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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  vesicles formed in the presence of PFOA are multilamellar and the smaller objects have a clear bilay
5 ous nanospheres, filomicelles and vesicular, multilamellar and tubular polymersomes from poly(ethylen
6                   Free radical oxidations of multilamellar and unilamellar liposomes of various mixtu
7 ow that the coacervate-supported membrane is multilamellar, and mediates the selective uptake or excl
8 ylene deformation modes, observed when lipid multilamellar assemblies are rapidly frozen from the liq
9  and transmission electron microscopy showed multilamellar axonal ensheathment.
10 rements and previous simulations of hydrated multilamellar bilayers (MLB) of DPPC.
11 particles surrounded by lipid shells, called multilamellar bodies (MLBs), reported in human age-relat
12 icroscopic analysis revealed the presence of multilamellar bodies resembling ceroid in the DV of the
13                 This causes the formation of multilamellar bodies typical of many lysosomal storage d
14 uronal cholesterol deposits, accumulation of multilamellar bodies, and age-dependent neurodegeneratio
15 cumulation of lipid droplets, lysosomes, and multilamellar bodies.
16 cumulation in PTs and the formation of large multilamellar bodies.
17 es, extracellular droplets and extracellular multilamellar bodies.
18 e multipotential glial cells that synthesize multilamellar, compacted myelin and secrete growth facto
19                  This novel multivesicular / multilamellar compartment, we suggest represents the sta
20  oppositely charged membrane surfaces in the multilamellar complex is responsible for DNA stabilizati
21 uced capture and release of lectins in dense multilamellar complexes is highly efficient, highly sele
22 arly complexes that assemble and function in multilamellar contexts in vivo.
23                       Electron microscopy of multilamellar crystals of CA(2+)-ATPase currently offers
24  Comparing the profile of molecules in these multilamellar crystals with that previously observed in
25 ty of morphologies, including large-diameter multilamellar cylinders and liposome-like structures, as
26                                CNS myelin, a multilamellar differentiation of the oligodendrocyte pla
27 ave been performed on fluid (L(alpha))-state multilamellar dispersions as a function of temperature f
28 -MASNMR yielded high-resolution spectra from multilamellar dispersions of unlabeled brain SM and Chol
29  as a model lipid, these domains can convert multilamellar DMPC vesicles into discoidal-shaped partic
30 poE3, apoE4, and a mutant form apoE4R158M to multilamellar DMPC vesicles was similar and was reduced
31 mography to observe that MDCs form as large, multilamellar domains that generate concentric spherical
32 on of protein and membrane in an exaggerated multilamellar endosomal compartment.
33                          The growth of large multilamellar fatty acid vesicles fed with fatty acid mi
34 plasm, and in ligand blots binds to purified multilamellar fibrous matrix.
35 f crystalline inclusions bound together by a multilamellar fibrous matrix.
36 ructural recovery of SC lipids to the native multilamellar form.
37 prefer loose layers or vesicular rather than multilamellar forms, thereby prolonging the structural r
38 and sequence of Man after self-assembly into multilamellar glycodendrimersomes (GDSs).
39  annulus fibrosus (AF) represents a complex, multilamellar, hierarchical structure consisting of coll
40 en closely appositioned membranes within the multilamellar interior of late endosomal/lysosomal prote
41   We use the fact that the repeat spacing of multilamellar lipid bilayers is a sensitive and accurate
42 d that 5'-mononucleotides organized within a multilamellar lipid matrix can produce oligomers in the
43 s initiate wrapping of neuronal axons with a multilamellar lipid structure called myelin.
44 he number of water molecules of hydration of multilamellar lipid vesicles using magic angle spinning
45  and nonpolar (phospholipid) environments in multilamellar lipid vesicles, where the cross-peak devel
46 ter in defects (lakes) that are intrinsic to multilamellar lipid vesicles; the result was inconsisten
47                        For randomly oriented multilamellar lipids or aligned membranes, solid-state (
48  cell-depleted by intravenous inoculation of multilamellar liposome-encapsulated dichloromethylene di
49 dansylated lecithin by incubation with donor multilamellar liposomes and isolated by centrifugation.
