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1 tricted in Napaeozapus insignis, an obligate hibernator.
2 , was also decreased in brain and liver from hibernators.
3  both consistent with an initiation block in hibernators.
4 ibernation compared to other small mammalian hibernators.
5 ousal, consistent with patterns in mammalian hibernators.
6 nfluence metabolism and thermogenesis in non-hibernators.
7 ch is prohibitive for these processes in non-hibernators.
8 is and may explain the enhanced longevity in hibernators.
9 tify cis elements with convergent changes in hibernators.
10 milar and distinct from those found in small hibernators.
11 tive, 0.47 +/- 0.08 pmol/mg protein per min; hibernator, 0.16 +/- 0.05 pmol/mg protein per min, P < 0
12 s from hibernators (active, 2.4 +/- 0.7 min; hibernator, 7.1 +/- 1.4 min, P < 0.001).
13  Patients were designated hibernators or non-hibernators according to the volume of hibernating myoca
14                                              Hibernators accumulated loss-of-function effects for CRE
15 ean transit times in cell-free extracts from hibernators (active, 2.4 +/- 0.7 min; hibernator, 7.1 +/
16  provides a genetic framework for harnessing hibernator adaptations to understand human metabolic con
17  change -0.4 [SE 0.9] and -0.4 [0.8] for non-hibernators and hibernators, respectively) but increased
18 p=0.011) and 3.6% (1.7-5.4; p=0.0002) in non-hibernators and hibernators, respectively.
19 rned by hypoxia tolerant vertebrate animals, hibernators, and freeze-tolerant animals (cryobiology);
20 Increased levels of eEF-2 phosphorylation in hibernators appear to be a component of the regulated sh
21                        Fat-storing mammalian hibernators are an extreme example of this strategy wher
22 dicating that the changes observed in torpid hibernators are defined by body temperature, not torpor
23                                              Hibernators are natural cold-stress adaptors; however, l
24 that underlie the intense activity cycles of hibernator BAT.
25 bsequently cellular aging, in a large-bodied hibernator, black bears (Ursus americanus).
26 torpor and rapid reperfusion during arousal, hibernator brains resist damage and the animals emerge n
27                      In brain and liver from hibernators, eEF-2 kinase activity was increased relativ
28                                              Hibernators have perfected internal mechanisms to mainta
29   Some diapausing insects and some mammalian hibernators have regular cyclic patterns of substantial
30       Previous studies, largely in mammalian hibernators, have shown that periodic arousal is driven
31  the dwarf lemurs of Madagascar are obligate hibernators, hibernating between 3 and 7 months a year.
32        Understanding mechanisms by which the hibernator host and its gut symbionts adapt to the alter
33         We isolated muscle fibers from small hibernators, Ictidomys tridecemlineatus and Eliomys quer
34 ns (TADs) enriched for convergent changes in hibernators, including the Fat Mass & Obesity (Fto) locu
35 hat show shallow torpor, but its activity in hibernators is at least damped if not absent.
36  temperature around 37 degrees C, whereas in hibernators it can approach 0 degrees C without triggeri
37                                 Migrants and hibernators may experience problems as a consequence of
38  ventriculography, in hibernators versus non-hibernators, on carvedilol compared with placebo.
39                     Patients were designated hibernators or non-hibernators according to the volume o
40                          All small mammalian hibernators periodically rewarm from torpor to high, eut
41 ur findings show how convergent evolution in hibernators pinpoints functional genetic mechanisms of m
42                                     Seasonal hibernators possess a remarkable suite of adaptations th
43  0.9] and -0.4 [0.8] for non-hibernators and hibernators, respectively) but increased with carvedilol
44 % (1.7-5.4; p=0.0002) in non-hibernators and hibernators, respectively.
45 her than protein breakdown could explain the hibernator's capacity for large, rapid, and repeated mic
46                            Winter fasting in hibernators shifts the microbiota to favor taxa with the
47                          In most fat-storing hibernator species, seasonal changes in food intake, tri
48                                    Effect of hibernator status on response of LVEF to carvedilol was
49 pite such a depressed physiologic phenotype, hibernators still maintain activity in their nervous sys
50                                              Hibernators, such as the 13-lined ground squirrel, endur
51                                     Seasonal hibernators, such as the arctic ground squirrel (AGS), d
52                                    Mammalian hibernators survive prolonged periods of cold and resour
53                  Female and underweight male hibernators terminate hibernation in spring when abovegr
54 occurring variant of ATP5G1 from a mammalian hibernator that critically contributes to intrinsic cyto
55 ls, Ictidomys tridecemlineatus, are obligate hibernators that transition annually between summer home
56 n gene expression in the brain of a seasonal hibernator, the golden-mantled ground squirrel, Spermoph
57 Urocitellus brunneus)-a federally threatened hibernator-to meet three objectives: (1) document season
58 cemlineatus and Eliomys quercinus and larger hibernators, Ursus arctos and Ursus americanus.
59 nual cycle, especially lipid reserves, makes hibernators valuable and promising models for research i
60 easured by radionuclide ventriculography, in hibernators versus non-hibernators, on carvedilol compar
61        Leveraging this knowledge gained from hibernators, we engineered a deliverable RNF114 complex
62  (Ictidomys tridecemlineatus) are obligatory hibernators who can survive over 6 months of the year in