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1 try, and bronchoconstriction was assessed by whole body plethysmography.
2 ut (eNOS-/-) mice of C57BL6 background using whole body plethysmography.
3 at the same time as measuring breathing via whole body plethysmography.
4 Ventilation was measured by whole-body plethysmography.
5 exposures by monitoring their sniffing with whole-body plethysmography.
6 HR to methacholine challenge was measured by whole-body plethysmography.
7 in 7- to 9-week-old unanaesthetized rats via whole-body plethysmography.
8 a, and severe airway hyperreactivity through whole-body plethysmography.
9 EEG and neck EMG recordings and breathing by whole-body plethysmography.
10 Minute ventilation (VE) was measured using whole-body plethysmography.
11 In this study, we established dwarf hamster whole-body plethysmography and assessed disease severity
12 challenges, lung function was determined by whole-body plethysmography and bronchoalveolar lavage fl
13 medullary respiratory circuits, we performed whole-body plethysmography and electrophysiological reco
15 which was observed through antinociception, whole-body plethysmography, and blood-brain biodistribut
17 -old intact, freely behaving rat pups, using whole-body plethysmography during breathing of room air
20 respiratory frequency (RF) was monitored by whole-body plethysmography immediately after the 4th cha
22 olume, and minute volume were measured using whole-body plethysmography in rats administered GHB.
24 of AR to inhaled methacholine by barometric whole-body plethysmography is a valid indicator of airwa
27 ompared with airway resistance measured with whole-body plethysmography (Raw-p) in 10 of the 16 infan
30 yper-reactivity was measured by non-invasive whole-body plethysmography, Th2 response and airway infl
31 rial gradient, and ventilatory parameters by whole body plethysmography to determine the responses el
33 res are impaired in the mutant mice, we used whole-body plethysmography to quantitatively measure odo
34 ext]e was recorded in newborn rat pups using whole-body plethysmography under normoxic and hypoxic co
35 s to inhaled methacholine were determined by whole body plethysmography using changes in enhanced pau
36 ventilation) or noninvasive techniques, like whole body plethysmography (WBP), assesses the severity
37 e models of pathology is the need to combine whole-body plethysmography (WBP) to measure respiration
38 eofluoroscopy, ultrasonic vocalizations, and whole-body plethysmography were used to assess VF motion