ライフサイエンスコーパス: beat

1 an the current state-of-the-art method (bead beating).

2 y state, Ca influx equals Ca efflux on every beat.

3 the action potential duration (APD) of that beat.

4 aptation mechanism controlling the flagellar beat.

5 s that propagate through the heart with each beat.

6 force to generate the ciliary and flagellar beat.

7 repolarize ventricular myocytes and end each beat.

8 than 10 successive detectable oscillometric beats.

9 lps protect against the formation of ectopic beats.

10 serotonergic cells are active when cilia are beating.

11 for characterizing the efficiency of ciliary beating.

12 bute importantly to CSF flow through ciliary beating.

13 ring vigorous activity such as cardiomyocyte beating.

14 e the greatest mechanical force from ciliary beating.

15 ablishing SACOs through to the initiation of beating.

16 ibution within the basal body during ciliary beating.

17 chloride permeability and increases ciliary beating.

18 no ectopy; 1, isolated premature ventricular beats; 2, bigeminy; 3, couplets; and 4, nonsustained ven

19 dence interval, 4.01-60.89; P<0.0001) and >7 beats (adjusted hazard ratio, 6.26; 95% confidence inter

20 , ERGC seems to be surprisingly good, easily beating all of the competitors.

21 Beat-to-beat alternation (alternans) of the cardiac action poten

22 layed a decisive role in shaping the beat-to-beat alternations in AP morphology observed during alter

23 iac alternans, described as periodic beat-to-beat alternations in contraction, action potential (AP)

24 Cardiac alternans--periodic beat-to-beat alternations in contraction, action potential (AP)

25 remains an unresolved issue whether beat-to-beat alternations in intracellular Ca(2+) ([Ca(2+)]i ) o

26 Beat-to-beat alternations of AP morphology and CaT amplitude rev

27 rodrugs increased beating rate and decreased beat amplitude in human induced pluripotent stem cell-de

28 The expression patterns of beat and side genes suggest that Beats are neuronal rece

29 ata showed that stroke rates, including tail beat and whole-body movements during feeding, were faste

30 leted zebrafish revealed compromised ciliary beating and developmental defects.

31 , except RV-B48 and HCoV-OC43, altered cilia beating and mucociliary clearance.

32 nitric oxide production to increase ciliary beating and mucociliary clearance.

33 r understanding of the regulation of ciliary beating and mucociliary transport is necessary for ident

34 a network formed by paralogs of Beaten Path (Beat) and Sidestep (Side), a ligand-receptor pair that i

35 er rate (>200 beats per minutes), longer (>7 beats), and repetitive runs of NSVT were more highly pre

36 ed based upon their beating frequency, their beating angle, and their distinct localization within th

37 pproximately 3-5-fold, and increases ciliary beating approximately 20-50%.

38 The beats are an observable signature of the ability to cont

39 patterns of beat and side genes suggest that Beats are neuronal receptors for Sides expressed on peri

40 feature vectors characterizing six types of beats are used as inputs for one-versus-one support vect

41 ng of the injection site identified matching beats arising from that site by week 1 after implantatio

42 In ciliary swimmers, ciliary beating, arrests, and changes in beat frequency are ofte

43 y monitoring bacterial motion and heart-cell beating as well as detecting infrasound power in solutio

44 These cilia beat at a native frequency and in a synchronized pattern

45 ted in form of 10-fold cross validation with beat-based and record-based training schemes.

46 , 99.82% and 99.70%, respectively, using the beat-based training scheme, and 44.40%, 88.88% and 81.47

47 increases in myocardial demand on a beat-to-beat basis and mitochondrial calcium release depends on

48 lar filling with cardiac output on a beat-to-beat basis.

49 om statistical measurements of the number of beats before initiation and before termination, respecti

50 tive and tempo-flexible synchronization to a beat, but that only certain vocal learning species are i

51 s of spatial and temporal coherence of cilia beat can be recovered and distinguished, and that if a c

52 stimulation or the patch-clamp technique in beating cardiac myocytes, we identified a neuronal NO sy

53 thin 3 min of beta-adrenergic stimulation in beating cardiac myocytes.

54 RATIONALE: During each beat, cardiac myocytes (CMs) generate the mechanical out

55 ; (2) 2-dimensional in vitro models, such as beating cardiomyocyte monolayers or small clusters of hu

56 nt stem cells (hiPSCs) and differentiated to beating cardiomyocytes (CMs).

