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1 a series of experiments using the monogamous prairie vole.
2 he formation of pair bonds in the monogamous prairie vole.
3  the effects of estrogen on the brain of the prairie vole.
4 [V1a receptor (V1aR)] antagonist in the male prairie vole.
5 ir bond formation in the socially monogamous prairie vole.
6  relate to the specialized life style of the prairie vole.
7 tors modulate pair bonding in the monogamous prairie vole.
8 1a receptor (V1aR) in a large sample of wild prairie voles.
9  is critical for pair-bond formation in male prairie voles.
10 total and selective social behaviors in male prairie voles.
11 a role in the preference for hind nipples in prairie voles.
12  estrus induction and pair bonding in female prairie voles.
13  labeling throughout the forebrain of female prairie voles.
14  role for the VNO in reproductive success in prairie voles.
15 inding in the ventral pallial region of male prairie voles.
16 al nitric oxide synthase (nNOS) in lactating prairie voles.
17  in the production of maternal aggression in prairie voles.
18 th maternal and mating-induced aggression in prairie voles.
19 ent in the control of maternal aggression in prairie voles.
20 n of postcopulatory aggression in adult male prairie voles.
21 mapping regional staining for c-fos) in male prairie voles.
22  montane voles, but it remained unchanged in prairie voles.
23 ne voles but did not change significantly in prairie voles.
24 erences (an index of pair bonding) in female prairie voles.
25 body mass distribution in this population of prairie voles.
26 ve different neurobiological actions in male prairie voles.
27 al circuitry mediate selective aggression in prairie voles.
28 nd consequences on social behavior in female prairie voles.
29 ological effects of AMPH treatment in female prairie voles.
30 iosus muscles in adult male, but not female, prairie voles.
31 ex difference would be similarly distinct in prairie voles.
32  drug experience in socially monogamous male prairie voles.
33 ression associated with pair bonding in male prairie voles.
34 ession is found in a chemosensory pathway in prairie voles.
35 idine (BrdU) in the amygdala and DG than did prairie voles.
36 and VMH, but not in the pMeA or DG, than did prairie voles.
37 nvolved in pair bond formation in monogamous prairie voles.
38 and medial (pMeA) nuclei, in meadow, but not prairie, voles.
39                                              Prairie voles also match the fear response, anxiety-rela
40  showing conserved neural mechanisms between prairie vole and human.
41 including differences between the monogamous prairie vole and its promiscuous congeners.
42 e brains of two monogamous vole species, the prairie vole and pine vole, and two promiscuous vole spe
43 n more egalitarian and monogamous ones, like prairie voles and humans, when there is no perceived cos
44 d peptide expression have been found between prairie voles and polygamous meadow voles.
45 in and behavior parallel differences between prairie voles and promiscuous congeners.
46 its maternal aggression and NO production in prairie voles and suggest that the central release of NO
47 septum regulates pair bond formation in male prairie voles and that this process requires access to b
48 eptor binding that is similar to that of the prairie vole, and exhibit increased affiliative behaviou
49 for the behavioral effects of AMPH in female prairie voles, and found that conditioning with low to i
50 h alloparenting in juvenile and adult female prairie voles, and oxytocin receptor antagonist infused
51  regulation of partner preferences in female prairie voles, and suggest that oxytocin receptor expres
52                  For example, sexually naive prairie voles are rarely aggressive.
53                           Here, we show that prairie voles are susceptible to mule deer CWD prions in
54 duced facilitation of pair bond formation in prairie voles, as well as potential sex differences in t
55 ctivation on partner preference formation in prairie voles, as well as the interaction between the MC
56                  In socially monogamous male prairie voles, AVP acts centrally via vasopressin V1a re
57 r the formation of social attachment in male prairie voles, because administration of haloperidol blo
58                                      In male prairie voles, both vasopressin and dopamine act in the
59 ion of kappa- and mu-opioid receptors in the prairie vole brain.
60                                              Prairie vole breeder pairs form monogamous pair bonds, w
61 enhanced partner preference formation in the prairie vole, but not in the non-monogamous meadow vole.
62 e behaviour in the highly social, monogamous prairie vole, but not in the relatively asocial, promisc
63                                       Female prairie voles, but not meadow voles, spent more time in
64 y psychiatric disorders, discoveries made in prairie voles can direct novel treatment strategies for
65                      Likewise, in adult male prairie voles, central (intracerebroventricular) injecti
66 peared to be disproportionately large in the prairie vole compared with other rodents.
