ライフサイエンスコーパス: rhythmic

1 e mammalian circadian clock encodes time via rhythmic action potential activity in the suprachiasmati

2 ing insight into the mechanism that produces rhythmic action potential firing in SCN.

3 Rhythmic action potentials and intercellular Ca(2+) wave

4 Rhythmic actions benefit from synchronization with exter

5 The synchronous rhythmic activation of cholinergic cells drives the coor

6 he homolog of yeast and mammalian GCN2), and rhythmic activation of CPC-3 was abolished under conditi

7 Cycling P-eIF2alpha levels required rhythmic activation of the eIF2alpha kinase CPC-3 (the h

8 itory interneuron are known to shape diverse rhythmic activities in the cortex, but how they interact

9 ANCE STATEMENT Slow forms of thalamocortical rhythmic activity are thought to be essential for memory

10 Respiration is a rhythmic activity as well as one that requires responsiv

11 which non-rhythmic Treg cells are driven to rhythmic activity by systemic signals to confer a circad

12 How mammalian neural circuits generate rhythmic activity in motor behaviors, such as breathing,

13 naptic mechanisms that mediate slow forms of rhythmic activity in thalamic circuits.

14 ace of circuit configurations giving rise to rhythmic activity in the crustacean stomatogastric gangl

15 chronization and for probing the function of rhythmic activity in the healthy brain.SIGNIFICANCE STAT

16 otide-gated (HCN) channels are essential for rhythmic activity in the heart and brain, and mutations

17 major regulators of synaptic plasticity and rhythmic activity in the heart and brain.

18 We show that fast rhythmic activity in the prefrontal cortex becomes promi

19 sm, as many of these images amplify 30-80 Hz rhythmic activity in the visual brain.

20 ice of either sex, we recorded slow forms of rhythmic activity in TRN neurons, which were driven by f

21 -type Ca(2+) channel that contributes to the rhythmic activity of adult DA neurons in the substantia

22 ted while crawling was monitored through the rhythmic activity of DE-3.

23 le contribution of thalamic circuits to slow rhythmic activity remain unclear.

24 nisms, only the latter accommodates observed rhythmic activity supporting rule-based decision making

25 The basic rhythmic activity that underlies stepping is generated b

26 receiving attended signals align their gamma-rhythmic activity to that of the sending populations, su

27 with >60% of channels presenting significant rhythmic activity were either mesial or temporal basal s

28 Theta-band (~6 Hz) rhythmic activity within and over the medial PFC ("midfr

29 tary action is also accompanied by prominent rhythmic activity, and recent behavioral evidence sugges

30 s tightly linked to the phase of local gamma-rhythmic activity, with maximal signal content occurring

31 may reciprocally organize subcortical theta-rhythmic activity.

32 ocal circuits to generate different forms of rhythmic activity.

33 abilities at the command of network-specific rhythmic activity.SIGNIFICANCE STATEMENT The cerebellum

34 the putative frontal eye field in marmosets, rhythmic alpha-band activity (9-14 Hz) was higher in dee

35 se data are consistent with a model in which rhythmic alpha-band activity in deeper layers inhibits s

36 They support a rhythmic, alpha-pulsed organization of dynamic attention

37 ividual-level analyses, 14% of profiles were rhythmic and 4% were linear.

38 roup-level analyses, 22% of metabolites were rhythmic and 8% were linear, whereas in individual-level

39 Of the group-rhythmic and group-linear metabolites, only 7% and 12% w

40 rmore, we show that gsn promoter activity is rhythmic and is directly controlled by core clock compon

41 ead, perhaps universal; that music varies in rhythmic and melodic complexity; and that elements of me

42 es but also demonstrate fundamental roles of rhythmic and metabolic genes in the physiology and behav

43 ng analysis showed that GmPRR3b(H6) displays rhythmic and photoperiod-dependent expression and is pre

44 German, a nonnative language that shares key rhythmic and prosodic properties with their own native l

45 oscillators in the SFO and OVLT are strongly rhythmic and require action potential-dependent communic

46 vioral circadian rhythms in bees that remain rhythmic, and impairs sleep.

47 Moreover, AS-related genes exhibited rhythmic AS and APA regulation, adding another layer of

48 Taken together, our characterization of the rhythmic B. distachyon transcriptome represents a founda

49 on-identical neurons and synapses underlying rhythmic behavior, we analyzed the circuits' response to

50 Endogenous rhythmic behaviors are evolutionarily conserved and esse

51 s modulate the neuronal circuits controlling rhythmic behaviors, including sleep [1].

