ライフサイエンスコーパス: second trimester

1 ked the presence of the CD44(+) cells in the second trimester.

2 vation in tissue resident neutrophils in the second trimester.

3 ostpartum, but fetal loss was highest in the second trimester.

4 100 healthy pregnant women, starting in the second trimester.

5 with moderate methyl bromide use during the second trimester.

6 ing outside of the guideline as early as the second trimester.

7 with adjustment for energy costs during the second trimester.

8 le the ventricle size decreases in the later second trimester.

9 with periodontitis when assessed during the second trimester.

10 surface remains smooth until the end of the second trimester.

11 erebral wall throughout the remainder of the second trimester.

12 e thrombocytopenia with bleeding only in the second trimester.

13 2 units, P < 0.03) trimesters but not in the second trimester.

14 nner) and snacks consumed per day during the second trimester.

15 red to women with a normal pregnancy, in the second trimester.

16 at the first antenatal visit, usually in the second trimester.

17 ase with maternal fever, particularly in the second trimester.

18 tussis in infant than vaccination during the second trimester.

19 es of pregnancies with CHDs diagnosed in the second trimester.

20 second trimester and long bones later in the second trimester.

21 ment that is apparent sonographically in the second trimester.

22 lular density declined from the first to the second trimester.

23 ollutant concentrations during the first and second trimester.

24 scores between the 2 groups at the first and second trimesters.

25 questionnaire administered in the first and second trimesters.

26 Mean second trimester (15-22 weeks' gestation) serum sTNFp55

27 yses showed that, compared with mothers with second-trimester 25(OH)D concentrations in the highest q

28 Fetal viability was low in the second trimester (29.2%) and much higher (95.3%) in the

29 ) and third (53%) trimesters than during the second trimester (33%).

30 ted with fetal demise was more common in the second trimester (55.3%), and preterm labor (52.3%) and

31 at least one study ultrasound in 5.1% by the second trimester, 7.9% by the third trimester, and 10.2%

32 ter, 9.7 g lower when it occurred during the second trimester (95% CI: -14.5, -4.8), and 3.3 g lower

33 ho had first-trimester abortion, 383 who had second-trimester abortion, and 163 who gave birth).

34 or chronic pain after first-trimester versus second-trimester abortion.

35 er abortion and 21% (CI, 18% to 25%) who had second-trimester abortion.

36 The median maternal second trimester alpha-T level was 63 muM (interquartile

37 PCR testing of second-trimester amniotic fluid for U. urealyticum can i

38 birth rates and rates of abortion during the second trimester among a subgroup of minors who were 17.

39 rate of weight gain was 306 g/wk during the second trimester and 247 g/wk during the third trimester

40 isoform levels were measured by HPLC at the second trimester and 3 years of age, respectively.

41 greater prevalence compared with that in the second trimester and a 5.1-fold greater prevalence compa

42 partum, and their diets were assessed in the second trimester and at 3 and 12 months postpartum (n =

43 al attachment level were recorded during the second trimester and following interviews on oral hygien

44 lled and were screened in the program by the second trimester and had at least 3 additional prenatal

45 lled and were screened in the program by the second trimester and had at least 3 additional prenatal

46 driven by an association with AC earlier in second trimester and long bones later in the second trim

47 r) of trihalomethanes experienced during the second trimester and pregnancy overall may affect fetal

48 ation between maternal IL-8 level during the second trimester and risk of schizophrenia spectrum diso

49 eptible to infection with RhCMV early in the second trimester and that intrauterine infection results

50 he first trimester with 26.1 to 36.1% in the second trimester and to 51.2% in the third trimester of

51 for subjects with exposure to famine in the second trimester and was increased significantly for sub

52 dence interval [CI], -32 to -1 g) during the second trimester and weighed 74 g less (95% CI, -140 to

53 globin <11.0 g/dL in first and <10.5 g/dL in second trimester) and iron deficiency (ID) by the iron i

54 0 (95% CI 0-6.49) after an infection in the second trimester, and 0 (95% CI 0-11.95) after an infect

55 egnancy, 18 in the first trimester, 4 in the second trimester, and 1 in the third trimester.

