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1                                              Thermotropic and enantiotropic liquid-crystalline phase
2 ic structure induces self-assembly into both thermotropic and lyotropic lamellar liquid crystalline (
3 les are mixed with layered materials such as thermotropic and lyotropic smectic liquid crystals and b
4 Cer acyl chains dramatically lowers the high thermotropic and pressure-induced transitions.
5 aturated acyl chains display relatively high thermotropic and pressure-induced transitions.
6                                          The thermotropic and structural properties of ganglioside GM
7 verse supramolecular structures that exhibit thermotropic and/or lyotropic behavior.
8                     Here, we investigate the thermotropic behavior and solid-state organizations of t
9 nucleation, size-dependent polymorphism, and thermotropic behavior of nanoscale crystals.
10  containing C24 sphingomyelin have a complex thermotropic behavior which may be related to the observ
11                                          The thermotropic behaviors of 1-deoxyDHCers alone and in mix
12                  In contrast to very similar thermotropic changes in the secondary structure of both
13       The resulting hybrid biomaterials form thermotropic columnar hexagonal mesophases in which the
14                      These complexes display thermotropic columnar liquid crystalline behavior in spi
15 tail side groups displays a new bicontinuous thermotropic cubic phase with symmetry Pn3 m and formed
16 s, they self-organize into a multicontinuous thermotropic cubic phase with the Im3m space group symme
17 li channels coincide with discontinuities in thermotropic fluorescence spectra and specific growth ra
18  hydrogen-bond-constrained backbone, exhibit thermotropic lamellar, discotic nematic, hexagonal, and
19 es should be thermodynamically stable in all thermotropic lipid systems.
20 and release of trehalose occurred during the thermotropic lipid-phase transition measured in pancreat
21                  A systematic study into the thermotropic liquid crystal behavior using polarizing op
22 r phases enable the study and application of thermotropic liquid crystal phase behavior without therm
23  we describe an anhydrous nanoDNA-surfactant thermotropic liquid crystal system, which exhibits disti
24 active nematic in contact with a hydrophobic thermotropic liquid crystal.
25 st free-standing hydrogels comprising unique thermotropic liquid crystalline (LC) domains and magneti
26 figurations) of micrometer-sized droplets of thermotropic liquid crystals (LCs) dispersed in aqueous
27 f phospholipids at planar interfaces between thermotropic liquid crystals and aqueous phases gives ri
28                                        Using thermotropic liquid crystals and biological materials, w
29 ied class of liquid crystals are a subset of thermotropic liquid crystals known as calamitic, in whic
30    We report the uniform planar anchoring of thermotropic liquid crystals on films of bovine serum al
31 subunits for the synthesis of a new class of thermotropic liquid crystals via palladium-catalyzed cro
32  simple generic method for the production of thermotropic liquid crystals.
33 urface-driven changes in the orientations of thermotropic liquid crystals.
34 as demonstrated through the synthesis of two thermotropic liquid-crystalline fluorescent benzobis(imi
35 ature of the material and induces reversible thermotropic liquid-crystalline transitions.
36 uid crystals are traditionally classified as thermotropic, lyotropic or polymeric, based on the stimu
37                              Discovering the thermotropic nature of thermal phase transitions in simp
38  gold nanorods are prepared and dispersed in thermotropic nematic liquid crystals.
39  observed to be much lower than the GO doped thermotropic nematic medium 5CB.
40 larized light microscopy to characterize the thermotropic phase behavior and microstructure of diC(14
41  cation exchange resin, Dowex 50WX2, and its thermotropic phase behavior and solute-adsorption proper
42  of the components of the lipid bilayer, the thermotropic phase behavior of dimyristoylphosphatidylch
43 ol- (DAG-) enriched and DAG-poor phases, the thermotropic phase behavior of the ternary mixtures dimy
44 e short-chain DMPC showed greater changes in thermotropic phase behavior than with DPPC on taxane add
45 g molecular dynamics, lateral lipid packing, thermotropic phase behavior, "fluidity", lateral mobilit
46 wo fractions are also quite similar in their thermotropic phase behavior, and their high levels of ga
47        The effect of alpha-tocopherol on the thermotropic phase behaviour of aqueous dispersions of d
48 re we report the experimental observation of thermotropic phase boundaries in these classic ferroelec
49 alorimetry (DSC) was used to investigate the thermotropic phase properties of binary mixtures of disa
50 ophospholipids (C14 to C18 chain length) the thermotropic phase transition is eliminated at the SML e
51  changes increased with temperature near the thermotropic phase transition of DPPG (about 40 degrees
52                          The peptide-induced thermotropic phase transition of MLVs formed of DMPC and
53 MPS-d54, the deuterated species exhibited no thermotropic phase transitions but revealed chain order
54         The effects of these peptides on the thermotropic phase transitions of 1-stearoyl-2-oleoylpho
55 C) between isotropic and chiral nematic (N*) thermotropic phases, which limits their practical applic
56 elatively minor effects on the structure and thermotropic properties of C18:0-SM.
57                           The structural and thermotropic properties of dipalmitoylphosphatidylethano
58                            The structure and thermotropic properties of N-palmitoyl sphingomyelin (C1
59                                          The thermotropic properties of triolein-rich, low-cholestero
60                                      It is a thermotropic (solvent-free) liquid crystal of cubic symm
61 ater), in a range of block copolymers and in thermotropic (solvent-free) liquid crystals.
62 lar dichroism spectroscopy showed no obvious thermotropic structural changes in membrane-bound NRne b
63 only those mutants which also demonstrated a thermotropic structural transition in the complex, and t
64             This assembly leads to the first thermotropic structure of the "double diamond" type.
65 ids in the sense that they show that for the thermotropic transition the approximation of phospholipi

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