ライフサイエンスコーパス: chorionic

1 The Drosophila eggshell, which has a pair of chorionic appendages (dorsal appendages) located asymmet

2 alysis confirmed AP-2alpha variants in ovine chorionic binucleate cell nuclear extracts, one of which

3 DNase I protection analysis using ovine chorionic binucleate cell nuclear protein, identified 19

4 ormone/prolactin gene family, is produced by chorionic binucleate cells at the maternal-fetal interfa

5 ent transactivation of the oPL gene in ovine chorionic binucleate cells.

6 al membranes, is expressed by leukocytes and chorionic cytotrophoblast cells.

7 eak extra-embryonic ectoderm and late-streak chorionic ectoderm - were microdissected into fractions

8 f the ectoplacental cavity via union between chorionic ectoderm and the ectoplacental cone, a decline

9 ning proliferation throughout the developing chorionic ectoderm and, thus, in supporting its stem cel

10 cone, a decline in the frequency of mitotic chorionic ectoderm cells in vivo, and of trophoblast ste

11 ential increased steadily in extra-embryonic/chorionic ectoderm until the first somite pairs formed,

12 e distributed throughout the extra-embryonic/chorionic ectoderm, an observation that is probably attr

13 AP-2alpha was localized in ovine chorionic epithelial cells by immunohistochemistry and a

14 e, we propose that the presence of placental chorionic fusion and the exchange of cell lines between

15 othesize that IL-22 cytokine produced by the chorionic girdle binds IL-22R1 on endometrium, serving a

16 triking increase in IL-22 mRNA expression in chorionic girdle from days 32 to 35 and an absence of IL

17 Our discovery of IL-22 in the chorionic girdle is a novel finding, as this cytokine ha

18 ation of mRNA encoding the cytokine IL-22 in chorionic girdle relative to noninvasive chorion.

19 e used to verify high expression of IL-22 in chorionic girdle.

20 experiments showed that treatment with human chorionic gonadatropin (hCG) prevented death and the exp

21 o regulate expression of the placental human chorionic gonado-tropin (hCG) alpha- and beta-subunit ge

22 ermine the modulation of uterine function by chorionic gonadotrophin (CG) in a nonhuman primate.

23 MP4-treated cells form syncytia that express chorionic gonadotrophin (CG).

24 High-affinity binding of LH and human chorionic gonadotrophin (hCG) causes secondary hormone o

25 mor marker alpha-fetoprotein (AFP) and human chorionic gonadotrophin (HCG) during the first two cycle

26 onths of trying to conceive or until a human chorionic gonadotrophin (hCG) test confirmed pregnancy.

27 s) of interactions between an antigen, human chorionic gonadotrophin (hCG), and antibodies, anti-alph

28 of mouse cell line-derived recombinant human chorionic gonadotrophin (r-alpha hCG), a protein that is

29 expression of differentiation markers human chorionic gonadotrophin and placental alkaline phosphata

30 placental (i.e., her offspring's) homologous chorionic gonadotrophin beta5 (CGB5) and CSH1 genes and

31 Using primers specific for human chorionic gonadotrophin gene, the presence of human DNA

32 tion provided by alpha-fetoprotein and human chorionic gonadotrophin in the management of germ cell t

33 microg/L; Ca-125 level, 15 U/mL; beta-human chorionic gonadotrophin level < 2 IU/mL).

34 The importance of accurate human chorionic gonadotrophin monitoring and the types of huma

35 adotrophin monitoring and the types of human chorionic gonadotrophin produced in cancer are also topi

36 nant purified beta-arrestin-1 mimicked human chorionic gonadotrophin to promote desensitization of hu

37 um tumor markers alpha-fetoprotein and human chorionic gonadotrophin were correlated with treatment o

38 rker decline (alpha-fetoprotein and/or human chorionic gonadotrophin) during the first two cycles of

39 nce of a variety of sequences, such as human chorionic gonadotrophin, ubiquitin, TFIIA, guanine nucle

40 otrophin to promote desensitization of human chorionic gonadotrophin-stimulated AC activity, in the p

