ライフサイエンスコーパス: acclimatization

1 adjustments in ventilation (i.e. ventilatory acclimatization).

2 After acclimatization.

3 ight play an adaptive or maladaptive role in acclimatization.

4 change resulting from local adaptations and acclimatization.

5 e frequency of oscillations was slower after acclimatization.

6 ventilatory system during and after altitude acclimatization.

7 hlights the important role of the kidneys in acclimatization.

8 plant architecture also contributed to this acclimatization.

9 e that is positively associated with quicker acclimatization.

10 climatization to high altitude and during de-acclimatization.

11 eptor sensitivity and successful ventilatory acclimatization.

12 mechanism underlying CBF normalization with acclimatization.

13 to identify genes underlying adaptation and acclimatization.

14 ts for erythrocyte hypoxic memory and faster acclimatization.

15 well with most other measures of ventilatory acclimatization.

16 e in ventilation and change in G(pO2) during acclimatization.

17 eja species exhibited high Cd resistance and acclimatization.

18 e across UHI decile groups, again suggesting acclimatization.

19 n of no acclimatization, but did not exclude acclimatization.

20 lue of 1.070 (1.057, 1.082) if there were no acclimatization.

21 G(pCO2) is a modest predictor of ventilatory acclimatization.

22 e chemoreflex and that caffeine abolishes CB acclimatization.

23 entral nervous system adaptations that allow acclimatization.

24 ude was 5% less than SL but normalized after acclimatization.

25 k decreased 12% acutely but normalized after acclimatization.

26 who ascend to high altitude without previous acclimatization.

27 nders; 12 Sherpa), and (2) following partial acclimatization (11 4 days) to 5050 m (18 lowlanders; 20

28 al trials at sea level and following partial acclimatization (14 to 20 days) at 5050 m; involving: (1

29 environments, which may lead to an increased acclimatization ability even during long-term exposure t

30 In less than 2 years, acclimatization achieves the same heat tolerance that we

31 We found strong evidence of acclimatization across cities.

32 attributed to several factors, such as true acclimatization, adaptive behaviors, or harvesting effec

33 at high altitude (ALT1) and after 16 days of acclimatization (ALT16) to 5260 m at rest and during sub

34 The hypoxia modelling of high-altitude acclimatization and adaptation in humans demonstrates th

35 on people living above 3,500 m, the study of acclimatization and adaptation to high altitude in human

36 tion on pulmonary vascular regulation during acclimatization and adaptation to high altitude.

37 Here, in the context of acclimatization and adaptation, we provide a contemporar

38 is a natural setting in which to study human acclimatization and adaptation.

39 appear to play major roles in high-altitude acclimatization and adaptation.

40 dance that are essential to the processes of acclimatization and biomineralization.

41 nses to hypoxia, abrogating both ventilatory acclimatization and carotid body cell proliferative resp

42 tonic activity in the process of ventilatory acclimatization and de-acclimatization during rest and e

43 at importance for understanding of microbial acclimatization and evolution in natural environments.

44 Local acclimatization and fixed effects, such as adaptation, c

45 croorganisms could assist with environmental acclimatization and help resource species to suppress ot

46 ystem a powerful candidate for investigating acclimatization and local adaptation of organisms to glo

47 romones than wet season males, partly due to acclimatization and partly due to developmental plastici

48 of individual susceptibilities and effective acclimatization and prevention options.

49 thaliana play a key regulatory role in cold acclimatization and the acquisition of freezing toleranc

50 Preventive measures include slow ascent, pre-acclimatization and, in some instances, medications.

51 d studies of the genomic basis of evolution, acclimatization, and adaptation in real ecological conte

52 cal mechanisms associated with high-altitude acclimatization, and provides insight into the relations

53 g exercise increased at high altitude during acclimatization, and this corresponded with increased in

54 bioavailability and participant acclimation/acclimatization are warranted to elucidate the influence

55 lower brain blood flow during ascent to and acclimatization at high altitude compared to lowlanders

56 We also have studied the fern acclimatization, at different shading conditions, findin

57 ped environmentally independent, avian-style acclimatization, becoming endothermic.(1)(,)(2) The abil

58 We assessed ventilatory and renal acclimatization between unacclimatized LL and TH during

59 ines shifted somewhat in the direction of no acclimatization, but did not exclude acclimatization.

60 nse protects oxygenation through ventilatory acclimatization, but elicits hypocapnia and respiratory

61 suggests that parallel habitat adaptation or acclimatization by larvae from S. salamandra and S. infr

62 ve relevance in clinical scenarios where PDL acclimatization can be exploited to optimize tooth movem

63 velopmental plasticity) or during adulthood (acclimatization) can both affect adult phenotypes.

