ライフサイエンスコーパス: heat loss

1 owing to more rapid heating rates and lower heat loss.

2 y balancing the rates of heat production and heat loss.

3 ace in a dose-dependent manner, resulting in heat loss.

4 ue provides an insulating layer that impedes heat loss.

5 using SU-8 on a glass wafer to minimize the heat loss.

6 e that had undergone divergent selection for heat loss.

7 r high heat loss and an inbred line with low heat loss.

8 thermoregulate almost exclusively by varying heat loss.

9 radiation it absorbs overwhelms its internal heat losses.

10 sent observational evidence that the surface heat loss actually strengthens the front during October-

11 s between a noninbred line selected for high heat loss and an inbred line with low heat loss.

12 5 billion years (Gyr) as a result of surface heat loss and declining radiogenic heat production.

13 rust more than 1 Myr old) results in greater heat loss and fluid flux than that at ridge crests and p

14 ) thermogenesis fails to compensate for body heat loss and heart rate declines, infant pups maintain

15 e to body warming, and when active stimulate heat loss and inhibit heat production.

16 But the mechanisms of interior heat loss and resurfacing are currently unclear, as is t

17 to skin and core cooling, thereby enhancing heat loss and the magnitude of the fall in deep body tem

18 sulations are typically used to minimize the heat losses and to confine the heat transport through th

19 diated by a lower sweating rate (evaporative heat loss) and reduced skin blood flow (dry heat loss) f

20 transepidermal water loss and transcutaneous heat loss, and have difficulty maintaining homeostasis.

21 ystem designs may be large, particularly the heat loss associated with pilot scale data resulting in

22 dent increase in metabolic rate results from heat loss at ambient temperatures below thermoneutrality

23 pat4(-/-) mice did not result from increased heat loss, because both cold tolerance and response to a

24 ostly high optical concentrations leading to heat loss by the hot bulk liquid and heated surfaces or

25 me extend it is beneficial to purposely open heat loss channels in order to establish a larger temper

26 kin resulting in greater skin blood flow and heat loss during cold exposure.

27 not be accounted for solely by modulation of heat loss effectors, but also involves other mechanisms.

28 from the core to the periphery, followed by heat loss exceeding metabolic heat production.

29 heat loss) and reduced skin blood flow (dry heat loss) for a given core temperature.

30 It revealed that elevated GST and heat loss from basements are dominant factors in the hea

31 ation between the tips and the flame reduces heat loss from the flame to the surrounding environment,

32 However, spontaneous heat loss from thermally charged phase-change materials

33 mperatures (GSTs) at artificial surfaces and heat losses from basements of buildings, sewage systems,

34 mixed layer and a strengthening of winds and heat losses from the ocean, as driven by the low frequen

35 The QTL for heat loss identified on chromosome 1 in the HB populatio

36 ch on average indicate significant advective heat loss in crust up to 65 Myr old.

37 alinity waters in the Levantine and enhanced heat loss in the Aegean Sea, coupled with surface water

38 ose from sea ice expansion and reduced ocean heat losses in the Nordic and Barents seas, driven by a

39 use of MWs compensates better for the strong heat losses in this reaction, associated with the boilin

40 or low (SL) stress response from high or low heat loss lines of mice, respectively.

41 were created from lines of mice differing in heat loss measured by direct calorimetry as an indicator

42 In the rat, approximately 20% of total body heat-loss occurs by sympathetically mediated increases i

43 al average of 50 to 100 mW m(-2) and a total heat loss of 7.5 to 15 terawatts.

44 energic agonist midodrine, the inappropriate heat loss over their tail surface was reduced, normalizi

45 tive evidence for additional QTL influencing heat loss, percentage subcutaneous fat, and percentage h

46 g that the physiologic response is to reduce heat loss rather than to generate heat.

47 de new insight into the mechanisms governing heat loss responses and suggest that the age-related dim

48 We have identified that autonomic heat loss responses at rest and during fixed-intensity e

49 eating and infer that ET-1 may attenuate the heat loss responses of cutaneous blood flow, but not swe

50 lts, cyclooxygenase (COX) contributes to the heat loss responses of cutaneous vasodilatation and swea

51 hat the age-related diminished COX-dependent heat loss responses reported in previous studies may be

52 e ageing is known to attenuate COX-dependent heat loss responses.

53 tle's radiogenic contribution to the surface heat loss, set limits on the composition of the silicate

54 ooling occurs via convective and evaporative heat loss, so right-to-left shunted blood flow through a

55 ng" of wing-like pectoral fins and minimizes heat loss through a series of counter-current heat excha

56 enesis in brown adipose tissue, and regulate heat loss through modulation of peripheral vasoconstrict

57 sms (i.e., intracerebral heat production and heat loss via skin surfaces) that underlie MDMA-induced

58 Evidence for significant QTL influencing heat loss was found on chromosomes 1, 2, 3, and 7.

59 These heat exchangers substantially reduce heat loss when these whales feed in cold waters.

60 Also, we found that to avoid unsustainable heat loss while swimming, bears employed unusual heterot