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1  and interactions of catecholamines with the biomembrane.
2 t on direct interactions between ILs and the biomembrane.
3 nd stability of pores formed in vesicles and biomembranes.
4 lipids in curved regions and vesicle buds of biomembranes.
5 nderstanding of lateral heterogeneity within biomembranes.
6 ets to test the effect of immunoglobulins on biomembranes.
7 n approach used during domain isolation from biomembranes.
8 es of distinct signal-triggering topology on biomembranes.
9 ically well-defined lipid bilayer models for biomembranes.
10 hydrophilic proteins can bind transiently to biomembranes.
11 idylcholine were used in this study to mimic biomembranes.
12 that mimics the composition and structure of biomembranes.
13 o create, manipulate, and analyze lipids and biomembranes.
14  that diffusion is highly localised in fluid biomembranes.
15 nel architecture for active transport across biomembranes.
16 the importance of the collective dynamics of biomembranes.
17 efficient to deplete cholesterol (Chol) from biomembranes.
18 properties notably determine the behavior of biomembranes.
19 rameter to monitor packaging and fluidity of biomembranes.
20  to muscle components like myofibrils and/or biomembranes.
21 ol transport of these charged species across biomembranes.
22 sion of the freezing point of transitions in biomembranes.
23 t can aid in the characterization of complex biomembranes.
24 ow that TX-100 has a restructuring action on biomembranes.
25 otein association and protein insertion into biomembranes.
26 the asymmetric distribution of components in biomembranes.
27 duce targeted binding of amyloid deposits to biomembranes.
28 omplex, stable, and impermeable phospholipid biomembranes.
29 -55,940 partitions with high efficiency into biomembranes.
30 f bubbles in foams, and pattern formation in biomembranes.
31 haracterization of composition variations in biomembranes.
32  lipids can induce dramatic shape changes in biomembranes.
33 triggering a dramatic change in the shape of biomembranes.
34 tudies on mass transport characterization of biomembranes.
35 teins in stabilizing nascent fusion pores in biomembranes; a function inferred from recent experiment
36 tly taking into account the mechanics of the biomembrane and cytoskeleton.
37 nce of methanol, and solvents in general, in biomembrane and proteolipid studies.
38 pyridine) were prepared as model systems for biomembranes and cells and studied by scanning electroch
39 redict passive permeation of peptides across biomembranes and for determining the thermodynamics of p
40  identify biofunctional lattice formation on biomembranes and galectin-reagents with therapeutic pote
41   Omega-3 and -6 PUFAs are key components of biomembranes and play important roles in cell integrity,
42 demonstrate an affinity of superwarfarins to biomembranes and suggest that cellular responses to thes
43     Molecular self-assembly, the function of biomembranes and the performance of organic solar cells
44 across the bilayer indicated that asymmetric biomembranes are assembled and maintained by specific me
45 e functional roles of the lipid asymmetry of biomembranes are attracting increasing attention.
46 rium steady state, our findings suggest that biomembranes are elastically more complex than previousl
47                                              Biomembranes are key objects of numerous studies in biol
48                                          How biomembranes are self-organized to perform their functio
49                                              Biomembranes are thin capacitors with the unique feature
50 nine, a dye that is commonly used in various biomembrane assays.
51 e catalysis demands the generation of intact biomembrane assemblies with structural integrity and lat
52  beta-sheet aggregates upon interacting with biomembranes at the onset of diseases, such as Parkinson
53 issue within a biomembrane requires that the biomembrane be biologically inert, and that the mean por
54 ng dynamic and topological information about biomembranes because the molecular interactions taking p
55 , simulations are a great technique to study biomembrane behavior.
56  GTP-loaded K-Ras4B with heterogeneous model biomembranes by using a combination of different spectro
57 ing the molecular evolution of ion-selective biomembrane channels/transporters, globular proteins, an
58                           Lipid bilayers are biomembranes common to cellular life and constitute a co
59 ncluding those (pi > or =30 mN/m) that mimic biomembrane conditions.