50 a fractions of l(o) phase lipids obtained in multilamellar liposomes by a fluorescence resonance ener
51 mplete-core LPSs, and then incorporated into multilamellar liposomes consisting of dimyristoyl phosph
52 lls in mice by intravenous administration of multilamellar liposomes containing dichloromethylene-bis
53 POPC), water, and ibuprofen were measured in multilamellar liposomes using pulsed field gradient magi
54       Lipid and ethanol 1H NMR resonances of multilamellar liposomes were resolved by magic-angle spi
55  previously reconstituted Z rings in tubular multilamellar liposomes with FtsZ-YFP-mts, where mts is
56 ted intravenously with 5-mg boluses of large multilamellar liposomes, and the ensuing hemodynamic, he
57 thy et al. for poly(ethylene glycol)-grafted multilamellar liposomes.
58  undergoes dehydration, a liquid crystalline multilamellar matrix is produced that organizes and conc
59 em is the ensheathment of axons by myelin, a multilamellar membrane containing a small group of prote
60 nosensitive axons are insulated by myelin, a multilamellar membrane formed by Schwann cells.
61 ized by ensheathment of axons with myelin, a multilamellar membrane greatly enriched in the galactoli
62 howed that the storage material consisted of multilamellar membrane profiles ("zebra bodies").
63 nalized gap junctions were incorporated into multilamellar membrane structures, with features charact
64 regardless of their source, have in common a multilamellar membrane wrapping, and long myelinated seg
65                   Myelin is synthesized as a multilamellar membrane, but the mechanisms of membrane t
66 od and to confer long-term stability on this multilamellar membrane.
67 esults agree with previous experiments using multilamellar membranes as well as with molecular dynami
68 ostable complex demonstrated the presence of multilamellar membranes with a periodicity 6.0 to 6.5 nm
69 re into liposomes during extrusion of large, multilamellar membranes.
70 ucture-directing agents were prepared from a multilamellar MFI (ML-MFI) zeolite.
71 e of GM-CSF and IL-4, empty HLA-DR reside in multilamellar MIIC, but are scarcely observed at the cel
72 ease or renal cancer patients contain round, multilamellar mineral particles of 50 to 1,500 nm, where
73 operties in a dipalmitoylphosphatidylcholine multilamellar model membrane bilayer system.
74 y to self-regulate the formation of compact, multilamellar myelin and generate sheaths of physiologic
75 an increase in glial cell size to generate a multilamellar myelin sheath.
76 eir plasma membrane around axons to generate multilamellar myelin sheaths.
77 orphous, to aggregates with a more extensive multilamellar nanostructure.
78  stable, and multifunctional unilamellar and multilamellar onion-like vesicles denoted dendrimersomes
79 mitoyl-2-oleoyl-sn-glycero-3-phosphocholine) multilamellar onions dispersed in deuterated dodecane.
80 ediated spontaneous solubilization of either multilamellar or unilamellar vesicles made of a membrane
81 membrane surfaces, which, in turn, fuse into multilamellar or unilamellar vesicles.
82 etween the central and inner plaques of this multilamellar organelle.
83 ed that PXo specifically marks non-canonical multilamellar organelles (PXo bodies).
84 V was less efficient than apoA-I at clearing multilamellar phospholipid liposomes and promoting ATP-b
85 sisting of single (unilamellar) or multiple (multilamellar) phospholipid bi-layers.
86 man trimers, efficiently coprecipitated with multilamellar PI liposomes in the presence of calcium.
87 l-sensitive binding to solid-phase PI and to multilamellar PI liposomes.
88 Ca(2+) gives rise to 100-mum-wide single- or multilamellar planar sheets of lipid and LPS formed from
89 ethod is based upon reconstituting DAGK into multilamellar POPC vesicles by dialyzing the detergent d
90 ocytic and late-Golgi markers in an aberrant multilamellar pre-vacuolar compartment.
