ライフサイエンスコーパス: inescapable

1 the cell cycle in a process that is largely inescapable and irreversible.

2 Acute, inescapable, and unpredictable stress can profoundly mod

3 An analogy can be made between the inescapable antigenic drive in chronic infection versus

4 DinB, indicating that mutagenesis is not an inescapable byproduct of repair.

5 ansform how cell biologists contend with the inescapable complexity of modern biology.

6 The inescapable conclusion is that it has a large metallic c

7 An inescapable conclusion of such studies has been the gros

8 An inescapable consequence for most living organisms is gre

9 An inescapable consequence of sex in eukaryotes is the evol

10 Thus, intercellular competition creates an inescapable double bind that makes aging inevitable in m

11 Given fundamental and inescapable effects of noise on nearly all aspects of ne

12 -escape deficits caused by prior exposure to inescapable electric shock in rats (learned helplessness

13 The effects of escapable and yoked inescapable electric tailshocks on extracellular levels

14 A regimen of inescapable electrical footshocks or no footshocks was t

15 etrieval emotional arousal (restraint stress/inescapable foot shock, exposure to the predator odor TM

16 posed to a shuttle box for 4 d or were given inescapable foot-shocks for the same time period.

17 mice, we found that repeated forced swim and inescapable footshock both produced aversive behaviors t

18 se upon presentation of a cue conditioned to inescapable footshock.

19 y old rats were exposed to unpredictable and inescapable footshocks, and fear memory for the shock co

20 im test and reduced levels of freezing after inescapable footshocks, suggesting that M(1)R(-/-) mice

21 The reality of hepatitis C is inescapable for the estimated 130 million people worldwi

22 that exposure of rats to randomly presented, inescapable loud sound, referred to as sound stress, inc

23 variations within each age, activities in an inescapable novel environment and novel object explorati

24 mal in their behavioral response to a novel, inescapable open field and in their preference for a nov

25 ; spontaneous locomotor activity in a novel, inescapable open field; and novelty place preference.

26 This presents an inescapable paradox for the current model of arrestin-me

27 Despite these inescapable pressures, high diversity and precision for

28 The inescapable price of the precision of knowledge generate

29 a new and general method for exploiting the inescapable protein corona to target nanomaterials to sp

30 of serotonergic neuronal function, show that inescapable, randomly presented sound pulses activate se

31 There is an inescapable requirement for local PMN recruitment and ac

32 Inescapable shock (IS) enhances analgesia to systemic mo

33 Exposure to a single session of inescapable shock (IS) induces peripheral and central pr

34 EPM) after exposure to escapable shock (ES), inescapable shock (IS) or fear conditioning (FC), result

35 Exposure of rats to inescapable shock (IS) potentiated the analgesic respons

36 Uncontrollable or inescapable shock (IS) produces behavioral changes that

37 Inescapable shock (IS) produces subsequent interference

38 The present experiments characterize inescapable shock (IS)-induced potentiation of morphine

39 rain IL-1beta was explored after exposure to inescapable shock (IS; 100 1.6 mA tail shocks for 5 sec

40 These deficits produced by inescapable shock and NBTI were reversed by the nonselec

41 ges occur in the dorsal raphe nucleus during inescapable shock and that such changes may contribute t

42 se inhibitor, mimicked the effect of earlier inescapable shock at a dose of 2.5 microM in previously

43 shuttle-escape performance in the manner of inescapable shock in a dose-dependent manner and acted s

44 eceptor impairs escape performance following inescapable shock in the learned helplessness paradigm.

45 to improve performance in rats preexposed to inescapable shock or pretreated with NBTI.

46 acid (5 ng) into the frontal cortex prior to inescapable shock prevented the escape deficit.

47 Experience with unsignaled, inescapable shock represents a profound challenge to bra

48 their own preshock baseline, rats exposed to inescapable shock showed an increase in extracellular 5-

49 s produced by EHNA or by earlier exposure to inescapable shock were reversed by intraperitoneal injec

50 precursor to adenosine release-precedes the inescapable shock-induced impairment.

51 may contribute to the behavioral effects of inescapable shock.

52 A single session of inescapable shocks (IES) in mice reduced FoxO3a phosphor

53 ynergistically with an ineffective number of inescapable shocks to maximally impair test performance.

54 spects of fear (i.e., fear conditioning) and inescapable stress (i.e., struggling and helplessness).

55 disorder wherein a subset of mice exposed to inescapable stress (IS) develop a deficit in escape beha

56 oral control over tail-shock termination, or inescapable stress (IS) without control.

57 Inescapable stress can induce learned helplessness in ma

58 Inescapable stress consisted of 100 1 mA tailshocks, and

59 Acute inescapable stress enhances classical eyeblink condition

60 Inescapable stress increased BDNF mRNA expression at 0 b

61 We found that uncontrollable and inescapable stress induced behavioral state-dependent ch

62 60 min in males, but there was no effect of inescapable stress on BDNF mRNA in females.

63 Here, we examine the effects of acute inescapable stress, an animal model of behavioral depres

64 swim is usually considered a consequence of inescapable stress, and is used to screen antidepressant

65 These results reveal sex differences in inescapable stress-induced gene expression that may have

66 re slower to escape, even before exposure to inescapable stress.

67 ssed animals but increased anxiety following inescapable stress.

68 al area in mediating behavioral responses to inescapable stress.

69 In the absence of an inescapable stressor, increased 5-HT(1B) autoreceptor ex

70 nimals are subjected to an unpredictable and inescapable stressor.

71 entricular (i.c.v.) IL-1beta and exposure to inescapable tail shock (IS) activate acute phase respons

72 In this study, male rats were exposed to inescapable tail shock, loud noise or restraint, and the

73 rats were exposed to a single session of 100 inescapable tail shocks (IS).

74 Exposure to 100 inescapable tail shocks (ISs) increased HMGB-1 and NLRP3

75 ut and passive coping behaviors during acute inescapable (tail suspension, TS) stress.

76 In addition, some stressors such as inescapable tailshock (IS) also produce elevated basal l

77 the caudal dorsal raphe nucleus (DRN) during inescapable tailshock (IS) has been shown to be critical

78 le Sprague-Dawley rats to escapable or yoked inescapable tailshock and assessed LC activity by measur

79 ve been observed following stressors such as inescapable tailshock and social isolation, while no cha

80 Inescapable tailshock led to greater serotonergic neural

81 N following exposure to escapable and yoked, inescapable tailshock.

82 A prior report indicated that exposure to inescapable tailshocks (IS) raised levels of brain IL-1b

83 he paradigm established by these data, it is inescapable that going forward, investigators will opera

84 the breadth of topics covered reflected how inescapable the influence of noncoding RNAs is in develo

85 e coping strategies to react to escapable or inescapable threats, respectively.

86 Wistar-Kyoto rats were exposed to inescapable, uncontrollable footshocks.

87 ochemical and behavioral changes that follow inescapable, uncontrollable tail shocks (ISs) in Sprague

88 eviously reported that rats that experienced inescapable-unpredictable stress subsequently exhibited