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1. |
Results demonstrate that intracellular galectin-9 transactivates inflammatory cytokine genes in monocytes through direct physical interaction with NF-IL6. |
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2. |
data indicate that the PRDM16-C/EBP-beta complex initiates brown fat formation from myoblastic precursors |
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3. |
Both CBF1 and C/EBP-beta bind the CR2 promoter in B cells raising the possibility that these factors facilitate or respond to alterations in chromatin structure to control the timing and/or level of CR2 transcription. |
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4. |
Results suggest that the C/EBPalpha and C/EBPbeta transcription factors enhance expression of the TNFR1 protein in cells. |
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5. |
C/EBPbeta regulated cell growth and conferred TNF-alpha resistance to prostate cancer cells, in part, via regulation of metastatic gene expression |
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6. |
C/EBPB is up-regulated in multiple myeloma; it directly influences expression of IRF4, BLIMP1, and BCL2 |
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7. |
C/EBPbeta is a mediator of the deleterious effects of unsaturated free fatty acids on beta-cell function. |
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8. |
C/EBP-beta binds to the CCAAT box in the CD1d promoter, required for its expression in keratinocytes |
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9. |
ERalpha is involved in the transcriptional regulation of HSD17B8 gene in response to E2 through its interaction with C/EBPbeta. |
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10. |
Two CCAAT/enhancer-binding protein (C/EBP) family members [C/EBP-homologous protein (CHOP) and C/EBPbeta] enhanced V2 transcription via different pathways. |
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11. |
C/EBPbeta directly binds to the MMP-13 promoter region and stimulates the expression of MMP-13 in chondrocytes in inflammatory arthritis. |
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12. |
a composite enhancer binding both PPARgamma and C/EBPa,b factors confers adipocyte-specific expression to Retn in mouse, and its absence from the human gene may explain the lack of adipocyte expression in humans. |
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13. |
Ha-Ras transformation of MCF10A cells leads to repression of Singleminded-2s through NOTCH and C/EBPbeta. |
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14. |
C/EBP beta is cyclically regulated during the human menstrual cycle and could have a role in endometrial receptivity. |
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15. |
C/EBPbeta regulates bcl-xl gene expression in human breast cancer cells in response to cigarette smoke condensate treatment |
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16. |
P. aeruginosa induces IL-8 promoter expression and protein production in conjunctival epithelial cells by activating RelA and C/EBPbeta and by promoting the cooperative binding of these transcription factors to the IL-8 promoter |
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17. |
Tumor necrosis factor-alpha upregulates 11beta-hydroxysteroid dehydrogenase type 1 expression by CCAAT/enhancer binding protein-beta in HepG2 cells. |
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18. |
the interplay between NF-kappaB and C/EBPbeta has an impact on the ability of C/EBPbeta to stimulate TGF-beta1 transcription |
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19. |
Regulates cytokine production in mature neutrophils; nuclear C/EBPbeta is rapidly phosphorylated upon cell stimulation, suggesting that it can activate cytokine promoters. |
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20. |
C/EBPbeta was found to have an important role in epithelial cell ICAM-1 regulation, while the adjacent NF-kappaB sequence binds the RelA/p65 and NF-kappaB1/p50 members of the NF-kappaB family to induce ICAM-1 expression in response to H. influenzae. |
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21. |
NRAMP1 proximal region binds CCAAT enhancer binding proteins alpha or beta and is crucial for transcription |
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22. |
/EBPbeta as a direct substrate of G9a-mediated post-translational modification that alters the functional properties of C/EBPbeta during gene regulation. |
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23. |
These data indicate that NF-IL6 is a natural inhibitor of APOBEC3G that facilitates HIV-1 replication. |
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24. |
Observational study of gene-disease association. (HuGE Navigator) |
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25. |
Quantitative reverse transcription-polymerase chain reaction (RT-PCR) showed decreased expression of HNF3 beta/FoxA2 and TTF-1 mRNA in papillary thyroid carcinoma cell lines, when compared with normal thyroid cells |
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26. |
C/EBP beta overexpression significantly upregulated promoter activities of IL-8, COX-2, and anti-apoptotic Bfl-1 genes in prostate cancer cells. |
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27. |
ERK-regulated site in Med1 protein is also essential for up-regulating interferon-induced transcription although not critical for binding to C/EBP-beta |
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28. |
Lysophosphatidic acid-induced transactivation of epidermal growth factor receptor regulates cyclo-oxygenase-2 expression and prostaglandin E(2) release via C/EBPbeta in human bronchial epithelial cells. |
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29. |
C/EBPbeta, which binds to multiple cis-regulatory elements in promoter I.3/II, is a key factor in the transcriptional complex controlling aromatase expression in uterine leiomyoma cells. |
