ライフサイエンスコーパス: estrous cycle

1 ulation, late onset of puberty, and abnormal estrous cycle).

2 uenced by season, gender and/or stage of the estrous cycle.

3 social behaviors change as a function of the estrous cycle.

4 ring days 2-6 of the follicular phase of the estrous cycle.

5 f an important biological rhythm, the female estrous cycle.

6 he activity of LAT and BA neurons across the estrous cycle.

7 male Syrian hamsters display a regular 4-day estrous cycle.

8 sleep and activity levels fluctuate over the estrous cycle.

9 e and visceral stimulation change across the estrous cycle.

10 root ganglia varied significantly across the estrous cycle.

11 immunity may be affected by the stage of the estrous cycle.

12 cervix or the kidney after monitoring their estrous cycle.

13 estrous (progesterone dominant) stage of the estrous cycle.

14 sic effectiveness of KOR agonists across the estrous cycle.

15 7 are expressed at similar stages of the rat estrous cycle.

16 t reflects steroidogenesis during the normal estrous cycle.

17 of the hippocampus, were detected across the estrous cycle.

18 the expression of sexual behavior during the estrous cycle.

19 the diestrus or the proestrus phase of their estrous cycle.

20 water maze during the various phases of the estrous cycle.

21 sal forebrain cholinergic neurons across the estrous cycle.

22 uctuations detected during the course of the estrous cycle.

23 mRNA were detected during the course of the estrous cycle.

24 estrus, metestrus and diestrus phases of the estrous cycle.

25 organization of synaptic function across the estrous cycle.

26 mically modulate its activity throughout the estrous cycle.

27 g ovulation, or surrounding follicles during estrous cycle.

28 y during the sexually receptive phase of the estrous cycle.

29 eres in adult males and in females along the estrous cycle.

30 y similar to that in IL-33 mRNA level during estrous cycle.

31 ified heifers were obtained on day 14 of the estrous cycle.

32 alpha oscillates in phase with the 4-d-long estrous cycle.

33 on, and PSD-95 protein expression across the estrous cycle.

34 icroscopy in male and female mice across the estrous cycle.

35 ose and frequency mimicking those during the estrous cycle.

36 are significantly changed as a result of the estrous cycle.

37 ith the cyclic changes in feeding across the estrous cycle.

38 , respectively, of rats without altering the estrous cycle.

39 female C57BL/6 mice in defined phases of the estrous cycle.

40 as highest during the diestrous phase of the estrous cycle.

41 y and associated with a bolus release at mid-estrous cycle.

42 r the proestrus or metestrus stages of their estrous cycle.

43 n female mice that may be independent of the estrous cycle.

44 orexia contributed to the disturbance of the estrous cycle.

45 Most mutant mice did not show normal estrous cycles.

46 gnaling, Pgr null female rats exhibit robust estrous cycles.

47 les that had regular (4-5 days) or irregular estrous cycles.

48 at hippocampal BDNF levels change across the estrous cycle, accompanied by neurophysiological respons

49 In females, the estrous cycle affected pellet, but not cocaine, self-adm

50 or training positively impacts the disrupted estrous cycle after an HX.

51 not affected regardless of the stage of the estrous cycle after cervix injection with PRV; (2) in co

52 ility due to prolonged diestrus phase of the estrous cycle and aberrant steroidogenesis.

53 t basal forebrain at different stages of the estrous cycle and at different time points after the adm

54 mouse brain is remarkably stable during the estrous cycle and demonstrates that the genes that do fl

55 pears to contribute to the disruption of the estrous cycle and elimination of sexual receptivity duri

56 mRNA and peptide levels fluctuate across the estrous cycle and have been shown to be modulated by est

57 in the hippocampus of female rats across the estrous cycle and male rats was analyzed by light micros

58 s were sacrificed at different stages of the estrous cycle and ovariectomized animals were sacrificed

59 maintains its epithelial identity during the estrous cycle and postpartum regeneration.

60 Both estrous cycle and sex affect the numbers and types of ne

61 hypothalamus may be a factor regulating the estrous cycle and sexual behavior in female rodents.

62 red for the cyclic changes in feeding across estrous cycle and that AgRP and NPY neurons are essentia

63 E signaling, in the hamster ovary during the estrous cycle and the role of gonadotropins and ovarian

64 lar 5-HT in the MBH varied with stage of the estrous cycle and with the light/dark cycle.

65 ty of the uterine horn is altered during the estrous cycle and, if so, which subpopulations are affec

66 he female null mutant mouse has asynchronous estrous cycles and a reduced number of surviving pups.

67 Mice deficient in BmprIB exhibit irregular estrous cycles and an impaired pseudopregnancy response.

68 wild-type ovary transplants displayed normal estrous cycles and corpora lutea, despite DHT treatment,

69 n with clozapine N-oxide resulted in delayed estrous cycles and decreased fertility.

