Molecular pathogenesis of Philadelphia chromosome negative myeloproliferative disorders
- 31 January 2005
- journal article
- review article
- Published by Elsevier in Blood Reviews
- Vol. 19 (1) , 1-13
- https://doi.org/10.1016/j.blre.2004.02.002
Abstract
No abstract availableKeywords
This publication has 94 references indexed in Scilit:
- Characteristics of circulating megakaryocyte progenitors (CFU-MK) in patients with primary myelofibrosisEuropean Journal of Haematology, 2009
- Clonal hematopoiesis in familial polycythemia vera suggests the involvement of multiple mutational events in the early pathogenesis of the diseaseBlood, 2003
- Disruption of oxygen homeostasis underlies congenital Chuvash polycythemiaNature Genetics, 2002
- Molecular basis of the neutrophil glycoprotein NB1 (CD177) involved in the pathogenesis of immune neutropenias and transfusion reactionsEuropean Journal of Immunology, 2001
- Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genesOncogene, 2000
- The gene encoding hematopoietic cell phosphatase (SHP-1) is structurally and transcriptionally intact in polycythemia veraOncogene, 1997
- Chromosome Studies in 104 Patients With Polycythemia VeraMayo Clinic Proceedings, 1991
- Circulating erythroid and megakaryocytic progenitors in polycythaemia vera and essential thrombocythaemiaEuropean Journal of Haematology, 1989
- Megakaryocytopoiesis in Polycythemia vera: Characterization by Megakaryocytic Progenitors (CFU-Meg) in vitro and Quantitation of Marrow MegakaryocytesActa Haematologica, 1988
- Familial Thrombocythemia and/or Thrombocytosis – Apparently a Rare DisorderActa Haematologica, 1987