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1 l as Poisson spike trains with long absolute refractory periods).
2 n by research on the so-called psychological refractory period.
3 ivity correlated in part with this transient refractory period.
4 stribution, cutaneous triggering and lack of refractory period.
5 s is true of tails both before and after the refractory period.
6 tion, an activity that correlates with their refractory period.
7  AF stability independent of baseline atrial refractory period.
8 urements or changes in ventricular effective refractory period.
9 response failure and recovery, followed by a refractory period.
10  isolated after the clusters had entered the refractory period.
11  TEP and JI observed in the non-regenerative refractory period.
12 le of Ca2+-activated K+ (BK) currents in the refractory period.
13  transition that expresses a threshold and a refractory period.
14 mol/L had no significant effect on effective refractory period.
15  re-excite the heart after expiration of the refractory period.
16  closure kinetics, which reduce the neuron's refractory period.
17 Ca2+ elevation to the onset of the prolonged refractory period.
18 ility, and increases in both tau(SD) and the refractory period.
19 lantable defibrillator electrodes during the refractory period.
20 ntial generation, reducing duration, and the refractory period.
21 itical determinant of the time course of the refractory period.
22 ositive potentials, and prolong the relative refractory period.
23 same S2-induced graded response prolongs the refractory period.
24 n S2 at intervals shorter than the effective refractory period.
25  atrial action potential duration and atrial refractory period.
26 ponent of the total duration of the relative refractory period.
27 erative capacity than the first, revealing a refractory period.
28  inner limit, however, was not its effective refractory period.
29 rical burst, and reduced activity during the refractory period.
30  potential repolarization and shortening the refractory period.
31 periods of nonresponsiveness indicative of a refractory period.
32 without a driving input pulse and exhibits a refractory period.
33 e controls without affecting the ventricular refractory period.
34 led Ca(2)(+) release units (CRUs) with fixed refractory period.
35 hances excitability by reducing the neuronal refractory period.
36 reshold excitatory inputs were followed by a refractory period.
37  4x threshold determined the shortest atrial refractory period.
38 h S1-S2 = 5 to 10 ms earlier than the atrial refractory period.
39 t transformations, for example thresholds or refractory periods.
40 id channel openings and subsequent prolonged refractory periods.
41 ion, the cycle of block and unblock shortens refractory periods.
42 tes and (2) decreasing absolute and relative refractory periods.
43 hetic stimulation did not change ventricular refractory periods.
44 characteristics, atrial activation times and refractory periods.
45 s, and atrial, AV, and ventricular effective refractory periods.
46 e significantly greater compared with atrial refractory periods.
47 reductions in CD16 expression and activation refractory periods.
48 fore, potentially, cellular excitability and refractory periods.
49 (IC; conduction velocity, 2.4 +/- 0.2 m/sec; refractory period, 0.6 +/- 0.1 msec) and were inhibited
50    Patients with DWR had a shorter effective refractory period (138.8+/-13.4 versus 163.8+/-12.2 ms,
51 -adaptive shortening of the atrial effective refractory periods (14+/-13 versus 12+/-14 ms; P=0.11).
52 ses in noninfarct zone ventricular effective refractory period, 3% to 5% increases in infarct zone ve
53 r assaying p(r), which utilizes the synaptic refractory period--a brief 5-6 ms period following relea
54 s; p = 0.05) and ventriculo-atrial effective refractory periods (AC(VI): 97 +/- 21 ms; control: 127 +
55 .1+/-1.0 Hz), suggesting a large gradient in refractory periods across the BZ.
56 al stimulation shortens the atrial effective refractory period (AERP) and maintains atrial fibrillati
57           In pace/controls, atrial effective refractory period (AERP) at a drive cycle length (DCL) o
58 y in the preclinical rabbit atrial effective refractory period (AERP) model.
59  (AF)-induced shortening of atrial effective refractory period (AERP), we examined the potential of K
60 te-dependent effects on the atrial effective refractory period (AERP).
61                             Atrial effective refractory period, AF inducibility, and duration of indi
62 on to sinus rhythm included atrial effective refractory periods, AF cycle lengths, left atrial dimens
63                          The duration of the refractory period affected only the low-frequency portio
64 ration and conduction time and the effective refractory period after delivery of the basic stimulus (
65 atrial premature beats and directly measured refractory periods after cardioversion) also increased f
66 table EBZ, pinacidil shortened the effective refractory period and abolished conduction block at shor
67                                   Effects on refractory period and AF duration in open chest pigs: Th
68                                    Effective refractory period and APD are closely related in the hum
69  three modified models that have no explicit refractory period and examine their ability to produce r
70             Nonactivity-dependent responses (refractory period and latency) at two stages of the circ
71 ntagonists and had a characteristic postwave refractory period and spatial boundaries between adjacen
72                   The first peak indicates a refractory period and the 400 Hz oscillation demonstrate
73 s recovery function vanishes for an absolute refractory period and then gradually increases to unity.
