ライフサイエンスコーパス: motor activity

1 anslocation consuming 1-2 ATP per base pair (motor activity).

2 in microtubules, cytoskeleton linkages, and motor activity.

3 ments sliding toward each other via Myosin-2 motor activity.

4 ic response to D1 stimulation, and augmented motor activity.

5 in vivo constriction rate scales with myosin motor activity.

6 ry that shapes their material properties and motor activity.

7 erant responding for a nondrug reinforcer or motor activity.

8 w these unusual spinal cord neurons regulate motor activity.

9 s of M18A in vivo do not depend on intrinsic motor activity.

10 els in midbrain GABA neurons did not enhance motor activity.

11 erator (CPG) that coordinate flexor-extensor motor activity.

12 stent with DNA damage induced by unregulated motor activity.

13 g notching, indicating the importance of the motor activity.

14 ition, whereby intermolecular contacts limit motor activity.

15 oplasm of cells and thereby probe stochastic motor activity.

16 fauna from flora: perception, cognition, and motor activity.

17 ent from both thermal diffusion and directed motor activity.

18 lament's ability to regulate ABPs and myosin motor activity.

19 ion of even a single mutant protomer poisons motor activity.

20 ta strains and analyzed Dyn1 single-molecule motor activity.

21 sphorylation of the MYO3A motor and reducing motor activity.

22 g RLC phosphorylation or nonmuscle myosin II motor activity.

23 ed actin polymerization as a function of its motor activity.

24 r's tract and the dorsal column and regulate motor activity.

25 ake of the palatable diet, without affecting motor activity.

26 novelty and olfactory responses, anxiety or motor activity.

27 in circadian entrainment and for masking of motor activity.

28 radigm, as well as assessment of spontaneous motor activity.

29 ice, at doses that did not inherently affect motor activity.

30 al dopamine signalling for proper control of motor activity.

31 by both actin depolymerization and myosin II motor activity.

32 at R3b-1 modulates the cycle period of crawl motor activity.

33 leading to deregulation of canonical kinesin motor activity.

34 nglia-thalamocortical network during ongoing motor activity.

35 eep with concomitant increases in waking and motor activity.

36 ubule binding without substantially reducing motor activity.

37 nstream from mast cells in the regulation of motor activity.

38 urons and in-phase with bouts of ipsilateral motor activity.

39 (CRF(1)) mediates the stress-induced colonic motor activity.

40 hat the interaction of Eg5 with TPX2 reduces motor activity.

41 ilitates force generation independent of its motor activity.

42 ies for perception, cognition and control of motor activity.

43 t a primary function of sleep is to suppress motor activity.

44 of Rho-kinase-dependent non-muscle myosin II motor activity.

45 c ankle plantarflexion force, or sat with no motor activity.

46 tivity shows a tight coupling to the singing motor activity.

47 t models of neurologic disorders that impact motor activity.

48 l network controlling the underlying singing motor activity.

49 t that ICC-SS contribute to regulation of LM motor activity.

50 l human disease mutations that affect myosin motor activity.

51 thway synapses and D1-mediated activation of motor activity.

52 the control of striatal circuits regulating motor activity.

53 an animal receives is directly linked to its motor activity.

54 nteract with the flagellar switch to control motor activity.

55 wing increasing, decreasing or no changes in motor activity.

56 ion and adenosine triphosphate-driven import motor activity.

57 erved response resulting in neurological and motor activity.

58 to the dynein-1 tail directly stimulates its motor activity.

59 function to lead to impaired motivation and motor activity.

60 e-stranded DNA (ssDNA)-specific nuclease and motor activities.

61 train the expression of respiratory rate and motor activities.

62 is class of kinesin and independent of their motor activities.

63 nd the interdependence of dynein and kinesin motor activities.

64 tribution of ensembles' cross-linking versus motoring activities.

65 irst breath that initiates a life-sustaining motor activity(1).

