ライフサイエンスコーパス: energy gain

1 y, which should be optimised to maximise net energy gain.

2 ibution of a particular membrane to the free energy gain.

3 on reaction with methane yields the greatest energy gain.

4 nd edibility and has been argued to increase energy gain.

5 mpared to fibrils, results in a smaller free energy gain.

6 substantial length to achieve a significant energy gain.

7 pesticide pollutants, respectively, per net energy gain.

8 forage fishes but did not show the greatest energy gains.

9 behaviour of an animal that maximizes total energy gained.

10 plasma with more than a gigaelectronvolt of energy gain, accelerating a trailing positron bunch in a

11 inding could benefit from the potential free energy gain accompanying the release of these water mole

12 the coefficient of variation of the rate of energy gain among patches, and the ratio of the expected

13 >100 MV m(-1) accelerating gradient, >50 MeV energy gain and excellent output beam quality.

14 High gradients of energy gain and high energy efficiency are necessary par

15 results for below-gap optical pumping reveal energy-gain and -loss Floquet replica valence bands that

16 days HRT, shifted from neutral to positive (energy gain around 2.7 GJ/d) after thermal pretreatment.

17 nce of the boundary energy, we show that the energy gain associated with boundary curvature relaxatio

18 he in-plane lattice constants diminishes the energy gain associated with the tetragonal distortion, a

19 Despite a focusing energy gain below unity, the unprecedented power gain is

20 We report the demonstration of the energy gain by a distinct trailing positron bunch in a p

21 which case the distance of acceleration and energy gain can be strongly limited by head erosion.

22 nfirmed by both the high negative Gibbs free energy gain, DeltaG = -115.95 kJ/mol, calculated using t

23 f possible dimer conformations, and that the energy gain depends on the interplay between structural

24 Prey profitability (energy gained divided by prey handling time) is an essen

25 routes shape animal movement and presumably, energy gains during migration.

26 Density functional theory showed that the energy gain from CO binding to low-coordinated Cu atoms

27 ase) is a transmembrane enzyme that utilizes energy gained from ATP hydrolysis to transport sodium an

28 The energy gained from intercalation is slightly greater tha

29 how that cooking substantially increases the energy gained from meat, leading to elevations in body m

30 ng not on molasses in reactor feed but using energy gained from oxidation of sulfur compounds produce

31 Within 18-h test, the energy gained from the MPPC was 76.8 J, 76 times higher

32 The docking energy gained from this induced fit is 0.7 kcal/mol for

33 foods, the idea that cooking meat increases energy gain has never been tested.

34 alternative, a biofuel should provide a net energy gain, have environmental benefits, be economicall

35 However, the energy gain in a single-stage LPA can be limited by lase

36 goal of achieving burning fusion plasmas and energy gain in the laboratory.

37 ein between the two GET phases by leveraging energy gained in ATP binding and hydrolysis to undergo s

38 ws the optical pulse, is primarily due to an energy gain involving the photoexcited charge carriers t

39 throttles reconnection so that the electron energy gain is a large fraction of the released magnetic

40 Although energy gain is a well-known effect from cooking starch-r

41 al/mol to the helix stability, while no free energy gain is detected if the two residues have the rev

42 Later in the photocycle, the free energy gain is transferred from the chromophore to the p

43 in terms of raw material, solvent, time and energy gained more importance to provide a sustainable l

44 The energy gain must reside in or near the photoisomerized r

45 field of the second stage is detected via an energy gain of 100 megaelectronvolts for a subset of the

46 -95% recovery efficiency, resulting in a net energy gain of 57-62 kJ/mol-CO2 captured.

47 ed barrier of 116 kJ mol(-1) and the overall energy gain of 72 kJ mol(-1).

48 application of the model to examine the net energy gain of a typical pause-travel predator (the Atla

49 dscape of fibril growth and reduces the free energy gain of Abeta peptide binding to the fibril by ap

50 mW/m(2) in 2011, which represents an annual energy gain of around 1.0 x 10(15) J.

51 piratory pathways, describing the respective energy gain of host-cell and PMP resulting from varying

52 on demonstrate that half of the binding free energy gain of m(7)GTP with respect to GTP can be attrib

53 Here we show that an energy gain of more than 42 GeV is achieved in a plasma

54 ectively doubles their energy, producing the energy gain of the 3-km-long SLAC accelerator in less th

55 photocathode wakefield acceleration combines energy gains of tens of GeV m(-1) with generation of ult

56 cene gives rise to a substantial anti-Stokes energy gain (PDI, 0.70 eV; tetracene, 0.86 eV).

57 charged particle beams at high gradients of energy gain per unit length is necessary to achieve an a

58 We show how energy gain, predation and damage can be combined in a s

59 indicate that the fundamental limitation to energy gain presented by laser depletion can be overcome

60 el also releases less air pollutants per net energy gain than ethanol.

61 se counteracting effects result in a maximum energy gain through a complete removal of water molecule

62 cificity (i.e. the result of greater binding energy gained through interactions with major histocompa

63 omplex suggests that there is a considerable energy gain upon binding of maltotriose in comparison to

64 te linear acceleration of electrons with keV energy gain using optically generated terahertz pulses.

65 ions illustrate that substantial anti-Stokes energy gains via a TTA process can be effortlessly reali

66 Large digestive organs increase rates of energy gain when food is plentiful but are costly to mai

67 self-assembly reflects a balance between the energy gain when particle cores approach and the entropy