ライフサイエンスコーパス: liquid-crystalline phase

1 ak hydrophobic interactions, indicative of a liquid crystalline phase.

2 and experimental results is very good in the liquid crystalline phase.

3 and on whether the bilayer was in the gel or liquid crystalline phase.

4 nsport and light emission is affected by the liquid crystalline phase.

5 nsport and light emission is affected by the liquid crystalline phase.

6 olate ellipsoidal type I hexagonal lyotropic liquid crystalline phase.

7 ty that averages the dipolar coupling in the liquid crystalline phase.

8 o 16:0-22:6PE-d(31)/SM (1:1) bilayers in the liquid crystalline phase.

9 umns assemble further into a two-dimensional liquid crystalline phase.

10 SM and increased acyl chain ordering in the liquid crystalline phase.

11 s from unbinding of dislocations-a 'hexatic' liquid crystalline phase.

12 liquid ordered phase that may coexist with a liquid crystalline phase.

13 ether the fluoroalkylated PC was in a gel or liquid-crystalline phase.

14 rs in bilayers of phosphatidylcholine in the liquid-crystalline phase.

15 nd in the design of new magnetically aligned liquid crystalline phases.

16 emble into nanoscale fibers, aggregates, and liquid crystalline phases.

17 ouplings for molecules dissolved in oriented liquid crystalline phases.

18 an in the SM dispersions in both the gel and liquid crystalline phases.

19 hose in DPPC dispersions in both the gel and liquid crystalline phases.

20 ilayers are fully hydrated and in the fluid (liquid-crystalline) phase.

21 ve also confirmed uptake by the resin in the liquid-crystalline phase and release in the gel phase.

22 n to self-assemble into a hexagonal columnar liquid crystalline phase, and respond to applied electri

23 .5 A, indicating that the bilayers were in a liquid-crystalline phase, and several sharp low-angle re

24 iched CHOL, the solubility of CHOL in the CE liquid-crystalline phase (approximately 8 mol %) was mea

25 eposited from the hexagonal (H(I)) lyotropic liquid crystalline phase are shown to be excellent amper

26 amer in both the solid state and the aqueous liquid crystalline phase are well reproduced.

27 nded compounds of molybdenum and tungsten in liquid crystalline phases are described.

28 ispersed with cellulose nanocrystals to form liquid crystalline phases are developed.

29 ely little is known about how defects in one liquid crystalline phase arise from defects or deformati

30 tive magneto-LC effect in columnar hexagonal liquid crystalline phase as probed by differential scann

31 s work provides new insights into the use of liquid crystalline phases as templates for nanocrystal s

32 chain and 1 is the methyl group) do not form liquid-crystalline phases as a consequence of strong alt

33 s of the 2H NMR spectra were observed in the liquid crystalline phase at and above 0 degrees C.

34 ning calorimetry indicates a transition to a liquid-crystalline phase at 81 degrees C.

35 We also report spontaneous formation of liquid-crystalline phases at high concentrations ( appro

36 We report the discovery of a lyotropic liquid crystalline phase based on a 3-D hexagonal close-

37 The liquid crystalline phase behavior of 4-[6-(4'-cyanobiphe

38 ensions were prepared in which the lyotropic liquid crystalline phase behavior of the hybrid material

39 The aqueous, lyotropic liquid-crystalline phase behavior of the alpha-helical p

40 between them, as the baseline, we report the liquid-crystalline phase behaviors of two other related

41 rface, similar to the formation of lyotropic liquid crystalline phases by common surfactants.

42 e addition of equimolar CHOL in the lamellar liquid crystalline phase causes a smaller increase in or

43 -like') macromolecules often exhibit nematic liquid crystalline phases characterized by orientational

44 N-H dipolar couplings, measured in uniaxial liquid crystalline phases, clearly establishes the relat

45 bient temperature (293 K), at which gel- and liquid-crystalline phases coexist in the peptide-free PO

46 responsible for the formation of the layered liquid crystalline phase consisting of hexagonally order

47 The liquid crystalline phase consisting of the potassium sal

48 unts of DP and other lipid components in the liquid-crystalline phase, correlating with a dramatic in

49 The bilayer periodicity in both the gel and liquid-crystalline phases decreases significantly at hig

50 e change between two distinct regions on the liquid-crystalline phase diagram: (i) a higher density h

51 g of graphene oxide flakes in self-assembled liquid-crystalline phases enables laser patterning of co

52 Thermotropic and enantiotropic liquid-crystalline phase formation of 1PnX salts is favo

53 type of lipid bilayer disk or bicelle, and a liquid crystalline phase formed by a cationic lipid.

54 n lipid bilayer in the biologically relevant liquid crystalline phase has been examined by performing

55 e with C16:0-SM bilayers in both the gel and liquid-crystalline phases; however, 30 mol % C16:0-SM re

56 suggested that freezing the LDL core into a liquid crystalline phase imposes structural constraints

57 ences of the formation of a novel electronic liquid crystalline phase in its vicinity.