66 some anesthetics can also increase brain and motor activity-a phenomenon known as paradoxical excitat

67 Depressed patients present with motor activity abnormalities, which can be easily record

68 rthermore, we show that this distribution of motor activity accords with models in which curvature, o

69 nt of the system that modulates the cortical motor activity, allowing individuals to express their in

70 he differential regulation of the kinase and motor activities allows for MYO3A to precisely self-regu

71 Myosin VIII's motor activity along actin provides a molecular mechanis

72 However, myosin motor activity also fragments actin filaments through mo

73 vement and is considered to reflect cortical motor activity and action-perception coupling.

74 In younger, pre-symptomatic animals, altered motor activity and anxiety-like behaviors have also been

75 s was preferentially active in states of low motor activity and arousal.

76 n of MYO6 binding partners demonstrates that motor activity and binding to endosomal membranes mediat

77 th high precision existing and new models of motor activity and coordination in vivo.

78 an essential role of the stalk in regulating motor activity and coupling conformational changes acros

79 t turnover, and shows a simple dependence on motor activity and crosslink dynamics.

80 emonstrate a distinctive pattern of vigorous motor activity and crying to specific unfamiliar visual,

81 ns of cocaine on circulating corticosterone, motor activity and degranulation of mast cells in both t

82 related limb movement kinematics to recorded motor activity and demonstrate that imposed alterations

83 o motoneurons were estimated during rhythmic motor activity and demonstrated primarily intense inputs

84 and the warm ambient temperature potentiated motor activity and elicited profound stereotypy and self

85 rmine the activation or inhibition of myosin motor activity and enable precise timing and spatial asp

86 ession in postnatal neurons causes increased motor activity and fatal epilepsy.

87 ne a novel regulatory mechanism by which the motor activity and function of the fission yeast type on

88 normal self-similar/fractal organization of motor activity and heart rate over a wide range of time

89 sts between sensory alterations and dystonic motor activity and how mechanisms underlying the sensory

90 ryptamine receptor 2A) receptors, suppressed motor activity and increased feeding bout duration-a pro

91 f these virus-induced bodies requires myosin motor activity and is dependent on the secretory pathway

92 ement of NMJs as well as positive effects on motor activity and life span.

93 s, including attentional and arousal states, motor activity and neuromodulatory input.

94 oth condensin I and II exhibit ATP-dependent motor activity and promote extensive and reversible comp

95 BA1A alpha-tubulin selectively impair dynein motor activity and severely and dominantly disrupt corti

96 ciated with domain-specific higher-cognitive motor activity and sound processing (dorsal premotor cor

97 ospital discharge based on early measures of motor activity and the actual hospital discharge date we

98 We discovered preferred patterns of motor activity and turning behavior.

99 CRF-induced stimulation of colonic secretory motor activity and urocortin 2-induced delayed gastric e

100 MIIA-F stack formation was regulated by both motor-activity and the availability of surrounding actin

101 ical change and having objective (observable motor activity) and related subjective (energy) levels.

102 by diffusible gradients, spatially selective motor activities, and adaptive changes in chromosome arc

103 ns, lower average and greater variability of motor activity, and a shift to later peak activity and s

104 tenuates neuronal responsiveness, suppresses motor activity, and alleviates motor abnormalities assoc

105 that the unique features of MYO3A, enhanced motor activity, and an extended tail with tail actin-bin

106 n actin-filament turnover regulators, myosin motor activity, and changes in the concentration of cros

107 -positive dopaminergic (DA) neurons, reduced motor activity, and increased oxidative stress.

108 ness measured by body weight loss, decreased motor activity, and reduced food intake.

