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1 r NO (thus maximizing oxygen delivery in the respiratory cycle).
2 eliminated the post-inspiration phase of the respiratory cycle.
3 cidence data to reconstruct any phase of the respiratory cycle.
4 eventing alveolar collapse at the end of the respiratory cycle.
5 wave speed remained unchanged throughout the respiratory cycle.
6 orants and active at different phases of the respiratory cycle.
7 cquires multiple low-dose CT images during a respiratory cycle.
8 ropharyngeal levels at each increment of the respiratory cycle.
9 d exclusively to the expiratory phase of the respiratory cycle.
10 n and hyperoxic vasconstriction in the human respiratory cycle.
11 tions in PaO2 as shunt varies throughout the respiratory cycle.
12 ion management (RPM), is used to monitor the respiratory cycle.
13 ty analysis was confined to one phase of the respiratory cycle.
14 ons that varied as a function of time in the respiratory cycle.
15 h and terminate the inspiratory phase of the respiratory cycle.
16 eartbeats increasing and decreasing within a respiratory cycle.
17 ion would alter the inspiratory phase of the respiratory cycle.
18 ive of fluctuations in inhibition during the respiratory cycle.
19 fire during the late expiratory phase of the respiratory cycle.
20 of inspiratory and expiratory phases of the respiratory cycle.
21 lar filling and ejection dynamics during the respiratory cycle.
22 tor activity was recorded as an index of the respiratory cycle.
23 bursts are coupled to specific phases of the respiratory cycle.
24 he variability of RR intervals in individual respiratory cycles.
25 icular system and in the spinal canal during respiratory cycles.
26 e synchronization of heartbeat intervals and respiratory cycles.
27 tory cycle, whereas PET occurs over multiple respiratory cycles.
28 ntragastric pressures were measured over 6-8 respiratory cycles.
29 that allowed resolution of both cardiac and respiratory cycles.
30 rcise to that recorded during the first five respiratory cycles after the abrupt cessation of exercis
31 ory activity would be entrained to the human respiratory cycle, albeit at the much slower rhythm of a
34 that Dbx1(+) neurons activate earlier in the respiratory cycle and discharge greater magnitude inspir
35 x-evoked prolongation of the PI phase of the respiratory cycle and excitation of PI neurones includin
36 gnals that recurred on the time scale of the respiratory cycle and whose range was approximately one
37 us work has demonstrated an influence of the respiratory cycle and, more specifically, rhythmic nasal
38 ith no activity related to either cardiac or respiratory cycles and their conduction velocity was 0.8
39 ate mechanisms underlying NO function in the respiratory cycle, and provide insight into the aetiolog
40 distinct portions of the centrally generated respiratory cycles; and (c) phasic synaptic inhibition,
42 necting distant brain regions, and posit the respiratory cycle as an important reference for neuronal
44 d a significant HR change in the first three respiratory cycles at 40 % of maximum voluntary contract
52 ind that many neurons become phase-locked to respiratory cycles in a stage-dependent manner, emphasiz
53 ty shows detectable changes during nonapneic respiratory cycles in adults evaluated for sleep-disorde
54 by occluding the tracheal cannula for thirty respiratory cycles; in the second series of experiments,
60 moter activity in both the cell division and respiratory cycles of the budding yeast Saccharomyces ce
61 ly 1 month of age, most Mecp2-/y mice showed respiratory cycles of variable duration; meanwhile, thei
64 ectroencephalographic power to vary with the respiratory cycle predicted next-day sleepiness as measu
65 aximum firing rate nor start time during the respiratory cycle predicted the occurrence of doublets.
66 Spectral analysis proved the existence of respiratory cycle-related electroencephalographic change
67 entilation, approximately 67,150 spontaneous respiratory cycles, represented by 3,592 16-sec epochs,
68 Motion of the tissue from the cardiac and respiratory cycles severely limits intravital microscopy
69 al for tissue oxygenation by RBCs within the respiratory cycle that is required for both normal cardi
70 tructures relatively immobile throughout the respiratory cycle, the efficiency and safety of these pr
71 preceding nontriggering efforts had shorter respiratory cycle times (p < 0.0005) and expiratory time
72 n this context, nitric oxide coordinates the respiratory cycle to acquire and deliver oxygen to targe
74 inputs during a portion of the lung or gill respiratory cycle was observed following a negative curr
76 e activity both lung and gill rhythm-related respiratory cycles were divided into three distinct phas
77 ical CT scan provides only a snapshot of the respiratory cycle, whereas PET occurs over multiple resp
79 and the L1 root consisted of two bursts per respiratory cycle with a silent period during inspiratio
81 performed for 10 seconds over a span of 2-3 respiratory cycles with supporting a continuous positive
82 the timing of SWR events is modulated by the respiratory cycle, with a significantly increased probab
83 aroresponsive neuronal assemblies during the respiratory cycle, without concomitant firing rate chang
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