56 ted in the first trimester, 8 (33.3%) in the second trimester, and 2 (8.3%) in the third trimester.

57 first trimester, 52% after infection in the second trimester, and 29% after infection in the third t

58 part of the first trimester, 8.5E-03 in the second trimester, and 5.1E-03 in the third trimester.

59 s increased substantially from early to late second trimester, and a shift was observed from 1-->4/1-

60 in the first trimester, by 350 kcal/d in the second trimester, and by 500 kcal/d in the third trimest

61 sis and deep anemia occur, especially in the second trimester, and endoscopic screening should be rec

62 ed intraperitoneally with RhCMV early in the second trimester, and pregnancies were terminated by hys

63 diverge and become nonoverlapping during the second trimester, and the generation of the intestinal g

64 eased mortality rate up to the middle of the second trimester, and then the mortality rate switched d

65 ns for three-months preconception, first and second trimester, and whole-pregnancy averages.

66 microGy, first trimester; 7.9-76.7 microGy, second trimester; and 51.3-130.8 microGy, third trimeste

67 facial dysmorphism, which was diagnosed on a second-trimester antenatal real-time three-dimensional u

68 in concentrations >120 g/L at the end of the second trimester are associated with a </=3-fold increas

69 n levels in mantle dentine formed during the second trimester (as (55)Mn:(43)Ca area under curve) wer

70 rolled at prenatal care clinics during their second trimester, at which time blood, stool, urine, and

71 ne (SVZ) expanded massively during the early second trimester, becoming densely populated with neural

72 ared with fetuses diagnosed with CHDs in the second trimester between 2007 and 2013.

73 abolism were measured from random nonfasting second-trimester blood samples.

74 lities, is most often identified in the late second trimester, carries a substantial mortality in the

75 The second trimester cells also engrafted secondary recipien

76 exposures (OR = 2.0; 95% CI: 1.1, 3.6), and second-trimester chlorpyrifos applications (OR = 3.3; 95

77 and child's age and sex, the top quartile of second-trimester choline intake was associated with a ch

78 me exercise (> or = 60 days in the first and second trimesters combined) had a protective effect on p

79 rotective against low weight gain during the second trimester compared with multivitamins alone.

80 were apparent early in pregnancy, during the second trimester: compared with uninfected women, women

81 placenta, yet little is known regarding the second-trimester decidual environment.

82 Yet, administration of alpha-GalCer in the second trimester did not cause pregnancy loss.

83 Second-trimester diet was assessed by food frequency que

84 We assessed first- and second-trimester diet with the use of food-frequency que

85 To characterize the differences between second trimester Down syndrome (DS) and euploid fetuses,

86 Women's second trimester EPDS scores negatively correlated with

87 -based vitamin D intake during the first and second trimesters (equivalent to the amount of vitamin D

88 In adjusted models, second-trimester exposure to UFPs (hazard ratio per inte

89 lbirth risk, and preconception and first and second trimester exposures were not.

90 tation < 37 weeks) births for the first- and second-trimester exposures in a logistic mixed model, an

91 ptomic changes were shared across first- and second-trimester exposures, including for the top differ

92 imaging presentation of CPAM type II in the second trimester, extensively involving all lobes of the

93 ssion was significantly reduced in first and second trimester fetal cerebral cortex compared with adu

94 site structures than those seen in first and second trimester fetal tissues.

95 with childhood kidney volume, whereas higher second trimester fetal weight was positively associated

96 cant effect on ZNF804A allelic expression in second-trimester fetal brain, with the schizophrenia ris

97 ells are the predominant blood subset in the second-trimester fetus, whereas Vdelta1(+) and Vdelta3(+

98 Our analyses of second trimester fetuses exposed at the time of meiotic

99 Second-trimester fetuses diagnosed with a CHD between 20

100 Second-trimester fetuses with trisomy 21 have a signific

101 Maternal exposure to second-trimester fever was associated with increased ASD

102 Studies were included if they recorded second-trimester findings of ultrasonographic markers, c

103 re likely to be managed operatively in their second trimester (First 43.9%, Second 59.1%, Third 34.2%

104 the authors studied associations of maternal second-trimester fish intake and erythrocyte mercury lev

105 edia of mixed cortical primary cultures from second trimester foetuses with Down syndrome (Down syndr

106 nd showed highest levels at the start of the second trimester followed by a gradual decline through t

107 III (532 fetuses diagnosed with a CHD in the second trimester from 1996 to 2001, the period before fi

108 The spectrum of CHDs seen in the second-trimester groups differed after first-trimester s

109 inferiority study comparing the influence of second-trimester (GW 13-25) vs third-trimester (>/=GW 26

110 were screened in the MIHP by the end of the second trimester had lower odds of VLBW (odds ratio [OR]

111 uman semilunar valve leaflets from first and second trimester hearts.

