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1 nward and leftward in healthy humans at high altitude.
2 er to characterize the water distribution by altitude.
3 thrust, the spacecraft is bounded to a given altitude.
4 ysfunction with hypoxia at sea level or high altitude.
5 rscoring their adapted capacity to thrive at altitude.
6 to the hypobaric hypoxia encountered at high altitude.
7 larly to the base of the ionosphere at 90 km altitude.
8 se capacity under chronic hypoxaemia at high altitude.
9 ty during hypoxic exposure on ascent to high altitude.
10 ose is famed for migratory flight at extreme altitude.
11 similar to that inside the cabin at cruising altitude.
12 fects compared to lowland natives at extreme altitude.
13 cise capacity associated with an increase in altitude.
14 abolism observed with exposure to hypoxia at altitude.
15 henotypes with adaptive significance at high altitude.
16 ous cerebral consequences than lowlanders at altitude.
17 influence exercise capacity at this moderate altitude.
18 s affecting growth shifted with latitude and altitude.
19 1.11), which could not be distinguished from altitude.
20  cloud close to the highest regions at 17 km altitude.
21 modynamic changes at both sea level and high altitude.
22  confirmed that the insects were captured at altitude.
23 chondria contribute to thermogenesis at high altitude.
24 n in healthy lowland natives exposed to high altitude.
25  according to the type of processing and the altitude.
26 ders with (n=6) and without (n=9) EE at high altitude.
27  and half during the rainy season and at low altitude.
28 ypical exospheric densities found at ~700 km altitudes.
29 chondria contribute to thermogenesis at high altitudes.
30 se thresholds might not be applicable at all altitudes.
31 ted with urbanization may also affect flight altitudes.
32 l were used to predict emissions at cruising altitudes.
33 r staple prey, moose (Alces alces), to lower altitudes.
34 ation and surface air temperature, on flight altitudes.
35  shifting their ranges poleward or to higher altitudes.
36  revealed lower drought resilience at higher altitudes.
37 nsfers among the bounded orbits in different altitudes.
38 es that are normal for children in different altitudes.
39 alse positives for tachypnoea increased with altitude: 0% in India (95% CI 0-0), 7.3% in Guatemala (4
40            404 participants were from India (altitude 1-919 m), 389 were from Guatemala (1036-2017 m)
41 erosols from South Asian countries to higher altitudes (12-18 km) where they form the Asian Tropopaus
42 r between two competing effects at different altitudes(14).
43  assessment at low altitude (Lowlanders, low altitude; 344 m, Sherpa, Kathmandu; 1400 m) and followin
44  (344 m) and following 14 to 21 days at high altitude (4300 m), and permanent Andean highlanders with
45 e studied 4-8 days following arrival at high altitude (4383 m; Cerro de Pasco, Peru), a setting that
46  conducted a 6-yr field experiment in a high-altitude (4600 m asl) alpine grassland on the Tibetan Pl
47 of neutral densities (<10(2) cm(-3)) at high altitudes (~5300 km) by the MESSENGER spacecraft.
48        For each 1000-m (3300-ft) increase in altitude above 2500 m (8200 ft), AMS prevalence increase
49 ere reduced to levels below detectability at altitudes above 40 kilometres.
50 horizontal approaches, the latter from three altitudes above ground level (AGL).
51  m to investigate any interactions with high altitude acclimatisation.
52 serts with flight bouts performed at various altitudes according to species and season, along a gradi
53 ime, we report variants associated with high-altitude adaptation in Iranian native chickens by whole
54           These findings suggested that high-altitude adaptation in response to hypoxemia has differe
55                                         High-altitude adaptation of Tibetans represents a remarkable
56 gical consequences of acute and chronic high altitude adaptation.
57 at MIR6644-2 is involved in hypoxia and high-altitude adaptations by regulation of embryo development
58 The atmospheric pressure that decreases with altitude affects lung physiology.
59  microbial diversity in near-ground and high-altitude air above the largest ice-free Antarctic habita
60    The present study has focused on the high altitude alga Spirogyra porticalis (Muell.) Cleve- a fil
61 rodent persists in large numbers in the high-altitude Alpine meadow [6, 7].
