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 thway synapses and D1-mediated activation of motor activity.

3 nteract with the flagellar switch to control motor activity.

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

5 stent with DNA damage induced by unregulated motor activity.

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

7 oplasm of cells and thereby probe stochastic motor activity.

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

9 ent from both thermal diffusion and directed motor activity.

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

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

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

13 sphorylation of the MYO3A motor and reducing motor activity.

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

15 g RLC phosphorylation or nonmuscle myosin II motor activity.

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

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

18 novelty and olfactory responses, anxiety or motor activity.

19 in circadian entrainment and for masking of motor activity.

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

21 ion and adenosine triphosphate-driven import motor activity.

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

23 al dopamine signalling for proper control of motor activity.

24 by both actin depolymerization and myosin II motor activity.

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

26 erved response resulting in neurological and motor activity.

27 nglia-thalamocortical network during ongoing motor activity.

28 eep with concomitant increases in waking and motor activity.

29 ubule binding without substantially reducing motor activity.

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

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

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

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

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

35 ntly triggered complex pattern of intestinal motor activity.

36 tone in the CNS, as reflected by spontaneous motor activity.

37 muli redirect attention and suppress ongoing motor activity.

38 function to lead to impaired motivation and motor activity.

39 on did not, revealing functional deficits in motor activity.

40 circuits involved in attention, reward, and motor activity.

41 anatomy or differences in general anxiety or motor activity.

42 nursing behavior, while causing stereotyped motor activity.

43 ng residues as couplers of NTP hydrolysis to motor activity.

44 C138 subcomplex is required to coordinate I1 motor activity.

45 nia did not show the expected habituation of motor activity.

46 ety-, stress- and fear-related behaviors and motor activity.

47 The HCs are responsible for motor activity.

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

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

50 in vivo constriction rate scales with myosin motor activity.

51 ry that shapes their material properties and motor activity.

52 erant responding for a nondrug reinforcer or motor activity.

53 w these unusual spinal cord neurons regulate motor activity.

54 the control of striatal circuits regulating motor activity.

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

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

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

58 train the expression of respiratory rate and motor activities.

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

60 nd the interdependence of dynein and kinesin motor activities.

61 rdinated dance of cognitive, perceptual, and motor activities.

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

63 bsequent experiments PSI (8 mg/kg) decreased motor activity after p.o. but not i.p. administration.

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

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

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

67 to approximately 10 microm and require Myo10 motor activity and actin filaments.

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

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

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

71 We analyzed spontaneous motor activity and cocaine-induced hyperactivity in wild

72 organelle mediates cytadherence and gliding motor activity and contains a cytoskeleton-like componen

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

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

75 re characterized at age 4 months by vigorous motor activity and crying in response to unfamiliar visu

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

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

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

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

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

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

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

83 controlling fission yeast myosin-II (Myo2p) motor activity and function during cytokinesis.

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

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

86 e exploratory pattern, characterized by high motor activity and increased object exploration.

87 sphorylation of DIC, which stimulates dynein motor activity and increases minus-end-directed runs of

88 to plus ends of growing MTs requires kinesin motor activity and interaction with EB1.

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

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

91 imuli, whereas low-reactive infants show low motor activity and low vocal distress to the same stimul

92 PSI and its route of administration have on motor activity and neuronal loss in rat brain.

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

94 how changes in the actin track influence the motor activity and spatial regulation of these myosins.

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

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

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

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

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

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

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

102 Caspase activity, myosin motor activity, and microtubules were required to initia

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

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

105 onds to changes in Myo2p cellular levels and motor activity, and the emergence of tropomyosin-bound a

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

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

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

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

110 /PP1 phosphorylation switch modulates CENP-E motor activity as an essential feature of chromosome con

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

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

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

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

115 ation Scale, Riker Sedation-Agitation Scale, Motor Activity Assessment Scale, or Ramsay over the thre

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

117 es, affect- and stress-related behaviors and motor activity at 1 and 2 months of age.

118 diated inhibition, ensuring maximal myosin-I motor activity at these sites.

