ライフサイエンスコーパス: burst-forming unit

1 ilineage colony-forming units, and erythroid burst-forming units.

2 (+) cells (2.7-fold/kg/apheresis), erythroid burst-forming units (1.8-fold/kg/apheresis), and colony-

3 Erythroid burst-forming unit and colony-forming unit numbers are g

4 ononuclear cells were cultured for erythroid burst-forming unit and granulocyte-macrophage colony-for

5 eir wild-type littermates, splenic erythroid burst-forming unit and high-proliferative potential colo

6 on of late-stage erythroid progenitors-day 3 burst-forming units and colony-forming units, associated

7 normal hematopoietic progenitors, erythroid burst-forming units and granulocyte/monocyte colony-form

8 and osteoclastogenic but a low proportion of burst-forming unit (BFU)e.

9 Using erythroid burst-forming unit (BFU-E) and CFU-E progenitors purifie

10 High-level MDR transduction of erythroid burst-forming unit (BFU-E) and colony-forming unit-granu

11 hood showed a moderate decrease in erythroid burst-forming unit (BFU-E) and erythroid colony-forming

12 e colony-forming unit (CFU-GM) and erythroid burst-forming unit (BFU-E) colonies.

13 early erythropoiesis encompassing erythroid burst-forming unit (BFU-E) differentiation to proerythro

14 e colony-forming unit (CFU-GM) and erythroid burst-forming unit (BFU-E) growth.

15 25 inhibitor reduced the number of erythroid burst-forming units (BFU-e's) but not the more different

16 A second wave of definitive-type erythroid burst-forming units (BFU-e's), erythroid colony-forming

17 Erythroid burst-forming units (BFU-E) were isolated from periphera

18 colony-forming units (CFU-GM) and erythroid burst-forming units (BFU-E) were performed on each harve

19 mpanied with decreased bone marrow erythroid burst-forming units (BFU-Es) and colony-forming units-er

20 f EFA to hematopoietic progenitors erythroid burst-forming units (BFU-Es) and granulocyte-macrophage

21 V617F-positive erythroid burst-forming units (BFU-Es) were more frequent in patie

22 requency and number of both early (erythroid burst-forming unit [BFU-E]) and late erythroid progenito

23 umber and frequency of both early (erythroid burst-forming unit [BFU-E]) and late erythroid progenito

24 e reported that SP stimulates erythroid (E) (burst-forming unit [BFU]-E and colony-forming unit [CFU]

25 ells (colony-forming unit-erythroid [CFU-E], burst-forming unit [BFU]-E, and CFU-granulocyte-macropha

26 globin-containing erythroblasts in erythroid burst-forming unit (BFUe) cultures from healthy adult in

27 n in erythroid progenitors (mature erythroid burst-forming units [BFUEs]) was observed between e14.5

28 ith discordant results and also in erythroid burst-forming unit colonies but not in those with clonal

29 macrophage colony-forming unit and erythroid burst-forming unit colonies compared with plasma from ca

30 macrophage colony-forming unit and erythroid burst-forming unit colony formation compared with BM of

31 common myeloid progenitors (CMPs), erythroid burst-forming units, colony-forming units in spleen, and

32 ac or embryo body by three different assays, burst-forming units, colony-forming units, and analysis

33 res, as indicated by more numerous erythroid burst-forming unit-derived colonies in low Epo concentra

34 k and E progenitors identified as CFU-Mk and burst forming unit-E.

35 locyte macrophage, but not other HPC such as burst-forming unit erythrocyte or CFU granulocyte, eryth

36 of cells in G1 phase (27.4%) was observed in burst-forming unit-erythrocytes (BFU-E)-derived erythrob

37 -EPOR antibodies stimulated the formation of burst forming unit erythroid colonies from human CD34(+)

38 ly supports the differentiation of wild-type burst-forming unit erythroid (BFU-e) and colony-forming

39 lf-renewal of an early erythroid progenitor, burst-forming unit erythroid (BFU-E), and increase the p

40 lony-forming unit granulocyte-macrophage and burst-forming unit erythroid cells revealed absence of t

