ライフサイエンスコーパス: myocyte enhancer factor 2

1 g MyoD, myogenin, serum response factor, and myocyte enhancer factor 2.

2 n II-dependent transcriptional activities of myocyte enhancer factor 2.

3 ic translocation, resulting in activation of myocyte enhancer factor 2.

4 the derepression of the transcription factor myocyte enhancer factor 2.

5 ess cardiac transcription factors GATA-4 and myocyte enhancer factor-2.

6 or-2, c-Fos, c-Jun, activator protein-1, and myocyte enhancer factor-2.

7 teraction with the beta-catenin promoter via myocyte enhancer factor-2.

8 transcription factors Sp1 and Sp3 and/or the myocyte enhancer factor 2D.

9 is and inhibit transcriptional activation by myocyte enhancer factors 2.

10 represses the transcriptional activities of myocyte enhancer factor 2 and cAMP response element-bind

11 Expression of myocyte enhancer factor 2 and genes encoding contractile

12 Furthermore, myocyte enhancer factor 2 and nuclear factor of activate

13 associated with class II histone deacetylase/myocyte enhancer factor-2 and calcineurin signaling path

14 e known downstream effectors of calcineurin (myocyte enhancer factor-2 and NFAT) cannot completely ac

15 ted pathological gene expression directed by myocyte-enhancer factor-2 and nuclear factor of activate

16 s, we identify rearrangements between MEF2D (myocyte enhancer factor 2D) and five genes (BCL9, CSF1R,

17 onal factors, such as stimulating protein 1, myocyte enhancer factor 2, and nuclear factor of activat

18 resses the levels of Kruppel-like factor 15; myocyte enhancer factor 2, and peroxisome proliferator-a

19 The transcription factors MyoD and myocyte enhancer factor-2 appear to be responsible for m

20 KLF4 promoter, and competitive blocking of a myocyte enhancer factor-2 binding site in the KLF4 promo

21 f KLF4 promoter identified a hypermethylated myocyte enhancer factor-2 binding site.

22 the transcriptional activation of Nur77 via myocyte enhancer factor 2-binding sites in its promoter.

23 novel Scl target gene, transcription factor myocyte enhancer factor 2 C (Mef2C) from Scl(fl/fl) feta

24 es Cabin1, a transcriptional corepressor for myocyte enhancer factor 2, creating a docking site for 1

25 of HDAC-1/2/3 with Nrf2 and HDAC-3/5/7 with myocyte enhancer factor-2; deacetylation of these factor

26 y by the pattern of expression of Drosophila myocyte enhancer factor 2 (DMEF2)-like immunoreactivity.

27 ion with GCA adenovirus resulted in improved myocytes enhancer factor-2 expression.

28 Three putative binding sites for the myocyte enhancer factor-2 family of transcription factor

29 ies suggest that KLF15 can inhibit GATA4 and myocyte enhancer factor 2 function.

30 ctionally interacts with TEF-1 and also with myocyte enhancer factor 2 in a mammalian two-hybrid assa

31 These data suggest that ERK5 activation of myocyte enhancer factor 2-induced gene expression may pl

32 E17 cortical neurons may be mediated through myocyte enhancer factor 2-induced gene expression.

33 lial KLF4 expression through DNMT enrichment/myocyte enhancer factor-2 inhibition mechanisms of KLF4

34 um response factor) box transcription factor myocyte enhancer factor-2D (MEF-2D) acts as the principa

35 n of muscle-specific genes by members of the myocyte enhancer factor 2 (MEF2) and MyoD families of tr

36 d by the ASD-associated transcription factor myocyte enhancer factor 2 (MEF2) and that Brg1 regulates

37 g pattern of the muscle transcription factor myocyte enhancer factor 2 (Mef2) by promoting exclusion

38 Myocyte enhancer factor 2 (MEF2) C, a member of the MEF2

39 The myocyte enhancer factor 2 (MEF2) consists of a family of

40 stinct regulatory elements, domain 1 and the myocyte enhancer factor 2 (MEF2) domain.

41 We studied the role of transcription factor myocyte enhancer factor 2 (MEF2) during HSC activation.

42 d COX7A(H) lack NRF sites but have conserved myocyte enhancer factor 2 (MEF2) elements.

43 n factors, including members of the MyoD and myocyte enhancer factor 2 (MEF2) families.

44 ein-protein interactions with members of the myocyte enhancer factor 2 (MEF2) family of MADS domain t

45 p-helix (bHLH) transcription factors and the myocyte enhancer factor 2 (MEF2) family of MADS-box tran

46 exists between PGC-1alpha and members of the myocyte enhancer factor 2 (MEF2) family of transcription

47 Members of the myocyte enhancer factor 2 (MEF2) family of transcription

48 There are four members of the myocyte enhancer factor 2 (MEF2) family of transcription

49 vely activates transcription mediated by the myocyte enhancer factor 2 (MEF2) family of transcription

50 ression of muscle-specific genes through the myocyte enhancer factor 2 (MEF2) family of transcription

51 Members of the Myocyte Enhancer Factor 2 (MEF2) family of transcription

52 The transcription factors in the myocyte enhancer factor 2 (MEF2) family play important r

53 tions with nuclear hormone receptors and the myocyte enhancer factor 2 (MEF2) family.

