ライフサイエンスコーパス: CFU-GEMM

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1 reased (P = 0.041) and increased (P = 0.076) CFU-GEMM progenitor cell colony formation in 29 benzene-

2 d human alpha-globin gene in their BFU-E and CFU-GEMM and the lack of its transcript.

3 oliferative capacities of CFU-GM, BFU-E, and CFU-GEMM were intact as colonies generated respectively

4 ded 2 degrees colonies of CFU-GM, BFU-E, and CFU-GEMM.

5 n the same time frame as those of CFU-GM and CFU-GEMM in BM, spleen, and PB, although the magnitude w

6 CFU over time, FL alone increased CFU-GM and CFU-GEMM threefold and fivefold, respectively.

7 The maximal number CFU-GM and CFU-GEMM were seen in PB on day 10, with 537- and 585-fo

8 and 108-fold increase in splenic CFU-GM and CFU-GEMM, respectively.

9 kinetics and magnitude to that of CFU-GM and CFU-GEMM.

10 , and megakaryocytes within the same colony (CFU-GEMM)] in comparison with the wild-type mice.

11 ed in 13 of 15 evaluable patients; including CFU-GEMM (12), BFU-E (8), and CFU-GM (6).

12 nulocyte erythroid megakaryocyte macrophage [CFU-GEMM]) from the bone marrow (BM) to peripheral organ

13 -erythrocyte, -monocyte, and -megakaryocyte (CFU-GEMM) were, respectively, 83 +/- 12, 95 +/- 16, 84 +

14 nulocyte macrophage-erythroid-megakaryocyte (CFU-GEMM).

15 ocyte, erythroid, macrophage, megakaryocyte (CFU-GEMM), colony-forming unit-macrophage (CFU-M), and b

16 ulocyte, erythroid, monocyte, megakaryocyte (CFU-GEMM) in PB, respectively, when compared with contro

17 ocyte, erythrocyte, monocyte, megakaryocyte (CFU-GEMM), respectively, compared with mouse serum album

18 ulocyte, erythroid, monocyte, megakaryocyte [CFU-GEMM]), erythroid (burst-forming unit-erythroid [BFU

19 e transduced cells formed significantly more CFU-GEMM and BFU-E colonies than did the controls.

20 inhibits erythroid (BFU-E), multipotential (CFU-GEMM), and granulocyte-macrophage (CFU-GM) progenito

21 and BM-stroma and promoted the formation of CFU-GEMM and burst-forming unit-erythroid in methylcellu

22 FU-E colonies and the erythroid progenies of CFU-GEMM.

23 Self-renewal of CFU-GEMM was also retained as replating efficiency of si

24 res grown in the absence of Epo, no BFU-E or CFU-GEMM colonies grew.

25 ting colony-forming unit (CFU)-GM, CFU-G, or CFU-GEMM numbers.

26 myeloid (CFU-GM), and primitive progenitor (CFU-GEMM, HPP-CFC, or CFU-A) colonies.

27 creased pluripotent hemopoietic progenitors (CFU-GEMM).

28 o retained as replating efficiency of single CFU-GEMM colonies into 2 degrees dishes was >96% and yie

29 (+)CD34(+)Lin(-) progenitor cells before the CFU-GEMM stage.

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