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30. |
Pyk2 is induced and involved in monocyte differentiation and C/EBPbeta is a critical regulator of the Pyk2 expression. |
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31. |
The effect of cell density and inflammatory conditions on the expression, compartmentalization, activation, and the anti-proliferative function of the GR in primary human lung fibroblast cultures, was studied. |
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32. |
PPARgamma agonists have diverging and overlapping mechanisms blocking transactivation of transcription factors NF-kappaB and C/EBPbeta. |
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33. |
C/EBPbeta was identified as the transcription factor regulating Tas1r3 promoter activity in HuCCT1 cells. |
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34. |
IL-17 induces MMP-1 in human cardiac fibroblasts directly via p38 MAPK- and ERK-dependent AP-1, NF-kappaB, and C/EBP-beta activation. |
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35. |
Results identify in Italians a suggestive linkage of early-onset type 2 diabetes (T2D) to chromosome 12q15, in the region of the CHOP gene, but no link to C/EBPbeta. |
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36. |
CCAAT/enhancer-binding protein beta may play a major role in interleukin-6-mediated inhibition of peroxisome proliferator activated receptor alpha gene expression. |
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37. |
C/EBP-beta participates in insulin-responsive expression of the F7 gene. |
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38. |
C/EBPbeta is essential for the transcription of the 17beta-HSD8 gene in the liver |
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39. |
The evidence is presented indicating that PDX-1 triggers hepatic dedifferentiation by repressing the key hepatic transcription factor CCAAT/enhancer-binding protein beta. |
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40. |
KGF increased integrin alpha(5) expression by phosphorylating C/EBP-beta |
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41. |
IL-17 is a potent inducer of CRP expression via p38 MAPK and ERK1/2-dependent NF-kappaB and C/EBPbeta activation. |
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42. |
diacylglycerol acyltransferase 2 expression is regulated by CAAT/enhancer-binding protein beta (C/EBPbeta) and C/EBPalpha during adipogenesis |
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43. |
Important constitutive gene regulatory functions for C/EBPbeta in differentiated macrophages but not in human blood monocytes. |
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44. |
There are high levels of FGF-BP expression in invasive human breast cancer, relative to normal breast and in situ carcinoma, and in MDA-MB-468 human breast cancer cells. |
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45. |
Calcitrio may signal cell differentiation of HL 60 cells which in turn regulates expresson of CEBPB |
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46. |
Identification of the CEBPB gene as a target of translational regulation in myeloid precursor cells transformed by the BCR/ABL oncogene. |
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47. |
transcriptional activation of the interleukin-8 promoter by bradykinin involves the prostanoid-independent activation of nuclear factor-kappaB, and prostanoid-dependent activation of activating protein-1 and nuclear factor-interleukin-6 |
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48. |
C/EBP beta is an essential signaling component for inhibition of NF-kappa B-mediated transcription in TNF-tolerant monocytic cells. |
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49. |
COX-2 is downregulated by PC-SPES via inhibition of NF-kappaB and C/EBPbeta in non-small cell lung cancer cells |
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50. |
A switch between C/enhancer-binding protein (CEBP) zeta and CEBP beta operates at the CEBP site on the C-reactive protein (CRP)promoter to regulate CRP transcription. |
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51. |
NF-kappaB- and C/EBPbeta-driven interleukin-1beta gene expression and PAK1-mediated caspase-1 activation play essential roles in interleukin-1beta release from Helicobacter pylori lipopolysaccharide-stimulated macrophages |
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52. |
The specific expression pattern of C/EBP-beta in gestational trophoblastic disease indicate that C/EBP-beta could potentially be an additional marker of such lesions. |
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53. |
Conditional expression of C/EBP alpha induced the C/EBP family members C/EBP beta and C/EBP epsilon and subsequent granulocyte differentiation. |
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54. |
PGE(2) induces HIV-1 LTR activity in t cells through a complex interplay between C/EBPbeta and CREB |
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55. |
C/EBPbeta plays an essential constitutive role in the expression of COX-2, but may not be directly involved in its regulation in association with human labour. |
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56. |
Conserved amino acids regulationregulate phosphoenolpyruvate carboxykinase (PEPCK) gene expression. |
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57. |
ATRA triggers an increase in the translation of C/EBPbeta-LIP that antagonizes C/EBP transactivators by interacting with their binding sites in the albumin promoter |
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58. |
5'-region from -252 to -175, containing a consensus site for CCAAT/enhancer binding proteins alpha,beta (C/EBPalpha,beta), was essential for SAA1 induction in HASMCs. |
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59. |
CCAAT/enhancer-binding protein beta gene expression is activated by endoplasmic reticulum stress through an unfolded protein response element downstream of the protein coding sequence |
