ライフサイエンスコーパス: command

1 be key communicating circuitry for 'central command'.

2 use; the whole pipeline is run from a single command.

3 ation maps neural states to changes in motor command.

4 ostly on the processing of the central motor command.

5 , or the electrosensory and trigeminal motor command.

6 t a transient, sensory stimulus into a motor command.

7 statistics and other reports using a single command.

8 indicating the presence of a latent movement command.

9 has features indicative of a hidden movement command.

10 ntegration of sensory information with motor commands.

11 simulation parameters using simple one-line commands.

12 adding it to the previously generated motor commands.

13 ependently and, hence, configure final motor commands.

14 bject dynamics to generate feedforward motor commands.

15 od to study short-term modification of motor commands.

16 gle trial basis, to the animals' major motor commands.

17 of the limb, and produces appropriate motor commands.

18 ns may also not be specified by unique motor commands.

19 ing retinal signals into saccadic oculomotor commands.

20 tor that generated the necessary multiphasic commands.

21 beliefs about how the limb responds to motor commands.

22 for generating temporally patterned outgoing commands.

23 f generating temporally patterned descending commands.

24 ntegration of sensory feedback and executive commands.

25 sensory information into task-specific motor commands.

26 the standard of reference irrespective of BH commands.

27 fect the expression of already-adapted motor commands.

28 e performance, we must generate better motor commands.

29 e sensory representation of error into motor commands.

30 ices, primarily enabled by voice recognition commands.

31 duce the improvement in the subsequent motor commands?

32 atures of movement encoded by changing motor commands?

33 ume signal (related to medullary ventilatory command), (3) autonomic function, and (4) compound muscl

34 Francis' office window (at the Salk) commanded a panorama of the Pacific.

35 a telangiectasia mutated) that is capable of commanding a plethora of signaling networks for DNA repa

36 a cell population until a specific stimulus commands a coordinated shut-off.

37 duced proliferation of defensive blood cells commands a diversion of dietary carbon away from somatic

38 In COMMAND, a single-blind, randomised controlled trial, el

39 tion of eye-velocity signals to eye-position commands, a transformation achieved by a hindbrain cell

40 this view, motor memory is a memory of motor commands, acquired through trial-and-error and reinforce

41 tant in plants, because their sessile nature commands adaptation for survival rather than escape from

42 -band power may directly relate to the motor-command adjustments activated after movement-execution e

43 eperiod beta-power might relate to the motor-command adjustments activated after movement-execution e

44 In addition to single-command analysis of an entire experiment from mapped rea

45 me time, deployment of these technologies in command and control as well as in entertainment roles is

46 In all scenarios, the legal command and control frameworks were the most important d

47 hen the relationship between voluntary motor command and its sensory consequences changes.

48 The neural circuits underlying central command and muscle afferent control of breathing remain

49 nated activation of motoneurons from central command and premotor networks.

50 During exercise, central command and reflexes from exercising muscles produce the

51 es that stores the learned efficacy of motor commands and adapts future locomotor drive for tens of s

52 sed the relationship between balancing motor commands and associated vestibular sensory feedback, the

53 circuitries is integrated with central motor commands and contributes importantly to the muscle activ

54 ortex is far from a stable conduit for motor commands and instead undergoes significant changes durin

55 in the relationship between their locomotor commands and the resulting distance moved, then adjust c

56 mating the time elapsed between the movement commands and their observed consequences.

57 closed head injury who were unable to follow commands and were enrolled within 6 hours of injury at n

58 ng, correct movement initiation (feedforward commands) and online corrections (feedback responses) we

59 hat determines both feedforward and feedback commands), and skill-learning tasks, requiring the acqui

60 technological and management options, legal command, and control frameworks including the Atlantic F

61 rm this visual information into useful motor commands, and implement these motor representations to p

62 Market-based and command-and-control policy instruments have, along with

63 esting that the circuit is organized to both command antennal grooming and control its duration.

64 rticospinal neurons that could function as a command apparatus for operation of the hand.

65 at the posterior parietal cortex contains a "command apparatus" for the operation of the hand in imme

66 that granule cell responses to the brief EOD command are sufficiently varied and prolonged.

67 els of sensorimotor control posit that motor commands are generated by combining multiple modules whi

68 where control rate indicates how often motor commands are sent from the brain to the prosthetic, and

69 a mechanistic account of how copies of motor commands are transformed into sensory predictions.