112 We isolated EVs from second trimester human cytotrophoblasts (CTBs) by differ

113 -immunopanned oligodendrocytes isolated from second trimester human fetal spinal cord.

114 nvestigate the development of these cells in second trimester human fetal tissues.

115 and tissue levels of endogenous steroids in second trimester human fetuses using multidimensional an

116 Functional in vitro assays showed that second-trimester human decidua conditioned medium stimul

117 -to-noise-ratio DTI data of fixed tissues of second-trimester human fetal brains were acquired and an

118 vivo transplantation model by transplanting second-trimester human fetal heart tissues s.c. into the

119 y initiated molecular cytogenetic studies of second-trimester human fetal ovaries, allowing us to dir

120 ch the brain is developmentally similar to a second-trimester human fetus.

121 Already in second-trimester human skin, the phenotype of blood and

122 The second-trimester IL-8 levels in mothers of offspring wit

123 Periodontal therapy during the second trimester improves maternal oral health but fails

124 wing i.v. rhCMV inoculation during the early second trimester in two of three rhCMV-seronegative preg

125 spectrum of CHDs diagnosed in the first and second trimesters in the same time period differed signi

126 In the second trimester, inadequate GWG was predicted with a se

127 exposure (> or = 70 microg/liter) during the second trimester increased the risk of term low birth we

128 In the second trimester, increased O(2) tension promotes protea

129 Mean second-trimester intakes were 328 (standard deviation (S

130 ry adverse consequences of DS evident in the second trimester, leading to testable hypotheses about p

131 g toward the tip along the fibrosal layer in second trimester leaflets.

132 High-activity lupus in the first and second trimesters led to a 3-fold increase in pregnancy

133 e did not see any consistent associations of second trimester levels of either alpha-T or gamma-T wit

134 goal of this study was to determine whether second-trimester levels of four cytokines-interleukin-8

135 ifications to assess the association between second-trimester levels of maternal serum alpha-fetoprot

136 ry in a previous pregnancy of preterm birth, second trimester loss, preterm premature fetal membrane

137 nd early pregnancy outcomes in the first and second trimester (<24 weeks of gestation)?

138 such as the Integrated test using first and second trimester markers.

139 Second trimester maternal plasma alpha-T concentration w

140 There is a direct association between second-trimester maternal serum alpha-fetoprotein levels

141 ernal age alone, 60-70% for maternal age and second-trimester maternal serum biochemical testing, 75%

142 k group by a combination of maternal age and second-trimester maternal serum biochemistry gives a det

143 schizoaffective disorder) who had available second-trimester maternal serum samples.

144 Early second-trimester maternal Tdap immunization significantl

145 A thickened nuchal fold in the second trimester may be useful in distinguishing unaffec

146 t obstruction, early intervention during the second trimester may prevent the development of ventricu

147 Second trimester median PlGF was 31% lower at 14 weeks (

148 revious pregnancy also was terminated in the second trimester medically due to the ultrasound diagnos

149 ate first trimester MIA (n = 6), and 2) late second trimester MIA (n = 7).

150 sh whether antibiotic treatment early in the second trimester might reduce these risks in a general o

151 omatic coronavirus disease who experienced a second-trimester miscarriage in association with documen

152 ere not associated with an increased risk of second-trimester miscarriage.

153 d with a significant increase in the risk of second trimester miscarriages.

154 could also be detected at high frequency in second-trimester mucosal tissues (e.g., the intestine an

155 ere obtained in early pregnancy (n = 1), the second trimester (n = 2), and the third trimester (n = 3

156 lammation (IAI), we studied 301 women during second trimester (n = 39), third trimester (n = 40), and

157 adder, and amniotic fluid of miniature pigs (second trimester, n = 2; third trimester, n = 2).

