ライフサイエンスコーパス: conscious

1 rtant as people are becoming diabetic health conscious.

2 which species can be ranked as more or less conscious.

3 patient is unresponsive or perhaps minimally conscious(1), and to predict whether they will recover.

4 Nowadays the world population has been more conscious about healthy food products based on bioactive

5 n, our findings reveal a common signature of conscious access across sensory modalities and illustrat

6 normal structural connectivity for disrupted conscious access and the relationship between these two

7 However, despite conscious access being impaired, the ability to decode t

8 Conscious access has been robustly associated with activ

9 a crucial role in conscious access, and that conscious access may mediate the association between imp

10 g to global neuronal workspace (GNW) theory, conscious access relies on long-distance cerebral connec

11 and more sustained P300 suggesting improved conscious access to auditory novelty.

12 ivity within the GNW plays a crucial role in conscious access, and that conscious access may mediate

13 owever, reaching full potential will require conscious adjustments to the skillsets and mind sets of

14 cit safety vs. threat) that is distinct from conscious affective experience and more closely tracks t

15 GROUND DATA: Novices are hypothesized to use conscious analysis (effortful DM) leading to activation

16 eso-parietal areas associated with minimally conscious and conscious states.

17 uide researchers and practitioners in making conscious and effective choices for each step of the gen

18 Understanding the distinction between conscious and unconscious cognition remains a priority i

19 daily behavior is dynamically influenced by conscious and unconscious processes.

20 are the neural signatures that differentiate conscious and unconscious processing in the brain?

21 the real predispositions, alignment between conscious and unconscious responses promises deeper insi

22 ectomy plus amlodipine), renal blood flow in conscious animals (but not anesthetized animals) was sti

23 BP was directly measured in conscious animals at the end of the treatment.

24 eal-time dynamics of renal autoregulation in conscious animals have not been characterized.

25 bility of renal autoregulation assessment in conscious animals with spontaneous BP fluctuations and i

26 These results reveal, in conscious animals, a novel mechanism of neuromodulation

27 ence for the power of emotional stimuli over conscious attention.

28 study cortical reactivity in a cohort of 30 conscious awake patients with chronic focal and multifoc

29 ntal processes that exist largely outside of conscious awareness and control in both male and female

30 had made a decision, supports the idea that conscious awareness occurs when evidence has accumulated

31 Thus, conscious awareness of having reached a decision appears

32 What happens in the brain when conscious awareness of the surrounding world fades?

33 A comprehensive neurocognitive account of conscious awareness will not be possible without a sound

34 rating at least partially below the level of conscious awareness) in generating moral judgments and d

35 parent future influences "earlier" events in conscious awareness, might affect people's most fundamen

36 emotional face processing occurs outside of conscious awareness.

37 tions influence moral assessments outside of conscious awareness.

38 e rather than continuous, and unavailable to conscious awareness.

39 jects, and interacts with pursuit outside of conscious awareness.

40 system modulates pursuit behavior outside of conscious awareness.

41 y be important for regulation and control of conscious awareness.

42 We conclude that, in conscious, behaving humans, ventilatory sensitivities to

43 cognitive content and function during awake, conscious behavior remains unclear.

44 We applied conscious bioimaging to the assessment of NFkappaB and S

45 The CMRglc of the conscious brain (e.g., right parietal region, 99.6 +/- 1

46 s consciousness and memory while sparing non-conscious brain activities.

47 by the central nervous system, muscles, and conscious brain is of interest since body sway carries i

48 signal complexity were revealed in minimally conscious but not unaware patients.

49 on in the near term than the possibility of "conscious" chimeric animals.

50 n macro-scale brain network organisation and conscious cognition requires direct investigations into

51 brain functional interactions in supporting conscious cognition that is relevant to our understandin

52 of this higher-order topological feature for conscious cognition.

53 and the control of functions external to the conscious cognitive world of mammals.

54 l and neural science of unconscious (C0) and conscious computations (C1 and C2) and outline how they

55 repare low-fat peanuts in response to health-conscious consumer demands.

56 allow a global neuronal ignition coding for conscious content.

57 versus the back of the cortex in specifying conscious contents and discuss promising research avenue

58 n activity evoked by either conscious or non-conscious contents, as well as during conscious or non-c

59 e LFN is real-time measure that is not under conscious control and which reflects conceptually-mediat

60 urther complex behaviors to occur outside of conscious control remain poorly understood [1].

61 of these misdiagnosed patients as minimally conscious, corroborating their behavioural diagnoses.