70 us electrophysiology recordings of all motor commands are typically not available.

71 Such commands are ultimately carried out by the limbs and mus

72 ls, such as efference copy of smooth pursuit commands, are required to compensate for the visual cons

73 state of visual cortex, including the motor command associated with the report of the decision, an i

74 Under this guidance law, turning is commanded at a rate proportional to the angular rate of

75 performed with and without breath-hold (BH) commands at 3.0 T.

76 rhythm, and that it dynamically adapts these commands based on the <3 Hz fluctuations of propriocepti

77 ng retinal signals lead to robust oculomotor commands because corrections are observed if the traject

78 awakening, defined as the ability to follow commands before hospital discharge.

79 he human brain is capable of producing motor commands, but appears to require greater than normal sub

80 ion potentials (APs) to depolarizing current commands, but are unable to discharge trains of APs.

81 eeds to predict how the body reacts to motor commands, but how a network of spiking neurons can learn

82 s provide positive feedback to ongoing motor commands, but this influence decays as feedback weakens

83 ensory afferents may focus the central motor command by opening or closing sensory feedback pathways.

84 -directed gaze-stabilizing eye movements are commanded by abducens motoneurons that combine different

85 basal actinopterygians, to an outflow tract commanded by the non-valved, elastic, bulbus arteriosus

86 are covertly aware and capable of following commands by modulating their neural responses in motor i

87 mal control of movement in which feedforward commands can play a significant role.

88 that predicted sensory consequences of motor commands cancel sensory signals.

89 have shown that the optic lobe is the motor command center for dynamic body patterning.

90 Our data support a model in which central command circuits recruit individual motoneurons to gener

91 Motor commands computed by the cerebellum are hypothesized to

92 is addition serves as an update to the motor commands, constituting the learning signal.

93 st that the central complex influences motor commands, directing the appropriate movement within the

94 erebellum is involved in the update of motor commands during error-dependent learning.

95 the large dynamic range of extraocular motor commands during gaze stabilization.SIGNIFICANCE STATEMEN

96 We report command electro-optical switching on photolithographical

97 Do motor commands encode movement independently or can they be re

98 Users typically command FES systems through other preserved, but unrelat

99 clinical variables but capable of behavioral command following (patient 2).

100 Command following was characterized by a further increas

101 differentiation was irrespective of whether command following was evident through overt external beh

102 attending toward a stimulus), and (3) aware (command following).

103 etic resonance imaging assessments of covert command following.

104 tabolic activity was further associated with command following.

105 maging and electroencephalography can detect command-following and higher-order cortical function in

106 ce imaging and electroencephalography detect command-following during a motor imagery task (i.e. cogn

107 A subset of patients had fMRI testing of command-following using motor imagery paradigms (26 pati

108 c resonance imaging (fMRI)-based evidence of command-following, and correlated the findings with stan

109 urons process a visually specified reference command for the intended arm/hand position trajectory wi

110 from the retina and visual cortex into motor commands for rapid eye movements (saccades).

111 tibular inputs into temporally precise motor commands for the lateral rectus eye muscle.

112 e transfer of sensory information into motor commands for vocal amplitude control in response to back

113 ckage and using the same data structures and command formats, phylogeo allows users to easily map and

114 rain-machine interfaces (BMIs) extract motor commands from a single brain to control the movements of

115 shaping descending signals and coordinating commands from higher brain areas with the step cycle.

116 nveying sensory information and higher-order commands from the brain to motor circuits in the ventral

117 These modulations in motor commands from the CNS may lead to altered activation of

118 be compensated for by an alteration of motor commands from the CNS.

119 ting touch information with descending motor commands from the cortex and cerebellum.

120 als differentiated patients who could follow commands from those who could not.

121 ates, the optic tectum (superior colliculus) commands gaze shifts by synaptic integration of differen

122 ," which may alert shell neurons to movement commands generated by the superior colliculus.

