ライフサイエンスコーパス: fetal cell

1 CTH secretion (alone or with CRH) from human fetal cells.

2 a male fetus or evidence of persistent male fetal cells.

3 sheathed more host axons per donor cell than fetal cells.

4 ions of neurotrophic factors and implants of fetal cells.

5 se attributable to transplacentally acquired fetal cells.

6 uclear transfer-derived sheep generated from fetal cells.

7 ty requires cytogenetic analysis of amniotic fetal cells.

8 n cell lines established from adults than in fetal cells.

9 ation process examined in this review, these fetal cells acquire properties of leukocytes and endothe

10 Fetal cells acquired during pregnancy provide a potentia

11 Fetal cells and cell-free DNA reach the maternal circula

12 rved from yeast to human cells, expressed in fetal cells and most adult tissues, and acting synergist

13 IGFBP2 gene, which is normally expressed in fetal cells and turned off in adult cells, becomes react

14 r is not continuously exposed to circulating fetal cells and, in fact, has the capacity to eliminate

15 e of activated cell types, including tumors, fetal cells, and cells of the immune system.

16 e of culture failure, maternal overgrowth of fetal cells, and poor chromosome morphology.

17 tion known to induce iNOS maximally in human fetal cells, and the expression of iNOS was determined b

18 The engrafted fetal cells are a potential source of growth factors and

19 Because fetal cells are a source of placental IFN-gamma and cord

20 Fetal cells are known to persist in mothers for many yea

21 s from patients with fragile X syndrome, and fetal cells as early as 8 weeks old.

22 ed in neonatal RBC, will direct parasites to fetal cells, as well as F cells, and less to the approxi

23 c cell sorting followed by isolation of pure fetal cells by microdissection.

24 native strategy, which suggested that intact fetal cells can be found in maternal plasma by use of si

25 Fetal cells can be found in the maternal circulation in

26 Rare fetal cells can be recovered from maternal blood, which

27 s in humans have shown that during pregnancy fetal cells can enter the maternal circulation and persi

28 lure, our objective was to determine whether fetal cells can migrate to the maternal heart and differ

29 Rare nucleated fetal cells circulate within maternal blood.

30 Human fetal cells contained OGF and the zeta receptor.

31 Although apoptotic intact fetal cells could contribute to the detection of fetal D

32 The mean number of male fetal-cell DNA equivalents detected in 109 women bearing

33 The mean number of male fetal-cell DNA equivalents detected in 16-ml blood sampl

34 significantly higher than the number of male fetal-cell DNA equivalents detected in 46,XY fetuses (P

35 The mean number of male fetal-cell DNA equivalents detected when the fetal karyo

36 The mean number of male fetal-cell DNA equivalents detected when the fetus was m

37 We determined the number of fetal-cell DNA equivalents present in maternal whole-blo

38 Male fetal-cell DNA-equivalent quantitation was determined by

39 ing of the interactions between maternal and fetal cells during early placentation and highlights nov

40 Fetal cells enter maternal blood during pregnancy and pe

41 Fetal cells enter the maternal circulation during most p

42 Fetal cells exhibited a comparatively short-lived or rap

43 postpartum, the result of an encounter with fetal cells expressing the appropriate MHC/peptide compl

44 er the mechanism by which two populations of fetal cells (fetal cortex derived Gli1-expressing cells

45 and fetal blood sampling are used to obtain fetal cells for genetic diagnosis.

46 In vivo, eGFP+ fetal cells form endothelial cells, smooth muscle cells,

47 However, recovery and analysis of fetal cells from blood is complex, and sensitivity is lo

48 is method of prenatal diagnosis by enriching fetal cells from maternal blood by magnetic cell sorting

49 nosis of single gene disorders by recovering fetal cells from maternal circulation appears to be a fe

50 iptome analyses of primary cultures of human fetal cells from pregnancies affected with trisomy 21 (t

51 idence existed for persistent circulation of fetal cells from prior pregnancies.

52 In addition, fetal cells have been implicated in the development of p

53 recent report that showed calves cloned from fetal cells have longer telomeres than their age-matched

54 s, we demonstrate engraftment of multipotent fetal cells in injury zones of maternal hearts.

55 Sc remains to be elucidated, the presence of fetal cells in internal organs suggests that they could

56 dies have confirmed the residual presence of fetal cells in maternal blood and tissues following preg

57 Fetal cells in maternal blood are a noninvasive source o

58 ckgrounds (e.g., circulating tumor cells and fetal cells in maternal blood), detection of cells/parti

59 s possible that persistent microchimerism of fetal cells in maternal circulation may, for some mother

60 tion with these systems for the detection of fetal cells in maternal circulation.

61 etal:maternal microchimerism and the role of fetal cells in maternal health and disease.