64 trial baseline), the model suggests that the acclimatization capacities of all ecogroups are limited

65 high CO2 experimental conditions do not show acclimatization capacity or physiological tolerance rela

66 Taken together, following acclimatization, CO(2) -mediated changes in cerebrovascu

67 Following partial acclimatization, despite Sherpa demonstrating a blunted

68 te to ventilation by assessing how adulthood acclimatization, developmental adaptation, and populatio

69 ic ventilation derives from a combination of acclimatization, developmental adaptation, and populatio

70 rocess of ventilatory acclimatization and de-acclimatization during rest and exercise conditions.

71 f carotid body tonic activity in ventilatory acclimatization during rest and exercise.

72 te, extent, and clinical significance of the acclimatization effect, there is irrefutable evidence th

73 le in ventilatory acclimatization to, and de-acclimatization from, high altitude, and this persists d

74 0.001 for both), indicating that significant acclimatization had occurred.

75 gh altitude) or pathological (lung disease), acclimatization has a homeostatic implication because it

76 l responses that are critical for successful acclimatization; however, these responses may induce app

77 ral blood throughout 3 days of high-altitude acclimatization in healthy sea-level residents (n = 15;

78 chemoreceptor tonic activity to ventilatory acclimatization in humans has not been directly demonstr

79 ed that (1) periodic breathing persists with acclimatization in lowlanders and the severity is propor

80 We examined developmental plasticity and acclimatization in pheromone production in the butterfly

81 ts reveal a three-tiered strategy of thermal acclimatization in Pocillopora underpinned by host-photo

82 -or acclimatizes--under warming and that the acclimatization is greater at high temperatures.

83 canopy biomass due to, e.g., disturbance or acclimatization) may cause a reduction in canopy storage

84 nriched in genes contributing to salt stress acclimatization, nutrient solubilization and competitive

85 llowing 8 h of hypoxia does not underlie the acclimatization observed in ventilation or pulmonary vas

86 nd find that maximum and minimum temperature acclimatization occurs along the elevation gradient in b

87 Cold shock proteins (CSPs) enhance acclimatization of bacteria to adverse environmental cir

88 his increase in activity underlies the early acclimatization of both ventilation and the pulmonary va

89 We suggest that the gradual acclimatization of chickens in the Southern Levant and i

90 Acclimatization of FAT-D2KO mice at thermoneutrality dis

91 mmarizes the current knowledge regarding the acclimatization of lactose processing in humans.

92 This acclimatization of soil respiration to warming may there

93 Analysis of seasonal acclimatization of the O. faveolata holobiont in this st

94 Acclimatization of the psychrotolerant Yersinia enteroco

95 The potential effects of seasonal acclimatization on coral sensitivity to heat-stress, has

96 Little is known about the potential for acclimatization or adaptation of corals to ocean acidifi

97 difference is due to long-term physiological acclimatization or genetic adaptation.

98 iratory and renally mediated blood acid-base acclimatization (PCO(2), [HCO(3)(-)], pH) in both groups

99 anges in breathing variability over a 16 day acclimatization period to altitude, when awake, were qua

100 After a 2-week acclimatization period, groups of 30 male F344 rats rece

101 After an acclimatization period, patients underwent three polysom

102 s of 30 degrees C and 34 degrees C; after an acclimatization phase of 1 week at 30 degrees C.

103 An acclimatization phase often moderated this effect.

104 ession patterns and substantial variation in acclimatization potential based on coral genotype.

105 the first few days at altitude to allow this acclimatization process to occur.

106 026, 1.034) (actual versus expected under no acclimatization, respectively).

107 Trimetaphan had no effect on the acclimatization response of any of these variables.

108 in concentrations, in contrast to the normal acclimatization response to hypoxia in lowland primates.

109 t sea-level, but the impact of maturation on acclimatization responses to high altitude is unknown.

110 I find no evidence that acclimatization, rising incomes, or other unobserved dri

111 by upward bursts and pauses, resembling the acclimatization routines of human mountain climbers, and

112 prevalence of acute HAIs varies according to acclimatization status, rate of ascent and individual su

113 high altitude showed evidence of successful acclimatization, supporting the hypothesis that such fet

114 esce with poor sleep quality such that, with acclimatization, there appears to be a lengthening of cy

115 the hearing protection device (HPD) or with acclimatization time, allowing a lifetime of playing wit

116 ring protection: These include (a) a lack of acclimatization time; (b) a loss of "fortissimo blare" f

117 altitude to 2500 m, and (3) after 5 days of acclimatization to 2500 m.

118 (n = 9) at sea level (SL) and after 14 days acclimatization to 4300 m (chronic HA) in Cerro de Pasco

119 Following partial acclimatization to 5050 m, there were differential influ

120 flow (CBF) regulation at sea level and with acclimatization to 5050 m.

121 n = 8) were made at SL and following partial acclimatization to 5050 m.

