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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
16 gene expression was also observed in Pkd2-/-placentae and in cystic kidneys of Pkd1cond/-; Meox2cre/
18 production of transthyretin by preeclamptic placentae and whether transthyretin is carried into the
22 ere present in higher levels in preeclamptic placentae compared to normotensive placentae (p < 0.05,
24 , the choline/lipid ratio was </=0.02 in all placentae, despite preservation of the lipid peak (p<0.0
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
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
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.
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
49 on GD 20, and total Cr was estimated in the placentae; ovaries were removed from the F1 offspring on
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
54 ntiated TS cell cultures and dissected mouse placentae resulted in proliferating colonies that expres
58 ng (PAS-Seq) of RNA from normal and PE human placentae to interrogate transcriptome-wide gene express
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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