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1 lasts, infect underlying cytotrophoblasts in chorionic villi.
2 es from cultured lymphocytes, amniocytes, or chorionic villi.
3 vitro culture of explants of human placental chorionic villi.
4  layer that forms the outer surface of human chorionic villi.
5 s and accumulation of fetal macrophages into chorionic villi.
6 V spreads from basal and parietal decidua to chorionic villi and amniochorionic membranes and that ta
7 al cells, fibroblasts, and Hofbauer cells in chorionic villi and amniotic epithelial cells and tropho
8                 An increase in the number of chorionic villi and blood vessels over that in controls
9 tly contacts syncytiotrophoblasts that cover chorionic villi and cytotrophoblasts that invade uterine
10  differentiated syncytiotrophoblast (STB) in chorionic villi and extravillous trophoblast (EVT) at th
11 low) and CD34(+)CD45(low)-that were found in chorionic villi and in the chorioamniotic membrane.
12  this hypothesis, we exposed first-trimester chorionic villi and isolated cytotrophoblasts to CMV in
13 hanges are also preserved in first-trimester chorionic villi and term placenta.
14 und in trophoblasts and endothelial cells of chorionic villi and uterine arteries.
15 es, and inflammatory infiltrate in placental chorionic villi are associated with adverse pregnancy re
16 metrial epithelium and the epithelium of the chorionic villi are juxtaposed with minimal extension in
17 etal cytotrophoblast stem cells in anchoring chorionic villi become invasive.
18 GF during explant culture of first-trimester chorionic villi enhanced extravillous trophoblast differ
19 yncytiotrophoblasts and cytotrophoblasts, in chorionic villi-in clinical cases of congenital infectio
20 filing of secreted immune factors from human chorionic villi isolated from placentas at mid and late
21                   Antigens were also seen in chorionic villi of one of the first trimester placentas.
22 alivary glands, uterine decidua, and injured chorionic villi of the placenta, demonstrating both its
23 s present in the syncytiotrophoblasts of the chorionic villi of the rhesus placenta, within villous c
24 either into syncytiotrophoblasts in floating chorionic villi or extravillous trophoblasts (EVTs) at t
25 vering trophoblastic lacunae or newly formed chorionic villi remained largely Mamu-AG-negative.
26 on of glycosaminoglycans on trophoblasts and chorionic villi, resulting in increased permeability of
27                                           In chorionic villi, syncytiotrophoblasts did not become inf
28  which give rise to the mature cell types of chorionic villi-syncytiotrophoblasts on the surfaces of
29                                           In chorionic villi that were infected with CMV in utero, sy
30           DNA methylation in first-trimester chorionic villi was assessed in chromosomally normal mis
31  placentas and explants from first-trimester chorionic villi with the prototype Ugandan and a recentl