Introduction Although the effects of U2 small nuclear RNA auxiliary factor 1 gene ( U2AF1 ) mutations on the outcomes of patients with myelodysplastic syndromes (MDS) have previously been investigated, their prognostic significance remains controversial. We performed a meta-analysis to investigate the impact of U2AF1 mutations on MDS progression. Methods Two reviewers independently extracted information such as hazard ratios (HRs) and 95% confidential intervals (CIs) for overall survival (OS) and leukemia-free survival (LFS) as well as the number of surviving patients each year after diagnosis from the included studies. Results Thirteen studies with a total of 3038 patients were included. The summary odds ratio (OR) for U2AF1 mutations with...
Abstract Mutations in the U2 small nuclear RNA auxiliary factor 1 (U2AF1) gene are the common featur...
PURPOSE: Recurrently mutated genes and chromosomal abnormalities have been identified in myelodyspla...
). mutations on OS and LFS in MDS. mutations were 1.62 (95% CI, 1.27–2.09) and 2.21 (95% CI, 1.48–3....
We aimed to analyze clinical impacts of the U2AF1 mutation on patients with myelodysplastic syndrome...
The recent application of gene-sequencing technology has identified many new somatic mutations in pa...
Background: Recent genomic sequencing efforts have identified a number of recurrent mutations in mye...
Somatic mutations of U2AF1 gene have recently been identified in myelodysplastic syndrome (MDS) and ...
Recent genomic sequencing efforts have identified a number of recurrent mutations in myelodysplastic...
[[abstract]]Myelodysplastic syndromes (MDS) are a heterogeneous group of hematologic malignancies. A...
<div><p>Somatic mutations of <em>U2AF1</em> gene have recently been identified in myelodysplastic sy...
[[abstract]]Myelodysplastic syndromes (MDS) are a heterogeneous group of hematologic malignancies. A...
Myelodysplastic syndromes (MDS) are a clonal disease arising from hematopoietic stem cells, that are...
High-throughput DNA sequencing significantly contributed to diagnosis and prognostication in patient...
Myelodysplastic neoplasms (MDS) form a broad spectrum of clonal myeloid malignancies arising from he...
[[abstract]]Gene mutations have not yet been included in the 2016 WHO classification and revised Int...
Abstract Mutations in the U2 small nuclear RNA auxiliary factor 1 (U2AF1) gene are the common featur...
PURPOSE: Recurrently mutated genes and chromosomal abnormalities have been identified in myelodyspla...
). mutations on OS and LFS in MDS. mutations were 1.62 (95% CI, 1.27–2.09) and 2.21 (95% CI, 1.48–3....
We aimed to analyze clinical impacts of the U2AF1 mutation on patients with myelodysplastic syndrome...
The recent application of gene-sequencing technology has identified many new somatic mutations in pa...
Background: Recent genomic sequencing efforts have identified a number of recurrent mutations in mye...
Somatic mutations of U2AF1 gene have recently been identified in myelodysplastic syndrome (MDS) and ...
Recent genomic sequencing efforts have identified a number of recurrent mutations in myelodysplastic...
[[abstract]]Myelodysplastic syndromes (MDS) are a heterogeneous group of hematologic malignancies. A...
<div><p>Somatic mutations of <em>U2AF1</em> gene have recently been identified in myelodysplastic sy...
[[abstract]]Myelodysplastic syndromes (MDS) are a heterogeneous group of hematologic malignancies. A...
Myelodysplastic syndromes (MDS) are a clonal disease arising from hematopoietic stem cells, that are...
High-throughput DNA sequencing significantly contributed to diagnosis and prognostication in patient...
Myelodysplastic neoplasms (MDS) form a broad spectrum of clonal myeloid malignancies arising from he...
[[abstract]]Gene mutations have not yet been included in the 2016 WHO classification and revised Int...
Abstract Mutations in the U2 small nuclear RNA auxiliary factor 1 (U2AF1) gene are the common featur...
PURPOSE: Recurrently mutated genes and chromosomal abnormalities have been identified in myelodyspla...
). mutations on OS and LFS in MDS. mutations were 1.62 (95% CI, 1.27–2.09) and 2.21 (95% CI, 1.48–3....