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1 tors modulate pair bonding in the monogamous prairie vole.
2 a series of experiments using the monogamous prairie vole.
3 he formation of pair bonds in the monogamous prairie vole.
4  the effects of estrogen on the brain of the prairie vole.
5 [V1a receptor (V1aR)] antagonist in the male prairie vole.
6 ss molecularly-defined NAc cell types in the prairie vole.
7 ir bond formation in the socially monogamous prairie vole.
8  relate to the specialized life style of the prairie vole.
9 idine (BrdU) in the amygdala and DG than did prairie voles.
10 and VMH, but not in the pMeA or DG, than did prairie voles.
11 nvolved in pair bond formation in monogamous prairie voles.
12 1a receptor (V1aR) in a large sample of wild prairie voles.
13  is critical for pair-bond formation in male prairie voles.
14 total and selective social behaviors in male prairie voles.
15 a role in the preference for hind nipples in prairie voles.
16  estrus induction and pair bonding in female prairie voles.
17  labeling throughout the forebrain of female prairie voles.
18  role for the VNO in reproductive success in prairie voles.
19 inding in the ventral pallial region of male prairie voles.
20 al nitric oxide synthase (nNOS) in lactating prairie voles.
21 body mass distribution in this population of prairie voles.
22  in the production of maternal aggression in prairie voles.
23 th maternal and mating-induced aggression in prairie voles.
24 ent in the control of maternal aggression in prairie voles.
25 n of postcopulatory aggression in adult male prairie voles.
26 mapping regional staining for c-fos) in male prairie voles.
27  montane voles, but it remained unchanged in prairie voles.
28 ne voles but did not change significantly in prairie voles.
29 romoted a partner preference in stress-naive prairie voles.
30 nged within the PrL of male, but not female, prairie voles.
31 ssive stress-coping in male, but not female, prairie voles.
32 innate immune system in both male and female prairie voles.
33 an occur in the absence of Oxtr signaling in prairie voles.
34 erences (an index of pair bonding) in female prairie voles.
35 ve different neurobiological actions in male prairie voles.
36 al circuitry mediate selective aggression in prairie voles.
37 nd consequences on social behavior in female prairie voles.
38 ological effects of AMPH treatment in female prairie voles.
39 iosus muscles in adult male, but not female, prairie voles.
40 ex difference would be similarly distinct in prairie voles.
41  drug experience in socially monogamous male prairie voles.
42 ression associated with pair bonding in male prairie voles.
43 ession is found in a chemosensory pathway in prairie voles.
44 and medial (pMeA) nuclei, in meadow, but not prairie, voles.
45 erpinnings of OXT receptor (OXTR) agonism in prairie voles, a rodent species with demonstrated transl
46 dy, we separated pair bonded male and female prairie voles after five days of co-housing, subjected t
47                                              Prairie voles also exhibit natural variation in the leve
48                                              Prairie voles also match the fear response, anxiety-rela
49  showing conserved neural mechanisms between prairie vole and human.
50 including differences between the monogamous prairie vole and its promiscuous congeners.
51 e brains of two monogamous vole species, the prairie vole and pine vole, and two promiscuous vole spe
52 n more egalitarian and monogamous ones, like prairie voles and humans, when there is no perceived cos
53 ecular mechanisms underlying pair-bonding in prairie voles and paves the way to further our understan
54 d peptide expression have been found between prairie voles and polygamous meadow voles.
55 in and behavior parallel differences between prairie voles and promiscuous congeners.
56 hin the brains of closely related monogamous prairie voles and promiscuous meadow voles, and compare
57 its maternal aggression and NO production in prairie voles and suggest that the central release of NO
58 septum regulates pair bond formation in male prairie voles and that this process requires access to b
59 eptor binding that is similar to that of the prairie vole, and exhibit increased affiliative behaviou
60 for the behavioral effects of AMPH in female prairie voles, and found that conditioning with low to i
61 h alloparenting in juvenile and adult female prairie voles, and oxytocin receptor antagonist infused
62  regulation of partner preferences in female prairie voles, and suggest that oxytocin receptor expres
