ライフサイエンスコーパス: term placenta

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1 talized TB cell lines and primary cells from term placenta.

2 PC2 function in human syncytiotrophoblast of term placenta.

3 were purified as a single protein from human term placenta.

4 s ligand (FasL) and TRAIL in human early and term placentas.

5 protein was localized in first-trimester and term placentas.

6 ll but BAFF-R are known to be synthesized in term placentas.

7 6 was identified in both first trimester and term placentas.

8 placentas and to the syncytiotrophoblast in term placentas.

9 d pathway genes-HSD11B2, NR3C1, and FKBP5-in term placentas.

10 cells, and targeted bisulfite sequencing in term placentas.

11 determine directions for functional studies, term placentas, amniochorion membranes, and purified cyt

12 Chorionic plate arteries from full-term placentas and spiral arteries from nonpregnant myom

13 xymethylation is uniquely distributed within term placenta, and is associated with gene expression.

14 ational ages, cytotrophoblasts isolated from term placenta, and JAR choriocarcinoma cells.

15 To conclude, the gene expression in term placentas are highly affected by fetal, maternal an

16 We discovered that PHT cells from full-term placentas are refractory to ZIKV infection.

17 ssion of the human PEG3 gene in the early to term placenta, as well as the uterus and ovary, using RT

18 cytiotrophoblast of both first trimester and term placenta, but the intensity was much greater in the

19 oter or gene-body DNA methylation in matched term placenta, cord blood, and 3-6 mo saliva samples fro

20 Human amniotic epithelial cells (hAECs) from term placenta express surface markers and gene character

21 Macrophages from at-term placentas expressed CD14, exhibited macrophage micr

22 levels of HIV transcripts in trophoblasts of term placentas from HIV-infected women, we studied the p

23 crease in CS/GH-V RNA levels was detected in term placentas from obese (body mass index (BMI) >/= 35

24 ify the extent of altered gene expression in term placentas from pregnant women with late-onset PE an

25 e maternal- and fetal-facing surfaces of the term placenta have been determined in isolated membrane

26 ytic activity in situ, in tissue sections of term placenta, is co-localized with gelatinase B.

27 CTs were isolated from term placentas of 12 normal, 12 PE, and 12 IUGR pregnanc

28 First trimester and term placentas, purified trophoblast cells, choriocarcin

29 viously that trophoblasts isolated from full-term placentas resist infection by diverse viruses, incl

30 ne to establish that CTB cells purified from term placentas resist LIGHT-induced apoptosis.

31 expression of the maternal PHLDA2 allele in term placenta (the normal imprinting pattern was maintai

32 may contribute to Ca(2+) transport in human term placenta, the regulatory mechanisms associated with

33 ve elements and gene-associated DNA in human term placenta tissue samples.

34 s 9 weeks after gestation (n = 7) and in all term placenta tissues (n = 5) but not in other normal ad

35 CPASMCs were isolated from normal human term placentas using enzymatic digestion.

36 cinoma cells, cytotrophoblasts isolated from term placenta, villous core cells, and possibly other no

37 The cells from term placentas, which resist infection, do not express g

38 as well as Mel 624 parental cells, and human term placenta whole tissue sections were used as control

39 Immunostaining of term placenta with a DC-SIGN1-specific antiserum showed

40 sis of a partially purified extract of human term placenta with an antiserum to human apo A-I yielded

41 Comparison of the transcriptome between term placentas without and with VUE revealed differentia

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