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1  not oscillate or possibly oscillated with a low amplitude.
2 mechanism that boosts cochlear vibrations of low amplitude.
3 tially evokes single local Ca(2+) signals of low amplitude.
4 nerated from micro seismicity have extremely low amplitude.
5  of pp4 results in short period rhythms with low amplitude.
6 pecially problematic in detecting peaks with low amplitudes.
7 ation were observed to have long periods but low amplitudes.
8                                One-megahertz low-amplitude (0.18 MPa) continuous wave ultrasound dire
9  activation (82+/-18 versus 37+/-11 ms); (3) low-amplitude (0.47+/-0.16 versus 3.74+/-1.60 mV) and fr
10 d that intermediate-frequency (100-300 kHz), low-amplitude (1-3 V/cm) EFs, which they called "tumor-t
11                       It has been found that low-amplitude (+/-1 V) square wave excitation can prolon
12 ltammetry, while a high-frequency (100 kHz), low-amplitude (10 mV rms) sine wave was added to the vol
13 n stiffness by up to 90% when subjected to a low-amplitude (5%), repetitive (dynamic) compression.
14                              At each step, a low-amplitude (6 cm H2O) sinusoidal signal was alternate
15 regular initiation, aberrant conduction, and low amplitude activity could contribute to the pathogene
16 tiated in dendritic layers associated with a low amplitude "afterdischarge termination oscillation" (
17 f the beta-barrel as a collective rocking of low amplitude and of hundreds of nanoseconds time scale.
18                           Li-NR rhythms were low amplitude and profoundly weakened.
19 ereas others expressed a diurnal rhythm with low amplitude and significant activity during the day.
20   However, when capillaries are not present, low amplitudes and high set points produce images with p
21 ght, but the WS2 appeared inverted except at low amplitudes and high set points.
22 ses, correctly identifying even neurons with low amplitudes and small spatial extents in high drift c
23 frq protein and mRNA are low, resulting in a low-amplitude and long-period oscillation of the clock.
24 higher frequencies, short inspiratory times, low amplitudes, and low mean airway pressures for healin
25 nvolves switching from a nearly symmetrical, low-amplitude, and flagellar beating pattern to an asymm
26  GB3, all three observables reflect the same low-amplitude anisotropic motions arising from fluctuati
27 orate the bilayers, followed by a prolonged, low-amplitude ( approximately 65 mV) voltage clamp to mo
28 ck-responsive element sufficient to confer a low-amplitude (approximately 2-fold) circadian oscillati
29 ynchronized and high amplitude to sparse and low amplitude as plasticity declines and the cortex matu
30  currents required for optimal encoding of a low-amplitude auditory signal differ from those for loud
31 ass via alpha-actinin, we observed frequent, low-amplitude barbed-end fluctuations of +/-2-6 subunits
32                                The region of low amplitude between the aorta and left ventricle, whic
33 /-35 ms), giving rise to broad and sometimes low-amplitude bifurcated T waves and an increased transm
34 onses to optogenetically delivered high- and low-amplitude BMP signaling pulses indicate that spatiot
35                          We demonstrate that low-amplitude, brief trains of microstimulation can lead
36 olypeptide isolated from SDS-PAGE displays a low-amplitude broad spectrum with a peak at 553 nm, simi
37 n amplitude of 3 N to simulate exercise; (2) low amplitude, broad frequency vibration with frequency
38                                            A low-amplitude, broad-duration (40-50 ms) central peak of
39 ructed into a rhythmogenic process producing low amplitude burstlets and preinspiratory activity that
40  We characterized the disrupted locus of the low amplitude but still rhythmic mutant (M16) as the rpo
41 th their stimulation by carbochol activating low-amplitude Ca(2+) transients.
42 not germ-free (GF) EECs, exhibit spontaneous low-amplitude Ca2+ fluctuation.
