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1 racterize the neuromuscular basis of rolling escape behavior.
2 dangerous environmental settings that led to escape behavior.
3 s elegans detects UV and blue light to evoke escape behavior.
4 ced dopamine and promoted the performance of escape behavior.
5 ke, locomotor activity as well as panic-like escape behavior.
6 circumferentially during bending and rolling escape behavior.
7 remains still fully capable of driving rapid escape behavior.
8 lticellular ensembles that predict motivated escape behavior.
9 ulation can produce robust modality-specific escape behavior.
10 ound that mGluR2 modulated the threshold for escape behavior.
11 oracic motoneurons, preventing light-induced escape behavior.
12 to regulate perception, attention, fear, and escape behavior.
13 ungi have shaped the evolution of C. elegans escape behavior.
14 pr4), we show that pr1 cells regulate larval escape behavior.
15  these neurons was sufficient to trigger the escape behavior.
16 ting a predatory strike, initiates a startle-escape behavior.
17 y neuron was at times sufficient to evoke an escape behavior.
18 lating the threshold of the acoustic startle-escape behavior.
19 rned helplessness, inhibitory avoidance, and escape behavior.
20 inescapable stress (IS) develop a deficit in escape behavior.
21 s of crayfish, which are command neurons for escape behavior.
22 l Fos-like immunoreactivity (FLI) induced by escape behavior.
23 pinal Mauthner (M) cell, which initiates the escape behavior.
24 o trigger memory-guided, rather than random, escape behavior.
25 ircuitry controlling high-speed swimming and escape behaviors.
26 ct noxious heat so that animals can initiate escape behaviors.
27  by optokinetic response and looming-induced escape behaviors.
28 li, animals engage in diverse forms of rapid escape behaviors.
29 induce migratory, reproductive, foraging, or escape behaviors.
30 he LH-to-LHb pathway impairs aversion-driven escape behaviors.
31 stem of giant axons and unique fast swimming/escape behaviors.
32 nse ultrasound, eared moths perform dramatic escape behaviors.
33 vent which has been related to the timing of escape behaviors.
34 ably control three distinct motor aspects of escape behaviors.
35 s, parental care, and altruistic cooperative escape behaviors.
36 ight but are mildly impaired in geotaxis and escape behaviors.
37 riate motor activation sequences to generate escape behaviors.
38 ned here have been shown to be active during escape behaviors.
39 n the interneurons activated in swimming and escape behaviors.
40 ocomotion is critical for animal hunting and escaping behaviors.
41  single dose of ketamine suffices to restore escape behavior after aversive learning.
42             A sudden aversive event produces escape behaviors, an innate response essential for survi
43 micked the effects of IS and interfered with escape behavior and increased fear conditioning 24 hr la
44 k (IS) produces subsequent interference with escape behavior and increased fear conditioning that has
45  (DA) depletion on circling behavior, stress-escape behavior and subcortical DA function were examine
46 sual stimuli while simultaneously monitoring escape behavior and the recruitment of multiple reticulo
47 e we show that that the lPBN is required for escape behaviors and aversive learning to noxious stimul
48 the literature concerning stimuli that evoke escape behavior, and we expect this tool will help recon
49 oles of Gyc-89Da and Gyc-89Db in the hypoxia escape behavior appeared to be identical, we also showed
50 ure, the sensory networks that mediate their escape behavior are not well defined.
51                                              Escape behaviors are crucial to survive predator encount
52 ing regulates multiple phenotypes, including escape behavior, associative learning, immunity and long
53 that tracks approaching objects and triggers escape behavior before an impending collision.
54 ent with examples of shell shapes that allow escape behaviors being mechanically weaker than those wh
55 nance of antidepressant effects on motivated escape behavior but not for their initial induction.
56 onophores employ distinct routine and steady escape behaviors but-in contrast to fishes-do so using a
57 al GABAergic neurons within the dPAG control escape behavior by setting the excitability of the dPAG
58 lly stressful environments, plants can adopt escape behaviors by modifying the relative timing of dis
59   These delta2YFP/sop(-/-) embryos can mount escape behavior close to that of their wild-type sibling
60                                              Escape behaviors deliver organisms away from imminent ca
61 tions and possibly triggering an approach or escape behavior depending on their identity.
62 by robustly activating a thermal nociceptive escape behavior during the second half of larval develop
63                                 The flexible escape behavior exhibited by C. elegans in response to t
64  not detect them and produce the appropriate escape behavior fast enough.
65 sided lesions and showed disrupted footshock-escape behavior following left sided lesions.
