1 tiation, and its expression is controlled by
Kruppel-like transcription factors.
2 ng binding sites for TBX5, GATA, NKX2.5, and
Kruppel-like transcription factors.
3 or KLF5) belongs to the family of mammalian
Kruppel-like transcription factors.
4 Kruppel-like transcription factor 10 (KLF10), also named
5 eam of the transcriptional start site of the
Kruppel-like transcription factor 11 (KLF11) gene.
6 ress-induced cellular transcription factors,
Kruppel-like transcription factor 15 (KLF15) and the glu
7 Additional studies revealed the PR and
Kruppel-like transcription factor 15 (KLF15) cooperated
8 effect on ICP0 promoter activity alone, the
Kruppel-like transcription factor 15 (KLF15) cooperated
9 udies demonstrated that the activated GR and
Kruppel-like transcription factor 15 (KLF15) cooperative
10 The PR and
Kruppel-like transcription factor 15 (KLF15), which regu
11 Herein, we identify the
Kruppel-like transcription factor 2 (KLF2) as a potent r
12 Kruppel-like transcription factor 2 (KLF2), a critical g
13 eloid anti-inflammatory transcription factor
Kruppel-like transcription factor 2 (KLF2).
14 OxPLs also induced nuclear translocation of
Kruppel-like transcription factor 4 (KLF4), a known repr
15 Two pioneer transcription factors, GR and
Kruppel-like transcription factor 4 (KLF4), cooperativel
16 rotein is transcriptionally regulated by the
Kruppel-like transcription factor 4 (KLF4), we determine
17 down-regulation of WNT-dependent inhibitory
Kruppel-like transcription factor 4 in miR-199a-5p-overe
18 In contrast,
Kruppel-like transcription factor 4 was induced in antim
19 Kruppel-like transcription factor 5 (Klf5) was detected
20 In this study, we identify the
Kruppel-like transcription factor 6 (KLF6) as a molecula
21 In the current study,
Kruppel-like transcription factor 6 (KLF6) deficiency at
22 In this study, we identify the
Kruppel-like transcription factor 6 (KLF6)-B cell leukem
23 Here, we demonstrate that knocking down
Kruppel-like transcription factor 9 (KLF9) via shRNA pro
24 an Inr in non-cell-specific regulation and a
Kruppel-like transcription factor and Sp1 in the cell-sp
25 Mammalian
Kruppel-like transcription factors are implicated in reg
26 The
Kruppel-like transcription factor Biklf is preferentiall
27 We identified ten efficient Sp/
Kruppel-like transcription-factor-
binding sites in the p
28 KLF5 is a
Kruppel-like transcription factor broadly involved in de
29 Here, we show that the
Kruppel-like transcription factor Dar1 determines the mu
30 Here, we provide evidence that the
Kruppel-like transcription factor datilografo (dati) is
31 ng reactivation from latency, SLUG and three
Kruppel-like transcription factor family members (KLF4,
32 at a basal level by the specificity protein/
Kruppel-like transcription factor family of members, whi
33 Klf5, a member of the
Kruppel-like transcription factor family, has essential
34 KLF7, a member of the
Kruppel-like transcription factor family, is believed to
35 Sp3 belong to the specificity proteins (Sp)/
Kruppel-like transcription factor family.
36 ible early gene 1 (TIEG1) is a member of the
Kruppel-like transcription factor family.
37 Kruppel-like transcription factors have been linked to c
38 Erythroid Kruppel-like factor (EKLF) is a
Kruppel-like transcription factor identified as a transc
39 ndings suggest a reciprocal role for related
Kruppel-like transcription factors in the regulation of
40 Kruppel-like transcription factors,
including KLF4 and K
41 nd tCpG, which contain two binding sites for
Kruppel-like transcription factors,
including SP1/SP3, r
42 KLF6, a ubiquitously expressed
Kruppel-like transcription factor,
is frequently inactiv
43 previous studies have demonstrated that the
Kruppel-like transcription factor (
KLF) 4 potently repre
44 glionic neurons: for example, SLUG and three
Kruppel-like transcription factor (
KLF) family members,
45 The
Kruppel-like transcription factor (
KLF) family participa
46 interaction with members of the zinc finger
Kruppel-like transcription factor (
KLF) family.
47 cruited to promoters by a well characterized
Kruppel-like transcription factor (
KLF), in a sequence-s
48 Kruppel-like transcription factor (
KLF)13, previously sh
49 Expression of four
Kruppel-like transcription factors (
KLF), i.e., KLF4, KL
50 Several
Kruppel-like transcription factors (
KLF), including KLF1
51 The
Kruppel-like transcription factor,
KLF10, is a pivotal e
52 id receptor S1P(1) and its regulation by the
Kruppel-like transcription factor KLF2.
53 The
Kruppel-like transcription factor KLF4 is among the most
54 tion reveal that these DNA elements bind the
Kruppel-like transcription factor KLF4.
55 vidence for the involvement of the mammalian
Kruppel-like transcription factor,
KLF4, in preventing c
56 The
Kruppel-like transcription factor KLF6 is a novel tumor-
57 To identify potential functions for the
Kruppel-like transcription factor KLF7, we have determin
58 Kruppel-like transcription factors (
Klfs) are essential
59 The
Kruppel-like transcription factors (
KLFs) are important
60 Across species,
Kruppel-like transcription factors (
KLFs) have been iden
61 uring development in concert with changes in
Kruppel-like transcription factors (
KLFs).
62 e we show that forced expression of the lung
Kruppel-like transcription factor (
LKLF) in Jurkat T cel
63 ZNF217 proteins resemble
Kruppel-like transcription factors,
localize predominate
64 is predicted to encode alternately spliced,
Kruppel-like transcription factors of 1,062 and 1,108 aa
65 We established previously that GLI2, a
Kruppel-like transcription factor that acts downstream o
66 TGFbeta)-inducible early gene-1 (TIEG1) is a
Kruppel-like transcription factor that is rapidly induce
67 rlier, we demonstrated the essential role of
Kruppel-like transcription factor,
TIEG1, in TGF-beta-in
68 arly gene (TIEG) encodes a three zinc-finger
Kruppel-like transcription factor whose overexpression h
69 Here, we report that knockdown of the
Kruppel-like transcription factor ZBP-89 in zebrafish em
70 The
Kruppel-like transcription factor ZBP-89 is a sequence-s