123 hese results reveal how a single adaptor can command global changes in proteome composition through p

124 pants were assigned to cognitive therapy for command hallucinations + treatment as usual and 99 (50%)

125 22 (28%) of 79 in the cognitive therapy for command hallucinations + treatment as usual group (odds

126 ned in a 1: 1 ratio to cognitive therapy for command hallucinations + treatment as usual versus just

127 cipants from three centres in the UK who had command hallucinations for at least 6 months leading to

128 Acting on command hallucinations in psychosis can have serious con

129 ssed the participant's ability to cortically command his paralysed arm to perform simple single-joint

130 The U.S. Army Medical Command implemented programmatic changes to ensure deliv

131 H bias when presented with a familiar spoken command in which the salience of meaningful phonemic (se

132 These are now typed as reaction-like commands in ASCII text files that are read by Pycellerat

133 Trains of 2 distinctive voltage commands in form of APs recorded during large and small

134 ror in sensory coordinates into better motor commands in muscle coordinates?

135 t minority of vegetative patients who follow commands in neuroimaging tests, they point to putative n

136 left-right desynchronized inspiratory motor commands in reduced brain preparations and breathing at

137 sed but a significant RH bias in response to commands in which the salience of intonational or speake

138 We find that ALA signalling inhibits command interneuron activity by abrogating excitatory si

139 y by abrogating excitatory signalling in the command interneurons, which is responsible for promoting

140 ruct a Kalman filter that incorporates motor commands into a previously established model of optimal

141 s organization defines the assembly of motor commands into a string of run-and-turn action sequence c

142 vocalize, their vocal organ transforms motor commands into vocalizations for social communication.

143 nd the splaying apart of pore-lining helices commanding ion passage.

144 Remaining completely still on command is a major achievement as involuntary fluctuatio

145 eeding or predicting a movement that a motor command is eliciting.

146 sory prediction errors into corrective motor commands is the basis for how we learn the physics of ob

147 ore complex environment where more number of commands is to be used to control with better results in

148 to predict the sensory consequences of motor commands, is critical for adapted motor behavior.

149 e based on internal signals related to motor commands, known as corollary discharge (CD), sensory fee

150 sized that internal signals related to motor commands, known as corollary discharge, serve to generat

151 information and relay their outputs to motor command layers of the spinal cord.

152 bilistic, persistent and (ii) deterministic, command-like components.

153 -2 (CP-2)] are released from the cholinergic command-like neuron cerebral buccal interneuron 2.

154 The Mauthner cell (M-cell) is a command-like neuron in teleost fish whose firing in resp

155 The pipeline is available as both a command line and a Galaxy graphical user interface tool.

156 utational literacy, including platforms with command line and graphical user interfaces.

157 The tools can both be run from the Unix command line and installed into visual workflow builders

158 n be run from the web as well as a dedicated command line application, which allows easy integration

159 A JAVA cross-platform command line executable of ARACNe, together with all sou

160 th TIGERi could use the software without any command line experience.

161 is project is implemented in Java 7, and the command line interface (CLI) is designed to integrate in

162 ead by Pycellerator, which includes a Python command line interface (CLI), a Python application progr

163 Both tools are available with a command line interface as well as a graphical user inter

164 It provides a command line interface for easy integration into a bioin

165 ne application features a simple and concise command line interface for easy integration into high-th

166 art database search engines and a convenient command line interface for high-performance data process

167 It uses a command line interface to automatically call other progr

168 imitations, ASCIIGenome runs exclusively via command line interface to display genomic data directly

169 Toolbox includes a graphical user interface, command line interface, and options for speed and accura

170 ducts, but GDBB has only been available on a command line interface, which is difficult to use for th

171 eatures are available via both graphical and command line interface.

172 Yet many immunoinformatics tools have command line interfaces only and can be difficult to ins

173 The software is a command line perl script freely available as open source

174 tegrated Genome Viewer or with a stand-alone command line program.

175 significant expertise in these software and command line scripting experience on Unix platforms, bes

176 We implemented a command line software tool and a web interface called w4

177 Synima runs quickly on a command line to generate informative and publication qua

178 BGT is a compact format, a fast command line tool and a simple web application for effic

179 A command line tool and a web interface are available to t

180 sis, we implement CGES both as a stand-alone command line tool available for download in GitHub and a

181 We present SeqLib, a C ++ API and command line tool that provides a rapid and user-friendl

182 GEScan provides four operational modes: as a command line tool, as a Galaxy Toolshed, on a Galaxy-bas

183 We have developed a new Python command line tool, which is compatible with the widely a

184 Reaction Decoder is a robust command line tool, which performs this task with high ac

185 Command line tools are available for performing integrat

186 ALEA provides a customizable pipeline of command line tools for allele-specific analysis of next-

187 Modelled after Unix/GNU/Linux command line tools, individual programs perform a single

188 ository, and we also provide source code for command line usage under Linux and Mac OS X.