41 lony-forming unit granulocyte-macrophage and burst-forming unit erythroid cells with the 11q deletion

42 Frs. 2 and 3, greater than 70% of the total burst-forming unit erythroid colonies in CB and PB were

43 Further, although burst-forming unit erythroid colonies of BM were distrib

44 Burst-forming unit erythroid progenitors (BFU-Es) are so

45 lony forming unit granulocyte-macrophage and burst-forming unit erythroid, while treatment with block

46 Normal burst forming unit-erythroid (BFU-E) growth (>30 bursts/

47 points representing the transition from late burst forming unit-erythroid (BFU-E) to basophilic eryth

48 nit-granulocyte-macrophage (CFU-GM)-derived, burst forming unit-erythroid (BFU-E)-derived, and CFU-me

49 nulocyte-macrophage [CFU-GM]; 17% inhibition burst forming unit-erythroid [BFU-E]) and 3.44 micromol/

50 lony-forming unit-granulocyte macrophage and burst forming unit-erythroid were detected in the BM of

51 in other hematopoietic cells including human burst forming unit-erythroid-derived erythroblasts and T

52 median slope per day, -0.57; P = .0008), and burst-forming unit-erythroid (BFU-E) (median slope per d

53 1 expression in human CD34(+) cells impaired burst-forming unit-erythroid (BFU-E) and colony-forming

54 le colony-forming unit-erythroid (CFU-E) and burst-forming unit-erythroid (BFU-E) colonies were not p

55 Burst-forming unit-erythroid (BFU-E) colony-formation wa

56 formation by promoting self-renewal of early burst-forming unit-erythroid (BFU-E) progenitors.

57 Studies with progeny of burst-forming unit-erythroid (BFU-E) suggest that the FR

58 colony-forming unit-macrophage (CFU-M), and burst-forming unit-erythroid (BFU-E) was markedly decrea

59 orming unit-granulocyte/macrophage (CFU-GM), burst-forming unit-erythroid (BFU-E), and CFU-erythroid

60 ming unit-granulocyte, -macrophage (CFU-GM), burst-forming unit-erythroid (BFU-E), and colony-forming

61 main (HBD), to promote adhesion of primitive burst-forming unit-erythroid (BFU-E), mature BFU-E, and

62 , levels of these factors were determined in burst-forming unit-erythroid (BFU-E)-derived cells at di

63 Burst-forming unit-erythroid (BFU-E)-derived colony grow

64 3 protein was also highly expressed in early burst-forming unit-erythroid (BFU-E)-derived erythroid p

65 ntirely in the SBA(+) fraction; in contrast, burst-forming unit-erythroid (BFU-E)-forming cells were

66 Erythroid progenitors (burst-forming unit-erythroid [BFU-E]) were significantly

67 ny-forming unit-megakaryocyte [CFU-Meg], and burst-forming unit-erythroid [BFU-E]), and CD34(+) cells

68 ocyte, megakaryocyte [CFU-GEMM]), erythroid (burst-forming unit-erythroid [BFU-E]), and granulocyte-m

69 ing unit-granulocyte-macrophage [CFU-GM] and burst-forming unit-erythroid [BFU-E]).

70 Similarly, in vitro burst-forming unit-erythroid and colony-forming unit-ery

71 Deletion of Stat1 increased burst-forming unit-erythroid and reduced colony-forming

72 Erythroblasts plucked from the burst-forming unit-erythroid colonies of one of these ch

73 onies, whereas Flt3low cells produced mostly burst-forming unit-erythroid colonies.

74 y erythroid progenitors showed inhibition of burst-forming unit-erythroid colony formation when inter

75 ing unit-granulocyte/macrophage (CFU-GM) and burst-forming unit-erythroid derived from CML over a 2-l

76 We focus on the regulated expansion of burst-forming unit-erythroid erythroid progenitors by gl

77 a and promoted the formation of CFU-GEMM and burst-forming unit-erythroid in methylcellulose cultures

78 lony-forming unit-granulocyte macrophage and burst-forming unit-erythroid numbers and preferentially

79 479 (Y8) were capable of supporting immature burst-forming unit-erythroid progenitor development.

