ライフサイエンスコーパス: uterus

1 uential placebo vaginal gel for women with a uterus).

2 ract to expel the fertilized embryo into the uterus.

3 pha-mediated transcription in the breast and uterus.

4 ed when the disease is still confined to the uterus.

5 s with metritis compared to cows with normal uterus.

6 haped left fallopian tube and a normal right uterus.

7 ciency, including the thyroid, prostate, and uterus.

8 e uterus or the presence of a non-functional uterus.

9 extrauterine growth should mimic that in the uterus.

10 s for tumors that have progressed beyond the uterus.

11 d of AA amyloid deposited exclusively in the uterus.

12 of progesterone receptor (PGR) action in the uterus.

13 ntiated leiomyomas at sites distant from the uterus.

14 anism present only in the full-term pregnant uterus.

15 ial tissue in aberrant locations outside the uterus.

16 imination of bacterial biofilm in the equine uterus.

17 receptor cross-talk in vivo is modest in the uterus.

18 rointestinal tract, blood vessels, lung, and uterus.

19 regulation of GPR64 expression in the murine uterus.

20 e to define the FOXA2 cistrome in the murine uterus.

21 red for successful implantation in the mouse uterus.

22 ll and kidneys, followed by the pancreas and uterus.

23 ing to failure in embryo implantation to the uterus.

24 e epithelial and stromal compartments of the uterus.

25 r the pancreas, and 0.030 +/- 0.0034 for the uterus.

26 tract to prevent bacterial infection of the uterus.

27 ulated in PGN+poly(I:C)-treated placenta and uterus.

28 teracting with progesterone receptor (PR) in uterus.

29 nk between stimulus, response, and reward in uterus.

30 orin expression was detected in the pregnant uterus.

31 contraction-associated genes in the pregnant uterus.

32 s of the brain while others project onto the uterus.

33 s independent clonal lesions within a single uterus.

34 rophoblasts anchor the villous region to the uterus.

35 (a semiallograft) to grow and develop in the uterus.

36 d directly inoculate C. trachomatis into the uterus.

37 vical area, without detectable signal in the uterus.

38 growth-promoting actions of estrogen in the uterus.

39 arterial vessels, intestinal organs, and the uterus.

40 compared with women with intact ovaries and uterus.

41 pha (ERalpha) in the hippocampus but not the uterus.

42 ral pain in urinary bladder, ureter, gut and uterus.

43 utant in the luminal epithelium of the mouse uterus.

44 strogen-sensitive tissues, such as ovary and uterus.

45 e steps in the development of the C. elegans uterus.

46 ith the organisms ascending into the sterile uterus.

47 lunted hormonal responsiveness of the ageing uterus.

48 ansit of embryos from the spermatheca to the uterus.

49 learance of this bacterium from the infected uterus.

50 ages to clear C. sordellii from the infected uterus.

51 ne-induced physiological angiogenesis in the uterus.

52 mal growth of endometrial tissue outside the uterus.

53 esion in cancers of kidney, liver, lung, and uterus.

54 ansferring the embryo from an old to a young uterus.

55 s, trachea, tongue, eye, bladder, testis and uterus.

56 nhibiting reversals within the hermaphrodite uterus.

57 arterial walls, skin, lung alveoli, and the uterus.

58 innervated endometriosis lesions outside the uterus.

59 and-specific genes were altered in the PUGKO uterus.

60 of early life phytoestrogen exposure on the uterus.

61 ucture visible post-copulation in the female uterus.

62 uding prostate, melanoma, breast, ovary, and uterus.

63 aster females eject male ejaculates from the uterus 1-6 hr after mating with a stereotypic behavior r

64 ly greater in the adult (8893) than neonatal uterus (1101).

65 ally (10 to 240 mug; n = 3 to 8) or into the uterus (20 mug) under ultrasound guidance (n = 7) or via

66 ced by the timing of sperm ejection from the uterus [3, 4].