74 of reentry necessitates a sufficiently short refractory period and/or delayed conduction, and AF has
75  of AP14145 and vernakalant on the effective refractory periods and acute burst pacing-induced AF wer
76  fast inactivated states, thereby shortening refractory periods and permitting rapid, repetitive, and
77 dren had similar accessory pathway effective refractory periods and supraventricular tachycardia indu
78 axons are adapted to produce extremely short refractory periods and that brief bursts of forward-prop
79                                       Atrial refractory periods and their spatial distribution are im
80 uences were used to measure atrioventricular refractory periods and to produce atrial echoes and epis
81 ction potential waveforms, automaticity, and refractory periods and, in most cardiac cells, multiple
82 reases in infarct zone ventricular effective refractory period, and 4% to 6% increases in QTc interva
83 ization, fast after-hyperpolarization, brief refractory period, and high firing frequency characteris
84 rugs prolong the atrial action potential and refractory period, and thereby prevent recurrent atrial
85   The changes in AVNW-CL, AV nodal effective refractory period, and ventricular response during AF we
86 terval, from 2 to 45 ms beyond the effective refractory period, and was associated with unidirectiona
87 o investigate conduction patterns, effective refractory periods, and inducibility of AF.
88 overy of AP excitability during the relative refractory period; and steady-state INa inactivation via
89  site and the other MAPs, and PRR (effective refractory period-APD90=PRR) and related to the inductio
90 tently (receptive period approximately 1 wk; refractory period approximately 3 wk).
91 ivity-dependent depression and we identify a refractory period ( approximately 2 s) after endogenous
92 fective refractory period (ERP) and absolute refractory period (ARP) were significantly longer in dog
93                   The effective and absolute refractory periods (ARP and ERP) were measured during an
94 produced AP shortening and reduced effective refractory period associated with altered IKs kinetics i
95 nized atrial electrograms and long effective refractory periods associated with disorganized electrog
96 tive refractory period, with short effective refractory periods associated with organized atrial elec
97                                The effective refractory period at the high right atrium remained unch
98 ect not related to a change in the effective refractory period at the site of block.
99 us 376 +/- 466 ms; P=0.86), atrial effective refractory periods at 90 bpm (250+/-32 versus 248+/-36 m
100 The majority (95% SUNCT and 89% SUNA) had no refractory period between attacks.
101              The difference in the effective refractory period between the high right atrium and the
102  changes in heart rates and atrial effective refractory period, but both significantly increased AF s
103      We demonstrate that the duration of the refractory period-but neither the cycle period nor the m
104 ociated with a prolongation of the effective refractory period by 18 +/- 2 ms (P < .05), an increase
105               Cooling increased the relative refractory period by 7.8% per degree C (P < 0.0001), slo
106 rrent treatments extend the atrial effective refractory period by nonselective blockade of cardiac io
107 d APD(-61 mV) (reflecting cellular effective refractory period) by 22% (P < 0.05 for each).
108                                          The refractory period can be manipulated, for example from 1
109  areas of the EBZ, nor was the EBZ effective refractory period changed.
110 rated significant prolongation of the atrial refractory period compared with vehicle controls without
111 wave fronts, we found that the cycle length, refractory period, conduction velocity, and wavelength a
112 for 45 minutes to determine atrial effective refractory periods, conduction velocity, conduction hete
113  as the spontaneous activation rate and sAHP refractory period contribute to critical wave size varia
114 ms (type I) and the longest atrial effective refractory period corresponding to disorganized atrial e
115 y period, with the shortest atrial effective refractory period corresponding to organized atrial elec
116                                The effective refractory period data were used to determine the inters
117            Concurrently, the right effective refractory period decreased.
118 nged action potential duration and effective refractory period, decreased LSG function were identifie
119                                The effective refractory period difference between the sites of pacing
120  the site with the shortest atrial effective refractory period, disorganized atrial electrograms were
121                                   Increasing refractory period dispersion without changing conduction
122 ton arrival and emergence of a QB), and (iv) refractory period distribution (time for a microvillus t
123  in male SP expression levels correlate with refractory period duration in females, it is unknown whe
124 n on ventricular myocardial action potential refractory period, duration, force and rhythm is evidenc
125 re: starting and minimum pressure, burst and refractory period durations, enhanced contractile activi
126 gest decreased excitability and an increased refractory period during HF.
