ライフサイエンスコーパス: erythroid precursor cell

1 ld the activity of the GATA-1 promoter in an erythroid precursor cell.

2 scue assay in murine Samd14-Enh(-/-) primary 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 ng protein 3 (RIP3)-dependent necroptosis in erythroid precursor cells.

11 potential mechanism for direct infection of erythroid precursor cells and deranged erythropoiesis in

12 scue, characterized by increased survival of erythroid precursor cells and improved hemoglobin produc

13 us, the Na pump isoform composition of human erythroid precursor cells and mature erythrocytes contai

14 ing the Na pump isoform composition of human erythroid precursor cells and mature human erythrocytes.

15 nergic receptors that are expressed in human erythroid precursor cells and red cell ghosts.

16 ively parallel sequencing in GATA1-deficient erythroid precursor cells and those that are GATA1 reple

17 sion of TfR2 mRNA was high in normal CD34(+) erythroid precursor cells, and levels decreased during e

18 ived from innate immune cells, megakaryocyte-erythroid precursor cells, and nonhematopoietic tissues

19 ression is confined exclusively to the CFU-E erythroid precursor cells, but not in mature erythrocyte

20 f placenta growth factor (PlGF), secreted by erythroid precursor cells, correlate with increased plas

21 High-level globin expression in erythroid precursor cells depends on the integrity of NF

22 esults indicate that bipotential endothelial/erythroid precursor cells do indeed exist in the Xenopus

23 nias, characteristic vacuoles in myeloid and erythroid precursor cells, dysplastic bone marrow, neutr

24 Exosome complex integrity in erythroid precursor cells ensures Kit receptor tyrosine

25 expressed by mature hematopoietic cells, and erythroid precursor cell expression of Gdf11 has been im

26 iderably earlier stage were found to contain erythroid precursor cells following culture in isolation

27 age in mice does not alter erythropoiesis or erythroid precursor cell frequency under normal conditio

28 y restored enzymatic activity in B cells and erythroid precursor cells from patients with G6PD defici

29 esis, but rather from localized expansion of erythroid precursor cells in the injured bone marrow.

30 ional exosome complex components, in primary erythroid precursor cells induced erythroid cell maturat

31 ore, loss of Foxo3 induced mitotic arrest in erythroid precursor cells, leading to a significant decr

32 he Samd14-CP interaction is a determinant of erythroid precursor cell levels and function.

33 iatric B-ALL cell line, SEM, and an immortal erythroid precursor cell line, HUDEP-2, to allow for acu

34 f was sufficient for enhancer activity in an erythroid precursor cell line, its enhancer function in

35 nd traps or neutralizing antibodies promotes erythroid precursor cell maturation and red blood cell f

36 tial at different stages of hematopoiesis or erythroid precursor cell maturation.

37 adult (beta)-globin expression occurs within erythroid precursor cells of the adult lineage.

38 Thus, erythroid precursor cells possess an efficient mechanism

39 ke genes HBG1 and HBG2 are silenced in adult erythroid precursor cells remain a fundamental question

40 Further analyses of erythroid precursor cells showed that their differentiat

41 ozygous hemoglobin S/hemoglobin A (SA) donor erythroid precursor cells that results in greater donor

42 a KY1070 modulates ferroportin expression on erythroid precursor cells, thereby lowering potentially

43 o major globin mRNAs characteristic of adult erythroid precursor cells were clearly expressed in huma

44 3 weeks and the retention of human EPCs and erythroid precursor cells within the BM of recipient mic