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1 ld the activity of the GATA-1 promoter in an erythroid precursor cell.
2 ng protein 3 (RIP3)-dependent necroptosis in erythroid precursor cells.
3 th cell cycle progression in Foxo3-deficient erythroid precursor cells.
4 c cells (HEL cells) were used as a model for erythroid precursor cells.
5 and suffered from a lack of Ter-119-positive erythroid precursor cells.
6 retention, which interrupts iron delivery to erythroid precursor cells.
7  other host factors, drives the expansion of erythroid precursor cells.
8 t TfR2-alpha may be a useful marker of early erythroid precursor cells.
9 essential for the survival and maturation of erythroid precursor cells.
10  potential mechanism for direct infection of erythroid precursor cells and deranged erythropoiesis in
11 scue, characterized by increased survival of erythroid precursor cells and improved hemoglobin produc
12 us, the Na pump isoform composition of human erythroid precursor cells and mature erythrocytes contai
13 ing the Na pump isoform composition of human erythroid precursor cells and mature human erythrocytes.
14 nergic receptors that are expressed in human erythroid precursor cells and red cell ghosts.
15 ively parallel sequencing in GATA1-deficient erythroid precursor cells and those that are GATA1 reple
16 sion of TfR2 mRNA was high in normal CD34(+) erythroid precursor cells, and levels decreased during e
17 ression is confined exclusively to the CFU-E erythroid precursor cells, but not in mature erythrocyte
18 f placenta growth factor (PlGF), secreted by erythroid precursor cells, correlate with increased plas
19              High-level globin expression in erythroid precursor cells depends on the integrity of NF
20 esults indicate that bipotential endothelial/erythroid precursor cells do indeed exist in the Xenopus
21                 Exosome complex integrity in erythroid precursor cells ensures Kit receptor tyrosine
22 iderably earlier stage were found to contain erythroid precursor cells following culture in isolation
23 y restored enzymatic activity in B cells and erythroid precursor cells from patients with G6PD defici
24 ional exosome complex components, in primary erythroid precursor cells induced erythroid cell maturat
25 ore, loss of Foxo3 induced mitotic arrest in erythroid precursor cells, leading to a significant decr
26 f was sufficient for enhancer activity in an erythroid precursor cell line, its enhancer function in
27 tial at different stages of hematopoiesis or erythroid precursor cell maturation.
28 adult (beta)-globin expression occurs within erythroid precursor cells of the adult lineage.
29                                        Thus, erythroid precursor cells possess an efficient mechanism
30 ozygous hemoglobin S/hemoglobin A (SA) donor erythroid precursor cells that results in greater donor
31 o major globin mRNAs characteristic of adult erythroid precursor cells were clearly expressed in huma
32  3 weeks and the retention of human EPCs and erythroid precursor cells within the BM of recipient mic

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