127 nconsistent with accounts of a psychological refractory period during sequential information processi
128 e to blood-borne bacteria was induction of a refractory period during which leukocyte activation by s
129 followed by a prolonged (approximately 18 h) refractory period during which the ability of both elect
130 ed pacing was again instituted, below atrial refractory period, during 2 min of apnea.
131 itation evoked is followed by a long-lasting refractory period, during which the previously excited n
132 ) activation of a signaling component with a refractory period (e.g. G protein), and 3) inactivation
133 he antegrade atrioventricular node effective refractory period (ERP) (from 252+/-60 to 303+/-70 ms; P
134 eity (p < 0.001); no change in the effective refractory period (ERP) (p > 0.8) or ERP heterogeneity (
135 lar (RV) and left ventricular (LV) effective refractory period (ERP) and absolute refractory period (
136 , and their effects on ventricular effective refractory period (ERP) and arrhythmia development were
137 uration (APD90), right ventricular effective refractory period (ERP) and blood pressure measurements
138 rillation (AF) shortens the atrial effective refractory period (ERP) and predisposes to further episo
139 rillation (AF) shortens the atrial effective refractory period (ERP) and predisposes to further episo
140              Standard restitution, effective refractory period (ERP) and VF threshold (VFT) were meas
141 vide a surrogate for measuring the effective refractory period (ERP) in human ventricle.
142 al fibrillation (AF) on the atrial effective refractory period (ERP) in humans is unknown.
143 de of membrane currents on APD and effective refractory period (ERP) in rat endocardial and epicardia
144 length, obese patients had shorter effective refractory period (ERP) in the left atrium (251 +/- 25 m
145 e action potential duration and/or effective refractory period (ERP) is thought to decrease the cycle
146 le, AP duration (APD) restitution, effective refractory period (ERP) restitution, and conduction velo
147                      The effect of effective refractory period (ERP) shortening on the vulnerability
148 repeat attempts at inducing AF and effective refractory period (ERP) testing.
149 ction potential duration (APD) and effective refractory period (ERP) than a noninducing site, resulti
150                                LAA effective refractory period (ERP) was measured before and after pa
151 ng AF and the width, area, weight, effective refractory period (ERP), and wavelength in atrial tissue
152                             Atrial effective refractory period (ERP), conduction velocity, wavelength
153 tential durations (APD(50,75,90)), effective refractory period (ERP), post repolarization refractorin
154              While approaching the effective refractory period (ERP), the tissue response is characte
155 n (APD), conduction velocity (CV), effective refractory period (ERP), tissue excitation threshold and
156 ted with attenuation of the atrial effective refractory period (ERP).
157 tructed restitution curves for the effective refractory period (ERP).
158 rillation interval (AFI) and local effective refractory period (ERP).
159 trial and ventricular effective and relative refractory periods (ERPs and RRPs) were significantly sh
160 ls (APs) at 90% repolarization and effective refractory periods (ERPs) (60 +/- 1 ms vs. 44 +/- 1 ms;
161                                    Effective refractory periods (ERPs) were determined at 5 myocardia
162                                The effective refractory periods (ERPs) were measured in the setting o
163 ropranolol (0.1 mg/kg), and atrial effective refractory periods (ERPs) were obtained at baseline (EPS
164                              Measurements of refractory period extension by shocks during ventricular
165                   These findings support the refractory period extension hypothesis for defibrillatio
166                                   A relative refractory period followed CICR.
167 n produced by each impulse, but with a short refractory period following each Triggered impulse.
168  the AF vulnerability zone and the effective refractory period for a BCL, decreased as BCL lengthened
169 F every 6 h, which falls within the putative refractory period for biochemical responses, resulted in
170              RATIONALE: The development of a refractory period for Ca(2+) spark initiation after Ca(2
171                                            A refractory period for Ca(2+) spark initiation and subseq
172                                   During the refractory period for Hsp70 induction, HSF (heat-shock t
173 munity observed at P45 is reminiscent of the refractory period for inhibitory plasticity reported by
174  plasticity, demonstrating the presence of a refractory period for the regulation of synaptic plastic
175 ery ligation in dogs, ventricular functional refractory periods (FRPs) were measured at five to eight
176 e first evoked burst, with no evidence for a refractory period greater than approximately 1 s, even w
177 n potentials, resulting in shorter effective refractory periods, greater beat-to-beat variability of
178 n potentials, resulting in shorter effective refractory periods, greater beat-to-beat variability of
179 o the failing myocardium during the absolute refractory period improved LV function without increasin
180 , endocardial APD90 or ventricular effective refractory period in Scn5a+/Delta and WT hearts followin
181 t first transcriptional burst, followed by a refractory period in the range of hours.