63                  Using adult male and female prairie voles, animals were either pair bonded, co-house
64                                              Prairie voles are among a small group of mammals that di
65                                 Like humans, prairie voles are among the few mammalian species that f
66                  For example, sexually naive prairie voles are rarely aggressive.
67                           Here, we show that prairie voles are susceptible to mule deer CWD prions in
68 ized pair bonding in the socially monogamous prairie vole as an example of socio-sexual experience th
69 duced facilitation of pair bond formation in prairie voles, as well as potential sex differences in t
70 ctivation on partner preference formation in prairie voles, as well as the interaction between the MC
71                  In socially monogamous male prairie voles, AVP acts centrally via vasopressin V1a re
72 r the formation of social attachment in male prairie voles, because administration of haloperidol blo
73                                      In male prairie voles, both vasopressin and dopamine act in the
74  exogenously administered OXT penetrates the prairie vole brain and showed that Receptor for Advanced
75 ion of kappa- and mu-opioid receptors in the prairie vole brain.
76                                              Prairie vole breeder pairs form monogamous pair bonds, w
77 enhanced partner preference formation in the prairie vole, but not in the non-monogamous meadow vole.
78 e behaviour in the highly social, monogamous prairie vole, but not in the relatively asocial, promisc
79                                       Female prairie voles, but not meadow voles, spent more time in
80 ential underlying mechanisms, the monogamous prairie vole can provide important insights.
81 y psychiatric disorders, discoveries made in prairie voles can direct novel treatment strategies for
82                      Likewise, in adult male prairie voles, central (intracerebroventricular) injecti
83 peared to be disproportionately large in the prairie vole compared with other rodents.
84 ution of CART mRNA and peptide in monogamous prairie voles compared to congener promiscuous meadow vo
85 re, our study presents an integrated view of prairie vole dentate gyrus transcriptome and epigenome t
86                                         Male prairie voles displayed strongly selective huddling pref
87 odialysis experiments were performed on male prairie voles displaying affiliation or aggression.
88 d AMPH administration in sexually naive male prairie voles enhanced V1aR expression in the AH and ind
89                                    In female prairie voles, exposure to a male or to male sensory cue
90                                      In male prairie voles, exposure to either the stress of swimming
91 thylome of hippocampal dentate gyrus of four prairie vole groups, namely attacker virgin males, paren
92                                  Virgin male prairie voles had a large number of TH-immunoreactive ce
93                                Virgin female prairie voles had far fewer TH-immunoreactive cells in t
94 is, and the central nucleus of the amygdala, prairie voles had higher AVP receptor binding at birth t
95 hicle-exposed controls, prenatal VPA-exposed prairie voles had lower body weight throughout postnatal
96 ong-term pair-bonds, the socially monogamous prairie vole has emerged as an excellent model to study
97 ny species, including humans, and monogamous prairie voles have become the predominant model for inve
98                                 Furthermore, prairie voles have higher densities of oxytocin receptor
99                                              Prairie voles have more Oxtr+ cells than meadow voles, b
100 rences in CB1 densities across species, with prairie voles having higher CB1 binding in regions impli
101 nvironment influences CART expression in the prairie vole in a region- and stimulus-specific manner.
102 s research, the author observed 8 litters of prairie voles in a seminatural environment to confirm th
103 erences in forebrain V1aR expression of male prairie voles in mixed-sex seminatural enclosures.
104 tated partner preference formation in female prairie voles in the absence of mating.
105 expression and impair social bonding in male prairie voles) increased D1, but not D2, receptor mRNA i
106                                              Prairie voles inoculated with sPMCA products developed c
107                                          The prairie vole is a socially monogamous rodent that is an
108                                          The prairie vole is a socially monogamous species in which b
109           Unlike most mammalian species, the prairie vole is highly affiliative, forms enduring socia
110 his selective aggression in pair-bonded male prairie voles is associated with increased release of va
111   The formation of monogamous pair bonds, by prairie voles, is facilitated by activation of dopamine
112 rs in selective peer attachment using female prairie voles lacking a functional oxytocin receptor gen
113                             Among monogamous prairie voles, levels of vasopressin receptor (encoded b
114 to generate three different Oxtr-null mutant prairie vole lines.