41 of prior therapy (P < .001), baseline human chorionic gonadotropin > or = 1,000 U/L (P = .01), and l

42 ease at the time of GCT diagnosis, and human chorionic gonadotropin >/= 1,000 mIU/mL at initiation of

43 istration of exogenous testosterone or human chorionic gonadotropin (an LH receptor agonist), respect

44 The rate of HBsAg in 6,976 B-human chorionic gonadotropin (B-hCG)-positive specimens, as de

45 iocarcinoma that was confirmed by beta human chorionic gonadotropin (beta-HCG) levels and histopathol

46 ssed for four mRNA tumor markers: beta-human chorionic gonadotropin (beta-hCG), oncogene receptor (c-

47 serum alpha-fetoprotein (AFP) and beta-human chorionic gonadotropin (betaHCG) levels were 483 ng/mL a

48 s, which include the placental hormone human chorionic gonadotropin (CG) and the anterior pituitary h

49 of all mammals, whereas the closely related chorionic gonadotropin (CG) beta subunit genes have been

50 rly pregnancy by the placental production of chorionic gonadotropin (CG) but regresses in the presenc

51 pressing either the luteinizing hormone (LH)/chorionic gonadotropin (CG) or follicle-stimulating horm

52 LH), follicle-stimulating hormone (FSH), and chorionic gonadotropin (CG), are cysteine-knot growth-fa

53 Production of the placental hormone, chorionic gonadotropin (CG), increases dramatically as c

54 The human glycoprotein hormones chorionic gonadotropin (CG), thyrotropin (TSH), lutropin

55 h the production of the glycoprotein hormone chorionic gonadotropin (CG), which is secreted into the

56 Following induction of ovulation by equine chorionic gonadotropin (eCG)/human CG (hCG) treatment an

57 ere alpha-fetoprotein (AFP) 2.0 ng/mL, human chorionic gonadotropin (hCG) 151,111 IU/L, and lactate d

58 Previous studies on human chorionic gonadotropin (hCG) and human follicle-stimulat

59 chimeras of two glycoprotein hormones, human chorionic gonadotropin (hCG) and human follitropin (hFSH

60 by adrenocorticotropic hormone (ACTH), human chorionic gonadotropin (hCG) and oestrogen, and in the l

61 In contrast, human chorionic gonadotropin (hCG) and other glycoprotein horm

62 noassays for two model cancer markers, human chorionic gonadotropin (hCG) and prostate specific antig

63 Bovine lutropin (bLH) and human chorionic gonadotropin (hCG) are heterodimeric glycoprot

64 Human luteinizing hormone (hLH) and human chorionic gonadotropin (hCG) are human glycoprotein horm

65 Using human chorionic gonadotropin (hCG) as a model analyte to descr

66 Human chorionic gonadotropin (hCG) binds to the exodomain, and

67 Human chorionic gonadotropin (hCG) binds to the extracellular

68 Serum human chorionic gonadotropin (hCG) concentration was 200 mIU/m

69 l trophoblastic disease include raised human chorionic gonadotropin (hCG) concentrations 6 months aft

70 we proposed that the pregnancy hormone human chorionic gonadotropin (hCG) efficiently attracts human

71 questioned whether women with PMs need human chorionic gonadotropin (hCG) follow-up.

72 ned by univariate analysis; only serum human chorionic gonadotropin (HCG) had an impact on survival.

73 Human chorionic gonadotropin (hCG) has been shown to reduce th

74 ropin-releasing hormone (GnRH) gene by human chorionic gonadotropin (hCG) in GT1-7 neurons.