109 NA expression analyses, proteasome activity, motor activity, and survival.

110 e than one microtubule dramatically enhances motor activity, and thus minimizes the effects of any op

111 n a dose-dependent manner but did not affect motor activity, anxiety or responses to noxious thermal

112 Our analysis over the adult life-span of motor activity, anxiety-like, and depressive-like behavi

113 CPG output that produce rhythmic extraocular motor activity appropriate for minimizing motion-derived

114 inhibitor in vitro that uses its processive motor activity as part of a feedback loop to further pro

115 tergic pathways that regulate motivation and motor activity as well as the sensitivity to threat.

116 span, body and spleen weight, gait and other motor activities, as well as acoustic startle responses

117 Scales with "low" properties included the Motor Activity Assessment Scale (11.5) and the Sedation

118 inhibitory neurons for the patterning of the motor activity associated with repetitive motor behavior

119 in mice and rats and are similar to those in motor activity at time scales from minutes up to 10 hour

120 ring in circuits enacting self-regulation of motor activity, attention, and emotion.

121 l domain and the motor head retain wild-type motor activity but exhibit enhanced offloading and corti

122 nto microtubules that support normal kinesin motor activity but fail to support the activity of dynei

123 4m ring neuron circuits both negatively gate motor activity but inversely control turning behavior.

124 s not deprive prestin of its voltage-induced motor activity, but it does significantly impair the fas

125 m 8 weeks onwards with striking reduction in motor activity by 12 weeks.

126 oviding a molecular basis for the control of motor activity by mechanical signals.

127 that KBP directly inhibits KIF18A and KIF15 motor activity by preventing microtubule binding.

128 l cord inhibitory interneurons in generating motor activity by showing that they can generate alterna

129 miR-128 governs motor activity by suppressing the expression of various

130 Here, we examine coordination of motor activity by the scaffolding protein JNK-interactin

131 t decision-making tasks to show (1) that FEF motor activity can direct accurate, visually informed ch

132 However, motor activity can serve as a scaffold to shape the sens

133 ies have questioned the importance of myosin motor activity cell and tissue shape changes.

134 e for many neurobiological processes such as motor activity, cognitive functions, and affective proce

135 Conscious contributions to motor activity come after our understanding of the world

136 and memory formation to decision making and motor activity control--have inspired their re-creation

137 s fused to the MYO3B motor demonstrated that motor activity correlates with formation and elongation

138 The neural circuits that control motor activities depend on the spatially and temporally

139 peared to be the same as prestin because the motor activity depended on the concentration of intracel

140 t can promote actomyosin ring assembly and a motor activity-dependent form that supports ring contrac

141 In adult mice, FLARE also gave light- and motor-activity-dependent transcription in the cortex.

142 nce of spatial constraints and cross-linking motor activities determining distinct microtubule archit

143 ldren with more out-of-sync intrinsic visual-motor activity displayed more severe autistic traits, wh

144 e depleting toxin DSP-4 (50 mg/kg), then the motor activity, dopaminergic neuron loss, colon gene exp

145 been implicated in the production of phasic motor activity during active sleep in adults.

146 examination of functional changes in gastric motor activity during diabetes has not yet been performe

147 they showed the typical sustained visual-to-motor activity during Go trials.

148 d action of which likely regulates patterned motor activity during locomotion.

149 ections all contribute to the suppression of motor activity during sleep and sleep-wake transitions,

150 ral dynamics in the oscillatory profiles and motor activity during sleep in this model and to evaluat

151 ns in the motor cortex and severely impaired motor activity during the neonatal stage.

152 t the rapid elevation in dopamine levels and motor activity elicited by cocaine involves alpha1 recep

153 for chromosome segregation independently of motor activity, except for kinesin-6 Klp9, which is requ

154 While intrinsic and extrinsic regulation of motor activity exists, what governs the overall distribu

155 aused an immediate and temporary increase in motor activity followed by a marked and prolonged decrea

156 s show a selective modulation of preparatory motor activity following PA in healthy participants but

157 e that generates rhythmic neural network and motor activity for 3 weeks.

