ライフサイエンスコーパス: receptivity

1 ng readiness and synchronisation with female receptivity.

2 rol song significantly affects female mating receptivity.

3 lagen and fibronectin, thus abolishing their receptivity.

4 s to a female during courtship, boosting her receptivity.

5 play both male-like mounting and female-like receptivity.

6 strocyte contact regulates neuronal synaptic receptivity.

7 the estrous cycle with elimination of sexual receptivity.

8 displays widespread, though not uniform, PDF receptivity.

9 t, amacrine contact does not induce synaptic receptivity.

10 sperm and peptides that decrease her sexual receptivity.

11 l preoptic nucleus, leading to female sexual receptivity.

12 important step for full expression of sexual receptivity.

13 clicity and showed evidence of normal sexual receptivity.

14 argely attributable to a reduction in female receptivity.

15 failure due to lack of attainment of uterine receptivity.

16 ion of NPY and MOR circuits regulates sexual receptivity.

17 al for, the nutritional inhibition of sexual receptivity.

18 ivated by estrogen and inhibit female sexual receptivity.

19 Y) have been implicated in regulating sexual receptivity.

20 w prothymocytes during each period of thymic receptivity.

21 ermine the duration of the window of uterine receptivity.

22 accharide-based ligands during the window of receptivity.

23 g of ovulation with the expression of sexual receptivity.

24 d not affect paced mating behavior or sexual receptivity.

25 not affect contact return latency or sexual receptivity.

26 the LE coinciding with the onset of uterine receptivity.

27 rotransmitters in the facilitation of sexual receptivity.

28 of female rats increases their female sexual receptivity.

29 duced rats with 2 different levels of sexual receptivity.

30 uring courtship and shown to increase female receptivity.

31 pled class of GPCRs as regulators of uterine receptivity.

32 ion is critical for the expression of female receptivity.

33 ed lordosis behavior in rats with low sexual receptivity.

34 size or mating experience or to male sexual receptivity.

35 diol&BSA applied to the MBH or POA inhibited receptivity.

36 was positively correlated with the degree of receptivity.

37 ssociation of endometriosis with endometrial receptivity.

38 s disrupts progesterone pathways and uterine receptivity.

39 ctopamine-dependent behaviors such as female receptivity.

40 or normal papilla cell senescence and flower receptivity.

41 increased physical activity with peak sexual receptivity.

42 lated genes that are involved in endometrial receptivity.

43 radiol signaling in the regulation of sexual receptivity.

44 oss to endometriosis-related endometrial non-receptivity.

45 luding preovulatory events and female sexual receptivity.

46 ge/use, ovulation, oviposition, and remating receptivity.

47 naling pathways in the regulation of uterine receptivity.

48 otential changes in vector distributions and receptivity.

49 a signal that indicates a state of increased receptivity.

50 adult Abd-B neurons significantly decreased receptivity.

51 the neural circuit controlling virgin female receptivity.

52 ing neurons for high levels of virgin female receptivity.

53 inished plasma progesterone and poor uterine receptivity.

54 neurons in females greatly diminishes sexual receptivity.

55 prognostic information were identified: (1) receptivity, (2) deflection/rejection, (3) emotion, (4)

56 n resulted in significantly increased sexual receptivity 20 and 40 min after infusion when compared t

57 diol-mediated spinogenesis for female sexual receptivity (81.43 +/- 7.05 to 35.00 +/- 11.76, p < 0.05

58 In contrast, the effect of mating on female receptivity (a component of ejaculate toxicity) was affe

59 acilitation of lordosis, induction of sexual receptivity, abbreviation of the period of sexual recept

60 in female egg laying and decrease in female receptivity after copulation.