62 rom the Tibetan/Sherpa lineage, but from low-altitude ancestors who migrated from China plausibly acr
63 he risks of which are higher in women of low-altitude ancestry.
64 s in BERK-SS were higher than WT at moderate altitude and also compared to BERK-SS at sea level (P <
65 (eENT1) levels are reduced in humans at high altitude and in mice under hypoxia.
66 putational fluid dynamics simulations of low-altitude and near-wall flights based on in vivo high-spe
67  with airborne microbial diversity from high-altitude and non-polar sources suggests that strong sele
68 atty acid content was strongly influenced by altitude and temperature.
69 or each of the five quantiles of bird flight altitude and their differences between urban and non-urb
70 F signaling pathway was associated with high altitude and therefore corresponding O(2) availability i
71 bral hypometabolic conservation of energy at altitude and/or decreased risk of other cerebral consequ
72 ide variety of landscape from plains to high altitudes and is a congruence of many languages and cult
73 breathing (PB) occurs in most humans at high altitudes and is characterised by low-frequency periodic
74 to discriminate among samples from different altitudes and latitudes.
75 s that they may have adapted to life at high altitudes and may have contributed such adaptations to m
76 n many children who live at moderate to high altitudes and show acute respiratory signs.
77  contrast, only younger trees grow at higher altitudes and we document a relatively fast upward shift
78 ons underpin human evolution to life at high altitude, and could have an impact upon our understandin
79 ade fully restored EDD in lowlanders at high altitude, and normalized EDD between EE and non-EE Andea
80               Furthermore, llamas under high altitude Andean climatic conditions exhibited a pronounc
81 ature and locomotion, under its natural high altitude Andean habitat.
82 we used whole-genome sequencing to scan high-altitude Andeans for signals of selection.
83 RBs in Meghalaya including data of location, altitude, approximate age and bridge length was performe
84 erentiation between the fertile north, where altitudes are lower, and the arid south, where the Andes
85                    Future studies at various altitudes are needed to validate our findings and recomm
86  Old World camel species inhabit hot and low-altitude as well as cold and high-altitude deserts.
87 d to a drag force can be bounded at specific altitudes as function of the parameters of the thrust.
88                                         High-altitude associated with variant discovery highlighted t
89 R and lower thresholds for SpO(2) by age and altitude at four sites, with altitudes ranging from sea
90 ars in the eastern United States to estimate altitudes at five quantiles of the vertical distribution
91  of CO(2) variability near the ground (~1 km altitude) at an airport was correlated with the intensit
92 tropical Pacific and Atlantic increased high-altitude atmospheric humidity and heavy rainfall events,
93 ochronological evidence that some of the low-altitude basement landforms on- and offshore southwester
94 tal displacement of 10 km developed at 50 km altitude before connecting to the lower ionosphere.
95                                       At all altitudes, BERK-SS mice had a significantly lower percen
96 e abundance of H(2)O and HDO was observed at altitudes between 40 and 80 kilometres.
97  have preserved endothelial function at high altitude, but less is known about the Ethiopian highland
98 owlanders at sea level and in Sherpa at high altitude, but not in Andean natives.
99 lume (SV) were decreased upon ascent to high altitude, but were comparable to sea level in the HA-PVX
100 le for respiratory control during hypoxia at altitude, by linking genetic factors with cardiovascular
101  in left heart failure, head trauma, or high altitude can lead to endothelial barrier disruption refe
102 ur at sites under positive selection in high-altitude catfishes, located at opposite ends of the RH1
103      In particular, chronic exposure to high altitude (CEHA) has been associated with deficits in cog
104 b global radiative balance by affecting high altitude cloud formation and properties.
105 re-climate link through sea ice melt and low altitude clouds that may have contributed to accelerate
106 during ascent to and acclimatization at high altitude compared to lowlanders and that this difference
107 n CMS+ compared to healthy HA (CMS-) and low-altitude controls.