67 Carcinoma in the uterus, a cancer-resistant organ, requires a second clon

68 ecreased supportive environment of the older uterus, add support to the notion that an older uterus n

69 There is little known about healing of the uterus after Cesarean delivery (CD).

70 egnancy-related prion infectivity within the uterus, amniotic fluid, and the placental structure reve

71 Prion infectivity was confirmed within the uterus, amniotic fluid, and the placentome, the semiperm

72 nhanced dissemination of bacteria out of the uterus and a more robust inflammatory response than did

73 e the undesirable effects of estrogen in the uterus and breast tissues and to allow the beneficial ef

74 The characteristic features are empty uterus and cervix, gestational sac in the anterior part

75 s a Med12 missense variant (c.131G>A) in the uterus and demonstrated that this alteration alone promo

76 unable to cause hyperplasia or cancer in the uterus and did not activate Akt as effectively as Pten d

77 yly, horseshoe kidney, abnormally positioned uterus and elevated liver enzymes.

78 ells were mainly located in the upper tract (uterus and fallopian tubes).

79 ascend from the lower genital tract into the uterus and fallopian tubes.

80 Here, we identified ILC2s in the mouse uterus and found that they express cell surface molecule

81 The uterus and growing fetus are protected from ascending in

82 n defective CD4(+) T cell trafficking to the uterus and high bacterial load.

83 d bone formation with reduced effects in the uterus and in sebaceous glands.

84 For example, we observed chiral loops in the uterus and in the upper common oviduct that relax and co

85 ecific NK cells are abundant in the pregnant uterus and interact with invading placental trophoblast

86 expressed specifically in the glands of the uterus and is a critical regulator of postnatal uterine

87 ravillous trophoblasts invading the maternal uterus and its spiral arteries.

88 ates into cells that aggressively invade the uterus and its vasculature, anchoring the progeny and re

89 rgeted nanoparticle directed to the pregnant uterus and loaded with a tocolytic for reducing its plac

90 ces cellular proliferation and growth of the uterus and mammary glands.

91 After this, pups were delivered from the uterus and manually stimulated to initiate breathing in

92 treated before menarche, irradiation of the uterus and ovaries at doses as low as 1.00-2.49 Gy signi

93 Macrophages are prominent in the uterus and ovary at conception.

94 ted form, LC3B-II) decrease significantly in uterus and placenta during IPTL but not NIPTL.

95 ation of Hes1 were significantly elevated in uterus and placenta during PGN+poly(I:C)-induced preterm

96 DLL-4 and VEGF were significantly reduced in uterus and placenta during PGN+poly(I:C)-induced preterm

97 proinflammatory cytokines/chemokines in both uterus and placenta.

98 nd M2 (anti-inflammatory) macrophages to the uterus and placenta.

99 lting pregnancy, virus was also found in the uterus and placental tissue.

100 leads to impaired energy homeostasis in the uterus and reduced fertility of G6pc3(-/-) mothers.

101 (PE), cytotrophoblast (CTB) invasion of the uterus and spiral arteries is often shallow.

102 for most postmenopausal women with an intact uterus and that estrogen alone has no net benefit for th

103 that P. aeruginosa produces a biofilm in the uterus and that the host immune response is modulated fo

104 s in accumulation of maternal T cells in the uterus and that these activated cells can produce effect

105 n-sensitive peripheral organs, including the uterus and the anterior pituitary, or the proliferation

106 The mass abutted and displaced the uterus and the ovaries but did not distort either of the

107 The main portion of the gravid uterus and the ovaries was not seen on these images, but

108 ng that ERalpha uses AF-1 differently in the uterus and the pituitary for TAM action.

109 cervix is the boundary structure between the uterus and the vagina and is key for the maintenance of

110 nd trabecular bone in long bones, as well as uterus and thymus being partly dependent (40-70% reducti

111 Next, the uterus and uterine luminal fluid (ULF) were obtained fro

112 ched compared with endogenous T cells in the uterus and uterine-draining lymph nodes.

113 sence of individual NP aggregates inside the uterus and within embryos.