57 nt-specific and control-iPSCs, spontaneously beating cardiomyocytes (iPSC-CMs) were observed.

58 CaCLEAN combined with 3D confocal imaging of beating cardiomyocytes provides a functional 3D map of a

59 When coupled to spontaneously beating cardiomyocytes via connexin-43-containing gap ju

60 osed to Activin differentiate precisely into beating cardiomyocytes without further treatment.

61 of fundamental properties of ECC couplons in beating cardiomyocytes without pharmacological intervent

62 They fail to form beating cardiomyocytes, generate neurons poorly, form sm

63 07 mm could supply basic energy needs in non-beating cardiomyocytes, suggesting that increased collat

64 In beating cardiomyocytes, synchronized localized Ca(2+) tr

65 ntration, showing autoregulation of Na(+) in beating cardiomyocytes.

66 and quality of cell conversion; we observed beating cells as early as 1 week after reprogramming com

67 ral-GMT and shortened the duration to induce beating cells from 30 to 10 days in mouse fibroblasts.

68 We acquired videos of single beating cells, of microbead displacement during contract

69 esia (PCD), a congenital disorder of ciliary beating, characterized by recurrent infections of the up

70 Inverted ALIs exhibit beating cilia and mucus production, consistent with conv

71 Ciliated surfaces harbouring synchronously beating cilia can generate fluid flow or drive locomotio

72 times and behavioral benefits are seen to on-beat compared with off-beat targets.

73 versed when targets are more frequent at off-beat compared with on-beat times, and that preparatory n

74 oncentrations, axonemes displayed the static beat component in absence of the dynamic component.

75 to investigate the relation between the two beat components.

76 xt]25 [Formula: see text]m) with metachronal beat creates a flow that focuses bacteria-sized particle

77 the microscopic motion of cilia during their beating cycle.

78 e maximum number of successive oscillometric beats detectable in a measurement was assessed.

79 as measured by, for example, tests of heart beat detection, perform better in laboratory studies of

80 ic ex vivo kidney perfusion (NEVKP) in heart-beating donor kidney transplantation.

81 Liver grafts procured from heart-beating donors and preserved by SCS served as controls.

82 transplantations, split grafts, or non-heart-beating donors were not included.

83 ted on a pronounced 20,000-year (precession) beat, driven by orbital forcing of summer insolation, gl

84 x providing a direct assessment of the cilia beating efficiency.

85 ective method to extract low-dimensional ECG beat feature vectors.

86 rises from hydrodynamic interactions between beating filaments.

87 ates by more than an order of magnitude; the beating flagellum is simply unable to draw enough water

88 ves rise to a thickness-independent temporal beating for transmitted pulses, an analogue of Zitterbew

89 ed to stabilize basal bodies against ciliary beating forces.

90 Here we report beat frequency (BF) QEPAS that can be used for ultra-sen

91 ical release of ATP, which increases ciliary beat frequency (CBF) and speeds up mucociliary clearance

92 nasal and bronchial cells, we imaged ciliary beat frequency (CBF), intracellular calcium, and nitric

93 rs to controls, these structures had reduced beat frequency and did not maintain hydrodynamic couplin

94 Cilia were functional with normal beat frequency and pattern.

95 rs, ciliary beating, arrests, and changes in beat frequency are often coordinated across extended or

96 It is shown that the ciliary beat frequency can be recovered to match conventional an

97 show in mouse models that ciliary length and beat frequency of the oviductal epithelial cells are reg

98 be obtained simultaneously by detecting the beat frequency signal generated when the transient respo

99 works result in cortical oscillations at the beat frequency, and that such entrained oscillations giv

100 hat not only can rapidly determine the cilia beat frequency, but also simultaneously visualize the te

101 he cholinergic rhythm, and increases ciliary beat frequency.

102 me that oral gavage of ethanol decreased the beating frequency of all three types of ependymal cilia

103 The beating frequency of each cardiac spheroid could be read

104 -II and type-III classified based upon their beating frequency, their beating angle, and their distin

105 The capacity to extract a periodic beat from a complex musical segment is remarkable, as it

106 Epinephrine increased rate of matching beats from 35+/-4.3 to 65+/-4.0 beats per minute.

107 Tested upon a total of 107049 beats from MIT-BIH arrhythmia database, our method has a

108 erage the emergence of a slowly oscillating "beat" from intersecting high-frequency electric fields t

109 fferent degrees of optionality, existence of beat gestures).

