ライフサイエンスコーパス: social behaviour

1 frank neuronal loss and FTD-like changes in social behaviour.

2 mechanism for the rapid evolution of complex social behaviour.

3 sts; and the identification of violations of social behaviour.

4 ught to play a crucial role in emotional and social behaviour.

5 ulate shoal cohesion, indicative of abnormal social behaviour.

6 ional asymmetry has evolved as an adjunct to social behaviour.

7 ve in mutants, but becomes hypoactive during social behaviour.

8 thesis linking directional lateralization to social behaviour.

9 ects of testosterone administration on human social behaviour.

10 ed in face expression processing involved in social behaviour.

11 minent, early and progressive impairments in social behaviour.

12 granulin deficiency is sufficient to disrupt social behaviour.

13 netic and epigenetic underpinnings of animal social behaviour.

14 (Esr1), and investigated their role in male social behaviour.

15 recognition is a key component of successful social behaviour.

16 imaging and can give important insights into social behaviour.

17 of diversity that may apply to many forms of social behaviour.

18 Cooperation is central to human social behaviour.

19 , possibly conferring benefits to health and social behaviour.

20 low-level network in more complex high-level social behaviour.

21 example of an imprinted gene that regulates social behaviour.

22 RMG activity is essential for all aspects of social behaviour.

23 ent model for investigating the evolution of social behaviour.

24 y in the VMHvl of male mice engaged in these social behaviours.

25 g normal and pathological sexually dimorphic social behaviours.

26 Animals display a repertoire of different social behaviours.

27 halamic neural assemblies controlling innate social behaviours.

28 trate for competition between these opponent social behaviours.

29 e they have fundamentally important roles in social behaviours.

30 Cplx1(-/-) mice have pronounced deficits in social behaviours.

31 skills (3.86, 1.41 to 6.31), and 0.2 for pro-social behaviours (0.07, 0.02 to 0.12).

32 skills (7.53, 5.14 to 9.92) and 0.2 for pro-social behaviours (0.08, 0.03 to 0.13).

33 ominance specifically among other aspects of social behaviour, a finding supported by the observed in

34 xually immature mice that controls an innate social behaviour, a response pathway through the accesso

35 Maladaptive social behaviour accordingly was a major force that cont

36 Maladaptive social behaviour accordingly was a major force that cont

37 imental work that addresses how kin-selected social behaviours affect virulence.

38 ess), imprinted genes may evolve to modulate social behaviour, although so far no such instance is kn

39 n identification, but significant changes in social behaviour and in subjective emotional state are r

40 marizes recent studies in the epigenetics of social behaviour and offers perspectives on emerging tre

41 le is known of the link between personality, social behaviour and population structure.

42 scourse comprehension is a hallmark of human social behaviour and refers to the act of interpreting a

43 tification, and the group had impairments in social behaviour and significant changes in their subjec

44 in humans including emotion identification, social behaviour and subjective emotional state, and tha

45 that PX-RICS-deficient mice exhibit ASD-like social behaviours and ASD-related comorbidities.

46 ant role in the evolution and maintenance of social behaviour, and 'helpers' can maximize indirect fi

47 pression identification, had some changes in social behaviour, and had significant changes in their s

48 xpression identification, had some change in social behaviour, and had significant changes in their s

49 nd face emotional expression identification, social behaviour, and the subjective experience of emoti

50 language development, positive and negative social behaviours, and independence; parenting risk; hom

51 emical changes underlying human emotions and social behaviour are largely unknown.

52 In particular, while changes in social behaviour are prominent in bvFTD alone, there may

53 Inappropriate social behaviours are early and distinctive symptoms of

54 he responding neurons that regulate specific social behaviours are largely unknown.

55 ssible role in processing whether particular social behaviours are, or are not, appropriate.

56 the mouse hypothalamus, that underlie innate social behaviours, are shaped by social experience.

57 n shown to affect social group structure and social behaviour as well as individual fitness of the pr

58 avioural classification system, LABORAS) and social behaviour (as a measure of anxiety) in rats follo

59 reproductive physiology and numerous related social behaviours, as do oxytocin (mammals) and its homo

60 vered do not include frequency dependence or social behaviour, but the approach is capable of extensi

61 populations, with potential implications for social behaviour by increasing the number of potential i

62 The coordination of social behaviours by RMG suggests an anatomical hub-and-

63 These mice show ASD-resembling social behaviour deficits.

64 has established that effects of hormones on social behaviour depend on characteristics of both indiv

65 When we tested social behaviour directly, Cplx1(-/-) mice failed to dem

66 files, showed higher levels of inappropriate social behaviours ('disinhibition') and demonstrated mor

67 This is partly because social behaviours do not fossilize, making it difficult

68 'social concepts' (i.e. concepts describing social behaviour: e.g. 'polite', 'stingy') as compared w

69 Innate social behaviours emerge from neuronal circuits that int

70 ave implicated the amygdala in emotional and social behaviours, especially those related to fear and

71 al of sociobiology is to explain how complex social behaviour evolves, especially in social insects,

72 in hunger or inebriation state affected the social behaviours exhibited by two closely-related nestm

73 r associated with genetic variation in a non-social behaviour: explorative genotypes elicited most ag

74 asopressin (AVP) seem to modulate a range of social behaviour from parental care to mate guarding.