52 The rhythmic behaviour of these systems corresponds to high

53 is by paired-end tag (ChIA-PET) reveals that rhythmic BMAL1 target gene expression correlates with rh

54 This rhythmic brain activity interacts in complex ways with r

55 Entrainment couples rhythmic brain activity to external and internal rhythmi

56 Highly rhythmic burst-firing parvalbumin-positive GABAergic med

57 The reciprocal rhythmic bursting by the pGABA and pNon-GABA neurons dro

58 in mice revealed that they can discharge in rhythmic bursts at theta frequencies and drive theta act

59 ction by their intrinsic ability to generate rhythmic bursts of action potential.

60 1) is in the CPG underlying swimming, firing rhythmic bursts of action potentials as part of the swim

61 signals should be transferred through gamma-rhythmic bursts of information, resulting in a modulatio

62 First doses from each order were also rhythmic but shifted by 2 h.

63 While individual sites displayed rhythmic Ca(2+) events, the overall pattern of Ca(2+) tr

64 nesis, temporal patterns of auxin arise from rhythmic centrifugal waves of high auxin travelling thro

65 DNA replication is essential for the rhythmic changes of nucleosome composition at the frq pr

66 for transmission delays and be predictive of rhythmic changes.

67 BMAL1 target gene expression correlates with rhythmic chromatin interactions.

68 omics efforts have found relationships among rhythmic chromatin modifications at clock-controlled gen

69 Focusing on a family of rhythmic circuits, we propose a computational approach t

70 However, rhythmic clock gene expression in other brain sites rais

71 Finally, rhythmic clock gene expression is lost in Liver-RE mice

72 ng durations of dynamic mixed perception are rhythmic clusters of durations whose incidence falls wit

73 Rhythmic collagen degradation by CTSK maintains collagen

74 Many of the rhythmic components were replicated in primary AECs cult

75 Under rhythmic conditions, in each cycle, an inspiratory burst

76 indicate that exercise hyperaemia following rhythmic contractions at 60% maximum voluntary contracti

77 Rhythmic contractions of the renal pelvis transport urin

78 ial environment and ion channels to generate rhythmic contractions.

79 cape and the 2 degrees Mn conferring weaker, rhythmic contractions.

80 hibited spontaneous and carbachol-stimulated rhythmic contractions.

81 onstructed a parsimonious model that depicts rhythmic control imposed upon basic mRNA expression and

82 the potential role of mWAKE(+) cells in the rhythmic control of diverse behaviors and physiological

83 ression of deadenylases, regardless of other rhythmic controls, can robustly cluster the rhythmic mRN

84 eously deployed high-density probes revealed rhythmic coupling of the retrosplenial cortex with anato

85 Stimulation (tACS) is a method that injects rhythmic currents into the human brain via electrodes at

86 on of GR in the bronchial epithelium blocked rhythmic CXCL5 production, identifying GR as required to

87 ing behaviorally relevant locations in theta-rhythmic cycles (3-6 Hz).

88 e and the model is easy to interpret complex rhythmic data.

89 Our findings highlight the critical role of rhythmic deadenylation in regulating poly(A) rhythms and

90 greater than or equal to 1.5 Hz lateralized rhythmic delta activity or generalized periodic discharg

91 ble analyses in the lobar group, lateralized rhythmic delta activity predicted electrographic seizure

92 intraparenchymal hemorrhage and lateralized rhythmic delta activity were six times as likely to have

93 riodic discharges, spike-wave complexes, any rhythmic delta other than generalized.

94 tion and reception of coordinated, entrained rhythmic displays is a co-evolved system for credibly si

95 r-PAC) can be used to relate the output of a rhythmic "driver" network (i.e., high gamma) to the inpu

96 Light-entrained circadian clocks confer rhythmic dynamics of cellular and molecular activities t

97 ronal populations, which display coordinated rhythmic dynamics that support interareal communication.

98 The mechanisms underlying these rhythmic dynamics, their interactions, and their functio

99 ext of a classical visual SL task, divergent rhythmic EEG activity in the interstimulus delay periods

100 dependent upon multiple mechanisms to ensure rhythmic electrical activity that varies between day and

101 Rhythmic electrical and mechanical behaviours of LM are

102 GNIFICANCE STATEMENT "Midfrontal theta" is a rhythmic electrophysiological signature of the competiti

103 an of a mouse relies on stem cell-maintained rhythmic endometrial regeneration.

