ライフサイエンスコーパス: impulse

1 urge to act and a failed inhibition of that impulse.

2 tion and propagation of the cardiac electric impulse.

3 activation and conduction of the electrical impulse.

4 tion tracts designed to propagate electrical impulses.

5 of sound, motion, and gravity into neuronal impulses.

6 ferent nerve endings to fire slowly adapting impulses.

7 ly compete with selfish and other antisocial impulses.

8 ased from astrocytes in response to afferent impulses.

9 rting willpower, the effortful inhibition of impulses.

10 the basis for saltatory conduction of nerve impulses.

11 t reflection can undermine these cooperative impulses.

12 n released from MCs initiates Abeta-afferent impulses.

13 stantial temporal integration across whisker impulses.

14 sion of ion channel subunits associated with impulse activity (Cav1.2, Cav1.3, HCN1, Nav1.2, and NavB

15 ), the phenomenon that brief, high-frequency impulse activity at synapses in the brain can lead to lo

16 e ubiquitous TRPV1 channel, thereby lowering impulse activity in the peripheral nociceptor endings un

17 acute apomorphine that normally inhibits the impulse activity of DA neurons.

18 xamined the effects of PSE on the electrical impulse activity of VTA DA neurons using the in vivo ext

19 lying cellular preselection, we recorded the impulse activity of VTA neurons in response to cocaine a

20 length of axons and enormous variability of impulse activity over time.

21 Nerve impulse activity produces both developmental and adult p

22 other discovery is that nerve-evoked muscle impulse activity, rather than putative trophic factors,

23 sm that likely contributes to the changes in impulse activity.

24 animals represents an actual increase in the impulse activity.

25 ptic transmission, and transmission of nerve impulses, all of which are biologically meaningful proce

26 d for the saltatory conduction of electrical impulses along axons.

27 er and in the rapid propagation of the nerve impulses along myelinated axons.

28 critical balance between the strength of an impulse and an individual's ability to inhibit the desir

29 ion and conduction of the cardiac electrical impulse and are associated with various arrhythmia pheno

30 recently with the demonstration using focal impulse and rotor modulation (FIRM) mapping that rotors

31 on of atrial fibrillation (AF) include focal impulse and rotor modulation (FIRM) mapping, and initial

32 ation (AF) sources, either directly by Focal Impulse and Rotor Modulation (FIRM) or coincidentally wh

33 Focal impulse and rotor modulation (FIRM) with an endocardial

34 =11; 19+/-8% slowing) with 2.5 minutes focal impulse and rotor modulation (interquartile range, 1.0-3

35 or Atrial Fibrillation With or Without Focal Impulse and Rotor Modulation [CONFIRM]; NCT01008722).

36 Ablation comprised source (focal impulse and rotor modulation [FIRM]) and then convention

37 nd focal impulses), whose elimination (focal impulse and rotor modulation [FIRM]) may improve outcome

38 revealed by contact panoramic mapping (focal impulse and rotor modulation mapping), but not by electr

39 of 36 cases and targeted for ablation (focal impulse and rotor modulation) before pulmonary vein isol

40 tional Ablation for AF With or Without Focal Impulse and Rotor Modulation) trial prospectively reveal

41 or Atrial Fibrillation With or Without Focal Impulse and Rotor Modulation) trial, in which 92 consecu

42 ochlea, the temporal gap between the primary impulse and the following coda ranges from once to thric

43 late cell division, circadian rhythms, nerve impulses and chemotaxis, and guide the development of or

44 in the brain communicate through electrical impulses and coordinate this activity in ensembles that

45 ent evidence regarding the reward aspects of impulses and desires, the neural mechanisms that underli

46 in the tendency to seek stimulation, act on impulse, and engage in substance use are correlated with

47 tasks often result from inappropriate action impulses, and are thought to signal the need for increas

48 lowing stirring, hypoxia or brief electrical impulses applied to the bathing water.

49 ays connected to the procession of the nerve impulse are major mechanisms involved in the development

50 and allow the fast propagation of electrical impulses, are produced by oligodendrocytes.