110 t time) and rhythm (appearing on beat vs off beat) had additive behavioral effects and also dissociab

111 Beat-to-beat heart rate and blood pressure responses to standing

112 ive energy sources remains superior to other beating heart techniques.

113 e ability to provide real-time images of the beating heart with good temporal resolution, combined wi

114 In the beating heart, cardiac myocytes (CMs) contract in a coor

115 lene (ePTFE) cords on mitral leaflets in the beating heart.

116 sly map Vm and epicardial contraction in the beating heart.

117 A novel device used for beating-heart image-guided MV repair demonstrates a sign

118 Transesophageal echocardiography-guided beating-heart MV repair with expanded polytetrafluoroeth

119 ene Bmi1 significantly enhanced induction of beating iCMs from neonatal and adult mouse fibroblasts.

120 SeV-GMT generated 100-fold more beating iCMs than retroviral-GMT and shortened the durat

121 easures, and how disease state and number of beats impact their reproducibility.

122 rils and to analyze loss of synchronicity of beating in cells with contractile defects.

123 physiological processes such as spontaneous beats in cardiac myocytes and glucose-dependent ATP incr

124 d delayed afterdepolarizations and triggered beats in intact cardiomyocytes.

125 As the number of paced beats increased from 1 to 5, SR Ca content (assessed wit

126 The null hypotheses were that heart beat interval fluctuations at usual breathing frequencie

127 The SERCA group shows longer heart beat intervals (Mean +/- SD: 1009.7 +/- 151.6 ms) as com

128 tracings were analyzed offline over 8 to 10 beat intervals.

129 oshock the cell, converting the breaststroke beat into a symmetric sperm-like beat, which causes a re

130 empo-flexible synchronization to an auditory beat is a fundamental component of human music.

131 t tube, the signaling mechanism coordinating beats is mechanical rather than electrical.

132 mechanisms alters the probability of ectopic beats is not understood.

133 y clearance, driven by the engine of ciliary beating, is the primary physical airway defense against

134 ndividual in a school, as well as their tail-beating kinematics.

135 ep tapping at a similar rate via an internal beat mechanism.

136 d PROP+GLYC treatment (83 +/- 5 and 85 +/- 5 beats min(-1) , P = 0.25).

137 the GLYC treatment (110 +/- 7 and 112 +/- 5 beats min(-1) , P = 0.28) and PROP+GLYC treatment (83 +/

138 increased at HA from 64 +/- 10 to 74 +/- 12 beats min(-1) during the CONT treatment (P = 0.007) and

139 nt (P = 0.007) and from 52 +/- 4 to 59 +/- 5 beats min(-1) during the PROP treatment (P < 0.001).

140 perature management (< 50, 50-59, and >/= 60 beats/min [reference]) at 12, 20, and 28 hours after ran

141 Heart rates less than 50 beats/min and 50-59 beats/min were recorded in 132 (30%)

142 nhibitory head-up tilt test (bradycardia <40 beats/min for 10 s or asystole >3 s).

143 Beta-blockers reduced ventricular rate by 12 beats/min in both sinus rhythm and AF.

144 Each increase of 5 beats/min in initial heart rate was associated with a 22

145 or patients in sinus rhythm (HR: 1.16 per 10 beats/min increase, 95% CI: 1.11 to 1.22; p < 0.0001).

146 86 had a stable heart rate, defined as </=20 beats/min variation between admission and discharge.

147 enting with a ventricular tachycardia of 190 beats/min was administered amiodarone through an acciden

148 A heart rate <70 beats/min was also associated with a lower risk for the

149 A baseline heart rate <60 beats/min was associated modestly with an increased risk

150 Bradycardia less than 50 beats/min was independently associated with lower 180-da

151 Heart rates less than 50 beats/min and 50-59 beats/min were recorded in 132 (30%) and 131 (29%) of th

152 ns of relative bradycardia (heart rate, < 80 beats/min) in septic shock are unknown.

153 during acquisition (515 +/- 35 [mean +/- SD] beats/min), whereas suboptimal heating led to a lower he

154 during acquisition (515 +/- 35 [mean +/- SD] beats/min), whereas suboptimal heating led to a lower he

155 lower heart rate and a higher SD (470 +/- 84 beats/min).

156 lower heart rate and a higher SD (470 +/- 84 beats/min).