182                VIP shortens atrial effective refractory periods in dogs.
183  hearts, and prolonged ventricular effective refractory periods in initially non-arrhythmogenic Scn5a
184 he first-degree AV block dose, AVN effective refractory period increased from 186+/-37 to 282+/-33 ms
185                                    Effective refractory periods increased from 149+/-16 to 208+/-26 m
186 suring prolongation of ventricular effective refractory period induced by bilateral vagal stimulation
187 l DeltaPsim loss because of the disparity of refractory periods inside and outside the metabolic sink
188 whether the BK current is altered during the refractory period, intact clusters were stimulated to af
189                     In excitable tissues the refractory period is a critical control mechanism preven
190            A shortened beta-cell replication refractory period is also observed.
191 o investigations have demonstrated that this refractory period is due in large part to the persistent
192                                    Effective refractory period is most closely reflected by APD70.
193 e SR, electrical inhibition is released, the refractory period is terminated and peristaltic contract
194                    The inclusion of absolute refractory periods is not a satisfactory solution since
195 ven its association with a reduced effective refractory period, it may contribute to the substrate fo
196                        Absolute and relative refractory periods largely accounted for the reliability
197       Furthermore, we identified a transient refractory period (lasting up to 120 min) following prec
198                                          The refractory period lasts only one to a few milliseconds,
199                  LLDs are followed by a long refractory period, limiting LLD generation to approximat
200                                In vivo, this refractory period limits the frequency of reproductive b
201 I ECG (hazard ratio [HR]: 4.20), ventricular refractory period &lt;200 ms (HR: 3.91), and QRS fragmentat
202 G, history of syncope, ventricular effective refractory period &lt;200 ms, and QRS fragmentation seem us
203 rial pacing</=250 ms (or antegrade effective refractory period&lt;/=250 ms if shortest preexcited RR int
204 e PEI comprises absolute and relative sexual refractory periods marked, respectively, by the presence
205                    What happens during this "refractory period" might hold the key to spinal cord reg
206 uscles neither the mechanisms underlying the refractory period nor the link between excitability and
207 e that the global effect of VOR results in a refractory period of >/= 24 hours.
208 ne (< or =0.01 microL L(-1)) with a relative refractory period of 5 h after ethylene is added.
209 we investigated the relationship between the refractory period of a neuron and its firing precision.
210                                  A postburst refractory period of circa 2 seconds that increases with
211                                We observed a refractory period of neuronal origin in a two-stimuli pa
212 s (as was previously believed), produced the refractory period of spontaneous retinal waves and set t
213  identified an optimal anterograde effective refractory period of the accessory pathway cutoff of 240
214 +-sensitive K+ (BK) channels, determines the refractory period of the action potential.
215                                Moreover, the refractory period of the afterdischarge itself may also
216 +/- 104 ms, P < .0001), as did the effective refractory period of the AV node (279 +/- 60 versus 304
217 hannel activity contributes to the prolonged refractory period of the bag cell neurons.
218 bility of food by significantly reducing the refractory period of the brain's feeding circuitry.
219                   The relative and effective refractory period of the His-Purkinje system increased i
220 free firing rate derived by allowing for the refractory period often exceeded the observed firing rat
221 n used to predict the effect of removing the refractory period on a cell-by-cell basis for two largel
222                                          The refractory period opposes saturation, dynamically and st
223 synaptic factors are unlikely to explain the refractory period or its modulation by Ca(2+).
224 AF had shorter left atrial APD and effective refractory period (p = 0.01).
225 ted with a short accessory pathway antegrade refractory period (P<0.001) and atrioventricular reentra
226 rated that short accessory-pathway effective refractory period (P<0.001) and atrioventricular reentra
227 s showed shorter accessory-pathway effective refractory period (P<0.001) and more often exhibited mul
228 P<0.0003), and reduction in atrial effective refractory periods (P<0.0001) compared with control.
229             Furthermore, the duration of the refractory period predicts the timing of the next activa
230                   The sinus cycle length and refractory periods prolonged on procainamide or quinidin
231 After stimulation, T cells enter a transient refractory period, promoted by IL-2, during which they a
232                                         This refractory period provides a simple explanation for not
233 y, refractoriness, such as the Psychological Refractory Period (PRP) has only been quantified in disc
234 es (from depleted ROS) and induces (from the refractory period) regeneration, TEP increase and JI rev
235            It also shows that egg laying and refractory period response to SP is at least partially u
236 ntervals (AIs) in VF may depend on the local refractory period (RP), and sustained VF may require a s
237 ured at the pacing site and was shorter than refractory periods (RPs) near the base, creating heterog
238      From each VRC was measured the relative refractory period (RRP), the supernormality and the time
239 ulation was at the beginning of the relative refractory period (RRP), transitional make-break stimula
240 al upstroke, a prolongation of the effective refractory period secondary to the development of postre