158 tic stimulation revealed a rapid increase in motor activity for CS+ versus CS-, preceding more vigoro

159 ssful NoGo trials resulted in suppression of motor activity for CS+, but not CS-.

160 as a fml1Delta mutant indicating that Fml1's motor activity, fuelled by ATP hydrolysis, is essential

161 d whose downstream components can be read as motor activity governing cellular reversals.

162 shows particularly strong and predictive pre-motor activity (>10 s before movement initiation), mainl

163 Human motor activity has a robust, intrinsic fractal structure

164 In this context, effects on motor activity have received comparatively little attent

165 ynamic-attending theory, it is proposed that motor activity helps to synchronize temporal fluctuation

166 We find that overt rhythmic motor activity improves the segmentation of auditory inf

167 e rhythm for breathing and other coordinated motor activities in mammals.

168 The SwLo rats exhibit decreased motor activity in a swim test and other depression-like

169 pes, whereas the SwHi rats display increased motor activity in a swim test.

170 mechanism at cranial motor nuclei increases motor activity in all sleep-wake states, and least of al

171 synaptic functions related to the control of motor activity in basal conditions.

172 eport that the circadian rhythm amplitude of motor activity in both AD subjects and age-matched contr

173 for a coupling of actin assembly and myosin motor activity in cells.

174 inforced instrumental responding and general motor activity in control experiments.

175 isms but indicate a vital role for preceding motor activity in determining whether and which actions

176 d effects of luminal CT on neurally mediated motor activity in ex vivo male and female mouse full len

177 cortisol profile, skin temperature and wrist motor activity in healthy young and older volunteers und

178 trafficking by modulating microtubule-based motor activity in leukocytes.

179 compared preBotC and hypoglossal (XII) nerve motor activity in medullary slices from neonatal mice in

180 in GABA neurons, diminished morphine-induced motor activity in mice.

181 s capable of integrating multiple metrics of motor activity in order to characterize relationships be

182 e circadian system and patterns of sleep and motor activity in people with BD.

183 ify, with a rigorous approach, the nature of motor activity in response to Deep Brain Stimulation (DB

184 nded older adults exhibited more ipsilateral motor activity in response to TMS; this effect was not p

185 I pyrethroid that causes tremors and impairs motor activity in rodents, is broadly used.

186 al judgments as well as the choice-selective motor activity in the 8-30 Hz frequency range before sti

187 ablished between these changes and disrupted motor activity in the colon, and we now know that some o

188 dy, the low dose of 2.5 nmol/kg ip. enhanced motor activity in the open field task, while total dista

189 s a long-lasting facilitation of respiratory motor activity in the phrenic nerve, we tested the hypot

190 The defect in the myosin motor activity in these mutants is evident in developing

191 ch spontaneously generates breathing-related motor activity in vitro.

192 stimulation of mouse brain and modulation of motor activity in vivo.

193 ors are known to be involved in a variety of motor activities, including locomotion, postural control

194 Motor activity increased during the admission in this sa

195 up, inhibition arriving in-phase with local motor activity increases, particularly in higher Rin mot

196 nt and essential modes during cytokinesis: a motor activity-independent form that can promote actomyo

197 roduce subtle effects on response time or on motor activity indexed by neuroimaging/neuroelectrophysi

198 Furthermore, impaired NMII-B motor activity inhibits outflow tract myocardialization,

199 ons, allowing for the integration of diverse motor activities into a single mechanical outcome.

200 ing motoric response-conflict, inappropriate motor activity is actively (and perhaps non-selectively)

201 seases, or both, but the mechanisms by which motor activity is affected in disease are unclear.

202 We have found that motor activity is decreased by autophosphorylation, alth

203 Molecular motor activity is driven by a heterotrimeric complex com

204 Thus, myosin II motor activity is emerging as a broad regulatory mechani

205 ork retains the longstanding hypothesis that motor activity is engaged only once a decision threshold

206 here the decision terminates in a choice and motor activity is engaged.

