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1 he uterus, expelling maternal blood from the intervillous space.
2 placenta are localized predominantly in the intervillous space.
3 lated with monocyte density in the placental intervillous space.
4 te to the accumulation of macrophages in the intervillous space.
5 leukin (IL)-10, in plasma collected from the intervillous space.
6 al endometrium to initiate blood flow to the intervillous space.
7 microm over the villous tips throughout the intervillous space.
8 of transport rates via ease of access to the intervillous space.
9 on where maternal macrophages infiltrate the intervillous space.
10 tin sulfate A (CS) abundantly present in the intervillous space.
11 recruit B cells to further produce Ig in the intervillous spaces.
12 depositions of IgG3 and IgM were observed in intervillous spaces.
14 it was found that IRBCs adhere mainly in the intervillous space and also at significant levels to the
15 to an accumulation of macrophages within the intervillous space and increased production of tumor nec
17 antigens caused immediate breaks, increased intervillous spaces, and increased IELs in the intestina
19 ous CSPGs, we conclude that the CSPGs of the intervillous spaces are the receptors for placental IRBC
20 ction showed parasitized erythrocytes in the intervillous space but no hemozoin in macrophages nor in
21 in sulfate A (CSA) to sequester in placental intervillous spaces, causing severe sequelae for mother
23 ly, monocyte infiltration into the placental intervillous space has been identified as a key risk fac
24 this model, the depth of diffusion into the intervillous space is inversely proportional to the effi
25 infected erythrocytes (IEs) sequester in the intervillous space (IVS) of the placenta causing placent
26 sulfate proteoglycans (CSPGs) present in the intervillous spaces mediate the adherence of IRBCs in th
27 lfated, extracellular CSPGs localized in the intervillous spaces, minor amounts of two cell-associate
29 -normal maternal blood velocity entering the intervillous space of the placenta, distortion of the co
31 cells (IRBCs) selectively accumulate in the intervillous spaces of placenta, leading to poor fetal o
32 droitin sulfate proteoglycans (CSPGs) in the intervillous spaces of the placenta are the receptors fo
33 infected erythrocytes (IE) accumulate in the intervillous spaces of the placenta by binding to chondr
34 an mediate the sequestration of IRBCs in the intervillous spaces of the placenta during the entire se
35 droitin sulfate proteoglycans (CSPGs) in the intervillous spaces of the placenta mediate the IRBC adh
38 tration of late-stage parasites in placental intervillous spaces that express VAR2CSA and bind specif
39 emonstrate that the CSPGs are present in the intervillous spaces throughout the second and third trim
40 a significant correlate of most components (intervillous space, villous, trophoblast, and capillary
43 uterus are suspended as cell columns in the intervillous space, where they experience significant am