122 of Oman corals was maintained after 6-month acclimatization to a common ambient environment and was

123 is work in three main areas of his research: acclimatization to amplified speech, auditory disability

124 ate the functional role of Rox1 in mediating acclimatization to anaerobic conditions in Saccharomyces

125 on the increase in normoxic ventilation with acclimatization to CH, indicating this is a distinct mec

126 ences expressed by each species suggest that acclimatization to changing ocean conditions may vary, e

127 m cell niche, which support CB growth during acclimatization to chronic hypoxia.

128 nia but alone do not account for ventilatory acclimatization to chronic increased InCO(2).

129 ng that transcriptome plasticity facilitates acclimatization to environmental change in S. siderea.

130 can be used as a mechanism for survival and acclimatization to environmental conditions.

131 olonies of P. compressa exhibited beneficial acclimatization to heat stress (i.e., less bleaching) fo

132 ethods to examine and quantify the degree of acclimatization to heat- and cold-related mortality in r

133 obin, explored the determinants of a human's acclimatization to high altitude and developed the field

134 eptor tonic activity in lowlanders following acclimatization to high altitude and during de-acclimati

135 er adrenergic restraint of blood flow during acclimatization to high altitude and provides evidence o

136 ations in acid-base balance with progressive acclimatization to high altitude have been well-establis

137 Ventilatory acclimatization to high altitude is an important adaptio

138 Faster acclimatization to high altitude upon re-ascent is seen

139 onic sustained hypoxia (CSH), such as during acclimatization to high altitude, an additional time-dep

140 nic activity is elevated and associated with acclimatization to high altitude, and this persists 3 da

141 metric in predicting successful ventilatory acclimatization to high altitude.

142 irments in endothelial function during early acclimatization to high altitude.

143 liana leaves accumulate more ascorbate after acclimatization to high light intensity.

144 onses to exercise, which may influence their acclimatization to high-altitude environments.

145 ry response (HVR) that is called ventilatory acclimatization to hypoxia (VAH).

146 iratory centres is necessary for ventilatory acclimatization to hypoxia (VAH); VAH is a time-dependen

147 Additionally, the change in G(pO2) during acclimatization to hypoxia correlated well with most oth

148 can induce the changes known as ventilatory acclimatization to hypoxia, in the absence of the primar

149 essively during the first few hours of human acclimatization to hypoxia.

150 in respiratory control known as ventilatory acclimatization to hypoxia.

151 pua New Guinea that have undergone long-term acclimatization to natural variation in pCO2 .

152 cle, resultant cellular hypoxia necessitates acclimatization to optimize energy metabolism and restri

153 c state-dependent "stress response" but that acclimatization to oxygen deprivation is a relatively sl

154 eceptors play a critical role in ventilatory acclimatization to prolonged hypoxia in animals.

155 ctivity plays a critical role in ventilatory acclimatization to prolonged hypoxia in animals; However

156 Scallops showed no acclimatization to repetitive pile driving across and wi

157 findings unravel the role of Mn-catalase in acclimatization to salt/oxidative stress and demonstrate

158 the hypoxic ventilatory response and altered acclimatization to sustained hypoxia.

159 re that the initial infusion does not affect acclimatization to the 8 h hypoxia exposure, and the use

160 lytical methods for estimating the degree of acclimatization to the heat- and cold-related mortality

161 ll results were inconsistent with short-term acclimatization to the local environment or adaptation t

162 sults for London suggest relatively complete acclimatization to the UHI effect on summer heat-related

163 iations with those expected under no or full acclimatization to the UHI.

164 ld between cool and hot areas, which we call acclimatization to the UHI.

165 Methods to estimate acclimatization to urban heat island effects on heat- an

166 ilient to these changes due to adaptation or acclimatization to warmer temperatures, or they may be m

167 a potential mechanism for intergenerational acclimatization to warming oceans, which has substantial

168 c activity plays a major role in ventilatory acclimatization to, and de-acclimatization from, high al

169 f chronic caffeine intake on CB function and acclimatization using four groups of rats: normoxic, caf

170 acclimatization was proportional to the pre-acclimatization value.

171 ve and cross-transplanted corals, indicating acclimatization via plasticity within just 3 mo.

172 The degree of ventilatory acclimatization was associated with the change in the hy

173 Substantial acclimatization was observed in both ventilation and PAS

174 ypoxia, the magnitude of the increase during acclimatization was proportional to the pre-acclimatizat

175 pressed genes on the first and third days of acclimatization were enriched for several inflammatory p

176 t to high altitude, or (2) following partial acclimatization, when compared to high-altitude adapted

177 a carotid body (CB) sensitization, known as acclimatization, which leads to an increase in carotid s

178 ortant for predicting successful ventilatory acclimatization with chronic altitude.

179 riodic breathing persists with high altitude acclimatization with no obvious negative consequences; h

180 Defining mechanisms of positive acclimatization, with potential implications for carry o

181 t the increase in ventilatory loop gain with acclimatization would exacerbate breathing variability a