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1                                              CsCl abolished the rectification and hyperpolarized the
2                                              CsCl density gradient centrifugation indicated that almo
3                                              CsCl thermal ionization data are extremely sensitive to
4 ions of salts of different natures (CaCl(2), CsCl, Na(2)SO(4)) in the same mobile phase agree very we
5 amplification, buoyant density analysis in a CsCl gradient, and immunoprecipitation with monoclonal h
6                            We show that in a CsCl gradient, Polycomb response elements, promoters of
7 hree cell types, because of an increase in a CsCl-sensitive, hyperpolarization-activated inward curre
8 triction enzymes, (ii) shift in density on a CsCl gradient of the products synthesized in the presenc
9 ions from the NaCl B1 crystal structure to a CsCl B2 structure, which may have implications for exopl
10 ed whole-cell patch electrodes filled with a CsCl-based solution to voltage clamp the currents.
11  green fluorescence under 470 nm light after CsCl purification.
12 s, receptor 3 is able to extract CsNO(3) and CsCl from an aqueous D(2)O layer into nitrobenzene-d(5)
13 ve used glass-fiber filter binding assay and CsCl density gradient ultracentrifugation to monitor the
14 ed both glass fiber filter binding assay and CsCl density gradient ultracentrifugation to monitor the
15      In contrast to what is seen for CsF and CsCl, single-crystal X-ray structural analyses and (1)H
16 on product nanoparticles, including CsOH and CsCl, proceeded via SiO2 condensation over aggregates of
17 s increased linearly with increasing KCl and CsCl concentrations.
18              The abilities of NaCl, KCl, and CsCl to enhance the stability to urea denaturation were
19 tal chloride solutions (LiCl, NaCl, KCl, and CsCl) at various concentrations.
20 rmeation of alkali chlorides (LiCl, KCl, and CsCl) through steric hindrance-free nanoporous membranes
21  of macroscopic I(h), ZD7288 (50 microM) and CsCl (1 mM), reduced the channel conductance to 8 pS and
22  pulsed field gel electrophoresis (PFGE) and CsCl/ethidium bromide equilibrium centrifugation demonst
23 aster, omits the selective precipitation and CsCl gradient steps, uses less expensive and toxic reage
24 ased on the reaction of (SO3CF3)SiH2GeH3 and CsCl.
25                      As expected, ZD7288 and CsCl increased latencies and decreased the properties of
26                         Other salts, such as CsCl, can give rise to a combination of the two scenario
27 t also synthesized AlNiFe alloy with the B2 (CsCl-type) structure and the metastable Al9Ni2 phase.
28 rent crystal symmetries, including FCC, BCC, CsCl, and AlB2.
29  reported to date binary superlattices (BCC, CsCl, AlB2, Cr3Si, and Cs6C60).
30 alysis to stratify the explorations of a bcc-CsCl crystallite into orthogonal directions according to
31 om common, high-coordinated FCC-CuAu and BCC-CsCl lattices, to more exotic symmetries for spherical p
32 ractions on the transformation of binary bcc-CsCl analog crystals into close-packed configurations.
33 essfully demonstrates the realization of BCC-CsCl, SC-NaCl, and a weakly ordered cubic diamond phase.
34 dPt, and NiFePdPtIr, convert to gamma-brass, CsCl, and NiAs-type high-entropy intermetallics of Zn, I
35 ed irreversible and stable to DNA banding by CsCl gradient ultracentrifugation.
36                  Somatic I(h) was blocked by CsCl (1 mM) and was partially sensitive to BaCl(2).
37 ard rectification (I(h)) that was blocked by CsCl (3 mM) or by ZD 7288 (30 microM).
38 cells, even when K+ channels were blocked by CsCl and intracellular Na+ was clamped by monensin.
39                   This effect was blocked by CsCl and ZD7288, consistent with a role of IH.
40  be effectively separated from each other by CsCl density gradient centrifugation alone.
41 l characterization of viruslike particles by CsCl and sucrose gradient centrifugation revealed biophy
42 t are active at large negative potentials by CsCl and BaCl2, respectively, did not affect DeltaVm, in
43 lary vector in 293 cells and was purified by CsCl banding.
44 tion and size fractionation were purified by CsCl density gradient centrifugation.
45                          Ba1 was purified by CsCl gradient centrifugation and was found to have an ic
46 ed into the cell supernatant and purified by CsCl gradient centrifugation.
47  purified from the wild-type helper virus by CsCl equilibrium density-gradient centrifugation and use
48                         The cesium chloride (CsCl) density gradient profile of virus particles contai
49     Mucins were isolated by cesium chloride (CsCl) gradient centrifugation and size fractionated on S
50 n be purified by banding in cesium chloride (CsCl) gradients.
51 e-centered cubic (fcc), and cesium chloride (CsCl)-type lattices were synthesized by the judicious ch
52         When the recording pipette contained CsCl, greater peak inward current values and densities w
53  Replacement of pipette solutions containing CsCl with solutions containing equimolar concentrations
54 ied fiber proteins than did the conventional CsCl method.
