ライフサイエンスコーパス: social recognition

1 adult heterozygous Dyrk1a mice also rescued social recognition.

2 ry bulb (GnRH(OB)) of adult mice can mediate social recognition.

3 forward inhibition of CA3 and CA2 to promote social recognition.

4 PV IN-mediated inhibition of CA3 and CA2 and social recognition.

5 campus to the posterior hippocampus to guide social recognition.

6 on or avoidance behavior is thought to guide social recognition.

7 gan, an olfactory substructure essential for social recognition.

8 s Spheniscus vocalisations are important for social recognition.

9 /- mice showed decreased social interest and social recognition.

10 (V1aR) or oxytocin receptor (OTR) related to social recognition.

11 801), cognitive impairments, and deficits in social recognition.

12 veral days before behavioral testing reduced social recognition.

13 iral vector resulted in a complete rescue of social recognition.

14 but not the medial amygdala, is critical for social recognition.

15 sensitive PFC to BLA circuit is required for social recognition.

16 easured by prepulse inhibition, and impaired social recognition.

17 insights about neuroendocrine regulation of social recognition.

18 n explored concerning its modulatory role in social recognition.

19 e estrogen control over the OT regulation of social recognition.

20 experimental social experience on subsequent social recognition.

21 OT treatment fully restores social recognition.

22 la during the initial exposure to facilitate social recognition.

23 asopressin in the olfactory bulb impairs the social recognition abilities of rats and that vasopressi

24 alian social behaviors such as pair bonding, social recognition and aggression causally increases hum

25 ptor (V1aR) exhibit a profound impairment in social recognition and changes in anxiety-like behavior.

26 core autism-like traits, including defective social recognition and communication, increased stereoty

27 stress-coping responses, and mildly impaired social recognition and communication.

28 er that corresponded with reduced short-term social recognition and enhanced background (pre-investig

29 ories in rodents, focusing on two paradigms: social recognition and fear conditioning, representing a

30 on and provide insight into the mechanism of social recognition and immunity.

31 Oxytocin (OT) is a critical molecule for social recognition and memory that mediates social and e

32 "knocked out" were deficient specifically in social recognition and social anxiety.

33 ove useful in studies of disorders affecting social recognition and social engagement, and the treatm

34 Magel2 inactivation induces a deficit in social recognition and social interaction and a reduced

35 n play a particularly prominent role both in social recognition and the expression of appropriate soc

36 physiological responses including alertness, social recognition, and hunger, yet, their mechanism of

37 es abnormalities in respiratory function and social recognition, and improves motor coordination in y

38 ts were tested in a short-term memory model, social recognition, and in a separate group cortical and

39 g the monkey delayed matching-to-sample, rat social recognition, and mouse inhibitory avoidance model

40 oning, object recognition, object placement, social recognition, and spatial reference memory.

41 d violence, perceived respect from patients, social recognition as well as physician-nurse coordinati

42 reated mice exhibit impaired sociability and social recognition at 72 h post-exposure, which correlat

43 type (wt) mice resulted in a potentiation of social recognition behavior and a mild increase in anxie

44 and vertebrates share similarities in their social recognition behavior, indicating that these behav

45 olved in species-typical behavior, including social recognition behavior, maternal behavior, social b

46 atal novelty exposure-induced enhancement in social recognition broadens the impact of early life sti

47 region-selective receptor deletion impaired social recognition but left odor discrimination and reco

48 Social recognition constitutes the basis of social life.

49 for both food odors and urine, an important social recognition cue.

50 knockout mouse (but not V1B) has a profound social recognition deficit.

51 The social recognition deficits seen in oxytocin knockout mi

52 letion is sufficient to cause early FTD-like social recognition deficits.

53 bition-like behavior, as well as deficits in social recognition from a relatively young age.

54 ons as well as the CA2-vCA1 pathway restored social recognition function to wildtype levels.

55 t a critical role for the oxytocin system in social recognition has been conserved across perceptual

56 Social learning and social recognition have become emerging areas of interes

57 Hits synergistically affected social recognition in adulthood: only mice exposed to al

58 A recent study of social recognition in crickets shows that decorated cric

59 cally in the amygdala is required for normal social recognition in female mice.

60 odel that binge alcohol consumption disrupts social recognition in females and potentiates sensorimot

61 descending control over a circuit mediating social recognition in mice.

62 ) expressing neurons in the PFC that impairs social recognition in mice.

63 PAK inactivation led to obliteration of social recognition in old 3xTg-AD mice, which was associ

64 ut not after, the initial encounter restores social recognition in OT knock-out mice.

65 mygdala is both necessary and sufficient for social recognition in the mouse.

66 extending previous findings of impairment in social recognition in these mutants.