104 Critically, evidence for conjoined full-body rhythmic entrainment in great apes that could help recon

105 daptations that are specific to music (e.g., rhythmic entrainment) and the effects of adaptations for

106 However, the molecular basis for rhythmic epigenetic modifications and circadian regulati

107 parasite population remains synchronous and rhythmic even in an arrhythmic clock mutant host.

108 hmic brain activity to external and internal rhythmic events, serving fine-grained routing and modula

109 This rhythmic excitability has been widely observed but, crit

110 explore two other possible manifestations of rhythmic excitability in the beta band; windows of reduc

111 ch the regular oscillations corresponding to rhythmic expiration and inspiration are modulated by slo

112 illator is a gene network which orchestrates rhythmic expression across the day/night cycle.

113 Additionally, a cosinor analysis found rhythmic expression for approximately 11.9% of all 17 66

114 Its daily rhythmic expression in Arabidopsis (Arabidopsis thaliana

115 We propose CIRBP to play a role because its rhythmic expression is i) sleep-wake driven and ii) nece

116 restingly, the PVH exhibits BMAL1-controlled rhythmic expression of GABA-A receptor gamma2 subunit, a

117 dicated that Clk disruption abolished normal rhythmic expression of miR-375 and the functional regula

118 rane procollagen transport by the sequential rhythmic expression of SEC61, TANGO1, PDE4D and VPS33B.

119 CREBH regulates the rhythmic expression of the genes encoding the rate-limit

120 Furthermore, CREBH regulates rhythmic expression of the key autophagy genes in the li

121 We found that the rhythmic expression of these genes was abolished in cloc

122 ription factor CLOCK:BMAL1 to coordinate the rhythmic expression of thousands of genes.

123 Bmal1 coordinates the rhythmic expression of transcriptome and regulates biolo

124 transcribed strand (TS) of these genes in a rhythmic fashion unique to each gene's phase of transcri

125 riven tissue autonomous clocks occur without rhythmic feeding behavior and are lost in constant darkn

126 Malarial rhythmic fevers are the consequence of the synchronous b

127 which increases neurotransmitter release and rhythmic firing activity of dopamine neurons.

128 ng literature indicating that ELA alters the rhythmic firing of neurons in brain regions associated w

129 The link established between rhythmic firing patterns and complex attractor dynamics

130 ippocampal formation, contains high- and low-rhythmic-firing neurons (HRNs and LRNs, respectively), w

131 imilar or different cortical regions to high-rhythmic-firing neurons (HRNs) and assessed their tempor

132 We investigated whether low-rhythmic-firing neurons (LRNs) innervated similar or dif

133 polarized as the Vm underwent high amplitude rhythmic fluctuations lasting 1-2 s in duration.

134 Brain oscillations involve rhythmic fluctuations of neuronal excitability and may p

135 FICANCE STATEMENT Brain oscillations involve rhythmic fluctuations of neuronal excitability.

136 insic circadian oscillators, suggesting that rhythmic function might be a consequence of external sig

137 veness in dynamic activity changes involving rhythmic GABAergic neurotransmission mediates diurnal rh

138 When considering the overlap in rhythmic gene expression and specific pathway behavior,

139 co-expression network approach to associate rhythmic gene expression changes with physiological resp

140 us biological functions under clock control, rhythmic gene expression is tissue-specific despite an i

141 d a molecular signature of seasonal-specific rhythmic gene expression that included several genes bel

142 nscriptional mechanisms collectively control rhythmic gene expression.

143 ar 24-h rhythms and regulates the downstream rhythmic gene expression.

144 which established that a large proportion of rhythmic genes are governed by the homeostatic process w

145 e it has become clear that the percentage of rhythmic genes varies among mouse tissues, it remains un

146 ignificantly altered expression of circadian rhythmic genes, inflammatory response genes, and iron me

147 Here, we reveal rhythmic genome-wide alternative splicing (AS) of pre-mR

148 lay integral roles in circadian biology, its rhythmic genomic actions have never been characterized.

149 i.e., Type II cells (64% of total) generated rhythmic, global Ca(2+) transients at the SW frequency t

150 l of pulmonary neutrophilia persists without rhythmic glucocorticoid availability.

