The recent application of gene-sequencing technology has identified many new somatic mutations in patients with myelodysplastic syndromes (MDS). Among them, serine and arginine rich splicing factor 2 (SRSF2) mutations belonging to the RNA splicing pathway were of interest. Many studies have already reported the potential prognostic value of SRSF2 mutations in MDS patients, with controversial results. Therefore, a meta-analysis was performed to investigate their prognostic impact on MDS.Databases, including PubMed, Embase and the Cochrane Library, were searched for relevant studies published up to 14 October 2016. Overall survival (OS) was selected as the primary endpoint, and acute myeloid leukemia (AML) transformation was the secondary end...
Abstract Myelodysplastic syndromes (MDS) are a group of neoplasms that are ineffectiv...
Myelodysplastic syndromes (MDS) are stem cell disorders caused by various gene abnormalities. We per...
Myelodysplastic Syndromes (MDS) are hematopoietic disorders characterized by myeloid dysplasia, inef...
Recurrent somatic mutation of SRSF2, one of the RNA splicing machinery genes, has been identified in...
. These authors contributed equally to this work. Hotspot mutations of serine/arginine-rich splicing...
Hotspot mutations of serine/arginine-rich splicing factor 2 (SRSF2) gene have been identified in a p...
Introduction Although the effects of U2 small nuclear RNA auxiliary factor 1 gene ( U2AF1 ) mutation...
High-throughput DNA sequencing significantly contributed to diagnosis and prognostication in patient...
PURPOSE: Recurrently mutated genes and chromosomal abnormalities have been identified in myelodyspla...
Background: Recent genomic sequencing efforts have identified a number of recurrent mutations in mye...
High-throughput DNA sequencing significantly contributed to diagnosis and prognostication in patient...
Myelodysplastic syndromes (MDS) are the most common myeloid malignancies of the elderly, characteriz...
Myelodysplastic syndromes (MDS) are a clonal disease arising from hematopoietic stem cells, that are...
Mutations in splicing factor (SF) genes are frequently detected in myelodysplastic syndrome, but the...
[[abstract]]Gene mutations have not yet been included in the 2016 WHO classification and revised Int...
Abstract Myelodysplastic syndromes (MDS) are a group of neoplasms that are ineffectiv...
Myelodysplastic syndromes (MDS) are stem cell disorders caused by various gene abnormalities. We per...
Myelodysplastic Syndromes (MDS) are hematopoietic disorders characterized by myeloid dysplasia, inef...
Recurrent somatic mutation of SRSF2, one of the RNA splicing machinery genes, has been identified in...
. These authors contributed equally to this work. Hotspot mutations of serine/arginine-rich splicing...
Hotspot mutations of serine/arginine-rich splicing factor 2 (SRSF2) gene have been identified in a p...
Introduction Although the effects of U2 small nuclear RNA auxiliary factor 1 gene ( U2AF1 ) mutation...
High-throughput DNA sequencing significantly contributed to diagnosis and prognostication in patient...
PURPOSE: Recurrently mutated genes and chromosomal abnormalities have been identified in myelodyspla...
Background: Recent genomic sequencing efforts have identified a number of recurrent mutations in mye...
High-throughput DNA sequencing significantly contributed to diagnosis and prognostication in patient...
Myelodysplastic syndromes (MDS) are the most common myeloid malignancies of the elderly, characteriz...
Myelodysplastic syndromes (MDS) are a clonal disease arising from hematopoietic stem cells, that are...
Mutations in splicing factor (SF) genes are frequently detected in myelodysplastic syndrome, but the...
[[abstract]]Gene mutations have not yet been included in the 2016 WHO classification and revised Int...
Abstract Myelodysplastic syndromes (MDS) are a group of neoplasms that are ineffectiv...
Myelodysplastic syndromes (MDS) are stem cell disorders caused by various gene abnormalities. We per...
Myelodysplastic Syndromes (MDS) are hematopoietic disorders characterized by myeloid dysplasia, inef...