108                                         High-altitude deer mice (Peromyscus maniculatus) and low-alti
109                             We examined high-altitude deer mice, which have evolved a high capacity f
110                                    Such high-altitude densities cannot be accounted for by the typica
111 ot and low-altitude as well as cold and high-altitude deserts.
112  direction and 22.59 +/- 5.81 degrees in the altitude direction, imaging of gamma rays using organic
113             We included effects of activity, altitude, direction of approach, distance, habitat, herd
114             Response triggers were linked to altitude, distance, habitat and target species.
115 ic legacy through gene flow into several low-altitude East Asian populations(4,5) and high-altitude m
116 tailwinds at intermediate and high migration altitudes east of the Caribbean.
117 d eastern regions above the Equilibrium Line Altitude (ELA) but away from the interior; hydrologicall
118 s suggest that exposure to mild and moderate altitude enhances the progression of SCD in BERK-SS mice
119                                         High-altitude environments require that animals meet the meta
120 nknown whether exposure to mild and moderate altitude exacerbates SCD associated cardiopulmonary and
121          These data demonstrate that chronic altitude exposure exacerbates the complications associat
122                                         High altitude exposure reduced plasma volume by 11% (P < 0.01
123                        Following 3 months of altitude exposure, right ventricular systolic pressure w
124           The existence of an analogous high-altitude feedback, however, has yet to be directly evalu
125                                         High-altitude flights are therefore not the general rule for
126  due to local regulations prohibiting higher-altitude flights without federal authorization.
127  reduced pressure/oxygen and fatigue on high-altitude flights.
128 viour increased during drone flights, at any altitude flown.
129 ergic; NN) and nine healthy controls in high altitude for 21 days were enrolled in the study.
130 nalogous to that previously reported at high altitude for hypoxia-inducible factor 1alpha.
131 esults can help to explain how to adapt high-altitude for men and women, respectively.
132      Highland native Andeans have resided at altitude for millennia.
133 , electrons and other particles circulate at altitudes from about 500 to 40,000 kilometres in the Van
134 ase in received signal intensity per 100' of altitude gain, up to 400'.
135                                  The extreme altitude (&gt;4,000 m) of the highland wild dogs' (HWD) obs
136     Long-term operations carried out at high altitude (HA) by military personnel, pilots, and astrona
137 a maladaptation syndrome encountered at high altitude (HA) characterised by severe hypoxaemia that ca
138 e of native Lowlanders during sustained high altitude (HA) exposure.
139            The environmental hypoxia of high altitude (HA) increases the incidence of intrauterine gr
140                             Exposure to high altitude (HA) is characterized by heightened muscle symp
141                          The hypoxia of high-altitude (HA) residence increases the risk of intrauteri
142 ions that were compared with SL values: high altitude (HA), Plasma Volume Expansion (HA-PVX), Sildena
143 he colonisation of lowland inland and higher altitude habitats by this aggressively invasive predator
144  that colonized the Andes from ancestral low-altitude habitats in South America.
145 adinus, with populations now thriving in low altitude habitats.
146 h the laboratory and the field (e.g. at high altitude) have demonstrated that endothelial function is
147 tive chickens distributed in a wide range of altitudes, have developed adaptive mechanisms to deal wi
148 sms by which the environment, including high-altitude, heat, and cold exposure, alters nutrition requ
149 t on vector populations in understudied high-altitude, high-incidence districts.
150 , presence of hypoxia, systemic hypotension, altitude higher than >500 m, and GDP per capita were sig
151 t sea level, lowlanders acclimatized to high altitude, Himalayan Sherpa, and Andean Quechua, and expl
152 ted pulmonary pressure is evident (e.g. high altitude); however, a causal link is not established.
153                           We argue that high altitude human populations require special attention to
154 tion are common strategies to cope with high-altitude hypoxia, but some changes require longer evolut
155 ocene epoch and successfully adapted to high-altitude hypoxic environments long before the regional a
156 or system with three satellites at 51,000 km altitude illustrates the feasibility of using radio-freq
157 ents of bar-headed geese flying at simulated altitude in a wind tunnel.