75 Treatment with human chorionic gonadotropin (HCG) increased levels of plasma

76 Human chorionic gonadotropin (hCG) induces de novo synthesis o

77 We show that human embryonic chorionic gonadotropin (hCG) induces sequential mRNA exp

78 n immune-compromised mice that secrete human chorionic gonadotropin (hCG) into the host mouse and inc

79 Human chorionic gonadotropin (hCG) is a glycoprotein hormone e

80 Human chorionic gonadotropin (hCG) is a glycoprotein secreted

81 Human chorionic gonadotropin (hCG) is a heterodimeric member o

82 Human chorionic gonadotropin (hCG) is an important biomarker f

83 Human chorionic gonadotropin (hCG) is necessary for the mainte

84 tudies do not establish a single serum human chorionic gonadotropin (hCG) level that is diagnostic of

85 f clinical grade crude preparations of human chorionic gonadotropin (hCG) on Kaposi's sarcoma, HIV, S

86 The impact of human chorionic gonadotropin (hCG) on prostate carcinoma viabi

87 Human chorionic gonadotropin (hCG) preparations contain activi

88 Recent clinical trials with human chorionic gonadotropin (hCG) prepared from early pregnan

89 Human chorionic gonadotropin (hCG) promotes proliferation of e

90 sitivity, affinity and specificity for human chorionic gonadotropin (hCG) protein.

91 The human chorionic gonadotropin (hCG) proteins constitute a diver

92 Treatment of mice with human chorionic gonadotropin (hCG) resulted in increased circu

93 The hormone human chorionic gonadotropin (hCG) serves to maintain the fetu

94 Human chorionic gonadotropin (hCG) suppresses cell-mediated al

95 on the basis of persistently positive human chorionic gonadotropin (hCG) test results in the absence

96 We detect human chorionic gonadotropin (hCG) using an antibody-based san

97 TH gene transcription is stimulated by human chorionic gonadotropin (hCG) via cyclic AMP-induced andr

98 resistance to EMA/CO, and because the human chorionic gonadotropin (hCG) was near normal, they were

99 In the present work human chorionic gonadotropin (hCG) was used as a model protein

100 rat breast cancer model indicate that human chorionic gonadotropin (hCG), a hormone that is present

101 Experimental observations suggest that human chorionic gonadotropin (hCG), a major hormone of pregnan

102 Results of recent studies suggest that human chorionic gonadotropin (HCG), a placental glycoprotein h

103 rs, human C-reactive protein (CRP) and human chorionic gonadotropin (hCG), by using fluorescent-label

104 s pregnancy-related hormones including human chorionic gonadotropin (hCG), estrogen, progesterone, an

105 e mechanisms of the human pregnancy hormone, chorionic gonadotropin (hCG), in the liver.

106 express a surface feature that mimics human chorionic gonadotropin (hCG), the cognate ligand for LHr

107 pha-fetoprotein, unconjugated estriol, human chorionic gonadotropin (hCG), the free beta subunit of h

108 rthermore, using the mediator molecule human chorionic gonadotropin (hCG), we interface the intracell

109 zes the peptide GVLPALPQV derived from human chorionic gonadotropin (hCG)-beta.

110 f the conceptus during implantation is human chorionic gonadotropin (hCG).

111 verified for the efficient binding of Human Chorionic Gonadotropin (hCG).

112 oma cells before and after exposure to human chorionic gonadotropin (hCG).

113 wo antigen/antibody pairs were investigated: chorionic gonadotropin (hCG)/mouse monoclonal anti-hCG a

114 y constrained than the beta-subunit of human chorionic gonadotropin (hCG-beta).

115 lactate dehydrogenase (LDH; .0001) and human chorionic gonadotropin (HCG; .0001).

116 and the intracellular beta subunit of human chorionic gonadotropin (hCGbeta) and peroxisome prolifer

117 t with induction of aromatase (hCYP19A1) and chorionic gonadotropin (hCGbeta) expression.

118 Activation of the luteinizing hormone/human chorionic gonadotropin (LH/hCG) receptor (LHR) in cultur

119 the regulation of luteinizing hormone/human chorionic gonadotropin (LH/hCG) receptor mRNA stability

120 The luteinizing hormone/human chorionic gonadotropin (LH/hCG) receptor, which belongs

121 eta-subunit of macaque (Macaca fascicularis) chorionic gonadotropin (mCG-beta) is more conformational

122 increased alpha fetoprotein (n = 18), human chorionic gonadotropin (n = 5), or both (n = 2); nine ha

123 hree markers (alpha-fetoprotein [AFP], human chorionic gonadotropin [hCG], and lactate dehydrogenase

124 the gonadotropin hormone alpha-subunit gene, chorionic gonadotropin alpha (Cga), is responsible for C