151 ary inflammatory responses is independent of rhythmic glucocorticoid signaling in airway epithelial c

152 letion of gpn abolished gsn mRNA rhythms and rhythmic glycogen accumulation.

153 d CSP-1, modulate the phase and amplitude of rhythmic gsn mRNA, and these changes are similarly refle

154 Recent work has identified rhythmic gut contractions in human, mice, and hydra to b

155 irectly for H3K4me3 modification, leading to rhythmic H3K4me3 changes in target genes.

156 g, healthy subjects performed maximal-effort rhythmic handgrip exercise for 5 min under control condi

157 ed forearm vascular conductance (FVC) during rhythmic handgrip exercise under control conditions and

158 knowledge gap, nine healthy males performed rhythmic handgrip exercise with simultaneous measurement

159 alignment (the latter to a higher extent for rhythmic high-beta patterns than random patterns) while

160 and JMJ14 expression, which in turn regulate rhythmic histone modification dynamics for the clock and

161 , however, most of these transcripts are not rhythmic in subjects with schizophrenia.

162 Rhythmic in-host parasite replication is responsible for

163 r the 24-h cycle and are responsible for the rhythmic induction of genes involved in autophagy during

164 Moreover, whether such rhythmic infra-slow activity patterns exist in awake beh

165 hat high dopamine-induced periodic FSI gamma-rhythmic inhibition enables switching between beta-rhyth

166 We find evidence for strong rhythmic inhibition in these neurons, suggesting that th

167 indbrain and spinal cord, where they provide rhythmic input to major motor control centers.

168 nisms could look very similar in the case of rhythmic input, but an oscillator might better provide t

169 es how novel oscillations are generated when rhythmic inputs converge on a nonlinearly activating tar

170 early day response of this circuit with dual rhythmic inputs is sensitive to the changes in daylength

171 urons types in the OB in response to dynamic rhythmic inputs.

172 others, like audition, are faced with mostly rhythmic inputs.

173 islets gain persistent chromatin changes and rhythmic insulin responses with a raised glucose thresho

174 hanistic explanation for previously observed rhythmic interactions and transitions, our model suggest

175 oscillations remained mostly unaffected but rhythmic Klf10 expression was abolished in this model.

176 cardiovascular complications, the role that rhythmic leukocyte adhesion plays in different vascular

177 rgic receptors to assess their relevance for rhythmic leukocyte adhesion.

178 suggest that specific compounds may counter rhythmic LFPs to produce superior signal-to-noise charac

179 intrinsic oscillator maintains Plasmodium's rhythmic life cycle.

180 hasically in bursts (>100 Hz) when driven by rhythmic light pulses at theta (4 or 8 Hz) frequencies.

181 e investigated the effects of DAA and DAQ on rhythmic local field potentials (LFPs) occurring in the

182 er cells may instantiate a subcortical theta-rhythmic loop of spatial feedback.

183 standing and locomotion after five weeks of rhythmic manual stimulation of triceps surae muscles (no

184 Defective rhythmic metabolism is associated with high-fat high-cal

185 nals and cell-cell communication controlling rhythmic metabolism.

186 This phase shift was governed by a rhythmic microenvironment and a vessel type-specific osc

187 We demonstrate that pulse trains of rhythmic MNS, delivered at 12 Hz, entrain sensorimotor m

188 stent with this idea, IRt inhibition blocked rhythmic motor and autonomic components of fictive swall

189 levant as excitation of T cells affected the rhythmic motor pattern, probably acting upon the rhythmo

190 generators (CPGs) that autonomously produce rhythmic motor patterns.

191 the command neuron initiates and accelerates rhythmic motor patterns.

192 on, airway and exocrine gland secretion, and rhythmic movements of the gastrointestinal system.

193 central pattern generator (CPG), coordinate rhythmic movements underlying locomotion.

194 During the generation of rhythmic movements, most spinal neurons receive an oscil

195 rhythmic controls, can robustly cluster the rhythmic mRNAs by their peak phases in poly(A) tail leng

196 Furthermore, we demonstrate that although rhythmic mu stimulation has statistically significant bu

197 tive for influencing the hippocampus because rhythmic neural activity in the theta band is associated

198 used to infer the direction and strength of rhythmic neural transmission between distinct brain netw

199 reby establish the direction and strength of rhythmic neural transmission.