158 nces O(2) delivery or use during exercise at altitude in Peruvian Quechua.
159 showed a direct relationship with geographic altitude in SCP 3 x 3-mm(2) scans in this group of healt
160 m above ground level, and possibly at higher altitude in spring.
161               We observe intense NPF at high altitudes in tropical convective regions over both Pacif
162 map the cellular network coverage at various altitudes in various terrains (flat, hilly, mountainous)
163                    Wolves selected for lower altitudes in winter, particularly in the area where bear
164 during dust storm conditions revealed a high-altitude increase in atmospheric water vapour that was m
165 osure to mild (1609 m) and moderate (2438 m) altitude increased rates of haemolysis and right ventric
166 ent wave interference is clearly observed in altitude independent interference patterns.
167 own to propagate ballistically: They have an altitude independent path loss consistent with minimal s
168                                         High altitude-induced hypoxia in humans evokes a pattern of b
169 on of sympathetic control abolished the high altitude-induced increase in heart rate.
170                                     The high altitude-induced reduction in LV filling and ejection wa
171                            Pregnancy at high altitude is associated with a greater incidence of fetal
172 decrease in apple leaf width with increasing altitude is controlled by a basic/helix-loop-helix trans
173  where bears and wolves are sympatric, where altitude is generally higher than where they are allopat
174  conclusion, the risk of miscarriage at high altitude is lower in Andean women.
175 the authors demonstrated that CMS at extreme altitude is not linked to elevation of hemoglobin, since
176 diate biotic interactions along low-latitude/altitude limits (44 of 68 studies).
177 sits that abiotic factors form high-latitude/altitude limits, whereas biotic interactions create lowe
178 arsh climatic conditions along high-latitude/altitude limits.
179  changes have arisen across independent high-altitude lineages or the speed at which such changes ari
180 tructuring within one of the world's highest altitude lizards, Phrynocephalus theobaldi, due to consi
181  rainfall only increases fertility in higher altitude locations (New Zealand, Romania, and Northern V
182 mic and sympathetic neural assessment at low altitude (Lowlanders, low altitude; 344 m, Sherpa, Kathm
183 xperienced in many situations including high altitude, lung disease, obstructive sleep apnea, and age
184                                      At both altitudes, LZC of the BF signals was significantly highe
185 ia Basin of Tanzania and Uganda in mid-level altitude, malaria-endemic settings.
186                         For aquatic and high-altitude mammals, our analysis highlights 15 and 16 gene
187                                         High-altitude mice had a more oxidative muscle phenotype than
188 d a more oxidative muscle phenotype than low-altitude mice.
189 ss, oxygen saturation <93% (when not at high altitude), moderate malnutrition, or an unknown human im
190 ltitude East Asian populations(4,5) and high-altitude modern Tibetans(6).
191                 Small mammals native to high altitude must sustain high rates of thermogenesis to cop
192                 Small mammals native to high altitude must sustain high rates of thermogenesis to cop
193 in some high-altitude taxa, and several high-altitude natives have evolved to resist the depressive e
194  the evolution of hypoxia resistance in high-altitude natives involves integrated functional changes
195 in the central nervous system; however, high-altitude natives of the Tibetan plateau, the Sherpa, exp
196 es in terahertz spectroscopy(8,9) and a high-altitude observatory(10), of the rotational ground-state
197 nalog, located 1000 km from the coast, at an altitude of 3232 m.
198  occultation profiles penetrating down to an altitude of 40 km.
199 tation of mice (genus Phyllotis) at a record altitude of 6,205 m.
200 ) from the planetary boundary layer up to an altitude of 80 kilometres.
201 lassification of olive oils according to the altitude of the olive grove and to the morphological asp
202 nce of several forms of perturbations in the altitude of the spacecraft is also investigated in this
203 e thrusts are proposed in order to bound the altitude of the spacecraft.
