ライフサイエンスコーパス: navigation

1 o processing the optic flow generated during navigation.

2 tand the cellular mechanisms of learning and navigation.

3 ng visual memories for successful view-based navigation.

4 bnormal expression of genes involved in axon navigation.

5 r biasing towards reliance on boundary-based navigation.

6 he availability of cues that can be used for navigation.

7 euronal firing to support memory and spatial navigation.

8 crotubules is especially critical for neuron navigation.

9 brain circuits, resulting in less efficient navigation.

10 at these birds rely on a geomagnetic map for navigation.

11 eases our reliance on familiar routes during navigation.

12 tics of both spontaneous and contrast-driven navigation.

13 nal subtypes, several of which contribute to navigation.

14 ant information-processing role in olfactory navigation.

15 nd mechanisms that migratory mammals use for navigation.

16 in learning and memory as well as in spatial navigation.

17 along with their cognitive functions beyond navigation.

18 previously been implicated in compass-based navigation.

19 nvironment could be relevant for large-scale navigation.

20 Both regions are involved in spatial navigation.

21 nctions, such as episodic memory and spatial navigation.

22 ereby supporting remembering and potentially navigation.

23 ocampal formation and is involved in spatial navigation.

24 hysiology driven by an image-based abdominal navigation.

25 , which is essential information for optimal navigation.

26 s adult flies' capacity to perform celestial navigation.

27 and provide an internal compass for spatial navigation.

28 rception and memory-based scene construction/navigation.

29 at approximates information maximization for navigation.

30 ns for two pertinent observations related to navigation.

31 employs the Earth's magnetic field to assist navigation.

32 may converge upon a common neural system for navigation.

33 and use this information for orientation and navigation.

34 e (MTL) that supports spatial processing and navigation.

35 hought to be critical for memory and spatial navigation.

36 e development of circuits that control adult navigation.

37 ntly registered to external landmarks during navigation.

38 al circuits, and to be implemented for robot navigation.

39 ation test, as a measure of entorhinal-based navigation.

40 ust verticality signal for three-dimensional navigation.

41 development, mediating axonal, and neuronal navigation.

42 tor, cospecific) or to control the course of navigation.

43 al intelligence and robotics with autonomous navigation.

44 enerated gradients are needed for successful navigation.

45 fic locations, typically their homes, during navigation.

46 ortex, is important in learning, memory, and navigation.

47 implicated in associative memory and spatial navigation.

48 ith silicon probes during head-fixed virtual navigation.

49 anization within the growth cone direct axon navigation.

50 ble firing rate changes during unconstrained navigation.

51 ct evidence that ants require MBs for visual navigation.

52 vement, implicating these signals in spatial navigation.

53 standing these important components of human navigation.

54 the body and head (the fly's heading) during navigation (1,2).

55 their current view for successful view-based navigation [11].

56 ts information necessary for visually guided navigation [3-9].

57 patial metrics predicted by rodent models of navigation [5].

58 onmental challenges and the ants' collective navigation abilities.

59 However, the impact of interindividual navigation ability and demographic risk factors (e.g., A

60 We also show that although baseline navigation ability differs between men and women, sex do

61 a single molecule study to characterize the navigation ability of KIF3AC, KIF3AA, and KIF3CC when en

62 ory storage and retrieval as well as spatial navigation across many species.

63 Spinal commissural axon navigation across the midline in the floor plate require

64 d during development for cellular and axonal navigation also play roles in synapse maturation and hom

65 , scaffold graphs have proven useful for the navigation and analysis of chemical space, being used fo

66 ars carries accelerometers normally used for navigation and attitude determination.

67 the neural mechanisms that underlie spatial navigation and awareness of others in real-world scenari

68 m cells in the LS and the hippocampus during navigation and conditioning tasks.

69 bias, including the potential impact on host-navigation and courtship.

70 omplex, a brain structure involved in visual navigation and decision making.

71 value in monitoring hazardous environments, navigation and detecting hidden adversaries.

72 ng climate change mitigation, flood control, navigation and engineering works.

73 The hippocampus is crucial for spatial navigation and episodic memory formation.

74 a brain region that is important for spatial navigation and episodic memory, benefits from a rich div

75 TL function encompassing its role in spatial navigation and episodic memory.

76 hysiological substrate for spatial coding in navigation and episodic recall.