43  the post-wave Ca2+ increase, and during the low-amplitude Ca2+ responses evoked by threshold histami
44                   Directly imposing high- or low-amplitude Ca2+ signals with an extracellular gradien
45 ast, phorbol 12-myristate 13-acetate induced low amplitude calcium oscillations, slower translocation
46  low binding capacity that transduced only a low amplitude calcium signal, suggesting the involvement
47 ptors that had normal binding but transduced low amplitude calcium signals, while other mutations in
48 ons demonstrate that only bats emitting such low-amplitude calls hear moth echoes before their calls
49                                              Low amplitude circadian oscillations in the molecular ci
50                     Furthermore, we observed low-amplitude circadian oscillatory transcription of kai
51 admission, mechanical ventilation and absent/low amplitude compound muscle action potentials.
52 ross different catalogs and is of remarkably low amplitude, consistent with an effective Omega approx
53  postsynaptic receptors generating sustained low-amplitude current and desensitize the receptors, the
54 and mechanisms of tonic inhibitory currents, low amplitude currents resulting from ambient GABA actin
55                                         Yet, low-amplitude currents at similar frequencies have been
56 se to photoperiod is observed, and this very low amplitude cycling of some phytochrome proteins is ou
57 ation of extrasynaptic NMDARs, produced only low-amplitude cytoplasmic Ca(2+) spikes and modest, nond
58  each precordial lead as the total number of low-amplitude deflections that deviated from their respe
59 ion potentials, but we found no evidence for low-amplitude dendritic spikes that have been reported f
60     The first stage consists of a sustained, low-amplitude depolarization (plateau activity) lasting
61 ling flanks) and compared them to periods of low amplitude (desynchronized) mu-alpha.
62 closion, egg-laying, and feeding) tend to be low amplitude, display large variations amongst replicat
63 y and high frequency LH pulses but with very low amplitude due to reduced responsiveness of the pitui
64 tate, whereas Gprk2 mutants produce constant low-amplitude EAG responses.
65 imb tonic rigidity and posttonic clonus; (6) low-amplitude EEG during postictal depression.
66 ized high-frequency stimulation (LHFS) using low-amplitude electric pulses instituted within a formed
67 ion between implanted CoCrMo metal alloy and low amplitude electrical oscillation, similar in magnitu
68 of which were immediately followed by brief, low-amplitude electrical stimulation to the amygdala.
69     Both frontal and parietal TMS elicited a low-amplitude electroencephalographic (EEG) slow wave co
70  (r=0.64, P<0.0001), many isthmuses had very low-amplitude electrograms, and EUS could not be identif
71 l dysfunction, including absent, delayed, or low amplitude electrophysiological responses from the au
72 es generated by self-initiated movements and low-amplitude environmental vibrations emanating from di
73 cally blind from birth with nonrecordable or low-amplitude ERGs.
74 standard approaches to identify these brief, low amplitude events are difficult, time consuming, and
75                                 Detection of low-amplitude events is critical to survival; for exampl
76  can be excited for fields ranging between a low amplitude excitation threshold and a high amplitude
77                                         When low-amplitude excitatory postsynaptic potentials (EPSPs)
78 i) sentinel spike; and (iii) spike burst and low amplitude fast activity onset.
79 evealed three patterns of seizure onset: (i) low amplitude fast activity; (ii) sentinel spike; and (i
80 ve largely been distinguished into two types-low amplitude fast oscillations (LAF), or high amplitude
81 oteins exhibited a minor contribution from a low-amplitude fast decay, consistent with local motion o
82 here vole dynamics shifted from a high- to a low-amplitude fluctuation regime in the mid-1990s.
83           LA AFL circuits had either flat or low-amplitude forces in the inferior leads.
84                           The termination of low-amplitude fractionated activity in the PVs preceded
85 in constant darkness, the dKO mice exhibited low-amplitude, fragmented rhythms and attenuated light r
86 formation about individual subjects (whereas low-amplitude frames carry little).
87   The focal ERG showed signals of borderline low amplitude from the fovea with the multifocal ERG, th
88                       As a practical matter, low-amplitude, genome-wide oscillations, a ubiquitous bu
89                      A notable exception are low-amplitude high-frequency (~600 Hz) somatosensory EEG
90 oad with rest periods and may be promoted by low-amplitude high-frequency stimuli.