204           Among numerous trapping records at altitudes of >5,000 m, we captured a specimen of the yel
205 etween the planet and its innermost ring, at altitudes of 2600 to 3900 kilometers above the cloud top
206 ts in that there is a low-stability layer at altitudes of 50-58 km and highly and moderately stratifi
207  We also found that the difference in flight altitudes of nocturnally migrating birds between urban a
208 valuate the effect of urbanization on flight altitudes of nocturnally migrating birds.
209 aric (HH)) conditions, at real and simulated altitudes of up to 3800 m.
210 rgies of tens of kiloelectron volts (keV) at altitudes of ~0.8-1.5 Earth radii on timescales over 10
211  should be advantageous under stressful high altitude or latitude environment where short growing sea
212  availability (hypoxia) of residence at high altitude or other conditions is generally thought to be
213 ions to climate, UV exposure, disease, diet, altitude, or cultural practice and have generated import
214                                      At high altitude oxygen delivery to the tissues is impaired lead
215 cantly lower in BERK-SS at mild and moderate altitude (P < 0.05).
216 erpa compared to lowlanders across ascent to altitude (P = 0.046).
217 applied especially to high latitude and high altitude peatlands and during phenological transition ph
218            We then used camera trap and high-altitude photographic data to compare our field and labo
219 ent in obtaining important insight into high altitude physiology.
220 e three-dimensional nature of a flood, where altitude plays a critical role as the third dimension, a
221 d synergies between the conservation of high altitude Polylepis woodlands and their associated avifau
222 ability of directional selection in the high-altitude populations.
223     Tibetan highlanders have adapted to high altitude, possibly in part via the selection of genetic
224                                         High altitude pregnancy is associated with increased frequenc
225 scarriage (pregnancy loss <20 weeks) in high-altitude pregnancy?
226 ressively earlier over time, that increasing altitude produced later phenologies and that a strong sp
227                                They cover an altitude range of 57-1211 m a.m.s.l.
228 en near present-day levels (~21%) within the altitude range where the micrometeorites were melted dur
229 , degraded and restored alpine grasslands at altitudes ranging between 3,900 and 4,200 m on the Tibet
230 erra Nevada mountain range at four different altitudes ranging from 10,000 ft to 40,000 ft.
231 O(2) by age and altitude at four sites, with altitudes ranging from sea level to 4348 m.
232                     Asthma treatment in high altitude reduced the type 2 immune response, corrected t
233 y sensitive phases in high latitude and high altitude regions.
234 hondrial plasticity in small mammals at high altitude remains unresolved.
235  the earliest evidence of a prehistoric high-altitude residential site.
236 benefit the global estimated 85 million high altitude residents.
237 mountaineering expedition to survey the high-altitude rodent fauna of Volcan Llullaillaco in the Puna
238 ndance of taxa changed significantly at each altitude sampled, and the diversity profile shifted acro
239                   Species differed in flight altitude, seasonality, and associated weather conditions
240 o in an African population located in a high-altitude setting in Nairobi, Kenya.
241      These findings indicate that geographic altitude should be accounted for when performing retinal
242  metabolism in flight muscle relative to low-altitude sister taxa.
243 ated model plant-soil ecosystems from a high-altitude site (600 m) to low-altitude sites at 300 and 3
244 ecent excavations at Chiquihuite Cave-a high-altitude site in central-northern Mexico-that corroborat
245  in all regions except for Peru (the highest altitude site).
246 ems from a high-altitude site (600 m) to low-altitude sites at 300 and 30 m to simulate warming by 1.
247 of April 2015 to September 2016) at two high altitude sites, i.e., Jungfraujoch (JFJ; Switzerland) an
248         The presence of nanoplastics in high-altitude snow indicates airborne transport of plastic po
249 e completely different to those forming high-altitude snowpack on Earth.
250       Comparative physiology studies of high-altitude species provide an exceptional opportunity to u
251 %) and following 3 to 6 days at 5050 m (high altitude; Spo(2)=83+/-3%).