75 tional facial expressions, its role in human social behaviour has remained unclear.

76 ficance of non-social selection pressures on social behaviours has received little attention.

77 al circuit that regulates parental-offspring social behaviour in C. elegans and that this provides ev

78 ly insults could result in severely impaired social behaviour in later childhood and adolescence.

79 Understanding the neurobiology of social behaviour in mammals has been considerably advanc

80 on interactions in humans, and mechanisms of social behaviour in non-human primates, and may have imp

81 al reproductive traits gives rise to complex social behaviour in non-reproductive helpers.

82 and virulence is crucially dependent on the social behaviour in question.

83 ver was used to investigate the evolution of social behaviour in repeated Prisoner's Dilemma, Chicken

84 siological state influences food sharing and social behaviour in social insects is poorly understood.

85 full-length mutant protein display abnormal social behaviour in the absence of acute neurodegenerati

86 ction, and initiating a surprising degree of social behaviour in these mostly solitary animals.

87 ffers new perspectives on the key drivers of social behaviour in wild populations.

88 the spread of disease and the prevalence of social behaviour in wildlife.

89 apted ecotypes and cryptic morphs, divergent social behaviours in birds and insects, as well as alter

90 on of oxytocin temporally mitigates autistic social behaviours in experimental settings, it remains i

91 functionally associated with species-typical social behaviours in male vertebrates.

92 vasopressin influences male reproductive and social behaviours in several vertebrate taxa through its

93 Social behaviours in species as diverse as honey bees an

94 on and exposure on a range of individual and social behaviours in young adult bees.

95 in has a conserved role in regulating animal social behaviour including parental-offspring interactio

96 acterium Myxococcus xanthus exhibits several social behaviours, including aggregation of cells into s

97 and psychiatric disorders in which disturbed social behaviour is commonplace.

98 In mice, social behaviour is driven by pheromones, chemical signa

99 Knowledge of social behaviour is essential for appropriate social con

100 n for its role in lactation, parturition and social behaviours--is required for proper muscle tissue

101 ice exhibit enlarged ventricles and impaired social behaviour, locomotor activity, and learning and m

102 These sex differences in social behaviour may underpin male-biased acquisition of

103 se in the non-SSLP areas, with more positive social behaviour (mean difference 0.45, 95% CI 0.09 to 0

104 Empathy is a complex social behaviour mediated by a network of brain structur

105 o norm violations are two important forms of social behaviour modelled in economic games.

106 teractions that are an important part of the social behaviour of M. xanthus.

107 have profound effects on the demography and social behaviour of tetrapods.

108 ged individuals were recorded along with the social behaviour of their groups.

109 estigate this, we examined the cognitive and social behaviours of complexin 1 knockout mice (Cplx1(-/

110 he group did not have significant changes in social behaviour or in their subjective emotional state.

111 stering of organisms can be a consequence of social behaviour, or of the response of individuals to c

112 ant implications for the evolution of animal social behaviour, particularly complex interactions such

113 tic and neural circuits can profoundly alter social behaviour, providing a potential molecular mechan

114 uggests that testosterone enhances strategic social behaviour rather than dominance seeking behaviour

115 However, primate social behaviour shows strong evidence for phylogenetic

116 ers of the same species, as cues to regulate social behaviours such as pup suckling, aggression and m

117 individuals is essential to many aspects of social behaviour, such as the maintenance of stable soci

118 es are shaped by valuation of other people's social behaviour, such that they empathize with fair opp

119 Social behaviours, such as aggression or mating, proceed

120 ons as components of pheromones that mediate social behaviours, such as caste and nestmate recognitio

121 Microorganisms are capable of remarkable social behaviours, such as forming transient multicellul

122 The ease of finding anti-social behaviours suggests that cheaters may be common i

123 a crucial determining effect on the type of social behaviour that evolves.

124 Biofilm formation is a social behaviour that generates favourable conditions fo

125 a gustatory-olfactory aspect of early infant social behaviour that is, in part, reliant on pre-natal

126 ore rigidly determined altricial patterns of social behaviour, the roles of post-reproductive group m

127 sian comparative methods to infer changes in social behaviour through time, thereby allowing us to ev

128 However, although mice show different social behaviours towards adults, juveniles and neonates

129 for measuring individual motor behaviour and social behaviour, we found that behaviours such as anten

130 changes in home cage behaviour and decreased social behaviour which, in contrast to motor function, a