ライフサイエンスコーパス: multilamellar

1 those possessing excess positive charge were multilamellar aggregates with the DNA effectively conden

2 ate endosome size and reduced the numbers of multilamellar and dense-tubule-containing late endosomes

3 als age-progressive accumulation of striking multilamellar and multivesicular organelles, preceding t

4 ous nanospheres, filomicelles and vesicular, multilamellar and tubular polymersomes from poly(ethylen

5 Free radical oxidations of multilamellar and unilamellar liposomes of various mixtu

6 ow that the coacervate-supported membrane is multilamellar, and mediates the selective uptake or excl

7 ylene deformation modes, observed when lipid multilamellar assemblies are rapidly frozen from the liq

8 and transmission electron microscopy showed multilamellar axonal ensheathment.

9 rements and previous simulations of hydrated multilamellar bilayers (MLB) of DPPC.

10 particles surrounded by lipid shells, called multilamellar bodies (MLBs), reported in human age-relat

11 icroscopic analysis revealed the presence of multilamellar bodies resembling ceroid in the DV of the

12 This causes the formation of multilamellar bodies typical of many lysosomal storage d

13 uronal cholesterol deposits, accumulation of multilamellar bodies, and age-dependent neurodegeneratio

14 e multipotential glial cells that synthesize multilamellar, compacted myelin and secrete growth facto

15 This novel multivesicular / multilamellar compartment, we suggest represents the sta

16 oppositely charged membrane surfaces in the multilamellar complex is responsible for DNA stabilizati

17 uced capture and release of lectins in dense multilamellar complexes is highly efficient, highly sele

18 arly complexes that assemble and function in multilamellar contexts in vivo.

19 Electron microscopy of multilamellar crystals of CA(2+)-ATPase currently offers

20 Comparing the profile of molecules in these multilamellar crystals with that previously observed in

21 ty of morphologies, including large-diameter multilamellar cylinders and liposome-like structures, as

22 CNS myelin, a multilamellar differentiation of the oligodendrocyte pla

23 ave been performed on fluid (L(alpha))-state multilamellar dispersions as a function of temperature f

24 -MASNMR yielded high-resolution spectra from multilamellar dispersions of unlabeled brain SM and Chol

25 as a model lipid, these domains can convert multilamellar DMPC vesicles into discoidal-shaped partic

26 poE3, apoE4, and a mutant form apoE4R158M to multilamellar DMPC vesicles was similar and was reduced

27 on of protein and membrane in an exaggerated multilamellar endosomal compartment.

28 The growth of large multilamellar fatty acid vesicles fed with fatty acid mi

29 plasm, and in ligand blots binds to purified multilamellar fibrous matrix.

30 f crystalline inclusions bound together by a multilamellar fibrous matrix.

31 ructural recovery of SC lipids to the native multilamellar form.

32 prefer loose layers or vesicular rather than multilamellar forms, thereby prolonging the structural r

33 and sequence of Man after self-assembly into multilamellar glycodendrimersomes (GDSs).

34 annulus fibrosus (AF) represents a complex, multilamellar, hierarchical structure consisting of coll

35 en closely appositioned membranes within the multilamellar interior of late endosomal/lysosomal prote

36 We use the fact that the repeat spacing of multilamellar lipid bilayers is a sensitive and accurate

37 d that 5'-mononucleotides organized within a multilamellar lipid matrix can produce oligomers in the

38 s initiate wrapping of neuronal axons with a multilamellar lipid structure called myelin.

39 he number of water molecules of hydration of multilamellar lipid vesicles using magic angle spinning

40 ter in defects (lakes) that are intrinsic to multilamellar lipid vesicles; the result was inconsisten

41 For randomly oriented multilamellar lipids or aligned membranes, solid-state (

42 cell-depleted by intravenous inoculation of multilamellar liposome-encapsulated dichloromethylene di

43 dansylated lecithin by incubation with donor multilamellar liposomes and isolated by centrifugation.

44 a fractions of l(o) phase lipids obtained in multilamellar liposomes by a fluorescence resonance ener

45 mplete-core LPSs, and then incorporated into multilamellar liposomes consisting of dimyristoyl phosph

46 lls in mice by intravenous administration of multilamellar liposomes containing dichloromethylene-bis

47 POPC), water, and ibuprofen were measured in multilamellar liposomes using pulsed field gradient magi

48 Lipid and ethanol 1H NMR resonances of multilamellar liposomes were resolved by magic-angle spi

49 previously reconstituted Z rings in tubular multilamellar liposomes with FtsZ-YFP-mts, where mts is

50 ted intravenously with 5-mg boluses of large multilamellar liposomes, and the ensuing hemodynamic, he

51 thy et al. for poly(ethylene glycol)-grafted multilamellar liposomes.

52 undergoes dehydration, a liquid crystalline multilamellar matrix is produced that organizes and conc

53 em is the ensheathment of axons by myelin, a multilamellar membrane containing a small group of prote

54 ized by ensheathment of axons with myelin, a multilamellar membrane greatly enriched in the galactoli

55 howed that the storage material consisted of multilamellar membrane profiles ("zebra bodies").

