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Thrombopoietin, flt3, and kit ligands together suppress apoptosis of human mobilized CD34+ cells and recruit primitive CD34+Thy-1+ cells into rapid division

1 Jun 1999

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PMID: 10378891
DOI: 10.1016/s0301-472x(99)00031-4

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Thrombopoietin, flt3, and kit ligands together suppress apoptosis of human mobilized CD34+ cells and recruit primitive CD34+Thy-1+ cells into rapid divisionPMID 10378891Read ↗

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The stem cell factor–c-KIT pathway must be inhibited to enable apoptosis induced by BCR–ABL inhibitors in chronic myelogenous leukemia cellsSemantic proximity Read ↗

Characterization of CD34+ cells mobilized to the peripheral blood during the recovery from cyclophosphamide chemotherapy.Semantic proximity Read ↗

Effects of thrombopoietin on the proliferation and differentiation of primitive and mature haemopoietic progenitor cells in cord blood.Semantic proximity Read ↗

Phenotypic and functional analyses of CD34NEG hematopoietic precursors from mobilized peripheral blood.Semantic proximity Read ↗

Gene expression profile of primary human CD34+CD38lo cells differentiating along the megakaryocyte lineageSemantic proximity Read ↗

Comparison of CD34+ subsets and clonogenicity in human bone marrow, granulocyte colony-stimulating factor-mobilized peripheral blood, and cord blood.Semantic proximity Read ↗

Gene expression profiling of normal and malignant CD34-derived megakaryocytic cellsSemantic proximity Read ↗

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