ライフサイエンスコーパス: late pregnancy

1 etal proteins in the maternal bloodstream in late pregnancy.

2 mg once daily in HIV-1-infected women during late pregnancy.

3 fetal growth acceleration or deceleration in late pregnancy.

4 increased overall NF-kappaB activity during late pregnancy.

5 is associated with exposure to SSRIs during late pregnancy.

6 ng concentrations of 25(OH)-vitamin D during late pregnancy.

7 of neutrophils in the blood of women during late pregnancy.

8 id not correlate with insulin sensitivity in late pregnancy.

9 as a result of impaired mammogenesis during late pregnancy.

10 rses the metabolic changes seen in hearts in late pregnancy.

11 pregnancy and regulate the onset of labor in late pregnancy.

12 dual RMRs increased from 456 to 3389 kJ/d by late pregnancy.

13 was used to reconstitute adiponectin during late pregnancy.

14 the four-compartment model in both early and late pregnancy.

15 response to the stress of chronic hypoxia in late pregnancy.

16 sin-1 underwent unscheduled apoptosis during late pregnancy.

17 ut transcripts decreased dramatically during late pregnancy.

18 rnal FM across a spectrum of body weights in late pregnancy.

19 l resource allocation to fetal growth during late pregnancy.

20 was quantified serially in early, mid-, and late pregnancy.

21 nal exposure to influenza circulation during late pregnancy.

22 entration in the maternal circulation during late pregnancy.

23 n with pregestational type 2 diabetes during late pregnancy.

24 ed distribution of the higher percentiles in late pregnancy.

25 egnancy (P < 0.001), but was restored during late pregnancy.

26 PHN associated with maternal use of SSRIs in late pregnancy.

27 women had 25(OH)D measured in both early and late pregnancy.

28 ed glucose intolerance and hyperlipidemia in late pregnancy.

29 for increased cervical distensibility during late pregnancy.

30 teine concentration that otherwise occurs in late pregnancy.

31 ws the substantial demand for choline during late pregnancy.

32 ine exposure is substantially lowered during late pregnancy.

33 gnancy (early pregnancy, 94.7+/-15.9 mg/min; late pregnancy, 122.7+/-9.3 mg/min; P = 0.003).

34 LV strain decreased significantly in late pregnancy (-19.5+/-2% to -17.6+/-1.6%, P<0.001) and

35 ancy (6-17 wk gestation) and 16 women during late pregnancy (21-37 wk gestation).

36 ight gain, increased skinfold thicknesses in late pregnancy (28 wk) and early postpartum (4-6 wk), an

37 sistance in nine obese women with GDM during late pregnancy (30-36 weeks) and 1 year postpartum.

38 markedly lower in Asians than Caucasians in late pregnancy (31 +/- 6 vs. 49 +/- 3 bursts min(-1) at

39 ased rates of bone calcium deposition during late pregnancy, a finding that was particularly evident

40 In late pregnancy, activity of the allopregnanolone-synthes

41 56%) of 545 assigned to usual care smoked at late pregnancy (adjusted odds ratio [AOR] 0.90, 97.5% CI

42 In late pregnancy, although there was an overall increase i

43 ctivity increased by approximately 2-fold in late pregnancy and after estrogen treatment.

44 ns between exposure to certain phthalates in late pregnancy and behavioral problems in boys.

45 For periods in late pregnancy and childhood, we estimated spatially and

46 the tracking of serum 25(OH)D from early to late pregnancy and factors that influence this.

47 zation of XOR in the non-secretory states of late pregnancy and induced involution compared with the

48 d maternal serum bile acid levels, occurs in late pregnancy and is often associated with poor perinat

49 Remarkably, defects are reverted during late pregnancy and lactation but return upon involution

50 y pregnancy with impaired development during late pregnancy and lactation followed by delayed postlac

51 cifically in mammary epithelial cells during late pregnancy and lactation resulted in efficient delet

52 ted protein 5 (Lrp5) that are induced during late pregnancy and lactation via use of the whey acidic

53 paraventricular nucleus are activated during late pregnancy and lactation, as measured by an increase

54 ssion is significantly down-regulated during late pregnancy and lactation.

