Sarcoma
|
0.310 |
GenomicAlterations
|
group |
CGI |
|
|
|
Other emphysema
|
0.200 |
Biomarker
|
phenotype |
MGD |
|
|
|
Malignant transformation
|
0.050 |
AlteredExpression
|
phenotype |
BEFREE |
The proto-oncogene C-jun acts as a transcriptional activator or repressor for numerous cellular genes, and the overexpression of these genes may cause malignant transformation.
|
1404666 |
1992 |
Renal Cell Carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
We investigated the expression of jun genes in renal cell cancer (RCC) and their regulation by cytokines and transforming growth factor beta 1 (TGF-b1).
|
1404666 |
1992 |
Myeloid Leukemia
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
The present work demonstrates that treatment of human myeloid leukemia cells (HL-60, U-937, and KG-1) with CDDP is associated with increased expression of the c-jun gene and that this effect is related to activation by a transcriptional mechanism.
|
1737349 |
1992 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
It recently has been reported that certain nuclear receptors can antagonize the tumor promoter 12-O-tetradeconylphorbol-13-acetate (TPA) by direct interaction with the transcription factor AP-1, and that the AP-1 constituents cJun and cFos can inhibit receptor activity.
|
1791843 |
1991 |
Chronic Lymphocytic Leukemia
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Expression of proto-oncogene c-jun during differentiation of B-chronic lymphocytic leukemia.
|
2113601 |
1990 |
Lyme Disease
|
0.020 |
Biomarker
|
disease |
BEFREE |
Ninety-four serum specimens from patients having Lyme borreliosis were tested for reactivity with P39.
|
2380361 |
1990 |
Neuroblastoma
|
0.050 |
Biomarker
|
disease |
BEFREE |
Finally, this study identified a breakpoint at 1p32 that was localized between the genes JUN and MYCL for one neuroblastoma thus establishing the order of these genes as centromere, JUN, MYCL, telomere.
|
2776489 |
1989 |
Central neuroblastoma
|
0.050 |
Biomarker
|
disease |
BEFREE |
Finally, this study identified a breakpoint at 1p32 that was localized between the genes JUN and MYCL for one neuroblastoma thus establishing the order of these genes as centromere, JUN, MYCL, telomere.
|
2776489 |
1989 |
Childhood Neuroblastoma
|
0.050 |
Biomarker
|
disease |
BEFREE |
Finally, this study identified a breakpoint at 1p32 that was localized between the genes JUN and MYCL for one neuroblastoma thus establishing the order of these genes as centromere, JUN, MYCL, telomere.
|
2776489 |
1989 |
Human immunodeficiency virus (HIV) II infection category B1
|
0.040 |
Biomarker
|
disease |
BEFREE |
Interactions of the transcription factor AP-1 with the long terminal repeat of different human immunodeficiency virus type 1 strains in Jurkat, glial, and neuronal cells.
|
7474072 |
1995 |
Asthma
|
0.060 |
Biomarker
|
disease |
BEFREE |
To study this reduced DNA binding, we examined the ability of the nuclear translocated transcription factors activator protein 1 (AP-1), nuclear factor kappa B (NF-kappa B) and cyclic AMP response element-binding protein (CREB) to bind to their DNA-binding sites and to interact with GR in PBMC from patients with steroid-sensitive and steroid-resistant asthma.
|
7500041 |
1995 |
Carcinogenesis
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Jun proteins can thus be key intermediates in regulatory cascades which result in the differential modulation of the AFP and albumin gene expression in the course of liver development and carcinogenesis.
|
7537266 |
1995 |
ovarian neoplasm
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
We evaluated the effects of recombinant human G-CSF, rhGM-CSF, rhM-CSF and rhIL-1 alpha on proliferation and regulation of c-jun gene expression in 4 human ovarian-carcinoma (HOC) cell lines, NIH:OVCAR-3, SK-OV-3, HEY and BG-1, and in one primary ovarian tumor in vitro.
|
7591243 |
1995 |
leukemia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In this work, we demonstrate that the levels of c-jun mRNA, c-Jun protein, and DNA binding activity of a nuclear transcription factor AP-1 to 12-o-tetradecanoylphorbol 13-acetate responsive elements all increased following treatment with the cell-permeable ceramide, N-acetylsphingosine in human leukemia HL-60 cells.
|
7592995 |
1995 |
Childhood Leukemia
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In this work, we demonstrate that the levels of c-jun mRNA, c-Jun protein, and DNA binding activity of a nuclear transcription factor AP-1 to 12-o-tetradecanoylphorbol 13-acetate responsive elements all increased following treatment with the cell-permeable ceramide, N-acetylsphingosine in human leukemia HL-60 cells.
|
7592995 |
1995 |
Asthma
|
0.060 |
Biomarker
|
disease |
BEFREE |
Secondary steroid resistance in asthma may arise in response to the release of cytokines that activate AP-1 and other transcription factors that bind directly to GR.
|
7633872 |
1995 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The c-fos and c-jun genes were also activated in these tumors.
|
7732661 |
1995 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Since P(+)-to-tumor phenotype progression occurred in cells overexpressing c-jun but not AP-1, we propose that P(+)-to-transformed phenotype progression is c-jun dependent and AP-1 independent.
|
7766308 |
1995 |
Reperfusion Injury
|
0.300 |
Biomarker
|
disease |
CTD_human |
Differential expression of c-jun, c-fos and hsp 70 mRNAs after folic acid and ischemia-reperfusion injury: effect of antioxidant treatment.
|
7922267 |
1994 |
Status Epilepticus
|
0.300 |
Biomarker
|
disease |
CTD_human |
Distinctive rat brain immediate early gene responses to seizures induced by lithium plus pilocarpine.
|
7984056 |
1994 |
Petit mal status
|
0.300 |
Biomarker
|
disease |
CTD_human |
Distinctive rat brain immediate early gene responses to seizures induced by lithium plus pilocarpine.
|
7984056 |
1994 |
Grand Mal Status Epilepticus
|
0.300 |
Biomarker
|
disease |
CTD_human |
Distinctive rat brain immediate early gene responses to seizures induced by lithium plus pilocarpine.
|
7984056 |
1994 |
Complex Partial Status Epilepticus
|
0.300 |
Biomarker
|
disease |
CTD_human |
Distinctive rat brain immediate early gene responses to seizures induced by lithium plus pilocarpine.
|
7984056 |
1994 |