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1  KO neonates showed severe apnea and altered respiratory pattern.
2  maintains upper airway patency and a normal respiratory pattern.
3  the stability and provide plasticity to the respiratory pattern.
4     The dorsolateral (DL) pons modulates the respiratory pattern.
5 hepatic translation, and the k-space-derived respiratory pattern.
6 roxia or dihydrocodeine) would influence the respiratory pattern.
7 =0.05), which correlated with improvement in respiratory pattern.
8 ptors may be involved in the genesis of this respiratory pattern.
9 vice is demonstrated by identifying specific respiratory patterns.
10 e ability of patients to determine their own respiratory pattern and to maintain forced exhalation du
11 ting capillary refill time, skin turgor, and respiratory pattern and using combinations of other sign
12 mosensitivity can reduce or abolish abnormal respiratory patterns and may be an option in the managem
13 itory inputs to the KF that lead to RTT-like respiratory patterns and proposes potential KF local cir
14 ibitory inputs to the KF leading to RTT-like respiratory patterns and suggest possible KF local circu
15 espondingly, we find that abnormal Rett-like respiratory patterns are alleviated, and survival is pro
16 lex (preBotC) SST(+) neurons, which modulate respiratory pattern but are not rhythmogenic, were trans
17 the degree of entrainment of the spontaneous respiratory pattern by the ventilator.
18      Acetylcholine and nicotine can modulate respiratory patterns by acting on nicotinic acetylcholin
19 een depth and duration of inspiration in the respiratory pattern, characterizing this specific state.
20            Our findings demonstrate distinct respiratory patterns during EPM exploration: slower brea
21 hy human volunteer breathing along different respiratory patterns during the MR acquisition.
22 ely interneurons, that communicated with the respiratory pattern generating network to effect changes
23 gesting that this region is critical for the respiratory pattern generation.
24     These cells were not part of the central respiratory pattern generator (CPG), because they were t
25 used by a synaptic feedback from the central respiratory pattern generator (CPG).
26 naffected by pharmacological blockade of the respiratory pattern generator and persists without carot
27             The carotid bodies stimulate the respiratory pattern generator directly and indirectly by
28 e, we studied the adaptive behaviours of the respiratory pattern generator in rat on repetitive vagal
29                                          The respiratory pattern generator modulates the sympathetic
30 phasically activated throughout breathing by respiratory pattern generator neurons.
31 laninergic subset, selectively innervate the respiratory pattern generator plus a portion of the dors
32 s (the central chemoreceptors) would drive a respiratory pattern generator that is not or minimally a
33 pH-regulated excitatory drive to the central respiratory pattern generator.
34 the lower brainstem regions that contain the respiratory pattern generator.
35 NMDA receptor-dependent pontine input to the respiratory pattern generator.
36 cs rarely coincide with abnormalities of the respiratory pattern generator.
37  glutamatergic and innervate principally the respiratory pattern generator; they regulate multiple as
38              Finally, we demonstrate how the respiratory pattern generators are part of a larger and
39                                      The two respiratory patterns have distinct influences on fMRI si
40 ncrease in ventilation and the regularity of respiratory patterns in perinatal rat preparations.
41 ogressive, increasingly severe disruption of respiratory pattern, initially during sleep and then als
42 gor (LR, 2.5; 95% CI, 1.5-4.2), and abnormal respiratory pattern (LR, 2.0; 95% CI, 1.5-2.7).
43   These findings add to our understanding of respiratory pattern modulation and suggest a novel mecha
44 nd in humans can explain gene expression and respiratory patterns observed in these eukaryotes.
45 ter no-I tests whether or not changes in the respiratory pattern occur in the subsequent cycles; and
46               Muscimol eliminated the on-off respiratory pattern of neurons in the rostral ventrolate
47                                         Self-respiratory pattern of StHEI realized through in situ in
48 pendent excitatory input to RVLM neurons and respiratory patterning of their activities via inputs fr
49 ggested possible factors contributing to the respiratory patterns of RTT, we take a novel computation
50                 These characteristics of the respiratory pattern persist in in situ preparations even
51 uctuations stemming from a specific periodic respiratory pattern (r=-0.49).
52        The reported wearable mask device and respiratory pattern recognition algorithms could be wide
53 atment with rhIGF1 in these animals improves respiratory patterns, reduces anxiety levels, and increa
54 s that vocal sequences are tightly linked to respiratory patterns that are modulated by ANS fluctuati
55 ven the importance of the KF in coordinating respiratory pattern, the mechanisms of mu opioid recepto
56 infants' bedding recorded body movements and respiratory patterns to measure sleep and wake states.
57                           Complex changes in respiratory pattern underpin the ventilatory manifestati
58                               To compare the respiratory pattern, variability, synchronization, and n
59                                              Respiratory pattern variables and capillary blood gases
60                                          The respiratory pattern was determined in three asphyxiated,
61                                              Respiratory pattern was measured by plethysmography and
62 ; and (2) that LTF causes complex changes in respiratory pattern which are responsible for the increa