ライフサイエンスコーパス: cord blood-derived

1 C9i also enhanced apoptosis in cord blood-derived CD19(+) B-lineage cells (but not myel

2 Human hematopoietic cell lines and cord blood-derived CD34(+) and CD34(+), CD38(-) cell pop

3 ression of the NUP98-HOXA9 fusion protein in cord blood-derived CD34(+) cells confers a proliferative

4 In vitro pDC generation from human cord blood-derived CD34(+) hematopoietic progenitors was

5 n immune system was generated from umbilical cord blood-derived CD34(+) hematopoietic stem cells in B

6 cooperates with MA4 to initiate leukemia in cord blood-derived CD34(+) hematopoietic stem/progenitor

7 EV treatment of human umbilical cord blood-derived CD34(+) HSPCs alters the expression o

8 f ligands for both P- and E-selectins on all cord blood-derived CD34+ cells.

9 Cord blood-derived CD4(+) T cells are largely naive and

10 Comparison with expanded cord blood-derived CD4(+)CD25(hi) tTreg and expanded Tef

11 mbined with ex vivo expanded human umbilical cord blood-derived CD8(+) T cells, that have been geneti

12 Cord blood-derived cells surrounding surfactant-immunore

13 ransplanted lineage-depleted human umbilical cord blood-derived cells with high aldehyde dehydrogenas

14 Human LAD2 cells and umbilical primary human cord blood-derived cultured mast cells were stimulated w

15 d TNF from LAD2 cells and of CCL2 from human cord blood-derived cultured MCs.

16 Cord blood-derived cultured suppressor cell function was

17 DNA methylation of cord-blood derived DNA from 134 infants involved in a pr

18 Cord blood-derived ECFC therapy may offer new therapeuti

19 Intrajugular administration of human cord blood-derived ECFCs after established arrested alve

20 We examined the effects of human umbilical cord blood-derived ECFCs and their extracellular vesicle

21 studies indicate protective effects of human cord blood-derived ECFCs in experimental AKI and suggest

22 deficient mice in the presence or absence of cord blood-derived ECFCs.

23 Cs, the endothelial layer consisted of human cord blood-derived endothelial progenitor cells (hCB-EPC

24 lating factor in cultures of human umbilical cord blood-derived eosinophil (CDE) precursor cells.

25 Umbilical cord blood-derived EPCs (cbEPCs) were analyzed in parall

26 generated by peripheral blood- and umbilical cord blood-derived EPCs in a model of in vivo vasculogen

27 However, similar to adult- and cord blood-derived EPCs, HUVECs and HAECs derived from v

28 racterized the dynamic adhesion of umbilical-cord-blood-derived EPCs (CB-EPCs) to surfaces coated wit

29 Umbilical cord blood-derived haematopoietic stem cells (HSCs) are

30 the stem cell activity of cultured umbilical cord blood derived hematopoietic cells.

31 splants by intrahepatic inoculation of human cord blood-derived hematopoietic progenitor cells (CD34(

32 ator of adhesive properties in primary human cord blood-derived hematopoietic stem and progenitor cel

33 udy, we genetically modified human umbilical cord blood-derived hematopoietic stem cells (HSCs) to ex

34 lts in a marked expansion of human umbilical cord blood-derived HSPCs following cytokine stimulation.

35 We found that umbilical cord blood-derived HSPCs showed the greatest transplanta

36 nt CD34(+) erythroleukemic cell line, and in cord blood-derived human CD34(+) cells.

37 Rag2(-)/(-)gammac(-)/(-) mice humanized with cord blood-derived human hematopoietic stem cells produc

38 erism were observed after transplantation of cord blood-derived human HSCs into nonirradiated adult a

39 ulation of the human LAD2 mast-cell line and cord blood-derived human mast cells (hMCs).

40 adenine nucleotide-specific P2Y receptors on cord blood-derived human mast cells (hMCs).

41 Fc epsilon RI expression in these umbilical cord blood-derived human mast cells, as well as in mouse

42 Cord blood-derived human MC (hMC) express functional rec

43 Cultured cord blood-derived human MCs (hMCs) express mRNA transcr

44 sion and CysLT(1)-dependent proliferation of cord blood-derived human MCs (hMCs).

45 Moreover, preparations of human umbilical cord blood-derived immature mast cells not only expresse

46 TB(4) was a potent chemoattractant for human cord blood-derived immature, but not mature, mast cells.

47 s prolong VEGFR-2 and Akt phosphorylation in cord blood-derived late outgrowth endothelial progenitor

48 leukotriene C(4) synthase (LTC(4)S) by human cord blood--derived mast cells (hMCs), augments their hi

49 We now demonstrate that human cord blood-derived mast cell progenitors are susceptible

50 protease tryptase in normal human umbilical cord blood-derived mast cells (hCBMCs).

51 howed that the native MCEMP1 is expressed in cord blood-derived mast cells and HMC-1 and THP-1 cell l

52 Human cord blood-derived mast cells and the HMC-1 mast cell li

53 rkC, whereas preparations of human umbilical cord blood-derived mast cells expressed mRNAs for trkA a

54 e of the type I interferon receptor on human cord blood-derived mast cells reduced the RSV-mediated i

55 uman leukemic mast cells and human umbilical cord blood-derived mast cells to release newly synthesiz

56 Human cord blood-derived mast cells undergo apoptosis upon exp

57 Human cord blood-derived mast cells were treated for 2 weeks w

58 le development and function were examined in cord blood-derived mast cells.

59 mRNA and protein were present only in human cord blood-derived mast cells.

60 c mast cell (HMC-1) line and human umbilical cord blood-derived mast cells.

61 ergic donors' basophils and sensitized human cord blood-derived mast cells.

62 s IgE-desensitized rat MC and human lung and cord blood-derived MC (CBMC) after priming with fibrobla

63 S1P accelerated the development of cord blood-derived MCs (CB-MCs) and strikingly increased

64 The LAD2 MC line or primary human cord blood-derived MCs (CBMCs) were infected with HRV or

65 We now report that human cord-blood-derived MCs (hMCs) express the CysLT1 recepto

66 nduction were similar to levels achieved for cord blood-derived MPP and up to 20-fold higher than tho

67 adoptive transfer of ex vivo expanded human cord blood-derived NK cells into humanized mice reconsti

68 w Notch influences terminal differentiation, cord blood-derived NK cells or sorted peripheral blood N

69 Overexpression of activated Notch on cord blood-derived NK cells resulted in a 2-fold increas

70 lthy donors were cultured in the presence of cord blood-derived normal AFP (nAFP) or HCC tumor-derive

71 MCs developed from cord blood-derived progenitors cultured with stem cell f

72 rily focused on the more extensively studied cord blood-derived stem cell.

73 CD8+,CD57+ T cells were cocultured with cord blood-derived stem cells, and percentage inhibition

74 the growth of normal cells, including human cord blood-derived stem cells.

75 hairpin RNA (shRNA) library transduced into cord blood-derived stem/progenitor cells.

76 Cord blood-derived surfactant-positive epithelial cells

77 e expression of these receptors on adult and cord blood-derived term and preterm neonatal B cells.