67 al hormones play a role in the modulation of social recognition including estrogen, oxytocin and argi

68 could provide a basis for different types of social recognition, including kin and species recognitio

69 Social recognition is crucial for survival in social spe

70 Social recognition is essential for the formation of soc

71 In male mice and rats, social recognition is known to be governed by the neurop

72 he site in the female brain for OT action on social recognition is still unknown.

73 Long-term social recognition is vital for species with complex soc

74 es typical behavioral functions that include social recognition, maternal-infant attachment, and modu

75 The proper operation of a social recognition mechanism allows for the expression o

76 hether CA2 OXTRs may contribute to long-term social recognition memory (SRM) formation.

77 Social recognition memory (SRM) is a key determinant of

78 Social recognition memory (SRM) is crucial for reproduct

79 s-relevant behaviors, specifically disrupted social recognition memory (SRM).

80 neuropeptide oxytocin is thought to mediate social recognition memory (SRM).

81 ons of hippocampal area CA2 are required for social recognition memory and aggression in mice.

82 k3-deficient rats exhibit impaired long-term social recognition memory and attention, and reduced syn

83 signaling in modulating short- and long-term social recognition memory and found that it is necessary

84 found that RAG1-deficient mice show impaired social recognition memory compared to mice wildtype for

85 In rats, social recognition memory for conspecifics typically las

86 R2B overexpression in the forebrain enhances social recognition memory for different strains and anim

87 in regulating short- and long-term forms of social recognition memory has not been fully investigate

88 e data trace the origin of the impairment in social recognition memory in RAG1-deficient mice to the

89 isition model in rat pups at 0.1 mg/kg and a social recognition memory model in adult rats at 0.01 mg

90 found that RAG1-deficient mice show impaired social recognition memory relative to heterozygous or RA

91 In vivo studies using a mouse model of social recognition memory showed that these derivatives

92 terone concentration, turning asymmetry, and social recognition memory suggest that stress hormones a

93 RAG1 plays a role in brain function using a social recognition memory task, an assessment of the acq

94 y undescribed role for the SuM in regulating social recognition memory via oxytocin signaling and rei

95 alamic-pituitary-adrenal axis, we found that social recognition memory was prolonged to at least 24 h

96 ion of food preference learning and impaired social recognition memory without affecting sociality.

97 ort that young adult AC1+ mice have enhanced social recognition memory, and normal fear and spatial m

98 ay an important role in the consolidation of social recognition memory, at least in part through enha

99 dependent learning and memory, as assayed by social recognition memory, novel object recognition, and

100 investigate the role of the NMDA receptor in social recognition memory, specifically the consequences

101 led to an impairment in short- and long-term social recognition memory.

102 ytocin plays an important role in modulating social recognition memory.

103 of food preference learning, sociality, and social recognition memory.

104 dal neurons and the persistence of long-term social recognition memory.

105 s that preferred to turn right showed better social recognition memory.

106 Relatively few studies have investigated how social recognition might be improved or enhanced.

107 d enhancement of cognitive function in a rat social recognition model at low doses.

108 The data strongly suggest the involvement in social recognition of the four genes coding for ER-alpha

109 social memory capabilities, the majority of social recognition papers explore short-term memories an

110 ng produced by a 120-min delay that impaired social recognition performance to 29% of 30-min delay co

111 ng specific roles for amygdala OTR in female social recognition potentially mediated by anxiety in a

112 Oxytocin supports social recognition, redirects behavior away from feeding

113 ing the functional genomics of OT and OTR in social recognition should help elucidate the neurobiolog

114 dors serve as important safety-promoting and social recognition signals, but their role in human brai

115 re critically involved in the development of social recognition skills within rodent species, primate

116 Social recognition (SR) enables rodents to distinguish b

117 Polymorphisms within TraA govern social recognition such that receptors cluster only betw

118 general understanding of the development of social recognition systems.

119 ed amnesia paradigms in the novel object and social recognition tasks, at very low dose levels.

120 ed with vehicle-treated Cplx2-/- mice in the social recognition test (34 compared with 13%, P<0.01).

121 In vivo evaluation of 14d in a social recognition test in mice revealed an amnesic effe

122 rference of MLIs during distinct phases of a social recognition test revealed the cerebellar engageme

123 c-Fos mapping after the social recognition test showed that cerebellar manipulat

124 chrogaster) to novel females in a multitrial social recognition test to investigate whether individua

125 nificantly improved short-term memory in rat social recognition that was not likely due to alteration

126 Social recognition, the ability to recognize individuals

127 roducts in a micronet required for mammalian social recognition, through which an individual learns t

128 ning, spontaneous alternation in the Y maze, social recognition, trace and contextual fear conditioni

129 avior enables the evolution and stability of social recognition, whereas conditional helping leads to

130 ated mice, iE-DAP-exposed mice show impaired social recognition while maintaining normal motor activi

131 ecent studies exploring neural substrates of social recognition with a focus on the potential role of