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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 NA-binding basic helix-loop-helix (bHLH) and GATA transcription factors.
5 rol of cardiac and neural gene expression by GATA transcription factors.
6 ion of cell type-specific gene expression by GATA transcription factors.
7 evealed potential binding sites for bHLH and GATA transcription factors.
8 of TORC1 signalling and depends on specific GATA transcription factors.
9 ivated in the Drosophila fat body by Rel and GATA transcription factors.
10 ting the cardiogenesis-promoting function of GATA transcription factors.
11 binding sites for AP-1, NF-kappaB, Ets, and GATA transcription factors.
12 gh functional and physical interactions with GATA transcription factors.
13 including a sequential cascade of redundant GATA transcription factors.
14 ed by the coordinate action of NF-kappaB and GATA transcription factors.
15 ity of endogenous globin genes to respond to GATA transcription factors.
16 angements, and suggests a novel function for GATA transcription factors.
17 two conserved consensus sites for binding of GATA transcription factors.
19 ed an SlKD1-interacting transcription factor GATA transcription factor 6 (SlGATA6), which is required
20 ced into consensus binding sites for AP-1 or GATA transcription factors abolished the pressure overlo
21 The friend of GATA (FOG)-1 protein regulates GATA transcription factor activity in several stages of
22 es (twist, snailA, snailB, forkhead, mef2, a GATA transcription factor and a LIM transcription factor
23 of distribution is, thus far, unique to the GATA transcription factors and suggests a protein-protei
24 e mechanism responsible for the silencing of GATA transcription factors and the subsequent loss of a
27 pancy determined by ChIP-seq, recruitment by GATA transcription factors appears to be a stronger dete
35 t the GATA motif is required in cis and that GATA transcription factors are required in trans for exp
41 blastoma susceptibility through differential GATA transcription factor binding and direct modulation
43 dependent upon highly conserved Forkhead and GATA transcription factor binding sites, which are bound
46 pecific genes identified multiple repeats of GATA transcription factor-binding sites (i.e. GATA eleme
48 of the intestine genes were enriched for the GATA transcription factor consensus binding sequence.
49 in accessibility studies revealed a role for GATA transcription factors downstream of IL-33 signaling
51 nstrate that a putative null mutation in the GATA transcription factor egl-18, which is involved in s
52 enhancer function, we demonstrated that the GATA transcription factor ELT-2 and the mediator subunit
53 ased analyses identified the tissue-specific GATA transcription factor ELT-2 as a major regulator of
57 bility shift assays show that the C. elegans GATA transcription factor ELT-2 specifically binds to th
58 show that endodermal expression involves the GATA transcription factor ELT-2, and that ELT-2 can bind
59 1294 age-regulated genes and found that the GATA transcription factors ELT-3, ELT-5, and ELT-6 are r
60 nesis and targets of the intestinal-specific GATA transcription factor, ELT-2, at multiple developmen
66 ded evidence to suggest that a member of the GATA transcription factor family (GATA-4) is responsible
67 GNC gene encodes a member of the Arabidopsis GATA transcription factor family and has been implicated
70 a transcriptional repression function for a GATA transcription factor for prolonging the onset of se
73 on of the Arabidopsis (Arabidopsis thaliana) GATA transcription factors GATA, NITRATE-INDUCIBLE, CARB
75 of the DNA sequence that mediates binding of GATA transcription factors, GATA motifs reside throughou
81 The paralogous and functionally redundant GATA transcription factors GNC (for GATA, NITRATE-INDUCI
89 expression and cellular localization of the GATA transcription factors in ovarian tumor tissues and
90 entified a conserved function for endodermal GATA transcription factors in regulating local epithelia
93 irect transcriptional target of Forkhead and GATA transcription factors in the lateral mesoderm, and
97 Gata4, a member of the zinc finger family of GATA transcription factors, is highly expressed in duode
98 pidermal cells is known to require the ELT-1 GATA transcription factor, little is known about how the
102 rther genetic manipulations suggest that the GATA transcription factor Pannier is synergistically inv
106 moted endothelium formation, indicating that GATA transcription factors promote vasculogenesis via ac
110 nduce DOC-2/DAB2 promoter activity, although GATA transcription factors share a very similar DNA-bind
111 enase promoter requires a binding site for a GATA transcription factor, suggesting that the insulator
112 his binding motif overlaps with that for the GATA transcription factors, (T/A)GATA(A/G), and GATA-1 c
115 We report the identification of ELT-1, a GATA transcription factor that specifies hypodermal fate
116 gulated transcription factors as well as two GATA transcription factors that act as repressors and ac
117 NL belong to the 11-member family of B-class GATA transcription factors that are characterized to dat
118 rdiac gene transcription by interfering with GATA transcription factors that are implicated in cardia
119 ession, and four predicted binding sites for GATA transcription factors that are required for endoder
120 first evidence that rs8023462 interacts with GATA transcription factors to influence gene expression.
123 and miR-217) also regulate the chondrogenic GATA transcription factor tricho-rhino-phalangeal syndro