115 recently established the socially monogamous prairie vole (Microtus ochrogaster) as an animal model w
116                                          The prairie vole (Microtus ochrogaster) exhibits parental be
117                                          The prairie vole (Microtus ochrogaster) is a highly social,
118                                          The prairie vole (Microtus ochrogaster) is a socially monoga
119                        Here we show, using a prairie vole (Microtus ochrogaster) model of social bond
120                                          The prairie vole (Microtus ochrogaster), a monogamous rodent
121 f intranasal OT given developmentally in the prairie vole (Microtus ochrogaster), a socially monogamo
122 nt species, the highly social and monogamous prairie vole (Microtus ochrogaster), greatly increases p
123                   In the socially monogamous prairie vole (Microtus ochrogaster), mating induces endu
124         Research on a monogamous rodent, the prairie vole (Microtus ochrogaster), suggests that these
125                                    Using the prairie vole (Microtus ochrogaster)--a socially monogamo
126  for drug-induced social deficits, using the prairie vole (Microtus ochrogaster)-a socially monogamou
127  mammalian CpGs, for the socially monogamous prairie vole (Microtus ochrogaster).
128  DA in social attachment of the "monogamous" prairie vole (Microtus orchrogaster).
129 he expression of pro-social behavior in male prairie voles (Microtus ochragaster), predicting that in
130 al species sympatric with cervids, including prairie voles (Microtus ochrogaster) and field mice (Per
131 accumbens (NAc) expression across monogamous prairie voles (Microtus ochrogaster) and promiscuous mea
132                                   Monogamous prairie voles (Microtus ochrogaster) and promiscuous mon
133 OTRs) impairs the formation of pair bonds in prairie voles (Microtus ochrogaster) and zebra finches (
134                                              Prairie voles (Microtus ochrogaster) are a valuable mode
135                                  Pair-bonded prairie voles (Microtus ochrogaster) are biparental afte
136                                              Prairie voles (Microtus ochrogaster) are exceptional amo
137                                              Prairie voles (Microtus ochrogaster) are monogamous and,
138                                              Prairie voles (Microtus ochrogaster) are monogamous rode
139                                              Prairie voles (Microtus ochrogaster) are monogamous rode
140                                     Although prairie voles (Microtus ochrogaster) are socially monoga
141 ry, and somatosensory cortex was examined in prairie voles (Microtus ochrogaster) by using electrophy
142                     After pair-bonding, male prairie voles (Microtus ochrogaster) display aggression
143                                         Male prairie voles (Microtus ochrogaster) display mating-indu
144                                              Prairie voles (Microtus ochrogaster) exhibit a monogamou
145                                         Male prairie voles (Microtus ochrogaster) form a pair bond wi
146             Like humans, socially monogamous prairie voles (Microtus ochrogaster) form opposite-sex p
147 Ralpha immunoreactivity (IR) was compared in prairie voles (Microtus ochrogaster) from Illinois (IL),
148                                   Studies in prairie voles (Microtus ochrogaster) have shown that alt
149                                   Monogamous prairie voles (Microtus ochrogaster) show mating-induced
150                                         Male prairie voles (Microtus ochrogaster) spontaneously exhib
151                     The authors exposed male prairie voles (Microtus ochrogaster) to novel females in
152 abitation of sexually nai;ve male and female prairie voles (Microtus ochrogaster) triggers a cascade
153                              Male and female prairie voles (Microtus ochrogaster) were cohabitated wi
154                                       Female prairie voles (Microtus ochrogaster) were exposed to 1 h
155                             Pair-bonded male prairie voles (Microtus ochrogaster) were infused with a
156 e meadow voles (Microtus pennsylvanicus) and prairie voles (Microtus ochrogaster) were injected with
157 uilding blocks of monogamous pair bonding in prairie voles (Microtus ochrogaster), as well as opportu
158                                              Prairie voles (Microtus ochrogaster), like humans, are b
159                       In socially monogamous prairie voles (Microtus ochrogaster), parental behaviors
160 vectors were used to enhance ERalpha in male prairie voles (Microtus ochrogaster), which display high
161 natal VPA exposure in the social, monogamous prairie voles (Microtus ochrogaster).
162 endency to form a partner preference in male prairie voles (Microtus ochrogaster).
163 mation and social contact in male and female prairie voles (Microtus ochrogaster).
164  partner preference (PP) formation in female prairie voles (Microtus ochrogaster).
165 cial behavior in monogamous mammals, such as prairie voles (Microtus ochrogaster).
166 oxy for pair bonding) in socially monogamous prairie voles (Microtus ochrogaster).
167 luencing socioreproductive behaviors in male prairie voles (Microtus ochrogaster).
