ライフサイエンスコーパス: endotherm

1 atitude, and highest in food webs containing endotherms.

2 s yield temperatures similar to large modern endotherms.

3 at schistosomes are exclusively parasites of endotherms.

4 h, 10.10% resistant starch (RS), and two DSC endotherms: 1) starch gelatinization, and 2) melting of

5 ful means for studying the thermal niches of endotherms across climatic gradients.

6 onsistent with predictions, both terrestrial endotherm and ectotherm predators have significantly pos

7 Both endotherms and ectotherms (e.g., fish) increase their bo

8 etabolic rates were intermediate to those of endotherms and ectotherms and closest to those of extant

9 gram of body mass in ectotherms resulted in endotherms and ectotherms having the same food consumpti

10 n diffusion to that of oxygen consumption in endotherms and ectotherms.

11 parameterize this mechanistic model for any endotherm, and its use can improve SDM predictions by ex

12 While endotherms are able to limit fever costs physiologically

13 f such events on parasitic infections within endotherms are poorly studied and rarely considered in t

14 ips, common to the regulatory systems of all endotherms, are found to relate the rate of oxygen consu

15 The major contribution to the DSC endotherm arises from unfolding HA1 domains.

16 les, the DSC thermograms showed two distinct endotherms associated with the melting of the individual

17 revealed the presence of a new denaturation endotherm at 32 degrees C following UV irradiation of co

18 lly in all three states, exhibiting a single endotherm at 76 degrees C.

19 distinctive differential scaning colorimetry endotherms at 26 and 125 degrees C, attributed to destru

20 O2 versus other uranyl iodate compounds with endotherms at 479 and 494 degrees C.

21 lthough top ectotherms were heavier than top endotherms at a given trophic level, lower metabolic rat

22 rams of frozen PA solutions display a single endotherm, at the onset of ice melting, (2) the sum of t

23 iratory barrier thickness for a diversity of endotherms (birds and mammals) and ectotherms (fishes, a

24 ps of vertebrate ectotherms (amphibians) and endotherms (birds) respond to spatial environmental grad

25 ls yield temperatures lower than most modern endotherms but approximately 6 degrees C higher than co-

26 nd Ca2+ both forms exhibited a broad complex endotherm consisting of a well expressed low-temperature

27 ebrates, and understanding how high-altitude endotherms cope with the combined effects of hypoxia and

28 ms of a given body mass relative to those of endotherms correspond to differences in oxygen diffusion

29 Each endotherm could be deconvoluted into at least eight tran

30 ate and body form in extant humans and other endotherms currently make climatic adaptation the most p

31 ution models (SDMs), mechanistic modeling of endotherm distributions remains limited in this literatu

32 Most of these studies are conducted on endotherms, especially mammals, which maintain constant

33 e evolution seems to be a general feature of endotherm evolution, regardless of wide differences in s

34 right arrow over left arrow dimer) exhibited endotherms for C- and N-terminal domain unfolding with T

35 The mucosal immune system of endotherms has evolved organized secondary mucosal lymph

36 nments, and using an arctic nematode with an endotherm host for illustration, we show that climate wa

37 have been identified in multiple terrestrial endotherms; however, comparable adaptations in aquatic e

38 capsulated gold particles show clear melting endotherms in the DTA scan with no accompanying weight l

39 its metabolic rates of microbes, ectotherms, endotherms (including those in hibernation), and plants

40 e, and visually broader peaks in the melting endotherms indicating a greater temperature was required

41 lower melting temperature than YkuN, and its endotherm is composed of a single transition, while that

42 ermoregulatory huddling interactions between endotherms is developed.

43 this challenge is especially acute for small endotherms like hummingbirds that have exceedingly high

44 the stage I material does not show a melting endotherm of the encapsulated metal and does not react w

45 the conditions, the presence of exotherms or endotherms on mixing, though small, are viewed as signat

46 ese conditions, the temperature at which the endotherm peaked, T(max), increased with chain concentra

47 ality and greater longevities than nonvolant endotherms, presumably because flight reduces exposure t

48 In such cases, the DSC endotherm reports on the presumably highly cooperative m

49 k whereby mechanism can be incorporated into endotherm SDMs.

50 the properties of the collagen denaturation endotherm showed that the collagen denaturation endother

51 For endotherms, size and shape define the thermal niche thro

52 t-rate, body and heart mass in 24 species of endotherms spanning 5 orders of body mass.

53 Endotherms such as rats and mice huddle together to keep

54 RVA studies and DSC endotherms suggested molecular damage and amylose-lipid

55 nditions showed insignificant changes in the endotherms, suggesting only slight insertion of the mole

56 by an organism, being considerably faster in endotherms than ectotherms.

57 of the thermal niche of an ellipsoid furred endotherm that accurately predicts field and laboratory

58 For small endotherms that are native to high-altitude environments

59 ological and morphological traits that allow endotherms to persist in a wide range of temperatures.

60 a temporary suspension of euthermia allowing endotherms to undergo reversible hypothermia and generat

61 We find that the metabolic rate of endotherms undergoing their primary mode of locomotion a

62 otherm showed that the collagen denaturation endotherm was determined only by the rate of unfolding,

63 the insoluble complexes, whereas no melting endotherm was observed in the soluble complexes.

64 A good fit of the endotherm was obtained with four two-state transitions s

65 In all cases the endotherms were easily described by four two-state trans

66 bilayers, whereas cholesterol abolished all endotherms when the mole fraction of cholesterol (X(chol

67 Streptokinase exhibited a complex endotherm whose shape was sensitive to changing pH.

68 re dinosaurs ectotherms or fast-metabolizing endotherms whose activities were unconstrained by temper

69 7.4 is characterized by a single cooperative endotherm with a transition temperature (Tm) of 66 degre

70 pressed in a wild-type strain (pts+) had two endotherms with Tm congruent with 50 and 57 degrees C an