Comprehensive mutational profiling in advanced systemic mastocytosis
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Title
Comprehensive mutational profiling in advanced systemic mastocytosis
Authors
Keywords
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Journal
BLOOD
Volume 122, Issue 14, Pages 2460-2466
Publisher
American Society of Hematology
Online
2013-08-20
DOI
10.1182/blood-2013-04-496448
References
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Related references
Note: Only part of the references are listed.- Systemic mastocytosis in adults: 2012 Update on diagnosis, risk stratification, and management
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- SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)
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- (2012) E. Soucie et al. BLOOD
- 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
- Recurrent somatic TET2 mutations in normal elderly individuals with clonal hematopoiesis
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- Single Nucleotide Polymorphism Array Lesions, TET2, DNMT3A, ASXL1 and CBL Mutations Are Present in Systemic Mastocytosis
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- EZH2 mutational status predicts poor survival in myelofibrosis
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- KIT-D816V-independent oncogenic signaling in neoplastic cells in systemic mastocytosis: role of Lyn and Btk activation and disruption by dasatinib and bosutinib
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- Molecular profiling of chronic myelomonocytic leukemia reveals diverse mutations in >80% of patients with TET2 and EZH2 being of high prognostic relevance
- (2011) V Grossmann et al. LEUKEMIA
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- (2011) Celalettin Ustun et al. LEUKEMIA RESEARCH
- Frequent pathway mutations of splicing machinery in myelodysplasia
- (2011) Kenichi Yoshida et al. NATURE
- IDH1 mutations are detected in 6.6% of 1414 AML patients and are associated with intermediate risk karyotype and unfavorable prognosis in adults younger than 60 years and unmutated NPM1 status
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- WHO subvariants of indolent mastocytosis: clinical details and prognostic evaluation in 159 consecutive adults
- (2010) A. Pardanani et al. BLOOD
- Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1
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- Detection of JAK2 exon 12 mutations in 15 patients with JAK2V617F negative polycythemia vera
- (2009) S. Schnittger et al. HAEMATOLOGICA
- Prognosis in adult indolent systemic mastocytosis: A long-term study of the Spanish Network on Mastocytosis in a series of 145 patients
- (2009) Luis Escribano et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Variable presence ofKITD816Vin clonal haematological non-mast cell lineage diseases associated with systemic mastocytosis (SM-AHNMD)
- (2009) Karl Sotlar et al. JOURNAL OF PATHOLOGY
- Frequent TET2 mutations in systemic mastocytosis: clinical, KITD816V and FIP1L1-PDGFRA correlates
- (2009) A Tefferi et al. LEUKEMIA
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- Systemic Mastocytosis Associated with Chronic Idiopathic Myelofibrosis
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