Characterization of 35 new cases with four different MPLW515 mutations and essential thrombocytosis or primary myelofibrosis
- PMID: 19029146
- PMCID: PMC2625421
- DOI: 10.3324/haematol.13224
Characterization of 35 new cases with four different MPLW515 mutations and essential thrombocytosis or primary myelofibrosis
Figures
References
-
- Pardanani AD, Levine RL, Lasho T, Pikman Y, Mesa RA, Wadleigh M, et al. MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients. Blood. 2006;108:3472–6. - PubMed
-
- Lasho TL, Pardanani A, McClure RF, Mesa RA, Levine RL, Gilliland DG, et al. Concurrent MPL515 and JAK2V617F mutations in myelofibrosis: chronology of clonal emergence and changes in mutant allele burden over time. Br J Haematol. 2006;135:683–7. - PubMed
-
- Schnittger S, Bacher U, Haferlach C, Dengler R, Krober A, Kern W, et al. Detection of an MPLW515 mutation in a case with features of both essential thrombocythemia and refractory anemia with ringed sideroblasts and thrombocytosis. Leukemia. 2007;22:453–555. - PubMed
-
- Schnittger S, Bacher U, Kern W, Schroder M, Haferlach T, Schoch C. Report on two novel nucleotide exchanges in the JAK2 pseudokinase domain: D620E and E627E. Leukemia. 2006;20:2195–7. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