67 ution of CART mRNA and peptide in monogamous prairie voles compared to congener promiscuous meadow vo
68 odialysis experiments were performed on male prairie voles displaying affiliation or aggression.
69 d AMPH administration in sexually naive male prairie voles enhanced V1aR expression in the AH and ind
70                                    In female prairie voles, exposure to a male or to male sensory cue
71                                      In male prairie voles, exposure to either the stress of swimming
72                                  Virgin male prairie voles had a large number of TH-immunoreactive ce
73                                Virgin female prairie voles had far fewer TH-immunoreactive cells in t
74 is, and the central nucleus of the amygdala, prairie voles had higher AVP receptor binding at birth t
75                                 Furthermore, prairie voles have higher densities of oxytocin receptor
76 nvironment influences CART expression in the prairie vole in a region- and stimulus-specific manner.
77 s research, the author observed 8 litters of prairie voles in a seminatural environment to confirm th
78 erences in forebrain V1aR expression of male prairie voles in mixed-sex seminatural enclosures.
79 tated partner preference formation in female prairie voles in the absence of mating.
80 expression and impair social bonding in male prairie voles) increased D1, but not D2, receptor mRNA i
81                                              Prairie voles inoculated with sPMCA products developed c
82                                          The prairie vole is a socially monogamous rodent that is an
83                                          The prairie vole is a socially monogamous species in which b
84           Unlike most mammalian species, the prairie vole is highly affiliative, forms enduring socia
85 his selective aggression in pair-bonded male prairie voles is associated with increased release of va
86   The formation of monogamous pair bonds, by prairie voles, is facilitated by activation of dopamine
87                             Among monogamous prairie voles, levels of vasopressin receptor (encoded b
88 recently established the socially monogamous prairie vole (Microtus ochrogaster) as an animal model w
89                                          The prairie vole (Microtus ochrogaster) exhibits parental be
90                                          The prairie vole (Microtus ochrogaster) is a highly social,
91                                          The prairie vole (Microtus ochrogaster) is a socially monoga
92                        Here we show, using a prairie vole (Microtus ochrogaster) model of social bond
93                                          The prairie vole (Microtus ochrogaster), a monogamous rodent
94 f intranasal OT given developmentally in the prairie vole (Microtus ochrogaster), a socially monogamo
95 nt species, the highly social and monogamous prairie vole (Microtus ochrogaster), greatly increases p
96                   In the socially monogamous prairie vole (Microtus ochrogaster), mating induces endu
97         Research on a monogamous rodent, the prairie vole (Microtus ochrogaster), suggests that these
98                                    Using the prairie vole (Microtus ochrogaster)--a socially monogamo
99  for drug-induced social deficits, using the prairie vole (Microtus ochrogaster)-a socially monogamou
100  DA in social attachment of the "monogamous" prairie vole (Microtus orchrogaster).
101 he expression of pro-social behavior in male prairie voles (Microtus ochragaster), predicting that in
102 al species sympatric with cervids, including prairie voles (Microtus ochrogaster) and field mice (Per
103                                   Monogamous prairie voles (Microtus ochrogaster) and promiscuous mon
104 OTRs) impairs the formation of pair bonds in prairie voles (Microtus ochrogaster) and zebra finches (
105                                              Prairie voles (Microtus ochrogaster) are a valuable mode
106                                  Pair-bonded prairie voles (Microtus ochrogaster) are biparental afte
107                                              Prairie voles (Microtus ochrogaster) are exceptional amo
108                                              Prairie voles (Microtus ochrogaster) are monogamous and,
109                                              Prairie voles (Microtus ochrogaster) are monogamous rode
110                                              Prairie voles (Microtus ochrogaster) are monogamous rode
111                                     Although prairie voles (Microtus ochrogaster) are socially monoga
112 ry, and somatosensory cortex was examined in prairie voles (Microtus ochrogaster) by using electrophy
113                     After pair-bonding, male prairie voles (Microtus ochrogaster) display aggression
114                                         Male prairie voles (Microtus ochrogaster) display mating-indu
115                                              Prairie voles (Microtus ochrogaster) exhibit a monogamou
116                                         Male prairie voles (Microtus ochrogaster) form a pair bond wi
117 Ralpha immunoreactivity (IR) was compared in prairie voles (Microtus ochrogaster) from Illinois (IL),
118                                   Monogamous prairie voles (Microtus ochrogaster) show mating-induced
119                                         Male prairie voles (Microtus ochrogaster) spontaneously exhib
120                     The authors exposed male prairie voles (Microtus ochrogaster) to novel females in
121 abitation of sexually nai;ve male and female prairie voles (Microtus ochrogaster) triggers a cascade
122                                       Female prairie voles (Microtus ochrogaster) were exposed to 1 h
123                             Pair-bonded male prairie voles (Microtus ochrogaster) were infused with a
124 e meadow voles (Microtus pennsylvanicus) and prairie voles (Microtus ochrogaster) were injected with
125 vectors were used to enhance ERalpha in male prairie voles (Microtus ochrogaster), which display high
126 endency to form a partner preference in male prairie voles (Microtus ochrogaster).