61 Uterine receptivity, also known as the window of implantation, l

62 f a female as an indication of her increased receptivity and accordingly coordinates his song choice,

63 ogaster, mating causes a reduction in sexual receptivity and an elevation in egg production for at le

64 ion is that because periods of female sexual receptivity and attractiveness are more extended in bono

65 ely down-regulated with the onset of uterine receptivity and blastocyst activation prior to implantat

66 ell types in the uterus to influence uterine receptivity and blastocyst implantation for the establis

67 ses in uterine stroma, affecting endometrial receptivity and decidualization, while not affecting E2-

68 prerequisite for the development of uterine receptivity and early pregnancy establishment.

69 The prolonged "sperm effect" on female receptivity and egg production is therefore entirely att

70 Mating induces changes in the receptivity and egg-laying behavior in Drosophila female

71 promised fertility due to defects in uterine receptivity and embryo implantation.

72 lectrical stimulation for maintaining muscle receptivity and enhancing functional recovery.

73 d therefore be paid to cultivar-specific AMF receptivity and function in the development of climate s

74 of progesterone in the regulation of sexual receptivity and given the importance of progestin recept

75 immunologic functions, including endometrial receptivity and implantation as well as defense against

76 ila melanogaster females reduce their sexual receptivity and increase egg laying [1, 2].

77 notypic switch resulting in decreased sexual receptivity and increased egg laying.

78 increased egg-laying rate and reduced sexual receptivity and is controlled by the products of the mal

79 ction in the bladder by promoting epithelial receptivity and local inflammation.

80 l PROK1 may play a pivotal role in enhancing receptivity and maintaining early pregnancy.

81 alization may play a key role in endometrial receptivity and offer a novel target for fertility treat

82 dsx(+) neurons play a pivotal role in sexual receptivity and post-mating behaviors [1, 2, 5-9].

83 ys of fluoxetine treatment eliminated sexual receptivity and proceptivity (hops/darts) in 40% and 46%

84 creased time spent in proximity to the male, receptivity and proceptivity.

85 x2 genes are critical for conferring uterine receptivity and readiness to implantation could have cli

86 embrane transport system regulating cellular receptivity and responsiveness.

87 bstantial genetic variation for both primary receptivity and speed of remating.

88 ptide (SP or Acp70A), which decreases female receptivity and stimulates egg production in the first m

89 l that these neurons are required for sexual receptivity and sufficient to induce dopamine release in

90 ion differentially according to their sexual receptivity and the genetic identity of both female and

91 to promote glutamate receptor clustering and receptivity and to induce the formation of postsynaptica

92 and genetic mechanisms governing endometrial receptivity and uterine competency for pregnancy.

93 We find that both continuous receptivity and very short lengths of receptivity are ab

94 female during copulation and mediate female receptivity and/or male courtship inhibition.

95 Our data suggest that AIP influences ligand receptivity and/or nuclear targeting of AhR.

96 ng rates and activity levels, reduced sexual receptivity, and activation of the immune system.

97 les, both retn and dsxF contribute to female receptivity, and both genes act to repress male-like cou

98 endometrial proliferation, decreased uterine receptivity, and increased implantation failure in anima

99 tivity, abbreviation of the period of sexual receptivity, and induction of twice-daily prolactin surg

100 -278, and miR-184) showed altered fecundity, receptivity, and lifespan responses to receipt of SP, wh

101 zoate (EB)-primed rats on sexual motivation, receptivity, and proceptivity were examined.

102 roductive behavior, e.g., sexual motivation, receptivity, and proceptivity.

103 econdary outcomes (knowledge, self-efficacy, receptivity, and willingness) were assessed via patient

104 the reproductive behaviour eliciting female receptivity, arb for male-specific fin morphogenesis and

105 inuous receptivity and very short lengths of receptivity are able to evolve.

106 Although many genes critical for uterine receptivity are primarily regulated by ovarian hormones,

107 ibrations, as well as their effect on female receptivity, are conserved in other Drosophila species.

108 showed significantly higher levels of female receptivity as compared with WT littermates.

