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1 /6J mice were tested for sociability towards gonadectomized A/J stimulus mice in a social choice task
2      That bone resorption cannot increase in gonadectomized Adrb2-deficient mice highlights the biolo
3 tradiol or vehicle was administered daily to gonadectomized, adrenalectomized (ADX) male (experiment
4 -diol), or vehicle was administered daily to gonadectomized, adrenalectomized male Long-Evans rats.
5 H(-/-)) mice develop gonadal tumors and-when gonadectomized-adrenocortical carcinoma.
6                                           We gonadectomized adult female and male geckos from an incu
7  The effects of testosterone replacements in gonadectomized adult male rats were investigated using t
8 nfluences cholesterol gallstones, we studied gonadectomized AKR/J mice of both genders that were impl
9             In the present study we used 487 gonadectomized and 376 intact age-matched F(2) mice gene
10 visual cortical circuit organization between gonadectomized and control animals.
11 homozygous alpha ERKO and wildtype mice were gonadectomized and given estradiol benzoate or vehicle.
12  the first experiment, female whiptails were gonadectomized and implanted for 6 weeks with either a S
13 a sham surgery, were gonadectomized, or were gonadectomized and implanted with a testosterone-filled
14 nock-out (ERalphaKO) and wild-type mice were gonadectomized and implanted with testosterone.
15 tomized (OVX), orchiectomized (ORX), or sham-gonadectomized and received replacement therapy with est
16 resentative areas of acutely and chronically gonadectomized and sham-operated adult male rats.
17 antified AVP-immunoreactive fiber density in gonadectomized and sham-operated male and female mice to
18                      Additionally, mice were gonadectomized and supplemented with 5-alpha-dihydrotest
19                    Adults of both sexes were gonadectomized and tested for lordosis behavior.
20                               Male rats were gonadectomized and treated with estrogen or dihydrotesto
21                  Sexually naive ferrets were gonadectomized and treated with sex steroids, after whic
22 ale-oriented or male-oriented, and ewes were gonadectomized and treated with subcutaneous implants of
23                                    Rats were gonadectomized and treated with testosterone, estrogen,
24 inguishable from males of similar species if gonadectomized and treated with testosterone.
25 ult female and male Sprague-Dawley rats were gonadectomized, and 1 week later, half of the animals re
26                   In contrast, supplementing gonadectomized animals with dihydrotestosterone provided
27 cantly reduced on P7, but after treatment of gonadectomized animals with estradiol benzoate on P0, le
28                         In vivo treatment of gonadectomized animals with testosterone or dihydrotesto
29 differences in NOS activity were detected in gonadectomized animals.
30 of male and female Long Evans rats that were gonadectomized as adults and treated for 30 days with ei
31                       Females and males were gonadectomized at 1 month of age and implanted either wi
32                                 In addition, gonadectomized ERalphaKO and WT mice rapidly learn to es
33                                              Gonadectomized, estradiol-treated male and female ferret
34                                              Gonadectomized FCG mice exhibited no sex differences in
35                                              Gonadectomized female and gonadectomized male DI rats bo
36  We have recently reported that treatment of gonadectomized female and male C57/B1 mice with the gona
37 toxicity of the NSDA system were examined in gonadectomized female and male CD-1 mice.
38 ns and testosterone in limbic brain areas of gonadectomized female and male rats.
39 d hormones: dihydrotestosterone treatment of gonadectomized female Dmp1Cre.Socs3 (f/f) mice restores
40                                              Gonadectomized female mice received an intracerebral inj
41 nuates MPP(+)-induced striatal DA release in gonadectomized female, but not male, rats.
42 dogenesis were most evident among intact and gonadectomized, female rats respectively.
43 ived and restored estrogens to young and old gonadectomized females and males and studied the morphol
44                                              Gonadectomized females and males exhibited similar amoun
45 l secretion and gallstone prevalence in both gonadectomized females and males.
46 hippocampus (but not other brain regions) of gonadectomized females.
47 efold overexpression relative to ovaries, or gonadectomized flies.
48 , adult Long-Evans male and female rats were gonadectomized for comparison with controls.
49 ale Fischer 344 rats at 3 months of age were gonadectomized (GDX'd) and implanted with Silastic capsu
50 ceptibility to malaria infection, intact and gonadectomized (gdx) C57BL/6 mice were inoculated with P
51                                              Gonadectomized (GDX) male and female mice were trained o
52                                              Gonadectomized (GDX) male and female rats implanted with
53       Young and middle-aged intact and young gonadectomized (GDX) male Fischer 344 rats were anaesthe
54        Interestingly, OFQ was ineffective in gonadectomized (GDX) males, whereas testosterone replace
55                                           In gonadectomized (GDX) mice with low testosterone and high
56            Adult male 3xTg-AD mice were sham gonadectomized (GDX) or GDX to deplete endogenous androg
57               We found that hormone-replaced gonadectomized GPR54 KO males and females displayed appr
58 ealed that visual and motor circuits in both gonadectomized groups resided in cortical areas with dim
59  implantation to female and male, intact and gonadectomized Long-Evans rats.
60                                              Gonadectomized male and female ferrets (Mustela putorius
61 eus basalis magnocellularis, and striatum of gonadectomized male and female rats to determine whether
62                   In the caudal VMH, in both gonadectomized male and female rats, the levels of CCK-R
63  low-dose ketamine (2.5 mg/kg) in intact and gonadectomized male and female rats.
