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1            Aging, for virtually all life, is inescapable.
2 after sleep deprivation is intense and seems inescapable.
3 s with time spent awake, until sleep becomes inescapable.
4 ain vasculature, areas of low blood flow are inescapable and cannot be removed by functional hyperemi
5  the cell cycle in a process that is largely inescapable and irreversible.
6  psychological, that are overwhelming (i.e., inescapable and unpredictable), can measurably affect su
7                                       Acute, inescapable, and unpredictable stress can profoundly mod
8           An analogy can be made between the inescapable antigenic drive in chronic infection versus
9 ral control but not when mice anticipated an inescapable aversive outcome.
10  DinB, indicating that mutagenesis is not an inescapable byproduct of repair.
11 ncing complex (RISC) complexes, resulting in inescapable cell death.
12 ansform how cell biologists contend with the inescapable complexity of modern biology.
13                                          The inescapable conclusion is that it has a large metallic c
14                                           An inescapable conclusion of such studies has been the gros
15                                           An inescapable consequence for most living organisms is gre
16         Sleep, like ageing(17,18), may be an inescapable consequence of aerobic metabolism.
17                         This disparity is an inescapable consequence of Eurocentric biases in genome-
18 ting from such neutrophil accumulation is an inescapable consequence of parenchymal cell death has no
19                                           An inescapable consequence of sex in eukaryotes is the evol
20   Thus, intercellular competition creates an inescapable double bind that makes aging inevitable in m
21                        Given fundamental and inescapable effects of noise on nearly all aspects of ne
22 -escape deficits caused by prior exposure to inescapable electric shock in rats (learned helplessness
23           The effects of escapable and yoked inescapable electric tailshocks on extracellular levels
24                                 A regimen of inescapable electrical footshocks or no footshocks was t
25 etrieval emotional arousal (restraint stress/inescapable foot shock, exposure to the predator odor TM
26 posed to a shuttle box for 4 d or were given inescapable foot-shocks for the same time period.
27 ntral medial striatum throughout training on inescapable footshock and signaled active avoidance task
28 mice, we found that repeated forced swim and inescapable footshock both produced aversive behaviors t
29 se upon presentation of a cue conditioned to inescapable footshock.
30 y old rats were exposed to unpredictable and inescapable footshocks, and fear memory for the shock co
31 im test and reduced levels of freezing after inescapable footshocks, suggesting that M(1)R(-/-) mice
32                The reality of hepatitis C is inescapable for the estimated 130 million people worldwi
33 e the death of neurons-the final, apparently inescapable, hallmark of the disease.
34         Light and temperature variations are inescapable in nature.
35 that exposure of rats to randomly presented, inescapable loud sound, referred to as sound stress, inc
36 variations within each age, activities in an inescapable novel environment and novel object explorati
37                Hence, there appears to be an inescapable obligatory dependence on sensory-prediction
38                                         This inescapable obstacle warrants alternative approaches, su
39 mal in their behavioral response to a novel, inescapable open field and in their preference for a nov
40 ; spontaneous locomotor activity in a novel, inescapable open field; and novelty place preference.
41                             This presents an inescapable paradox for the current model of arrestin-me
42               These differences highlight an inescapable physical tradeoff between hydrodynamic stabi
43                                Despite these inescapable pressures, high diversity and precision for
44                                          The inescapable price of the precision of knowledge generate
45 s in the absence of glomerular lesions, with inescapable progression to end-stage renal disease.
46  a new and general method for exploiting the inescapable protein corona to target nanomaterials to sp
47 of serotonergic neuronal function, show that inescapable, randomly presented sound pulses activate se
48                                  There is an inescapable requirement for local PMN recruitment and ac
49 bility time and were resilient to developing inescapable shock (IES)-induced escape deficits.
50                                              Inescapable shock (IS) enhances analgesia to systemic mo
51              Exposure to a single session of inescapable shock (IS) induces peripheral and central pr
52 EPM) after exposure to escapable shock (ES), inescapable shock (IS) or fear conditioning (FC), result
53                          Exposure of rats to inescapable shock (IS) potentiated the analgesic respons
54                            Uncontrollable or inescapable shock (IS) produces behavioral changes that
55                                              Inescapable shock (IS) produces subsequent interference
56 g network analysis, we find that exposure to inescapable shock (IS), compared to context training, re
57         The present experiments characterize inescapable shock (IS)-induced potentiation of morphine
58 rain IL-1beta was explored after exposure to inescapable shock (IS; 100 1.6 mA tail shocks for 5 sec
59                   These deficits produced by inescapable shock and NBTI were reversed by the nonselec
60 ges occur in the dorsal raphe nucleus during inescapable shock and that such changes may contribute t
61 se inhibitor, mimicked the effect of earlier inescapable shock at a dose of 2.5 microM in previously
62  shuttle-escape performance in the manner of inescapable shock in a dose-dependent manner and acted s
63 eceptor impairs escape performance following inescapable shock in the learned helplessness paradigm.