62 ive intensive care units (ICUs), we enrolled conscious, critically ill adults who had a tracheostomy

63 Telemetric analysis from conscious Cx36 KO mice revealed higher variance in heart

64 delivered intravesically to SCI rats during conscious cystometry significantly decreased the frequen

65 n invoking them is thought to be guided by a conscious decision.

66 behaviorally, the attentional blink impairs conscious decisions about the presence of integrated sur

67 From 0-240 min, 2 groups of conscious dogs (n = 9 dogs/group) received a duodenal in

68 olfactory epithelium of rodents, and in live conscious dogs.

69 Guilt, a self-conscious emotion, includes self-focused role taking and

70 neural signals in the cognitive assembly of conscious emotional experiences.

71 vention, attributions of charitability, self-conscious emotions, and moral condemnation.

72 neural decision processes and components of conscious experience are tightly linked.

73 es whose temporal dynamics determine whether conscious experience arises.

74 advances that are important for dissociating conscious experience from related enabling and executive

75 Although the neural bases of conscious experience have been extensively investigated

76 ocesses to inform decisions and give rise to conscious experience is a longstanding question.

77 lusters is involved in tracking the distinct conscious experience of a particular motion axis.

78 We hypothesized that the conscious experience of a specific visual motion axis is

79 The conscious experience of fear, he tells us here, is not w

80 uli into working memory with little, if any, conscious experience of them.

81 e, features of volition, namely, its link to conscious experience, and reviews stimulation and patien

82 art of a subcortical network that influences conscious experience.

83 y to trigger actions), its subjectivity (the conscious experiences associated with initiating volunta

84 oux and Hakwan Lau argue that everyday human conscious experiences cannot be understood separately fr

85 Compared with unconsciousness, conscious experiences during NREM sleep were associated

86 g that it may constitute a core correlate of conscious experiences in sleep.

87 ur understanding of the neural correlates of conscious experiences in sleep.

88 r which brain states determine whether these conscious experiences will occur and what prevents us fr

89 etwork of cognition, a network essential for conscious experiences.

90 NCC, the neural substrates supporting entire conscious experiences.

91 ng of the neural underpinnings of dreams and conscious experiences.

92 ost relevant node for inducing distortion of conscious face processing by direct electrical stimulati

93 science, allowing controlled intervention on conscious feelings and their downstream effects on highe

94 distinct from the circuits that give rise to conscious feelings of fear and anxiety.

95 al circuits are not directly responsible for conscious feelings, they provide nonconscious inputs tha

96 terest in the development of environmentally conscious formulations.

97 In conscious freely behaving animals blockade of Ca(2+)-dep

98 using whole-body bioluminescence imaging, in conscious, freely moving rodents.

99 In addition to conscious goals and stimulus salience, an observer's pri

100 rward: through education and awareness, cost-conscious guideline development, government regulation,

101 data, which are the first to be obtained in conscious humans, demonstrate that the administration of

102 ogical consequences have not been studied in conscious humans.

103 ry note for purely behavioral studies of non-conscious information processing.

104 pseudo-imitative behavior can occur without conscious intent or other higher-order cognitive process

105 s override ascending sensory information and conscious intention, leading to maladaptive and disablin

106 from sensory features, because it requires a conscious, intentional attitude toward the object.

107 inent pursuit trial but rather was immune to conscious intervention.

108 p this approach out of reach for many budget-conscious laboratories.

109 for wakeful rest than for states with lower conscious level like propofol-induced anesthesia.

110 erged from minimally conscious, to the fully conscious locked-in syndrome.

111 AF reversion in conscious long-term tachypaced pigs: Pigs were subjected

112 hing or the ventilatory response to CO(2) in conscious male Wistar rats.

113 For the first time in conscious males and females, the findings of the present

114 Thus, in conscious mammals, breathing is subject to a dual and in

115 ding that you are in harm's way based on non-conscious memories, schemas, and mental models.

116 gation, particularly because of its roles in conscious memory consolidation, spatial navigation, emot

117 of ischemia in a specific cortical region of conscious mice of any postnatal age, including perinatal

118 Urodynamic cystometry in conscious mice revealed overactive bladder, reduced maxi

119 The new method to chronically pace conscious mice yields stable atrial and ventricular capt

120 ities for NFkappaB and STAT3 in the brain of conscious mice.

121 mains a technical challenge, particularly in conscious mice.

122 eously record cardiac electrical activity in conscious mobile mice.