91 lectroencephalogram (EEG) recordings display low-amplitude, high-frequency fluctuations.
92 topic exchange mechanism involving localized low-amplitude, high-frequency motions that do not requir
93 putational studies suggested that additional low-amplitude, high-frequency oscillations were also pos
94 eflex effects on inspiratory motor output of low-amplitude, high-frequency pressure oscillations (HFP
95  system to an ecologically relevant range of low-amplitude, high-frequency stimuli.
96 egular and fast spiking units) by presenting low-amplitude, high-frequency vibrissa stimulation.
97 sing evidence suggests that a high-velocity, low-amplitude (HVLA) thrust directed at a dysfunctional
98                                              Low-amplitude hyperpolarizing potentials were recorded i
99                                              Low-amplitude ICMS at different PM locations thus evokes
100                In a multivariate analysis, a low amplitude in lead II (<34.6 uV) and high dominant ra
101             The f-waves combined with both a low amplitude in lead II and high dominant rate in lead
102 nocturnal switch in myometrial activity from low amplitude, infrequent contractures to high amplitude
103  rat resulted in robust apneusis (lengthened low amplitude inspiration due to loss of post-inspirator
104           Age was mainly correlated with the low-amplitude introduction and build-up phases, dominanc
105 in all four phases, but most strongly in the low-amplitude introduction and high-amplitude climax pha
106 it and impaired contralateral pursuit, (2) a low-amplitude ipsilesional right-beating nystagmus witho
107 scillations of KaiC phosphorylation, whereas low-amplitude KaiC phosphorylation rhythms persist in th
108 (reflecting activity of the caller) with the low-amplitude let-down phase.
109 owing Gaboxadol exposure is characterized by low-amplitude LFPs, during which dFB-induced effects are
110 s substantially more complex compared to the low-amplitude linear regime, due to the inevitable emerg
111 solitons-high-intensity nonlinear pulses-and low-amplitude linear waves.
112 Structural failures resulting from prolonged low-amplitude loading are particularly problematic.
113 the MOD-1 receptor in AIY neurons to promote low-amplitude locomotor behavior characteristic of well
114                  Depletion of TRAP150 caused low-amplitude, long-period rhythms, identifying it as a
115 enuinely in a straight conformation or was a low-amplitude, long-wavelength helix.
116     As the CaM C lobe sites are populated by low amplitude/low frequency (global) Ca2+ signals, but o
117 The simulations show that there is a slower, low-amplitude (&lt;7%) decay component not accessible by th
118 ing AFM under ambient conditions through the low-amplitude (&lt;= 1 nm) excitation of higher eigenmodes
119                During the SII acquisition, a low-amplitude mechanical vibration is applied to the hea
120 such as fixational drift, smooth pursuit and low-amplitude mechanical vibrations of the eyes.
121 cluding depolarization block and depolarized low amplitude membrane oscillations (DLAMOs), have been
122  no membrane activity or display depolarised low-amplitude membrane oscillations, to neurones that we
123 s at kHz frame rates, is also accompanied by low amplitude modulation.
124 activity and other physiological rhythms but low amplitude molecular rhythms.
125 scale, whereas those in Switch II experience low-amplitude motion on the nanosecond time scale and ch
126 trometry, were used to locate differences in low-amplitude motion when SH2 was bound to the peptide.
127 xperimental investigation of these harmonic, low-amplitude motions, however, has proven challenging.
128 emonstrate the ability of SCD in identifying low-amplitude motor unit action potentials and effective
129                                              Low amplitude muscle vibration (0.5 ms; 80 Hz; duration
130  one short period (22 h) mutant (M2) and two low amplitude mutants, one of which showed apparent arhy
131                                        Among low-amplitude mutants, one mutant, tnp6, had an insertio
132 ectrocochleography (ECochG) showed prolonged low amplitude negative potentials without auditory nerve
133 ed chloride current (ICl(Ca)) and sustained, low amplitude non-selective cation current (ICat).
