ライフサイエンスコーパス: inert gas

1 d by in-situ bubble formation from dissolved inert gas.

2 which reversibly loses NO on purging with an inert gas.

3 gas can also be measured using dilution with inert gas.

4 tion triggered by exposures to high pressure inert gases.

5 nient to carry out without the protection of inert gases.

6 real-time analysis of several impurities in inert gases.

7 emperature without the special protection of inert gases.

8 nd thus, would be more favorable solvent for inert gases.

9 esthetized swine received an infusion of six inert gases.

10 idated by comparative measurements using the inert gas [11C]CH4 in four greyhounds.

11 tment of polymer substrates by a reactive or inert gas aiming at a specific surface functionalization

12 aqueous reaction mixture via purging with an inert gas, allowing for the preparation of pure chlorine

13 ly exposing epitaxial graphene to controlled inert gases and ambient humidity conditions, while measu

14 iltration, the filtrate is blown dry with an inert gas, and the dried porphyrinogen can be dissolved

15 us solvents and liquid water in solvation of inert gases are not principally due to the hydrogen-bond

16 nd closed through heat treatments in air and inert gas at various temperatures.

17 was monitored in the presence and absence of inert gases at normal and elevated pressures and under b

18 anotubes that are undergoing collisions with inert gas atoms or small molecules.

19 from the intact complex by colliding it into inert gas atoms such as argon or xenon.

20 acuumised extraction cell, (3) holding in an inert gas buffer tank, (4) pasteurisation, (5) and refri

21 ed to less than 1 ppb from nitrogen or other inert gas by passing through an oxygen trap.

22 tension, in random order, using the multiple inert gas elimination technique (MIGET).

23 Multiple inert gas elimination technique study showed that the tr

24 To test this we used the multiple inert gas elimination technique to study eight women and

25 gas exchange, the latter using the multiple inert gas elimination technique.

26 evaluated by blood gas analysis and multiple inert gas elimination technique.

27 smatching was analyzed by using the multiple inert gas elimination technique.

28 ution (VA/Q) was analyzed using the multiple inert gas elimination technique.

29 of VA and Q were determined by the multiple inert gas elimination technique.

30 onchoconstriction measured with the multiple inert gases elimination technique is frequently bimodal.

31 e black phosphorus channels passivated in an inert gas environment, without any prior exposure to air

32 Inert gas exchange in tissue has been almost exclusively

33 ly reversible and independent of the type of inert gas exposure.

34 ve been prepared from an aluminum flux under inert gas flow.

35 A simple, rapid extraction under inert gas followed promptly by LC-MS analysis minimized

36 The inert gases helium and xenon are effective neuroprotecta

37 An auxiliary inert gas (hot N(2)) was used to enhance the drying proc

38 The partial pressure of a given inert gas in mixed-venous blood flowing back to the lung

39 ir underwater results in increased dissolved inert gas in tissues and organs.

40 s enables the in situ conversion of SF6 , an inert gas, into an active fluorinating species by using

41 based on the fact that when a pulsed flow of inert gas is introduced into the conjunction between a p

42 served at low gas phase concentrations or in inert gas matrices.

43 gy-ion-beam deposition into a (co-condensed) inert gas matrix and UV laser-induced visible-region pho

44 uss environmental effects of the solid-state inert-gas matrix on the reaction rate.

45 ere taken before (hemodynamics, blood gases, inert gas measurements) and 10 (hemodynamics, blood gase

46 od gases) and 20 (hemodynamics, blood gases, inert gas measurements) minutes after induction of ventr

47 cycle of protein activation is initiated by inert gas-mediated singlet O2 production.

48 to the co-gas N2, since substitution of the inert gas N2 by either Ar or He has no effect on measure

49 rees < theta < 127 degrees ; in contrast, an inert gas, N2, was nonwetting with a smaller range of co

50 n that also uses nitrogen, and for different inert gases, no significant effects upon performance are

51 or spatial as well as temporal variations in inert gas partial pressure in tissue.

52 del does not allow for spatial variations in inert gas partial pressure.

53 ctivation of the ions via collisions with an inert gas produces isotopically derivatized fragment ion

54 er echocardiography, pulmonary blood flow by inert gas re-breathing, and vasoactive exchange via the

55 udy was to validate CO measurement using the inert gas rebreathing (IGR) method against other noninva

56 The scaled particle model of inert gas solubility in liquid water predicts cavity wor

57 omena of cavity formation and association of inert gas solutes.

58 nitric oxide, which is then entrained in an inert gas stream and detected, usually through chemilumi

59 understanding of the effects of pressure and inert gas supersaturation on organ function and knowledg

60 uid, droplets of the reaction mixture and an inert gas that maintains a uniform droplet spacing and s

61 ld not be used if an accurate calculation of inert gas transport to tissue is required.

62 impulse oscillometry (IOS), multiple breath inert gas washout (MBW), body plethysmography, single-br

63 metry, body plethysmography, multiple-breath inert gas washout (with the tracer gas sulfur hexafluori

64 The multiple-breath inert gas washout parameter acinar ventilation heterogen

65 y control subjects performed multiple-breath inert gas washout, plethysmography, and spirometry.

66 ith EDTA/NaCl/Tris buffer, and spraying with inert gases, were used to reduce the nonspecific adsorpt

67 tion assumes that the partial pressure of an inert gas (which is proportional to the content of that

68 The "inert" gas xenon has been shown to be an effective neuro