125 Antibodies to human serum albumin and chorionic gonadotropin also developed.

126 nt mare serum gonadotropin followed by human chorionic gonadotropin also stimulated cumulus expansion

127 n an increased blood level of the beta human chorionic gonadotropin and a histopathological examinati

128 day on days 1, 8, and 15]), patients' human chorionic gonadotropin and alfa-fetoprotein concentratio

129 Patients with a favourable decline in human chorionic gonadotropin and alfa-fetoprotein continued BE

130 be induced by two placental hormones: human chorionic gonadotropin and human chorionic somatotropin

131 ignificantly, directly associated with human chorionic gonadotropin and inversely with estrone-3-gluc

132 Increased leptin levels, as well as human chorionic gonadotropin and luteinizing hormone receptors

133 two maternal serum hormones, free beta-human chorionic gonadotropin and pregnancy-associated plasma p

134 rnal age, maternal levels of free beta human chorionic gonadotropin and pregnancy-associated plasma p

135 rnal age, maternal levels of free beta human chorionic gonadotropin and pregnancy-associated plasma p

136 cessful (91 percent), the mean (+/-SD) serum chorionic gonadotropin and progesterone concentrations w

137 y, biochemically (by the production of human chorionic gonadotropin and progesterone), and immunohist

138 Pretreatment serum concentrations of human chorionic gonadotropin and progesterone, the size and vo

139 ing levels of the free beta subunit of human chorionic gonadotropin and stillbirth risk.

140 ted protein domains (F(c)) of two anti-human chorionic gonadotropin antibodies were proteolytically r

141 H), luteotropin (LH), follitropin (FSH), and chorionic gonadotropin are members of the heterodimeric

142 Measurements of serum chorionic gonadotropin are of little clinical value for

143 nt of effective treatments, the use of human chorionic gonadotropin as a biomarker, and centralisatio

144 firm the primary site and the level of human chorionic gonadotropin as independent factors.

145 [PAPP-A], and the free beta subunit of human chorionic gonadotropin at 10 weeks 3 days through 13 wee

146 nizes the GVL peptide (GVLPALPQV) from human chorionic gonadotropin beta presented by the peptide-HLA

147 Disrupting disulfide loops in the human chorionic gonadotropin beta subunit (CGbeta) inhibits co

148 Co-expression of the wild-type chorionic gonadotropin beta subunit with double cysteine

149 urothelial carcinoma-associated 1 and human chorionic gonadotropin beta type II genes.

150 ellular kinetic folding pathway of the human chorionic gonadotropin beta-subunit (hCG-beta) reveals t

151 ity to secretion and assembly with the human chorionic gonadotropin beta-subunit (hCG-beta).

152 ons of trophoblast cells that produce equine chorionic gonadotropin between days 40 and 120 of normal

153 d signaling despite moderate levels of human chorionic gonadotropin binding in transfected cells.

154 treatment with a desensitizing dose of human chorionic gonadotropin caused transcriptional down-regul

155 with tubal ectopic pregnancies, a high serum chorionic gonadotropin concentration is the most importa

156 ion analysis revealed the pretreatment serum chorionic gonadotropin concentration to be the only fact

157 There was no relation between higher serum chorionic gonadotropin concentrations and the risk of ge

158 Higher serum chorionic gonadotropin concentrations were associated wi

159 Higher serum chorionic gonadotropin concentrations were associated wi

160 tant receptors and is dependent on the human chorionic gonadotropin dose, the surface concentration o

161 pre-mRNA encoding the beta-subunit of human chorionic gonadotropin gene 6 and pre-trans-splicing mol

162 CSF levels of alpha-fetoprotein or betahuman chorionic gonadotropin had normalization with chemothera

163 onography and sensitive tests for beta-human chorionic gonadotropin have evolved, the presentation of

164 s and real immunorecognition assays of human chorionic gonadotropin hormone are well below the visual

165 a single-copy equine (e) luteinizing hormone/chorionic gonadotropin hormone beta subunit gene (eLH/CG

166 include genes located in the promoter of two chorionic gonadotropin hormone genes.