56 nalized gap junctions were incorporated into multilamellar membrane structures, with features charact

57 regardless of their source, have in common a multilamellar membrane wrapping, and long myelinated seg

58 Myelin is synthesized as a multilamellar membrane, but the mechanisms of membrane t

59 od and to confer long-term stability on this multilamellar membrane.

60 esults agree with previous experiments using multilamellar membranes as well as with molecular dynami

61 ostable complex demonstrated the presence of multilamellar membranes with a periodicity 6.0 to 6.5 nm

62 re into liposomes during extrusion of large, multilamellar membranes.

63 ucture-directing agents were prepared from a multilamellar MFI (ML-MFI) zeolite.

64 e of GM-CSF and IL-4, empty HLA-DR reside in multilamellar MIIC, but are scarcely observed at the cel

65 ease or renal cancer patients contain round, multilamellar mineral particles of 50 to 1,500 nm, where

66 operties in a dipalmitoylphosphatidylcholine multilamellar model membrane bilayer system.

67 y to self-regulate the formation of compact, multilamellar myelin and generate sheaths of physiologic

68 an increase in glial cell size to generate a multilamellar myelin sheath.

69 eir plasma membrane around axons to generate multilamellar myelin sheaths.

70 orphous, to aggregates with a more extensive multilamellar nanostructure.

71 stable, and multifunctional unilamellar and multilamellar onion-like vesicles denoted dendrimersomes

72 mitoyl-2-oleoyl-sn-glycero-3-phosphocholine) multilamellar onions dispersed in deuterated dodecane.

73 ediated spontaneous solubilization of either multilamellar or unilamellar vesicles made of a membrane

74 membrane surfaces, which, in turn, fuse into multilamellar or unilamellar vesicles.

75 etween the central and inner plaques of this multilamellar organelle.

76 V was less efficient than apoA-I at clearing multilamellar phospholipid liposomes and promoting ATP-b

77 sisting of single (unilamellar) or multiple (multilamellar) phospholipid bi-layers.

78 man trimers, efficiently coprecipitated with multilamellar PI liposomes in the presence of calcium.

79 l-sensitive binding to solid-phase PI and to multilamellar PI liposomes.

80 Ca(2+) gives rise to 100-mum-wide single- or multilamellar planar sheets of lipid and LPS formed from

81 ethod is based upon reconstituting DAGK into multilamellar POPC vesicles by dialyzing the detergent d

82 ocytic and late-Golgi markers in an aberrant multilamellar pre-vacuolar compartment.

83 rformed on randomly oriented, fully hydrated multilamellar samples.

84 nervous system produce myelin, a lipid-rich, multilamellar sheath that surrounds axons and promotes t

85 g axons in helical or concentrically wrapped multilamellar sheets of insulating plasma membrane--the

86 immune response elicited by NPs composed of multilamellar "stapled" lipid vesicles carrying a recomb

87 phobic, interactions are responsible for the multilamellar structure and stability of myelin.

88 LPS in water spontaneously forms a multilamellar structure composed of symmetric bilayers.

89 This periodic multilamellar structure was retained at temperatures as

90 and cationic liposomes self-assemble into a multilamellar structure where two-dimensional lipid shee

91 diffraction of the globules revealed a novel multilamellar structure with alternating lipid bilayer a

92 The Schwann cell myelin sheath is a multilamellar structure with distinct structural domains

93 action patterns of dried samples suggested a multilamellar structure with the beta-folded P0-cyt loca

94 rrangement of each component to form compact multilamellar structures comprised of alternating layers

95 ganize collagen fibril bundles into complex, multilamellar structures essential for transparency in t

96 uced by rapamycin and was highly enriched on multilamellar structures induced by dysfunctional ESCRT-

97 We use multilamellar structures of common lipids to identify an

98 -derived lines consistently exhibit abundant multilamellar structures that are positive for markers o

99 mesomorpholgy and resulted in myelinic-like, multilamellar structures.

100 nd causes accumulation of autophagosomes and multilamellar structures.

101 of Atg5-positive puncta and the formation of multilamellar structures.

102 ics of polymer films, of liquid crystals and multilamellar surfactant films, and of metal surfaces, a

103 hase in sphingomyelin-containing mixed lipid multilamellar suspensions with 0.4 mol % EqtII.

104 al volume adiabatic compressibilities of the multilamellar vesicle assemblies.

105 in lipid, vacuole and endoplasmic reticulum/multilamellar vesicle-like structures, and altered cellu

106 ), (ii) faster rate of association with DMPC multilamellar vesicles (MLV), (iii) greater reduction in

107 ) as the neutral lipid and preparing them as multilamellar vesicles (MLV), we increased the efficienc

108 PO (chiPO), or DM (chiDM) in DMPC/DMPS (1:1) multilamellar vesicles (MLVs) and of chiDO in large unil

109 ion of large unilamellar vesicles (LUVs) and multilamellar vesicles (MLVs) are very different.