207 Regulation of cytoplasmic dynein's motor activity is essential for diverse eukaryotic funct

208 Here we ask how this choice-selective motor activity is modified by prior expectation during a

209 Myosin-II motor activity is not always required, and there is evid

210 Motor activity is not essential, but the actin binding s

211 n motors, in which active stress produced by motor activity is opposed by passive resistance to netwo

212 These results indicate that motor activity is shaped by a cognitive variable that dr

213 However, motor activity is supplemented by other passive targetin

214 inistered to rodents, a resulting upsurge of motor activity is thought to share face and predictive v

215 tegration of nociceptive inputs with ongoing motor activities leading to the initiation of complex, y

216 he actin filaments and changes due to myosin motor activity leading to enhanced F-actin severing of p

217 rainstem disinhibit rapid eye movement sleep motor activity, leading to dream enactment.

218 ead-to-tail orientations, we could show that motor activity leads to activation of the nuclease domai

219 ivity via the thalamus, play a major role in motor activity, learning and memory, sensory processing,

220 elated processes including the regulation of motor activity, learning, motivated behavior, psychostim

221 by repetitive sounds, whisker deflection or motor activity led to a near arrest of angiogenesis in b

222 r the intraspinal circuitry that coordinates motor activity likewise uses cell position as an interna

223 s with different levels of brain arousal and motor activity: locomotion, nonlocomotor movement, quiet

224 rterial pressure (MAP), heart rate (HR), BT, motor activity (MA), and oxygen consumption (Vo2) were m

225 This motor activity may allow p68 to transport Ca-calmodulin

226 The extent to which actigraphically recorded motor activity may predict inpatient clinical course and

227 In addition, Myo52 motor activity may pull on cables to provide the tension

228 Measurements of the effects on motor activity measured via electroencephalography (EEG)

229 letion of CB2Rs in dopamine neurons enhances motor activities, modulates anxiety and depression-like

230 sh Memory and Aging Project who had baseline motor activity monitoring up to 11 days and were followe

231 The increase in body temperature and gross motor activity observed during the SD procedure was decr

232 substrate transfer, and highlight how ATPase/motor activities of AAA+ proteases can be critical for s

233 and uncover a novel mechanism modulating the motor activity of cardiac MHC isoforms.

234 resection and define the involvement of the motor activity of DNA2 in this process.

235 sine 5'-triphosphate (ATP) hydrolysis-driven motor activity of DNA2 involved in the long-range resect

236 sents a barrier, explaining the need for the motor activity of DNA2 to displace RPA prior to resectio

237 eedback that likely accounts for the altered motor activity of dSod1 (G85R) We found cell-autonomous

238 over, actin binding during ATP turnover, and motor activity of F. graminearum myosin-1.

239 ut has little or no inhibitory effect on the motor activity of Fusarium solani myosin-1, human myosin

240 Motor activity of nuclear myosin was dependent on the Hs

241 rical stimulation aims to restore functional motor activity of patients with disabilities resulting f

242 How the motor activity of TgMyoA is regulated during these criti

243 Here, we report on the motor activity of the different myosin-1C isoforms measu

244 We conclude that the diminished motor activity of this mutant is most likely responsible

245 acquired for awake animals, showed increased motor activity on a memantine challenge (total distance

246 The influence of motor activity on sensory processing is crucial for perc

247 cohol pharmacokinetics, significantly reduce motor activity or intrabout operant response speed, or p

248 rganization as mutant forms of Kif3a lacking motor activity or the motor domain can restore p150(Glue

249 microtubule dynamics, their well-established motor activity, or additional, unknown functions.

250 search should shift focus on sleep, physical/motor activity, or circadian patterns to identify common

251 known how the nonmotor domain contributes to motor activity, or how a kinesin-5 tetramer utilizes a c

252 Breathing is an essential, enduring rhythmic motor activity orchestrated by dedicated brainstem circu

253 s a brain mechanism that globally suppresses motor activity, ostensibly via the subthalamic nucleus (

254 h UV light; illumination at 400 nm initiates motor activity over a broad range of intensities, wherea

255 ociate with dynein/dynactin and activate the motor activity pulling on astral microtubules.

