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1 squirrels before any of the animals began to hibernate.
2 utside of Madagascar was previously known to hibernate.
3 Toolkit, and server-side data storage using Hibernate.
4 axis, increases its body weight, and finally hibernates.
6 584 segments, 24% (n = 140) were labeled as hibernating; 23% (n = 136) as stunned; 30% (n = 177) as
7 mine, was observed in 83% of stunned, 59% of hibernating, 35% of remodeled and 13% of scarred myocard
8 l because only 55% of segments classified as hibernating actually improved resting function after rev
10 osmolarity and pH outside the incubator with Hibernate and density gradient separation of neurons fro
11 -altitude inhabitants, as well as those that hibernate and interrupt their development when exposed t
12 but kinase-knockout clones still are able to hibernate and recover, indicating that this pathway does
13 me, and hematological features of blood from hibernating and active free-ranging subadult brown bears
15 utyric acid ([GABA](ecf)) in striatum of non-hibernating and hibernating arctic ground squirrels to t
17 nconsistent bloodstream amino acid supply by hibernating and waiting for more nutrient to be provided
18 d by fibrosis from that arising from viable (hibernating and/or stunned) myocardium has important imp
19 ptable mammals, spending up to half the year hibernating, and the remainder of the year attempting to
20 It may also be induced in nonhibernators via hibernating animal serum factors or delta-opiate peptide
21 emical findings were compared with untreated hibernating animals (n = 7), sham-normal animals (n = 5)
23 respect from nature: Diving, burrowing, and hibernating animals living in diverse environments are m
24 similarities between calorie-restricted and hibernating animals suggest the effects of CR may be par
25 shutdown of cellular functions that permits hibernating animals to tolerate severe reductions in cer
27 SCs were observed postsynaptic to cones from hibernating animals, although depolarized cones were abl
29 34 interactions were disrupted in brain from hibernating animals, in which eIF-2alpha was highly phos
30 imer-like phosphorylation is also present in hibernating animals, mitosis, or during embryonic develo
33 BA](ecf)) in striatum of non-hibernating and hibernating arctic ground squirrels to test the hypothes
34 neural microstructure from groups of animals hibernating at different ambient temperatures revealed t
35 ose syndrome (WNS) is an emerging disease of hibernating bats associated with cutaneous infection by
36 drome (WNS) is an emerging disease affecting hibernating bats in eastern North America that causes ma
39 proliferates at low temperatures and targets hibernating bats, resulting in their premature arousal f
41 on and delayed recovery of metabolic rate in hibernating bears suggest that the majority of metabolic
43 w temperatures, and perhaps their ability to hibernate below the permafrost, might explain the abilit
44 sured metabolic rate and body temperature in hibernating black bears and found that they suppress met
46 ranscription-PCR products from euthermic and hibernating brain and compared them using differential d
47 as reduced 3-fold in cell-free extracts from hibernating brain at 37 degreesC, eliminating hypothermi
48 rpose of this study was to determine whether hibernating brain tissue is tolerant to penetrating brai
50 Among patients with ischemic cardiomyopathy, hibernating, but not ischemic, myocardium identifies whi
52 approximately 124% and 99%, respectively, in hibernating compared with cold control preparations with
53 The remaining SCNx squirrels that did not hibernate continuously displayed CARs in body mass withi
60 Western fat-tailed dwarf lemurs are known to hibernate for seven months per year inside tree holes.
64 d for weeks in brain and other organs of the hibernating ground squirrel, Spermophilus tridecemlineat
65 uirrels (T(b) range 34.7-38.9 degrees C) and hibernating ground squirrels (T(b) range 2.9-3.9 degrees
66 BA](ecf) was determined in unrestrained, non-hibernating ground squirrels (T(b) range 34.7-38.9 degre
67 , suggest that light can reach the retina of hibernating ground squirrels maintained in the laborator
68 rites, and spines from several cell types in hibernating ground squirrels retract on entry into torpo
69 ng hibernation and arousal in two species of hibernating ground squirrels suggest that it could play
70 d shutdown of cellular function that permits hibernating ground squirrels to tolerate "trickle" blood
71 bular epithelial cells (RTECs) isolated from hibernating ground squirrels would be protected against
72 eriments, we looked at mlEPSCs from cones of hibernating ground squirrels, which exhibit dramatically
77 ificantly enhanced in both cold controls and hibernating groups, while vasoconstriction in response t
78 ificantly increased in the renal arteries of hibernating hamsters compared with controls, but not com
80 y in the pancreas, but when expressed in the hibernating heart it liberates fatty acids from triglyce
85 teristics of the cardiac interstitium in the hibernating human myocardium and evaluate whether active
87 g perfusion was significantly reduced in the hibernating LAD region in comparison with the normal rem
88 increased from 2.4+/-0.04 to 4.7+/-0.7 mm in hibernating LAD regions (P<0.05) whereas remote wall-thi
89 and a long-term (1976-2008) data set from a hibernating mammal (the yellow-bellied marmot) inhabitin
93 shortage and/or reduced ambient temperatures hibernating mammals become heterothermic, allowing their
99 ypothermic and hypometabolic torpid state in hibernating mammals, we investigated the potential for t
102 Apoptotic myocytes were observed in the hibernating myocardial region in all pigs (4.8 +/- 2.3%)
103 vidence for a local inflammatory reaction in hibernating myocardial segments from patients undergoing
107 nt in LVEF was associated with the volume of hibernating myocardium (viable myocardium with contracti