70 PNA mice had irregular estrous cycles and elevated testosterone and luteinizing

71 assessed, because PR-/- mice do not exhibit estrous cycles and fail to become pregnant.

72 F1 estrous cycles and fertility were unaffected, and F2 lit

73 e AR(-/-) mice appear normal but show longer estrous cycles and reduced fertility.

74 Homozygous mutant females have normal estrous cycles and reproductive and mating behavior but

75 ctuations in anxiety-like behaviors over the estrous cycle, and, as adults, differ from wild-type mic

76 (lox/lox) mice were infertile, with abnormal estrous cycles, and exhibited a complete failure of the

77 ibited delayed puberty onset, no evidence of estrous cycles, and minimal fecundity.

78 differentially expressed as a result of the estrous cycle are related to myelin and oligodendrocytes

79 l cell physiology and the mean length of its estrous cycle are similar to those in humans.

80 hin/kappa-opioid receptor signaling over the estrous cycle, as well as the nature of the endogenous m

81 Estrous cycle assessments were made during a 5-8 week pe

82 rats with either normal length or elongated estrous cycles, but stressed females gained less weight

83 n eminence, regulate LHRH release during the estrous cycle by undergoing plastic changes that alterna

84 ction of solid foods, resumption of maternal estrous cycling, cessation of nursing, or maternal inter

85 eptors on mossy fibers seems responsible for estrous cycle changes in area CA3.

86 a significant delay in the pubertal onset of estrous cycles compared with control animals.

87 ats was assessed at identified points in the estrous cycle corresponding to low (estrus) and high (pr

88 icate that progesterone variation during the estrous cycle could be responsible for a component of th

89 t RAM performance was influenced by specific estrous cycle day, particularly during proestrus.

90 is regulated in a manner that is gender and estrous cycle dependent.

91 ine sex differences, hormonal influences and estrous cycle-dependent changes in AMPH-induced immediat

92 ring following hyperpolarizing stimuli in an estrous cycle-dependent manner.

93 However, the estrous cycle did not impact the level of cocaine choice

94 Accordingly, we assessed sex and estrous cycle differences in choice between food (45 mg

95 It is well established that there are estrous cycle differences in cocaine-induced behavioral

96 These results suggest that estrous cycle disruption after a major SCI is a conseque

97 Estrous cycle disruption after spinal cord injury (SCI)

98 (BLA), whose activity fluctuates across the estrous cycle due to a shift in the balance of inhibitio

99 ertile and exhibit a substantial increase in estrous cycle duration as revealed by examination of vag

100 ioral measures, irrespective of the stage of estrous cycle during the task.

101 s affected significantly by the stage of the estrous cycle during viral infection of the cervix; (3)

102 Estrous cycle effects on reinstatement were also assesse

103 their reproductive status" (having 4-5 days estrous cycles, > 60% successful pregnancies after matin

104 tion length, puberty onset in males, growth, estrous cycles, hormone levels, immunological end points

105 hormone loss, how and whether to monitor the estrous cycle if animals are ovary-intact, dose of hormo

106 During estrous cycle, IL-33 expression levels fluctuated along

107 spine density and synaptic number across the estrous cycle in female rats correlate with increased hi

108 trating the importance of accounting for the estrous cycle in females, our data set the ground for a

109 the estrous cycle, resulting in a shortened estrous cycle in GREKO(-/-) mice.

110 ons in specific GABA(A)R subunits during the estrous cycle in mice, causing cyclic changes of tonic i

111 We conclude that the estrous cycle in rat is accompanied by structural remode

112 in CA1 and CA3 electrophysiology across the estrous cycle in rats.

113 ated uptake was present in all phases of the estrous cycle in reproductive organs and mammary glands

114 asing hormone (GnRH) and thus coordinate the estrous cycle in rodents; however, the precise role of k

115 he density of V(1a)R would change across the estrous cycle in several subcortical regions implicated

116 x differences and their interaction with the estrous cycle in the adult medial prefrontal cortex tran

117 significant effects of time of day or day of estrous cycle in the medial preoptic nucleus, median emi

118 dimorphic and variable throughout the female estrous cycle in the rat posterodorsal medial amygdala (

119 essed nectin-1 only during the stages of the estrous cycle in which mice are susceptible to vaginal H

120 f GH in females depended on the stage of the estrous cycle in which they were exposed to the stressfu

121 , exogenous progesterone treatment inhibited estrous cycles in wild-type female rats but not in Pgr-n

122 e nuclear proteins important for puberty and estrous cycling in mammals.

123 In vivo, elevated estrogen during estrous cycling in mice, and estrogen treatment of mice

124 tric label retention, functional response to estrous cycling in vivo by proliferation, enhanced growt

125 nges in ovarian steroid secretion during the estrous cycle influenced GABAergic neuronal activity in

126 It remains unknown, however, if the aberrant estrous cycle is a result of an injury to the spinal cor

127 ch uterine innervation may change during the estrous cycle is uncertain.