91 rformed on randomly oriented, fully hydrated multilamellar samples.
92 nervous system produce myelin, a lipid-rich, multilamellar sheath that surrounds axons and promotes t
93 g axons in helical or concentrically wrapped multilamellar sheets of insulating plasma membrane--the
94            The poly(A)-LNP were structurally multilamellar spheres without blebs, but the mRNA vaccin
95  immune response elicited by NPs composed of multilamellar "stapled" lipid vesicles carrying a recomb
96 phobic, interactions are responsible for the multilamellar structure and stability of myelin.
97           LPS in water spontaneously forms a multilamellar structure composed of symmetric bilayers.
98                                This periodic multilamellar structure was retained at temperatures as
99  and cationic liposomes self-assemble into a multilamellar structure where two-dimensional lipid shee
100 diffraction of the globules revealed a novel multilamellar structure with alternating lipid bilayer a
101          The Schwann cell myelin sheath is a multilamellar structure with distinct structural domains
102 action patterns of dried samples suggested a multilamellar structure with the beta-folded P0-cyt loca
103 rrangement of each component to form compact multilamellar structures comprised of alternating layers
104 ganize collagen fibril bundles into complex, multilamellar structures essential for transparency in t
105 uced by rapamycin and was highly enriched on multilamellar structures induced by dysfunctional ESCRT-
106                                       We use multilamellar structures of common lipids to identify an
107 -derived lines consistently exhibit abundant multilamellar structures that are positive for markers o
108 elevated lysophosphatidylcholine species and multilamellar structures visualized by cryo-electron tom
109 mesomorpholgy and resulted in myelinic-like, multilamellar structures.
110 nd causes accumulation of autophagosomes and multilamellar structures.
111 of Atg5-positive puncta and the formation of multilamellar structures.
112 ics of polymer films, of liquid crystals and multilamellar surfactant films, and of metal surfaces, a
113 hase in sphingomyelin-containing mixed lipid multilamellar suspensions with 0.4 mol % EqtII.
114 al volume adiabatic compressibilities of the multilamellar vesicle assemblies.
115  in lipid, vacuole and endoplasmic reticulum/multilamellar vesicle-like structures, and altered cellu
116  large unilamellar vesicles (LUVs) and giant multilamellar vesicles (GMVs) from unrefined, deoiled so
117 lified using a ToF-SIMS image of dried large multilamellar vesicles (LMVs), loaded with the antibioti
118 ), (ii) faster rate of association with DMPC multilamellar vesicles (MLV), (iii) greater reduction in
119 ) as the neutral lipid and preparing them as multilamellar vesicles (MLV), we increased the efficienc
120 PO (chiPO), or DM (chiDM) in DMPC/DMPS (1:1) multilamellar vesicles (MLVs) and of chiDO in large unil
121 ion of large unilamellar vesicles (LUVs) and multilamellar vesicles (MLVs) are very different.
122 mbrane packing, and volumetric properties in multilamellar vesicles (MLVs) composed of the polar lipi
123 protonated in a weak acid) was inserted into multilamellar vesicles (MLVs) consisting of either 1-pal
124 lpha-helical conformation in the bilayers of multilamellar vesicles (MLVs) containing dipalmitoylphos
125 olid-state NMR data of PLB and P-PLB in POPC multilamellar vesicles (MLVs) indicates that a direct in
126 , DMPS/DO, and [DMPC/DMPS (1:1, mol/mol)]/DO multilamellar vesicles (MLVs).
127  were encapsulated in lipid-based onion-type multilamellar vesicles (MLVs).
128 es against OVA in comparison with the larger multilamellar vesicles (MLVs).
129 ge unilamellar vesicles (LUV) and sedimented multilamellar vesicles (sMLV), as opposed to SUV, form l
130 produce higher order morphologies, including multilamellar vesicles and micelles depending on the pH.
