ライフサイエンスコーパス: hibernator

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1 milar and distinct from those found in small hibernators.

2 , was also decreased in brain and liver from hibernators.

3 both consistent with an initiation block in hibernators.

4 tive, 0.47 +/- 0.08 pmol/mg protein per min; hibernator, 0.16 +/- 0.05 pmol/mg protein per min, P < 0

5 s from hibernators (active, 2.4 +/- 0.7 min; hibernator, 7.1 +/- 1.4 min, P < 0.001).

6 Patients were designated hibernators or non-hibernators according to the volume of hibernating myoca

7 ean transit times in cell-free extracts from hibernators (active, 2.4 +/- 0.7 min; hibernator, 7.1 +/

8 change -0.4 [SE 0.9] and -0.4 [0.8] for non-hibernators and hibernators, respectively) but increased

9 p=0.011) and 3.6% (1.7-5.4; p=0.0002) in non-hibernators and hibernators, respectively.

10 rned by hypoxia tolerant vertebrate animals, hibernators, and freeze-tolerant animals (cryobiology);

11 Increased levels of eEF-2 phosphorylation in hibernators appear to be a component of the regulated sh

12 dicating that the changes observed in torpid hibernators are defined by body temperature, not torpor

13 that underlie the intense activity cycles of hibernator BAT.

14 torpor and rapid reperfusion during arousal, hibernator brains resist damage and the animals emerge n

15 In brain and liver from hibernators, eEF-2 kinase activity was increased relativ

16 Understanding mechanisms by which the hibernator host and its gut symbionts adapt to the alter

17 hat show shallow torpor, but its activity in hibernators is at least damped if not absent.

18 Migrants and hibernators may experience problems as a consequence of

19 ventriculography, in hibernators versus non-hibernators, on carvedilol compared with placebo.

20 Patients were designated hibernators or non-hibernators according to the volume o

21 All small mammalian hibernators periodically rewarm from torpor to high, eut

22 0.9] and -0.4 [0.8] for non-hibernators and hibernators, respectively) but increased with carvedilol

23 % (1.7-5.4; p=0.0002) in non-hibernators and hibernators, respectively.

24 her than protein breakdown could explain the hibernator's capacity for large, rapid, and repeated mic

25 Winter fasting in hibernators shifts the microbiota to favor taxa with the

26 In most fat-storing hibernator species, seasonal changes in food intake, tri

27 Effect of hibernator status on response of LVEF to carvedilol was

28 pite such a depressed physiologic phenotype, hibernators still maintain activity in their nervous sys

29 Hibernators, such as the 13-lined ground squirrel, endur

30 Seasonal hibernators, such as the arctic ground squirrel (AGS), d

31 Female and underweight male hibernators terminate hibernation in spring when abovegr

32 ls, Ictidomys tridecemlineatus, are obligate hibernators that transition annually between summer home

33 n gene expression in the brain of a seasonal hibernator, the golden-mantled ground squirrel, Spermoph

34 nual cycle, especially lipid reserves, makes hibernators valuable and promising models for research i

35 easured by radionuclide ventriculography, in hibernators versus non-hibernators, on carvedilol compar

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