158 ward flow velocity increased, peaking in the second trimester (nonsignificant), but returned to basel

159 = 1.12, 95% confidence interval: 0.79, 1.59; second trimester odds ratio = 1.30, 95% confidence inter

160 the lateral ganglionic eminence late in the second trimester of development (23-24 weeks postconcept

161 t to the facial skin of human fetuses in the second trimester of development.

162 ve decrease in ZNF804A expression during the second trimester of fetal brain development.

163 l and paternal psychological distress at the second trimester of gestation and 3 years after delivery

164 ventricular zone of human fetal brain at the second trimester of gestation and to study their progeny

165 stress) was obtained by questionnaire in the second trimester of gestation by using the Brief Symptom

166 fferentially to cortical neurogenesis at the second trimester of gestation in human cerebral cortex.

167 zations in the human fetal cortex during the second trimester of gestation.

168 and in human brain tissue from the first and second trimester of gestation.

169 abundant in the airway epithelium during the second trimester of human development than after birth.

170 During the second trimester of human fetal development, neural stru

171 sidered comparable with exposure late in the second trimester of humans.

172 th higher maternal glucose levels during the second trimester of pregnancy (2-h glucose after the ora

173 that syncytiotrophoblasts isolated from the second trimester of pregnancy also constitutively releas

174 Serum samples were collected during the second trimester of pregnancy and analyzed for levels of

175 t count of greater than 150 x 10(9)/L by the second trimester of pregnancy and only 2% of term infant

176 We found that in the second trimester of pregnancy and postpartum women did n

177 atio of omega-6-to-omega-3 PUFAs in the late-second trimester of pregnancy are associated with less w

178 Vitamin D supplementation from the second trimester of pregnancy did not influence maternal

179 Women given albendazole in the second trimester of pregnancy had a lower rate of severe

180 serum level of alpha-fetoprotein during the second trimester of pregnancy is a marker of placental d

181 amined the effects of cocaine use during the second trimester of pregnancy on cerebral neocortical vo

182 d nitrogen dioxide, UFPs exposure during the second trimester of pregnancy remained positively associ

183 ) or matched placebo (n=1205) daily from the second trimester of pregnancy until delivery.

184 ids, especially 16:1t and 18:2tc, during the second trimester of pregnancy was associated with greate

185 pecific maternal serum IgG levels during the second trimester of pregnancy were evaluated in relation

186 ing before pregnancy and during the first or second trimester of pregnancy with preterm birth in a la

187 echocardiography is usually done during the second trimester of pregnancy, but waiting until that ti

188 rette consumption during either the first or second trimester of pregnancy, even as low as 1-2 cigare

189 trophoblast cell line (HTR8), from first and second trimester of pregnancy, express receptors relevan

190 mation and reorganization is apparent in the second trimester of pregnancy, making it a crucial and v

191 orionic gonadotropin was measured during the second trimester of pregnancy, seeking information about

192 ies visualized on ultrasound scan during the second trimester of pregnancy.

193 ted food frequency questionnaires during the second trimester of pregnancy.

194 case when cessation occurred in the first or second trimester of pregnancy.

195 experienced intrauterine fetal demise in the second trimester of pregnancy.

196 syndrome is now routinely offered during the second trimester of pregnancy.

197 cy cohort using a 3-d food record during the second trimester of pregnancy.

198 -369.1) given ZIKV infection in the first or second trimester of pregnancy; however, because ZIKV inf

199 ous group of 448 women was followed from the second trimester of their first pregnancy.

200 ealing occurs in fetal skin in the first and second trimesters of development.

201 12, betaine, and folate during the first and second trimesters of pregnancy and offspring visual memo

202 ures of maternal intake during the first and second trimesters of pregnancy and serum 25-hydroxyvitam

203 de screening and treatment) in the first and second trimesters of pregnancy compared to the third tri

204 tritional deficiency during the first and/or second trimesters of pregnancy exhibited increased risk

205 rentiation and invasion during the first and second trimesters of pregnancy were associated with down

206 ternal uterine arteries during the first and second trimesters of pregnancy.

