Age, JAK2V617F and SF3B1 mutations are the main predicting factors for survival in refractory anaemia with ring sideroblasts and marked thrombocytosis
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Age, JAK2V617F and SF3B1 mutations are the main predicting factors for survival in refractory anaemia with ring sideroblasts and marked thrombocytosis
Authors
Keywords
-
Journal
LEUKEMIA
Volume 27, Issue 9, Pages 1826-1831
Publisher
Springer Nature
Online
2013-04-18
DOI
10.1038/leu.2013.120
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Mutations affecting mRNA splicing define distinct clinical phenotypes and correlate with patient outcome in myelodysplastic syndromes
- (2012) F. Damm et al. BLOOD
- Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes
- (2012) F. Thol et al. BLOOD
- SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes
- (2012) V. Visconte et al. BLOOD
- Biologic and clinical significance of somatic mutations of SF3B1 in myeloid and lymphoid neoplasms
- (2012) M. Cazzola et al. BLOOD
- The development and application of small molecule modulators of SF3b as therapeutic agents for cancer
- (2012) Thomas R. Webb et al. DRUG DISCOVERY TODAY
- Clinical features and course of refractory anemia with ring sideroblasts associated with marked thrombocytosis
- (2012) J. Broseus et al. HAEMATOLOGICA
- High frequencies of SF3B1 and JAK2 mutations in refractory anemia with ring sideroblasts associated with marked thrombocytosis strengthen the assignment to the category of myelodysplastic/myeloproliferative neoplasms
- (2012) S. Jeromin et al. HAEMATOLOGICA
- Emerging roles of the spliceosomal machinery in myelodysplastic syndromes and other hematological disorders
- (2012) V Visconte et al. LEUKEMIA
- Spliceosome-related gene mutations in myelodysplastic syndrome can be used as stable markers for monitoring minimal residual disease during follow-up
- (2012) Kazuyuki Matsuda et al. LEUKEMIA RESEARCH
- SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value
- (2011) M. M. Patnaik et al. BLOOD
- Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms
- (2011) L. Malcovati et al. BLOOD
- SF3B1 mutations in myelodysplastic syndromes: clinical associations and prognostic implications
- (2011) F Damm et al. LEUKEMIA
- SF3B1, a splicing factor is frequently mutated in refractory anemia with ring sideroblasts
- (2011) V Visconte et al. LEUKEMIA
- Frequent pathway mutations of splicing machinery in myelodysplasia
- (2011) Kenichi Yoshida et al. NATURE
- SomaticSF3B1Mutation in Myelodysplasia with Ring Sideroblasts
- (2011) E. Papaemmanuil et al. NEW ENGLAND JOURNAL OF MEDICINE
- Molecular and clinical features of refractory anemia with ringed sideroblasts associated with marked thrombocytosis
- (2009) L. Malcovati et al. BLOOD
- Detection of JAK2 exon 12 mutations in 15 patients with JAK2V617F negative polycythemia vera
- (2009) S. Schnittger et al. HAEMATOLOGICA
- Mutations of JAK2 and TET2, but not CBL are detectable in a high portion of patients with refractory anemia with ring sideroblasts and thrombocytosis
- (2009) J. Flach et al. HAEMATOLOGICA
- Is refractory anaemia with ring sideroblasts and thrombocytosis (RARS-T) a necessary or useful diagnostic category?
- (2008) Douglas Wardrop et al. BRITISH JOURNAL OF HAEMATOLOGY
- JAK2V617F mutation status identifies subtypes of refractory anemia with ringed sideroblasts associated with marked thrombocytosis
- (2008) A. H. Schmitt-Graeff et al. HAEMATOLOGICA
- Characterization of 35 new cases with four different MPLW515 mutations and essential thrombocytosis or primary myelofibrosis
- (2008) S. Schnittger et al. HAEMATOLOGICA
- Refractory anemia with ringed sideroblasts associated with thrombocytosis: comparative analysis of marked with non-marked thrombocytosis, and relationship with JAK2 V617F mutational status
- (2008) J. M. Raya et al. INTERNATIONAL JOURNAL OF HEMATOLOGY
- The Role of JAK2 Mutations in RARS and Other MDS
- (2008) E. Hellstrom-Lindberg et al. Hematology-American Society of Hematology Education Program
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now