123 tion may therefore be seen as a kind of self-conscious motivation.

124 ial question of whether machines may ever be conscious must be based on a careful consideration of ho

125 Smog Study-2 (AHSMOG-2), a cohort of health conscious nonsmokers where 81% have never smoked.

126 visuomotor encoding occurs independently of conscious object perception.

127 hat contrast brain activity evoked by either conscious or non-conscious contents, as well as during c

128 or non-conscious contents, as well as during conscious or non-conscious states, particularly general

129 ant difference in luciferase expression when conscious or unconscious throughout development.

130 ification between unresponsive and minimally conscious patients.

131 e, on single trials we could decode both the conscious percept and the suppressed stimulus.

132 single cells multiplex representation of the conscious percept and veridical physical stimulus, rathe

133 prior to that stage differ from the eventual conscious percept even though they provide input to it.

134 ge proportions of IT neurons represented the conscious percept even without active report.

135 represent the act of report rather than the conscious percept itself.

136 g a no-report paradigm in which the animal's conscious percept was inferred from eye movements.

137 transform these sensory inputs into a final conscious percept.

138 e cortical visual pathway and with an evoked conscious percept.

139 a constant visual stimulus evokes a varying conscious percept.

140 d that cortical activity trajectories during conscious perception are fast evolving and robust to sma

141 (8-13 Hz), bias sensory responses and change conscious perception but not, surprisingly, the underlyi

142 two distinct heartbeat-related influences on conscious perception differentially related to early vs.

143 The tight relationship between attention and conscious perception has been extensively researched in

144 ce of supramodal neural processes related to conscious perception has not been convincingly shown so

145 connectivity and an increased threshold for conscious perception have been reported.

146 cious perception in one modality can predict conscious perception in a different modality.

147 y investigating whether neural correlates of conscious perception in one modality can predict conscio

148 Conscious perception is crucial for adaptive behaviour y

149 We find that conscious perception is influenced and signaled by ventr

150 While conscious perception is robustly associated with sustain

151 this response can be observed regardless of conscious perception is still unknown.

152 decision and report from the neural basis of conscious perception itself.

153 iatal responses to a first target determined conscious perception of a second target.

154 neural activity in visual cortex predicting conscious perception of auditory near-threshold stimulat

155 visual working memory is known to affect our conscious perception of concurrent visual input.

156 m underlies important functions relevant for conscious perception of differing natural images.

157 ble known electrophysiological correlates of conscious perception of near-threshold visual stimuli.

158 Subjective tinnitus is the conscious perception of sound in the absence of any acou

159 temporal neural activity patterns predicting conscious perception of the feeble stimulation.

160 The conscious perception of the hedonic sensory properties o

161 Moreover, conscious perception of the second target was signaled b

162 internal signals can be integrated into our conscious perception of the world.

163 responses being measured are associated with conscious perception or with postperceptual processes in

164 l response to surprisal outside the scope of conscious perception points to the fundamental relations

165 g its presence or absence and the associated conscious perception remain elusive.

166 pendent of the type of report (i.e., whether conscious perception was reported by pressing or withhol

167 f consciousness is the prevalent confound of conscious perception with the requirement of reporting i

168 previously associated with metacognition and conscious perception, including some areas in the prefro

169 Despite escaping conscious perception, manipulable objects activated an o

170 d paradigms for probing neural correlates of conscious perception, our findings reveal a common signa

171 ventral striatum activity may contribute to conscious perception, presumably by gating cortical info

172 decoded from the cortex and transformed into conscious perception, significantly augmenting function.

173 rtunity to examine the mechanisms underlying conscious perception.

174 te cortical information flow, contributes to conscious perception.

175 cortical information flow, may contribute to conscious perception.

176 for both changes due to attentional task and conscious perception.

177 visual space that is an essential aspect of conscious perception.

178 ing neural activity as a robust correlate of conscious perception.

179 ated effects have been reported to influence conscious perception.

180 vity in prefrontal cortex (PFC) critical for conscious perception?

181 Null Findings Falsify Prefrontal Theories of Conscious Perception?, by Brian Odegaard, Robert T.Knigh

182 before or after a target stimulus can hinder conscious perceptual processing of the target via an emo

183 ing his four-decade career exploring how non-conscious processes involving the amygdala detect and re

184 how his four-decade career exploring how non-conscious processes involving the amygdala detect and re

185 the P3b itself is not a neural signature of conscious processing and highlights the importance of ca

186 tions regarding the elementary mechanisms of conscious processing in the human brain.