207 uency questionnaire in each of the first and second trimesters of pregnancy.

208 ed with dichorionic twin fetal growth in the second trimester only, driven by an association with AC

209 In contrast, bleeding in the second trimester only, of a single episode, on a single

210 g/m(3) increase in PM2.5 exposure during the second trimester only, which remained unchanged after ad

211 Recommending immunization from the second trimester onward would widen the immunization opp

212 ith fetal growth was observed from the early second trimester onwards, while no major growth deficit

213 recommend a monthly dose of IPTp-SP from the second trimester onwards.

214 (first trimester OR, 5.1; 95% CI, 1.9-13.2; second trimester OR, 0.5; 95% CI, 0.2-1.2; and third tri

215 t trimester (OR = 1.93; 95% CI: 1.55, 2.40), second trimester (OR = 1.67; 95% CI: 1.35, 2.08), third

216 es demonstrate high expression in first- and second-trimester placenta, specifically in EVTs and sync

217 First and second trimester placental tissues from normal pregnanci

218 lines were generated by isolating first and second trimester placental villous cytotrophoblasts foll

219 -3 (n-3) and omega-3 (n-6) PUFAs measured in second-trimester plasma; n-6/n-3 ratios were calculated.

220 Second trimester PlGF measurements are of limited value.

221 We used residential addresses to estimate second-trimester PM2.5 and black carbon exposure via a c

222 ght, P < 0.0007, and 1-kg weight gain in the second trimester predicted a 26-g increase in newborn we

223 nders, maternal weight gain in the first and second trimesters predicted newborn weight (1-kg weight

224 other hand, preterm cervical ripening in the second trimester predicts preterm birth.

225 umbilical cord serum collected from elective second trimester pregnancy terminations.

226 We present a case of second trimester pregnancy with symptomatic COVID-19 com

227 ratio, 4.68; 95% CI, 3.74 to 5.86); loss of second-trimester pregnancy, 16.4% vs. 1.7% (hazard ratio

228 PBDEs and their metabolites (OH-PBDEs) among second trimester pregnant women recruited from San Franc

229 een intra-amniotic U. urealyticum in healthy second-trimester pregnant women and subsequent pregnancy

230 Second-trimester prenatal ultrasound is widely used in a

231 y low-dose aspirin beginning as early as the second trimester prevented clinically important health o

232 1-SD (0.36 g . kg(-1) . d(-1)) increment in second-trimester protein intake corresponded to a -0.10

233 Mean (range) second-trimester protein intake was 1.4 g . kg(-1) . d(-

234 ys through 13 weeks 6 days of gestation) and second-trimester quadruple screening (measurement of alp

235 ning at 11 weeks of gestation is better than second-trimester quadruple screening but at 13 weeks has

236 at 11, 12, and 13 weeks, respectively; with second-trimester quadruple screening, 81 percent; with s

237 ening but at 13 weeks has results similar to second-trimester quadruple screening.

238 cohort, we examined associations of maternal second trimester red blood cell mercury (RBC-Hg) concent

239 nulliparous women with a short cervix in the second trimester require further exploration.

240 R) for 1 mug/L=1.05; 95% CI: 1.00, 1.11] and second trimesters (RR for 1 mug/L=1.03; 95% CI: 1.00, 1.

241 gnancies; two LB (no malformations), and one second trimester SA.

242 in isolation or with bacteria in first- and second-trimester samples.

243 ial was conducted to evaluate the effects of second-trimester scaling and root planing and the use of

244 We did second-trimester scans and neonatal follow-up for the wo

245 tuses we diagnosed small muscular VSD on the second-trimester scans.

246 Second trimester screening for Down's syndrome is widely

247 adruple test should be the test of choice in second trimester screening for Down's syndrome.

248 iocentesis, or 3 times greater if they had a second trimester screening test (Quadruple test) and tre

249 itive rate) and is more effective than other second trimester screening tests.