109 We assessed queen sexual receptivity (as measured by likelihood to take mating fl

110 vels of cortisol were associated with sexual receptivity, as indicated by species-typical tail-waggin

111 e relationship between PAPPA and endometrium receptivity, as well as the regulation of N-fucosylation

112 re we perform a meta-analysis of endometrial-receptivity associated genes on 164 endometrial samples

113 microRNAs that could regulate 30 endometrial-receptivity associated genes, and we confirm experimenta

114 In mice, uterine receptivity begins with the secretion of LIF from uterin

115 in an elevated egg-laying rate and decreased receptivity, behaviors whose persistence (but not initia

116 integrin alphaVbeta3, a critical endometrium receptivity biomarker, was up-regulated by PAPPA, thereb

117 FOXA2-regulated genes that influence uterine receptivity, blastocyst implantation, and stromal cell d

118 les mated to SP null males exhibited altered receptivity, but not reproductive output, in comparison

119 s to blastocysts and uterine preparation for receptivity, but, remarkably, blocks blastocyst competen

120 idatory estrogen (E2) stimulates endometrial receptivity by activating a network of signaling pathway

121 ts protein targets contribute to endometrial receptivity by altering cell polarity and adhesion.

122 ses contributing to the regulation of sexual receptivity by estradiol and progesterone are compromise

123 of activin signaling by FST enables uterine receptivity by preserving critical BMP signaling.

124 NCOA6 controls E(2) sensitivity and uterine receptivity by regulating multiple E(2)-signaling compon

125 opment of competence by oligodendrocytes and receptivity by target axons.

126 pic glutamate vesicular release or glutamate receptivity can independently modify the severity of RGC

127 , a novel behavioral aspect of virgin female receptivity characterized in this study.

128 2014) in this issue of Neuron, dissected the receptivity circuit of female Drosophila, providing insi

129 Females displayed receptivity continuously for 14 days in both conditions.

130 pecies exhibit three ontogenetic patterns of receptivity: cyclic, in which females alternately become

131 lectively, these findings point to a uterine receptivity deficit that underpins the frequent failure

132 ehaviours during mating with variable sexual receptivity depending on hormonal status(1-4).

133 etween male pollen release and female pistil receptivity (dichogamy), and self-pollen rejection.

134 the estrous cycle and elimination of sexual receptivity during fluoxetine treatment.

135 However, latent receptivity during mating contact can be uncovered in mu

136 However, female receptivity during mating contact is odr-7 independent.

137 ila melanogaster significantly alters female receptivity, egg production, lifespan, hormone levels, i

138 vernment health authorities increase vaccine receptivity, endorsements from non-state customary autho

139 unctional pheromone components: Plethodontid Receptivity Factor (PRF), Sodefrin Precursor-Like Factor

140 proteinaceous pheromone, termed plethodontid receptivity factor (PRF), was experimentally delivered t

141 s on Exo70A1, a previously identified stigma receptivity factor essential for pollination.

142 g and sought-after biomarkers of endometrial receptivity, fertility and infertility.

143 ne and its roles in regulating female sexual receptivity, fertility and interactions with Plasmodium

144 Thamnophis sirtalis parietalis), the loss of receptivity following intromission during mating can be

145 t bioactive substances that regulate uterine receptivity for blastocyst implantation.

146 epigenome-transcriptome networks for uterine receptivity for embryo implantation and the pathogenesis

147 Development of uterine endometrial receptivity for implantation is orchestrated by cyclic s

148 mone action and its critical role in uterine receptivity for implantation.

149 ynchronizing embryo development with uterine receptivity for implantation.

150 omen due, in part, to inadequate endometrial receptivity for support of embryo implantation.

151 plantation, decidualization, and endometrial receptivity from disruption of the LIF-STAT3-EGR1 pathwa

152 In these affected rats, reduced sexual receptivity generally preceded disruption of vaginal cyc

153 A number of known uterine receptivity genes and gland-specific genes were altered

154 prevented expression of certain endometrial receptivity genes, perturbed uterine fluid handling and

155 e fly Drosophila melanogaster, virgin female receptivity has received relatively little attention, an

156 portant site for modulation of female sexual receptivity, has a sexual dimorphism in dendritic spine

157 r of pathways involved in regulating uterine receptivity have been identified in the mouse, less is u

158 Uterine receptivity implies a dialogue between the hormonally pr

159 pidly disrupted estrous cyclicity and sexual receptivity in adult, regularly cycling Fischer rats.

