ライフサイエンスコーパス: social recognition

1 gan, an olfactory substructure essential for social recognition.

2 s Spheniscus vocalisations are important for social recognition.

3 campus to the posterior hippocampus to guide social recognition.

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

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

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

7 veral days before behavioral testing reduced social recognition.

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

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

10 easured by prepulse inhibition, and impaired social recognition.

11 insights about neuroendocrine regulation of social recognition.

12 n explored concerning its modulatory role in social recognition.

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

14 experimental social experience on subsequent social recognition.

15 OT treatment fully restores social recognition.

16 la during the initial exposure to facilitate social recognition.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

34 Social recognition constitutes the basis of social life.

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

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

37 The social recognition deficits seen in oxytocin knockout mi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

56 Social recognition memory (SRM) is crucial for reproduct

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

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

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

60 In rats, social recognition memory for conspecifics typically las

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

78 Oxytocin supports social recognition, redirects behavior away from feeding

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

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

81 Social recognition (SR) enables rodents to distinguish b

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

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

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

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

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

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