250 mester (Group I, 127 fetuses) or only in the second-trimester screening (Group II, 344 fetuses), were

251 erform first-trimester screening, to perform second-trimester screening, or to use strategies incorpo

252 rations of 10 BFRs were measured in maternal second trimester serum samples stored from routine scree

253 Maternal second-trimester serum levels of IL-8, IL-1beta, IL-6, a

254 PCB congeners and 2 OCPs measured in banked second-trimester serum samples were compared between the

255 vaginosis with oral clindamycin early in the second trimester significantly reduces the rate of late

256 Second-trimester spatiotemporal exposures ranged from 8.

257 On the basis of second-trimester-specific guidelines, inadequate GWG can

258 A second-trimester stillbirth occurred during the course o

259 rofiles of progenitors between the first and second trimesters suggest that these cells had gestation

260 Especially in the second trimester, symptoms such as nausea and vomiting,

261 bacteria were detected more often during the second trimester than during the first--Ureaplasma ureal

262 01), whereas for those who smoked during the second trimester, the corresponding ORs were 1.37 (1.35-

263 In the second trimester, the estimated mean (+/-SD) total trans

264 sease and acute leukemia diagnosed after the second trimester, therapeutic termination of the pregnan

265 ause of the exposure to antimalarials in the second trimester, there were limited numbers of malaria

266 )) increase in PM2.5 in the first trimester, second trimester, third trimester, and whole pregnancy w

267 high supplemental folic acid intakes in the second trimester, those with the lowest tertile of vitam

268 eived saline injections at the same first or second trimester time points or were untreated.

269 Women were randomized during their second trimester to blinded weekly doses of placebo or 4

270 y Doppler ultrasound is commonly used in the second trimester to identify pregnancies destined to dev

271 mester fetal sheep previously exposed in the second trimester to maternal alcohol "binges" (1.5 g/kg

272 of uterine artery resistance index from the second trimester to the third were associated with the r

273 nd lifestyle characteristics, track from the second trimester to the third, and are associated with t

274 haracteristics and track moderately from the second trimester to the third.

275 We performed similar analyses with maternal second trimester tocopherol isoform levels.

276 r dust samples and mother's blood during the second trimester; umbilical cord blood at birth; and she

277 5% increase in odds of preterm birth, while second-trimester unemployment was associated with a 3% d

278 en antibodies were present from early in the second trimester until term.

279 sed in utero arsenic exposure using maternal second-trimester urinary arsenic, maternal prepregnancy

280 ds ratio=0.77, 95% CI=0.43-1.36), first- and second-trimester use (odds ratio=0.84, 95% CI=0.40-1.77)

281 ds ratio=0.56, 95% CI=0.25-1.24), first- and second-trimester use (odds ratio=0.90, 95% CI=0.37-2.17)

282 ated risk increase for Caucasians during the second trimester was 37% (95% CI: 0.80, 2.36), while for

283 Dietary intake during the second trimester was assessed with a food-frequency ques

284 l proximity to methyl bromide use during the second trimester was associated with markers of restrict

285 ing untreated genital herpes during first or second trimester was associated with more than double th

286 Higher maternal wheat intake during the second trimester was associated with reduced atopic derm

287 no use) within 5 km of the home during the second trimester was negatively associated with birth we

288 NO2 in the second trimester was negatively associated with spontane

289 rsenic measured in maternal urine during the second trimester was not associated with methylation in

290 otal trans fatty acid consumption during the second trimester was positively associated with the feta

291 l weight gain from 14 to 20 and 21 to 27 wk (second trimester) was significantly associated with incr

292 tionnaires administered during the first and second trimesters, we assessed maternal intake of common

293 Blood TCM concentrations in the second trimester were associated with an elevated risk o

294 folate and maternal supplement intake during second trimester were associated with higher cord UMFA.

295 the women who contracted ZVD in the first or second trimester were still pregnant at the time of this

296 ations between GWG beginning as early as the second trimester with fetal cord blood leptin and strong

297 concentrations were lowest in the first and second trimesters with levels comparable to those observ

298 nd 2 with PET/CT), 2 were scanned during the second trimester (with PET/MR imaging), and 1 was scanne

299 e acetylcholinesterase inhibitors during the second trimester, with hazard ratios of 1.3 (95% confide

300 ounger than 8 GW, older than 10-12 GW, or in second trimester xenografted testes (14-17 GW).