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「"Guesnu M "[Author]」の検索結果

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Deciphering leukemic B-cell chronic lymphoproliferative disorders.

Erythropoiesis abnormalities contribute to early-onset anemia in patients with septic shock.

Erythroleukaemia and RAEB-t: a same disease?

Isodicentric/pseudoisodicentric chromosome 21 amplification in four cases of acute myelocytic leukemia or myelodysplasia.

Erythroleukemia: a comparison between the previous FAB approach and the WHO classification.

Pure red cell aplasia associated with myelodysplastic syndromes.

Activity of the caspase-3/CPP32 enzyme is increased in "early stage" myelodysplastic syndromes with excessive apoptosis, but caspase inhibition does not enhance colony formation in vitro.

Megakaryocyte growth and development factor-induced proliferation and differentiation are regulated by the mitogen-activated protein kinase pathway in primitive cord blood hematopoietic progenitors.

Preliminary evaluation of the new hematology analyzer COULTER GEN-S in a university hospital.

Ineffective erythropoiesis in myelodysplastic syndromes: correlation with Fas expression but not with lack of erythropoietin receptor signal transduction.

Analysis of megakaryocyte growth and development factor (thrombopoietin) effects on blast cell and megakaryocyte growth in myelodysplasia.

Fas/Apo-1 (CD95) expression and apoptosis in patients with myelodysplastic syndromes.

Expression of the transcription factor Evi-1 in human erythroleukemia cell lines and in leukemias.

Molecular detection of t(8;21)/AML1-ETO in AML M1/M2: correlation with cytogenetics, morphology and immunophenotype.

High doses of intravenous recombinant erythropoietin for the treatment of anaemia in myelodysplastic syndrome.

Increase in double-positive CD4+CD8+ peripheral T-cell subsets in an HIV-infected patient.

Massive thrombosis of venous cerebral sinuses in a 2-year-old boy with a combined inherited deficiency of antithrombin III and protein C.

Detection of the chromosome 16 CBF beta-MYH11 fusion transcript in myelomonocytic leukemias.

Expression of the Evi-1 gene in myelodysplastic syndromes.

[Pancytopenia and gelatinous transformation of the bone marrow in anorexia nervosa].

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