Liver Cirrhosis, Experimental
|
0.300 |
Biomarker
|
disease |
CTD_human |
Systems level analysis and identification of pathways and networks associated with liver fibrosis.
|
25380136 |
2014 |
Malignant tumor of colon
|
0.210 |
Biomarker
|
disease |
RGD |
In colon cancer, apobec-1 protein levels decreased by 90% in the cancer tissue as compared to normal tissue, suggesting an inhibitory effect of the 5'UTR on apobec-1 translation.
|
12020819 |
2002 |
Malignant tumor of colon
|
0.210 |
AlteredExpression
|
disease |
BEFREE |
Apobec-1 mRNA was detectable in normal and colon cancer tissue, metastatic nodules, and certain colon cancer-derived cell lines.
|
9797364 |
1998 |
Hyperlipidemia
|
0.200 |
Biomarker
|
disease |
RGD |
Effects of a thyromimetic on apolipoprotein B-100 in rats.
|
11116209 |
2000 |
Hyperlipoproteinemias
|
0.200 |
Biomarker
|
disease |
RGD |
Effects of a thyromimetic on apolipoprotein B-100 in rats.
|
11116209 |
2000 |
Obesity
|
0.200 |
Biomarker
|
disease |
RGD |
In contrast, the hepatic mRNA encoding APOBEC-1, the catalytic subunit of the RNA editing activity, demonstrated an increased abundance of 1.8-fold in obese Zucker rats versus lean controls.
|
8781289 |
1996 |
Liver and Intrahepatic Bile Duct Epithelial Neoplasm
|
0.200 |
Biomarker
|
disease |
RGD |
Low expression of the apolipoprotein B mRNA-editing transgene in mice reduces LDL levels but does not cause liver dysplasia or tumors.
|
9633945 |
1998 |
Liver and Intrahepatic Bile Duct Neoplasm
|
0.200 |
Biomarker
|
disease |
RGD |
Low expression of the apolipoprotein B mRNA-editing transgene in mice reduces LDL levels but does not cause liver dysplasia or tumors.
|
9633945 |
1998 |
Arteriosclerosis
|
0.030 |
Biomarker
|
disease |
BEFREE |
RE4 APOBEC-1 transgenic mice should prove valuable for studying the roles of apoB-containing lipoproteins in lipid metabolism and atherosclerosis.
|
9633945 |
1998 |
Arteriosclerosis
|
0.030 |
Biomarker
|
disease |
BEFREE |
Whereas Ldlr(-/-)Apobec1(-/-) mice fed a western-type diet and injected with a control AAV8.null vector experienced a further 65% progression in atherosclerosis over 2 months compared with baseline mice, Ldlr(-/-)Apobec1(-/-) mice treated with AAV8.mLDLR realized an 87% regression of atherosclerotic lesions after 3 months compared to baseline mice.
|
20976059 |
2010 |
Arteriosclerosis
|
0.030 |
Biomarker
|
disease |
BEFREE |
Here, we placed hypercholesterolemic Ldlr-/-Apobec1-/- mice on a high-fat diet and treated them with either 25 mg/kg/day of clopidogrel (CLO) or 180 mg/kg/day of TIC for 16 weeks and evaluated the extent of atherosclerosis.
|
31242230 |
2019 |
Atherosclerosis
|
0.030 |
Biomarker
|
disease |
BEFREE |
Here, we placed hypercholesterolemic Ldlr-/-Apobec1-/- mice on a high-fat diet and treated them with either 25 mg/kg/day of clopidogrel (CLO) or 180 mg/kg/day of TIC for 16 weeks and evaluated the extent of atherosclerosis.
|
31242230 |
2019 |
Atherosclerosis
|
0.030 |
Biomarker
|
disease |
BEFREE |
Whereas Ldlr(-/-)Apobec1(-/-) mice fed a western-type diet and injected with a control AAV8.null vector experienced a further 65% progression in atherosclerosis over 2 months compared with baseline mice, Ldlr(-/-)Apobec1(-/-) mice treated with AAV8.mLDLR realized an 87% regression of atherosclerotic lesions after 3 months compared to baseline mice.
|
20976059 |
2010 |
Atherosclerosis
|
0.030 |
Biomarker
|
disease |
BEFREE |
RE4 APOBEC-1 transgenic mice should prove valuable for studying the roles of apoB-containing lipoproteins in lipid metabolism and atherosclerosis.
|
9633945 |
1998 |
Epilepsy
|
0.020 |
Biomarker
|
disease |
BEFREE |
Corrigendum: A Novel RNA Editing Sensor Tool and a Specific Agonist Determine Neuronal Protein Expression of RNA-Edited Glycine Receptors and Identify a Genomic APOBEC1 Dimorphism as a New Genetic Risk Factor of Epilepsy.
|
31105523 |
2019 |
Epilepsy
|
0.020 |
Biomarker
|
disease |
BEFREE |
A Novel RNA Editing Sensor Tool and a Specific Agonist Determine Neuronal Protein Expression of RNA-Edited Glycine Receptors and Identify a Genomic APOBEC1 Dimorphism as a New Genetic Risk Factor of Epilepsy.
|
29375302 |
2017 |
Neurofibromatosis 1
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
C-->U editing of neurofibromatosis 1 mRNA occurs in tumors that express both the type II transcript and apobec-1, the catalytic subunit of the apolipoprotein B mRNA-editing enzyme.
|
11727199 |
2002 |
Neurofibromatosis 1
|
0.020 |
AlteredExpression
|
disease |
LHGDN |
Taken together, the data support the hypothesis that C-->U RNA editing of the NF1 transcript occurs both in a subset of PNSTs and in an alternatively spliced form containing a downstream exon, presumably an optimal configuration for enzymatic deamination by apobec-1.
|
11727199 |
2002 |
Neurofibromatosis 1
|
0.020 |
Biomarker
|
disease |
BEFREE |
Overexpression of APOBEC-1 in transgenic animals caused liver dysplasia and APOBEC-1 has been identified in neurofibromatosis type 1 tumours, suggesting that RNA editing may be another mechanism for tumourigenesis.
|
11072063 |
2000 |
Liver carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
However, high-level expression of APOBEC-1 in transgenic mouse and rabbit livers causes liver dysplasia and hepatocellular carcinoma.
|
9633945 |
1998 |
Liver carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
The transgene expression of the catalytic subunit APOBEC-1 of the apo B mRNA editing enzyme-complex can cause hepatocellular carcinoma in mice and rabbits.
|
10597235 |
1999 |
Anaplasia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Apobec1 Promotes Neurotoxicity-Induced Dedifferentiation of Müller Glial Cells.
|
28150227 |
2017 |
Barrett Esophagus
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
APOBEC1 could be involved in cancer promotion at the very early stages of carcinogenesis, as it is highly expressed in Barrett's esophagus, a condition often associated with esophageal adenocarcinoma.
|
25085003 |
2014 |
Cerebral Infarction
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Apobec-1 could upregulate COX-2 expression in neurogenic cells by stabilizing COX-2 mRNA, and might aggravate injury of oxygen-glucose deprivation in neurogenic cells as well as in rats with cerebral ischemia.
|
23609497 |
2013 |
Cholelithiasis
|
0.010 |
Biomarker
|
disease |
BEFREE |
To investigate APOBEC1 and PPARG as candidate genes for common symptomatic gallstone disease in humans.
|
17696929 |
2007 |