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1 riable, ranging from violent to tolerant and affiliative.
2 ikely to be aggressive and more likely to be affiliative.
3  appropriate social behaviors, aggressive or affiliative.
4 ur data show that Sept5 deficiency decreased affiliative active social interaction, but this phenotyp
5 ffers social advantages, pointing towards an affiliative, adaptive function.
6 g videos of social interactions labelled as "affiliative", "aggressive", or "ambiguous".
7 chanisms-physical avoidance, social support, affiliative, aggressive and displacement behaviours-to c
8 direct causal role of the MeA in controlling affiliative allogrooming and identify a select, tachykin
9               Here we show that mice exhibit affiliative allogrooming behaviour towards distressed pa
10 icly searchable and standardised database on affiliative and agonistic animal social behaviour.
11 sequent social cues in a variety of socially affiliative and avoidant ways.
12              Foraging bats demonstrated both affiliative and competitive interactions with different
13 iably recognized, and the majority of highly affiliative and cooperative dyads are actually unrelated
14                      While some species have affiliative and even cooperative interactions between in
15 ferences between cats' facial signals during affiliative and non-affiliative intraspecific interactio
16 teractions and responded differently to both affiliative and threatening signals.
17  three social-functional subtypes: pleasure, affiliative, and dominance.
18  in human bonding in different reproductive, affiliative, and kinship-based relationships remains unr
19 nspecifics making expressions of aggressive, affiliative, and neutral valence.
20                   We measured frequencies of affiliative behavior (grooming, play, approaches and pro
21  that prosocial behavior may be predicted by affiliative behavior and activity in the prosocial neura
22 ) has an important role in the regulation of affiliative behavior and social bonding in both nonhuman
23 relative to the continuum of species-typical affiliative behavior and supports the hypothesis that ER
24     Openers showed significantly more social affiliative behavior both before and after door opening
25 hibited increased levels of both anxiety and affiliative behavior compared with control males.
26 wing that individuals who show high rates of affiliative behavior form stronger social bonds with oth
27  the well-described influence of oxytocin on affiliative behavior in voles could also be of importanc
28 ting that females who manifest high rates of affiliative behavior may also be more motivated to antic
29 eptide systems involved in the regulation of affiliative behavior may contribute to abnormalities in
30                                 The frequent affiliative behavior of African elephants is posited as
31 the endogenous opioid system in maternal and affiliative behavior of group-living rhesus macaque (Mac
32          Changes in both negative affect and affiliative behavior were significantly related to volun
33 er, PAC1-deficient females exhibited delayed affiliative behavior when housed with novel males, and P
34 es indicate that OT administration increases affiliative behavior, including trust, empathy, and soci
35 rticostriatal network predicted the onset of affiliative behavior, while another predicted the amount
36  negative affective experience and increased affiliative behavior.
37 ens of Cape mole-rats reflects their lack of affiliative behavior.
38 mans, which promotes interpersonal touch and affiliative behavior.
39 c effects, suggesting a role in grooming and affiliative behavior.
40  (d = 1.09), and at 4-5 weeks exhibited more affiliative behaviors (d = 0.64), including gesturing, l
41 ostromedial basal forebrain are critical for affiliative behaviors and social attachment.
42 egy for elucidating the mechanisms of social affiliative behaviors and the alteration of these behavi
43 n, serve a crucial role in the regulation of affiliative behaviors and thus may be altered in borderl
44      The results suggest that protective and affiliative behaviors are pivotal in bonobo society and
45 e with frequencies of observed parenting and affiliative behaviors between partners.
46 stnatal development, engaged in fewer social affiliative behaviors in a familial context, exhibited l
47 vioral domains such as sex-naive anxiety and affiliative behaviors, but does not alter other domains
48 nogamous rodents that display high levels of affiliative behaviors, including pair-bonding, biparenta
49 f sCAMs often manifests in changes in social affiliative behaviors, likely through alterations in syn
50 ) predicted oxytocin-associated increases in affiliative behaviors--lip smacking, visual attention to
51                                       Social affiliative behaviors-engagement in positive (i.e., nona
52 eins, including SHANKs and others, on social affiliative behaviors.
53 ductions, or other dysregulations, of social affiliative behaviors.
54 iety disorders due to its ability to promote affiliative behaviors.
55 s methamphetamine had only modest effects on affiliative behaviors.
56 he literature on the role of sCAMs in social affiliative behaviors.
57 ving perceptual abilities and one subserving affiliative behaviors.
58  studies indicate its association with human affiliative behaviors.
59 oxytocin binding and signaling in sexual and affiliative behaviors.
60 t of the prairie vole, and exhibit increased affiliative behaviour after injection with arginine vaso
61 nflict on grooming interactions: we examined affiliative behaviour at the evening sleeping burrow, 30
62 tigated how the occurrence of aggressive and affiliative behaviour during inter-group encounters was
63  administered arginine vasopressin increases affiliative behaviour in the highly social, monogamous p
64 is dynamically modulated to enhance females' affiliative behaviour towards a partner.