55 ssed microRNA declined precipitously between late pregnancy and lactation.

56 ammary gland, with maximum expression during late pregnancy and lactation.

57 acid and glucose kinetics are altered during late pregnancy and might suggest a mechanism for higher

58 inol and beta-carotene concentrations during late pregnancy and offspring bone mineralization assesse

59 n the ST(dl), DA turnover was highest during late pregnancy and on the day of parturition, while no c

60 structural and functional differentiation at late pregnancy and parturition to produce and secrete mi

61 mes, the hypercoaguable state that occurs in late pregnancy and postpartum, and the progressively dec

62 ciation between the maternal use of SSRIs in late pregnancy and PPHN in the offspring; further study

63 conclusion, PBDEs may impair fetal growth in late pregnancy and reduce birth size.

64 onsumption of gluten-containing foods during late pregnancy and subsequent risk of celiac disease in

65 d exposure to ultraviolet B radiation during late pregnancy and the maternal use of vitamin D supplem

66 Expression of all four Cxs peaks during late pregnancy and throughout lactation suggesting essen

67 (HPA) axis is known to be attenuated during late pregnancy and throughout lactation.

68 protein-3 (IGFBP-3) to mammary tissue during late pregnancy and throughout lactation.

69 the developing CNS, adult testes, breasts in late pregnancy, and germinal centers of secondary B cell

70 Little is yet known about zinc absorption in late pregnancy, and no information on absorption from th

71 doses are higher in early pregnancy than in late pregnancy, and there can be considerable intersubje

72 l administration of L. salivarius PS2 during late pregnancy appears to be an efficient method to prev

73 tions of UBF during the follicular phase and late pregnancy are partially mediated by ER-dependent me

74 tudy measured insulin sensitivity in mice in late pregnancy at day 16 (D16) and near term at D19.

75 d self-reported tobacco use by the mother at late pregnancy, birthweight of the baby, the proportion

76 , channel mRNA and total protein increase in late pregnancy, but current density decreases as in rats

77 subjects had low insulin sensitivity during late pregnancy, but neither glucose clamp nor minimal mo

78 Higher maternal systolic blood pressure in late pregnancy, but not in middle pregnancy, was associa

79 d oxidation remained similar between mid and late pregnancy, but there was wide variation between the

80 e and N1-methylnicotinamide were measured in late pregnancy by mass spectrometry (n = 497) and relate

81 SnoN expression is induced at late pregnancy by the coordinated actions of TGF-beta an

82 ggests that consumption of a high LA diet in late pregnancy can enhance placental PG production and m

83 while more limited deficiency during mid- to late pregnancy causes deficits in hippocampal plasticity

84 e PCR and Western blots demonstrate that, in late pregnancy, channel transcript quantities and total

85 >/=30 ng/ml) was observed in both early and late pregnancy compared with insufficient levels (25OHD

86 to oxidative metabolism has been observed in late pregnancy compared with pregravid states.

87 utoreactive T cells from mice induced during late pregnancy compared with virgin controls.

88 eproductive failure linking subfertility and late pregnancy complications and has allowed us to rejec

89 Late pregnancy complications include gestational diabete

90 t heparin effectively prevents recurrence of late pregnancy complications, 135 women with previous hi

91 erapies, in particular better prophylaxis of late pregnancy complications, are urgently needed for ob

92 ry outcomes included the live-birth rate and late pregnancy complications.

93 eight heparin in the prevention of recurrent late pregnancy complications.

94 Thus, nadroparin did not prevent late-pregnancy complications in women at risk of recurre

95 Primary outcome was a composite end point of late-pregnancy complications.

96 5; however, development recovered by mid- to late pregnancy (d14.5).

97 r drinking water for 5 day periods in mid to late pregnancy (day, D, 11-16 or D14-19).

