ライフサイエンスコーパス: ego

1 ego-1 interacts genetically with him-17, another regulat

2 ego-2 activity also promotes aspects of development not

3 dancy, average number of edges in the step-1 ego network, and natural connectivity.

4 st robust: the number of edges in the step-1 ego network, as well as the leave-one-out differences in

5 ed to identify high (n = 11) and low (n = 9) ego-involved individuals.

6 kers to derive continuous measurements about ego motion from ground contacts.

7 ocytes, the astrocyte even takes on an alter ego of the stem cell itself (S. Goldman, this issue of T

8 ntinuum between the fibroblast and its alter ego, the myofibroblast.

9 m severity (PANSS positive score, SAPS, AMDP ego-disorder) as well as response latencies during the e

10 t CSR-1 directly binds to histone mRNA in an ego-1-dependent manner using biotinylated 2'-O-methyl RN

11 Here, we show that atx-2 is an ego gene.

12 es of such changes on the distribution of an ego's network ties are not well understood.

13 more information, replacing up to 94% of an ego's predictability, significant information is also pr

14 own colocators, that contain up to 85% of an ego's predictive information.

15 k to distinguish the mobility patterns of an ego's social ties from those not socially connected to t

16 obtain such nodes, with the alter-based and ego-based strategy.

17 "I" accounting for individual behavior, and ego psychologists' concepts of the organizing functions

18 ttern of pregnancy denial, dissociation, and ego disorganization.

19 al experiences, out-of-body experiences, and ego-dissolution); (6) emotional responses (including pos

20 %) at baseline, experienced as intrusive and ego-dystonic, and associated with higher suspiciousness

21 Features of mystical and ego-dissolution experiences were common.

22 ses distortions of space-time perception and ego dissolution, produces rapid and persistent therapeut

23 resources by the pressures of reputation and ego might interfere with the thought processes needed to

24 ate that the volume of communication between ego and its transient alters does not display such a sys

25 tial-temporal contextual information between ego- and allocentric reference frames to compute predict

26 ent a complex phenotypic interaction between ego-2 and alx-1, consistent with their relationship bein

27 of inversity determines the ordering between ego-based or alter-based means for any network, with imp

28 lf-transcendent experiences characterized by ego dissolution, nondual awareness, and bliss.

29 symptoms, global functioning, self-concept, ego defenses, work and social functioning, and readmissi

30 le in the recovery of object movement during ego movement.

31 ary psychological/physical resources (i.e., "ego depletion").

32 were associated with negatively experienced ego dissolution, lower levels in hippocampal glutamate w

33 were associated with positively experienced ego dissolution.

34 bit system may play a key role in explaining ego-dystonic or self-destructive behaviour.

35 ance to male egos is stronger than to female egos, wealth correlations are larger along patrilineal l

36 se of young children and the case of fragile egos.

37 redictive information about the fly's future ego-rotation, potentially crucial for ongoing flight con

38 For a number of germ-line-expressed genes, ego-1 mutants were resistant to a form of PTGS called RN

39 Notably, for a given ego, these social signatures tend to persist over time,

40 negative affect, lower anxiety, and greater ego resilience in youth.

41 negative affect, lower anxiety, and greater ego resilience.

42 (dmPFC) throughout all key moments for high ego-involved participants, but particularly during criti

43 Those with high ego involvement might show more activation within evalua

44 of small RNAs and the rise of mRNA levels in ego-1(-) animals.

45 We show that alters with longer lifetimes in ego's network receive more calls, with the lifetime of t

46 rteen more deaths per 100, 000 population in ego counties.

47 nd centrality measures as well as individual ego measures and further constructed sociograms.

48 nieces, cousins, etc) of a focal individual ego, structured by the class of ego and of its kin.