189 Meta-eqtl is a set of command line utilities written in R, with some computati

190 SplicePlot is a simple command line utility that produces intuitive visualizati

191 Genome aims to be easily integrated with the command line, including batch processing of data, and th

192 t is written in C and can be run from a Unix command line.

193 GLANET can be run using its GUI or on command line.

194 Queries can also be run from the command-line and the database can be queried directly th

195 e VCF files and organized these tools into a command-line based utility named VCF-kit.

196 In addition, the package provides a command-line interface for users with scripting and prog

197 MSMBuilder boasts an easy to use command-line interface, as well as clear and consistent

198 rieve annotation from these catalogs via the command-line interface.

199 n Core standard, includes both Web-based and command-line interfaces, and is fully open-source softwa

200 phisticated analyses that are independent of command-line knowledge.

201 In contrast to most command-line or batch interactions with Rosetta, Foldit

202 The toolbox, available as command-line or with a graphical user interface, enables

203 Genomic Integration Site Tracker (GeIST), a command-line pipeline designed to map the integration si

204 StochHMM provides a command-line program and C++ library that can implement

205 to (i) execute and manage otherwise complex command-line programs, (ii) launch multiple exploratory

206 The Ruby-based web framework and the command-line software (implemented in Java, with visuali

207 e HaploPOP software is freely available as a command-line software at www.ieg.uu.se/Jakobsson/softwar

208 neration, and support for running both R and command-line software on local computers and computer cl

209 ling of the web interface, (ii) links to the command-line stand-alone and web versions of the MToolBo

210 In summary, through the command-line tool and the web server, these protocols pr

211 resent BISQUE, a web server and customizable command-line tool for converting molecular identifiers a

212 cture of RNA) is an integrated and automated command-line tool for the analysis and annotation of RNA

213 We present Epock, an efficient command-line tool that calculates pocket volumes from MD

214 ating data stored in NMR-STAR files and as a command-line tool to convert from NMR-STAR file format i

215 Many of the BiopTools command-line tools act as filters, taking a PDB (or PDBM

216 esentation of parameters, inputs, outputs of command-line tools in so-called Common Tool Descriptor d

217 The application can be executed using either command-line tools or a user-friendly Graphical User Int

218 We present a training model for use of command-line tools when the learner has little to no pri

219 g protein structure, and BiopTools, a set of command-line tools which exploit BiopLib.

220 r interface (GUI) to streamline usage of the command-line tools, calculate data from structure librar

221 the capabilities of many R/Bioconductor and command-line tools, it makes efficient use of existing s

222 of medical images, overcoming limitations of command-line tools.

223 GLINT is a user-friendly command-line toolset for fast analysis of genome-wide DN

224 a queries and downloads, alignment programs, command-line utilities and more.

225 le as a web-server or a platform-independent command-line version.

226 KBase) and are publicly available via API or command-line web interface.

227 Unfortunately, Rosetta is largely a command-line-driven software package which restricts its

228 an be used through a web interface or in the command-line.

229 Acoustic stimuli that activate ASR-command Mauthner cells also activate dorsal raphe nucleu

230 The capability to induce REM sleep on command may offer a powerful tool for investigating its

231 Similar local command mechanisms that selectively activate the pattern

232 of matching perceived objects with the motor commands needed to grasp them.

233 ished the ability to update subsequent motor commands needed to reduce motor errors.

234 cusing on key structures that might form the command network.

235 hanges in the excitabilities of the Mauthner command neuron for escape and the inhibitory interneuron

236 ng that these neurons are not simply feeding command neurons but likely play a more general role in e

237 The serotonergic HSN command neurons initiate the active state, but accumulat

238 iculospinal neurons, tectal steering/turning command neurons should have minimal frequency adaptive p

239 ause activation of P1 neurons, male-specific command neurons that trigger courtship.

240 lder is required to periodically demonstrate command of a body of knowledge that is essential to curr

241 eir expression is specialized when under the command of a common regulator.

242 n in task compliance, cognitive ability, and command of language.

243 ment for testing a certification candidate's command of the body of knowledge.

