ライフサイエンスコーパス: receptivity

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

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

3 strocyte contact regulates neuronal synaptic receptivity.

4 the estrous cycle with elimination of sexual receptivity.

5 displays widespread, though not uniform, PDF receptivity.

6 t, amacrine contact does not induce synaptic receptivity.

7 sperm and peptides that decrease her sexual receptivity.

8 l preoptic nucleus, leading to female sexual receptivity.

9 important step for full expression of sexual receptivity.

10 clicity and showed evidence of normal sexual receptivity.

11 argely attributable to a reduction in female receptivity.

12 failure due to lack of attainment of uterine receptivity.

13 ion of NPY and MOR circuits regulates sexual receptivity.

14 al for, the nutritional inhibition of sexual receptivity.

15 ivated by estrogen and inhibit female sexual receptivity.

16 Y) have been implicated in regulating sexual receptivity.

17 w prothymocytes during each period of thymic receptivity.

18 ermine the duration of the window of uterine receptivity.

19 luding preovulatory events and female sexual receptivity.

20 accharide-based ligands during the window of receptivity.

21 g of ovulation with the expression of sexual receptivity.

22 d not affect paced mating behavior or sexual receptivity.

23 not affect contact return latency or sexual receptivity.

24 the LE coinciding with the onset of uterine receptivity.

25 rotransmitters in the facilitation of sexual receptivity.

26 of female rats increases their female sexual receptivity.

27 duced rats with 2 different levels of sexual receptivity.

28 uring courtship and shown to increase female receptivity.

29 lated genes that are involved in endometrial receptivity.

30 ion is critical for the expression of female receptivity.

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

32 ed lordosis behavior in rats with low sexual receptivity.

33 size or mating experience or to male sexual receptivity.

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

35 naling pathways in the regulation of uterine receptivity.

36 otential changes in vector distributions and receptivity.

37 a signal that indicates a state of increased receptivity.

38 adult Abd-B neurons significantly decreased receptivity.

39 radiol signaling in the regulation of sexual receptivity.

40 the neural circuit controlling virgin female receptivity.

41 ing neurons for high levels of virgin female receptivity.

42 inished plasma progesterone and poor uterine receptivity.

43 neurons in females greatly diminishes sexual receptivity.

44 rol song significantly affects female mating receptivity.

45 lagen and fibronectin, thus abolishing their receptivity.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

71 embrane transport system regulating cellular receptivity and responsiveness.

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

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

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

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

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

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

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

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

80 -278, and miR-184) showed altered fecundity, receptivity, and lifespan responses to receipt of SP, wh

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

101 2014) in this issue of Neuron, dissected the receptivity circuit of female Drosophila, providing insi

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

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

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

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

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

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

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

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

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

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

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

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

114 ynchronizing embryo development with uterine receptivity for implantation.

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

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

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

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

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

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

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

122 Uterine receptivity implies a dialogue between the hormonally pr

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

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

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

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

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

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

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

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

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

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

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

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

135 um of trophoblast cells promoted endometrium receptivity in vitro.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

151 Uterine receptivity is therefore under dual control and is regul

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

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

154 Receptivity (lordosis quotients and ratings) and procept

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

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

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

158 in and altered the expression of endometrial receptivity markers.

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

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

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

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

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

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

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

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

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

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

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

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

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

172 Female sexual receptivity offers an excellent model for complex behavi

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

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

175 Multiple signals may be used for receptivity or unreceptivity.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

196 Uterine receptivity to embryo implantation is coordinately regul

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

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

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

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

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

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

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

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

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

206 stimulate increased fecundity and decreased receptivity to remating.

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

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

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

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

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

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

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

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

215 Receptivity to television alcohol advertising predicted

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

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

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

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

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

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

222 Sexual receptivity was again monitored 30 min after injection o

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

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

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

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

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

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

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

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

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

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