131 ielding compressed interbilayer distances in multilamellar vesicles at equilibrium with unaltered bil
132 ion of dimyristoylphosphatidylcholine (DMPC) multilamellar vesicles by apolipoprotein A-I (apoA-I) to
133 or the microsolubilization of dimyristoyl-PC multilamellar vesicles by apolipoprotein A-I.
134 DT-diaphorase to either large unilamellar or multilamellar vesicles containing homologs of CoQ, inclu
135          In contrast, powder x-ray data from multilamellar vesicles does not yield information about
136  demonstrated that novel transferrin-bearing multilamellar vesicles entrapping alpha-T3 resulted in a
137   Here, we describe interbilayer-crosslinked multilamellar vesicles formed by crosslinking headgroups
138                          In contrast, NMR of multilamellar vesicles gives evidence for smaller ( appr
139 sulation efficiency of 36.3 +/- 18.9%, while multilamellar vesicles have an encapsulation efficiency
140 yl-L-alpha-phosphatidylethano lam ine (POPE) multilamellar vesicles have been determined fluorometric
141  2,2'-azobis(2,4-dimethylvaleronitrile) into multilamellar vesicles in the presence of NADH and DT-di
142  Furthermore, 2H NMR experiments on DMPC-d54 multilamellar vesicles indicate that the acyl chains of
143 ture of headgroups and interbilayer water in multilamellar vesicles is investigated by electron spin
144 the emission intensity profile in stationary multilamellar vesicles obtained with a polarized excitat
145                                              Multilamellar vesicles of 0.1-5.5 mm in diameter in the
146                                           In multilamellar vesicles of dioleoylphosphatidylethanolami
147 and the other specifically (19)F labeled) in multilamellar vesicles of dipalmitoylphosphatidylcholine
148 igh instrumental resolution are reported for multilamellar vesicles of L alpha phase lipid bilayers o
149 igh instrumental resolution are reported for multilamellar vesicles of L alpha phase lipid bilayers o
150 r spontaneous solubilization of phospholipid multilamellar vesicles or the ABCA1-mediated efflux of c
151 ational echo double-resonance experiments in multilamellar vesicles support the helical conformation
152 volves the evolution of small unilamellar to multilamellar vesicles to lamellar liquid crystals and f
153 fusion of small unilamellar vesicles to form multilamellar vesicles was detected.
154 ure of dipalmitoylphosphatidylcholine (DPPC) multilamellar vesicles was studied by cw-ESR using a cha
155                               Low numbers of multilamellar vesicles were present, some of which were
156 g solid-state NMR experiments carried out on multilamellar vesicles were used to corroborate the heli
157  lamellar liquid crystals, and large uni- or multilamellar vesicles where the large torus {Mo(154)} a
158 m originally large unilamellar vesicles into multilamellar vesicles with a collapsed interbilayer spa
159 alpha-helix, particularly at 37 degrees C in multilamellar vesicles with compositions that mimic the
160 inder/arachoid), large unilamellar vesicles, multilamellar vesicles, and cholesterol monohydrate crys
161 le of binding dimyristoylphosphatidylcholine multilamellar vesicles, unless its multimeric structure
162 dgroup mobility, and the repeat distances in multilamellar vesicles, we found that DMSO exclusively w
163 ane of small (approximately 100 nm) uni- and multilamellar vesicles, which were composed of 1-palmito
164 orescence data previously obtained from PLFE multilamellar vesicles.
165  (SM) colipid interactions in fluid uni- and multilamellar vesicles.
166 al types of particles, some of which are not multilamellar vesicles.
167 id-disordered (Ld) domains in fully hydrated multilamellar vesicles.
168 headgroups of adjacent lipid bilayers within multilamellar vesicles.
169 1,2-dimyristoyl-sn-glycero-3-phosphocholine) multilamellar vesicles.
170 ither ABCA1-expressing cells or phospholipid multilamellar vesicles.
171 nt storage material organized as exaggerated multilamellar whorls, striated belts and 'fingerprint bo
172 ke the protein-free cylinders, the cones are multilamellar with essentially identical interlamellar s
173                                 Furthermore, multilamellar wrapping of myelin membranes around axons

 
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