127 mation and social contact in male and female prairie voles (Microtus ochrogaster).
128  partner preference (PP) formation in female prairie voles (Microtus ochrogaster).
129 cial behavior in monogamous mammals, such as prairie voles (Microtus ochrogaster).
130 oxy for pair bonding) in socially monogamous prairie voles (Microtus ochrogaster).
131 luencing socioreproductive behaviors in male prairie voles (Microtus ochrogaster).
132 segment of a 25-year study of the monogamous prairie vole, Microtus ochrogaster, in Illinois, USA.
133                                           In prairie voles, Microtus ochrogaster, females exhibit a d
134                                In monogamous prairie voles, Microtus ochrogaster, males are parental
135                                In monogamous prairie voles, OT and dopamine interact to promote partn
136 umber of TH-immunoreactive cells in the male prairie vole pBST and MeAPd, an effect that could be rev
137                            Within the normal prairie vole population, both the type and the amount of
138                                              Prairie vole pups (Microtus ochrogaster) in laboratory c
139                                              Prairie vole pups in seminatural environments preferred
140                                   Adult male prairie voles received a sham surgery, were gonadectomiz
141 r show that mice that are transgenic for the prairie vole receptor gene have a neuroanatomical patter
142  and/or changes in promoter structure of the prairie vole receptor gene may contribute to the species
143  corticosterone, a stress hormone, in female prairie voles recovering alone but not the female prairi
144 ie voles recovering alone but not the female prairie voles recovering with their male partner.
145 he cingulate cortex, AVP receptor binding in prairie voles showed a peak in early development with a
146  organization, sexual differentiation of the prairie vole spinal cord differs from that found in most
147                                    In female prairie voles, swim stress interferes with the developme
148  of aggression in sexually naive, adult male prairie voles that are comparable to those levels observ
149                                 Adult female prairie voles that overexpress oxytocin receptor in the
150                               Ovariectomized prairie voles that were treated with estradiol benzoate
151 and behavioral consequences of exposing male prairie voles to a pup.
152                           Here, we used male prairie voles to examine the effects of drug exposure on
153                                           In prairie voles, trade-offs in the fitness consequences of
154 rphic microsatellite in the 5' region of the prairie vole vasopressin 1a receptor (avpr1a) gene modif
155 may narrow the behavioral repertoire of male prairie voles via a DA receptor-specific mechanism in th
156           A group of gonadally intact female prairie voles was included to reveal possible sex differ
157                                   Here, male prairie voles were administered intracerebroventricularl
158 es on the parental behavior of virgin female prairie voles were examined.
159             Reproductively naive, adult male prairie voles were implanted with radiotransmitters used
160                        Male and female adult prairie voles were placed in a cage either alone, or wit
161                                   Adult male prairie voles were transfected with ERalpha in the MeA (
162 e investigated Oxtr expression in monogamous prairie voles, which have a well-characterized OXT syste
163  genetic and genomic tools for this species, prairie voles will likely maintain their current traject
164 essive behavioral testing of female and male prairie voles with immunohistochemistry for citrulline,
165          Overall, our data indicate that the prairie vole would be a useful model for exploring how i
166   We hypothesized that PR expression in male prairie voles would differ from that described in other
167  we initially predicted that male and female prairie voles would exhibit similar behavioral responses
168                                              Prairie vole young on hind nipples, however, were dislod

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