187 are suggested to provide a scaffold for the conscious processing of information, with marked topolog

188 parahippocampal cortex and frontal areas in conscious processing of object-context relations, which

189 Conscious processing of shapes was indexed by the visual

190 tionship between the intertwined concepts of conscious processing, attention, and working memory.

191 nctions contribute to a holistic approach to conscious processing.

192 ne of the proposed canonical "signatures" of conscious processing.

193 Studies in conscious rats demonstrate that these antagonists are or

194 l blood flow to baseline after BP changes in conscious rats occurs rapidly, in 5-10 seconds.

195 e prefrontal cortex and nucleus accumbens of conscious rats were assessed using microdialysis.

196 l blood flow stability is not compromised in conscious rats with impaired renal autoregulation.

197 corded concurrent BP and renal blood flow in conscious rats, comparing animals with renal autoregulat

198 ctivation via electrical CSN stimulation, in conscious rats, controls the innate immune response to l

199 In conscious rats, selective chemogenetic activation of Sub

200 luated their regional hemodynamic effects in conscious rats.

201 e the contribution of these neurons to BP in conscious rats.

202 n E(2) production and increased heat loss in conscious rats.

203 to posterior parietal locations activated by conscious recollection.

204 hat do not require training are based on sub-conscious, reflex responses (e.g. optokinetic nystagmus)

205 ort a close relationship between IPS and the conscious representation of the body external appearance

206 vocal, and gestural expressions, before ( c) conscious representation or experience of these changes

207 However, whether this response arises as a conscious response or reflects a more fundamental mechan

208 ts that spontaneous, but stimulus-dependent, conscious retrieval processes, that are generally intact

209 techniques are excitingly friendly to budget conscious scientific research organizations where probab

210 In clinical practice, local anesthesia with conscious sedation (CS) is performed in roughly 50% of p

211 Guidelines to triage patients to conscious sedation (CS) or monitored anaesthesia care (M

212 o investigate whether the sedation mode (ie, conscious sedation [CS] vs general anesthesia [GA]) affe

213 n raw analyses, intraprocedural success with conscious sedation and general anesthesia was similar (9

214 nesthesia was noted in 102 of 1737 (5.9%) of conscious sedation cases.

215 The conscious sedation group was less likely to experience i

216 These results suggest the safety of conscious sedation in this population, although comparat

217 In US practice, conscious sedation is associated with briefer length of

218 Conscious sedation is used during transcatheter aortic v

219 MT performed under conscious sedation non-GA had significantly shorter onse

220 ctomy (MT) under general anaesthesia (GA) or conscious sedation non-GA through a systematic review an

221 nesthesia with patients undergoing TAVR with conscious sedation on an intention-to-treat basis for th

222 Conversion from conscious sedation to general anesthesia was noted in 10

223 tment-weighted adjustment for 51 covariates, conscious sedation was associated with lower procedural

224 Conscious sedation was associated with reductions in pro

225 Conscious sedation was used in 1737/10 997 (15.8%) cases

226 Conscious sedation was used in 59.9% of transfemoral pro

227 l conditions for enabling the development of conscious self-awareness, the absence of which leaves us

228 ts across all ganglia types, suggesting that conscious sensation and homeostatic regulation are the r

229 mplicated in both homeostatic regulation and conscious sensations are found at all anatomic levels, s

230 muli and innocuous stimuli that do not reach conscious sensations from visceral organs to the central

231 ch to determine a sense of agency, i.e. the (conscious) sense of authorship and control over our acti

232 mediate this effect and is it restricted to conscious sensory events (suprathreshold), or does it al

233 mon brain regions and processes in mediating conscious sensory experience.

234 intravenous AITC only evoked bradycardia in conscious SH and WKY rats.

235 jection of AITC caused similar bradypnoea in conscious SH and WKY rats.

236 Conversely, inhaled AITC in conscious SH rats evoked complex brady-tachycardia with

237 premature ventricular contractions (PVCs) in conscious SH rats.

238 In conscious sheep, infusion of Escherichia coli decreased

239 voked bradycardia but no tachycardia/PVCs in conscious SHs, while inhalation and injection of AITC ca

240 e wakefulness syndrome (VS/UWS) or minimally conscious state (MCS).

241 ness syndrome (VS/UWS; n = 70) and minimally conscious state (MCS; n = 57) were presented with the lo

242 y across the cortex is characteristic of the conscious state and is reduced during anesthesia.