114 Trials who were aged 50-79 y, had an intact uterus, and completed a baseline food-frequency question

115 n the glandular epithelial (GE) cells of the uterus, and conditional deletion of Foxa2 after birth im

116 ch has tissue-specific distribution (kidney, uterus, and crypt epithelia of intestinal tissues), in g

117 se reporter, ER-regulated genes in the mouse uterus, and eNOS enzyme activation further indicated tha

118 d in the blood, lymph nodes, vagina, cervix, uterus, and fallopian tubes.

119 a2V decreased significantly in the placenta, uterus, and fetal membranes during PGN+poly(I:C)-induced

120 actor in small-cell carcinoma of the cervix, uterus, and ovary.

121 Preconception radiation doses to the gonads, uterus, and pituitary gland and administered chemotherap

122 tion radiation doses to the testes, ovaries, uterus, and pituitary gland, and related these to the ri

123 ormone-responsive cancers, including breast, uterus, and prostate cancer.

124 he actin cytoskeleton in the spermatheca and uterus, and to allow the exit of embryos from the sperma

125 in the regulation of steroid hormones in the uterus, and to overcome P4 resistance in human reproduct

126 mations of the reproductive tracts, with the uterus anteriorized towards oviduct and the vas deferens

127 meiotic resumption, while the pituitary and uterus appear to be normal.

128 luminal epithelial cells of a C/EBPbeta-null uterus are able to proceed through the G1 phase of the c

129 m-negative bacteria isolated from the equine uterus are capable of producing a biofilm in vitro, and

130 Glands of the uterus are essential for establishment of pregnancy in m

131 s in endocrine glands, intestinal villi, and uterus are the most affected in response to VEGF or VEGF

132 de at the interface between the placenta and uterus are thought to play many important roles in pregn

133 epithelial cells that line the inside of the uterus are unable to grow due to a lack of growth factor

134 estational sac onto the anterior wall of the uterus at the site of previous LSCS scar in a multipara

135 All women had an intact uterus at the time of study entry.

136 In mice, the uterus becomes receptive to blastocyst implantation on d

137 A blastocyst will implant only when the uterus becomes receptive.

138 Benign tumors of the breast and uterus, both of which are key target tissues of estrogen

139 ted side-effects impacting, for example, the uterus, breast and blood.

140 tment of L. monocytogenes to the gestational uterus but rather is due to compromised local innate cel

141 Inadequate invasion of the uterus by cytotrophoblasts is speculated to result in pr

142 ing renal development) by the former and the uterus by Mullerian ducts.

143 ostpartum bacterial infections of the bovine uterus cause endometritis but the risk of disease is inc

144 a may translocate directly into the pregnant uterus, causing localized inflammation and adverse pregn

145 organ modules for the ovary, fallopian tube, uterus, cervix and liver, with a sustained circulating f

146 t organs of mammals, including the oviducts, uterus, cervix and upper vagina, are derived from the Mu

147 for anomalies and aneuploidy; examining the uterus, cervix, placenta, and amniotic fluid; and guidin

148 sed leukocyte infiltration in the cervix and uterus compared to AZ2.

149 ed actions of glucocorticoids, and the mouse uterus contains high levels of the glucocorticoid recept

150 EP(3) receptors, the laxative effect and the uterus contraction induced via ricinoleic acid are absen

151 lantation and stromal decidualization in the uterus contribute to significant numbers of pregnancy lo

152 plantation of the embryo before reaching the uterus could result in ectopic pregnancy and lead to mat

153 onses [1, 3-6] via SP sensory neurons in the uterus defined by coexpression of the proprioceptive neu

154 In C. elegans, the ventral uterus develops through coordinated signaling between th

155 ngenital urogenital anomaly characterised by uterus didelphys with blind hemivagina and ipsilateral r

156 ompensatory hypertrophy of the right kidney, uterus didelphys with haematometra and haematocervix in

157 nephric ducts which leads to unfused uterus (uterus didelphys).

158 It is characterised by a triad of symptoms - uterus didelphys, obstructed hemivagina and ipsilateral

159 Embryo implantation requires that the uterus differentiate into the receptive state.

160 re, the results show the feasibility of live uterus donation, even from a postmenopausal donor.

161 t inclusion and at 3, 6, and 12 months after uterus donation.

