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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

24 -1 gene structure and the molecular basis of ego-1 alleles.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

53 concepts of the organizing functions of the ego.

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