167 mplantation was defined by the appearance of chorionic gonadotropin in maternal urine.

168 e in three, alpha-fetoprotein and beta human chorionic gonadotropin in one) suffered a relapse, compa

169 chimeric receptor could not respond to human chorionic gonadotropin in producing cAMP, co-expression

170 Synthesis and secretion of chorionic gonadotropin in trophoblast cells of the place

171 Human chorionic gonadotropin increased GRTH gene expression an

172 Chorionic gonadotropin is a heterodimeric glycoprotein h

173 Maternal serum chorionic gonadotropin is measured to screen for fetal c

174 l/L]), and serum alpha-fetoprotein and human chorionic gonadotropin levels were normal.

175 d six weeks or more, the first appearance of chorionic gonadotropin occurred 6 to 12 days after ovula

176 stillbirth (odds ratio for every increase in chorionic gonadotropin of 1 multiple of the median, 1.4;

177 oprotein of 100 ng/mL or greater or of human chorionic gonadotropin of 5,000 U/L or greater (group B)

178 cal evidence and highly elevated serum human chorionic gonadotropin or alfa-fetoprotein concentration

179 hem either after the administration of human chorionic gonadotropin or during the physiologic rise in

180 ts expression is increased 2.5-fold by human chorionic gonadotropin over a 12-h period.

181 Treatment of Leydig cells with human chorionic gonadotropin rapidly induced free radical, PBR

182 tide and two subunits), whereas the lutropin/chorionic gonadotropin receptor (LH/CGR) is a single cha

183 helix (TM3) of the luteinizing hormone/human chorionic gonadotropin receptor (LH/hCGR) in regulating

184 The luteinizing hormone/human chorionic gonadotropin receptor (LH/hCGR) undergoes palm

185 ly as an agonist for the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) and suggested to

186 The luteinizing hormone chorionic gonadotropin receptor (LHCGR) is a G(s)-couple

187 The luteinizing hormone/chorionic gonadotropin receptor (LHR) is a heptahelical

188 alized expression of the luteinizing hormone/chorionic gonadotropin receptor, PROK1, PROKR1, and LIF

189 assay) was inhibited by 57 %, and both human chorionic gonadotropin secretion and L-leucine influx th

190 ed CTBs in low oxygen leads to reduced human chorionic gonadotropin secretion and STB-associated gene

191 h WT mice by both in vivo and in vitro human chorionic gonadotropin stimulation.

192 e was defined as a negative serum beta-human chorionic gonadotropin test (beta-hCG < 6 IU/L) 17 days

193 eriod, and a combination of a positive human chorionic gonadotropin test and an outpatient obstetric

194 of a pregnancy outcome was a positive human chorionic gonadotropin test; least predictive was an obs

195 ncy by interview and selective urinary human chorionic gonadotropin tests.

196 acts independently or additively with human chorionic gonadotropin to enhance androstenedione secret

197 pply this platform to the detection of human chorionic gonadotropin using surface plasmon resonance.

198 of the risk of an adverse outcome than serum chorionic gonadotropin values.

199 GRTH is transcriptionally up-regulated by chorionic gonadotropin via cyclic AMP-induced androgen f

200 pecimens for up to 1 year, and urinary human chorionic gonadotropin was assayed to detect conception

201 Daily urinary human chorionic gonadotropin was assayed to detect conception

202 Daily urinary human chorionic gonadotropin was assayed to detect conception

203 al records of 28,743 girls and women in whom chorionic gonadotropin was measured during the second tr

204 Using purified plasma membranes, human chorionic gonadotropin was similarly observed to have no

205 istologic subtype and increase of beta-human chorionic gonadotropin were not significantly correlated

206 For anti-hCG (human chorionic gonadotropin) mAb 8F11, studied at two incorpo

207 f tumor markers (alpha fetoprotein and human chorionic gonadotropin), and imaging.