134 s, trpv1(-/-) mice had a higher frequency of low-amplitude, non-voiding bladder contractions.
135 ex beam can confine a microbubble by forcing low-amplitude, nonspherical, shape oscillations, enablin
136 ictable component of the QRS and manifest as low-amplitude notches and slurs.
137        Repetitive nerve stimulation revealed low amplitude of compound muscle action potential at res
138 weak currents are remarkable considering the low amplitude of the electric fields acting on the brain
139                                          The low amplitude of water signatures could be explained by
140                          Specifically, under low amplitudes of physiological force, PAK2 is protected
141 , and the existing sic-1 mutant both exhibit low-amplitude or arrhythmic expression of core circadian
142  mutations of these sites show short period, low amplitude, or arrhythmic conidiation rhythms in cons
143 hase with cycles in Per1 and Per2; there was low-amplitude oscillation of Cry1 and Cry2.
144 mutant flies manifest high trough values and low amplitude oscillations.
145                                   We imposed low-amplitude oscillations on individual globus pallidus
146  preBotC neuronal activity has revealed that low-amplitude oscillations persist at physiological leve
147 est electrical energy from low-frequency and low-amplitude oscillations such as ocean wave.
148 l deletion, displays increased stability and low-amplitude oscillations, consistent with previous rep
149 s: an initial postmitotic pulse, followed by low-amplitude oscillations.
150  (nRT) play a critical role in generation of low-amplitude oscillatory bursting involving mutually in
151 ese results demonstrate that high-frequency, low-amplitude oscillatory pressure waves in the UA, simi
152 e a preserved bacillary layer on SS-OCT with low-amplitude outer retinal corrugations (ORCs) compared
153           The 2:1 ventricular conduction and low-amplitude P waves challenged the diagnosis of 4 of 2
154 nt decreasing-velocity or linear drift and a low-amplitude periodic oscillation.
155 ations between small earthquakes and ongoing low-amplitude periodic stresses indicate increased fault
156 ed by a transition from dominant 41,000-year low-amplitude periodicity to dominant 100,000-year high-
157 eased during high-amplitude as compared with low-amplitude periods.
158 t disturbing the sample being studied due to low amplitude perturbations.
159                                            A low-amplitude phase, detected in concurrence with the ma
160                    During eupnoeic activity, low-amplitude post-inspiratory (post-I) discharge was on
161 he core of the reentry registered no or very low amplitude potentials.
162  >/=114 ms; root mean square 40 <20 muV, and low-amplitude potentials 40 >38 ms) were defined as havi
163 se include internal electric field-dependent low-amplitude protein motions and the reorganization of
164                 We achieved this using brief low-amplitude pulsatile mechanical stimuli to selectivel
165 ion methods while operating under relatively low-amplitude pulses (20 V).
166 g series (up to 45 s) of hundreds of regular low-amplitude pulses.
167 t with high-risk features including wide and low-amplitude QRS complexes.
168 sional electroanatomic voltage maps revealed low-amplitude regions in the inferior or posterior left
169 contrast, stroke patients exhibited the same low-amplitude response to all stimuli.
170 ) for high amplitudes, but failed to predict low amplitude responses.
171                                              Low-amplitude responses were influenced by both starting
172 While some experimental studies suggest that low-amplitude RF radiation may influence cellular metabo
173 anifested within the inter-spike interval as low amplitude rhythmic oscillations in the 4-12 Hz frequ
174 cadian rhythms, others have irregular and/or low-amplitude rhythms.
175 pecies adapted to high mean temperatures and low-amplitude seasonal fluctuations; an increase in seas
176 strategic imposition of a high-frequency and low-amplitude shear perturbation orthogonal to the prima
177 was obtained and analyzed for fQRS duration, low amplitude signal duration<40 mV (LAS40), and root-me
178 he detection and identification of transient low-amplitude signals across the entire frequency spectr
179 h the cochlea also uses resonance to amplify low-amplitude signals and to generate a spatial map of f
180  of this molecular network; amplification of low-amplitude signals by hair bundles seems to be univer
181 the small nature of autonomic nerves and the low-amplitude signals from their small axons.