168 segment of a 25-year study of the monogamous prairie vole, Microtus ochrogaster, in Illinois, USA.
169                                           In prairie voles, Microtus ochrogaster, females exhibit a d
170                                In monogamous prairie voles, Microtus ochrogaster, males are parental
171         Previous studies revealed that adult prairie vole offspring who received either high (HC) or
172 lationships with mates and peers (monogamous prairie voles) or peers (group-living meadow voles).
173                                In monogamous prairie voles, OT and dopamine interact to promote partn
174 umber of TH-immunoreactive cells in the male prairie vole pBST and MeAPd, an effect that could be rev
175                            Within the normal prairie vole population, both the type and the amount of
176                                              Prairie vole pups (Microtus ochrogaster) in laboratory c
177                                              Prairie vole pups in seminatural environments preferred
178                                   Adult male prairie voles received a sham surgery, were gonadectomiz
179 r show that mice that are transgenic for the prairie vole receptor gene have a neuroanatomical patter
180  and/or changes in promoter structure of the prairie vole receptor gene may contribute to the species
181  corticosterone, a stress hormone, in female prairie voles recovering alone but not the female prairi
182 ie voles recovering alone but not the female prairie voles recovering with their male partner.
183 he cingulate cortex, AVP receptor binding in prairie voles showed a peak in early development with a
184 bits alcohol intake in male, but not female, prairie voles socially housed in the presence of untreat
185 l (IN) OXT administration in male and female prairie voles socially housed in the presence of untreat
186  organization, sexual differentiation of the prairie vole spinal cord differs from that found in most
187          We confirmed the presence of CB2 in prairie vole spleen tissue using [3H] CP-55,940.
188 e oxytocin is knocked out, normally amicable prairie voles struggle to make friends.
189 ess both dopamine receptors (Drd1+/Drd2+) in prairie voles, suggesting these cells may be particularl
190                                    In female prairie voles, swim stress interferes with the developme
191  of aggression in sexually naive, adult male prairie voles that are comparable to those levels observ
192                                 Adult female prairie voles that overexpress oxytocin receptor in the
193                               Ovariectomized prairie voles that were treated with estradiol benzoate
194 VN) in male prairie voles, whereas in female prairie voles the morphological activation within the wh
195 cial defeat model in the socially monogamous prairie vole to investigate the impact of this stress on
196 and behavioral consequences of exposing male prairie voles to a pup.
197                           Here, we used male prairie voles to examine the effects of drug exposure on
198                                           In prairie voles, trade-offs in the fitness consequences of
199 rphic microsatellite in the 5' region of the prairie vole vasopressin 1a receptor (avpr1a) gene modif
200 may narrow the behavioral repertoire of male prairie voles via a DA receptor-specific mechanism in th
201           A group of gonadally intact female prairie voles was included to reveal possible sex differ
202                             Using monogamous prairie voles, we first employed receptor pharmacology i
203 -photon in vivo Ca(2+) imaging in monogamous prairie voles, we found that pair bonding does not elici
204                                   Here, male prairie voles were administered intracerebroventricularl
205 es on the parental behavior of virgin female prairie voles were examined.
206             Reproductively naive, adult male prairie voles were implanted with radiotransmitters used
207                        Male and female adult prairie voles were placed in a cage either alone, or wit
208                   Thirty-two male and female prairie voles were scanned at baseline, 24 hr, and 2 wee
209                                   Adult male prairie voles were transfected with ERalpha in the MeA (
210 ar nucleus of the hypothalamus (PVN) in male prairie voles, whereas in female prairie voles the morph
211 e investigated Oxtr expression in monogamous prairie voles, which have a well-characterized OXT syste
212 cleus of the stria terminalis (BNST) in male prairie voles, while defeat experience increased BNST CR
213  genetic and genomic tools for this species, prairie voles will likely maintain their current traject
214 essive behavioral testing of female and male prairie voles with immunohistochemistry for citrulline,
215 ed pair-bonding in Microtus ochrogaster, the prairie vole, with plastic changes in several brain regi
216          Overall, our data indicate that the prairie vole would be a useful model for exploring how i
217   We hypothesized that PR expression in male prairie voles would differ from that described in other
218  we initially predicted that male and female prairie voles would exhibit similar behavioral responses
219                                              Prairie vole young on hind nipples, however, were dislod

 
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