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1 c glycoforms were reported to be enriched in fetal circulation.
2 ring waste products and xenobiotics from the fetal circulation.
3 placental uptake of organic anions from the fetal circulation.
4 ge was observed between the placenta and the fetal circulation.
5 to drive accumulation of substrates from the fetal circulation.
6 chnique for studying the distribution of the fetal circulation.
7 ity in the way blood is streamed through the fetal circulation.
8 nificantly secreted by the placenta into the fetal circulation.
9 to cells located closely to the maternal and fetal circulation.
10 roxychromans (alpha- and gamma-CEHCs) in the fetal circulation.
11 with levels of interleukin-6 and S100beta in fetal circulation.
12 missing enzyme across the placenta into the fetal circulation.
13 G and mediates transcytosis from maternal to fetal circulation.
14 ing boluses of specific amino acids into the fetal circulation.
15 minants of the amino acid composition in the fetal circulation.
16 Much weaker relations were seen in the fetal circulation.
17 ve barrier to prevent maternal atRA reaching fetal circulation.
18 and/or persistence of maternal cells in the fetal circulation.
19 derived trophoblasts separates maternal from fetal circulation.
20 AA and DHA from the mother and enriches the fetal circulation.
21 es (anti-SSA/Ro and/or anti-SSB/La) into the fetal circulation.
22 e nitric oxide synthase (iNOS) regulates the fetal circulation.
23 ta modulates metabolites in the maternal and fetal circulation.
24 ation parameters and maintain patency of the fetal circulation.
25 by the human placenta into the maternal and fetal circulations.
26 these metabolites into both the maternal and fetal circulations.
27 levels were substantial in the placenta and fetal circulation (109.7 +/- 125.4 nmol g(-1) in the pla
28 levels were substantial in the placenta and fetal circulation (109.7 125.4 nmol g(-1) in the placent
29 1 and NGM-SZ21 were transported equally into fetal circulation (8.9% vs 8.7%, respectively, P = .58).
31 es aids in understanding the function of the fetal circulation and may be helpful in detecting the hu
32 promised the integration of the maternal and fetal circulation and presumably the transfer of methylT
33 the principal backdoor androgen in the male fetal circulation and that DHT is undetectable (<1 ng/mL
34 od cell Hb content within both the adult and fetal circulations and contributed to meeting the elevat
35 which form the barrier between maternal and fetal circulations and thus govern the cross talk betwee
36 composition of amino acids delivered to the fetal circulation, and impaired placental amino acid sup
37 opment by crossing the placenta and entering fetal circulation, and indirectly through AT(1)-AA-induc
38 at AT(1)-AAs cross the mouse placenta, enter fetal circulation, and lead to small fetuses with organ
39 (Ang II) concentrations in the maternal and fetal circulations are associated with dramatic increase
40 ed cytokines in the amniotic fluid or in the fetal circulation be viewed as a humoral expression and
41 ne, was transferred from the maternal to the fetal circulation by non-exchange mechanisms also (P<0.0
43 ramen ovale is an essential component of the fetal circulation contributing to oxygenation and carbon
44 Previous techniques for the study of the fetal circulation did not permit assessment of phasic ev
45 erangement of CXC chemokines in maternal and fetal circulation distinguishes VUE from acute chorioamn
47 Very little drug passively diffuses to the fetal circulation during the first trimester, when organ
49 ng maternal IgG across the human placenta to fetal circulation has not been identified, although the
50 s such as meconium aspiration and persistent fetal circulation have fostered clinical trials demonstr
51 h uptake of metformin into the placental and fetal circulation highlights the potential for direct im
52 We measured flow in the major vessels of the fetal circulation in 40 late-gestation normal human fetu
53 f contrast material between the maternal and fetal circulation in gravid mice through the use of dyna
55 ntal proteome secreted into the maternal and fetal circulations in normal pregnancy based on 4-vessel
56 the present review was to compare changes in fetal circulation, in terms of both velocimetry and actu
58 when maternal antibodies gain access to the fetal circulation, just prior to the clinical detection
59 al microchimerism, and maternal cells in the fetal circulation, known as maternal microchimerism.
60 e data suggest that intact beta(2)GPI in the fetal circulation may be a novel cardioprotective factor
61 s of the known vasoconstrictor Ang II in the fetal circulation may indeed play a role in the marked i
62 processes, the high levels of Ang II in the fetal circulation may serve to modulate overall fetoplac
63 ed transport of cholesterol from maternal to fetal circulation might attenuate congenital malformatio
64 ncoding the human factor IX protein into the fetal circulation of immunocompetent hemophiliac and nor
65 whereas the brain-sparing remodelling of the fetal circulation resulting from placental insufficiency
66 n increased metabolite concentrations in the fetal circulation, suggesting increased maternal or feta
67 l boluses of unlabelled amino acids into the fetal circulation to provide substrates for exchange (tr
68 easured in the absence of amino acids in the fetal circulation (transfer by non-exchange mechanisms)
69 late and UMFA concentrations in maternal and fetal circulation warrant additional investigation becau
70 lls in the transport of IgG from maternal to fetal circulation, we studied Fc gamma receptor (Fc gamm
71 exchangers, all amino acids appearing in the fetal circulation were substrates of TAT1, LAT3 or LAT4.