65 do not engage in any immediate post-conflict affiliative behaviour with the protagonists or other bys
66 uit brain reward systems to drive changes in affiliative behaviour.
67 d on macaque-macaque allogrooming behaviour, affiliative behaviours of short duration (agonistic supp
68 a major benefit of sociality, facilitated by affiliative behaviours such as grooming and communal nes
69 s of social communication: their relation to affiliative behaviours, their sensitivity to social cont
70 ort of socially aversive (malevolent) versus affiliative (benevolent) traits.
71                                         Male affiliative bonding depends upon release of both vasopre
72 ater emphasis on facial signals that promote affiliative bonding.
73 trinsically social animals, forming enduring affiliative bonds [1].
74 ormal infant monkeys, which developed strong affiliative bonds and little or no behavioral disturbanc
75 h adult partners with whom they share strong affiliative bonds, aligning with the idea that play is a
76 striatal connectivity similar to other human affiliative bonds; highlight specific corticostriatal pa
77 t correlated with how quickly animals become affiliative but causally accelerates it.
78 lowing AVP administration, they reciprocated affiliative communication cues with species-typical affi
79 einforcement training and the addition of an affiliative conspecific), and data collected on their be
80 nd strength, whistle exchange frequency, and affiliative contact behavior rates to test this hypothes
81  time in close proximity and engage in fewer affiliative contact behaviors to reinforce and maintain
82 failed to console distressed conspecifics by affiliative contact.
83  vocalisations are enhanced when paired with affiliative contexts but inhibited when paired with aggr
84 ic cats exhibit more rapid facial mimicry in affiliative contexts than non-affiliative ones, which is
85 tive vocalizations, taken from agonistic and affiliative contexts, of humans and three other primates
86 to geladas) and made by males during various affiliative contexts.
87 This second sympathetic network may subserve affiliative, defensive and sexual behaviors.
88 inship-related social scenarios evocative of affiliative emotion induce septal-preoptic-anterior hypo
89  area, may play a key role in enabling human affiliative emotion.
90 ial molecule that nonselectively facilitated affiliative emotions and behavior, it is now recognized
91   Our finding of a neural signature of human affiliative experience bears direct implications for the
92 t theory, we focused instead on the socially affiliative experience of sex.
93 obiological mechanisms underpinning impaired affiliative experiences and behaviors in neuropsychiatri
94  remains obscure whether the neural bases of affiliative experiences can be differentiated from the e
95 126) imitate lipsmacking gestures (a macaque affiliative expression) performed by a human experimente
96 c-cardiac discrimination of threatening from affiliative facial cues.
97        In contrast, in women, AVP stimulates affiliative facial motor patterns in response to the fac
98 ammalian species, the prairie vole is highly affiliative, forms enduring social bonds between mates a
99 communicative signals, enriched mirroring to affiliative gestures).
100 cifically impairs social, but not nonsocial, affiliative grouping preferences.
101 ncounter, predicts how quickly animals begin affiliative huddling with their partner.
102 ree social contexts (aggressive, submissive, affiliative) in 389 animals, using the Facial Action Cod
103  warfare, whilst also engaging in the strong affiliative inter-group relationships necessary for larg
104                                              Affiliative interaction, proximity, and nearest neighbor
105     In humans, stress can promote protective affiliative interactions and prosocial behavior.
106 their tendencies to engage in short-duration affiliative interactions and tolerance of conspecifics,
107 hine learning classifier for affiliative/non-affiliative interactions based on manual CatFACS codings
108                                  We recorded affiliative interactions of 29 two-year-old rhesus monke
109  We examined the social partners involved in affiliative interactions of female orphans and non-orpha
110 ore agonistic interactions to more positive, affiliative interactions over their life span.
111 s' facial signals during affiliative and non-affiliative intraspecific interactions.
112            These findings demonstrate social-affiliative learning in the Mongolian gerbil.
113 ience of pleasant images increased (exciting<affiliative&lt;erotica).
114                                         This affiliative motivation ensures that people experience an
115 vidence that inflammation may promote social affiliative motivation, the present research proposes a
116             Next, we describe how heightened affiliative need can interact with adolescent transition
117 ocial and hormonal mechanisms that stimulate affiliative needs for females at puberty.
118 nfamiliar monkeys (movie monkeys) displaying affiliative, neutral, and aggressive behaviors.
119 we develop a machine learning classifier for affiliative/non-affiliative interactions based on manual
120 yteles hypoxanthus), a species known for its affiliative, nonhierarchical relationships.
121 ial mimicry in affiliative contexts than non-affiliative ones, which is consistent with the proposed
122 ns in domestic cats are often categorised as affiliative or agonistic.
123 portant role in facilitating and maintaining affiliative or cooperative interactions in social animal
124 ssive responses to conspecific aggressive or affiliative overtures.