60 urface pressures (> or = 30 mN/m) that mimic biomembrane conditions.
61                                              Biomembranes constitute a basis for all compartments of
62 cked using an activity-based probe, with the biomembranes delineated by carbocyanine lipid reporters.
63  binding to serum proteins, interaction with biomembranes, differences in subcellular localization, a
64 apparently new possibilities in the study of biomembrane electrostatics and other bioelectric phenome
65 ganic mixed ionic-electronic parameters, and biomembrane features.
66 ay be correlated with the lipid diversity of biomembranes, for example, with regard to membrane curva
67 novel single-cell based nanotool termed dual biomembrane force probe (dBFP).
68                                      Using a biomembrane force probe capable of measuring single bond
69        Adhesion frequency experiments with a biomembrane force probe could not detect interactions of
70                               We have used a biomembrane force probe decorated with P-selectin to for
71 ve dynamics simulations, we demonstrate that biomembrane force probe measurements of various P- and L
72                                              Biomembrane force probe was used to determine VWF-GPIb m
73 robes (e.g., the atomic force microscope and biomembrane force probe), P-selectin:PSGL-1 adhesion bon
74                                      Using a biomembrane force probe, we observed biphasic force-dece
75                                      Using a biomembrane force probe, we observed real-time reversibl
76                     Using a flow chamber and biomembrane force probe, we show a triphasic force depen
77 al fluctuation and force-clamp assays with a biomembrane force probe.
78 tly larger than previously published for the biomembrane force probe.
79 ease/resumption in thermal fluctuations of a biomembrane force probe.
80                                    Using the biomembrane force-probe, the bond system was exposed to
81 nd is highly enriched in detergent-resistant biomembrane fractions associated with microdomains, i.e.
82 understanding how lipid diversity relates to biomembrane function.
83  rate model shows that for proteins to drive biomembrane fusion at observed rates, they have to perfo
84 ative predictions about how proteins mediate biomembrane fusion.
85 oaded K-Ras4B with neutral and anionic model biomembranes has been investigated by a combination of d
86 roviding new insight into dynamic changes in biomembranes; however, few reports in the literature hav
87 termine whether a structurally heterogeneous biomembrane, human stratum corneum (SC), behaved as a ho
88 t setting, the use of fibrin in a collagenic biomembrane impairs B-MSCs proliferation and migration i
89 Here, through an integrated bioenergetic and biomembrane integrity probing in three different human c
90                                              Biomembrane interfaces create regions of slowed water dy
91                          Integrity of animal biomembranes is critical to preserve normal cellular fun
92 o probing for lipid phase domains in natural biomembranes is discussed.
93  The results show that PLA2 binding to model biomembranes is not significantly affected by pressure a
94 er study, the lipid composition of fusogenic biomembranes is quite complex.
95 based on partition constants of PFAS between biomembrane lipids and water exist.
96 eptides could increase the susceptibility of biomembrane lipids to fusion through an effect on lipid
97  understanding of how lipids and proteins in biomembranes may be obstructed by very small obstacles c
98 namics of small vesicles, diffusing close to biomembranes, may be spatially restricted by altering lo
99     These results show a new method to probe biomembrane mechanical properties using light as well as
100 m to interrogate lipid phase behavior, study biomembrane mechanics, reconstitute membrane proteins, a
101 and linear elasticity theories combined with biomembrane mechanics.
102 though lipid-dependent protein clustering in biomembranes mediates numerous functions, there is littl
103 , activity, and inhibition in a controllable biomembrane microenvironment.
104 yer, describes the conformation of TM-A in a biomembrane mimic, presents a peptide-bilayer model usef
105 0/C10-EPC remained lamellar in mixtures with biomembrane-mimicking lipid formulations [e.g., dioleoyl
106                                      The new biomembrane model challenges the standard model (the flu
107  giant unilamellar vesicles (GUVs, used as a biomembrane model) made by electroformation with varying
108                         The assay applies to biomembrane models as well.
109 vide a basis for the construction of complex biomembrane models, which exhibit fluidity barriers and
110 opy has impeded distinction between numerous biomembrane models.
