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1 gher in female rats during proestrus than in diestrus.
2 Ralpha included PGR and cohesin, only during diestrus.
3 e receptor 1 in male rats and female rats in diestrus.
4 F9):bone morphogenetic protein 15 (BMP15) at diestrus.
5 ic (EM) techniques, compared with estrus and diestrus.
6 els of LENK-ir in CA3a-c compared to rats in diestrus.
7 as well as decreased POMC mRNA expression on diestrus.
8 ve at the time of the LH surge as well as on diestrus.
9 surge, but virtually none coexpressed Fos on diestrus.
10 prevents the lowering of excitability during diestrus.
11 regulated in GCNF(fl/fl)Zp3Cre(+) females at diestrus.
12 of normally-cycling female rats in estrus or diestrus.
13 levels are highest) compared with estrus and diestrus.
14 or metestrus, and 31.1 (26.7, 36.3) mmHg for diestrus.
15 nt marking tend to occur at higher levels on diestrus 1 and diestrus 2 than on proestrus or estrus.
16 highest levels of ChAT mRNA were detected on diestrus 1.
17 mals during proestrus compared with those at diestrus-1.
18 observed for those that were stressed during diestrus 2 and perfused 24 hr later during proestrus.
19  to occur at higher levels on diestrus 1 and diestrus 2 than on proestrus or estrus.
20 ariable, with the highest levels detected on diestrus 2.
21 us females at estrus (27.2+/-2.3) but not at diestrus-2 (39.1+/-3.4).
22  lower in females at estrus versus males and diestrus-2 (I(K,slow): male 21.9+/-1.8, estrus 14.6+/-0.
23 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
24 I(to,f): male 26.8+/-1.9, estrus 14.9+/-1.6, diestrus-2 22.1+/-2.1).
25 ), respectively) were lower in estrus versus diestrus-2 and male.
26 consisted of significantly longer periods of diestrus and less estrus.
27 esterone receptor (PGR) were co-bound during diestrus and lost during estrus.
28 nated with ERalpha and PGR co-binding during diestrus and non-hormone receptor transcription factors
29 trated the Cxcr4-deficient epithelium in the diestrus and proestrus stages.
30 iated reinstatement was only observed during diestrus and proestrus.
31  but is also differentially regulated during diestrus and proestrus.
32 age of the rat estrous cycle: minimal during diestrus and prominent during proestrus.
33 elayed or absent vaginal opening, persistent diestrus, and atrophic reproductive tracts with absent c
34 reatment period, mice were euthanized during diestrus, and colon tissue samples were subjected to mor
35  4-day cycles (proestrus, estrus, metestrus, diestrus), as determined during the 2 weeks prior to inj
36 ycling rats in proestrus (uterus, cervix) or diestrus (colon); OVX+E2 did not restore the inhibitory
37 roestrus (P), estrus (E), metestrus (M), and diestrus (D).
38 n 0800 and 1000 h (females ovariectomized on diestrus day 1).
39 enchymal state of breast cancer cells during diestrus, decreased blood vessel diameters, and higher n
40           Conversely, mice inoculated during diestrus did not show a decreased response to Ag by eith
41 in the MePD of males and cycling females (in diestrus, early proestrus, late proestrus, and estrus).
42                           We also found that diestrus ELA mice had higher levels of progesterone and
43 w estrogen estrous phases (estrus/metaestrus/diestrus (EMD)) froze more during extinction retrieval t
44 s revealed that proestrus rats compared with diestrus, estrus, and male rats contained significantly
45 mented ovariectomized females) compared with diestrus, estrus, or male rats.
46 ptic proteins and spine density in IS and in diestrus female rats could not be reversed by ketamine.
47 hytoestrogen supplements on anxiety in male, diestrus female, and proestrus female rats were examined
48 males) than low-estradiol states (estrus and diestrus females and males).
49 gesterone) females compared to proestrus and diestrus females and males.
50 directed social behaviors between estrus and diestrus females via anterior hypothalamic outputs.
51 ex differences in proestrus when compared to diestrus females, and we discovered a direct role for Ea
52 milarly, ERbeta-ir was highest in estrus and diestrus females, mainly in dendritic spines and glia.
53                    ERalpha-ir was highest in diestrus females, particularly in dendritic spines, axon
54            No effect of diet was seen in the diestrus females.
55 n males, whereas it caused persistent APS in diestrus females.
56 ation of BNST(DL)-CRF neurons reduced APS in diestrus females.