244 that tectum can elaborate gaze reorientation commands on its own, rather than merely acting as a rela

245 rned from these errors and altered the motor commands on the subsequent reach.

246 ination revealed an ability to follow simple commands only and abnormal movements, including myoclonu

247 d by the alignment algorithms using multiple command option values.

248 ulatta) while they produced vocalizations on command or passively listened to monkey calls.

249 0.1-0.8) and assigned to Special Operations Command (OR = 0.0 [95% CI, 0.0-0.0]).

250 t so that on the very next attempt our motor commands partially compensate for the unfamiliar physics

251 ming neural activity into control signals to command prostheses to allow human patients to dexterousl

252 between vestibular sensory signals and motor commands related to maintaining balance.

253 with and without alternation in the voltage command shape.

254 val of functionally related volitional motor commands signaled by muscle activity in the impaired for

255 etinal image motion with smooth eye movement command signals to signal depth sign from motion paralla

256 The participant successfully cortically commanded single-joint and coordinated multi-joint arm m

257 ("spatial" synergies) or time-varying muscle commands ("spatiotemporal" synergies).

258 The demonstrated commanding strategy should be compatible with other viab

259 nd the resulting distance moved, then adjust command strength to achieve a desired travel distance.

260 Whereas motor command strength was independent of projection allocatio

261 ween the trigeminal sensory and electromotor command system, or the electrosensory and trigeminal mot

262 re part of the phylogenetically oldest motor command system, spontaneously arborize and form contacts

263 rse range of clients including web browsers, command terminals, programming languages and standalone

264 lows for a better user correction of control commands than classification.

265 the combined result of descending unilateral commands that change the leg motor output via task-speci

266 hey are one of the few sources of descending commands that directly influence motor output.

267 neuron's firing modulated strongly only with commands that evolved along a single direction within po

268 arm, changing the relationship between motor commands that our brain sends to our arm muscles and the

269 rception to action by providing the premotor commands that release hunting responses.

270 transforming sensory information into motor commands that support postural and locomotor control.

271 that the cortex sends population-level motor commands that tend to structure according to the approxi

272 omplexity of this heterogeneous disorder has commanded the need to better define asthma phenotypes ba

273 iability, influencing the population readout commanding the owl's sound-orienting behavior.

274 NIFICANCE STATEMENT When generating movement commands, the brain is believed to use internal models o

275 The challenge lies in commanding their chaotic behavior.

276 accepts various combinations all by one-line command, therefore allowing highly flexible yet fully au

277 ithout explicit spinal transmission of motor commands through the lesion.

278 nge as needed through the remapping of motor command to action goal, with strong implications for reh

279 ation and converts it into appropriate motor command to keep the contraction force steady.

280 nt signal by the efference copy of the motor command to produce the action.

281 ur movements and establishing the best motor commands to achieve our ends.

282 gation requires sensory perception and motor commands to be intertwined in a feedback loop, yet the n

283 an internal dynamic model that relates motor commands to changes in body state (e.g. arm position and

284 es of varying intensities rely on descending commands to heterogeneous pools of motoneurons.

285 vioral goal (reach a spatial goal) and motor commands to move the limb.

286 in the world, an animal's brain must produce commands to move, change direction, and negotiate obstac

287 error during a movement, we update our motor commands to partially correct for this error on the next

288 at use (efferent) information from our motor commands to predict and attenuate the sensory consequenc

289 lone computer program that reads a script of commands to represent complex macromolecules, including

290 primary efferent pathway that conveys motor commands to the spinal cord, the dysfunction of movement

291 e corollary discharge, or copies of outgoing commands, to accelerate motor corrections.

292 tic errors that trigger trial-to-trial motor-command updates influenced beta-activity during the fore

293 hand, reanimated through implanted FES, and commanded using his own cortical signals through an intr

294 cordings of calcium current in response to a command waveform based on the motorneuron AP show, direc

295 pping) based projection of EMG into external commands were applied while artificially introducing non

296 vention allocation, but statistical analysis commands were constructed masked to group.

297 Only those patients who followed commands, whether overtly with behavior or covertly with

298 e ability to initiate and terminate sleep on command will also help us to elucidate its functions wit

299 gle sensory internal model can combine motor commands with vestibular and proprioceptive signals opti

300 stributed preparatory activity into movement commands within hierarchically organized cortical circui