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1 PC2 function in human syncytiotrophoblast of term placenta.
2 talized TB cell lines and primary cells from term placenta.
3 were purified as a single protein from human term placenta.
4 erved in first-trimester chorionic villi and term placenta.
5 , Slug and Snail, were detected in the human term placenta.
6  cells, and targeted bisulfite sequencing in term placentas.
7 s ligand (FasL) and TRAIL in human early and term placentas.
8 protein was localized in first-trimester and term placentas.
9 ll but BAFF-R are known to be synthesized in term placentas.
10 6 was identified in both first trimester and term placentas.
11  placentas and to the syncytiotrophoblast in term placentas.
12 d pathway genes-HSD11B2, NR3C1, and FKBP5-in term placentas.
13 determine directions for functional studies, term placentas, amniochorion membranes, and purified cyt
14 essed ~1300-fold higher than LIN28A in human term placenta and is the predominant paralog expressed i
15           Chorionic plate arteries from full-term placentas and spiral arteries from nonpregnant myom
16 xymethylation is uniquely distributed within term placenta, and is associated with gene expression.
17 ational ages, cytotrophoblasts isolated from term placenta, and JAR choriocarcinoma cells.
18          To conclude, the gene expression in term placentas are highly affected by fetal, maternal an
19       We discovered that PHT cells from full-term placentas are refractory to ZIKV infection.
20 t a set of quantitative metrics from healthy term placentas as a baseline for future assessments of p
21  differentiated from trophoblast stem cells, term placenta, as well as HTR8/SVneo, we demonstrate tha
22 ssion of the human PEG3 gene in the early to term placenta, as well as the uterus and ovary, using RT
23 cytiotrophoblast of both first trimester and term placenta, but the intensity was much greater in the
24 oter or gene-body DNA methylation in matched term placenta, cord blood, and 3-6 mo saliva samples fro
25 Human amniotic epithelial cells (hAECs) from term placenta express surface markers and gene character
26                          Macrophages from at-term placentas expressed CD14, exhibited macrophage micr
27 levels of HIV transcripts in trophoblasts of term placentas from HIV-infected women, we studied the p
28 crease in CS/GH-V RNA levels was detected in term placentas from obese (body mass index (BMI) >/= 35
29 ify the extent of altered gene expression in term placentas from pregnant women with late-onset PE an
30       In this study, we examined preterm and term placentas, from unassisted conceptions and those co
31 e maternal- and fetal-facing surfaces of the term placenta have been determined in isolated membrane
32 ytic activity in situ, in tissue sections of term placenta, is co-localized with gelatinase B.
33                       CTs were isolated from term placentas of 12 normal, 12 PE, and 12 IUGR pregnanc
34                          First trimester and term placentas, purified trophoblast cells, choriocarcin
35 viously that trophoblasts isolated from full-term placentas resist infection by diverse viruses, incl
36 ne to establish that CTB cells purified from term placentas resist LIGHT-induced apoptosis.
37 cental tissue from second-trimester and full-term placentas separated into decidua, placental villi a
38  expression of the maternal PHLDA2 allele in term placenta (the normal imprinting pattern was maintai
39  may contribute to Ca(2+) transport in human term placenta, the regulatory mechanisms associated with
40 ve elements and gene-associated DNA in human term placenta tissue samples.
41 s 9 weeks after gestation (n = 7) and in all term placenta tissues (n = 5) but not in other normal ad
42      CPASMCs were isolated from normal human term placentas using enzymatic digestion.
43 s can be derived from CTBs isolated from the term placenta, using TSCM supplemented with a low concen
44 cinoma cells, cytotrophoblasts isolated from term placenta, villous core cells, and possibly other no
45 phoblast cells isolated from GDM and non-GDM term placentas were cultured for 8-hour (CTB) and follow
46                               The cells from term placentas, which resist infection, do not express g
47 as well as Mel 624 parental cells, and human term placenta whole tissue sections were used as control
48                            Immunostaining of term placenta with a DC-SIGN1-specific antiserum showed
49 sis of a partially purified extract of human term placenta with an antiserum to human apo A-I yielded
50      Comparison of the transcriptome between term placentas without and with VUE revealed differentia