160 ual conditioning increases sexual arousal or receptivity in both sexes but the increase has different

161 ted by E19, is sufficient to induce synaptic receptivity in E17 RGCs.

162 diate in progesterone (P)-facilitated sexual receptivity in female rats and mice.

163 The facilitative effect of P on sexual receptivity in female rats was blocked by antisense olig

164 rogesterone- and dopamine-facilitated sexual receptivity in female rats.

165 ced pheromone, which provokes initial sexual receptivity in females, and which has not been previousl

166 copulation cause a reduction of post-coital receptivity in females, referred to as the "copulation e

167 ed to male infertility nor to lack of sexual receptivity in males paired with previous mates.

168 Thus, P-facilitated receptivity in mice involves P and 3alpha,5alpha-THP and

169 le there has been limited research on sexual receptivity in primates, this has been one recurring top

170 p in progestin receptor regulation of sexual receptivity in rats and mice.

171 is not responsible for the absence of sexual receptivity in suboptimally hormonally primed ovariectom

172 tically regulates the acquisition of uterine receptivity in the female mouse, and disruption of such

173 tically regulates the acquisition of uterine receptivity in the female mouse.

174 The lack of Gb(3) and of Stx receptivity in the gastrointestinal tract raised questio

175 l group of pheromones known to affect female receptivity in vertebrates.

176 um of trophoblast cells promoted endometrium receptivity in vitro.

177 ntrol pausing, a key aspect of female sexual receptivity, in response to male courtship.

178 ng increased egg laying and decreased sexual receptivity, in the mated female.

179 Msxgenes play important roles during uterine receptivity including modulation of epithelial junctiona

180 gulated genes in the GE during the window of receptivity, including leukemia inhibitory factor (LIF),

181 fluid or semen resulted in decreased sexual receptivity, increased attractiveness of queens to worke

182 Collectively, uDCs appear to govern uterine receptivity, independent of their predicted role in immu

183 d abdominal ganglion neurons inhibits female receptivity, indicating the importance of these neurons

184 In contrast, the levels of a key receptivity-inhibiting Sfp (sex peptide) were the same i

185 ternity in M matings through the transfer of receptivity-inhibiting Sfps.

186 We identify a meta-signature of endometrial receptivity involving 57 mRNA genes as putative receptiv

187 al significance, because compromised uterine receptivity is a major cause of pregnancy failure in IVF

188 Thus, virgin female receptivity is controlled at least in part by neurons th

189 esterone following ovulation (PostOv), while receptivity is correlated with estrogen preceding it (Pr

190 rojection pathway critical for female sexual receptivity is extensively remodelled during the estrous

191 Sexual receptivity is female behavior that allows or helps a ma

192 (PND 30 and PND 60) the period when pathway receptivity is lost.

193 Thus, synaptic receptivity is not induced simply by dendritic elaborati

194 Abnormal endometrial receptivity is one of the major causes of embryo implant

195 mination, so the pheromone-induced change in receptivity is the only known function of PRF.

196 Uterine receptivity is therefore under dual control and is regul

197 EMENT Lordosis, the measure of female sexual receptivity, is a sexually dimorphic behavior regulated

198 Rats with low sexual receptivity (L/M<0.5) were bilaterally infused with the

199 Normally, the "window" of uterine receptivity lasts for a limited time.

200 is there such prominent variation in sexual receptivity length among primate species?

201 olutionary trade-offs associated with sexual receptivity length using mathematical modeling.

202 r reproductive state: virgins display sexual receptivity (lordosis behavior), while lactating mothers

203 Receptivity (lordosis quotients and ratings) and procept

204 Sexual proceptivity and receptivity (lordosis) during the postpartum estrus were

205 e (P) and its metabolites' effects on sexual receptivity (lordosis) of mice was examined.