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60. |
IRF-1-CEBPbeta complex activate the promoter of IL-18 binding protein. |
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61. |
Pretreatment of monocytic cells with low TNF doses inhibited TNF-induced (restimulation with a high dose) IL-8 promoter-dependent transcription as well as IL-8 production, which was prevented by overexpression of C/EBPbeta, but not p65 or Oct-1. |
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62. |
C/EBPbeta is involved in enhancing transcription from the P670 promoter of HPV16 during keratinocyte differentiation |
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63. |
identifies new function of C/EBPbeta in LDLR transcription as an oncostatin M-induced transactivator by itself in addition to its role as an EGR-1 co-activator |
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64. |
Papillomavirus E2 protein binds to C/EBP factors and may contribute to enhancing keratinocyte differentiation, which is suppressed by the viral oncoproteins E6 and E7 in HPV-induced lesions |
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65. |
Expression levels of C/EBPbeta isoforms in breast tumors were correlated with clinicopathological tumor parameters, expression of estrogen and progesterone receptors (ER, PR), Ki67 immunostaining, and expression of 7 cell-cycle regulatory proteins. |
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66. |
Ras-induced structural alteration of C/EBPbeta determines differential gene activation through selective interaction with distinct Mediator complexes |
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67. |
Transactivators C/EPB-beta and GATE-binding factor 1 (GBF1) physically interact to induce interferon-gamma-regulated transcription; an intact GTPS motif in C/EBP beta regulatory domain 2 is required for an interaction with GBF1. |
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68. |
data demonstrated that chronic inflammation appeared to play roles in induction of CCAAT/enhancer-binding protein beta expression in prostate epithelium which was associated with increased Cyclooxygenase-2 expression and androgen receptor downregulation |
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69. |
These findings provide new insight into the regulation of cyclooxygenase-2 promoter by an interplay between two opposite beta isoforms and p300 co-activator. |
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70. |
the level of basal as well as cAMP-stimulated IL-10 transcription depends on the expression of C/EBP alpha and beta and their binding to three motifs in the promoter/enhancer region |
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71. |
Calreticulin interacts with C/EBPalpha and C/EBPbeta mRNAs and represses translation of C/EBP proteins. |
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72. |
MEK2 and p38 in IFN-gamma-mediated signal transduction and induction of C/EBP beta expression and activity associated with interleukin-6 (IL-6) secretion in colon epithelial cells. |
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73. |
EBPbeta could be an important gene in acute promyelocytic leukemia pathogenesis |
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74. |
Defective thermoregulation owing to the lack of C/EBPbeta is associated with the reduced capacity to supply fatty acids as fuels to sustain brown fat thermogenesis. |
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75. |
Activation by C/EBP alpha and beta did not depend on their binding to the C/EBP site, since they still activated IGFBP-5 promoter. |
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76. |
Positively functioning NF-IL6 (C/EBPbeta)is not constitutively multiubiquinated by the proteasome. Deletion of leucine zipper domain in NF-IL6 caused the loss of its homodimerization activity & its degradation by the ubiquitin-proteasome system. |
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77. |
Regulates HIV-1 transcription in activated Jurkat T cells |
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78. |
Data show that epidermal growth factor receptor signaling results in phosphorylation of CUG-BP1, and leads to increased binding of CUG-BP1 to CCAAT/enhancer binding protein beta (C/EBP beta) mRNA and elevated expression of the C/EBPbeta LIP isoform. |
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79. |
GBF1 is recruited to the endogenous IRF-9 promoter, and interacts with C/EBP-beta, IL-1, and IL-6 |
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80. |
Several DNA:transcription factor complexes were formed with the conserved regulatory regions identified in multi-species sequence alignment. |
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81. |
Decreased activity and enhanced nuclear export of CCAAT-enhancer-binding protein beta during inhibition of adipogenesis by ceramide. |
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82. |
These results suggest that CSF-induced and HIV-1-mediated regulation of Hck and C/EBPbeta represent the heterogeneous susceptibility of tissue macrophages to HIV-1 infection. |
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83. |
Overexpression of C/EBP beta was sufficient to increase basal expression of a Dlx3 reporter gene in a dose-dependent manner. |
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84. |
both phosphorylation and dephosphorylation of C/EBPbeta in response to growth hormone coordinately modulate its ability to activate transcription by modulating its DNA binding activity and its transactivation capacity |
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85. |
cooperation with cyclic AMP-induced forkhead transcription factor in differentiating human endometrial stromal cells |
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86. |
findings show that expression of C/EBPbeta, which contributes to the regulation of amino-acid-responsive genes, is itself controlled by amino acid availability through transcription |