51 TCL stiffness using acoustic radiation force impulse (ARFI) imaging.

52 SI), FibroScan, and acoustic radiation force impulse (ARFI) in a cohort of NAFLD patients who underwe

53 ging technique, and acoustic radiation force impulse (ARFI), an ultrasound-based imaging technique, a

54 An integrative model in which ensembles of impulses arising from physiologically distinct LTMRs are

55 h the presynaptic membrane (PM) when a nerve impulse arrives.

56 actical applications, its predicted specific impulse as a solid rocket propellant would be 333 s.

57 treated with extracorporeal shock wave [280 impulses at 0.1 mJ/mm]), and group 5 (combined bone marr

58 inated axons can conduct sustained trains of impulses at high frequency, but this involves substantia

59 hold mechanoreceptors (Abeta-LTMRs) generate impulses at their terminals in the skin.

60 anterior cingulum are shown to be related to impulse, attention, and executive problems in neurodevel

61 tion solving the transient mass, energy, and impulse balance.

62 l (AVC) is essential for delay of electrical impulses between atria and ventricles, and defects in AV

63 ar excitation-consists of not only a primary impulse but also a coda of delayed secondary responses w

64 current stimulation (tDCS) preserves action impulses but prevents their behavioral expression.

65 units did not effectively integrate whisker impulses, but instead combined weak impulse responses wi

66 , elevated the generation and propagation of impulses by LTMRs, and altered the spinal cord circuitry

67 PIGD patients show poorer control over motor impulses compared to TD patients.

68 susceptibility to acting on prepotent motor impulses compared to TD patients.

69 around axons in the CNS, enables rapid nerve impulse conduction and sustains neuronal health.

70 Remarkably, impulse conduction continued throughout, and all these c

71 Myelination is essential for rapid impulse conduction in the CNS, but what determines wheth

72 ge-gated sodium channel (Na(V)1.5) underlies impulse conduction in the heart, and its depolarization-

73 myelination is essential for rapid saltatory impulse conduction in the nervous system, and malformati

74 channels (Nav) and thus underpin rapid nerve impulse conduction in the vertebrate nervous system [1].

75 in is a membrane system that fosters nervous impulse conduction in the vertebrate nervous system.

76 , but it is not known how this is related to impulse conduction in vivo.

77 logical changes in axons following sustained impulse conduction that appear to result from osmosis an

78 Transseptal impulse conduction was significantly slower in LBBB+HF t

79 pace after they have entered the axon during impulse conduction.

80 re associations between neural correlates of impulse control and out-of-scanner measures of impulsivi

81 n the relatively slow, linear development of impulse control and response inhibition during adolescen

82 duced brain function in regions intrinsic to impulse control and taste responsiveness, risk allele ca

83 a motor test, aimed at assessing changes in impulse control and visuomotor performance, respectively

84 Impaired response inhibition and poor impulse control are hallmarks of the manic phase of bipo

85 t LHb dysfunction may contribute to impaired impulse control associated with drug addiction.

86 Alterations in mood, cognition, and impulse control associated with these changes might cont

87 nectivity were in turn associated with lower impulse control at 24 months of age, and mediated the as

88 lications for studies examining deviances in impulse control by showing that the developmental path b

89 impulses varies greatly, and difficulty with impulse control can have severe consequences; in the ext

90 Here, we test the hypothesis that this impulse control capacity is driven by increased maturati

91 l Mn exposure causes lasting attentional and impulse control deficits in adulthood, and whether conti

92 trol, and may point to avenues for improving impulse control deficits in various neurologic and psych

93 cutive dysfunctions (i.e. hypervigilance and impulse control deficits, respectively).

94 o verify whether creativity is related to an impulse control disorder (ICD) as a complication of dopa

95 Emerging evidence suggests impulse control disorder subtypes have dissociable corre

96 Impulse control disorders (ICD) are commonly associated

97 Impulse control disorders (ICD), including pathological

98 rkinson's disease (PD) patients suffers from impulse control disorders (ICDs), which are side effects

99 ts with Parkinson's disease (PD) suffer from impulse control disorders (ICDs).