128 lock mutant females have extended, irregular estrous cycles, lack a coordinated luteinizing hormone (

129 ight gain by stressed subjects and unaltered estrous cycle lengths, but was not associated with enhan

130 simulating the estrogen fluctuations of the estrous cycle may be more effective than the widely used

131 Furthermore, estrous cycle mean length was shorter in the trained tha

132 orary interruption in the progression of the estrous cycle (mean of 9.4 days delay), which was not co

133 to be expressed during only one stage of the estrous cycle (metestrus).

134 ociception that varies with stage of the rat estrous cycle: minimal during diestrus and prominent dur

135 ly in AIB1(-/-)-ras virgin mice with natural estrous cycles, multiparous mice with cyclically elevate

136 n fertility, failing to progress through the estrous cycle normally, show any signs of successful ovu

137 region of the dorsal hippocampus during the estrous cycle of the female rat, and the functional cons

138 region of the dorsal hippocampus during the estrous cycle of the female rat.

139 and physiology of the hippocampus across the estrous cycle of the female rat.

140 in rat neocortex varied as a function of the estrous cycle of the rat, we asked whether either or bot

141 eceptors that occurs in neocortex during the estrous cycle of the rat.

142 In contrast, the estrous cycles of their pair-fed counterparts remained d

143 nstruct for understanding the effects of the estrous cycle on BLA-dependent behaviors.

144 We uncover a critical influence of the estrous cycle on the adult rat medial prefrontal cortex

145 was unaffected by strain, age, stage of the estrous cycle, or ovariectomy.

146 ts of female reproductive biology, including estrous cycling, ovulation, embryonic implantation, onse

147 eromotor responses between the phases of the estrous cycle (P < 0.001).

148 mpal levels of phosphorylated DORs vary with estrous cycle phase and that acute stress may dampen the

149 ows synaptic laterality depending on sex and estrous cycle phase in mature MePD neurons.

150 The estrous cycle phase in the female dogs enrolled in the s

151 differences in pDOR levels were seen across estrous cycle phase or sex.

152 nt and types of profiles varied with sex and estrous cycle phase.

153 The effects of neonatal age, estrous cycle, pregnancy, and progesterone on expression

154 t between LAT and BA predominance across the estrous cycle provides a simple construct for understand

155 hormone treatments that mimic the 4-day rat estrous cycle provoke a chemically coded reorganization

156 Fluoxetine treatment also elongated the estrous cycle, reduced blood levels of progesterone, and

157 anging concentration of estradiol during the estrous cycle regulates ERalpha to augment and then term

158 Estrous cycle-related variations of spatial reference me

159 oestrus and diestrus-metestrus phases of the estrous cycle, resulting in a shortened estrous cycle in

160 Molecular probing throughout a simulated estrous cycle revealed a significant surge in ovarian Gl

161 mpus, neocortex, and cerebellum to determine estrous cycle-specific changes in these four brain regio

162 we tested the impact of this SNP on age and estrous-cycle-specific expression of anxiety-like behavi

163 ctuations in anxiety-like behaviors over the estrous cycle-specifically, more anxiety-like behaviors

164 ncreasing effects of U-50488, independent of estrous cycle stage in females or gonadectomy in males.

165 use hormonal profiles are known to vary with estrous cycle stage, the purpose of this study was to ev

166 n hormone were temporally altered, revealing estrous cycle stage-specific modifications to the hypoth

167 y task between injured females regardless of estrous cycle stage.

168 e numbers of BrdU-labeled cells at different estrous cycle stages and after ovarian steroid manipulat

169 intact and castrated males and in females at estrous cycle stages associated with low and high estrog

170 intact female rats would be expressed during estrous cycle stages in which 17beta-estradiol (E2) is n

171 incides with the onset of alterations in the estrous cycle, suggesting that a decline in the estrogen

172 in female rats in the diestrous phase of the estrous cycle, the proestrous phase, and after ovariecto

173 rd of female rats in different stages of the estrous cycle to examine the influence of hormonal statu

174 a spinal cord HX returns the duration of the estrous cycle toward normal.

175 c virus infection at different stages of the estrous cycle was assessed in a rodent model after direc

176 of mid-thoracic spinal contusions on the rat estrous cycle was examined.

177 Although the Mutant estrous cycle was extended, comprehensive endocrine chan

178 By contrast, estrous cycling was more likely in mice on lower P:C (1:

179 st one brood of young and expressed a normal estrous cycle were exposed to an acute stressful event t

180 e rats showed a transient disturbance of the estrous cycle with elimination of sexual receptivity.

181 After controlling the macaque estrous cycle with progesterone, anti-HIV-1 neutralizing

182 of ovarian hormones, the interaction of the estrous cycle with sex differences in gene expression in

183 ception in proestrous rats, the phase of the estrous cycle with the highest levels of circulating est

184 ramatic changes in V(1a)R binding across the estrous cycle within any of the neuroanatomical areas me