206 eptivity involving 57 mRNA genes as putative receptivity markers, where 39 of these we confirm experi

207 in and altered the expression of endometrial receptivity markers.

208 on kyphotic nursing, sexual proceptivity and receptivity, maternal aggression, and daily litter weigh

209 Primary (initial) receptivity may be stimulated or inhibited by diet, ovar

210 Several single-gene mutations reduce female receptivity; most of these mutations also impair sensory

211 dulated behavior, sodium appetite and sexual receptivity, novel mechanisms of steroid action have eme

212 when dealing with other intermediate-to-low receptivity nuclei.

213 aria transmission, and could monitor malaria receptivity of a population to sustain malaria transmiss

214 el role for growth factors in regulating the receptivity of axons to myelination and reveal that diff

215 and ejaculation of males and reduced sexual receptivity of females.

216 y of diabetogenic T cells induces a state of receptivity of islets to subsequent immunological insult

217 ated upon mating, accounting for the reduced receptivity of mated females.

218 the attacks by learning how to minimize the receptivity of mostly ordinary people to recruiting orga

219 T cell motility is critical for the antigen receptivity of naive CD4 T cells.

220 hernes scorpioides, that assessed the sexual receptivity of once-mated females presented after a laps

221 To determine the receptivity of prenatal care providers and their patient

222 ual recovery of estrous cyclicity and sexual receptivity of the fluoxetine-treated animals.

223 of TECs diminish early in life, whereas the receptivity of the thymus to TEC engraftment remains rel

224 d postmating responses (fecundity and sexual receptivity) of Drosophila melanogaster females after th

225 Female sexual receptivity offers an excellent model for complex behavi

226 ances to the female that suppress her sexual receptivity or antagonize the behavior of competing male

227 and visual cues frequently advertise sexual receptivity or phenotypic quality [5].

228 Multiple signals may be used for receptivity or unreceptivity.

229 in all significantly increased female sexual receptivity over vehicle or estradiol plus oxytocin infu

230 gaster, seminal fluid proteins affect female receptivity, ovulation, oogenesis, sperm storage, sperm

231 go dramatic behavioral (e.g., reduced sexual receptivity), physiological (e.g., ovary activation, ovu

232 ocial behaviors, including female rat sexual receptivity, quantified as the copulatory stance known a

233 erentiation because of insufficient cytokine receptivity rather than signal quality.

234 Dendrite growth is not sufficient to trigger receptivity; rather, the ability of newly generated RGCs

235 eir brains encode the dynamics of mating and receptivity remains largely unknown.

236 antation, we find that the window of uterine receptivity remains open for an extended period at lower

237 In species with cyclic receptivity, remating may be inhibited by copulation its

238 the male-typical mounting and female-typical receptivity, respectively.

239 derage participants, the alcohol advertising receptivity score independently predicted the onset of d

240 An alcohol advertising receptivity score was derived (1 point each for having s

241 trols, as measured by lordosis quotients and receptivity scores, at 40, and 90 min after their infusi

242 lly "nondiapausing" mammals when the uterine receptivity signal is blocked or delayed.

243 astocyst stage when it waits for the uterine receptivity signal to implant.

244 ation (IGFBP1, prolactin) and c) endometrial receptivity (SPP1, MAOA, EDNRB) were measured.

245 Endometrial receptivity testing is purported to improve live birth f

246 ion yielded a euploid blastocyst, the use of receptivity testing to guide the timing of frozen embryo

247 We characterize two components of receptivity that are elicited in sexually mature females

248 vealed potential changes in antennal odorant receptivity that coincided with the shift from host-seek

249 h show a role for pheromones in induction of receptivity, these data show that exposure to pheromones

250 ons; and (v) restores endometrial functional receptivity through multiple mechanisms.

251 e saline washing, did not reveal any altered receptivity to 5-HT application.