77 otion hand detection, resulting in intuitive navigation and exploration of various types of biologica

78 e detection of CO(2) is important for upwind navigation and for enhancing the attraction to body heat

79 n into allocentric cognitive maps to support navigation and foraging in such spaces.

80 and trained an ANN to perform heat gradient navigation and found striking similarities in computatio

81 ed to 6 months of EE showed improved spatial navigation and had significantly fewer plaques in M1 and

82 aditional bioinformatics use for tagging and navigation and has necessitated the development of a new

83 ute to network operations supporting spatial navigation and learning in the hippocampus.

84 st known for their cognitive role in spatial navigation and memory corresponds to precise physiologic

85 Several types of neurons involved in spatial navigation and memory encode the distance and direction

86 ocampal place cells actively support spatial navigation and memory.

87 l temporal lobe is critical for both spatial navigation and memory.

88 rection codes represent cognitive spaces for navigation and memory.

89 es while they carried out real-world spatial navigation and observation tasks.

90 ly involved in memory consolidation, spatial navigation and pattern separation, complex functions oft

91 eference genome, UMD3.1.1, with cross-genome navigation and queries supported in JBrowse and BovineMi

92 of the brain are important for memory-guided navigation and rely on visual inputs.

93 The combination of navigation and robotics in spine surgery has the potenti

94 By recording from MEC cell ensembles during navigation and sleep, we found that spatial phase offset

95 rols a variety of adult behaviors, including navigation and sleep.

96 environment of hippocampal-dependent spatial navigation and striatal-dependent approach of a visual c

97 thalamic environment is instructive for TCA navigation and that the molecular cues netrin 1 and sema

98 e signaling systems required for pollen tube navigation and the potential roles of Ca(2+) signals.

99 adjacent locations into trajectories during navigation and their navigational experience-dependent r

100 nctions, including scene perception, spatial navigation, and autobiographical memory retrieval.

101 g memory recall, visual scene processing and navigation, and is a core component of the default mode

102 ing, memory, pattern separation, and spatial navigation, and its dysfunction is associated with neuro

103 y and scientifically for time dissemination, navigation, and long-baseline interferometric imaging.

104 eatures allow for easy network partitioning, navigation, and node positioning, SAMMI also offers a wi

105 del species for the study of olfaction-based navigation, and sequence OR gene-positive cosmid clones

106 tigate which cues mammals use for long-range navigation, and, surprisingly for nocturnal animals, sun

107 During spatial navigation, animals use self-motion to estimate position

108 If episodic memory and spatial navigation are 2 sides of the same coin, we hypothesized

109 Ageing effects on spatial navigation are characterized mainly in terms of impaired

110 The mechanisms underlying killer cell's navigation are not well understood.

111 regions and neural codes supporting spatial navigation are recruited when humans use language to org

112 the treatment plans of interest, can provide navigation around these sources of bias and elucidate th

113 tic-like vesicles at specific points in axon navigation as regulators of growth cone microenvironment

114 sensory repertoire in that it contributes to navigation, awareness of moving objects, and communicati

115 uring adequate potency in human whole blood, navigation away from Ames mutagenic amine fragments whil

116 influence of place cell activity on spatial navigation behavior has not yet been demonstrated.

117 ed in hippocampus-associated LS cells during navigation behavior that requires working memory.

118 mplements coordinate transformation to guide navigation behavior.

119 for the investigation of the neural basis of navigation behaviors and the evolution of these strategi

120 low-risk participants using big-data spatial navigation benchmarks.

121 tomizations made by the users allowing quick navigation between instances.

122 In the current study, we use spatial navigation big data (n = 27,108) from the Sea Hero Quest

123 ex (CX) is thought to underlie goal-oriented navigation but its functional organization is not fully

124 or detailed obstacle location information in navigation, but rely heavily on optical flow.

125 res are critical for both memory and spatial navigation, but we do not fully understand the neuronal

126 they are consistent with the hypothesis that navigation by boundaries and features may involve distin

127 The hippocampus is thought to guide navigation by forming a cognitive map of space.

128 he impact of ship traffic in the vicinity of navigation channels in a wide shallow waterbody.

