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 e marrow myeloid colonies compared with sham-
gonadectomized females.
47 hippocampus (but not other brain regions) of
gonadectomized females.
48 efold overexpression relative to ovaries, or
gonadectomized flies.
49 , adult Long-Evans male and female rats were
gonadectomized for comparison with controls.
50 ale Fischer 344 rats at 3 months of age were
gonadectomized (
GDX'd) and implanted with Silastic capsu
51 ceptibility to malaria infection, intact and
gonadectomized (
gdx) C57BL/6 mice were inoculated with P
52 Gonadectomized (
GDX) male and female mice were trained o
53 Gonadectomized (
GDX) male and female rats implanted with
54 Young and middle-aged intact and young
gonadectomized (
GDX) male Fischer 344 rats were anaesthe
55 Interestingly, OFQ was ineffective in
gonadectomized (
GDX) males, whereas testosterone replace
56 In
gonadectomized (
GDX) mice with low testosterone and high
57 Adult male 3xTg-AD mice were sham
gonadectomized (
GDX) or GDX to deplete endogenous androg
58 We found that hormone-replaced
gonadectomized GPR54 KO males and females displayed appr
59 ealed that visual and motor circuits in both
gonadectomized groups resided in cortical areas with dim
60 implantation to female and male, intact and
gonadectomized Long-Evans rats.
61 Gonadectomized male and female ferrets (Mustela putorius
62 eus basalis magnocellularis, and striatum of
gonadectomized male and female rats to determine whether
63 In the caudal VMH, in both
gonadectomized male and female rats, the levels of CCK-R
64 low-dose ketamine (2.5 mg/kg) in intact and
gonadectomized male and female rats.
65 sessed in postpubertal (> 60 days) normal or
gonadectomized male and female rats.
66 Gonadectomized female and
gonadectomized male DI rats both responded to high salt
67 In the second experimental series, adult
gonadectomized male hamsters were subjected to a right T
68 ns of intratracheal instillation of siRNA in
gonadectomized male mice exposed to hypoxia and monitore
69 regulated by estrogen during development, we
gonadectomized male rat pups at postnatal day 0 (P0) and
70 Gonadectomized male rats administered T, DHT, or 3alpha-
71 Gonadectomized male rats were implanted with a placebo,
72 The AAS effects on body weight in
gonadectomized male rats were modest, and no effects on
73 Peripheral injections of
gonadectomized male rats with DHT or T for 48 h reduced
74 ) testosterone replenishment restores LTF in
gonadectomized male rats, and (2) that the conversion of
75 Testosterone replenishment restores LTF in
gonadectomized male rats, and this is dependent on the c
76 LTF is similarly impaired in middle-aged and
gonadectomized male rats, suggesting that gonadal hormon
77 xiolytic- and antidepressant-like effects in
gonadectomized male rats, while similarly regulating cri
78 ctive effects on depressive-like behavior in
gonadectomized male rats.
79 re stereotaxically implanted near the PVN of
gonadectomized male rats.
80 ement results in decreased mortality in both
gonadectomized males and females.
81 ollowed by progesterone treatment (E + P) of
gonadectomized males evokes Fos activation in LHRH and A
82 the intact and axotomized sides of N.IX-X of
gonadectomized males that were either hormonally untreat
83 e marrow myeloid colonies compared with sham-
gonadectomized males, although local adipose inflammatio
84 In intact and androgen-replaced
gonadectomized males, gonadotropin significantly increas
85 intact males and was reduced in females and
gonadectomized males.
86 ed by ovariectomy while having no effects in
gonadectomized males.
87 expression in testes vs. ovaries, heads, and
gonadectomized males.
88 Interestingly, male
gonadectomized mice exhibited decreased sensitivity to G
89 the formation of gallstones, we investigated
gonadectomized mice treated with synthetic ER subtype-se
90 or, nonsignificant increases in bone mass in
gonadectomized mice, all the while inducing hypertrophy
91 Gonadectomized mice, GH-releasing hormone receptor-defic
92 ty occurring as frequently as every 9 min in
gonadectomized mice.
93 gonadal hormones, because they persisted in
gonadectomized mice.
94 tected for brain lesions in either intact or
gonadectomized mice.
95 gnificant changes in trkB mRNA or protein in
gonadectomized or estrogen-replaced animals.
96 ison of immunoreactivity in rats perinatally
gonadectomized or sham-operated revealed complex changes
97 e and female Sprague-Dawley rats were either
gonadectomized or studied intact.
98 prairie voles received a sham surgery, were
gonadectomized,
or were gonadectomized and implanted wit
99 Treatment of
gonadectomized,
peripubertal males and females with exog
100 Gonadectomized pre- and postpubertal male hamsters (Meso
101 Administration of E2 to
gonadectomized rats (0.2 mg/kg per day for 7 days) resul
102 ham operated male F344 rats were compared to
gonadectomized rats implanted with Silastic tubing conta
103 timal proliferation after vascular injury in
gonadectomized rats of both sexes (P < .05).
104 timal proliferation after vascular injury in
gonadectomized rats of both sexes (P < .05).
105 Gonadectomized rats of both sexes were implanted with es
106 This study tested whether, in
gonadectomized rats of both sexes.
107 the carotid artery in intact female rats and
gonadectomized rats of both sexes.
108 These effects are seen in
gonadectomized rats of both sexes.
109 he neointimal response to vascular injury in
gonadectomized rats of both sexes; addition of a progest
110 Gonadectomized rats received hormone treatments that ind
111 ithin the dentate gyrus induced anhedonia in
gonadectomized rats receiving testosterone supplementati
112 corresponding data from control and acutely
gonadectomized rats revealed that administration of the
113 Subsequent experiments in
gonadectomized rats suggest that circulating hormones in
114 lase-immunoreactive) were also quantified in
gonadectomized rats supplemented with testosterone propi
115 Corresponding analyses in
gonadectomized rats supplemented with testosterone revea
116 These decreases were attenuated in
gonadectomized rats that were supplemented with testoste
117 e ventromedial hypothalamic nucleus (VMH) of
gonadectomized rats treated with estrogen or testosteron
118 ine afferents but that supplementing acutely
gonadectomized rats with dihydrotestosterone provides no
119 2 (ERK2) expression in the dentate gyrus in
gonadectomized rats with testosterone replacements.
120 ferences in DA reuptake in DLS of intake and
gonadectomized rats, and we report sensitization of ES-i
121 However, in the DLS of both intact and
gonadectomized rats, DA reuptake was slower in females t
122 rexpression of ERK2 rescued this behavior in
gonadectomized rats.
123 F was not restored in T + ADT or DHT-treated
gonadectomized rats.
124 mark the association cortices of chronically
gonadectomized rats.
125 d production of MUA volleys and LH pulses in
gonadectomized rats.
126 sed anti-anxiety behavior of intact, but not
gonadectomized,
rats.
127 ross vertebrates and increased healthspan in
gonadectomized rodents.
128 We implanted
gonadectomized Sternopygus with either empty SILASTIC ca
129 iate early gene immunoreactivity (IEG-IR) in
gonadectomized,
steroid-treated mice in response to pher
130 or sham-operated revealed complex changes in
gonadectomized subjects; in cingulate cortex, TH immunor
131 Adult male ERbeta knockout and WT mice were
gonadectomized,
treated with female priming hormones, an
132 se urine overlapped maps for juvenile and/or
gonadectomized urine of both sexes, whereas maps for sex
133 hesis that LTF is similar in middle-aged and
gonadectomized young male rats of an inbred rat strain c