66  we uncovered a circuit that gates selective escape behavior for noxious light through acute and inpu
67                                              Escape behaviors help animals avoid harm from predators
68 he trajectory of temperature change, priming escape behavior if unsafe thermal conditions are imminen
69 and moderate-threat environments but induced escape behavior in high-threat environments, and that mo
70 e a poly-synaptic pathway that can transform escape behavior in mice under restraint to acute stress
71 nsory neurons that generate a characteristic escape behavior in response to mechanical, osmotic, or o
72 dworm Caenorhabditis elegans exhibits robust escape behavior in response to rapidly rising temperatur
73 l crush injury of the right trigeminal root, escape behavior in response to stimulation of the right
74 f glutamate, but not GABA, neurons abolishes escape behavior in response to threatening stimuli.
75 visual motion-detection circuits and related escape behavior in the tractable locust system.
76 Our findings demonstrate a visually mediated escape behavior in zebrafish larvae exposed to objects a
77 pulations of somatosensory neurons triggered escape behaviors in 24-hr-old zebrafish.
78  foot-shocks, excite LHb neurons and promote escape behaviors in mice.
79            Drosophilids show a wide range of escape behaviors in response to noxious cues, including
80 estigate the similarities and differences of escape behaviors in response to noxious stimuli and thei
81 iking changes in movement and posture (e.g., escape behaviors in response to noxious stimuli vs freez
82 us heat and irritant chemicals elicit robust escape behaviors in the planarian Schmidtea mediterranea
83 e dispensable for touch-evoked activation of escape behaviors in zebrafish.
84                             We studied mouse escape behavior, in which mice are known to memorize sub
85  must be particularly fast and well tuned in escape behaviors, in which both the speed and accuracy o
86 ry interneurons in the hindbrain network for escape behaviors initiated by the Mauthner cell.
87                                              Escape behavior is a set of locomotor actions that move
88                                We found that escape behavior is also decreased by chemogenetic inhibi
89  that the action selection process mediating escape behavior is constantly updated by recent threat h
90 ophyll degradation suggests that this stress-escape behavior is regulated independently and upstream
91 , which is used for social communication and escape behaviors, is an exquisitely sensitive detector o
92                               Flexibility in escape behavior may also add an element of unpredictabil
93  capture prey, suggesting that unpredictable escape behavior may be advantageous to prey in fewer cir
94                                 To this end, escape behaviors must be adaptive.
95 iral drugs and therapeutics on the endosomal escape behavior of enveloped viruses.
96                             We evaluated the escape behavior of grasshoppers to hypothetical visual f
97                           A new study of the escape behavior of the cockroach has found that its spat
98                               We studied the escape behavior of the fruit fly, Drosophila, and found
99  the hindbrain important for the lateralized escape behavior of zebrafish and then test the role of n
100 ant fiber system elicited the characteristic escape behaviors of jumping, wing beating, and flight; p
101 this, we have investigated the dependence of escape behavior on learned knowledge about the spatial e
102 ing cue-shock association learning, reactive escape behaviors, or expression of previously learned av
103 t the vlPAG neurons encoding nociceptive and escape behaviors provide synaptic inputs to the dLS-LHA-
104 ay (vlPAG), a known anatomical substrate for escape behaviors, provides inputs to the dLS.
105 t DA release was correlated with stimulation-escape behavior, rather than the aversiveness of automat
106 s these neural circuits to ultimately prompt escape behaviors remains unclear.
107 ctivity was assessed measuring avoidance and escape behavior, self-reports of anxiety and panic sympt
108 , a fly responds with either a long-duration escape behavior sequence that initiates stable flight or
109                          If this is correct, escape behavior should lower extracellular ACh.
110                           New work on innate escape behavior shows that mice spontaneously form a spa
111 , whereas dark stimuli activate SC and drive escape behaviors, suggesting that vLGN enables rapid mov
112 s such as fishes and tadpoles, these include escape behaviors, swimming across a range of speeds, and
113 t serve to control the directionality of the escape behavior that fish use to avoid predators.
114 fic synaptic sites involved in activation of escape behavior, the direction of the modulation by sero
115   Fish are elusive prey with a short-latency escape behavior--the C-start--initiated to either the le
116 , being tightly correlated with the animal's escape behavior to light and dark stimuli of variable co
117 er the computational challenges required for escape behaviors to be implemented, discuss possible alg
118 tionarily ancient neural systems to generate escape behavior, to which cortical encephalization has b
119  shelter during shelter experiences, guiding escape behavior toward the goal location-a shelter-when
120 serotonin on the neural circuit for tailflip escape behavior was found to depend on the animal's soci
121 y how the activity of this neuron relates to escape behaviors, we monitored jumps evoked by looming s
122                    Animals display selective escape behaviors when faced with environmental threats.
123 or lateral periaqueductal gray (lPAG) drives escape behaviors, whereas activation of lPBN efferents t
124 esions blocked the fall in pAVP and enhanced escape behaviors, whereas the hippocampal lesions produc
125 eing distances, altered freezing, and active escape behaviors, which would increase predation risk in
126 ory of engulfment time which integrates prey escape behavior with the mechanics of the whale's body,

 
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