162 Tregs are rapidly recruited to uterus-draining lymph nodes and activated in the first d

163 In uterus-draining lymph nodes of pregnant dams, the freque

164 ith a destructive bacterial infection of the uterus driven by commensal microbes, an alteration likel

165 a spatiotemporal expression of GPR64 in the uterus during early pregnancy.

166 temperature within the gravid miniature pig uterus during magnetic resonance (MR) imaging at 3 T.

167 Its location within the uterus, especially early during development when embryon

168 In the epithelial compartment of the uterus, estradiol-17beta (E(2)) induces cell proliferati

169 opical microbicides do not need to reach the uterus for efficacy.

170 Estrogen and progesterone prepare the uterus for embryo implantation and placental development

171 ch as transporting fertilized oocytes to the uterus for implantation.

172 of excess spermatozoa and preparation of the uterus for implantation.

173 erum miRNAs in cows with metritis and normal uterus (four cows per group), integrate miRNAs to their

174 In the adult uterus, FOXA2-bound and GE-expressed genes (3730) were e

175 In the neonatal uterus, FOXA2-bound and GE-expressed genes (469) were en

176 The uterus frequently develops benign fibroid tumors but ute

177 Blood vessels enter the uterus from the mesometrium, demarcating the uterus into

178 period, postmenopausal women with an intact uterus had a better benefit/risk index for raloxifene th

179 ghly linearly associated with cancers of the uterus (hazard ratio [HR] 1.62, 99% CI 1.56-1.69; p<0.00

180 d that 580 genes were decreased in the PUGKO uterus, however ULF secrotome analysis revealed that man

181 pancreas, prostate, small bowel, stomach, or uterus in 2005 and who underwent an extirpative procedur

182 imaging (MRI) findings in a case of Robert's uterus in a young woman.

183 er of PIBF1 in human choriodecidua and mouse uterus in late gestation.

184 n in the epithelial and stromal cells of the uterus in ovariectomized wild-type mice, but not in PRKO

185 c changes to the luminal structure of murine uterus in preparation for implantation.

186 y syndrome) underwent transplantation of the uterus in Sahlgrenska University Hospital, Gothenburg, S

187 contraction-associated genes in the pregnant uterus in the mouse and human.

188 ancers and precancerous abnormalities of the uterus in women who undergo myomectomy with or without e

189 rect delivery of C. muridarum into the mouse uterus increased both uterine horn/glandular duct dilati

190 IGF-I expression post-pubertally whereas the uterus increased expression.

191 bronectin that EVT encounter on invading the uterus increased HLA-G, EGF-Receptor-2, and LIF-Receptor

192 ary appears to be different from that in the uterus, indicating that ERalpha uses AF-1 differently in

193 inability of some embryos to implant in the uterus, indicating that stromal ESR1 is crucial for uter

194 uterus from the mesometrium, demarcating the uterus into mesometrial (M) and antimesometrial (AM) dom

195 oor support leading to the herniation of the uterus into or through the vagina.

196 Leukocyte infiltration into the uterus is a characteristic feature in early to midpregna

197 ation-competent blastocyst and the receptive uterus is a prerequisite for mammalian reproduction.

198 n abdominal ultrasonic transverse section of uterus is a reliable indicator for selection of recipien

199 Robert's uterus is a very rare anomaly which can be very well cha

200 Robert's uterus is a very rare mullerian duct anomaly which is ch

201 TGFbeta family signaling in the uterus is critical for establishing and maintaining preg

202 Microarray indicated the Ex3alphaERKO uterus is free of residual estrogen responses.

203 Although the presence of GR in the uterus is well established, uterine glucocorticoid signa

204 Ablation of Mig-6 in the murine uterus leads to the development of endometrial hyperplas

205 in various tissues, including mammary gland, uterus, lung, and pituitary.

206 vivo expression of KLF15 in an estrogenized uterus mimics P(4)'s action by inhibiting E(2)-induced u

207 of endometrial tissue (lesions) outside the uterus, most commonly on the peritoneum.