129 The analysis considers navigation channels in the Venice Lagoon using a new lar

130 NCE STATEMENT Motion perception is vital for navigation, communication, and the awareness of moving o

131 erred to the electronic domain, where radar, navigation, communications, and fundamental research rel

132 Netrin-1, a navigation cue during embryonic development, is upregula

133 s and neuronal networks that mediate spatial navigation, decision-making, sociality, and creativity e

134 For that reason, a neural substrate for navigation demands spatial and environmental information

135 However, an alternative hypothesis is that navigation difficulties in aged people are associated wi

136 s the gCMs into tumor tissues under magnetic navigation, effectively promoting their systemic circula

137 ons inspired by floral shapes streamline the navigation efficacy of sonar-guided robot systems.

138 inting tasks, which are theorized to measure navigation efficiency and cognitive mapping.

139 sentation of the environment, reduce spatial navigation efficiency, distort distance estimation and m

140 s in conscious memory consolidation, spatial navigation, emotion, and motivated behaviors.

141 Navigation engages many cortical areas, including visual

142 During navigation, fMRI responses in entorhinal cortex and vent

143 N (PADN group; n = 25) using remote magnetic navigation for ablation or medical therapy with riocigua

144 oducing a wide range of behaviors, including navigation, foraging, prey capture, and conspecific inte

145 the circuitry underlying memory and spatial navigation functions of the parasubiculum.SIGNIFICANCE S

146 ey at high-speed using the same proportional navigation guidance law as homing missiles.

147 that, unlike navigation guided by landmarks, navigation guided by boundaries is robust to "blocking"

148 daries explains the observation that, unlike navigation guided by landmarks, navigation guided by bou

149 ensation, experience, and directed action in navigation has been facilitated by the development of vi

150 Navigation has typically been studied as a spatial infor

151 al formation to encode physical space during navigation have been suggested as a suitable format.

152 using two-photon calcium imaging and virtual navigation have identified "spatially" modulated neurons

153 epresent locations in the environment during navigation, how this spatial tuning relates to memory fo

154 hippocampus that underlie spatial memory and navigation: how these neurons represent 3D space is cruc

155 standing the neural basis of visually guided navigation, however, little is known about how this syst

156 on, but most HD cell studies have focused on navigation in 2D environments.

157 s and in particular how can we describe this navigation in a concise way.

158 During navigation in a real arena, they showed spatially stable

159 We present navigation in a synthetic vessel tree based on our mappi

160 ore we investigated their role in view-based navigation in a visually oriented ant, Myrmecia midas.

161 Visual navigation in ants has long been a focus of experimental

162 The largely vision-based navigation in Cataglyphis requires sophisticated neurona

163 nt sensory modalities during the ontogeny of navigation in Cataglyphis.

164 n, rheotactic cell sorting, and microswimmer navigation in complex flow environments.

165 the fly brain circuitry underlying flexible navigation in complex multisensory environments.

166 ity and probabilistic behavior during animal navigation in different odor gradients and across a broa

167 Half of the patients were randomized to MRI navigation in each group.

168 al for a wide range of applications, such as navigation in GPS-denied environments.

169 RSC damage impairs navigation in humans and rodents [6-8], and the RSC is c

170 ics revealed a preference for geometry-based navigation in older adults, and for landmark-based navig

171 y and efficacy of PADN using remote magnetic navigation in patients with residual CTEPH after PEA.

172 functionality of PiVR by focusing on sensory navigation in response to gradients of chemicals (chemot

173 s sp., uses its active electric sense during navigation in the dark.

174 same neuronal coding schemes characterizing navigation in the physical space (tuned to distance and

175 rete swim-bout events that subserve the fish navigation in the presence of a distant light source.

176 ough loss of leaders crucial to younger male navigation in unknown, risky environments.

177 computations that are essential for flexible navigation in varied surroundings.

178 dying how geometry and landmark cues control navigation in young and older adults in a real, ecologic

179 tion in older adults, and for landmark-based navigation in younger ones.

180 Here, we focus on light-seeking navigation in zebrafish larvae.

181 Patient navigation included an assessment of barriers to surveil

182 d with brain regions known to play a role in navigation, including the hippocampus and anterior thala

183 During virtual navigation, individual cue cells exhibited firing fields

184 ogether, we reveal a novel mechanism of cell navigation involving APC-dependent assembly of branched

185 Spatial navigation is emerging as a critical factor in identifyi

186 s magnetic field for orientation and compass-navigation is fascinating and puzzling in equal measure.

