ライフサイエンスコーパス: air breathing

1 different from the control (attached retina, air breathing).

2 he pulmonary artery during the transition to air breathing.

3 els of SatPC essential for the transition to air breathing.

4 inner retinal Po(2) in lesioned areas during air breathing.

5 fore birth and is required for adaptation to air breathing.

6 sion of moderately severe PAH in mice during air breathing.

7 eostasis that are critical for adaptation to air breathing.

8 SP-SAP-treated rats also slept less during air breathing.

9 - 1.9 ml/kg(0.75)/min, p < 0.05) during room air breathing.

10 Hg) was 8.9% from the mean amplitude during air breathing.

11 irregularity in respiratory rate during room-air breathing.

12 en), compared to values measured during room air breathing.

13 oxygen from air when in isolation, and group air-breathing.

14 ent with existing definitions of synchronous air-breathing.

15 The transition to air breathing after birth requires both anatomic and bio

16 vide a single cell view of the adaptation to air breathing after birth.

17 Air-breathing allowed fishes at the water's edge to expl

18 y) were measured continuously during ambient air breathing (Amb) and a 6 min inhalation of the vasodi

19 ements that effect lung ventilation in other air-breathing amniotes.

20 onitored with a canopy apparatus during room-air breathing and 15 minutes of carbon dioxide exposure

21 antagonist, on ventilation (V E) during room air breathing and during hypoxic (10% O2) and hypercapni

22 bullfrogs acclimatized to semi-terrestrial (air-breathing) and aquatic-overwintering (no air-breathi

23 Tumor-cell survival for DDFP treatment with air-breathing animals was not significantly different fr

24 Although the lung is a defining feature of air-breathing animals, the pathway controlling the forma

25 In air-breathing animals, voluntary changes in respiratory

26 ous surface area, and enable gas exchange in air-breathing animals.

27 Conclusions: The commencement of air breathing at birth generates unique flow and volume

28 Rationale: The transition to air breathing at birth is a seminal respiratory event co

29 Adaptation to air breathing at birth is dependent on formation and fun

30 During the transition to air breathing at birth, biophysical forces are thought t

31 s susceptible to injury during transition to air breathing at birth.

32 eostasis that is necessary for adaptation to air breathing at birth.

33 entiation that is required for transition to air breathing at birth.

34 l cell maturation required for transition to air breathing at birth.

35 nctional changes necessary for adaptation to air breathing at birth.

36 fetal lung maturation and the transition to air-breathing at birth using isobaric hypoxic chambers w

37 preparation for the successful transition to air-breathing at birth.

38 preparation for the successful transition to air-breathing at birth.

39 r catfish in a laboratory arena and recorded air-breathing behaviour, activity and agonistic interact

40 content, and displayed temporally clustered air-breathing behaviour, consistent with existing defini

41 The cuvett-based air-breathing biobattery powered by isoamylase-treated s

42 ssure (RPP) was prevented from rising during air breathing by using an occluder on the dorsal aorta.

43 Within species, individual air-breathing can be influenced by metabolic rate as wel

44 d previously with a dry hydrogen feed and an air-breathing cathode.

45 zymatic fuel cells (EFCs), EFCs with laccase air-breathing cathodes prepared from TBA(+) modified Aqu

46 Under an air-breathing condition, mean P(O2) in the choroid, reti

47 ecreased compared with measurements under an air-breathing condition.

48 g) and 20 s of normoxia (n = 9), or a 40 min air-breathing control (n = 7).

49 ents when compared with term and term + 2-mo air-breathing controls.

50 ivocal results in some species, particularly air-breathing divers.

51 Hyperoxia is preferable to air breathing during retinal arterial occlusion not only

52 potheses that (1) hyperoxia is preferable to air breathing during retinal arterial occlusion, (2) hyp

53 olic pathway that comprises 13 enzymes in an air-breathing enzymatic fuel cell.

54 ccounts for as much as 35-40% of the normal, air-breathing eupnoeic drive to breathe.

55 systemic blood before entering the heart of air-breathing fishes, lung ventilation may supply the my

56 usly breathed 12% O2 followed by a switch to air breathing for 20 min.

57 air-breathing) and aquatic-overwintering (no air-breathing) habitats.