125 eural synchrony to social interactions among affiliative partners.
126 ed juveniles (peers) and the total number of affiliative peer relationships.
127  more closely related peers, those with more affiliative peers or more frequent play bouts had lower
128 time together, while the opposite occurs for affiliative physical contact behavior.
129 ion within the amygdala compared to the more affiliative pigtailed and moor macaques.
130  we demonstrate that individuals have strong affiliative preferences for full and maternal siblings o
131 account argues that oxytocin mainly enhances affiliative prosocial behaviors; the fear/stress theory
132 ty, decreased social avoidance, and promoted affiliative proximity and huddling with a novel, previou
133 ales were investigative and prosocial (e.g., affiliative proximity), they exhibited significant socia
134 nal relations were an excellent predictor of affiliative relations among daughters, explaining up to
135                                     Maternal affiliative relations may be transmitted to offspring, s
136 ysis compared relations among age peers with affiliative relations, kinship, and rank distance among
137 ther nonhuman primate species organize their affiliative relationships following the same pattern.
138 e males form strong, enduring, and equitable affiliative relationships similar to human friendships.
139  importance of studying agonistic as well as affiliative relationships to understand fully the connec
140 es indicated this only occurred after strong affiliative relationships were established between the o
141 y benefit by maintaining cohesive and strong affiliative relationships, and by increasing opportuniti
142 ineated dominance hierarchies and a range of affiliative relationships.
143 cs of conspicuous visual stimuli and display affiliative response to them.
144 tecture during development and to acquire an affiliative response toward conspecifics.SIGNIFICANCE ST
145 tive communication cues with species-typical affiliative responses.
146 xcitability, along with reduced responses to affiliative signals.
147              The stable group exhibited more affiliative social behavior and less agonistic behavior
148 here is less data to support the notion that affiliative social behavior can slow disease progression
149          These results support the idea that affiliative social behavior is subject to natural select
150 sized that nebulized oxytocin would increase affiliative social behaviors and such effects would be m
151           MDMA and its enantiomers increased affiliative social behaviors and vocalizations, whereas
152  We found that mWSD offspring initiated less affiliative social behaviors as well as proximity to a p
153 man primates show MDMA-specific increases in affiliative social behaviors following MDMA administrati
154  linked and play a crucial role in promoting affiliative social bonds.
155  structures varies with the number of direct affiliative social connections and suggest that this rel
156                                              Affiliative social connections facilitate well-being and
157 after the hurricane and found an increase in affiliative social connections, driven largely by monkey
158 g suggests that giving rather than receiving affiliative social contact may be more beneficial for ch
159 protein in the amygdala and increased active affiliative social interaction in C57BL/6J mice.
160 tent, the amygdala elevated levels of active affiliative social interaction in C57BL/6J mice.
161 etic background, selectively impaired active affiliative social interaction in mice.
162             Operated monkeys engaged in more affiliative social interactions with control partners th
163 ial threat posed by rival groups, intragroup affiliative social interactions, or coordinated behavior
164 maintained through positive reinforcement of affiliative social interactions.
165 ographics, and macaque-macaque agonistic and affiliative social interactions.
166 ation in cats has predominantly examined non-affiliative social interactions.
167                                              Affiliative social relationships have clear links to fit
168 tes, can benefit group members by developing affiliative social relationships, enhancing access to re
169  relationships, maternal-infant bonding, and affiliative social relationships.
170                                              Affiliative social touch, such as allogrooming (grooming
171                                       Highly affiliative species have receptors in brain circuits rel
172  care can facilitate the rapid responding to affiliative stimuli by reducing importance of threatenin
173 utbursts, suggesting that the attachment and affiliative system may be implicated in the disorder.
174 ng by showing that adult fish exhibit strong affiliative tendencies and that social interactions can
175                                              Affiliative tendencies were predicted by genetic variati
176  that food sharing reflects a combination of affiliative tendency and high tolerance.
177 ey respectively fulfill (material vs. social/affiliative), to account for flexibility in action inter
178 m that underlies the encoding and control of affiliative touch during prosocial interactions.
179 , the neural circuits that promote prosocial affiliative touch have remained unclear.
180                                              Affiliative touch serves to establish and strengthen soc
181 tunities for social influence and acted less affiliative toward virtual characters.
182 ts of parenting and the mutual regulation of affiliative versus agonistic infant-directed behaviors i
183 acial fur patch-is linked to their degree of affiliative vocal responding.
184                    For example, responses to affiliative vocalisations are enhanced when paired with
185 e a 5-HT1A receptor antagonist did not alter affiliative vocalizations and increased MDMA-induced soc
186  from agonistic human voices, but chimpanzee affiliative vocalizations were significantly closer to h
187 lizations were significantly closer to human affiliative vocalizations, than those of bonobos, indica
188 increased repetitive behaviors and decreased affiliative vocalizations.

 
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