ライフサイエンスコーパス: fetal blood

1 .6/10(6) nucleated cells (69.6 +/- 10/microL fetal blood).

2 tal transfer of amino acids from maternal to fetal blood.

3 ormal, healthy adults and in placental cord (fetal) blood.

4 tissue mass, with a significant elevation in fetal blood adiponectin.

5 el of ethanol in utero (average maternal and fetal blood alcohol level of 25 mg/dl) promotes prematur

6 triads of human placenta and of maternal and fetal blood and found large subject-to-subject variabili

7 of nutrients and gases between maternal and fetal blood and is the principal site for synthesizing h

8 Monocytes from fetal blood and lung isolated from U. parvum 70 d + LPS

9 isorganized, with thickening of the maternal-fetal blood barrier and an associated reduction in diffu

10 D-OH was more effective in crossing the fetal blood-brain barrier, and targeting activated micro

11 NT virus transmission: the placenta and the fetal blood-brain barrier.

12 id (~10 samples tested/animal), maternal and fetal blood by culture and polymerase chain reaction.

13 uded that PTHrP is an important regulator of fetal blood calcium and placental calcium transport.

14 These results suggest that full-term fetal blood can engraft allogeneic hosts across the majo

15 ce-activated cell sorter analysis on EGFP(+) fetal blood cells revealed that surface expression of CX

16 Similar behavior was displayed when fetal blood cells were tested in vitro on immobilized re

17 cell-depleted adult bone marrow or full-term fetal blood cells, as a model of cord blood in a murine

18 al fate giving rise to a normal yolk sac and fetal blood cells.

19 ation [Ca(2+)] was significantly lower in P0 fetal blood compared with both WT and maternal blood at

20 The lower fetal blood concentrations are likely due to active effl

21 primary murine brain-derived ECs (MBECs) or fetal blood-derived ECs (FBECs).

22 immunophenotype were comparable to those of fetal blood-derived MSCs and similarly differentiated al

23 eless data acquisition system able to record fetal blood flow signals in addition to fetal blood pres

24 index ratio as an indicator of preferential fetal blood flow to the upper body parts at the expense

25 A preferential fetal blood flow to the upper body parts at the expense

26 essfully discriminated the maternal from the fetal blood flows; the two orders of magnitude differenc

27 Cardiac nerve blockade exaggerated the fetal blood gas response to haemorrhage somewhat but did

28 Fetal blood glucose and insulin were increased (P<0.01,

29 e DNA-based methods has been for determining fetal blood group in pregnancies when the fetus is at ri

30 Allogeneic full-term fetal blood has poorer radioprotective capacity but grea

31 f a positive B19V-IgG or B19V-IgM finding in fetal blood increased with gestational age.

32 Fetal blood ionized calcium was significantly reduced in

33 Oxygen transport from maternal blood to fetal blood is a primary function of the placenta.

34 The normal calcium concentration in fetal blood is raised above the maternal level, an incre

35 Fetal blood lactate concentrations reached a peak at 8 h

36 solated and characterized in first-trimester fetal blood, liver, and bone marrow.

37 We transplanted human first-trimester fetal blood mesenchymal stem cells (MSCs) into homozygou

38 Fetal blood MSCs could be expanded for at least 20 passa

39 Fetal blood MSCs cultured in adipogenic, osteogenic, or

40 Fetal blood MSCs supported the proliferation and differe

41 In their undifferentiated state, fetal blood MSCs were CD29(+), CD44(+), SH2(+), SH3(+),

42 cyte recruitment.(1) They report that murine fetal blood neutrophil rolling, adhesion, and extravasat

43 We show that fetal blood neutrophils acquire the ability to roll and

44 pment, but that before embryonic day (E) 15, fetal blood neutrophils display little ability to roll o

45 When 10(6) fetal blood nucleated cells (median gestational age, 10(

46 that individual PHSC from adult marrow, late fetal blood, or newborn blood each produce similar fract

47 g of the exchange properties of maternal and fetal blood pools--and thereby of placental function.

48 cord fetal blood flow signals in addition to fetal blood pressure and heart rate from free moving ewe

49 Fetal blood pressure and heart rate were monitored and f

50 nd dexamethasone induce similar increases in fetal blood pressure and similar falls in the incidence

51 A pronounced increase in fetal blood pressure occurred following both betamethaso

52 ith the phenotype (c-kit(high)Thy-1(low)) of fetal blood promastocytes at 3 wk of culture that progre

53 At a per-cell level, B cells from fetal blood recipients did not proliferate as well as th

54 Allogeneic full-term fetal blood recipients had decreased absolute numbers of

55 In addition, reconstituting T cells in fetal blood recipients had decreased mouse T-cell recept

56 Splenic T cells in allogeneic full-term fetal blood recipients proliferated poorly, were unable

57 Immunohistochemical examination of fetal blood revealed primitive pyrenocytes that were con

58 enous fetal blood saturation quantified from fetal blood samples by using a hemoximeter.

59 DNA and anti-B19V antibodies in maternal and fetal blood samples obtained from 41 pregnancies that we

60 Fetal blood samples were drawn from the fetal brachial a

61 d pressure and heart rate were monitored and fetal blood samples were drawn to measure the response t

62 V-IgG were detected in 100%, 28%, and 24% of fetal blood samples, respectively.

63 multiple organs and virus was isolated from fetal blood samples.

64 nuous cardiotocography (1.39; 1.33-1.45) and fetal blood sampling (1.30; 1.14-1.47) with admission ca

65 Serial fetal blood sampling (FBS) and intrauterine platelet tra

66 entesis, chorionic villus sampling (CVS) and fetal blood sampling are used to obtain fetal cells for

67 At the time of fetal blood sampling, all mothers were B19V-DNA positive

68 apparent, probably because of liberal use of fetal blood sampling.

69 Good agreement was found between fetal blood saturation determined by the transabdominal

70 two-layer diffusion model to deconvolve the fetal blood saturation from that of the pregnant ewe.

71 abdominal NIR method and arterial and venous fetal blood saturation quantified from fetal blood sampl

72 ucose carbohydrates and polyols are found in fetal blood, some in concentrations higher than maternal

73 vessel patterning and over 50% reduction in fetal blood space.

74 NKPs were also found in the fetal blood, spleen, and thymus.

75 Fetal blood stem/stromal cells engrafted in bones, diffe

76 duced in HLA-A*0201(-) mothers and enter the fetal blood system.

77 These data suggest that impaired fetal blood to the abdominal organs and smaller fetal ki

78 on of the placenta, due to a decrease in the fetal blood vessels, and decreased expression of the gap

79 ic retinal vasculature and the regression of fetal blood vessels, causing persistent hyperplasia of t

80 Furthermore, these fetal blood Vgamma9Vdelta2 T cells are functionally prep

81 Fetal blood Vgamma9Vdelta2 T cells are phosphoantigen re

82 The presence of B19V-IgG in fetal blood was accompanied by lower B19V-DNA levels and

83 NK)/T-cell-restricted progenitor cell in the fetal blood, with a phenotype of NK1.1(+) CD117 (c-kit)+