208 40 attempts to transfer embryos to their own uterus (n = 18) or via the use of a gestational carrier

209 rogesterone acetate (2.5 mg/d) if they had a uterus (N=16 608) or to conjugated equine estrogens only

210 reased local P(4) metabolism in the pregnant uterus near term and provide insight into the importance

211 rus, add support to the notion that an older uterus negatively selects the less fit trisomic embryos.

212 ation of eggs and transfer of embryos to the uterus occurred in 92% (49/53) of kisspeptin-54-treated

213 in the fetus, its amniotic membrane, and the uterus of experimental and control rats.

214 Conceptus expansion throughout the uterus of mammalian species with a noninvasive epithelio

215 However, morphological changes in the uterus of marsupials at term mimic those that occur duri

216 t ICI 182,780 (ICI) acts as an ER agonist in uterus of mice with mutations in the ERalpha AF-2.

217 rylation and epithelial proliferation in the uterus of mutant mice.

218 s fails after embryos are transferred to the uterus of recipients before or during the implantation w

219 in the vasculature, without stimulating the uterus or enhancing growth of breast cancer xenografts.

220 fertility, which is caused by absence of the uterus or the presence of a non-functional uterus.

221 days of each 30-day cycle] for women with a uterus) or placebo (plus sequential placebo vaginal gel

222 all sites except paratesticular, vagina, and uterus, or with alveolar RMS were randomly assigned to r

223 d female reproductive organs (penis, testes, uterus, ovaries).

224 sperm cells retrieved from the mated female uterus partially rescue in vitro fertilization (IVF) tha

225 phils from the colon, blood, thymus, spleen, uterus, peritoneal cavity, and allergen-challenged lung.

226 ave demonstrated RT-QuIC seeding activity in uterus, placentome, ovary, and amniotic fluid but not in

227 ly predictable and stable environment of the uterus, postnatal development can be affected by a multi

228 formed worldwide, and the techniques of both uterus procurement and transplantation are still develop

229 g the logistical workflow for deceased donor uterus procurement in a deceased multiorgan donor settin

230 procured, our approach now is to perform the uterus procurement prior to the procurement of other org

231 eric-vaginal fistula developed 2 weeks after uterus procurement.

232 We detail a new approach to deceased donor uterus procurement.

233 The development of the C. elegans uterus provides a model for understanding the regulatory

234 Women with an intact uterus received conjugated equine estrogens (CEE; 0.625

235 Women with a uterus received estrogen plus progestin (medroxyprogeste

236 The trend in women with intact uterus receiving estrogen plus progestin, considered sep

237 ract with adjacent organs namely the vagina, uterus, rectum and colon.

238 results demonstrate that the preimplantation uterus relies on Notch signaling to inhibit apoptosis of

239 labor requires greater insight into how the uterus remains in a noncontractile state until term and

240 the brain expedites sperm ejection from the uterus, resulting in marked reduction of sperm in the st

241 show that the overexpression of N1ICD in the uterus results in complete infertility as a consequence

242 ear-old woman with congenital absence of the uterus (Rokitansky syndrome) underwent transplantation o

243 ts support that it is feasible to retrieve a uterus safely from a live donor.

244 Smooth muscle of the uterus stays remarkably quiescent during normal pregnanc

245 pecificity, DPTL prevents contraction of rat uterus stimulated by PGF(2alpha) and induces relaxation

246 a substantially greater luminance within the uterus than previously thought [5].

247 develops, and it is during this time in the uterus that the risk of later obesity in the child may d

248 For postmenopausal women without a uterus, the benefit/risk ratio was similar.

249 At the time of implantation in the maternal uterus, the mouse blastocyst possesses an inner cell mas

250 In caudal regions of the uterus, the normal simple columnar epithelium flanking t

251 o increase their ability to migrate into the uterus, thereby promoting one of the earliest and most i

252 The uterotropic response of the uterus to 17beta-estradiol (E2) is genetically controlle

253 is and interact with other cell types in the uterus to influence uterine receptivity and blastocyst i

254 ) is an H-shaped syncytium that connects the uterus to the body wall.