157 with albiglutide and dulaglutide (1.4 to 3.2 beats/min).

158 of patients with heart rate <70 versus >/=70 beats/min, balanced on 58 baseline characteristics.

159 opensity scores for discharge heart rate <70 beats/min, estimated for each of the 6,286 patients, wer

160 R interval and at heart rates from 70 to 110 beats/min, in increments of 10 beats/min.

161 with a discharge heart rate <70 versus >/=70 beats/min, respectively (hazard ratio [HR]: 0.86; 95% co

162 ,369 (38%) had a discharge heart rate of <70 beats/min.

163 rom 70 to 110 beats/min, in increments of 10 beats/min.

164 CI, -12 to -1; p = 0.02), and heart rate (-6 beats/min; 95% CI, -10 to -1; p = 0.03).

165 1) but not in AF (n = 3,034; HR: 1.03 per 10 beats/min; 95% CI: 0.97 to 1.08; p = 0.38).

166 rhythm (n = 14,166; adjusted HR: 1.11 per 10 beats/min; 95% confidence interval [CI]: 1.07 to 1.15; p

167 Heart rate (98 +/- 4 vs 89 +/- 4 vs 65 +/- 2 beats/min; all p < 0.05) and cardiac output (6.7 +/- 0.3

168 d heart rate at 2 minutes recovery (44 vs 43 beats/min; P = .28).

169 .7; P = .80), maximum heart rate (174 vs 175 beats/min; P = .41), and heart rate at 2 minutes recover

170 er peak heart rates (159+/-20 versus 184+/-9 beats/min; P<0.001).

171 parable heart rates (114+/-6 versus 115+/-11 beats/min; P=0.54), the QTc interval had prolonged signi

172 from minimal hibernation levels (mean 20-25 beats/minute [bpm]; min 10 bpm) to summer active levels

173 The combination of a fast and simple bead-beating module for the disruption of the bacterial cell

174 ution imaging to characterize MT behavior in beating mouse myocytes.

175 roneurography, and blood pressure by beat-to-beat noninvasive technique.

176 To beat obesity, the least fattening of widely recognised e

177 e is in excellent agreement with vibrational beating observed in time-resolved spectroscopy experimen

178 reinhardtii swims, it uses the breaststroke beat of its two flagella to pull itself forward [1].

179 tic inclination to tap, clap, or move to the beat of music.

180 ate that a plasma undulator generated by the beating of a mixture of high-order laser modes propagati

181 ch different functions as the high-frequency beating of a wing in a hummingbird, the dilation of the

182 The periodic beating of an isolated flagellum from Chlamydomonas rein

183 ll shape and size, misplacement and abnormal beating of cilia, blebbing of the microvilli.

184 ult of leftward flow generated by asymmetric beating of nodal cilia, which eventually induces asymmet

185 d oscillations give rise to the percept of a beat or a pulse.

186 arm and hand) was performed in 9 human heart-beating organ donors.

187 me (57.2+/-12.8 mL/beat versus 30.8+/-6.9 mL/beat; P<0.001) were observed.

188 s discovered a network formed by paralogs of Beaten Path (Beat) and Sidestep (Side), a ligand-recepto

189 d by high-speed video-microscopy and ciliary beat pattern is inferred.

190 hat anchor forces produced by the asymmetric beat pattern of motile cilia.

191 simultaneously visualize the temporal cilia beating pattern which plays critical roles in cilia func

192 nfrared brightness evolution is dominated by beat patterns caused by planetary-scale wave pairs and b

193 Characterization of cardiomyocyte beat patterns is needed for quality control of cells int

194 multiple orbital state admixtures, observing beat patterns produced by Zeeman splitting.

195 tificial cilium that could mimic the complex beating patterns of its biological counterpart.

196 mm, (-2.3 to 0.3, p=0.0128), heart rate -3.0 beats per min (-5.1 to -0.8, p=0.0070), and N-terminal p

197 zanimod-treated participants was less than 2 beats per min (bpm) compared with baseline, with no pati

198 omen (1.72, 1.19-2.49); and heart rate 60-90 beats per minute (1.21, 0.89-1.63) and >/=90 beats per m

199 beats per minute (1.21, 0.89-1.63) and >/=90 beats per minute (2.35, 1.03-5.33).