54 ta(B) or delta(C) induced transactivation of myocyte enhancer factor 2 (MEF2) gene expression and up-

55 The transcription factor family known as myocyte enhancer factor 2 (MEF2) has been implicated as

56 Myocyte enhancer factor 2 (Mef2) has been implicated in

57 Myocyte enhancer factor 2 (MEF2) has been shown recently

58 ted the importance of the myogenic regulator myocyte enhancer factor 2 (MEF2) in muscle differentiati

59 The activity-dependent transcription factor myocyte enhancer factor 2 (MEF2) induces excitatory syna

60 The transcription factor myocyte enhancer factor 2 (MEF2) is expressed throughout

61 Myocyte enhancer factor 2 (MEF2) is in the MADS (MCM1aga

62 sphorylation of the neuronal survival factor myocyte enhancer factor 2 (MEF2) leading to its inactiva

63 The transcription factor myocyte enhancer factor 2 (MEF2) plays a critical role i

64 Myocyte enhancer factor 2 (MEF2) plays essential roles i

65 Myocyte enhancer factor 2 (MEF2) proteins are important

66 Myocyte enhancer factor 2 (MEF2) proteins serve as impor

67 his conserved region is a consensus site for myocyte enhancer factor 2 (MEF2) proteins that we show i

68 Myocyte enhancer factor 2 (MEF2) regulates specific gene

69 Cabin1 binds calcineurin and myocyte enhancer factor 2 (MEF2) through its COOH-termin

70 gate the contribution of ERK5 and its target myocyte enhancer factor 2 (MEF2) to neurotrophin-3/TrkC-

71 The myocyte enhancer factor 2 (MEF2) transcription factor ac

72 vious studies have shown that members of the myocyte enhancer factor 2 (MEF2) transcription factor fa

73 unction as transcriptional repressors of the myocyte enhancer factor 2 (MEF2) transcription factor, f

74 ifferentiation through associations with the myocyte enhancer factor 2 (MEF2) transcription factor.

75 Here, we show that activation of myocyte enhancer factor 2 (Mef2) transcription factors (

76 Emerging evidence suggests that myocyte enhancer factor 2 (MEF2) transcription factors a

77 Myocyte enhancer factor 2 (MEF2) transcription factors c

78 The myocyte enhancer factor 2 (MEF2) transcription factors h

79 In response to neuronal activity, myocyte enhancer factor 2 (MEF2) transcription factors i

80 Myocyte enhancer factor 2 (MEF2) transcription factors p

81 Myocyte enhancer factor 2 (MEF2) transcription factors p

82 Myocyte enhancer factor 2 (MEF2) transcription factors p

83 The Myocyte Enhancer Factor 2 (MEF2) transcription factors s

84 We show that myocyte enhancer factor 2 (MEF2) transcription factors s

85 We find that cocaine regulates myocyte enhancer factor 2 (MEF2) transcription factors t

86 vel MHCI signaling pathway that requires the myocyte enhancer factor 2 (MEF2) transcription factors.

87 t corepressor that inhibits transcription by myocyte enhancer factor 2 (MEF2) transcription factors.

88 r localization and reduced expression of the myocyte enhancer factor 2 (MEF2) transcriptional target

89 ent fashion, the transactivation activity of myocyte enhancer factor 2 (MEF2), a protein known to coo

90 on is controlled by the transcription factor myocyte enhancer factor 2 (MEF2), but how MEF2 is activa

91 lves SOST expression reduction by inhibiting myocyte enhancer factor 2 (MEF2), which activates a dist

92 on, we have identified a perfectly conserved myocyte enhancer factor 2 (MEF2)-binding domain (-CTAAAA

93 ctivation of both Tcon and Treg cells led to myocyte enhancer factor 2 (Mef2)-induced expression of g

94 the present study we have determined that a myocyte enhancer factor 2 (MEF2)-related nuclear factor,

95 iptional activators critical for myogenesis, myocyte enhancer factor 2 (MEF2).

96 in conjunction with the transcription factor myocyte enhancer factor 2 (MEF2).

97 lates MuRF1 expression by acting through the myocyte enhancer factor 2 (MEF2).

98 ction by inhibiting the transcription factor myocyte enhancer factor 2 (MEF2).

99 by repressing myogenic transcription factor myocyte enhancer factor 2 (MEF2).

100 atory factors (MRFs)--MyoD and myogenin--and Myocyte Enhancer Factor 2 (MEF2).