110 ibitory cytokines are elevated in regions of hibernating myocardium and account in part for the depre
111 GF-5 may afford a way to restore function in hibernating myocardium and ameliorate heart failure in c
112 renergic receptor densities occur in viable, hibernating myocardium and may account in part for the o
115 that can accurately determine the amount of hibernating myocardium as well as the presence and degre
116 re is evidence to suggest that patients with hibernating myocardium benefit most from revascularizati
117 coplasmic reticulum proteins were present in hibernating myocardium but absent in stunned myocardium
119 umented with a proximal LAD stenosis develop hibernating myocardium characterized by relative reducti
120 ysiological and molecular characteristics of hibernating myocardium develop rapidly after a critical
123 proved clinically useful for distinguishing hibernating myocardium from irreversibly injured myocard
124 nuclear density to 995+/-100 nuclei/mm(2) in hibernating myocardium from the instrumented group versu
126 acked necrosis, might have been mistaken for hibernating myocardium had only histology been evaluated
127 rsibility of protein changes that develop in hibernating myocardium have an impact on functional reco
131 ced flow and increased FDG characteristic of hibernating myocardium in similarly instrumented pigs af
134 cyte >10%) and increased glycogen typical of hibernating myocardium in the LAD region (33+/-3% of myo
136 lts indicate that icMSCs improve function in hibernating myocardium independent of coronary flow or r
142 his study was performed to determine whether hibernating myocardium is adaptive or is destined to und
143 lation of oxygen consumption and function in hibernating myocardium is an adaptive response that prev
145 ata indicate that the proteomic phenotype of hibernating myocardium is dynamic and has similarities t
146 0.65+/-0.08 (mean+/-SEM) mL.min(-1).g(-1) in hibernating myocardium of instrumented pigs compared wit
147 F-A improves contractile function of chronic hibernating myocardium of pigs to a level comparable to
148 on tomography identified ischemia, scar, and hibernating myocardium on the survival benefit associate
151 Thus, physiologic and structural features of hibernating myocardium remain constant for at least two
152 ster and more precise method for determining hibernating myocardium remains the holy grail of noninva
153 , can be initiated by regional dysfunctional hibernating myocardium resulting from a severe coronary
154 in function and oxygen consumption at rest, hibernating myocardium retains the ability to increase m
155 and the presence of ischemia and/or stunned/hibernating myocardium should be assessed for optimal ma
156 designed to study apoptosis in hypoperfused hibernating myocardium subtending severe coronary stenos
157 tricular dysfunction (LVD) may have areas of hibernating myocardium that improve functionally after r
158 gene expression is regionally upregulated in hibernating myocardium to a level intermediate between t
159 te the serial changes in the response of the hibernating myocardium to dobutamine stimulation after r
161 f contractile reserve and thallium uptake in hibernating myocardium to myocardial structure in humans
162 descending artery (LAD) stenosis to produce hibernating myocardium underwent percutaneous revascular
163 egion (33+/-3% of myocytes from animals with hibernating myocardium versus 15+/-4% of myocytes from s
164 ascularization in the setting of significant hibernating myocardium was associated with improved surv
167 n the fasting state, FDG uptake in pigs with hibernating myocardium was heterogeneous and was increas
176 ing artery (LAD) stenosis to produce chronic hibernating myocardium with regional contractile dysfunc
177 n reversible loss of cardiomyocyte function (hibernating myocardium), which is amenable to therapeuti
178 t persistent myocardial stunning can lead to hibernating myocardium, 13 pigs were chronically instrum
180 emodeling in the cardiac interstitium of the hibernating myocardium, an important predictor of recove
182 identification of candidates with regions of hibernating myocardium, because these patients stand to
183 measured the expression of survival genes in hibernating myocardium, both in patients surgically trea
184 hat dobutamine echocardiography can identify hibernating myocardium, but laboratory studies suggest t
187 ion in coronary BF in conscious pigs induced hibernating myocardium, ie, perfusion-contraction matchi
191 this preclinical swine model of ischemic and hibernating myocardium, the combined delivery of circula
192 t in perfusion reserve is well recognized in hibernating myocardium, there is substantial controversy
193 tensive defects in HED uptake were found for hibernating myocardium, with regional retention approxim
232 reas of nonfunctional but viable (stunned or hibernating) myocardium can also contribute to the devel
234 olonged torpor and in squirrels that did not hibernate or had not been hibernating for several weeks.
238 factors ribosome modulation factor (RMF) and hibernating promoting factor (HPF) were shown to directl
240 ed transmural variation in FDG uptake in the hibernating region (LAD/normal), which averaged 2.5 +/-
241 p, NTG alone improved wall thickening in the hibernating region modestly from 11.4+/-7.2% at baseline
247 a marker of active remodeling, was higher in hibernating segments than in segments with persistent dy
248 duced a torpor-like state similar to that in hibernating species and characterized by a marked fall i
251 The results show that [GABA](ecf) in non-hibernating squirrels was 73 nM and this level was decre
252 the changes from a state of activity to the hibernating state are poorly understood; however, the se
255 yzes the regulation of ischemic tolerance in hibernating thirteen-lined ground squirrels (Spermophilu
257 e observation that eastern dwarf lemurs also hibernate, though in self-made underground hibernacula.
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