200 was associated with NSVT runs at a rate >200 beats per minute (adjusted hazard ratio, 15.63; 95% conf

201 -75th percentile) baseline heart rate was 63 beats per minute (bpm) (57-71 bpm).

202 (standard deviation) in the AF group and 63 beats per minute +/- 14 in the SR group (P < .01).

203 sults Mean heart rate during scanning was 83 beats per minute +/- 21 (standard deviation) in the AF g

204 CI, 340-358; P < .01), resting HR (mean, 84 beats per minute [bpm]; 95% CI, 82-86 to 74 bpm; 95% CI,

205 scription) with resting heart rates above 82 beats per minute had a 69% (95% CI, 46%-94%) increased r

206 hodromic reciprocating tachycardia (176+/-44 beats per minute versus 229+/-31 beats per minute; P=0.0

207 y predicted resting heart rate increase of 5 beats per minute was associated with a 20% increase in m

208 tachycardia/ventricular fibrillation >/= 240 beats per minute was equivalent to the control survival

209 ss II-IV, sinus rhythm, and heart rate >/=70 beats per minute) and non-SHIFT type.

210 on (extreme bradycardia with heart rate </=4 beats per minute) superimposed on exercise up-regulation

211 Slower (</=200 beats per minute), shorter (</=7), or a single run of NS

212 picardially tested in a euthanized pig at 60 beats per minute, 2 V amplitude, and 1 ms pulse width, r

213 f matching beats were 53+/-6.9 and 69+/-10.4 beats per minute, respectively, at 4 weeks.

214 a generic rate threshold between 185 and 200 beats per minute, which exceeds the rate tested in clini

215 an 90 mm Hg or a heart rate greater than 120 beats per minute.

216 cardiac chronotropic response upon tilt > 10 beats per minute.

217 d with men with resting heart rates below 62 beats per minute.

218 0.5 +/- 3.2 with median 0 (range, -8 to 17) beats per minute.

219 al biological pacemaker rates were 45 and 75 beats per minute.

220 raphy demonstrated normal sinus rhythm at 73 beats per minute.

221 of matching beats from 35+/-4.3 to 65+/-4.0 beats per minute.

222 a (176+/-44 beats per minute versus 229+/-31 beats per minute; P=0.001), and longer ventriculo-atrial

223 Faster rate (>200 beats per minutes), longer (>7 beats), and repetitive ru

224 s help narrow the search for valid models of beat perception.SIGNIFICANCE STATEMENT Humans perceive m

225 targets appearing frequently at a fixed off-beat position; (2) a rhythmic stream with targets appear

226 e) when a larger Ca(2+) transient at a given beat prolongs (shortens) the action potential duration (

227 ic electrical signals regulate the intrinsic beating properties of cardiomyocytes.

228 potentiated doxorubicin-induced decrease in beating rate and amplitude of iPS-derived cardiomyocytes

229 with amiodarone, L-ala,SP prodrugs increased beating rate and decreased beat amplitude in human induc

230 r cardiomyocyte differentiation capacity and beating rate and suppressed the smooth muscle cell forma

231 Cardiomyocytes adapt their autonomous beating rate to the frequency at which they were stimula

232 cardiomyocytes are characterised by a lower beating rate, disorganised sarcomeres and sarcoplasmic r

233 nipulation, PHOX2B::eGFP+ neurons controlled beating rates of cardiomyocytes, and the physical intera

234 ification are two main tasks in abnormal ECG beat recognition.

235 ding to perceptual and motor benefits for on-beat, relative to off-beat, times, even if the rhythmic

236 Voluntary movement and the heart beat require this calcium flow to be massive and fast.

237 erent beats to be categorized by the loading beat RR duration and beat RR duration.

238 egorized by the loading beat RR duration and beat RR duration.

239 rillatory cycle lengths with varying beat-to-beat sequences suggestive of unstable trajectories attac

240 mon model systems, and the complex flagellar beating shapes that power it make its quantitative descr

241 sheltered zones; there, a field of randomly beating short cilia ([Formula: see text]10 [Formula: see

242 , we 'deorphanized' four more members of the Beat-Side network.

243 and biasing of pairs of lasers, the optical beat signal can be tuned continuously over the range fro

244 nstrate control over the presence of quantum-beating signals by packing structurally flexible synthet

245 Understanding the origin of beating signals in the spectra of photosynthetic complex

246 olonged coherence lifetimes revealed through beating signals in the spectra of some systems may resul

247 re necessary to enhance the observed quantum-beating signals.