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87. |
Our data suggest that Tat-C/EBPbeta association is mediated through cdk9, and that phosphorylated C/EBPbeta may influence AIDS progression by increasing expression of HIV-1 genes. |
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88. |
CCAAT/enhancer binding protein-beta is a mediator of PPAR delta-dependent 14-3-3 epsilon gene regulation in human endothelial cells. |
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89. |
C/EBP beta binding to the C/EBP site, which is in part mediated via activation of RSK, can primarily explain the TPA responsiveness of the IGF-I gene promoter |
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90. |
Organization of the promoter regions involved in transcriptional activation of the human NF-IL6 gene |
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91. |
isoform LAP* is the primary isoform of C/EBP beta that regulates, through a redox switch, the LPS-induced expression of the IL-6 gene. |
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92. |
C/EBP-beta may have a role in promoting tumor invasiveness |
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93. |
C/EBP beta is identified as a new partner for HIV-1 Tat in stimulating monocyte chemoattractant protein 1 (MCP-1) transcription in astrocytes. |
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94. |
HMGI-Y physically interacts with Sp1 and C/EBP beta and facilitates the binding of both factors to the insulin receptor promoter |
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95. |
ATF3-FL and C/EBPbeta act as transcriptional suppressors for the ASNS gene to counterbalance the transcription rate activated by ATF4 following amino acid deprivation |
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96. |
A new distal enhancer site is identified in the CYP3A4 gene where C/EBPbeta-LAP binds and activates transcription, whereas the truncated form, C/EBPbeta-LIP (liver inhibitory protein), antagonizes LAP activity and causes gene repression. |
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97. |
C/EBPbeta is involved in the down-regulating of trefoil factor 1 (TFF1) gene expression. |
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98. |
negative cross-talk between p53 and C/EBPbeta is likely to impact expression of their respective target genes |
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99. |
Data imply that the comparison of C/EBP beta expression could be a prognostic marker for patients with glioma. |
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100. |
study provides strong evidence that early growth response 1 regulates low density lipoprotein receptor transcription via a novel mechanism of protein-protein interaction with CCAAT enhancer-binding protein beta |
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101. |
This factor plays important roles in the regulation of thyroid specific genes and processes, and its functions are altered in human thyroid carcinoma. |
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102. |
We conclude that C/EBPalpha and C/EBPbeta contribute to the deregulated expression of Bcl-2 in t(14;18) lymphoma cells |
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103. |
Transfection of NF-IL63'UTR nduced tumor suppression in a human hepatoma cell line. |
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104. |
demonstrate a novel role for C/EBP-beta in interleukin-1beta-induced connective tissue disease and define a new nuclear target for the Extracellular Signal-Regulated MAP Kinases pathway in matrix metallopeptidase 1 gene activation |
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105. |
C/EBPbeta plays a key role in the coordination of TGFbeta cytostatic gene responses, and its malfunction may trigger evasion of these responses in breast cancer |
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106. |
A C/EBP beta element in the FasL promoter, identified by a functionally significant single-nucleotide polymorphism, affects FasL expression in vitro and ex vivo and is associated with systemic lupus erythematosus in African American patients. |
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107. |
mechanisms of MDR1 activation by C/EBPbeta include C/EBPbeta binding of the chromatin of the MDR1 gene and interactions of C/EBPbeta with the Y box and Y box-associated proteins. |
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108. |
IL-1 induces CRP expression through 2 overlapping response elements, the binding sites for CCAAT-box/enhancer-binding protein-beta (C/EBP-beta) and p50-nuclear factor-kappaB (p50-NFkappaB). |
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109. |
Direct interaction between the IL6 promoter and the C/EBP beta protein in myxoid lipoarcoma. |
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110. |
Together this shows that glucocorticoids increase DNA-binding activity of C/EBPbeta via post-translational mechanism(s) involving phosphorylation. |
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111. |
constitutive expression of C/EBPbeta in ALK-positive anaplastic large cell lymphoma and its relationship to NPM-ALK |
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112. |
CCAAT/enhancer binding proteins alpha and beta have roles in growth and differentiation of hepatoblastomas |
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113. |
c-Rel((1-300)) binding to C/EBPbeta increases the affinity of C/EBPbeta for the C/EBP binding site at -53 on the CRP promoter |
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114. |
The activities of several functional C/EBPbeta responsive elements in the promoter region and in the intron of CCR5 suggest regulatory roles for C/EBPbeta in CCR5 gene expression and in the pathogenesis of HIV disease. |
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115. |
CCAAT/enhancer binding protein-beta is a mediator ofkeratinocyte survival and skin tumorigenesis involving oncogenic Ras signaling. |