182                ECGI noninvasively imaged the low-amplitude signals of AF in a wide range of patients
183       This study investigates low-frequency, low-amplitude signals preceding the 2023 M(W) 7.8 Kahram
184 ithin scar characterized by fractionated and low-amplitude signals usually occurring late during sinu
185 ifies more motor units, including those with low-amplitude signals, and performs well even in challen
186 l systems which use SR to detect and amplify low-amplitude signals, to demonstrate how a simple elect
187                            A transition from low-amplitude sinusoidal obliquity (~41 ky) and precessi
188                      Increasing intervals of low-amplitude small herbivore population fluctuations ar
189 aveform from sharp, high-amplitude to broad, low-amplitude spikes.
190 sway dependence was most apparent when using low amplitude stiffness-measuring perturbations, and the
191 his study, the first to our knowledge to use low-amplitude stimulation of LDT in freely moving cats,
192                        Five hours of chronic low-amplitude stimulation of the LDT induced a highly si
193 ata during epochs of high-amplitude or zero-/low-amplitude stimulation.
194 SOAE generation and the cochlear response to low amplitude stimuli.
195 ally, we demonstrate that the application of low-amplitude stimuli can entrain bundle motility either
196 es two types of energy waves: high-frequency low-amplitude stress waves and long-duration low-frequen
197 sphorylation of ERK1/2, while high-, but not low-, amplitude stretch caused phosphorylation of JNKs.
198                  These results indicate that low-amplitude, subthreshold current pulses are sufficien
199  that preceded particle uptake followed by a low amplitude sustained calcium increase.
200                                    Prolonged low-amplitude synaptic currents in biopsied anconeus mus
201 rome (CMS) associated with rapidly decaying, low-amplitude synaptic currents, and trace its cause to
202                  Among control animals, some low-amplitude T(b) rhythms during torpor were driven by
203 inger as in (a) whilst performing self paced low amplitude tapping of the (i) index finger, (ii) thum
204 e circadian mechanism in Neurospora, we used low-amplitude temperature cycles to compare WT and frq-n
205 ased on the ecology of nematodes, we applied low-amplitude temperature cycles to synchronize populati
206  required for behavioural synchronization to low-amplitude temperature cycles.
207 e by performing frequent relocation jumps of low amplitude that seem unrelated to localized hydrodyna
208 heir IN was converted to waveforms with very low amplitudes that yielded higher NAFX values and allow
209 es induced in the worm, but is beneficial at low amplitudes to ensuring homogeneous ultrasound exposu
210 0 Hz), rather than the low-frequency (2 Hz), low-amplitude, tonic GABAergic drive common to wild-type
211  seismic instruments often record coincident low-amplitude tremor in a narrow (1-5 cycles per second)
212 g) as compared with wild-type mice that have low amplitude (Type 1) phase resetting.
213         Furthermore, the prolonged action of low-amplitude ultrasound enables the elongation of amylo
214 o-generated dark continuous noise comprising low-amplitude unitary events occurring at a very high mo
215 onically increasing applied strain numerous, low-amplitude unloading/reloading cycles, and extracting
216               The anomaly, which consists of low-amplitude variance in obliquity (a node) and a minim
217 accelerometer suitable for low frequency and low amplitude vibration sensing.
218  tested by applying short (1.5 s) periods of low amplitude vibration to single intrinsic hand muscles
219                                   We applied low-amplitude vibration to the abductor pollicis brevis
220 onfined, high-restitution grains, subject to low-amplitude vibration, can serve as experimentally-acc
221 urfaces encountered by the animal, including low-amplitude vibrations initiated over 2 m away.
222 REM) sleep is the shift from high-frequency, low-amplitude wake EEG to low-frequency, high-amplitude
223  rate during sinusoidal vibration stimuli at low amplitudes was higher in the presence of alpha-bunga
224                                           On low-amplitude wave substrates, actomyosin contractility
225 e required for polarization and migration on low-amplitude wave substrates, they did not localize to

 
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