62 l microchimerism (FCM) is the persistence of fetal cells in the maternal circulation and organs follo

63 This results in the presence of fetal cells in the maternal circulation, known as fetal

64 ion-independent manner; approximately 40% of fetal cells in the maternal heart express Caudal-related

65 fficking results in long-term persistence of fetal cells in the mother and maternal cells in her offs

66 Proposed hypotheses about the function of fetal cells in the pathogenesis of maternal cancer inclu

67 pes in ways more closely resembling those of fetal cells, including increased LCR-gamma-globin contac

68 Maternal and fetal cells intermingle at the site of placental attachm

69 maternal cell trafficking, or the passage of fetal cells into the maternal circulation, is now a well

70 nces its mother's immune response by sending fetal cells into the maternal circulation.

71 lex (MHC) expressed by the trophoblasts, the fetal cells invading the maternal decidua during pregnan

72 In vitro, fetal cells isolated from maternal hearts recapitulate t

73 shows that compared with well-differentiated fetal cells, less differentiated embryonal and undiffere

74 rodents with TLE, but the scarcity of human fetal cells limits applicability in patient populations.

75 The human fetal cell line RPE 28 SV4 has been useful for studies o

76 ter in adult-derived fibroblasts than in the fetal cell lines.

77 es established from postnatal donors than in fetal cell lines.

78 Loss of Ackr2 specifically from fetal cells makes a key contribution to the placental de

79 These data suggest that fetal cells may be associated with SLE.

80 Fetal cells may mimic these events to selectively delete

81 interactions with CD1d expressed on invading fetal cells may play an immunoregulatory role at the mat

82 Fetal cells may respond to maternal injury by developing

83 Fetal cell microchimerism (FCM) is the persistence of fe

84 gate whether there is an association between fetal cell microchimerism and thyroid disease in women.

85 Our findings suggest a relation between fetal cell microchimerism and thyroid disease.

86 We reviewed all reports of studies on fetal cell microchimerism, defined as male DNA in matern

87 of factors that influence the development of fetal cell microchimerism.

88 The results of this study suggest that fetal cells migrate from the peripheral circulation into

89 We found that fetal cell migration is not universal but occurs in only

90 The sixfold elevation of fetal cells observed in maternal blood when the fetus ha

91 Metaphase karyotype analysis of fetal cells obtained by amniocentesis or chorionic villu

92 ononuclear cytotrophoblasts, the specialized fetal cells of the placenta that invade the uterus, play

93 The realization that fetal cells pass into the maternal circulation and can s

94 Recent studies indicate that fetal cells persist in maternal blood for decades after

95 ound in the maternal circulation and if male fetal cells persist in maternal tissues postdelivery.

96 This finding suggests that fetal cells persisting in the maternal circulation or ti

97 eatures include extended in vitro culture of fetal cells preceding nuclear transfer, as well as in vi

98 nstrated that after inflammatory stimulation fetal cells secreted more IL-8 (LPS, 8-fold; IL-1beta, 2

99 We report that fetal cells selectively home to injured maternal hearts

100 ammalian oocytes and spermatozoa derive from fetal cells shared by the sexes.

101 Various cell types including porcine fetal cells, stem cells, immortalized cell lines, and ma

102 have been directed towards the enrichment of fetal cells, such as erythroblasts, from maternal blood

103 vasion of the uterine lining by trophoblast, fetal cells that are the major cell type of the placenta

104 h villous and extravillous trophoblasts, the fetal cells that invade the maternal decidua.

105 al tissue specimens suggests the presence of fetal cells that may have multilineage capacity.

106 ined by mAb FDC6, and expressed in cancer or fetal cells/tissues, but not in normal adult cells/tissu

107 with a reduced capacity of the TCDD-exposed fetal cells to compete with control cells in a mixed com

108 Maternal-fetal cell transfer during pregnancy can lead to long-la

109 orts the very long-term clinical outcomes of fetal cell transplantation in 2 patients with Parkinson

110 Fetal cell transplantation therapies are being developed

111 ntact between maternal cells and specialized fetal cells (trophoblasts) in the human placenta: firstl

112 omical interfaces between maternal cells and fetal cells (trophoblasts): (i) the villous region where

113 Complete functionality of fetal cells was also restored; tritiated thymidine incor

114 The function of fetal cells was better maintained in the air-liquid inte

115 ellular localization of transcripts in human fetal cells, we show that human TSIX antisense transcrip

116 L against fetal Ags, we found that migrating fetal cells were cleared by the maternal immune system.

117 More fetal cells were detected in maternal blood when the fet

118 Fetal cells were detected in maternal peripheral blood i

119 GFP(+) fetal cells were detected in the blood and migrated to a