Published in Neonatology on October 31, 2013
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The evolution of cellular deficiency in GATA2 mutation. Blood (2013) 1.36
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Endogenous erythropoietin signaling is required for normal neural progenitor cell proliferation. J Biol Chem (2007) 1.32
New syndrome of paraganglioma and somatostatinoma associated with polycythemia. J Clin Oncol (2013) 1.32
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The JAK kinase inhibitor CP-690,550 suppresses the growth of human polycythemia vera cells carrying the JAK2V617F mutation. Cancer Sci (2008) 1.14
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Novel HIF2A mutations disrupt oxygen sensing, leading to polycythemia, paragangliomas, and somatostatinomas. Blood (2013) 1.07
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miR-451 enhances erythroid differentiation in K562 cells. Leuk Lymphoma (2010) 1.06
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Sickle cell disease resulting from uniparental disomy in a child who inherited sickle cell trait. Blood (2010) 1.04
Treatment target in polycythemia vera. N Engl J Med (2013) 1.02
The phenotype of polycythemia due to Croatian homozygous VHL (571C>G:H191D) mutation is different from that of Chuvash polycythemia (VHL 598C>T:R200W). Haematologica (2013) 0.97
New onset of myelofibrosis in association with pulmonary arterial hypertension. Ann Intern Med (2005) 0.97
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Chuvash polycythemia VHLR200W mutation is associated with down-regulation of hepcidin expression. Blood (2011) 0.94
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Allogeneic haematopoietic cell transplantation for myelofibrosis in 30 patients 60-78 years of age. Br J Haematol (2011) 0.93
Metabolic insight into mechanisms of high-altitude adaptation in Tibetans. Mol Genet Metab (2012) 0.93
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Severe hypochromic microcytic anemia caused by a congenital defect of the iron transport pathway in erythroid cells. Blood (2004) 0.91
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Novel homozygous VHL mutation in exon 2 is associated with congenital polycythemia but not with cancer. Blood (2013) 0.89
The heterozygote advantage of the Chuvash polycythemia VHLR200W mutation may be protection against anemia. Haematologica (2011) 0.89
Congenital polycythemia with homozygous and heterozygous mutations of von Hippel-Lindau gene: five new Caucasian patients. Haematologica (2005) 0.88
Imatinib effect on growth and signal transduction in polycythemia vera. Exp Hematol (2007) 0.87
The constitutive mobilization of bone marrow-repopulating cells into the peripheral blood in idiopathic myelofibrosis. Blood (2004) 0.86
JAK2 kinase inhibitors and myeloproliferative disorders. Curr Opin Hematol (2010) 0.86
Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia. Br J Haematol (2010) 0.86
The HIF2A gene in familial erythrocytosis. N Engl J Med (2008) 0.86
EPO receptor gain-of-function causes hereditary polycythemia, alters CD34 cell differentiation and increases circulating endothelial precursors. PLoS One (2010) 0.85
A quantitative allele-specific PCR test for the BRAF V600E mutation using a single heterozygous control plasmid for quantitation: a model for qPCR testing without standard curves. J Mol Diagn (2013) 0.85
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DMT1 mutation: response of anemia to darbepoetin administration and implications for iron homeostasis. Blood (2006) 0.85
HIF-mediated increased ROS from reduced mitophagy and decreased catalase causes neocytolysis. J Mol Med (Berl) (2015) 0.84
Oxygen-dependent regulation of erythropoiesis. Methods Enzymol (2004) 0.84
Increased size of solid organs in patients with Chuvash polycythemia and in mice with altered expression of HIF-1alpha and HIF-2alpha. J Mol Med (Berl) (2010) 0.84
Neonatal hemolytic jaundice: morphologic features of erythrocytes that will help you diagnose the underlying condition. Neonatology (2014) 0.84
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Elevated homocysteine, glutathione and cysteinylglycine concentrations in patients homozygous for the Chuvash polycythemia VHL mutation. Haematologica (2008) 0.84
Emerging molecularly targeted therapies in castration refractory prostate cancer. Prostate Cancer (2013) 0.83
Differential sensitivity to JAK inhibitory drugs by isogenic human erythroblasts and hematopoietic progenitors generated from patient-specific induced pluripotent stem cells. Stem Cells (2014) 0.83