243 raumatic brain injured patients in minimally conscious state based on a clinical trial using amantadi

244 Fear is a conscious state caused by exposure to real or imagined t

245 gn that can accurately distinguish minimally conscious state from VS/UWS.

246 A number of studies suggest that the awake, conscious state is not the default behavior of an assemb

247 of dopaminergic neuromodulation in minimally conscious state is undemonstrated.

248 d cognitive interpretation of each minimally conscious state item is still unclear and debated.

249 current behavioural repertoire of minimally conscious state items is limited and restricted to a few

250 In addition to enlarging the minimally conscious state items repertoire, and therefore decreasi

251 namic approaches in post-traumatic minimally conscious state patients should be tested in clinical tr

252 olunteers and seven post-traumatic minimally conscious state patients using 11C-raclopride PET to est

253 us state without language (n = 3), minimally conscious state with language (n = 4) or post-traumatic

254 (n = 2), vegetative state (n = 3), minimally conscious state without language (n = 3), minimally cons

255 igns of fluctuating consciousness (Minimally Conscious State).

256 The GNW hypothesis proposes that, in the conscious state, a non-linear network ignition associate

257 sment remains the gold standard to determine conscious state, EEG has proven to be a promising comple

258 ld help illuminate the neuronal basis of the conscious state.

259 municating patients who are in the minimally conscious state.

260 ionecrosis resulting in an ongoing minimally conscious state.

261 ive wakefulness syndrome (UWS)-and minimally conscious state.

262 less of their spike rate profile at baseline conscious state.

263 er he was in a vegetative state or minimally conscious state.

264 Psychedelic drugs are potent modulators of conscious states and therefore powerful tools for invest

265 riminated between unresponsive and minimally conscious states at the group level.

266 d involve what we call islands of awareness: conscious states that are neither shaped by sensory inpu

267 contents, as well as during conscious or non-conscious states, particularly general anesthesia.

268 functional integration of cortical areas in conscious states.

269 f advancing knowledge on the neurobiology of conscious states.

270 unresponsive wakeful syndrome and minimally conscious states.

271 reas associated with minimally conscious and conscious states.

272 props that can be utilized to perform PDT in conscious subjects without the need of extensive infrast

273 g signs of criticality were performed in non-conscious systems (in vitro neuronal cultures) or uncons

274 We found that conscious T2 perception was influenced and signaled by v

275 e to the attentional blink by revealing that conscious target perception may be determined by T1 proc

276 METHODS AND In conscious telemetered mice, acute intraperitoneal and or

277 unction by echocardiography, surface ECG and conscious telemetry, intracardiac electrograms and pacin

278 tivation of S1 and vPM) was more frequent in conscious than unconscious states.

279 Are some animals 'more conscious' than others?

280 patients in the new pandemic scenario, being conscious that availability and local situations are ext

281 le in the "piercing of consciousness" by non-conscious thought processes.

282 hrough those who have emerged from minimally conscious, to the fully conscious locked-in syndrome.

283 GFR was assessed in conscious TRPC6 wild type and knockout mice, and in anes

284 We have evaluated luciferase bioimaging in conscious, unrestrained mice after neonatal intracranial

285 ubsystems, image-forming circuits that drive conscious vision and non-image-forming circuits for beha

286 ensory attentional system that underlies our conscious visual experience.

287 Two main subcortical pathways serving conscious visual perception are the midget-parvocellular

288 sults suggest that brain dynamics underlying conscious visual perception belongs to the class of init

289 What contribution melanopsin makes to conscious visual perception is less studied.

290 Conscious visual perception is proposed to arise from th

291 erse, light-evoked behaviors that range from conscious visual perception to subconscious, non-image-f

292 f primary visual cortex (V1) lead to loss of conscious visual perception with significant impact on h

293 Here, for the first time, we show that 'conscious' visual discrimination abilities are often pre

294 and patient studies of the cortical basis of conscious volition down to the single-neuron level.

295 ether these changes represent state-related (conscious vs unconscious) or drug-related (anesthetic vs

296 ther the observed changes are state-related (conscious vs unconscious) or drug-related (drug vs no dr

297 ion evoked atropine-sensitive bradycardia in conscious WKY rats, and evoked atropine-sensitive bradyc

298 cardia with atrial-ventricular (AV) block in conscious WKY rats, thus indicating a parasympathetic re

299 ie the recently discovered phenomenon of non-conscious WM, which permits even subliminal stimuli to b

300 indings challenge the concept of genuine non-conscious "working" memory, argue that activity-silent s