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

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

124 t crosslinking protein fimbrin rescues Myo1p motor activity by displacing tropomyosin from actin fila

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

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

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

128 Thus, comodulation of rhythmic motor activity can result from convergent activation, vi

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

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

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

132 n nor prior treatment with cocaine increased motor activity compared to saline-injected controls, how

133 These findings suggest that sleep-related motor activity contributes to the development of neocort

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

135 In mice that received only saline, motor activity correlated positively with mast cell degr

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

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

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

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

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

141 Coordination of voluntary motor activity depends on the generation of the appropri

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 d that alteration of MT polymerization or MT motor activity does not induce organelle redistribution

145 1-3, MfdN), and a C-terminal part harboring motor activity (domains 4-7, MfdC).

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

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

148 comotor circuitry that coordinate left-right motor activity during movements.

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

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

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

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

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

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

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

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

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

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

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

160 Human motor activity has a robust, intrinsic fractal structure

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

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

163 Here, we compared the motor activity, histopathology, and individual muscle fo

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

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

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

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

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

169 General motor activity in anticipation of food was not diminishe

170 All three myosins exhibited robust motor activity in ATPase and actin filament gliding assa

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 Inhibition of CENP-E motor activity in cultured cells and tumor xenografts ca

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

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

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

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

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

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

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

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

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

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

191 ized CNS arousal is characterized by greater motor activity, increased responsivity to sensory stimul

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

193 sms by which IC/LC complexes regulate dynein motor activity independent of effects on cargo binding o

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

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

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

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

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

199 In this study, we show that myosin II motor activity is downstream of LTP induction and is nec

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

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

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

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

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

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

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

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

208 Motor activity is precisely regulated to avoid futile AT

209 ed only in the presence of She2p, and, thus, motor activity is regulated by cargo binding.

210 Our results suggest that Myo3A motor activity is regulated through a mechanism involvin

211 In addition, we found that motor activity is required for Myo1b localization in fil

212 Myosin motor activity is required to condense the nodes into a

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

214 However, motor activity is supplemented by other passive targetin

215 A key regulator of motor activity is the dynein regulatory complex (DRC), b

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

217 the relationship between colonic transit and motor activity is unclear.

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

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

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

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

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

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

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

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

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

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

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

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

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

233 n; however, how phosphorylation controls the motor activity of HM3A is obscure.

234 Previous findings suggested that the motor activity of human myosin IIIA (HM3A) is influenced

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

236 ion of histamine into the VLPO increases the motor activity of rats.

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

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

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

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

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

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

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

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

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

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

247 rylation at Ser-1444 is not needed for Myo2p motor activity, phosphorylation at this site promotes th

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

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

250 e it recruits kinesin-1 to provide the major motor activity required for nuclear migration in embryon

251 anced network of cooperative and competitive motor activity, required for fungal morphogenesis.

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

253 In transcription-coupled DNA repair, motor activity serves to remove RNA polymerase stalled o

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

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

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

257 The amount of motor activity, spatial patterns of activity, and explor

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

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

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

261 spinal cord generate the simple patterns of motor activity that are necessary for breathing and loco

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

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

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

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

266 fire rhythmically with ventral root-recorded motor activity; the rhythmic V2a interneurons fired duri

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

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

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

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

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

272 gulatory defect that leads to an increase in motor activity to generate heat.

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

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

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

276 an actin-based motor hypothesized to use its motor activity to move forward along actin filaments to

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

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

279 tribute, in part, to maintaining respiratory motor activity under immobilizing anesthetic conditions.

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

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

282 Stimulation of motor activity was observed following administration of

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

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

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

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

287 ignals elicited by both external stimuli and motor activity, we recorded from rats trained to rhythmi

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

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

290 Skin temperature and wrist motor activity were continuously recorded.

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

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

293 Receptor potentials and neural-motor activity were recorded in response to difference t

294 ies have demonstrated dynamic modulations in motor activity when we execute actions.

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 attentional shifts and cessation of ongoing motor activity with the appearance of salient environmen

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