In this issue ofBlood, Ho and colleagues report the independent predictive value of single genemutations in theCEBPA gene in pediatric acutemyeloid leukemia. The outcome for this group of patients was excellent with 83 % ( 13%) overall survival at 5 years from study entry. TheCCAAT/enhancer bindingprotein, en-codedby theCEBPA gene, is a transcription factor that induces the expression of genes in-volved in terminal differentiation of granulo-cytes.Recently,CEBPAmutations have been added to the list of single-genemutations that maydefine a separate disease entity in cytoge-netically normal acutemyeloid leukemia (CN-AML),which is increasingly recognized as a molecularly heterogeneousdisease.1Apart from CEBPAmutations,mutations in nucleophosm...
SummaryMutations in the CEBPA gene are present in 7%–10% of human patients with acute myeloid leukem...
PURPOSE: The transcription factor CCAAT/enhancer binding protein-alpha (CEBPA) is crucial for normal...
Purpose To determine the clinical relevance of mutations in the CCAAT/enhancer binding protein α (CE...
In this issue of Blood, Ho and colleagues report the independent predictive value of single gene mut...
The transcription factor CCAAT enhancer binding protein alpha (CEBPA) is crucial for normal developm...
We evaluated concurrent gene mutations, clinical outcome, and gene expression signatures of CCAAT/en...
Purpose: The transcription factor CCAAT/enhancer binding protein , encoded by the CEBPA, is crucial ...
Background Dysfunctioning of CCAAT/enhancer binding protein α (C/EBP α) in acute myeloid leukemia ca...
OBJECTIVES: The CCAAT/enhancer-binding protein-alpha (CEBPA) is lineage-specifi c transcription fact...
textabstractMutations in CCAAT/enhancer binding protein α (CEBPA) are seen in 5% to 14% of acute mye...
none11C/EBP is a transcription factor that regulates terminal granulocytic differentiation. CEBPA mu...
CCAAT/enhancer-binding protein alpha (CEBPA) mutations are a favorable prognostic factor in adult ac...
The CEBPA gene encodes a transcription factor protein that is crucial for granulocytic differentiati...
textabstractSince the introduction of molecular genetics, our knowledge about the abnormalities unde...
In this issue of Blood, based on a retrospective analysis of 4708 acute myeloid leukemia (AML) cases...
SummaryMutations in the CEBPA gene are present in 7%–10% of human patients with acute myeloid leukem...
PURPOSE: The transcription factor CCAAT/enhancer binding protein-alpha (CEBPA) is crucial for normal...
Purpose To determine the clinical relevance of mutations in the CCAAT/enhancer binding protein α (CE...
In this issue of Blood, Ho and colleagues report the independent predictive value of single gene mut...
The transcription factor CCAAT enhancer binding protein alpha (CEBPA) is crucial for normal developm...
We evaluated concurrent gene mutations, clinical outcome, and gene expression signatures of CCAAT/en...
Purpose: The transcription factor CCAAT/enhancer binding protein , encoded by the CEBPA, is crucial ...
Background Dysfunctioning of CCAAT/enhancer binding protein α (C/EBP α) in acute myeloid leukemia ca...
OBJECTIVES: The CCAAT/enhancer-binding protein-alpha (CEBPA) is lineage-specifi c transcription fact...
textabstractMutations in CCAAT/enhancer binding protein α (CEBPA) are seen in 5% to 14% of acute mye...
none11C/EBP is a transcription factor that regulates terminal granulocytic differentiation. CEBPA mu...
CCAAT/enhancer-binding protein alpha (CEBPA) mutations are a favorable prognostic factor in adult ac...
The CEBPA gene encodes a transcription factor protein that is crucial for granulocytic differentiati...
textabstractSince the introduction of molecular genetics, our knowledge about the abnormalities unde...
In this issue of Blood, based on a retrospective analysis of 4708 acute myeloid leukemia (AML) cases...
SummaryMutations in the CEBPA gene are present in 7%–10% of human patients with acute myeloid leukem...
PURPOSE: The transcription factor CCAAT/enhancer binding protein-alpha (CEBPA) is crucial for normal...
Purpose To determine the clinical relevance of mutations in the CCAAT/enhancer binding protein α (CE...