208 n harbors positional candidate genes such as chorionic gonadotropin, alpha chain; collagen, type XIX,

209 Thyroid function, human chorionic gonadotropin, and estradiol were measured befo

210 -linked sugar chains found in fetuin, equine chorionic gonadotropin, and glycophorin can be analyzed

211 pregnancy, serum concentration of beta-human chorionic gonadotropin, and stage of disease, with both

212 ic glycoprotein substrates by agalacto human chorionic gonadotropin, comprising 29 nM for beta4GalNAc

213 , cortisol, and reproductive hormones (human chorionic gonadotropin, estradiol, progesterone, human p

214 urine samples were collected to assess human chorionic gonadotropin, estrone-3-glucuronide, and pregn

215 detection of three markers: beta-chain human chorionic gonadotropin, hepatocyte growth factor recepto

216 of a set of three fertility hormones: human chorionic gonadotropin, human luteinizing hormone, and f

217 pharmacologically rescued by exogenous human chorionic gonadotropin, indicating that LH-responsivenes

218 used to bind the glycoprotein hormone, human chorionic gonadotropin, produced during normal pregnancy

219 ver time, produce extensive amounts of human chorionic gonadotropin, progesterone, placental growth f

220 n a modified commercial strip test for human chorionic gonadotropin, the hormone used to detect pregn

221 easurement of alpha-fetoprotein, total human chorionic gonadotropin, unconjugated estriol, and inhibi

222 block release of the secreted protein human chorionic gonadotropin-alpha.

223 ered hCG-SNAP fusion reporter protein (human chorionic gonadotropin-O(6) -alkylguanine-DNA alkyltrans

224 The human chorionic gonadotropin-stimulated phosphorylation of ERK

225 rogen and progesterone metabolites and human chorionic gonadotropin.

226 ociated with the beta-core fraction of human chorionic gonadotropin.

227 ly levels of estrone-3-glucuronide and human chorionic gonadotropin.

228 the day of induction of ovulation with human chorionic gonadotropin.

229 ein hormone alpha subunit gene, a subunit of chorionic gonadotropin.

230 ng hormone, thyroid-stimulating hormone, and chorionic gonadotropin.

231 by high circulating concentrations of human chorionic gonadotropin.

232 ndant in the serum and ovaries of beta-human chorionic growth hormone-stimulated frogs.

233 occurs fully when the embryos hatch from the chorionic membrane and encounter normal oxidative stress

234 rom the endometrial stalk (maternal side) to chorionic plate (fetal side).

235 Chorionic plate and myometrial artery relaxation was inc

236 Chorionic plate arteries from full-term placentas and sp

237 genitors of fetal origin were present in the chorionic plate of the placenta before the onset of feto

238 al expression and that inflammatory cells in chorionic plate or umbilical cord blood vessel walls be

239 Adequate blood flow through placental chorionic plate resistance arteries (CPAs) is necessary

240 ly expressed in ectoplacental cone cells and chorionic plate, and later in the labyrinthine trophobla

241 itor tissue of the umbilical cord), with the chorionic plate.

242 ired for normal organization of cells in the chorionic plate.

243 Human chorionic somatomammotropin (CS) and placental growth ho

244 previously reported placenta elements TSE or chorionic somatomammotropin enhancer factor 1 (CSEF-1) m

245 ropes, whereas the remaining four genes, the chorionic somatomammotropin genes (hCS-L, hCS-A, and hCS

246 , mammalian muscle-specific genes, and human chorionic somatomammotropin genes.

247 ones: human chorionic gonadotropin and human chorionic somatotropin hormone (CSH) produced by the pla

248 are crucial for development of the anterior chorionic structures.

249 chorionic trophoblast cells, including basal chorionic trophoblast (BCT) cells located at the chorioa

250 transcription factor, is highly expressed in chorionic trophoblast cells, including basal chorionic t

251 s led to a complete loss of undifferentiated chorionic trophoblasts after embryonic day 9.5 and preve

252 sement membranes located at the interface of chorionic trophoblasts and allantoic mesoderm.

253 embryos, however, restored the integrity of chorionic trophoblasts and enabled placental labyrinth f

254 ngly, Arnt-null TS cells differentiated into chorionic trophoblasts and syncytiotrophoblasts, as demo

255 ected in the placental syncytiotrophoblasts, chorionic trophoblasts, decidual cells, and amniotic epi

256 and HAI-1 were expressed in a population of chorionic trophoblasts.

