Colorectal Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Deficiency of 15-LOX-1 Induces Radioresistance through Downregulation of MacroH2A2 in Colorectal Cancer.
|
31717983 |
2019 |
Malignant neoplasm of colon and/or rectum
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Deficiency of 15-LOX-1 Induces Radioresistance through Downregulation of MacroH2A2 in Colorectal Cancer.
|
31717983 |
2019 |
Anus Neoplasms
|
0.010 |
Biomarker
|
group |
BEFREE |
Loss of histone variant macroH2A2 expression is associated with the progression of anal neoplasm and can be used as a prognostic biomarker for high-grade AIN and SCC.
|
26658220 |
2016 |
Neoplasms
|
0.010 |
Biomarker
|
group |
BEFREE |
Patients with AIN with macroH2A2-negative lesions showed earlier recurrence than those with macroH2A2-positive neoplasm (p=0.017).
|
26658220 |
2016 |
Dysplasia of anus
|
0.010 |
Biomarker
|
disease |
BEFREE |
Loss of histone variant macroH2A2 expression is associated with the progression of anal neoplasm and can be used as a prognostic biomarker for high-grade AIN and SCC.
|
26658220 |
2016 |
Carcinoma of anal margin
|
0.010 |
Biomarker
|
disease |
BEFREE |
Loss of histone variant macroH2A2 expression is associated with the progression of anal neoplasm and can be used as a prognostic biomarker for high-grade AIN and SCC.
|
26658220 |
2016 |
Anal squamous cell carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Loss of histone variant macroH2A2 expression is associated with the progression of anal neoplasm and can be used as a prognostic biomarker for high-grade AIN and SCC.
|
26658220 |
2016 |
Anal intraepithelial neoplasia I and II (AIN I and II) (histologically confirmed)
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
macroH2A2 was expressed in normal squamous tissue and lower grade AIN (I and II).
|
26658220 |
2016 |
Malignant Neoplasms
|
0.010 |
Biomarker
|
group |
BEFREE |
MacroH2A1.1 and macroH2A2 inhibit proliferation and are associated with better cancer prognosis; while macroH2A1.2 is associated to cancer progression.
|
25003966 |
2014 |
Tumor Progression
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
MacroH2A1.1 and macroH2A2 inhibit proliferation and are associated with better cancer prognosis; while macroH2A1.2 is associated to cancer progression.
|
25003966 |
2014 |
Primary malignant neoplasm
|
0.010 |
Biomarker
|
group |
BEFREE |
MacroH2A1.1 and macroH2A2 inhibit proliferation and are associated with better cancer prognosis; while macroH2A1.2 is associated to cancer progression.
|
25003966 |
2014 |
Malignant neoplasm of lung
|
0.010 |
Biomarker
|
disease |
BEFREE |
Here, we show that expression of histone macroH2A1.1 and macroH2A2 predicts lung cancer recurrence, identifying these histone variants as a novel tool for an improved risk stratification of cancer patients.
|
19648962 |
2009 |
Carcinoma of lung
|
0.010 |
Biomarker
|
disease |
BEFREE |
Here, we show that expression of histone macroH2A1.1 and macroH2A2 predicts lung cancer recurrence, identifying these histone variants as a novel tool for an improved risk stratification of cancer patients.
|
19648962 |
2009 |
Primary malignant neoplasm of lung
|
0.010 |
Biomarker
|
disease |
BEFREE |
Here, we show that expression of histone macroH2A1.1 and macroH2A2 predicts lung cancer recurrence, identifying these histone variants as a novel tool for an improved risk stratification of cancer patients.
|
19648962 |
2009 |
Carcinogenesis
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
Three genes (Notch2, H2AFY2, and CDC5L) showed similar expression differences between microsatellite instability and chromosomal instability cell lines as observed between the young and old cell cultures suggesting that they may play a role in tumorigenesis.
|
15574761 |
2004 |