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1 nits, multilineage colony-forming units, and erythroid burst-forming units.
2 more CD34(+) cells (2.7-fold/kg/apheresis), erythroid burst-forming units (1.8-fold/kg/apheresis), a
5 ed with their wild-type littermates, splenic erythroid burst-forming unit and high-proliferative pote
6 9 than the normal hematopoietic progenitors, erythroid burst-forming units and granulocyte/monocyte c
9 into adulthood showed a moderate decrease in erythroid burst-forming unit (BFU-E) and erythroid colon
11 well as in early erythropoiesis encompassing erythroid burst-forming unit (BFU-E) differentiation to
13 the SP600125 inhibitor reduced the number of erythroid burst-forming units (BFU-e's) but not the more
16 macrophage colony-forming units (CFU-GM) and erythroid burst-forming units (BFU-E) were performed on
17 egaly accompanied with decreased bone marrow erythroid burst-forming units (BFU-Es) and colony-formin
18 toxicity of EFA to hematopoietic progenitors erythroid burst-forming units (BFU-Es) and granulocyte-m
21 absolute number and frequency of both early (erythroid burst-forming unit [BFU-E]) and late erythroid
22 fetal hemoglobin-containing erythroblasts in erythroid burst-forming unit (BFUe) cultures from health
23 d reduction in erythroid progenitors (mature erythroid burst-forming units [BFUEs]) was observed betw
24 persons with discordant results and also in erythroid burst-forming unit colonies but not in those w
25 anulocyte-macrophage colony-forming unit and erythroid burst-forming unit colonies compared with plas
26 anulocyte-macrophage colony-forming unit and erythroid burst-forming unit colony formation compared w
27 erm HSCs, common myeloid progenitors (CMPs), erythroid burst-forming units, colony-forming units in s
28 lose cultures, as indicated by more numerous erythroid burst-forming unit-derived colonies in low Epo
29 throid, monocyte, megakaryocyte [CFU-GEMM]), erythroid (burst-forming unit-erythroid [BFU-E]), and gr
30 (colony-forming granulocytic-macrophage) and erythroid (burst-forming unit-erythroid) progenitor colo
31 lony-forming unit-granulocyte-monocytic) and erythroid (burst-forming unit-erythroid) progenitors.
32 ormal donor and chemotherapy patient-derived erythroid (burst-forming units-erythroid [BFU-E]), myelo
33 +) hematopoietic cells and completely blocks erythroid burst-forming unit formation in normal human b
34 fects because granulocyte-macrophage CFU and erythroid burst-forming units from STAT1(-/-) mice were
36 nulocyte-macrophage colony forming unit, and erythroid burst forming unit growth in rats subjected to
37 anulocyte-macrophage colony forming unit and erythroid burst forming unit) hematopoietic progenitor c
38 rogenitor cells (19-39% growth inhibition of erythroid burst-forming units, multilineage colony-formi
40 plete mobilization of BMP4-responsive stress erythroid burst-forming units; therefore, new stress pro
41 ells that can generate BMP4-dependent stress erythroid burst-forming units when cultured under stress
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