257 V spreads from basal and parietal decidua to chorionic villi and amniochorionic membranes and that ta

258 al cells, fibroblasts, and Hofbauer cells in chorionic villi and amniotic epithelial cells and tropho

259 An increase in the number of chorionic villi and blood vessels over that in controls

260 tly contacts syncytiotrophoblasts that cover chorionic villi and cytotrophoblasts that invade uterine

261 differentiated syncytiotrophoblast (STB) in chorionic villi and extravillous trophoblast (EVT) at th

262 low) and CD34(+)CD45(low)-that were found in chorionic villi and in the chorioamniotic membrane.

263 this hypothesis, we exposed first-trimester chorionic villi and isolated cytotrophoblasts to CMV in

264 und in trophoblasts and endothelial cells of chorionic villi and uterine arteries.

265 es, and inflammatory infiltrate in placental chorionic villi are associated with adverse pregnancy re

266 etal cytotrophoblast stem cells in anchoring chorionic villi become invasive.

267 GF during explant culture of first-trimester chorionic villi enhanced extravillous trophoblast differ

268 Antigens were also seen in chorionic villi of one of the first trimester placentas.

269 alivary glands, uterine decidua, and injured chorionic villi of the placenta, demonstrating both its

270 s present in the syncytiotrophoblasts of the chorionic villi of the rhesus placenta, within villous c

271 either into syncytiotrophoblasts in floating chorionic villi or extravillous trophoblasts (EVTs) at t

272 vering trophoblastic lacunae or newly formed chorionic villi remained largely Mamu-AG-negative.

273 In chorionic villi that were infected with CMV in utero, sy

274 DNA methylation in first-trimester chorionic villi was assessed in chromosomally normal mis

275 placentas and explants from first-trimester chorionic villi with the prototype Ugandan and a recentl

276 In chorionic villi, syncytiotrophoblasts did not become inf

277 yncytiotrophoblasts and cytotrophoblasts, in chorionic villi-in clinical cases of congenital infectio

278 which give rise to the mature cell types of chorionic villi-syncytiotrophoblasts on the surfaces of

279 lasts, infect underlying cytotrophoblasts in chorionic villi.

280 es from cultured lymphocytes, amniocytes, or chorionic villi.

281 vitro culture of explants of human placental chorionic villi.

282 dition, using organotypic human midgestation chorionic villous explants, we show that syncytiotrophob

283 ophan has been studied using human placental chorionic villous explants.

284 cells and in the trophoblast layer of human chorionic villus but not in a gonadotrope cell line that

285 One case of mosaicism in a chorionic villus sample, and two cases indicating somati

286 sector submitted data for amniotic fluid or chorionic villus samples referred from April, 1999, to M

287 Of 34,995 amniotic fluid and 3049 chorionic villus samples that had karyotyping and a rapi

288 amniotic fluid samples and 152 (45%) of 327 chorionic villus samples were associated with a substant

289 1148 amniotic fluid samples, 188 chorionic villus samples, and 37 fetal tissue samples we

290 Of 119,528 amniotic fluid and 23,077 chorionic villus samples, rapid aneuploidy testing repla

291 foetus diagnosed with del(4)(q33) following chorionic villus sampling (CVS) at 14 weeks, and the pre

292 We did a cost-utility analysis of chorionic villus sampling and amniocentesis versus no in

293 e of predisposing gene mutation according to chorionic villus sampling and testing of the neonate's b

294 of fetal cells obtained by amniocentesis or chorionic villus sampling is the current standard for pr

295 use of the cells from the amniotic fluid or chorionic villus sampling that are used for prenatal dia

296 idelines recommend offering amniocentesis or chorionic villus sampling to women aged 35 years or olde

297 d-old embryos, (ii) induced abortions, (iii) chorionic villus sampling, (iv) amniocentesis, and (v) f

298 00) were offered diagnostic amniocentesis or chorionic villus sampling.

299 ages (Hofbauer cells) that reside within the chorionic villus stroma.

300 o came to 16 prenatal diagnostic centers for chorionic-villus sampling or early amniocentesis at 9 to