101 , flow induced the dissociation of HDAC5 and myocyte enhancer factor-2 (MEF2) and enhanced MEF2 trans

102 iation is controlled by interactions between myocyte enhancer factor-2 (MEF2) and myogenic basic heli

103 Class II histone deacetylases (HDACs) bind myocyte enhancer factor-2 (MEF2) and repress specific ge

104 report tripartite co-operation between MyoD, myocyte enhancer factor-2 (MEF2) and the thyroid hormone

105 Members of the myocyte enhancer factor-2 (MEF2) family of MADS (MCM1, a

106 ription in collaboration with members of the myocyte enhancer factor-2 (MEF2) family of MCM1-agamous-

107 The myocyte enhancer factor-2 (MEF2) family of transcription

108 Members of the myocyte enhancer factor-2 (MEF2) family of transcription

109 at mediates interactions with members of the myocyte enhancer factor-2 (MEF2) family of transcription

110 Members of the myocyte enhancer factor-2 (MEF2) family of transcription

111 hat mediate interactions with members of the myocyte enhancer factor-2 (MEF2) family of transcription

112 tic enzymes that depends on interaction with Myocyte Enhancer Factor-2 (MEF2) for their recruitment t

113 Myocyte enhancer factor-2 (MEF2) is a transcription fact

114 xpression of the muscle differentiation gene Myocyte enhancer factor-2 (Mef2) is normally delayed in

115 nmuscle bHLH proteins E12 or E47 or with the myocyte enhancer factor-2 (MEF2) protein, which acts coo

116 arval muscle splitting is likely mediated by myocyte enhancer factor-2 (MEF2) since in Mef2 hypomorph

117 sitide dependent protein kinase-1 (Pdk1) and myocyte enhancer factor-2 (Mef2) to trigger neurodegener

118 In Drosophila, the Myocyte Enhancer Factor-2 (MEF2) transcription factor is

119 The myocyte enhancer factor-2 (MEF2) transcription factor pl

120 The myocyte enhancer factor-2 (MEF2) transcription factor re

121 ig MAPK-1 (BMK1), an MAPK that activates the myocyte enhancer factor-2 (MEF2) transcription factor.

122 Myocyte enhancer factor-2 (MEF2) transcription factors a

123 Myocyte enhancer factor-2 (MEF2) transcription factors c

124 Myocyte enhancer factor-2 (MEF2) transcription factors s

125 on (CGN) survival depends on activity of the myocyte enhancer factor-2 (MEF2) transcription factors.

126 ses GnRH gene expression via homeodomain and myocyte enhancer factor-2 (MEF2) transcription factors.

127 MMP10 gene transcription by associating with myocyte enhancer factor-2 (MEF2), a direct activator of

128 ter containing an essential binding site for myocyte enhancer factor-2 (MEF2), a stress-responsive tr

129 Three sites within the proximal promoter (myocyte enhancer factor-2 (MEF2), E-box, and CACC box) w

130 determine if hypertrophic signals activated myocyte enhancer factor-2 (Mef2), we studied mice carryi

131 is a member of class IIa HDACs that regulate myocyte enhancer factor-2 (MEF2)-mediated transcription

132 in the Nur77 promoter are binding sites for myocyte enhancer factor-2 (MEF2).

133 of the critical muscle transcription factor myocyte enhancer factor-2 (MEF2).

134 sitide dependent protein kinase-1 (Pdk1) and myocyte enhancer factor-2 (Mef2).

135 between the p38 pathway and a member of the myocyte-enhancer factor 2 (MEF2) group of transcription

136 The transcription factor myocyte-enhancer factor 2 (MEF2) has been shown to be re

137 dzelm, Cherry et al. (2015) demonstrate that myocyte enhancer factor 2D (MEF2D) binds and activates r

138 We reported here that myocyte enhancer factor 2D (MEF2D), a nuclear transcript

139 mediated autophagy regulated the activity of myocyte enhancer factor 2D (MEF2D), a transcription fact

140 ngs on the dysregulation of survival factor, myocyte enhancer factor 2D (MEF2D), by extrasynaptic NMD

141 lates and activates the transcription factor myocyte enhancer factor 2D (MEF2D), which plays a critic

142 emi-restricted transcription factors such as myocyte enhancer factor 2, nuclear factor of activated T

143 peptide) and transcription factor activity [myocyte enhancer factor-2, nuclear factor kappa B (NF-ka

144 tor), SRF (serum response factor), and MEF2 (myocyte enhancer factor 2) play critical roles in the me

145 MEF2 (myocyte enhancer factor 2) proteins are a small family o

146 it can associate with and phosphorylate the myocyte enhancer factor-2 repressor, HDAC5.

147 In contrast, HDAC4 is directly recruited to myocyte enhancer factor 2 sites within target promoters

148 HDAC5 formed a complex with myocyte enhancer factor-2 to down-regulate beta-catenin

149 The myocyte enhancer factor 2 transcription factor target of

150 n of nuclear factor of activated T cells and myocyte enhancer factor 2 transcription factors.

151 ated reduction of shear stress-mediated ERK5/myocyte enhancer factor 2 transcriptional activity, as w

152 nucleus and acts as a dominant inhibitor for myocyte enhancer factor 2 transcriptional activity.

153 r showed that the PKD-HDAC5 pathway mediated myocyte enhancer factor-2 transcriptional activation and

154 ctors, the serum response factor, Oct-1, and myocyte enhancer factor-2, whereas the other two genes (

155 d the pleiotropic transcription factor Mef2 (myocyte enhancer factor 2), which profoundly influences

156 Gene expression assays with myocyte enhancer factor 2, which is activated by calmodu