252  station), and Rigi mountain (rural and high altitude station) in Switzerland and further investigate
253 ross deserts in intermittent flights at high altitude, stopping in the desert during the day, while r
254 our forms of wet-processing in six different altitude strata, aiming to potentiate the final quality
255 t intermediate and especially high migration altitudes, strong headwinds at low and intermediate migr
256 ined with regionally rising equilibrium line altitudes strongly limit mass replenishment of the glaci
257  was found to have an advantage over the low altitude subtropical accession (CAN1).
258               Convergent changes across high-altitude taxa included increased hydroxyacyl-coA dehydro
259  trait under positive selection in some high-altitude taxa, and several high-altitude natives have ev
260 creased in only the longest established high-altitude taxa, whereas hexokinase activity increased in
261 inoids, alkaloids, and fatty acids, the high altitude temperate Himalayan accession (CAN2) was found
262 nts grown at various conditions (considering altitude, temperature, and precipitation/rainfall) and i
263 iates for geographical (latitude, longitude, altitude), temporal (year, season) and habitat terms (wo
264 ally, the estimated numbers of mosquitoes at altitude that cross a 100-km line perpendicular to the p
265 f capturing Anopheles species increased with altitude (the height of the sampling panel above ground
266  CO(2) variability increased with decreasing altitude, the magnitude of which varied from city to cit
267                             After 21 days of altitude therapy, CRTH2-expressing ILC2, CD4(+) and CD8(
268   However, many animals have adapted to high altitude through enhanced Hb binding affinity for oxygen
269 ion, which may confine water vapour to lower altitudes through gravitational fall and subsequent subl
270 the genetic adaptation of humans to the high-altitude Tibetan Plateau(7,8), which was inherited from
271          In contrast to Andean natives, high-altitude Tibetans present with a lower hemoglobin concen
272                                     The high altitude trans-Himalayan region indeed is hostile domain
273                   Clinicians evaluating high-altitude travelers who report moderate to severe limitat
274  study was to investigate the impact of high-altitude treatment on the clinical and immunological res
275 f ILC2 was significantly reduced in EA after altitude treatment.
276 Tregs which partially normalized during high-altitude treatment.
277 decreased significantly in EA patients after altitude treatment.
278 is heavily photopolluted environment, and to altitudes up to 4 km.
279  numerical experiments with different uplift altitudes using the Nanjing University of Information Sc
280                                              Altitude was a strong predictor of vitamin D status in t
281  years, while the effect of cultivation area altitude was also evaluated.
282                                              Altitude was one of the strongest correlates of VDD and
283 ing and summer stormy seasons show that high-altitude water is preferentially supplied close to perih
284                       We examined seven high-altitude waterfowl that have inhabited the Andes (3812-4
285 SCD mice that had lived at mild and moderate altitude were accompanied by changes in the balance betw
286   More than half of the SNPs associated with altitude were within large structural variants (inversio
287 ry (CDO(2) ) by 12-19% at sea level and high altitude, whereas core heating by 1.5 degrees C did not
288 2) by 12-19% (both P < 0.01) irrespective of altitude, whereas heating did not reliably change either
289  display high aerobic capacity (VO(2)max) at altitude, which may be a reflection of genetic adaptatio
290 e deer mice (Peromyscus maniculatus) and low-altitude white-footed mice (P. leucopus) were born and r
291 r understanding of vascular function at high altitude will clinically benefit the global estimated 85
292  North Pacific jet stream (NPJ), winter high-altitude winds that influence regional hydroclimate and
293 Atmospheric composition varies strongly with altitude within a PCAP at night with lower NOx and highe
294  headwinds at low and intermediate migration altitudes within the Caribbean that increase in strength
295                             Exposure to high altitude worsens symptoms and crises in patients with si
296 a level, mild (1609 m) and moderate (2438 m) altitude would have a higher rate of haemolysis, impaire
297 ed exercise tolerance, and that the level of altitude would worsen these decrements.
298  attracted to ALAN; hence, we predicted that altitudes would be lower over urban than over non-urban
299 e cerebral side effects of ascent to extreme altitude, yet little is known as to whether or not they
300 constitutes a relevant alternative for lower-altitude zones, and that spontaneous fermentations have

 
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