CCAAT/enhancer binding protein alpha (CEBPA) mutations in AML are associated with favourable prognosis and are divided into N- and C-terminal mutations. The majority of AML patients have both types of mutations. We assessed the prognostic significance of single (n 7) and double (n 12) CEBPA mutations among 224 AML patients. Double CEBPA mutations conferred a decisively favourable overall (P 0.006) and disease-free survival (P 0.013). However, clinical outcome of patients with single CEBPA mutations was not different from CEBPA wild-type patients. In a multivariable analysis, only double – but not single – CEBPA mutations were identified as independent prognostic factors. These findings indicate heterogeneity within AML patients with CEB...
Purpose: The transcription factor CCAAT/enhancer binding protein , encoded by the CEBPA, is crucial ...
CCAAT/enhancer binding protein-α (CEBPA) mutations in acute myeloid leukemia (AML) patients with a n...
Aim : The aim of this work is to study the prognostic impact of muta-tions in the myeloid transcript...
CCAAT/enhancer binding protein alpha (CEBPA) mutations in AML are associated with favourable prognos...
We evaluated concurrent gene mutations, clinical outcome, and gene expression signatures of CCAAT/en...
textabstractMutations in CCAAT/enhancer binding protein α (CEBPA) are seen in 5% to 14% of acute mye...
Purpose To determine the clinical relevance of mutations in the CCAAT/enhancer binding protein α (CE...
Biallelic mutations of the CEBPA gene (CEBPAbi) define a distinct entity associated with favorable p...
C/EBP is a transcription factor that regulates terminal granulocytic differentiation. CEBPA mutation...
Purpose CEBPA mutations are found as either biallelic (biCEBPA) or monoallelic (moCEBPA). We set out...
International audienceMutations of the CCAAT/enhancer binding protein alpha (CEBPA) gene have been a...
In this issue of Blood, based on a retrospective analysis of 4708 acute myeloid leukemia (AML) cases...
Despite recent refinements in the diagnostic and prognostic assessment of CEBPA mutations in AML, se...
The transcription factor CCAAT enhancer binding protein alpha (CEBPA) is crucial for normal developm...
We and others have shown that cytogenetically normal (CN)-AML patients with biallelic CEBPA gene mut...
Purpose: The transcription factor CCAAT/enhancer binding protein , encoded by the CEBPA, is crucial ...
CCAAT/enhancer binding protein-α (CEBPA) mutations in acute myeloid leukemia (AML) patients with a n...
Aim : The aim of this work is to study the prognostic impact of muta-tions in the myeloid transcript...
CCAAT/enhancer binding protein alpha (CEBPA) mutations in AML are associated with favourable prognos...
We evaluated concurrent gene mutations, clinical outcome, and gene expression signatures of CCAAT/en...
textabstractMutations in CCAAT/enhancer binding protein α (CEBPA) are seen in 5% to 14% of acute mye...
Purpose To determine the clinical relevance of mutations in the CCAAT/enhancer binding protein α (CE...
Biallelic mutations of the CEBPA gene (CEBPAbi) define a distinct entity associated with favorable p...
C/EBP is a transcription factor that regulates terminal granulocytic differentiation. CEBPA mutation...
Purpose CEBPA mutations are found as either biallelic (biCEBPA) or monoallelic (moCEBPA). We set out...
International audienceMutations of the CCAAT/enhancer binding protein alpha (CEBPA) gene have been a...
In this issue of Blood, based on a retrospective analysis of 4708 acute myeloid leukemia (AML) cases...
Despite recent refinements in the diagnostic and prognostic assessment of CEBPA mutations in AML, se...
The transcription factor CCAAT enhancer binding protein alpha (CEBPA) is crucial for normal developm...
We and others have shown that cytogenetically normal (CN)-AML patients with biallelic CEBPA gene mut...
Purpose: The transcription factor CCAAT/enhancer binding protein , encoded by the CEBPA, is crucial ...
CCAAT/enhancer binding protein-α (CEBPA) mutations in acute myeloid leukemia (AML) patients with a n...
Aim : The aim of this work is to study the prognostic impact of muta-tions in the myeloid transcript...