49 Classic psychedelic-induced ego dissolution involves a shift in the sense of self an

50 ve flight maneuvers according to its initial ego-rotation at the time of detection of the visual thre

51 uct problems, oppositional behavior, and low ego control; withdrawal or passivity (12 studies), inclu

52 trust and self-compassion while maintaining ego functioning as well as cognitive and perceptual luci

53 : Family members' wealth resemblance to male egos is stronger than to female egos, wealth correlation

54 We first sample a set of multiple ego networks of varying orders that form a patch, or a n

55 Drawing from the nationwide ego-network surveys of 41,033 Americans from 2020 to 202

56 ngs cast further doubts about the ability of ego-depletion manipulations to affect actual behavior in

57 -1 gene structure and the molecular basis of ego-1 alleles.

58 l individual ego, structured by the class of ego and of its kin.

59 of friends and characterize the concepts of ego-based and alter-based means.

60 We investigated the effect of ego depletion on risk taking.

61 the studies revealed a significant effect of ego depletion on risk taking.

62 cost model offers an ultimate explanation of ego depletion that helps to move the field beyond biolog

63 tal cortex during game play as a function of ego involvement, using video clips featuring key moments

64 sentation of object-centered and not just of ego-centered space.

65 00,000 population in the social proximity of ego counties in the contiguous United States, is associa

66 re, we provide more insight into the role of ego-1 in germ-line development.

67 Here, we investigate the role of ego-1 in germline proliferation.

68 ll three countries, which include samples of egos at different life stages.

69 This means that the communication volume of egos to groups of similar transient alters is stable.

70 x (RSC) correlated strongly with ratings of "ego-dissolution" and "altered meaning," implying the imp

71 r LSD correlated with subjective reports of "ego dissolution." The present results provide the first

72 network maintained by a focal individual, or ego, is intrinsically dynamic and typically exhibits som

73 ar circuit for the maintenance of "self" or "ego" and its processing of "meaning." Strong relationshi

74 mortality produce larger numbers of kin per ego and decrease the inequality of the distribution of k

75 onism, neuroticism, highly sensitive person, ego resiliency, need for structure, and negative emotion

76 Putative ego-1 null mutants had multiple, previously unreported d

77 Putting ego aside, the 'astrocyte' is also (and perhaps more imp

78 r-1, the RNA-dependent RNA polymerase (RdRP) ego-1, or the dicer-related helicase drh-3, leads to def

79 y (the inclusion of community in self scale, ego-dissolution inventory, communitas scale, and the MEQ

80 in the subjective experience of one's self (ego dissolution).

81 We previously identified several ego (enhancer of glp-1) genes that promote germline prol

82 gly in line with prospect theory, i.e., that ego depletion reduces risk taking for gains, increases r

83 total n = 1,716) to test the prediction that ego depletion results in decisions that are more strongl

84 Here, we show that ego-2 positively regulates signaling in various tissues

85 The ego-1 gene is also required for a robust response to RNA

86 The ego-1 gene is the first example of a gene encoding an Rd

87 The ego-1 gene was originally identified on the basis of gen

88 The ego-1 transcript was found predominantly in the germ lin

89 rrive at a location at a similar time as the ego.

90 Stimulated by the ego-dystonic nature of obsessive-compulsive disorder (OC

91 We have determined the ego-1 gene structure and the molecular basis of ego-1 al

92 We originally identified the ego-1 gene on the basis of a genetic interaction with gl

93 We previously identified the ego-2 (enhancer of glp-1) gene as a positive regulator o

94 le turnover in the identity of alters in the ego network.

95 alls and survey data to track changes in the ego networks and communication patterns of students maki

96 n which they transcend the boundaries of the ego and the confines of time and space.

97 cal systems and that his descriptions of the ego are consistent with the functions of the default-mod

98 cells and for the nature and severity of the ego- mutant defect.

99 concepts of the organizing functions of the ego.

100 mily, kinship, and strong social ties of the ego.

101 ies from those not socially connected to the ego but who arrive at a location at a similar time as th

102 as the perceived vaccination rate within the egos' social contact network.

103 ownstream neurons driving motor responses to ego-rotation receive inputs primarily from a small subse

104 lective areas) is significantly sensitive to ego-motion in scenes, thus distinguishing the role of PI

105 e a key neural mechanism of LSD and underlie ego dissolution.