100 mpulsivity is mild for some patients, severe impulse control disorders affect approximately 10% of ca

101 ioural side-effects, such as dyskinesias and impulse control disorders also known as behavioural addi

102 We compared PD patients with impulse control disorders and age-matched and gender-mat

103 Mechanisms underlying impulse control disorders and dyskinesias could provide

104 n-interventional, multicentre study (ICARUS (Impulse Control disorders And the association of neuRops

105 Impulse control disorders are commonly associated with d

106 Impulse control disorders are typically managed by reduc

107 ds to motor complications and, occasionally, impulse control disorders caused by intermittent stimula

108 PD patients with impulse control disorders demonstrate enhanced dopamine

109 treat patients with Parkinson's disease and impulse control disorders have shown efficacy in randomi

110 ation appears to be modest, PD patients with impulse control disorders may be differentially sensitiv

111 nergic striatal activity in PD patients with impulse control disorders may be partly related to decre

112 Those with impulse control disorders showed significantly lower DAT

113 -matched and gender-matched controls without impulse control disorders using [(123)I]FP-CIT (2beta-ca

114 d between 15 PD patients with and 15 without impulse control disorders using independent t tests.

115 In patients with Parkinson's disease and impulse control disorders, impairments are observed acro

116 Impulse control disorders, including gambling disorder,

117 n Parkinson's disease even in the absence of impulse control disorders.

118 ned because they are efficacious in treating impulse control disorders.

119 rol patients without hypersexuality or other impulse control disorders.

120 hich may ultimately mediate vulnerability to impulse control disorders.

121 further implicating this STN subdivision in impulse control disorders.

122 Impulse control disorders/other compulsive behaviours ('

123 dolescence impairs attention performance and impulse control during adulthood.

124 n association with intersubject variation in impulse control in 114 young adults.

125 ircuitry associated with decision-making and impulse control in alcohol-dependent humans and rodents,

126 Understanding the neural basis of poor impulse control in Internet addiction (IA) is important

127 A deficit in impulse control is a prominent, heritable symptom in sev

128 Improving impulse control is a promising target for the treatment

129 In contrast, the association of PMd with impulse control is consistent with the role of this area

130 Difficulty with impulse control is heightened in children with a family

131 for higher rates of smoking in patients with impulse control issues, as the smoking may represent an

132 I as a novel neural substrate of maladaptive impulse control mechanisms that may facilitate the devel

133 resonance imaging studies have shown altered impulse control processing in adolescents with a positiv

134 , whereas associative ability (learning) and impulse control were spared.

135 ty, longer duration of the index MDE, poorer impulse control, a more chronic and severe long-term cou

136 techniques clarifies the neurophysiology of impulse control, and may point to avenues for improving

137 cidal behavior, lifetime comorbid diagnoses, impulse control, and measures associated with bipolarity

138 disorders, are characterized by deficits in impulse control, however the relationship between orexin

139 n other disorders with altered D2R-dependent impulse control, such as addiction.

140 was associated with a reduced efficiency in impulse control, whereas DS led to a relative impairment

141 ALX5407 in the vmPFC alleviated deficits in impulse control.

142 ernal interleukin-6 concentrations and lower impulse control.

143 function within neural systems important for impulse control.

144 ing DRN activity to response suppression and impulse control.

145 rest of the population and show deficits in impulse control.

146 ms of alcohol dependence include compromised impulse control.

147 n stress, emotion and reward regulation, and impulse control.

148 ecreases inhibition associated with response impulse control.

149 ldren completed a snack delay task to assess impulse control.

150 ead to premature movements mimicking lack of impulse control.

151 and impulsiveness, emotional regulation, and impulse control/error monitoring.

152 Recent evidence indicates that impulse-control deficits may contribute to the severity

153 ar disorder (BPD); however, the emergence of impulse-control disorders has been documented in Parkins

154 ple neurotransmitter systems associated with impulse-control disorders, we hypothesized that KOR acti

155 tions, such as fluctuations, dyskinesias and impulse-control disorders.

