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1 s, isolated from villous tissue of full-term placentae.
2  and blunted STB differentiation seen in T21 placentae.
3 ratio 1.35-1.79) was detected in all healthy placentae.
4  inner fruit tissue containing the seeds and placentae.
5 ssociation with hypotrophic and hypovascular placentae.
6 ) from female placentae than those from male placentae.
7 ssion in response to maternal diet than male placentae.
8 cotyledon VEGF was decreased (P<0.05) in FGR placentae.
9 HIV-1-suppressive factor produced locally in placentae.
10 istinct from both each other and from normal placentae.
11 total transthyretin compared to normotensive placentae (2352 +/- 2949 ng/mL vs. 3250 +/- 1864 ng/mL,
12   We detected microorganisms in 10.6% of 535 placentae (443 were delivered late preterm and 92 were d
13 etic DNA-methylation pattern in pathological placentae affecting placentogenesis, but also the develo
14                    The Gd content of excised placentae and fetuses was measured, using inductively co
15          PinT pregnancies resulted in larger placentae and heavier foals relative to PinP (P < 0.05).
16  gene expression was also observed in Pkd2-/-placentae and in cystic kidneys of Pkd1cond/-; Meox2cre/
17                             TinP had smaller placentae and lighter foals relative to TinT (P < 0.05).
18  production of transthyretin by preeclamptic placentae and whether transthyretin is carried into the
19 ogy samples with known CN, including tonsil, placentae, and FFPE melanoma cell lines.
20                                          The placentae are smaller but do not reveal any evidence of
21 proteins in trophoblast cell lines and human placentae at different gestational ages.
22 ere present in higher levels in preeclamptic placentae compared to normotensive placentae (p < 0.05,
23                                       Female placentae demonstrated more striking alterations in gene
24 , the choline/lipid ratio was </=0.02 in all placentae, despite preservation of the lipid peak (p<0.0
25  and moderate apoptosis, was associated with placentae expressing intermediate levels of HB-EGF.
26  methylation analysis was performed on human placentae from first, second and third trimesters to det
27 pressing cells were significantly greater in placentae from HIV-1-infected women who did not transmit
28 cific isoform of TP (TPbeta) is increased in placentae from IUGR pregnancies, compared to healthy pre
29  tissues, was not observed in blastocysts or placentae from later stage clones, although fetuses reca
30        Analysis of MAOA expression in bovine placentae from natural reproduction revealed imprinted X
31 easuring mRNA and protein expression in term placentae from normotensive (NT) and PE women who delive
32  P = 0.002) were all significantly higher in placentae from NT women at altitude, despite mRNA expres
33 ion preserved placental architecture whereas placentae from untreated infected mice had widespread he
34 phoblast cells up to week 35 of gestation in placentae from women who delivered preterm.
35                                          IVF placentae, however, displayed hypomethylation of imprint
36  preterm infants (n = 477) and their infants/placentae (n = 535) were recruited, and swab specimens o
37 ntas from HIV-infected women, we studied the placentae of 30 HIV-positive and 13 control gravidae.
38                                Additionally, placentae of both groups of manipulated concepti exhibit
39                          By day 90, however, placentae of conceptuses from the high PE group expresse
40  exhibits pronounced sexual dimorphism, with placentae of females more sensitive to nutritional pertu
41 ue factor was significantly increased in the placentae of infected C57BL/6 mice but was reduced in mi
42  sensitive to nutritional perturbations than placentae of males.
43 lish whether HB-EGF expression is altered in placentae of pre-eclamptic women.
44          In contrast, we found random XCI in placentae of the deceased clones but completely skewed X
45 t they were not significantly different from placentae of uninfected mothers.
46 e the microbes most frequently isolated from placentae of women who deliver preterm.
47 r levels of HB-EGF protein were found in the placentae of women who were not in labour.
48                   HB-EGF is downregulated in placentae of women with preeclampsia, a disorder associa
49  on GD 20, and total Cr was estimated in the placentae; ovaries were removed from the F1 offspring on
50 amnionitis in moderate/late preterm and term placentae (P < .001).
51 eclamptic placentae compared to normotensive placentae (p < 0.05, n = 7), however the levels of trans
52  complications can occur, including abruptio placentae, renal failure, subcapsular hematomas, and hep
53 se to chorio-allantoic and visceral yolk sac placentae, respectively.
54 ntiated TS cell cultures and dissected mouse placentae resulted in proliferating colonies that expres
55                                 Preeclamptic placentae secreted similar levels of total transthyretin
56               Microarray analysis of Pkd1-/- placentae showed upregulation of a set of apolipoprotein
57 higher in genes (651 out of 700) from female placentae than those from male placentae.
58 ng (PAS-Seq) of RNA from normal and PE human placentae to interrogate transcriptome-wide gene express
59                      Human TfR isolated from placentae was used to characterize the structure of the
60 day (GD) 9.5 to 14.5 through drinking water, placentae were removed on GD 20, and total Cr was estima
61 = 3), PE/IUGR (n = 3) and HELLP/IUGR (n = 2) placentae were used to determine the mean methylation le
62  mice resulted in growth restricted pups and placentae with poor syncytialisation and diminished grow

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