255 exclusive deposition of SAA3 amyloid in the uterus, together with elevated uterine SAA3 transcripts,

256 rization was skewed in PGN+poly(I:C)-treated uterus toward double-positive CD11c(+) (M1) and CD206(+)

257 The molecular mechanism by which the uterus transitions from the prereceptive to the receptiv

258 This report is a proof-of-concept for uterus transplantation as a treatment for uterine factor

259 Eleven human uterus transplantation attempts have been done worldwide

260 Uterus transplantation has proven successful when perfor

261 Uterus transplantation is the first available treatment

262 using living donors or brain-dead donors in uterus transplantation programs, 2 years after the first

263 The first prospective observational study of uterus transplantation was initiated in 2013 with live d

264 We describe the first livebirth after uterus transplantation.

265 s after the first worldwide live birth after uterus transplantation.

266 ients in whom the disease is confined to the uterus, treatment results in successful remission; howev

267 r endometrial cancer involves removal of the uterus, tubes, ovaries, and lymph nodes.

268 n the rat hippocampal CA1 region but not the uterus undergoes enhanced interaction with the E3 ubiqui

269 d a conditional knockout (cKO) of Fst in the uterus using progesterone receptor-cre to study the role

270 nditionally deleted FOXA2 in the adult mouse uterus using the lactotransferrin Cre (Ltf-Cre) model an

271 re (Ltf-Cre) model and in the neonatal mouse uterus using the progesterone receptor Cre (Pgr-Cre) mod

272 paramesonephric ducts which leads to unfused uterus (uterus didelphys).

273 small-cell carcinomas of the cervix, ovary, uterus, vagina, and vulva.

274 ccharide (LPS) is commonly injected into the uterus via minilaparotomy, which is invasive, and can ca

275 of pregnancy, in whom activity in the whole uterus was considered, and the fetal dose was estimated

276 ionately more of the glucose taken up by the uterus was consumed by the uteroplacental tissues while

277 The uterus was donated from a living, 61-year-old, two-parou

278 Conditional knockout (cKO) of ALK3 in the uterus was obtained by producing Alk3(flox) (/flox)-Pgr-

279 Volumetry of the tumor and uterus was performed during the six sequences, with manu

280 In contrast, E2 action in the uterus was preserved in C451A-ERalpha mice and endometri

281 tial experience, in which the deceased donor uterus was procured post cross-clamp and after other org

282 The dose to the uterus was used as a proxy for early pregnancy (up to 10

283 egnancy [5 wk]), in whom the activity in the uterus was used as a proxy.

284 ectious potential of enJSRV particles in the uterus, we transferred bovine blastocysts into synchroni

285 s ovulated, fertilized, and implanted in the uterus were normal in these mice; however, pregnancies w

286 uctive tract structures and histology of the uterus were observed in the heifers.

287 A total of 16,608 women with a uterus were randomized to conjugated equine estrogens (0

288 nt mediator of progesterone signaling in the uterus, where it mediates tumor suppression by modulatin

289 DC population dynamics in the pregnant mouse uterus, where rapid tissue growth facilitated a dissecti

290 e at the site of placental attachment in the uterus, where the arteries are remodeled to supply the f

291 eported to be expressed in the epidermis and uterus, where the protein in keratinocytes is thought to

292 ithin the oviduct and are transported to the uterus, where they implant onto the uterine wall.

293 s physiological vascular permeability in the uterus, whereas misexpression of PR in the endothelium o

294 Endometrium is the inner lining of the uterus which is composed of epithelial and stromal tissu

295 se-1 were increased in PGN+poly(I:C)-treated uterus, which could induce pyroptosis.

296 lvic ultrasound demonstrated a normal- sized uterus with a well- circumscribed, heterogeneous mass lo

297 h haematometra and haematocervix in the left uterus with evidence of blood in a dilated retort-shaped

298 ct anomaly which is characterised by septate uterus with obstruction of a one-sided cavity and format

299 Ultrasonography shows a modestly enlarged uterus with three uterine fibroids.

300 elected for embryo transfer to the patient's uterus, yielding a clinical twin pregnancy and birth of