156 ve functions, including planning, reasoning, impulse-control, and making decisions based on contingen

157 nts who use deliberation to override selfish impulses: Deliberation only serves to undermine cooperat

158 persal by the parent fungus is limited to an impulse delivered to the spores to carry them clear of t

159 To measure aggressive impulses, each evening participants stuck between 0 and

160 Here, we use single-impulse electrical stimulation of the whisker pad in the

161 In columns with intact whiskers, brief light impulses evoked recurrent excitation and supralinear inh

162 o be exceptional, with a calculated specific impulse exceeding that of AP, leading to its high potent

163 ic generator (FO-TEG) is applicable for both impulse excitation and sinusoidal vibration which univer

164 For the impulse excitation, the generated current sustains and s

165 Using laboratory high-current impulse experiments, this research shows that within the

166 in DRG neurons, HA decreases TRPV1-mediated impulse firing and channel sensitization by bradykinin.

167 further strengthening even in the absence of impulse flow.

168 t to these results, we hope to give a strong impulse for further investigation on studying possible r

169 tron microscope (SEM) is a technique gaining impulse for its ability to enable rapid and contactless

170 filter was also found to recover deconvolved impulses for single photon counting from highly distorte

171 turn pathway for the sodium ions involved in impulse formation.

172 The model shows that the impulse frequency of different modules can differ from e

173 HMI impulses from a diagnostic transducer, combined with a c

174 bubble infusion, high mechanical index (HMI) impulses from a diagnostic ultrasound (DUS) transducer m

175 gauge the ability to prevent these incorrect impulses from turning into overt action errors.

176 reveals critical values for the shear-stress impulse generated by the cavitation bubble dynamics gove

177 The sinoatrial node is the main impulse-generating tissue in the heart.

178 We were able to rescue the failure of impulse generation and conduction by additional genetic

179 expressed in the specialized myocytes of the impulse generation and conduction system.

180 be triggered from large standoff distances, impulse generators for microvehicles, microfluidic valve

181 t but not the right ventral striatum of high-impulse (HI) rats compared with low-impulse (LI) rats.

182 es in nerve conduction velocity following an impulse (i.e. velocity recovery cycles) reflect after-po

183 ing system in which acoustic radiation force impulse imaging (ARFI) and shear wave elasticity imaging

184 ssociated with increases in sexual drive and impulse in both men and women.

185 inear increase across steppes, and an abrupt impulse in desert-steppes following a slight increase in

186 on, demonstrates the primacy of shear-stress impulse in determining cellular outcome resulting from p

187 increases with blast overpressure (BOP) and impulse in dose-dependent manner.

188 ing body sway, as revealed by an early force impulse in the opposite direction to that seen in LG.

189 hysiology because they transmit depolarizing impulses in enteric neurons, thereby enabling the coordi

190 the generation and propagation of electrical impulses in excitable cells.

191 tly reduced, whereas capsaicin-induced nerve impulses in the skin-nerve preparation increased in mice

192 In this work, we demonstrate that a voltage-impulse-induced ferroelastic domain switching in the (01

193 A voltage-impulse-induced non-volatile magnetization switching was

194 In particular, a voltage-impulse-induced two-step ferroelastic switching pathway

195 that interaction between these two types of impulse is central to cerebellar cortical information pr

196 mary impulse (the group delay of the primary impulse is on the order of a few hundred microseconds).

197 fically, cellular exposure to a shear-stress impulse J greater, similar0.1 Pa s ensures cell lysis or

198 sker impulse sequences that varied in single-impulse kinematics (5-20-ms time scale) and mean speed (

199 ostly 5-10 ms), accurately reflecting single impulse kinematics.

200 The temperature dependence of peak impulse latency was weakened at temperatures above 30 de

201 of high-impulse (HI) rats compared with low-impulse (LI) rats.