98 posed to 30 min immobilisation stress during late pregnancy (days 19-21), early lactation (days 3-4)

99 GWG in late pregnancy (defined as 28 weeks onward on the basis

100 autocrine prolactin or activate Stat5 during late pregnancy despite normal levels of circulating seru

101 ogical stages: virgin, early pregnancy (e7), late pregnancy (e20), lactating (day 4), involuting day

102 Late pregnancy elevated C-reactive protein (> or = 12 mi

103 coupled from the circadian clock, whereas in late pregnancy, energy availability is mediated by coord

104 ers with high concentrations of androgens in late pregnancy exhibit higher rates of aggression and mo

105 ts and 2) the relative effects of early- and late-pregnancy exposure to tobacco on infant birth weigh

106 During late pregnancy, female mice show no evidence of chronic

107 In late pregnancy, fetal weight in the folate deficient gro

108 epartures from trend lines in maternal FM in late pregnancy for any of the methods.

109 LdT and LAM use in late pregnancy for highly viremic mothers was equally ef

110 telbivudine (LdT) or lamivudine (LAM) use in late pregnancy for preventing hepatitis B mother-to-chil

111 uropean ancestry; 85 [41.3%] primiparous) in late pregnancy from December 19, 2012, through March 17,

112 During late pregnancy, full-length CDP levels decline, and a 15

113 In the late-pregnancy group, 3-HIA excretion decreased (P < 0.0

114 Midpregnancy and late pregnancy GWGs were associated with fat-free mass.

115 Women who smoked into late pregnancy had a much higher risk for schizophrenia

116 e mother was switched from MMF to SRL during late pregnancy had cleft lip and palate and microtia) an

117 parison with NPNL control subjects, women in late pregnancy had higher energy intakes and BMRs.

118 is of cervical hyaluronan (HA) from early to late pregnancy has long been proposed to play an essenti

119 In conclusion, serum from late pregnancy has the capacity to down-regulate T cell

120 In late pregnancy, hearts show eccentric hypertrophy, as ex

121 ffspring of rats exposed to dexamethasone in late pregnancy, hepatic expression of glucocorticoid rec

122 ng perturbed maternal insulin sensitivity in late pregnancy; hepatic insulin sensitivity was higher,

123 In late pregnancy, HPA axis responses to stressors, includi

124 red using a radioimmunoassay on samples from late pregnancy in 109 women delivering a child who devel

125 ravid, insulin resistance was evident during late pregnancy in all women (12.4 +/- 1.2 vs. 8.1 +/- 0.

126 glucose tolerance and insulin sensitivity in late pregnancy in association with dysregulated lipid an

127 sma leptin was analyzed in maternal blood in late pregnancy, in cord blood, and at 8, 16, and 52 wk i

128 tions occur in normal fetal membranes during late pregnancy, in preparation for labor.

129 In late pregnancy, inhibition of 5alpha-reductase (an allop

130 These results indicate that late pregnancy is associated with decreased ubiquitin-pr

131 Thus, the extreme hyperleptinemia of late pregnancy is attributable to binding of the leptin

132 usual increase in insulin resistance seen in late pregnancy is enhanced in obese mothers, causing mar

133 nd hence the HPA axis, following IL-1beta in late pregnancy is explained by presynaptic inhibition of

134 of gluten-containing food consumption during late pregnancy is not associated with risk of celiac dis

135 diomyocytes and that elevated PDK4 levels in late pregnancy lead to inhibition of PDH (pyruvate dehyd

136 We hypothesized that IH during late pregnancy (LG-IH) may increase the propensity for m

137 ly pregnancy (EP; weeks 10-12 of gestation), late pregnancy (LP; weeks 34-36 of gestation), and early

138 In late pregnancy, many women consuming contemporary Wester

139 In late pregnancy maternal hypothalamo-pituitary-adrenal (H

140 In late pregnancy, maternal insulin resistance occurs to su

141 In late pregnancy, maternal serum retinol and beta-carotene

142 at antibiotics taken during early life or in late pregnancy may be associated with childhood asthma.

143 The risk of stillbirth in late pregnancy may be determined by placental function i

144 concentration of ADAMTS13 that occurs during late pregnancy may combine to increase the risk for occu

145 ious effect of malaria during both early and late pregnancy on fetal growth.