187 tested the hypothesis that entorhinal-based navigation is impaired in pre-dementia Alzheimer's disea

188 In early Alzheimer's disease (AD) spatial navigation is impaired; however, the precise cause of th

189 Path integration plays a vital role in navigation: it enables the continuous tracking of one's

190 The spatial-navigation literature presents a parallel dichotomy betw

191 actors (e.g., APOE, age, and sex) on spatial navigation make it difficult to identify persons "at hig

192 ve gray whale strandings suggests that their navigation may be disrupted by increased radio frequency

193 The MRI navigation method (-32.4%) did not yield better antidepr

194 rategies have been incorporated into several navigation models [8, 12, 13], we still know little abou

195 ound (n = 600), mailed outreach plus patient navigation (n = 600), or usual care with visit-based scr

196 t, a process we refer to as "visually guided navigation." Neuroimaging work in adults suggests this a

197 In this paper we explore the navigation of a network taking into account the alternat

198 d to distance and direction) should underlie navigation of abstract semantic spaces, even if they are

199 ualize the role of synaptic-like vesicles in navigation of dorsal root ganglia pioneer axons.

200 upled receptor signaling is required for the navigation of immune cells along chemoattractant gradien

201 facilitation of effective communication and navigation of problems that arise.

202 nefit from neural mechanisms that enable the navigation of salt gradients to avoid high salinity.

203 ty gene programs that shape Th1 and Th2 cell navigation of the inflamed dermis.

204 Reproducible navigation of the pacing lead to predetermined HBP locat

205 ion regulation capacities develop to aid the navigation of the social environment during adolescence.

206 Successful navigation of the social environment is dependent on a n

207 ans were used for target selection and neuro-navigation of the transcranial magnetic stimulation.

208 Navigation of this new era will require genetic literacy

209 Navigation often requires movement in three-dimensional

210 c resonance imaging with a naturalistic maze-navigation paradigm, we identified functionally segregat

211 veillance was performed in 23.3% of outreach/navigation patients, 17.8% of outreach-alone patients, a

212 inology, and machine learning with a virtual navigation planning task.

213 inhibiting eye movements in humans impaired navigation precision.

214 s for mediating essential tasks that include navigation, predation and foraging, predator avoidance,

215 implementation of an OTP-based screening and navigation protocol has enabled significant gains in the

216 known to support episodic memory and spatial navigation, raising the possibility that its true functi

217 We discovered that, during active navigation, rat hippocampal CA1 place cell ensembles are

218 w, with potential applications in autonomous navigation, reconnaissance, and even medical imaging.

219 in cortisol, a biomarker of stress, disrupts navigation-related brain circuits, resulting in less eff

220 Navigation-related neural activity is seen in humans [11

221 T Path integration is the most basic form of navigation relying on self-motion cues.

222 f the information used by migratory bats for navigation remains unclear.

223 Successful visual navigation requires a sense of the geometry of the local

224 Fluid navigation requires constant updating of planned movemen

225 Spatial navigation requires landmark coding from two perspective

226 rvey included patients per provider/trainee, navigation, RIC posters/brochures, laboratory test timin

227 During navigation, rodents continually sample the environment w

228 field derived from the combination of Global Navigation Satellite System (GNSS) and satellite radar i

229 all stations that record signals from Global Navigation Satellite Systems(2,3) (GNSS), enabling us to

230 the firing rates of many MTL neurons during navigation significantly changed depending on the positi

231 Conclusion: Mailed outreach invitations and navigation significantly increased HCC surveillance vers

232 Here, we study longhorn crazy ant collective navigation skills within the context of a semi-natural,

233 n in a useful format, rather than relying on navigation-specific neural circuitry.

234 While view-based navigation strategies have been incorporated into severa

235 rature presents a parallel dichotomy between navigation strategies.

236 found that the contributions of proportional navigation strategy are negligible.

237 Navigation support is provided for linkage or relinkage

238 equipped with an augmented reality surgical navigation system (ARSN).

239 aboratory work [4-6] that turtles use a true navigation system in the open ocean, but their map sense

240 This novel navigation system provides a highly efficient way for re

241 complex environments necessitates a flexible navigation system that incorporates memory of recent beh

242 the ligand-receptor pair WNT5A-RYK acts as a navigation system to instruct filopodial pathfinding, a

243 ts were treated under CT guidance using a 3D navigation system.