241                         The atrial effective refractory period shortened in ATR and CAF groups.
242                             Atrial effective refractory period shortened progressively from 78+/-3 ms
243 er establishing chronic AF, atrial effective refractory period shortening, increases in spontaneous P
244       Using vagally induced atrial effective refractory period shortening, slowing of spontaneous sin
245  in the PCL shortened atrial and ventricular refractory periods significantly more than did the incre
246 nchronize (bursts) and generate a population refractory period (silence).
247 llatory stimulation, NFLs but not IFFLs show refractory-period stabilization (robustness to changes i
248 stimulations induce PIP3 responses without a refractory period, suggesting that GPCR-mediated inhibit
249 duced gene expression nor for the subsequent refractory period, suggesting that these phenomena depen
250  circuit, the resulting changes in effective refractory periods tend to stabilize reentry in this rem
251            This is mediated by shortening of refractory periods termed electrical remodeling.
252 ammed extra stimuli at 10 ms above effective refractory period than with stable pacing (13.4 +/- 16.5
253 ctive of the length of the stimulation and a refractory period that is shared with that generated by
254 niform self-renewal, slowed by a replication refractory period that prevents beta cells from immediat
255 ics was limited by absolute and relative tic refractory periods that were derived from an internal st
256              Given the tight distribution of refractory periods, the ability of refractoriness to imp
257 eled as probabilistic firing combined with a refractory period: the instantaneous firing rate is the
258 ulnerability zone for a BCL was its relative refractory period; the inner limit, however, was not its
259 ther rate-limiting step that may impact this refractory period, thereby providing an additional regul
260 tion bottleneck underlying the psychological refractory period to a frontoparietal network.
261 t effect on postsynaptic spiking, as did the refractory period to a smaller extent.
262                             The ratio of the refractory period to the stimulus period predicted the i
263 ite of shortest and longest atrial effective refractory periods until atrial fibrillation induction i
264       We also measured ventricular effective refractory period (V-ERP) and QT interval in separate gr
265 lthough action potential shapes and relative refractory periods varied little between genotypes, Kv1.
266 lar fibrillation (VF), ventricular effective refractory period (VERP) and defibrillation threshold (D
267  a prolongation of the ventricular effective refractory period (VERP) in the models, although there m
268  hearts, and prolonged ventricular effective refractory periods (VERPs) in non-arrhythmogenic Scn5a+/
269 ammed extra stimuli at 10 ms above effective refractory period versus 66.1 +/- 22.9 ms with pacing at
270                  Under these conditions, the refractory period was 147 ms; the action potential durat
271 l electrogram type with the atrial effective refractory period was further demonstrated by the effect
272 uced by more than fourfold, and the relative refractory period was increased in AdHERG-infected myocy
273                                 However, the refractory period was transient as a later fourth transf
274 el of cardiac action potential, in which the refractory period was variably shortened by a progressiv
275 ion, but not differences in atrial effective refractory periods, was associated with the development
276 dal function and right ventricular effective refractory period were impaired in the mutant mice, wher
277 DeltaV(m) produced by shocks in the absolute refractory period were measured with electrodes and a la
278 atrial fibrillation and the atrial effective refractory period were obtained from multiple sites of t
279               In the present study, auditory refractory periods were compared in a group of 24 young
280 setting response curves and atrial effective refractory periods were determined with single extrastim
281                       In simulations, longer refractory periods were found to make the response more
282                                    Effective refractory periods were increased homogeneously througho
283                       Changes in ventricular refractory periods were significantly greater compared w
284                                              Refractory periods were tightly distributed, with a mean
285 ining disease dynamics is illustrated during refractory periods, when population susceptibility level
286 d at sites with the longest atrial effective refractory period, whereas 1:1 atrial capture was still
287 to contribute to pacemaker potentials and to refractory periods which control the rhythmical motility
288 roadening the action potential lengthens the refractory period, which may in turn be antiarrhythmogen
289 s) and extraordinarily long (more than 10 s) refractory periods, which prevent urine reflux and kidne
290 location are related to the atrial effective refractory period, with short effective refractory perio
291 losely followed that of the atrial effective refractory period, with the shortest atrial effective re
292 olonged atrial action potential duration and refractory period without affecting ventricular electrop

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