110 mbrane packing, and volumetric properties in multilamellar vesicles (MLVs) composed of the polar lipi

111 protonated in a weak acid) was inserted into multilamellar vesicles (MLVs) consisting of either 1-pal

112 lpha-helical conformation in the bilayers of multilamellar vesicles (MLVs) containing dipalmitoylphos

113 olid-state NMR data of PLB and P-PLB in POPC multilamellar vesicles (MLVs) indicates that a direct in

114 , DMPS/DO, and [DMPC/DMPS (1:1, mol/mol)]/DO multilamellar vesicles (MLVs).

115 were encapsulated in lipid-based onion-type multilamellar vesicles (MLVs).

116 es against OVA in comparison with the larger multilamellar vesicles (MLVs).

117 ge unilamellar vesicles (LUV) and sedimented multilamellar vesicles (sMLV), as opposed to SUV, form l

118 produce higher order morphologies, including multilamellar vesicles and micelles depending on the pH.

119 ielding compressed interbilayer distances in multilamellar vesicles at equilibrium with unaltered bil

120 ion of dimyristoylphosphatidylcholine (DMPC) multilamellar vesicles by apolipoprotein A-I (apoA-I) to

121 or the microsolubilization of dimyristoyl-PC multilamellar vesicles by apolipoprotein A-I.

122 DT-diaphorase to either large unilamellar or multilamellar vesicles containing homologs of CoQ, inclu

123 In contrast, powder x-ray data from multilamellar vesicles does not yield information about

124 demonstrated that novel transferrin-bearing multilamellar vesicles entrapping alpha-T3 resulted in a

125 Here, we describe interbilayer-crosslinked multilamellar vesicles formed by crosslinking headgroups

126 In contrast, NMR of multilamellar vesicles gives evidence for smaller ( appr

127 sulation efficiency of 36.3 +/- 18.9%, while multilamellar vesicles have an encapsulation efficiency

128 yl-L-alpha-phosphatidylethano lam ine (POPE) multilamellar vesicles have been determined fluorometric

129 2,2'-azobis(2,4-dimethylvaleronitrile) into multilamellar vesicles in the presence of NADH and DT-di

130 Furthermore, 2H NMR experiments on DMPC-d54 multilamellar vesicles indicate that the acyl chains of

131 ture of headgroups and interbilayer water in multilamellar vesicles is investigated by electron spin

132 the emission intensity profile in stationary multilamellar vesicles obtained with a polarized excitat

133 Multilamellar vesicles of 0.1-5.5 mm in diameter in the

134 In multilamellar vesicles of dioleoylphosphatidylethanolami

135 and the other specifically (19)F labeled) in multilamellar vesicles of dipalmitoylphosphatidylcholine

136 igh instrumental resolution are reported for multilamellar vesicles of L alpha phase lipid bilayers o

137 igh instrumental resolution are reported for multilamellar vesicles of L alpha phase lipid bilayers o

138 r spontaneous solubilization of phospholipid multilamellar vesicles or the ABCA1-mediated efflux of c

139 ational echo double-resonance experiments in multilamellar vesicles support the helical conformation

140 volves the evolution of small unilamellar to multilamellar vesicles to lamellar liquid crystals and f

141 fusion of small unilamellar vesicles to form multilamellar vesicles was detected.

142 ure of dipalmitoylphosphatidylcholine (DPPC) multilamellar vesicles was studied by cw-ESR using a cha

143 Low numbers of multilamellar vesicles were present, some of which were

144 g solid-state NMR experiments carried out on multilamellar vesicles were used to corroborate the heli

145 alpha-helix, particularly at 37 degrees C in multilamellar vesicles with compositions that mimic the

146 inder/arachoid), large unilamellar vesicles, multilamellar vesicles, and cholesterol monohydrate crys

147 le of binding dimyristoylphosphatidylcholine multilamellar vesicles, unless its multimeric structure

148 dgroup mobility, and the repeat distances in multilamellar vesicles, we found that DMSO exclusively w

149 ane of small (approximately 100 nm) uni- and multilamellar vesicles, which were composed of 1-palmito

150 (SM) colipid interactions in fluid uni- and multilamellar vesicles.

151 orescence data previously obtained from PLFE multilamellar vesicles.

152 al types of particles, some of which are not multilamellar vesicles.

153 1,2-dimyristoyl-sn-glycero-3-phosphocholine) multilamellar vesicles.

154 id-disordered (Ld) domains in fully hydrated multilamellar vesicles.

155 headgroups of adjacent lipid bilayers within multilamellar vesicles.

156 ither ABCA1-expressing cells or phospholipid multilamellar vesicles.

157 nt storage material organized as exaggerated multilamellar whorls, striated belts and 'fingerprint bo

158 ke the protein-free cylinders, the cones are multilamellar with essentially identical interlamellar s

159 Furthermore, multilamellar wrapping of myelin membranes around axons