64 to improve performance in rats preexposed to inescapable shock or pretreated with NBTI.
65 acid (5 ng) into the frontal cortex prior to inescapable shock prevented the escape deficit.
66                  Experience with unsignaled, inescapable shock represents a profound challenge to bra
67 their own preshock baseline, rats exposed to inescapable shock showed an increase in extracellular 5-
68 s produced by EHNA or by earlier exposure to inescapable shock were reversed by intraperitoneal injec
69 tex (PFC) relative to uncontrollable stress (inescapable shock, IS).
70  precursor to adenosine release-precedes the inescapable shock-induced impairment.
71  may contribute to the behavioral effects of inescapable shock.
72                          A single session of inescapable shocks (IES) in mice reduced FoxO3a phosphor
73 ynergistically with an ineffective number of inescapable shocks to maximally impair test performance.
74 spects of fear (i.e., fear conditioning) and inescapable stress (i.e., struggling and helplessness).
75 disorder wherein a subset of mice exposed to inescapable stress (IS) develop a deficit in escape beha
76 oral control over tail-shock termination, or inescapable stress (IS) without control.
77                                              Inescapable stress can induce learned helplessness in ma
78                                              Inescapable stress consisted of 100 1 mA tailshocks, and
79                                        Acute inescapable stress enhances classical eyeblink condition
80 l raphe nucleus increases active coping with inescapable stress in rats and mice in a time-locked man
81                                              Inescapable stress increased BDNF mRNA expression at 0 b
82                                     However, inescapable stress increased resistance to auditory-cued
83             We found that uncontrollable and inescapable stress induced behavioral state-dependent ch
84  60 min in males, but there was no effect of inescapable stress on BDNF mRNA in females.
85 e (HC), during passive coping in response to inescapable stress under tail suspension (TS), and durin
86        Here, we examine the effects of acute inescapable stress, an animal model of behavioral depres
87  swim is usually considered a consequence of inescapable stress, and is used to screen antidepressant
88 uisition, either with or without exposure to inescapable stress, consistent with the hypothesis that
89      These results reveal sex differences in inescapable stress-induced gene expression that may have
90 e to passive coping behavior when exposed to inescapable stress.
91 fear extinction, with or without exposure to inescapable stress.
92 re slower to escape, even before exposure to inescapable stress.
93 ssed animals but increased anxiety following inescapable stress.
94 al area in mediating behavioral responses to inescapable stress.
95                         In the absence of an inescapable stressor, increased 5-HT(1B) autoreceptor ex
96 nimals are subjected to an unpredictable and inescapable stressor.
97  task in which mice were exposed to repeated inescapable stressors followed by an active avoidance ta
98 at ACh levels in the mPFC during exposure to inescapable stressors were positively correlated with la
99 neuroendocrine activation during exposure to inescapable stressors.
100 entricular (i.c.v.) IL-1beta and exposure to inescapable tail shock (IS) activate acute phase respons
101 al responses assessed 24 h after exposure to inescapable tail shock stress (IS) in adult male rats.
102     In this study, male rats were exposed to inescapable tail shock, loud noise or restraint, and the
103 rats were exposed to a single session of 100 inescapable tail shocks (IS).
104                              Exposure to 100 inescapable tail shocks (ISs) increased HMGB-1 and NLRP3
105 ut and passive coping behaviors during acute inescapable (tail suspension, TS) stress.
106          In addition, some stressors such as inescapable tailshock (IS) also produce elevated basal l
107 the caudal dorsal raphe nucleus (DRN) during inescapable tailshock (IS) has been shown to be critical
108 le Sprague-Dawley rats to escapable or yoked inescapable tailshock and assessed LC activity by measur
109 ve been observed following stressors such as inescapable tailshock and social isolation, while no cha
110                                              Inescapable tailshock led to greater serotonergic neural
111 N following exposure to escapable and yoked, inescapable tailshock.
112    A prior report indicated that exposure to inescapable tailshocks (IS) raised levels of brain IL-1b
113 he paradigm established by these data, it is inescapable that going forward, investigators will opera
114  the breadth of topics covered reflected how inescapable the influence of noncoding RNAs is in develo
115 l defensive behavior that is triggered by an inescapable threat.
116 e coping strategies to react to escapable or inescapable threats, respectively.
117                            Aging is a nearly inescapable trait among organisms yet lifespan varies tr
118            Wistar-Kyoto rats were exposed to inescapable, uncontrollable footshocks.
119 ochemical and behavioral changes that follow inescapable, uncontrollable tail shocks (ISs) in Sprague
120 eviously reported that rats that experienced inescapable-unpredictable stress subsequently exhibited
121 wed how a similar condition, if perceived as inescapable, would result in a downregulation of interoc

 
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