202 Here we employ an impulse-like forcing to quantify this yield strain of RB

203 se variations can be characterized by single impulse-like progression patterns.

204 ensity along the length of axons during high impulse load, supporting the increased metabolic demand

205 ssess the expression and inhibition of motor impulses may help identify PD patients who have difficul

206 By fitting a representative impulse model to each gene, it reports differentially ex

207 The speed of electrical impulse movement through axons is increased by myelin, a

208 re randomized to either DUS intermittent HMI impulses (n = 20) just prior to emergent percutaneous co

209 ly correct trials, revealing covert response impulses not discernible in overt behavior.

210 Exposure to shear-stress impulses of J less, similar0.035 Pa s leaves the cells u

211 e self-control necessary to reign in selfish impulses, or does self-interested deliberation restrain

212 eak expiratory flow, diffusing capacity, and impulse-oscillometric findings.

213 nd (ii) small airway involvement measured by impulse oscillometry (IOS) in adolescence.

214 We previously showed that impulse oscillometry (IOS) indices of peripheral airway

215 Impulse oscillometry (IOS) is an objective and noninvasi

216 We used impulse oscillometry (IOS) to compare single and repeate

217 ma and 18 healthy control subjects underwent impulse oscillometry (IOS), multiple breath inert gas wa

218 luated by conventional clinical tests and by impulse oscillometry in female late-onset, nonallergic p

219 Levels of impulse oscillometry reactance area indicating periphera

220 In multivariate analyses higher impulse oscillometry reactance area was associated (P =

221 rized with spirometry, body plethysmography, impulse oscillometry, alveolar and bronchial exhaled nit

222 Lung function was assessed by impulse oscillometry, and Feno measurements were perform

223 l airway function assessed by spirometry and impulse oscillometry, as well as Borg dyspnea scores at

224 cilitates the rapid conduction of electrical impulses over long distances.

225 The NaV1.5 is essential for cardiac impulse propagation and its dysfunction has been linked

226 of gap junctions during normal and abnormal impulse propagation are essential in the control of arrh

227 conductive biomaterial polymer that restores impulse propagation could synchronize contraction and re

228 Impulse propagation in the heart depends on the excitabi

229 Rapid impulse propagation in the heart is a defining property

230 Myelination of axons facilitates rapid impulse propagation in the nervous system.

231 er resemble native heart tissue; the fastest impulse propagation is along the long axis of the aligne

232 Neuronal electrical impulse propagation is facilitated by the myelin sheath,

233 rvous system, myelination of axons for rapid impulse propagation requires the synthesis of large amou

234 N), the central connection point that delays impulse propagation to optimize cardiac performance.

235 caused a lesion with interruption of cardiac impulse propagation using this respective target volume.

236 ay structural abnormalities likely to affect impulse propagation.

237 eath generated by oligodendrocytes for rapid impulse propagation.

238 , action potential duration, and velocity of impulse propagation.

239 g a temperature-sensitive process that slows impulse propagation.

240 ) caused slowing and interruption of cardiac impulse propagation.

241 our survival of rats in 0-450 kPa (0-800 Pas impulse) range at 10 discrete levels (60, 100, 130, 160,

242 o shows that, if correlations of the average impulse rate between different modules decreases, there

243 ere is a concomitant decrease in the average impulse rate in the modules, consistent with the observe

244 se regions, the freeze-out phenomenon in the impulse region, especially, the scaling law of the excit

245 e.g., the boundary between the adiabatic and impulse regions, the freeze-out phenomenon in the impuls

246 he neural mechanisms underlying this type of impulse regulation capacity.

247 ons are commonly modeled using linear finite impulse response (FIR) filters.

248 Here, we employ a zero-phase (infinite impulse response (IIR)) filter to remove the noise from

249 nvestigate (i) the generation of the primary impulse response and the dependence of the group delay o

250 omponents of a RF can be separated; (ii) the impulse response can be reconstructed at sample rates of

251 iated to provide an estimate of the system's impulse response function and is used to convolute the a

252 ts (both genders), with the subject-specific impulse response function period determined from a separ

253 ches the period of participant's oscillatory impulse response function reverberating in alpha.

