Therapeutically validated oncoproteins in myeloproliferative neoplasms (MPN) include BCR-ABL1 and rearranged PDGFR proteins. The latter are products of intra- (e.g. FIP1L1-PDGFRA) or inter-chromosomal (e.g. ETV6-PDGFRB) gene fusions. BCR-ABL1 is associated with chronic myelogenous leukaemia (CML) and mutant PDGFR with an MPN phenotype characterized by eosinophilia and in addition, in case of FIP1L1-PDGFRA, bone marrow mastocytosis. These genotype–phenotype associations have been effectively exploited in the development of highly accurate diagnostic assays and molecular targeted therapy. It is hoped that the same will happen in other MPN with specific genetic alterations: polycythemia vera (JAK2 V617F and other JAK2 mutations), essential thr...
The clonal bone marrow stem cell disorders essential thrombocythemia (ET), polycythemia vera (PV) an...
Myeloproliferative neoplasms (MPNs) are clonal disorders characterized by increased production of ma...
Background: The elucidation of the genetic background of the myeloproliferative neoplasms completely...
Therapeutically validated oncoproteins in myeloproliferative neoplasms (MPNs) include BCR-ABL in chr...
The tyrosine kinase encoding genes ABL1 and FGFR1 are involved in fusion genes underlying the myelop...
peer reviewedBIOLOGICAL ASPECTS OF JAK/STAT SIGNALING IN BCR-ABL-NEGATIVE MYELOPROLIFERATIVE NEOPLAS...
The BCR-ABL negative myeloproliferative disorders (MPDs) are poorly understood at both the clinical ...
This review focuses on topical issues in the biology and treatment of the myeloproliferative neoplas...
BCR::ABL1-negative myeloproliferative neoplasms (MPNs) include three major subgroupspolycythemia ver...
This review focuses on topical issues in the biology and treatment of the myeloproliferative neoplas...
BCR::ABL1-negative myeloproliferative neoplasms (MPNs) include three major subgroups—polycythemia ve...
The past 7 years have witnessed remarkable progress in our understanding of the genetics of BCR-ABL–...
Myeloproliferative neoplasms (MPNs) are a group of related clonal hematologic disorders characterize...
Somatic mutations in JAK2, calreticulin, and MPL genes drive myeloproliferative neoplasms (MPN), and...
This review is based on the presentations and deliberations at the 7th John Goldman Chronic Myeloid ...
The clonal bone marrow stem cell disorders essential thrombocythemia (ET), polycythemia vera (PV) an...
Myeloproliferative neoplasms (MPNs) are clonal disorders characterized by increased production of ma...
Background: The elucidation of the genetic background of the myeloproliferative neoplasms completely...
Therapeutically validated oncoproteins in myeloproliferative neoplasms (MPNs) include BCR-ABL in chr...
The tyrosine kinase encoding genes ABL1 and FGFR1 are involved in fusion genes underlying the myelop...
peer reviewedBIOLOGICAL ASPECTS OF JAK/STAT SIGNALING IN BCR-ABL-NEGATIVE MYELOPROLIFERATIVE NEOPLAS...
The BCR-ABL negative myeloproliferative disorders (MPDs) are poorly understood at both the clinical ...
This review focuses on topical issues in the biology and treatment of the myeloproliferative neoplas...
BCR::ABL1-negative myeloproliferative neoplasms (MPNs) include three major subgroupspolycythemia ver...
This review focuses on topical issues in the biology and treatment of the myeloproliferative neoplas...
BCR::ABL1-negative myeloproliferative neoplasms (MPNs) include three major subgroups—polycythemia ve...
The past 7 years have witnessed remarkable progress in our understanding of the genetics of BCR-ABL–...
Myeloproliferative neoplasms (MPNs) are a group of related clonal hematologic disorders characterize...
Somatic mutations in JAK2, calreticulin, and MPL genes drive myeloproliferative neoplasms (MPN), and...
This review is based on the presentations and deliberations at the 7th John Goldman Chronic Myeloid ...
The clonal bone marrow stem cell disorders essential thrombocythemia (ET), polycythemia vera (PV) an...
Myeloproliferative neoplasms (MPNs) are clonal disorders characterized by increased production of ma...
Background: The elucidation of the genetic background of the myeloproliferative neoplasms completely...