252 ) cascade is required for maintaining stigma receptivity to accept compatible pollen.

253 odulating its structure and consequently its receptivity to activation by cofactors.

254 erine endometrium are required to facilitate receptivity to an implanting blastocyst.

255 dsx-expressing neurons mediate virgin female receptivity to courting males.

256 egulators prepares the human endometrium for receptivity to embryo implantation and maintains pregnan

257 Uterine receptivity to embryo implantation is coordinately regul

258 nuates E(2) sensitivity to determine uterine receptivity to embryo implantation under normal physiolo

259 e endometrial epithelial cells to facilitate receptivity to implantation in species with different im

260 nction of the tissue, including establishing receptivity to implanting embryo, is also unclear.

261 otent progenitor cells and to increase their receptivity to lineage commitment and differentiation in

262 la species D. santomea, where females signal receptivity to male courtship songs by spreading their w

263 on focused on female advertisement of sexual receptivity to males or mother-offspring communication.

264 ' egg production and ovulation, reduce their receptivity to mating, mediate sperm storage, cause part

265 Females exhibited a high level of receptivity to new males, irrespective of intermating in

266 stimulate egg production, and reduce female receptivity to other males by releasing a complex mixtur

267 whereas in females their activation promotes receptivity to other males.

268 en matings exerted a strong effect on female receptivity to previous mates.

269 nowledge, self-efficacy for decision making, receptivity to receiving more information, and general w

270 stimulate increased fecundity and decreased receptivity to remating.

271 These changes include decreasing receptivity to remating; affecting sperm storage paramet

272 or change; however, family members expressed receptivity to smoking outdoors.

273 traparietal sulcus, a region associated with receptivity to stimuli at unexpected locations.

274 receptor globotriaosylceramide (Gb(3)), for receptivity to Stx binding in vitro, and for susceptibil

275 To assess public receptivity to such strategies, we compared adoption of

276 We conclude that the loss of pathway receptivity to sympathetic nerve ingrowth is associated

277 In addition, patients reported high receptivity to teledermoscopy for short-term monitoring

278 entional office-based visit, and (3) patient receptivity to teledermoscopy for short-term monitoring

279 Receptivity to television alcohol advertising predicted

280 f implantation--a brief phase of endometrial receptivity to the blastocyst--and were released into th

281 ut also on morphogenetic events that control receptivity to those differentiation cues, and we explai

282 In the first, age-dependent receptivity to thymic chimerism was studied in nonirradi

283 lecular markers for endometrial function and receptivity, to enhance conceptus survival and developme

284 emales did not differ significantly in their receptivity toward previous mates and different males, w

285 l refugee groups influence local policymaker receptivity toward refugee resettlement.

286 additional Acps that affected egg laying or receptivity upon ectopic expression.

287 that while these mice exhibit normal uterine receptivity, uterine cell proliferation and decidualizat

288 f, including nurses and physicians, and that receptivity varied among staff.

289 ogenetic proteins (BMPs) control endometrial receptivity via a conserved activin receptor type 2 A (A

290 Sexual receptivity was again monitored 30 min after injection o

291 whether SP accounts for the "sperm effect." Receptivity was higher and egg production lower in femal

292 Fast-food advertising receptivity was not associated with any drinking outcome

293 Tumor characteristics (grade, hormone receptivity) were similar across age groups.

294 bited minimal levels of P-facilitated sexual receptivity when compared to their wild-type littermates

295 s in either the pCd or pC1 clusters promotes receptivity, while silencing these neurons makes females

296 anandamide levels is associated with uterine receptivity, while up-regulation is correlated with uter

297 the molecular mechanisms underlying uterine receptivity will enable the development of new intervent

298 Failure to attain uterine receptivity will impede blastocyst attachment and result

299 -embryo dialog exists to synchronize uterine receptivity with the concomitant activation of the blast

300 pha-diol:BSA or 3 alpha-diol&BSA facilitated receptivity within 90 min.