200 ts support the hypothesis that a cross-areal rhythmic neuronal coordination is intrinsic to cognitive

201 y recurring and predictable changes, such as rhythmic nutrient availability, and to adapt cellular fu

202 The top pathways identified in transcripts rhythmic only in subjects with schizophrenia are associa

203 implications for clinical interpretation of rhythmic onset seizures.

204 an neocortex and mesial temporal lobe during rhythmic onset seizures.

205 sting for causal significance, we found that rhythmic optogenetic activation of retrosplenial cortex

206 tes, only 7% and 12% were also significantly rhythmic or linear, respectively, in >=50% of participan

207 task, while they received brief patterns of rhythmic or random transcranial magnetic stimulation (TM

208 dings highlight GR's fundamental role in the rhythmic orchestration of hepatic metabolism.

209 tion provided by the hormone auxin regulates rhythmic organ production at the shoot apex, but the spa

210 Cortical tremor is a fine rhythmic oscillation involving distal upper limbs, linke

211 For example, yeast cultures exhibit rhythmic oscillatory behavior in high cell-density conti

212 ttern generator (CPG) circuitry produces the rhythmic output necessary for limb coordination during l

213 fects were accompanied by a reduction in the rhythmic output of subthalamic nucleus (STN) neurons and

214 Finally, loss of rhythmic P-eIF2alpha levels led to reduced linear growth

215 This rhythmic pattern is altered by high-fat diet in a ligand

216 pecific neuronal circuits control the actual rhythmic pattern of movements.

217 n that activity in the STN is modulated in a rhythmic pattern when Parkinson's patients perform stepp

218 contraction phase temporarily disrupted the rhythmic pattern.

219 sing this control approach for generation of rhythmic patterns for synchronized limb movement.

220 ncy Modulated Mobius (FMM) model to describe rhythmic patterns in oscillatory systems.

221 n the peripheral system as phase shifting in rhythmic patterns.

222 ngaging an evolutionary perspective on human rhythmic perception and cognition.

223 Rhythmic, periodic, or ictal patterns were referred to a

224 how different tissues achieve a synchronized rhythmic physiology.

225 To understand the role of rhythmic poly(A) regulation in circadian gene expression

226 evidence has demonstrated the importance of rhythmic post-transcriptional controls, and it remains u

227 These 5-10 Hz rhythmic potentials increase the background firing rate

228 Rhythmic preBotC population activity consists of strong

229 at environmental sampling is a fundamentally rhythmic process.

230 n the biosynthetic pathway(s) regulating the rhythmic production of the pineal hormone melatonin, whi

231 ation between calcium transient activity and rhythmic proneuronal transcription factor expression in

232 ental mechanism by which the clock regulates rhythmic protein production, and provide key insights in

233 d the impact of this potential regulation on rhythmic protein synthesis, were not known.

234 Surprisingly, rhythmic pulmonary neutrophilia persisted, despite nonrh

235 We investigated whether rhythmic pulses of median nerve stimulation (MNS) could

236 hat the downstream effect of synchronous and rhythmic Purkinje cell discharges depends on the type of

237 that the onset of tremor is coincident with rhythmic Purkinje cell firing, which alters the activity

238 network (i.e., high gamma) to the input of a rhythmic "receiver" network (i.e., theta) and thereby es

239 ve transcription factors, we discovered that rhythmic redox control of CLOCK directly by endogenous H

240 hiasmatic nucleus (SCN) of mice, disturb the rhythmic redox control of CLOCK function, reprogram hepa

241 ammalian circadian clock is deeply rooted in rhythmic regulation of gene expression.

242 iptional repressors REV-ERBalpha and beta as rhythmic regulators of Srebp1 in BAT.

243 ose administration and was necessary for the rhythmic release of insulin and diurnal glycemic control

244 This clock drives rhythmic repression of inflammatory arthritis during the

245 This rhythmic reweighting alternately promotes either samplin

246 A rhythmic reweighting of pulvino-cortical interactions th

247 Underlying this rhythmic sampling are intrinsic theta oscillations in fr

248 d pulvino-cortical interactions during theta-rhythmic sampling by simultaneously recording from macaq

249 suprachiasmatic nucleus which regulates the rhythmic secretion of melatonin.