248 We also observe quantum beats, so-called vacuum Rabi oscillations, between the u

249 Cardiac tissue patches of all cell ratios beat spontaneously after 3D bioprinting.

250 h our stiffness measurements at the onset of beating, suggesting that mechanical signaling may initia

251 vation by considering the advantages of tail-beating synchronization between neighbors, which we have

252 EHTs beat synchronously by day five and exhibited robust leng

253 hich began generating calcium transients and beating synchronously within 1 day of seeding; the speed

254 expressed in the slowing of responses to on-beat targets, but not in the facilitation of off-beat ta

255 targets, but not in the facilitation of off-beat targets.

256 nefits are seen to on-beat compared with off-beat targets.

257 s, achieving performance that equals or even beats that of humans in some respects.

258 ns even with orders in the millions and thus beat the curse of dimension.

259 eparatory neural activity peaks at rhythm-on-beat times and behavioral benefits are seen to on-beat c

260 Shifting resources away from on-beat times was expressed in the slowing of responses to

261 In the second experiment, off-beat times were jittered, resulting in a similar CNV adj

262 e more frequent at off-beat compared with on-beat times, and that preparatory neural activity, previo

263 sly thought to be driven by the rhythm to on-beat times, is adjusted toward off-beat times.

264 tomatic, bottom-up resource attractors to on-beat times-preparatory neural activity peaks at rhythm-o

265 ing rhythms to direct resources away from on-beat times.

266 thm to on-beat times, is adjusted toward off-beat times.

267 ream with targets appearing frequently at on-beat times; and (3) a nonrhythmic stream with matched ta

268 motor benefits for on-beat, relative to off-beat, times, even if the rhythmic stream is not intentio

269 aging with patient ECG allowed for different beats to be categorized by the loading beat RR duration

270 Beat-to-beat alternation (alternans) of the cardiac acti

271 ICaCC played a decisive role in shaping the beat-to-beat alternations in AP morphology observed duri

272 Cardiac alternans, described as periodic beat-to-beat alternations in contraction, action potenti

273 Cardiac alternans--periodic beat-to-beat alternations in contraction, action potenti

274 ever, it remains an unresolved issue whether beat-to-beat alternations in intracellular Ca(2+) ([Ca(2

275 Beat-to-beat alternations of AP morphology and CaT ampli

276 ction to increases in myocardial demand on a beat-to-beat basis and mitochondrial calcium release dep

277 ventricular filling with cardiac output on a beat-to-beat basis.

278 Beat-to-beat heart rate and blood pressure responses to

279 A by microneurography, and blood pressure by beat-to-beat noninvasive technique.

280 the fibrillatory cycle lengths with varying beat-to-beat sequences suggestive of unstable trajectori

281 The cardiac beat-to-beat variation evoked at the moment of lung infl

282 Beat-to-beat variation in heart rate (f H ) has been use

283 For each beat type, global volumes were quantified via summation

284 depending on the frequency of each observed beat type.

285 obal functional measurement of the different beat types based on timing demonstrated differences in p

286 rements of a Newtonian flow induced by cilia beating (using micro-beads as tracers) and a mathematica

287 beat-V genes, encoding Side-VI receptors, are expressed

288 The cardiac beat-to-beat variation evoked at the moment of lung inflation ac

289 Beat-to-beat variation in heart rate (f H ) has been used as a t

290 001), and regurgitant volume (57.2+/-12.8 mL/beat versus 30.8+/-6.9 mL/beat; P<0.001) were observed.

291 odies against the forces produced by ciliary beating via distinct yet interdependent mechanisms.

292 vs irrelevant time) and rhythm (appearing on beat vs off beat) had additive behavioral effects and al

293 The beating waves have similar amplitudes but slightly diffe

294 defibrillation, return of spontaneous heart beat, weanability from extracorporeal cardiopulmonary re

295 Maximum night and day rates of matching beats were 53+/-6.9 and 69+/-10.4 beats per minute, resp

296 By week 4, 20% of beats were electronically paced, 60% to 80% of beats wer

297 ats were electronically paced, 60% to 80% of beats were matching, and mean and maximal biological pac

298 reaststroke beat into a symmetric sperm-like beat, which causes a reversal of the direction of swimmi

299 the frequencies of sounds generated by their beating wings [5].

300 A single-photon beating with itself can produce even the most elaborate