind the consensus sequence W

37 blastoma susceptibility through differential GATA transcription factor binding and direct modulation

38 with tumour formation resides in a conserved GATA transcription factor binding motif.

39 dependent upon highly conserved Forkhead and GATA transcription factor binding sites, which are bound

40 e contained a neuronal-specific enhancer and GATA transcription factor binding sites.

41 Site-specific mutagenesis of a GATA transcription factor-binding motif in the promoter

42 pecific genes identified multiple repeats of GATA transcription factor-binding sites (i.e. GATA eleme

43 We show that GATA transcription factors can either stimulate or suppr

44 of the intestine genes were enriched for the GATA transcription factor consensus binding sequence.

45 reinforcing regulatory network of Nkx2.5 and GATA transcription factors during cardiogenesis.

46 enhancer function, we demonstrated that the GATA transcription factor ELT-2 and the mediator subunit

47 ased analyses identified the tissue-specific GATA transcription factor ELT-2 as a major regulator of

48 Knockdown of the gut-specific GATA transcription factor ELT-2 by RNA interference simi

49 bility shift assays show that the C. elegans GATA transcription factor ELT-2 specifically binds to th

50 show that endodermal expression involves the GATA transcription factor ELT-2, and that ELT-2 can bind

51 1294 age-regulated genes and found that the GATA transcription factors ELT-3, ELT-5, and ELT-6 are r

52 nesis and targets of the intestinal-specific GATA transcription factor, ELT-2, at multiple developmen

53 The GATA transcription factor encoded by pannier (pnr) is a

54 elt-2 responds to overexpression of the GATA transcription factors END-1 and END-3, which specif

55 We report that GtaC, a GATA transcription factor, exhibits rapid nucleocytoplas

56 We propose that alterations of GATA transcription factor expression and aberrant nucleo

57 Scl/Gata transcription factor expression was significantly r

58 ded evidence to suggest that a member of the GATA transcription factor family (GATA-4) is responsible

59 GNC gene encodes a member of the Arabidopsis GATA transcription factor family and has been implicated

60 n B-GATAs are a subfamily of the 30-membered GATA transcription factor family from Arabidopsis.

61 ults in a new consensus binding site for the GATA transcription factor family.

62 a transcriptional repression function for a GATA transcription factor for prolonging the onset of se

63 The GATA transcription factors function in cell lineage spec

64 Although the GATA transcription factor GATA-2 is expressed in endothe

65 on of the Arabidopsis (Arabidopsis thaliana) GATA transcription factors GATA, NITRATE-INDUCIBLE, CARB

66 Here, we show that the two paralogous GATA transcription factors GATA, NITRATE-INDUCIBLE, CARB

67 of the DNA sequence that mediates binding of GATA transcription factors, GATA motifs reside throughou

68 All 3 hematopoietic GATA transcription factors, GATA-1, GATA-2, and GATA-3,

69 based conversion or by overexpression of the GATA transcription factor Gata6.

70 The Caenorhabditis elegans GATA transcription factor genes elt-1 and elt-3 are expr

71 DAL5 expression depends on the GATA transcription factors Gln3p and Gat1p.

72 The paralogous and functionally redundant GATA transcription factors GNC (for GATA, NITRATE-INDUCI

73 T-box, NK, and GATA transcription factors have known associations with

74 end-1 and end-3 are GATA transcription factors important for specifying endo

75 Serpent functions as the major GATA transcription factor in the larval fat body.

76 The function of GATA transcription factors in diverse developmental cont

77 ression program accessible for activation by GATA transcription factors in ESCs.

78 The nuclear distribution of GATA transcription factors in murine haemopoietic cells

79 expression and cellular localization of the GATA transcription factors in ovarian tumor tissues and

80 entified a conserved function for endodermal GATA transcription factors in regulating local epithelia

81 th chromatin accessibility changes linked to GATA transcription factors in single cells.

82 These findings indicate a role for GATA transcription factors in the differentiation of the

83 irect transcriptional target of Forkhead and GATA transcription factors in the lateral mesoderm, and

84 Furthermore, we show that GATA transcription factors in turn directly regulate Wnt

85 GATA transcription factors interact with FOG proteins to

86 Interplay among GATA transcription factors is an important determinant o

87 Gata4, a member of the zinc finger family of GATA transcription factors, is highly expressed in duode

88 pidermal cells is known to require the ELT-1 GATA transcription factor, little is known about how the

89 GATA transcription factors mediate cell differentiation

90 To elucidate the role of specific GATA transcription factors on globin gene expression, we

91 We go on to show that the GATA transcription factor pannier acts early in dorsal m

92 rther genetic manipulations suggest that the GATA transcription factor Pannier is synergistically inv

93 We present evidence that the Gata transcription factor, Pannier, and its binding part

94 GATA transcription factors play critical roles in restri

95 We provide evidence that AP1, ETS, and GATA transcription factors play key roles in HAEC transc

96 moted endothelium formation, indicating that GATA transcription factors promote vasculogenesis via ac

97 GATA transcription factors regulate proliferation, diffe

98 GATA transcription factors represent a family of highly

99 As such, GATA transcription factors represent a group of proteins

100 nduce DOC-2/DAB2 promoter activity, although GATA transcription factors share a very similar DNA-bind

101 enase promoter requires a binding site for a GATA transcription factor, suggesting that the insulator

102 his binding motif overlaps with that for the GATA transcription factors, (T/A)GATA(A/G), and GATA-1 c

103 We report the identification of ELT-1, a GATA transcription factor that specifies hypodermal fate

104 gulated transcription factors as well as two GATA transcription factors that act as repressors and ac

105 NL belong to the 11-member family of B-class GATA transcription factors that are characterized to dat

106 rdiac gene transcription by interfering with GATA transcription factors that are implicated in cardia

107 ession, and four predicted binding sites for GATA transcription factors that are required for endoder

108 first evidence that rs8023462 interacts with GATA transcription factors to influence gene expression.

109 The ability of GATA transcription factors to modulate myocardin activit

110 GATA transcription factors, together with Friend of GATA

111 and miR-217) also regulate the chondrogenic GATA transcription factor tricho-rhino-phalangeal syndro

112 AREA is a GATA transcription factor which mediates nitrogen metabo

113 ELT-2 is an intestinal GATA transcription factor with a conserved role in immun

114 Thus, integration of GATA transcription factors with BMP signaling, through c