111 rotein function in a mixture as complex as a biomembrane, one must know whether the lipid composition
112 c dimers and slowing down probe diffusion in biomembranes open the route to significant enhancement o
113  oxygen species that may damage organisms by biomembrane oxidation or mediate environmental transform
114  River humic acid (SRHA) causes an increased biomembrane perturbation (percent leakage of the fluores
115        The temperature studies revealed that biomembrane perturbation increases with decreasing tempe
116 nolamines (PEs), which are a common class of biomembrane phospholipids, typically display direct L(al
117 t the development of a microsphere supported-biomembrane platform enabling characterization of gamma-
118 Cu(+), Ag(+), Zn(2+), Cd(2+), Co(2+)) across biomembranes, playing a key role in homeostasis and in t
119 r solvents, or with combinations of multiple biomembranes, polymers, and nanomaterials remains challe
120 taining membranes and to translocate through biomembranes, presumably because of a higher propensity
121 has been shown to mimic the protein-mediated biomembrane process.
122  of allogeneic or xenogeneic tissue within a biomembrane requires that the biomembrane be biologicall
123 terest, which will open new opportunities in biomembrane research.
124 eltaM2 segments were shown to oligomerize in biomembranes resulting in ion-channel activity with char
125                             Self-assembly of biomembranes results from the intricate interactions bet
126                  Overall, the notion that in biomembranes selected lipids could laterally aggregate t
127                               Our electronic biomembrane sensing platform recreates distinct SARS-CoV
128                                              Biomembranes serve barrier functions and serve as a stor
129                  The mechanisms that mediate biomembrane shape transformations are of considerable in
130   We propose that by modeling these observed biomembrane shapes as fluid lipid bilayers in mechanical
131 yers as well as potential caveats in current biomembrane simulation methodology, including force-fiel
132   We discuss the current state-of-the-art of biomembrane simulations that, until now, have largely fo
133  surface pressures (>30 mN/m) that mimic the biomembrane situation.
134   Phospholipid self-assembly is the basis of biomembrane stability.
135 e thermodynamic effects of anionic lipids on biomembrane stability.
136 e peroxidase, resulting in greater leaf cell biomembranes stability in vines under saline condition c
137                               Most models of biomembrane structure and function include the implicit
138 ase as well as effects on biomacromolecules, biomembranes, subcellular structures and cells are discu
139 n the transmembrane region of SERCA near the biomembrane surface and interfere with calcium transport
140 esent a promising and extremely useful model biomembrane system for systematic measurements of mechan
141 (POPC) large unilamellar vesicle (LUV) model biomembrane system was studied by fluorescence spectrosc
142 possible to obtain structural parameters for biomembrane systems where isotope labeling may be prohib
143 mer backbone to facilitate interactions with biomembrane systems, and (ii) "rigid" dendronized side c
144 affect the fusion rate in model membrane and biomembrane systems.
145 e a guideline for understanding more complex biomembrane systems.
146              In the environment of a typical biomembrane, the higher proportion of saturated fatty ac
147 ess transport or conductance activity across biomembranes through the formation of nanopores.
148 odetermines the complex lipid composition of biomembranes through tuning of kappa .
149 uence ranges from domain formation in intact biomembranes to membrane protein reconstitution and crys
150  the investigation of molecular processes at biomembranes using EW-CRDS for chemical species showing
151 tates in the absence and presence of a model biomembrane was probed by pressure perturbation.
152         The substrate loading into supported biomembranes was detergent-dependent, as evidenced by ev
153  rapidly extracted from the lipid bilayer by biomembranes, which jeopardizes membrane stability and r
154 mechanics can play in imaging multicomponent biomembranes with AFM.
155 s of active gamma-secretase within supported biomembranes with native-like fluidity.
156   The phenomenon of thermal fluctuation of a biomembrane within a stack of like membranes was introdu
157 and triggered its lipoplex to permeate model biomembranes within the time span of endosome processing

 
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