ライフサイエンスコーパス: diestrus

1 e receptor 1 in male rats and female rats in diestrus.

2 F9):bone morphogenetic protein 15 (BMP15) at diestrus.

3 ic (EM) techniques, compared with estrus and diestrus.

4 els of LENK-ir in CA3a-c compared to rats in diestrus.

5 as well as decreased POMC mRNA expression on diestrus.

6 ve at the time of the LH surge as well as on diestrus.

7 surge, but virtually none coexpressed Fos on diestrus.

8 prevents the lowering of excitability during diestrus.

9 regulated in GCNF(fl/fl)Zp3Cre(+) females at diestrus.

10 of normally-cycling female rats in estrus or diestrus.

11 gher in female rats during proestrus than in diestrus.

12 levels are highest) compared with estrus and diestrus.

13 or metestrus, and 31.1 (26.7, 36.3) mmHg for diestrus.

14 nt marking tend to occur at higher levels on diestrus 1 and diestrus 2 than on proestrus or estrus.

15 highest levels of ChAT mRNA were detected on diestrus 1.

16 mals during proestrus compared with those at diestrus-1.

17 observed for those that were stressed during diestrus 2 and perfused 24 hr later during proestrus.

18 to occur at higher levels on diestrus 1 and diestrus 2 than on proestrus or estrus.

19 ariable, with the highest levels detected on diestrus 2.

20 us females at estrus (27.2+/-2.3) but not at diestrus-2 (39.1+/-3.4).

21 lower in females at estrus versus males and diestrus-2 (I(K,slow): male 21.9+/-1.8, estrus 14.6+/-0.

22 K,slow): male 21.9+/-1.8, estrus 14.6+/-0.6, diestrus-2 20.3+/-1.4; I(to,f): male 26.8+/-1.9, estrus

23 I(to,f): male 26.8+/-1.9, estrus 14.9+/-1.6, diestrus-2 22.1+/-2.1).

24 ), respectively) were lower in estrus versus diestrus-2 and male.

25 consisted of significantly longer periods of diestrus and less estrus.

26 but is also differentially regulated during diestrus and proestrus.

27 age of the rat estrous cycle: minimal during diestrus and prominent during proestrus.

28 elayed or absent vaginal opening, persistent diestrus, and atrophic reproductive tracts with absent c

29 4-day cycles (proestrus, estrus, metestrus, diestrus), as determined during the 2 weeks prior to inj

30 ycling rats in proestrus (uterus, cervix) or diestrus (colon); OVX+E2 did not restore the inhibitory

31 roestrus (P), estrus (E), metestrus (M), and diestrus (D).

32 n 0800 and 1000 h (females ovariectomized on diestrus day 1).

33 Conversely, mice inoculated during diestrus did not show a decreased response to Ag by eith

34 in the MePD of males and cycling females (in diestrus, early proestrus, late proestrus, and estrus).

35 w estrogen estrous phases (estrus/metaestrus/diestrus (EMD)) froze more during extinction retrieval t

36 s revealed that proestrus rats compared with diestrus, estrus, and male rats contained significantly

37 mented ovariectomized females) compared with diestrus, estrus, or male rats.

38 ptic proteins and spine density in IS and in diestrus female rats could not be reversed by ketamine.

39 hytoestrogen supplements on anxiety in male, diestrus female, and proestrus female rats were examined

40 males) than low-estradiol states (estrus and diestrus females and males).

41 gesterone) females compared to proestrus and diestrus females and males.

42 ex differences in proestrus when compared to diestrus females, and we discovered a direct role for Ea

43 milarly, ERbeta-ir was highest in estrus and diestrus females, mainly in dendritic spines and glia.

44 ERalpha-ir was highest in diestrus females, particularly in dendritic spines, axon

45 No effect of diet was seen in the diestrus females.

46 uperficial dorsal horn revealed that rats in diestrus had significantly lower KOR densities than thos

47 In late diestrus (high-progesterone phase), enhanced expression

48 er infected neurons than animals infected in diestrus I or diestrus II (proestrous and estrous animal

49 had less than 20% of infected cells found in diestrus I or diestrus II rats).

50 PRV infection compared to animals in either diestrus I or diestrus II.

51 urons than animals infected in diestrus I or diestrus II (proestrous and estrous animals had less tha

52 20% of infected cells found in diestrus I or diestrus II rats).

53 compared to animals in either diestrus I or diestrus II.

54 follicular tissue from Large White gilts in diestrus (LD, n = 3) and estrus (LE, n = 3), and Chinese

55 Diestrus-level E(2) implants alone provided no benefit,

56 Diestrus (<100 pg/ml in serum) levels of 17beta-estradio

57 , n = 3), and Chinese indigenous Mi gilts in diestrus (MD, n = 2) and estrus (ME, n = 3) were investi

58 cant decrease in the length of proestrus and diestrus-metestrus phases of the estrous cycle, resultin

59 Diestrus mice (low estradiol) exhibited a higher basal g

60 not ERalpha rescued synaptic potentiation in diestrus mice by enhancing GluN2B-mediated NMDA receptor

61 determine mRNA expression within the MBH in diestrus, never pregnant (nulliparous) controls, postpar

62 g proestrus nights than during metestrus and diestrus nights.

63 in the right MePD in males, or in females in diestrus or estrus.

64 ity (ir) in the DG hilus compared to rats in diestrus or proestrus.

65 ats that received ketamine during either the diestrus or the proestrus phase of their estrous cycle.

66 f the caudal striatum compared to females in diestrus, ovariectomized (OVX) females, castrated (CAST)

67 ice displayed hypofertility due to prolonged diestrus phase of the estrous cycle and aberrant steroid

68 gen, in the proestrus, estrus, metestrus and diestrus phases of the estrous cycle.

69 T13--L1, and L6--S1 in either the estrus or diestrus phases.

70 Females from the stages of diestrus, proestrus, and estrus were used.

71 Coronal hippocampal sections from diestrus rats were immunolabeled with antibodies to ERbe

72 , postpartum day 5 (PPD5), PPD10, PPD18, and diestrus, reproductively experienced (primiparous) femal

73 exposure of an ICR male to an ICR female in diestrus resulted in activation of cells located predomi

74 replacement (OVX+E2), or sham OVX (tested in diestrus; shamOVX-D).

75 cell activation in the estrus but not in the diestrus stage of the menstrual cycle of females was inh

76 oups of female mice: i) non pregnant (NP) at diestrus stage, ii) late pregnant (LP), iii) one day pos

77 down-regulation leads to prolonged metestrus-diestrus, superovulation, increased numbers of mature fo

78 BA had relatively greater inhibition during diestrus that paralleled more rapid contextual fear exti

79 estrus cycle, increasing 10-fold from early diestrus to a relative maximum in proestrus.

80 tion from an EM2 nonresponsive state (during diestrus) to an analgesically responsive state (during p

81 ne estrogen receptor alpha (mERalpha; during diestrus) versus glutamate (during proestrus), concomita

82 Female rats were sacrificed as either diestrus virgins, on pregnancy day 10 or 20, on the day

83 ments, when rats were infected at estrus and diestrus without prior progesterone priming, chlamydial

84 set of male-emitted pheromone ligands during diestrus yet fully detect and respond to the same ligand