256 ised nodes of the Bohland speech-production (motor activity regulation), default-mode (attention regu

257 l and the accessory chains it binds regulate motor activity remain to be determined.

258 ilament compliance, spatial heterogeneity of motor activity, reversible cross-links and filament turn

259 rding to this view, during action selection, motor activity should integrate cognitive information (e

260 mechanical modeling, varying amounts of OHC motor activity should provide varying degrees of feedbac

261 pertoire of behavioral responses that engage motor activity, spatial learning, and emotional processi

262 strate that prolonged release of 5-HT during motor activity spills over from its release sites to the

263 e spinal cord has the capacity to coordinate motor activities such as locomotion.

264 on or if they may result from other nonvocal motor activity such as orofacial motor movement.

265 adapted tendons to support high performance motor activities, such as sprinting and jumping.

266 e, it is tempting to speculate that it has a motor activity that assists the necessary severing actio

267 further suggest an energy landscape model of motor activity that couples the free-energy profile of m

268 rphology but exhibited decreased spontaneous motor activity that resolved as gene expression recovere

269 These data suggest that without its motor activity, the binding of Fml1 to its DNA substrate

270 extrusion occurs by 2 independent, uncoupled motor activities; the motors translocate on DNA in oppos

271 signaling controls complex functions such as motor activity through regulation of cell firing and het

272 e D2 receptors (D2R) are major regulators of motor activity through their signaling on striatal proje

273 Locomotion requires coordinated motor activity throughout an animal's body.

274 ule-associated proteins selectively regulate motor activity to achieve unidirectional nuclear transpo

275 rvation that diseased animals show decreased motor activity to facilitate recovery suggests that norm

276 n, suggesting a high degree of regulation of motor activity to maintain transport in a given directio

277 phosis enables spinal CPG-driven extraocular motor activity to match the changing requirements for ey

278 erial motors and unfolds mechanisms that tie motor activity to mechanical cues and bacterial surface

279 We extended the models by allowing motor activity to occur before a commitment to a choice

280 ody weight supported treadmill or open field motor activities, to target a high range of variations i

281 nectivity from left central, associated with motor activity, to mid-frontal, associated with performa

282 e basal ganglia pathways modulating cortical motor activity underlie both Parkinson disease (PD) and

283 r transport potential under load, we assayed motor activity using interferometric scattering microsco

284 General motor activity was comparable to that of wild-type mice

285 Stimulation of motor activity was observed following administration of

286 SWS, while increased cerebellar and cortical motor activity was related to time in rapid eye movement

287 Instead, myosin motor activity was required for the formation of the act

288 ct was ATP dependent, indicating that dynein motor activity was required.

289 ces on the nuclear surface through molecular motor activity, we conclude that the intermediate filame

290 ockdowns, and mutants with known deficits in motor activity, we showed that the myosin 2 motor is req

291 appetite changes, delusions, and repetitive motor activity were additionally more common in overtly

292 Skin temperature and wrist motor activity were continuously recorded.

293 intake, feeding microstructure, and general motor activity were measured under two motivational cond

294 No changes in motor activity were observed after seven injections of c

295 nd spindle bursts in M1 were driven by early motor activity, whereas 23.7% of the M1 bursts triggered

296 t the relationship between streaming and the motor activity which drives it.

297 subcortical regions drives early spontaneous motor activity, which is a hallmark of the developing se

298 pattern generators (CPGs) trigger bursts of motor activity with precise timing.

299 nology caused dramatic changes in in gastric motor activity, with disrupted slow waves, abnormal phas

300 pamine neuron transplantation, and increased motor activity, without a need for immunosuppression.