ライフサイエンスコーパス: rhythmical

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1 We demonstrate that observation of everyday rhythmical actions biases subsequent motor execution of

2 These features may favor occurrence of rhythmical activities in thalamocortical networks.

3 The recovery of rhythmical alternating movements, such as locomotion, is

4 This change in rhythmical brain activity leads to modulation of visual

5 ribed subthreshold membrane oscillations and rhythmical burst discharge in Mes V neurons from rats ag

6 ection, which has been suggested to underlie rhythmical bursting in Parkinson's disease, we first mea

7 from an irregular discharge to a pattern of rhythmical bursting in synchrony with hippocampal theta

8 to the MS/DB may normally act to inhibit the rhythmical bursting of MS/DB neurons, thereby producing

9 Spontaneous rhythmical [Ca2+]i oscillations were observed in ICCs af

10 g normal excitation-contraction coupling and rhythmical contraction.

11 in cued gait performance with three external rhythmical cues (ERC) (auditory, visual and somatosensor

12 ocimetry, we show that fertilization induces rhythmical cytoplasmic movements that coincide with puls

13 Spontaneous rhythmical depolarizations with superimposed action pote

14 Consequently, we suggest that such rhythmical discharges are neither a 'local sign' sympath

15 We suggest that the rhythmical discharges following the initial excitatory r

16 The characteristic rhythmical discharges of single postganglionic sympathet

17 a period of reduced discharge and subsequent rhythmical discharges seemingly phase-locked to the stim

18 inal ganglia responded to CCAP by generating rhythmical ecdysis bursts.

19 resulting in dissociation of the average and rhythmical effects of sympathetic activity.

20 the retrogradely labeled pTRG neurons showed rhythmical excitatory currents in tune with respiratory

21 In vivo, XIIts MNs displayed rhythmical, expiratory-related activity.

22 and coherence analyses demonstrated that the rhythmical firing pattern of MS/DB neurons strongly corr

23 rn of MS/DB neurons strongly correlated with rhythmical fluctuations in the hippocampal EEG during pe

24 e water reabsorption were counterbalanced by rhythmical glucocorticoid release, with excretion of end

25 mical mineralocorticoid release and elevated rhythmical glucocorticoid release.

26 aptic input to trigeminal motoneurons during rhythmical jaw movements.

27 ctivity of CVC(like) SPNs was underpinned by rhythmical membrane potential oscillations suggestive of

28 umans regulate osmolyte and water balance by rhythmical mineralocorticoid and glucocorticoid release,

29 crease in salt intake decreased the level of rhythmical mineralocorticoid release and elevated rhythm

30 evels of salt intake, half-weekly and weekly rhythmical mineralocorticoid release promoted free water

31 and to refractory periods which control the rhythmical motility of many hollow organs.

32 muscle homologues were induced to express a rhythmical motor pattern by experimental methods that ac

33 te oviposition were found to also activate a rhythmical motor pattern in pregenital abdominal segment

34 A release channel with a rhythmical nature is discussed as a possible molecular p

35 the mollusc Lymnaea, one of the best-studied rhythmical networks, intracellular stimulation of either

36 nd perhaps myenteric neuronal activity, into rhythmical, propagated motor programs, such as swallowin

37 escale invariance, multisensory integration, rhythmical structure, and attentional time-sharing.

38 ulation during action patterns that required rhythmical unimanual or bimanual (iso-directional/anti-d

39 he KaiB and KaiC protein levels are robustly rhythmical, whereas the KaiA protein abundance undergoes

40 uring the mid-flexion phase of contralateral rhythmical wrist flexion-extension.

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