64 sessed in postpubertal (> 60 days) normal or gonadectomized male and female rats.
65                    Gonadectomized female and gonadectomized male DI rats both responded to high salt
66     In the second experimental series, adult gonadectomized male hamsters were subjected to a right T
67 regulated by estrogen during development, we gonadectomized male rat pups at postnatal day 0 (P0) and
68                                              Gonadectomized male rats administered T, DHT, or 3alpha-
69                                              Gonadectomized male rats were implanted with a placebo,
70            The AAS effects on body weight in gonadectomized male rats were modest, and no effects on
71                     Peripheral injections of gonadectomized male rats with DHT or T for 48 h reduced
72 ) testosterone replenishment restores LTF in gonadectomized male rats, and (2) that the conversion of
73   Testosterone replenishment restores LTF in gonadectomized male rats, and this is dependent on the c
74 LTF is similarly impaired in middle-aged and gonadectomized male rats, suggesting that gonadal hormon
75 xiolytic- and antidepressant-like effects in gonadectomized male rats, while similarly regulating cri
76 ctive effects on depressive-like behavior in gonadectomized male rats.
77 re stereotaxically implanted near the PVN of gonadectomized male rats.
78 ement results in decreased mortality in both gonadectomized males and females.
79 ollowed by progesterone treatment (E + P) of gonadectomized males evokes Fos activation in LHRH and A
80 the intact and axotomized sides of N.IX-X of gonadectomized males that were either hormonally untreat
81              In intact and androgen-replaced gonadectomized males, gonadotropin significantly increas
82  intact males and was reduced in females and gonadectomized males.
83 expression in testes vs. ovaries, heads, and gonadectomized males.
84 the formation of gallstones, we investigated gonadectomized mice treated with synthetic ER subtype-se
85 or, nonsignificant increases in bone mass in gonadectomized mice, all the while inducing hypertrophy
86                                              Gonadectomized mice, GH-releasing hormone receptor-defic
87 ty occurring as frequently as every 9 min in gonadectomized mice.
88 tected for brain lesions in either intact or gonadectomized mice.
89 gnificant changes in trkB mRNA or protein in gonadectomized or estrogen-replaced animals.
90 ison of immunoreactivity in rats perinatally gonadectomized or sham-operated revealed complex changes
91 e and female Sprague-Dawley rats were either gonadectomized or studied intact.
92  prairie voles received a sham surgery, were gonadectomized, or were gonadectomized and implanted wit
93                                 Treatment of gonadectomized, peripubertal males and females with exog
94                                              Gonadectomized pre- and postpubertal male hamsters (Meso
95                      Administration of E2 to gonadectomized rats (0.2 mg/kg per day for 7 days) resul
96 ham operated male F344 rats were compared to gonadectomized rats implanted with Silastic tubing conta
97 timal proliferation after vascular injury in gonadectomized rats of both sexes (P < .05).
98 timal proliferation after vascular injury in gonadectomized rats of both sexes (P < .05).
99                                              Gonadectomized rats of both sexes were implanted with es
100                This study tested whether, in gonadectomized rats of both sexes.
101 the carotid artery in intact female rats and gonadectomized rats of both sexes.
102                    These effects are seen in gonadectomized rats of both sexes.
103 he neointimal response to vascular injury in gonadectomized rats of both sexes; addition of a progest
104                                              Gonadectomized rats received hormone treatments that ind
105 ithin the dentate gyrus induced anhedonia in gonadectomized rats receiving testosterone supplementati
106  corresponding data from control and acutely gonadectomized rats revealed that administration of the
107                    Subsequent experiments in gonadectomized rats suggest that circulating hormones in
108 lase-immunoreactive) were also quantified in gonadectomized rats supplemented with testosterone propi
109                    Corresponding analyses in gonadectomized rats supplemented with testosterone revea
110           These decreases were attenuated in gonadectomized rats that were supplemented with testoste
111 e ventromedial hypothalamic nucleus (VMH) of gonadectomized rats treated with estrogen or testosteron
112 ine afferents but that supplementing acutely gonadectomized rats with dihydrotestosterone provides no
113  2 (ERK2) expression in the dentate gyrus in gonadectomized rats with testosterone replacements.
114 rexpression of ERK2 rescued this behavior in gonadectomized rats.
115 F was not restored in T + ADT or DHT-treated gonadectomized rats.
116 mark the association cortices of chronically gonadectomized rats.
117 d production of MUA volleys and LH pulses in gonadectomized rats.
118 sed anti-anxiety behavior of intact, but not gonadectomized, rats.
119                                 We implanted gonadectomized Sternopygus with either empty SILASTIC ca
120 iate early gene immunoreactivity (IEG-IR) in gonadectomized, steroid-treated mice in response to pher
121 or sham-operated revealed complex changes in gonadectomized subjects; in cingulate cortex, TH immunor
122  Adult male ERbeta knockout and WT mice were gonadectomized, treated with female priming hormones, an
123 se urine overlapped maps for juvenile and/or gonadectomized urine of both sexes, whereas maps for sex
124 hesis that LTF is similar in middle-aged and gonadectomized young male rats of an inbred rat strain c

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