58 Air-breathing has evolved in many fish lineages, allowin

59 ulus-response curves were defined during (i) air breathing, (ii) hypoxia (12% O(2) in N(2)), and (iii

60 Air breathing in CH rats induced hypoventilation, a 12%

61 nd tidal volume (V(T)) were decreased during air breathing in sleep and wakefulness (group 2; P < 0.0

62 We examined social air-breathing in African sharptooth catfish Clarias gari

63 Air breathing is an essential motor function for vertebr

64 For C. gariepinus, synchronous air-breathing is strongly influenced by agonistic intera

65 gmentation model (U-Net) to extract dives of air-breathing krill predators from more than 30,000 h of

66 At birth, pulmonary vasodilation occurs as air-breathing life begins.

67 transition of an infant from intrauterine to air-breathing life is developmentally regulated, as the

68 However, in air-breathing mammals with compliant lungs susceptible t

69 some stem tetrapods suggests that spiracular air breathing may have been an important respiratory str

70 ss achieved by some fleets, the reduction of air-breathing megafauna bycatch is both an urgent and ac

71 the global nature of bycatch are lacking for air-breathing megafauna.

72 The spontaneously oxygen- or air-breathing mice were kept conscious or anesthetized w

73 ithin groups was the main factor influencing air-breathing of the entire group.

74 at SP-A and SP-D, which are ubiquitous among air breathing organisms, could contribute to the protect

75 In air-breathing organisms, an organic chemical's susceptib

76 Lung alveoli, which are unique to air-breathing organisms, have been challenging to genera

77 on of airborne xenobiotics in foliage and in air-breathing organisms.

78 d serve as the surfactant-producing cells of air-breathing organisms.

79 DPAT (30 mM) changed room air breathing pattern by increasing f and decreasing VT.

80 rior hyperventilation, caused a reduction in air-breathing PET,CO2 (P < 0.05, ANOVA), and a leftwards

81 of Adelie penguins and observations of other air-breathing predators (penguins, seals, and whales), a

82 ce edge) or inaccessible (solid fast ice) to air-breathing predators.

83 During room-air breathing, probands had significantly larger minute

84 The ability of air breathing R2* measurements to reflect tissue hypoxia

85 oral surface electrode during eupnea or room air breathing (RA), hypercapnia (HYP), and CPAP applicat

86 DA increased lung edema clearance in room air breathing rats (from 0.50 +/- 0.02 to 0.75 +/- 0.06

87 EF5 binding of "moderately" hypoxic cells in air breathing rats was identified using these techniques

88 In air breathing rats, for a given radiation dose, a large

89 as personality, but the mechanisms of group air-breathing remain unexplored.

90 t-efficient depth-use pattern for migrating, air-breathing species that do not feed in transit is to

91 considered in bioaccumulation assessments of air-breathing species.

92 The discovery of air-breathing structures in eurypterids indicates that c

93 tures known as Kiemenplatten represent novel air-breathing structures.

94 ia-exposed subjects (FIO2, 0.12); or c) room air breathing subjects whose dam food intake was matched

95 uplication of genes associated with obligate air-breathing, such as lung surfactants and the expansio

96 nvironmental conditions were unfavorable for air-breathing, terrestrial animals.

97 reous signal intensity on changing from room air breathing to oxygen inhalation (i.e., 5 minutes).

98 of predation, so some species perform group air-breathing, to reduce individual risk.

99 edatory communities, through introduction of air-breathing top predators, such as marine reptiles.

100 ous PO(2) measurements were made during room air breathing using (19)F magnetic resonance spectroscop

101 dothermic fishes, reproductive physiology of air breathing vertebrates, and endocrine physiology of r

102 Dive capacities of air-breathing vertebrates are dictated by onboard O(2) s

103 Air-breathing vertebrates incorporate a fraction of isot

104 is a physiological phenomenon present in all air-breathing vertebrates.

105 low of oxygenated and de-oxygenated blood in air-breathing vertebrates.

106 By contrast, room-air breathing was unaffected, suggesting that the drive

107 ean (+/- SE) baseline Qaw during quiet (room air) breathing was 6.6 +/- 0.6 ml/min (range, 3.9 to 10.

108 Responses during air breathing were assessed both prior to and after eith

109 hat the diuresis and natriuresis seen during air breathing were mediated by the increase in RPP; neit

110 ification occurring in food webs composed of air-breathing wildlife.

111 room air hyperventilation separated by room air breathing with continuous spirometry.