254 uperposition of two hypothetical oscillatory impulse response functions generated in response to each

255 on Climate Change's Fourth Assessment Report impulse response functions.

256 it can accurately recover the spatial RF and impulse response of ganglion cells recorded on a multi-e

257 s probed with electron pulses to observe the impulse response of the specimen in space and time.

258 m-specific information is decodable from the impulse response, even in the absence of attention and l

259 with space-invariant and -variant nonlinear impulse response.

260 statistical regularities exist, we measured impulse responses (IRs) of 271 spaces sampled from the d

261 17% of units, mostly in L5, showed weaker impulse responses and a slow firing rate increase during

262 The stimuli were spatialized using measured impulse responses and presented via earphones.

263 Our algorithm starts from the recorded impulse responses and proceeds by learning the correct a

264 mixtures are well described by odor-specific impulse responses convolved with the odorant's temporal

265 The same impulse responses convolved with the respiratory airflow

266 t analysis (LDA) is developed for recovering impulse responses in photon counting from a high speed p

267 whisker impulses, but instead combined weak impulse responses with a distinct, slow signal correlate

268 processing were done offline using recorded impulse responses, before presentation over headphones.

269 We trained rats to discriminate whisker impulse sequences that varied in single-impulse kinemati

270 Localized electrical rotors and focal impulse sources are prevalent sustaining mechanisms for

271 rdia (VT) supporting channels have very slow impulse spread and possess low entropy because of their

272 In ventricular scar, impulse spread is slow because it traverses split and zi

273 sion and the inability to control aggressive impulses takes a tremendous toll on society.

274 e factor induced localized thrombin activity impulse that propagated in space and possessed all chara

275 ct and transduce sound waves into electrical impulses that are sent to the brain.

276 maker cells autonomously generate electrical impulses that initiate and maintain the rhythmic contrac

277 ical cues from the environment into neuronal impulses that propagate throughout the gut and into othe

278 nce to thrice the group delay of the primary impulse (the group delay of the primary impulse is on th

279 r hair cells (IHCs) encode sounds into nerve impulses through fast and indefatigable Ca(2+)-dependent

280 e of TCR and BCR repertoires give a powerful impulse to adaptive immunity studies.

281 Ca(2+) from intracellular stores upon nerve impulse to trigger skeletal muscle contraction.

282 individual's long-term interest, short-term impulses to cheat present a self-control problem.

283 l discs transduce touch into slowly adapting impulses to enable tactile discrimination, but their tra

284 the brain can be stimulated with electrical impulses to reversibly change their activity and allevia

285 n sensory neurons is a regulator of afferent impulse traffic.

286 ty is also required for natural filtering of impulse trains as they travel through the sensory neuron

287 3 mum; p = 0.002), and impaired cell-to-cell impulse transmission (24% reduction in Connexin-43 level

288 e excitability of individual cardiomyocytes, impulse transmission between adjacent myocytes, and the

289 Instead, impulse transmission in RVF was hampered by reduction in

290 In a subset of hearts, impulse transmission tends to fall into two distinct con

291 lls around axons that is essential for rapid impulse transmission, but how glial cells accomplish thi

292 h on vertebrate axons is critical for neural impulse transmission, but whether electrically active ax

293 g their neurotransmitter to mediate synaptic impulse transmission.

294 sheath surrounding axons ensures that nerve impulses travel quickly and efficiently, allowing for th

295 The ability to control impulses varies greatly, and difficulty with impulse con

296 tate gyrus were well described by varying an impulse vector in a two-dimensional dynamical system, re

297 The first powerful impulse was provided by the completion of the black cott

298 Localized rotors or focal impulses were detected in 98 (97%) of 101 cases with sus

299 (detonation velocity, pressure and specific impulse) were obtained using the EXPLO v6.01 program.

300 calized sources (electrical rotors and focal impulses), whose elimination (focal impulse and rotor mo