58 han that of this spin label in SM in gel and liquid crystalline phases (in absolute values), indicati

59 mol % PCer, PSM and PCer mix ideally in the liquid crystalline phase; in the gel phase, PCer becomes

60 When cooled from the untilted L(alpha) liquid-crystalline phase into the tilted gel phase, vesi

61 The liquid crystalline phase is a necessary requirement for

62 These data suggest that the LDL core in the liquid crystalline phase is characterized by the appeara

63 Interestingly, a smectic-type liquid crystalline phase is observed at temperatures bet

64 For liquid crystalline phases, it is important to understand

65 oundaries between the ordered and disordered liquid crystalline phases (L and L) were similar for SM

66 ng uniform lattice orientation in frustrated liquid-crystalline phases, like cubic blue phases, is a

67 ional constraints obtained from samples in a liquid-crystalline phase lipid bilayer.

68 nment tensors through steric interactions, a liquid crystalline phase of cetylpyridinium bromide alig

69 The chiral nematic liquid crystalline phase of d(GpG) consists of long colu

70 The fully hydrated liquid crystalline phase of the dimyristoylphosphatidych

71 deposited from the hexagonal (H1) lyotropic liquid crystalline phase of the nonionic surfactant octa

72 ese copolymers form uncrosslinked, lyotropic liquid crystalline phases of large micelles between whic

73 The liquid crystalline phases of matter each possess distinc

74 Liquid crystalline phases of matter permeate nature and

75 C(n)PyPtSnSe were templated by the lyotropic liquid-crystalline phase of alkylpyridinium surfactant [

76 ese measurements point to the formation of a liquid-crystalline phase of P3HT solutions within a spec

77 TP-I and TPF4 are both highly mobile in the liquid-crystalline phase of the membrane while the inact

78 to the trends mentioned for the 1PnX salts, liquid-crystalline phases of mPnYX are found more freque

79 The observation that the liquid-crystalline phases of mPnYX salts have lower clea

80 Liquid-crystalline phases of stacked lipid bilayers repr

81 It is based on the formation of a lyotropic liquid crystalline phase on the surface of the liquid fi

82 ed to approximately 5-15 microm, whereas the liquid-crystalline phase P-d31OPC permeated to substanti

83 phase in equilibrium with an ordered nematic liquid crystalline phase, results in a clear phase separ

84 he expression of metastability, a feature of liquid crystalline phases that might be exploited in low

85 esicle dispersions, even though the lamellar liquid crystalline phase thickness of C20BAS is only 32

86 The half-time for the liquid crystalline phase to switch is very fast and prop

87 This is the first new inverse lyotropic liquid-crystalline phase to be reported for two decades

88 se of NFA-CER during the transition from the liquid-crystalline phase to the stable gel phase.

89 rimetry (DSC) was used to monitor the gel-to-liquid crystalline phase transition as a function of the

90 Kdo(2)-Lipid A suspensions revealed a gel-to-liquid crystalline phase transition at 36.4 degrees C (T

91 uld exert noticeable influence on the gel-to-liquid crystalline phase transition behavior of the lipi

92 The gel-to-liquid crystalline phase transition is successively weak

93 ented, with which the behavior of the gel-to-liquid crystalline phase transition observed for lipid b

94 But below the gel-to-liquid crystalline phase transition temperature, an addi

95 chain of C(20):C(20)PE can affect the gel-to-liquid crystalline phase transition temperature, Tm, of

96 roup mobility of SM both above and below the liquid crystalline phase transition temperature, whereas

97 ly efficient (3.8 +/- 2.1%) above the gel to liquid crystalline phase transition temperature.

98 ent 31P NMR was used to determine the gel-to-liquid crystalline phase transition temperatures of the

99 metry, we found that the width of the gel-to-liquid crystalline phase transition was 2 degrees C broa

100 eta was examined below and above the gel-to-liquid crystalline phase transition.

101 tidylcholine phospholipids during the gel-to-liquid crystalline phase transition.

102 rature during treatment was above the gel to liquid crystalline phase transition.

103 ospholipid alone undergoes a lamellar gel to liquid-crystalline phase transition at 66 degrees C duri

104 greater reduction in the enthalpy of gel to liquid-crystalline phase transition of DMPC MLV, (iv) hi

105 e conducted at temperatures below the gel to liquid-crystalline phase transition of the membrane lipi

106 ring has confirmed the retention of a gel to liquid-crystalline phase transition of the surfactant, o

107 C24 acyl chains, both having similar gel to liquid-crystalline phase transition temperatures).

108 oss-linked polymer is controlled by a gel to liquid-crystalline phase transition.

109 Both chiral liquid crystalline phase transitions and competing inter

110 The Tm values associated with the gel-to-liquid crystalline phase transitions for these PEs are f

111 ructural specificity effect of polyamines on liquid crystalline phase transitions of DNA and suggest

112 bility and monitor the gel-to-gel and gel-to-liquid crystalline phase transitions of SM as a function

113 The gel-to-liquid crystalline phase transitions of these 15 mixed-c

114 ing of highly unsaturated acyl chains in the liquid crystalline phase was examined for a series of sy

115 ibed here, large vesicle preparations in the liquid crystalline phase were most effective.

116 Films deposited from the hexagonal liquid crystalline phase were shown to be ion selective,

117 on could be suppressed, and room-temperature liquid crystalline phases were obtained.

118 The morphologies of three dilute liquid crystalline phases, which are widely used for bio

119 cular model for phosphocholine lipids in the liquid-crystalline phase, with a rigid backbone in the c