57 evealed a novel role for HIF2A in regulating diestrus gene expression patterns that were independent
58 uperficial dorsal horn revealed that rats in diestrus had significantly lower KOR densities than thos
59                                      In late diestrus (high-progesterone phase), enhanced expression
60 cycle stages were chosen for these analyses, diestrus (highest estrogen) and estrus (highest progeste
61 er infected neurons than animals infected in diestrus I or diestrus II (proestrous and estrous animal
62 had less than 20% of infected cells found in diestrus I or diestrus II rats).
63  PRV infection compared to animals in either diestrus I or diestrus II.
64 urons than animals infected in diestrus I or diestrus II (proestrous and estrous animals had less tha
65 20% of infected cells found in diestrus I or diestrus II rats).
66  compared to animals in either diestrus I or diestrus II.
67 terone and allopregnanolone signaling during diestrus increases avoidance behavior in ELA mice.
68 ggest that the transition between estrus and diestrus is underpinned by well-orchestrated changes in
69  follicular tissue from Large White gilts in diestrus (LD, n = 3) and estrus (LE, n = 3), and Chinese
70                                              Diestrus-level E(2) implants alone provided no benefit,
71                                              Diestrus (<100 pg/ml in serum) levels of 17beta-estradio
72   Placenta (n = 7) and homogenized tissue of diestrus mares (n = 6) were evaluated using protein dete
73 , n = 3), and Chinese indigenous Mi gilts in diestrus (MD, n = 2) and estrus (ME, n = 3) were investi
74 cant decrease in the length of proestrus and diestrus-metestrus phases of the estrous cycle, resultin
75                                              Diestrus mice (low estradiol) exhibited a higher basal g
76 not ERalpha rescued synaptic potentiation in diestrus mice by enhancing GluN2B-mediated NMDA receptor
77 en receptors in the VTA before stress during diestrus mimics the stress susceptibility found during e
78  determine mRNA expression within the MBH in diestrus, never pregnant (nulliparous) controls, postpar
79 g proestrus nights than during metestrus and diestrus nights.
80 in the right MePD in males, or in females in diestrus or estrus.
81  acquired value during estrus-but not during diestrus or in males-increased motivation.
82 ct adult male rats and female rats in either diestrus or proestrus.
83 ity (ir) in the DG hilus compared to rats in diestrus or proestrus.
84 ats that received ketamine during either the diestrus or the proestrus phase of their estrous cycle.
85 f the caudal striatum compared to females in diestrus, ovariectomized (OVX) females, castrated (CAST)
86 ice displayed hypofertility due to prolonged diestrus phase of the estrous cycle and aberrant steroid
87 gen, in the proestrus, estrus, metestrus and diestrus phases of the estrous cycle.
88  T13--L1, and L6--S1 in either the estrus or diestrus phases.
89                   Females from the stages of diestrus, proestrus, and estrus were used.
90            Coronal hippocampal sections from diestrus rats were immunolabeled with antibodies to ERbe
91 , postpartum day 5 (PPD5), PPD10, PPD18, and diestrus, reproductively experienced (primiparous) femal
92  exposure of an ICR male to an ICR female in diestrus resulted in activation of cells located predomi
93 replacement (OVX+E2), or sham OVX (tested in diestrus; shamOVX-D).
94 cell activation in the estrus but not in the diestrus stage of the menstrual cycle of females was inh
95 oups of female mice: i) non pregnant (NP) at diestrus stage, ii) late pregnant (LP), iii) one day pos
96 down-regulation leads to prolonged metestrus-diestrus, superovulation, increased numbers of mature fo
97 to excitatory synaptic inputs (proestrus and diestrus) than males.
98  BA had relatively greater inhibition during diestrus that paralleled more rapid contextual fear exti
99  estrus cycle, increasing 10-fold from early diestrus to a relative maximum in proestrus.
100 tion from an EM2 nonresponsive state (during diestrus) to an analgesically responsive state (during p
101 f the GLP-1 precursor glucagon (Gcg), during diestrus-to-proestrus and proestrus-to-estrus and greate
102 id not consume more of the different food in diestrus-to-proestrus and proestrus-to-estrus.
103 ne estrogen receptor alpha (mERalpha; during diestrus) versus glutamate (during proestrus), concomita
104        Female rats were sacrificed as either diestrus virgins, on pregnancy day 10 or 20, on the day
105                   A number of changes during diestrus were identified that may reduce chemosensitivit
106                         We found that during diestrus, when progesterone levels are relatively high,
107 ments, when rats were infected at estrus and diestrus without prior progesterone priming, chlamydial
108 set of male-emitted pheromone ligands during diestrus yet fully detect and respond to the same ligand

 
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