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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
35 a telangiectasia mutated) that is capable of commanding a plethora of signaling networks for DNA repa
37 duced proliferation of defensive blood cells commands a diversion of dietary carbon away from somatic
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
45 me time, deployment of these technologies in command and control as well as in entertainment roles is
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
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
65 at the posterior parietal cortex contains a "command apparatus" for the operation of the hand in imme
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
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
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
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
90 Our data support a model in which central command circuits recruit individual motoneurons to gener
93 st that the central complex influences motor commands, directing the appropriate movement within the
95 the large dynamic range of extraocular motor commands during gaze stabilization.SIGNIFICANCE STATEMEN
101 differentiation was irrespective of whether command following was evident through overt external beh
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
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
121 ates, the optic tectum (superior colliculus) commands gaze shifts by synaptic integration of differen
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
129 ssed the participant's ability to cortically command his paralysed arm to perform simple single-joint
131 H bias when presented with a familiar spoken command in which the salience of meaningful phonemic (se
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
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.
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
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
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
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
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
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
175 significant expertise in these software and command line scripting experience on Unix platforms, bes
180 sis, we implement CGES both as a stand-alone command line tool available for download in GitHub and a
182 GEScan provides four operational modes: as a command line tool, as a Galaxy Toolshed, on a Galaxy-bas
186 ALEA provides a customizable pipeline of command line tools for allele-specific analysis of next-
191 Genome aims to be easily integrated with the command line, including batch processing of data, and th
199 n Core standard, includes both Web-based and command-line interfaces, and is fully open-source softwa
203 Genomic Integration Site Tracker (GeIST), a command-line pipeline designed to map the integration si
205 to (i) execute and manage otherwise complex command-line programs, (ii) launch multiple exploratory
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
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
214 ating data stored in NMR-STAR files and as a command-line tool to convert from NMR-STAR file format i
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
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
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
238 iculospinal neurons, tectal steering/turning command neurons should have minimal frequency adaptive p
240 lder is required to periodically demonstrate command of a body of knowledge that is essential to curr
244 that tectum can elaborate gaze reorientation commands on its own, rather than merely acting as a rela
246 ination revealed an ability to follow simple commands only and abnormal movements, including myoclonu
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
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
259 nd the resulting distance moved, then adjust command strength to achieve a desired travel distance.
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
265 the combined result of descending unilateral commands that change the leg motor output via task-speci
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
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
274 NIFICANCE STATEMENT When generating movement commands, the brain is believed to use internal models o
276 accepts various combinations all by one-line command, therefore allowing highly flexible yet fully au
278 nge as needed through the remapping of motor command to action goal, with strong implications for reh
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
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
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
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
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