250 While it is known that rhythmic sensory events can entrain brain oscillations a

251 Two largely independent research lines use rhythmic sensory stimulation to study visual processing.

252 rimentally investigated and even modified by rhythmic sensory stimuli or invasive and non-invasive ne

253 EEG was recorded while subjects listened to rhythmic sequences.

254 Here we show that in woodpecker drumming, a rhythmic signal used during mating and territorial defen

255 ed between reward deliveries, found that the rhythmic signals persisted during periods of dry licking

256 actors while subjects attend to a controlled rhythmic sound sequence, we find that salient events in

257 It is not known whether this "inaudible" rhythmic sound stream also induces entrainment.

258 found that significant phase locking to the rhythmic sounds preceded participants' detection of them

259 ocampal sites to study spatial modulation of rhythmic spike timing in rats freely exploring an open e

260 ic inhibition enables switching between beta-rhythmic SPN cell assemblies representing the currently

261 A rhythmic stimulation cycle was programmed to create a mo

262 ng post-hoc only those participants in which rhythmic stimulation enhanced visual detection, the magn

263 le for synchronization of auditory cortex to rhythmic structure in sounds including speech and music.

264 to tones in one ear only, while keeping the rhythmic structure of tones constant.

265 The escape response and rhythmic swimming in zebrafish are distinct behaviors me

266 ole cord, V1 hyperpolarization increased the rhythmic synaptic drive to flexor and extensor motoneuro

267 he period, amplitude, duration, and shape of rhythmic synaptic input.

268 g the day in vitro and was necessary for the rhythmic synthesis of select proteins in vivo.

269 inally, a better tapping performance in this rhythmic task was related to alpha power modulations in

270 evidence that selective attention relies on rhythmic temporal coordination between visual areas, and

271 ing by the pGABA and pNon-GABA neurons drove rhythmic theta activity in the EEG.

272 ysis of the model demonstrates that accurate rhythmic time keeping can be achieved over a range of fr

273 The effect of rhythmic TMS on WM performance was dependent on whether

274 ole of these neural oscillations, we applied rhythmic transcranial magnetic stimulation (TMS) in eith

275 nvasively stimulating with theta versus beta rhythmic transcranial magnetic stimulation.

276 that BMAL1 ability to drive tissue-specific rhythmic transcription is associated with not only the a

277 In mammals, BMAL1 and CLOCK activate rhythmic transcription of genes including the nuclear re

278 eceptor alpha, inducing microbiota-dependent rhythmic transcription of the lipid transporter gene Cd3

279 cked feedback loop in Drosophila is to drive rhythmic transcription required for overt rhythms.

280 egulation of metabolism is largely driven by rhythmic transcriptional activation of clock-controlled

281 Rhythmic transcriptional control mediated by the circadi

282 ing, but strikingly also the gain of a novel rhythmic transcriptome in Bmal1-targeted cells.

283 the loss of hepatocyte REV-ERBs remodels the rhythmic transcriptomes and metabolomes of multiple cell

284 There was only partial overlap of our rhythmic transcripts with published animal adipose and h

285 expression is restricted to ~10% of normally rhythmic transcripts.

286 s with schizophrenia have a different set of rhythmic transcripts.

287 roduction, and provide key insights into how rhythmic translation, cellular energy, stress, and nutri

288 These data support a model in which non-rhythmic Treg cells are driven to rhythmic activity by s

289 tetanic contraction (100 Hz, 500 ms) and to rhythmic twitch contractions (4 Hz, 30 s) was impaired a

290 During rhythmic twitch contractions, slow onset vasodilatation

291 Most transcripts that were rhythmic under AL lost their rhythms, and many new trans

292 For most transcripts that were rhythmic under all conditions, including many known cloc

293 s, including the circadian clock genes, were rhythmic under both diets.

294 icosterone concentrations were significantly rhythmic under LD, but not under LLbright and DLAN.

295 Cortical tremor is considered a rhythmic variant of cortical myoclonus and is part of th

296 mpt to phase lock, or entrain, alpha through rhythmic visual stimulation under the assumption that th

297 ed human EEG data, recorded during bilateral rhythmic visual stimulation, we find the typical SSR gai

298 ial control via phosphorylation also governs rhythmic WCC binding to the promoters of clock-controlle

299 We found that during rhythmic whisker movement, 54 of 115 active neurons (47%

300 ere able to completely synchronize their own rhythmic wrist or arm movement with the movement of the