Cholestasis
|
0.300 |
Biomarker
|
disease |
CTD_human |
Classification of Cholestatic and Necrotic Hepatotoxicants Using Transcriptomics on Human Precision-Cut Liver Slices.
|
26881866 |
2016 |
Hepatitis, Toxic
|
0.300 |
Biomarker
|
disease |
CTD_human |
Classification of Cholestatic and Necrotic Hepatotoxicants Using Transcriptomics on Human Precision-Cut Liver Slices.
|
26881866 |
2016 |
Drug-Induced Liver Disease
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Classification of Cholestatic and Necrotic Hepatotoxicants Using Transcriptomics on Human Precision-Cut Liver Slices.
|
26881866 |
2016 |
Hepatitis, Drug-Induced
|
0.300 |
Biomarker
|
disease |
CTD_human |
Classification of Cholestatic and Necrotic Hepatotoxicants Using Transcriptomics on Human Precision-Cut Liver Slices.
|
26881866 |
2016 |
Drug-Induced Acute Liver Injury
|
0.300 |
Biomarker
|
disease |
CTD_human |
Classification of Cholestatic and Necrotic Hepatotoxicants Using Transcriptomics on Human Precision-Cut Liver Slices.
|
26881866 |
2016 |
Chemical and Drug Induced Liver Injury
|
0.300 |
Biomarker
|
disease |
CTD_human |
Classification of Cholestatic and Necrotic Hepatotoxicants Using Transcriptomics on Human Precision-Cut Liver Slices.
|
26881866 |
2016 |
Chemically-Induced Liver Toxicity
|
0.300 |
Biomarker
|
disease |
CTD_human |
Classification of Cholestatic and Necrotic Hepatotoxicants Using Transcriptomics on Human Precision-Cut Liver Slices.
|
26881866 |
2016 |
Anorexia Nervosa
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa.
|
31308545 |
2019 |
Skin callus
|
0.020 |
Biomarker
|
disease |
BEFREE |
In contrast, exogenous JA treatment during callus formation on CIM did not influence the plant regeneration process.
|
31094274 |
2019 |
Skin callus
|
0.020 |
Biomarker
|
disease |
BEFREE |
The 74-88% callus induction frequency was obtained on CIM-1 to CIM-5.
|
31218181 |
2019 |
Neoplasms
|
0.020 |
Biomarker
|
group |
BEFREE |
Tumours were selected with the following phenotypical features, using mucin histochemical and immunohistochemical analyses, in addition to their morphological features: (1) tumours with an extremely well-preserved gastric foveolar phenotype (foveolar-type); (2) tumours with an extremely well-preserved complete-type intestinal metaplastic phenotype (CIM-type); and (3) ordinary tumours without extreme phenotypes (ordinary-type).
|
10878546 |
2000 |
Neoplasms
|
0.020 |
Biomarker
|
group |
BEFREE |
The incidence of MSI-H was found to be significantly higher in foveolar-type tumors (100%; 4 of 4) than in ordinary-type (19%; 10 of 52) or CIM-type tumors (0%; 0 of 5) (P < .01).
|
11014567 |
2000 |
Syringomyelia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Scoliotic patients with CIM were generally offered surgery only when there was a large syrinx.
|
29532166 |
2018 |
Syrinx formation
|
0.010 |
Biomarker
|
disease |
BEFREE |
Scoliotic patients with CIM were generally offered surgery only when there was a large syrinx.
|
29532166 |
2018 |
Acute encephalopathy
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Our results revealed that having at least one CIM allele is a risk factor for the onset of acute encephalopathy, regardless of its antecedent infections.
|
20934285 |
2011 |
Neoplasm Metastasis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
In this study, we report the identification of a novel cancer invasion and metastasis-related gene (hereafter referred to as CIM, also called ERLEC1), which influences both of these stress-response pathways to promote metastasis.
|
21118962 |
2010 |
Malignant neoplasm of lung
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Ectopic expression of CIM in lung cancer cells increased their tolerance to hypoxia.
|
21118962 |
2010 |
Carcinoma of lung
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Ectopic expression of CIM in lung cancer cells increased their tolerance to hypoxia.
|
21118962 |
2010 |
Primary malignant neoplasm of lung
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Ectopic expression of CIM in lung cancer cells increased their tolerance to hypoxia.
|
21118962 |
2010 |