ライフサイエンスコーパス: artificial membrane

1 P radically alters how it interacts with the artificial membranes.

2 tic GPCR, into both lipid- and polymer-based artificial membranes.

3 functional significance of this FP by using artificial membranes.

4 the binding and kinetics of Arf and Brag2 in artificial membranes.

5 lar processes and important to the design of artificial membranes.

6 e toxin pores in both human erythrocytes and artificial membranes.

7 two or three dimensions into non-lipid-based artificial membranes.

8 mediate effective fusion of both native and artificial membranes.

9 mucin mimetics and their incorporation into artificial membranes.

10 from the spontaneity of the interaction with artificial membranes.

11 etergent micelles, and when reconstituted in artificial membranes.

12 n detergent micelles compared with native or artificial membranes.

13 of PC2 forms an alpha-helix and inserts into artificial membranes.

14 -2, and BAX can form ion-conductive pores in artificial membranes.

15 aphorase functions as an antioxidant in both artificial membrane and natural membrane systems by acti

16 Permeability through artificial membranes and Caco-2 cell monolayers in vitro

17 -step model applies to biological as well as artificial membranes and that a limiting step in the hyd

18 applications, such as in molecular sensors, artificial membranes, and as catalysts.

19 lipids, opening ion conductance pathways in artificial membranes, and integrating into natural membr

20 eral principles identified from studies with artificial membranes apply to biological systems.

21 Experiments on artificial membranes are revealing many details about th

22 rnary lipid mixture, we demonstrate that the artificial membrane-associated cytoskeleton, on the one

23 crometer-sized rafts are readily observed in artificial membranes, attempts to observe analogous doma

24 p7 and myristoylated p15 fragments of BID to artificial membranes bearing the lipid composition of mi

25 aAPC are based on artificial membrane bilayers containing discrete membran

26 mbrane interaction than the charge-dependent artificial membrane binding, and the mode of interaction

27 Artificial membrane-bound vesicles, known as liposomes,

28 c issues, we assessed the binding of StAR to artificial membranes by fluorescence resonance energy tr

29 tion capacity factor (k(IAM)) on immobilized artificial membrane chromatography columns (IAM-HPLC) is

30 atographic measurements using an immobilized artificial membrane column provide the most precise esti

31 The dynamics of water at the surface of artificial membranes composed of aligned multibilayers o

32 Quantitative kinetic studies using artificial membranes confirm that receptor dimerization

33 e have mimicked this interaction by using an artificial membrane containing synthetic Galcer and reco

34 In vitro, synuclein fragments artificial membranes containing the mitochondrial lipid

35 ere we report on the design and synthesis of artificial membranes embedded with synthetic, self-repro

36 bic substrates in a detergent-free native or artificial membrane environment.

37 boid proteins in both detergent micelles and artificial membrane environments.

38 es and feeding them to mosquitoes through an artificial membrane followed by assessment of infection

39 ion in living systems or reconstitution into artificial membranes; however these approaches have inhe

40 data and an in vitro parameter, immobilized artificial membrane (IAM) chromatography was performed.

41 nts, as determined by HPLC on an immobilized artificial membrane (IAM) column, and serum rhGH concent

42 5R, have been immobilized on the immobilized artificial membrane (IAM) liquid chromatographic station

43 the phospholipid monolayer of an immobilized artificial membrane (IAM) liquid chromatography (LC) sta

44 a chromatographic tool based on immobilized artificial membranes (IAM-HPLC) and with quantum-chemist

45 zes to the nerve terminal and interacts with artificial membranes in vitro but binds weakly to native

46 ssential for the fusion of alphaviruses with artificial membranes (liposomes).

47 tor (beta(2)-AR) have been immobilized on an artificial membrane liquid chromatographic stationary ph

48 holipid analogue monolayer of an immobilized artificial membrane liquid chromatographic stationary ph

49 ention coefficients, measured by immobilized artificial membrane liquid chromatography (IAM-LC) and b

50 Artificial membranes may be resistant or susceptible to

51 the blood-brain barrier, as predicted in an artificial membrane model assay and demonstrated in ex v

52 en major brain gangliosides were adsorbed as artificial membranes on plastic microwells, only GT1b an

53 clamp uses computer simulation to introduce artificial membrane or synaptic conductances into biolog

54 s amphiphilic self-assembled systems such as artificial membranes or cell walls.

55 tudies are normally obtained in vitro and in artificial membranes or detergent.

56 s paves the way for practical application of artificial membranes or droplet networks in diverse area

57 ere obtained experimentally using a parallel artificial membrane permeability assay (PAMPA) and showe

58 ological pH) were studied using the parallel artificial membrane permeability assay (PAMPA) at pH 6.5

59 mbrane permeability was assessed by parallel artificial membrane permeability assay and Caco-2 assay.

60 16 (PhPro)4 stereoisomers using the parallel artificial membrane permeability assay and looked at dif

61 ilico model as well as a customized parallel artificial membrane permeability assay indicated good sk

62 ention measurements determined by a parallel artificial membrane permeability assay was drawn.

63 nhibition activities, anti-fIIa activity and artificial membrane permeability were considerably impro

64 ed liquid membrane, is based on the parallel artificial membrane permeation assay (PAMPA), widely use

65 Data sets for the artificial membrane permeation rate and for clearance in

66 by immobilization on either the immobilized artificial membrane-phosphatidyl choline (IAM-PC) statio

67 ly, addition of the cytosolic preparation to artificial membranes resulted in the transient, charge-i

68 the recombinant, non-lipidated protein into artificial membranes results in bilayer destabilization

69 ll out within 12 h, induction continued with artificial membrane rupture and oxytocin, administered t

70 s expressing the subtypes and an immobilized artificial membrane stationary phase.

71 mbrane binding, which is concordant with the artificial membrane studies.

72 soforms respond differently to properties of artificial membranes such as surface charge, they should

73 subunits was analyzed by crosslinking to an artificial membrane surface and by electron microscopy o

74 nar lipid bilayers are still the best-suited artificial membrane system for the study of reconstitute

75 An artificial membrane system was optimized for application

76 a protein anchor and reconstituted inside an artificial membrane system.

77 and compared in rat liver microsomes and an artificial membrane system.

78 Artificial membrane systems allow researchers to study t

79 eins have been successfully reconstituted in artificial membrane systems for sensing purposes.

80 Artificial membrane tethering of centralspindlin restore

81 Artificial membrane tethering of Ste5(R407S K411S) resto

82 Artificial membrane tethering of the PTEN mutants effect

83 BAX and BCL-2 each form channels in artificial membranes that have distinct characteristics

84 ater dynamics may guide the future design of artificial membranes that rapidly transport protons and

85 However, contrary to the interaction with artificial membranes, the interaction with biological me

86 have shown that cholesterol may nucleate in artificial membranes to form thick two-dimensional bilay

87 he transferability of conclusions drawn from artificial membranes to live cells.

88 re have been tremendous advances in creating artificial membranes to model the properties of native m

89 SNARE proteins are sufficient to fuse artificial membranes together.

90 Lipid mixtures within artificial membranes undergo a separation into liquid-di

91 Herein the influence of limonene on artificial membranes was studied to verify the effect of

92 s disease forms calcium permeant channels in artificial membranes, we have proposed that the intracel

93 found that alpha-synuclein binds directly to artificial membranes whose lipid composition mimics that

94 Irradiation of this artificial membrane with visible light results in the un

95 lpha-synuclein binds with higher affinity to artificial membranes with the PS head group on the polyu