80 r, only gp55-P induces erythroid bursts from burst-forming unit-erythroid progenitors and only gp55-P

81 eLV-C impairs the in vivo differentiation of burst-forming unit-erythroid to colony-forming unit-eryt

82 Maximal numbers of CFU-E and burst-forming unit-erythroid were increased, and CFU-E d

83 ming granulocytic-macrophage) and erythroid (burst-forming unit-erythroid) progenitor colony formatio

84 g unit-granulocyte-monocytic) and erythroid (burst-forming unit-erythroid) progenitors.

85 colony-forming unit-granulocyte-macrophage, burst-forming unit-erythroid, and high proliferative pot

86 oid progenitors (CFU-granulocyte-macrophage, burst-forming unit-erythroid, CFU-granulocyte-erythrocyt

87 colony-forming unit-granulocyte-macrophage, burst-forming unit-erythroid, or colony-forming unit-ery

88 ently detected on red blood cell precursors, burst-forming unit-erythroid- (BFU-E) derived cells.

89 yocyte [CFU-MK], CFU-granulocyte/macrophage, burst-forming unit-erythroid/CFU-erythroid, and CFU-gran

90 y transiently delaying erythropoiesis at the burst-forming unit-erythroid/colony-forming unit-erythro

91 iest erythroid-restricted precursors (BFU-E [burst-forming unit-erythroid]) is also detected in the I

92 eous cell population, we analyzed individual burst-forming units-erythroid (BFU-E) and nonerythroid c

93 Progeny of normal human burst-forming units-erythroid (BFU-E) contained Mpl rece

94 Single burst-forming units-erythroid (BFU-E) from 1 patient wer

95 , and greater than 10-fold higher numbers of burst-forming units-erythroid (BFU-E) in the Wnt-express

96 Burst-forming units-erythroid (BFU-E) increased in the s

97 acrophage colony-forming cells (GM-CFC), and burst-forming units-erythroid (BFU-E) per kilogram in th

98 0(4)/kg, respectively; the median numbers of burst-forming units-erythroid (BFU-e) were 0.20, 6.94, a

99 ethasone selectively increased the number of burst-forming units-erythroid (BFU-E), whereas lenalidom

100 p67(+) cells were significantly enriched for burst-forming units-erythroid (BFU-Es) and depleted of c

101 and chemotherapy patient-derived erythroid (burst-forming units-erythroid [BFU-E]), myeloid (colony-

102 It has been previously shown that burst-forming units-erythroid and colony-forming units-e

103 ma-globin expression in K562 cells and human burst-forming units-erythroid and that increase prolifer

104 AT1 protein was detected in 7-d-old burst-forming units-erythroid colonies by Western blotti

105 progenitors, defined as increased numbers of burst-forming units-erythroid colonies.

106 Fura-2 loaded day-10 burst-forming units-erythroid-derived erythroblasts were

107 oietic cells and completely blocks erythroid burst-forming unit formation in normal human bone marrow

108 use granulocyte-macrophage CFU and erythroid burst-forming units from STAT1(-/-) mice were resistant

109 ing units were also inhibited, but erythroid burst-forming units grew normally.

110 acrophage colony forming unit, and erythroid burst forming unit growth in rats subjected to hemorrhag

111 macrophage colony forming unit and erythroid burst forming unit) hematopoietic progenitor cell growth

112 forming unit-megakaryocytes and occasionally burst-forming unit-megakaryocytes, with a plating effici

113 No inhibition of either burst-forming unit-MK- or colony-forming unit-MK-derived

114 cells (19-39% growth inhibition of erythroid burst-forming units, multilineage colony-forming units,

115 t significantly alter steady-state erythroid burst-forming unit numbers.

116 lization of BMP4-responsive stress erythroid burst-forming units; therefore, new stress progenitors m

117 can generate BMP4-dependent stress erythroid burst-forming units when cultured under stress erythropo