244 it was outweighed by impaired landmark-based navigation (t(980) = 6.374, p < 0.001) resulting in an o

245 rsal lateral septum in rat during a rewarded navigation task and compared spatial firing in the two a

246 ty of thousands of cortical neurons during a navigation task and reveals that features of the task en

247 t an entorhinal cortex-based virtual reality navigation task can differentiate patients with mild cog

248 ns as mice performed a goal-directed spatial navigation task in new visual virtual reality (VR) conte

249 task paradigm that we implement as an aerial navigation task in virtual reality and which creates cog

250 We used a continuous place navigation task in which male rats navigate to one of tw

251 tive patients exhibited larger errors in the navigation task than biomarker-negative patients, whose

252 ncurrent with fMRI) performed a planning and navigation task that could be most efficiently solved by

253 ted that claim by returning to a spontaneous navigation task with rats and domestic chicks, using a s

254 an enhanced incidence of errors in a spatial navigation task, but it did not affect spatial correlate

255 ental study, 25 healthy subjects performed a navigation task, with the retrofit attachment and withou

256 about latent variables using a naturalistic navigation task.

257 urgical subjects performed a virtual spatial navigation task.

258 s) may be the substrate for visual memory in navigation tasks [5-7], while computational modeling sho

259 This study provides evidence that navigation tasks may aid early diagnosis of Alzheimer's

260 Here we develop a series of navigation tasks that separately manipulate the statisti

261 n the clustering model is applied to spatial navigation tasks, so-called place and grid cell-like rep

262 has been repeatedly observed during spatial navigation tasks.

263 and constriction devices, and intraoperative navigation techniques were used.

264 d potential of this novel bioimpedance-based navigation technology as a non-fluoroscopic technique to

265 s adversely affected by disparities, patient navigation, telephone calls and prompts, and reminders i

266 bility for most interventions except patient navigation, telephone calls and prompts, and reminders i

267 d higher cancer screening rates with patient navigation; telephone calls, prompts, and other outreach

268 ce cells in marmoset hippocampus during free navigation that exhibit remarkable parallels to analogou

269 d into a comprehensive Markov-chain model of navigation that quantitatively predicts the stationary d

270 During spatial navigation, the frequency and timing of spikes from spat

271 t, akin to a ship's pilot, guides lymphocyte navigation, the nature of this pilot is unknown.

272 brain regions typically involved in spatial navigation: the medial prefrontal cortex and the right e

273 Paralleling its role in navigation, these data implicate the entorhinal/subicula

274 designed to tap boundary- and landmark-based navigation (thought to rely on hippocampal and striatal

275 work demonstrated directional coding during navigation through a continuous stimulus feature space a

276 reatment of vascular disease demands dynamic navigation through complex blood vessel pathways and acc

277 deficiency virus (HIV) includes facilitating navigation through the HIV continuum of care: timely dia

278 Understanding transcription factor navigation through the nucleus remains critical for deve

279 d factors associated with successful patient navigation through two steps of the continuum using mult

280 behaviors, such as foraging orientation and navigation, time-memory for food sources, sleep, and lea

281 ock neurons, to potentially impair honey bee navigation, time-memory, and social communication.

282 at lesions of MB calyces impair ants' visual navigation to a remembered food location yet leave their

283 We tested this using virtual navigation to grant participants 'X-ray' vision during e

284 ge rate undergoes transient increases during navigation to increase electrosensory sampling.

285 pacing lead on the HB cloud and reproducible navigation to predetermined HB capture sites.

286 oritization and drug design, and serves as a navigation tool for medicinal chemists, structural and c

287 The journey of sperm navigation towards ovum is one of the most important que

288 g from biomedical diagnostics, to autonomous navigation, trace gas sensing, and scientific exploratio

289 anosensory and visual cues, it should enable navigation under conditions where no single cue is consi

290 ntorhinal cortex is critically implicated in navigation underpinned by the firing of spatially modula

291 d the availability of body-based cues during navigation using an omnidirectional treadmill and a head

292 the hippocampus supports episodic memory and navigation via the theta oscillation, a ~4-10 Hz rhythm

293 We found that navigation was stochastic and did not rely on the contin

294 road network structure has on our real world navigation, we aimed to explore the relationship between

295 e observed neurons whose firing rates during navigation were tuned to specific heading directions in

296 arallels between interval timing and spatial navigation, where direct analogies can be made between t

297 he ability to integrate objects into spatial navigation, which would be an advantage for migrating he

298 guidance law, coupling low-gain proportional navigation with a low-gain proportional pursuit element.

299 ectively anchored, potentially providing for navigation without a stable externally anchored directio

300 le inland waterways should meet the needs of navigation without compromising the health of riverine e