146 y (tenofovir-unexposed) were enrolled during late pregnancy or within 72 hours of birth.

147 ive hormones, and fat mass were increased in late pregnancy (P < 0.001).

148 For women immunized with Tdap during late pregnancy, pertussis-specific immunoglobulin G leve

149 ERG-encoded K(+) channels as a precursor to late pregnancy physiological activity.

150 The data also explain how late pregnancy poses a threat to cardiac homeostasis, an

151 irected metabolic imprinting once set during late pregnancy prior to the first parturition persistent

152 Maternal social stress during late pregnancy programs hypothalamo-pituitary-adrenal (H

153 ta indicate that the hormonal environment of late pregnancy promotes metabolic remodeling in the hear

154 dels, and early pregnancy, midpregnancy, and late pregnancy rates of GWG (0-17, 17-27, and 27 wk to d

155 Early pregnancy, midpregnancy, and late pregnancy rates of GWG were independently associate

156 - 5 vs. 30 +/- 3 bursts min(-1) in early and late pregnancy, respectively; P = 0.023).

157 seasonal variation in 25(OH)D for early and late pregnancy separately, and the difference between th

158 ized decrease in miRNAs, such as miR-150, at late pregnancy serves to allow translation of targets cr

159 f wild-type and ERBB4-null mammary glands at late pregnancy showed that ERBB4 expression was required

160 virus (HIV) infection who took tenofovir in late pregnancy (tenofovir-exposed) or no tenofovir durin

161 f all live births and stillbirths (including late-pregnancy terminations) delivered at >/=20 weeks' g

162 piratory quotient is significantly higher in late pregnancy than postpartum.

163 r enzymes, and low platelets), a disorder of late pregnancy that involves the liver as one of the tar

164 found evidence for a serum factor present in late pregnancy that suppresses T cell activation.

165 Except in late pregnancy, the doses estimated with realistic voxel

166 We found that during the period of late pregnancy there is protection against paralysis, du

167 In middle and late pregnancy, there also is a four-fold increase in va

168 During late pregnancy, TNF-alpha was inversely correlated with

169 n supraoptic and paraventricular nuclei from late pregnancy to late lactation may reflect the functio

170 is condition when orally administered during late pregnancy to women who had experienced infectious m

171 r conditions of marked insulin resistance in late pregnancy, to predict abnormalities of glucose tole

172 between PI use and lower increase in BMI in late pregnancy warrants further study.

173 Malaria both in early and late pregnancy was associated with a reduction in fetal

174 Higher oily fish consumption in late pregnancy was associated with lower childhood aorti

175 Higher maternal serum retinol in late pregnancy was associated with lower offspring total

176 ration of 25(OH)-vitamin D in mothers during late pregnancy was associated with reduced whole-body (r

177 A questionnaire on the mother's diet in late pregnancy was completed by 3-4.5 mo postpartum.

178 auterine growth retardation, and exposure in late pregnancy was necessary to the association.

179 r confounders, reported maternal drinking in late pregnancy was negatively associated with childhood

180 Anaemia (haemoglobin <11 g/dL) in late pregnancy was negatively associated with forced vit

181 y, the change in TNF-alpha from pregravid to late pregnancy was the only significant predictor of the

182 apoptosis when expressed ectopically during late pregnancy, we found that during post-lactational in

183 Moderate and heavy drinkers in late pregnancy were also more likely to have an SGA birt

184 era of patients and comparison subjects from late pregnancy were assayed by enzyme-linked immunosorbe

185 of 30 ng/ml or higher at trial entry and in late pregnancy were associated with a lower risk of pree

186 ternal serum beta-carotene concentrations in late pregnancy were associated with greater total body B

187 Current densities in late pregnancy were lower than in female controls.

188 Exposures to PM2.5 and BC in late pregnancy were positively associated with newborn S

189 al contractility is drastically increased in late pregnancy when compared to non-pregnant conditions.

190 SSRI exposure during late pregnancy-whether a causal factor or not-might iden

191 ll and in early pregnancy, midpregnancy, and late pregnancy with neonatal adiposity.