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1 T in males than in females during estrous or diestrous.
2 g) increased hypothalamic 5-HT in males, and diestrous and estrous females to approximately 2 pg/samp
3 ly more resistant to seizure-induction, than diestrous and males rats.
4 mented differences in sleep patterns between diestrous and pregnant rats, reproductive state did not
5              AVP exerted the same effects on diestrous and proestrous days of the ovarian cycle, whet
6 oxetine while smaller responses were seen in diestrous and proestrous rats.
7 n in brain slices from ovariectomized (OVX), diestrous, and proestrous kisspeptin-GFP mice.
8 roductive tract-draining LN from estrous and diestrous animals.
9 ver was about 2-fold greater in male than in diestrous day one (D(1)) female rats in the diagonal ban
10               The authors exposed estrous or diestrous female hamsters (Mesocricetus auratus) to sali
11                                           In diestrous female mice, only 20-Hz activation generated s
12                                    Levels in diestrous females (0.98 +/- 0.09 pg, n=38) were not sign
13 evalent in the spinal cord of proestrous vs. diestrous females and vs. males.
14                                              Diestrous females had the highest levels during the dark
15     However, gonadally intact males, but not diestrous females, were able to discriminate object loca
16           No such difference was observed in diestrous females.
17  posterior MeA was higher in estrous than in diestrous females.
18             They found that estrous (but not diestrous) females investigated conspecific male odors l
19 arizing sag and was increased across OVX --> diestrous --> proestrous mice.
20 aled that AVP increased [Ca(2+)]i in >80% of diestrous kisspeptin neurons via a mechanism involving v
21 ochemically identified supraoptic neurons of diestrous or lactating female rats.
22 rmine (18)F-FES uptake in female rats in the diestrous phase of the estrous cycle, the proestrous pha
23 nd mammary glands but was highest during the diestrous phase of the estrous cycle.
24 er during the estrous (estrogen dominant) or diestrous (progesterone dominant) stage of the estrous c
25  of immunoreactive FOS in early pregnant and diestrous rats in the medial septum (MS), vertical and h
26 on of OFQ in male, ovariectomized (OVX), and diestrous rats produced a significant antinociceptive ef
27 ent, older, persistent estrous or persistent diestrous rats were infected by kidney injection and giv
28 e BSTv did not differ between postpartum and diestrous rats, but serotonin turnover was lower in moth
29 virus per gram of tissue than the persistent diestrous rats.
30 ediate early gene expression between OVX and diestrous rats.
31 n anxiety-related behaviors in postpartum or diestrous rats.
32                           Female rats showed diestrous smears during the first week of treatment and
33 ignificantly greater in male rats and during diestrous than during estrous.
34        Postpartum rats are less anxious than diestrous virgin females, a phenomenon requiring that mo
35                                    Groups of diestrous virgins were also examined.
36 ut had no effect on the open-arm behavior of diestrous virgins.

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