55  be problematic using conventional two-cycle CsCl gradient ultracentrifugation.
56 DNase, (iii) FeCl3 precipitation and DNase + CsCl and (iv) FeCl3 precipitation and DNase + sucrose.
57 tangential flow filtration (TFF) and DNase + CsCl, (ii) FeCl3 precipitation and DNase, (iii) FeCl3 pr
58  outward currents more effectively than does CsCl.
59  of the transducing particles by equilibrium CsCl density-gradient centrifugation showed that the par
60  sensitive to low concentrations of external CsCl.
61  identical to those where it is observed for CsCl and CsBr.
62 h maximizes the recovery of labeled DNA from CsCl gradients.
63  indicate that the CuAu-I crystals form from CsCl parent crystals by a diffusionless transformation,
64 mistry-synthesized Cs(2)SnCl(6) powders from CsCl salt solutions are successfully encapsulated into a
65 les into different crystal structures, e.g., CsCl, AlB2, and Cr3Si.
66  addition, we argue that Cs 5p-5p bonding in CsCl occurs already at ambient pressure, stabilizing the
67                       Similar disparities in CsCl sensitivity were observed in myocytes isolated from
68 ent sedimentation equilibrium experiments in CsCl with UV detection were also generated.
69  dye binds to the negatively charged GAGs in CsCl-fractionated extracts from chicken tendons.
70 yant density of the cross-linked particle in CsCl led to the total mass of the particles and their fr
71 yant density of the cross-linked particle in CsCl we could deduce the total mass of the particle, hen
72                  A comparison of proteins in CsCl density gradient centrifugation fractions from supe
73 how that this mineral should dissociate into CsCl-type MgO cotunnite-type SiO2 at pressures and tempe
74 from the medium of Sf9 cultures by isopycnic CsCl gradient centrifugation followed by rate-zonal cent
75                                     In 1.0 M CsCl, the conductance of each analogue channel is approx
76 eld the intrinsic pKain of PS lipid in 0.1 M CsCl to be in the range 2.5-3.0.
77 M NaCl, 30% ammonium sulfate (mu = 7.0); 3 M CsCl, 30% ammonium sulfate (mu = 7.0); and 2.5 M NaCl, 3
78 ning of all chloride salts of alkali metals (CsCl, RbCl, KCl, NaCl, and LiCl) from the aqueous phase
79 It was blocked by external perfusion of 1 mM CsCl but was unaffected by BaCl(2).
80            The micropipette contained 130 mM CsCl and 1 microM QX-314.
81 asured with patch pipettes containing 130 mM CsCl was 10-15 pS (n = 15 cell pairs); despite this low
82 sured using patch pipettes containing 130 mM CsCl was 220 +/- 13.1 pS (12 cell pairs).
83 under voltage clamp in the presence of 15 mM CsCl and 15 mM tetraethylammonium chloride (TEA-Cl) to e
84 1,000 picosiemens (pS) in symmetrical 150 mm CsCl were observed.
85 (G-T)] and poly[d(A-T)].poly[d(A-T)] in 5 mM CsCl, 0.2 mM HEPES, pH 7.5 at 20 degrees C.
86 naturing conditions in the presence of NaCl, CsCl, and tetrabutyl ammonium chloride (NBu4Cl).
87 mes increase by a factor of 2 on addition of CsCl as the electrolyte.
88                               In the case of CsCl, an unprecedented 2:2 complex is observed in the so
89 th groups then received incremental doses of CsCl until sustained VT resulted.
90  by isopycnic centrifugation in a mixture of CsCl and guanidine HCl.
91 rizing current injections in the presence of CsCl.
92 e purified from Extract PBS by two rounds of CsCl/guanidine HCl ultracentrifugation as well as in vit
93 en PTX3 and AM HC-HA withstands four runs of CsCl ultracentrifugation in the presence of 4 m GnHCl.
94 VC2.null) were isolated by sequential use of CsCl step gradients followed by isopycnic centrifugation
95                 With 1 mEq/kg body weight of CsCl, MAPD90 rose by 86 +/- 100 ms in dogs with HF versu
96 d to high titer (> 10(8)/ml) and purified on CsCl gradients due to their buoyancy difference relative
97  mm (where m denotes molality) NaCl, KCl, or CsCl.
98                  In current-clamp recording, CsCl, which inhibits only I(H) in nodose neurons, hyperp
99 stable complexes with the test cesium salts, CsCl and CsNO(3), in solution (10% methanol-d(4) in chlo
100 es suspended in different density solutions, CsCl for microbeads and Percoll for cells.
101                               In symmetrical CsCl solutions with minimal concentrations of internal E
102            At the sensory receptor terminal, CsCl decreased the threshold pressure for initiation of
103 luid, but does have a lower free energy than CsCl.
104                                We found that CsCl induced larger early afterdepolarizations and a gre
105                                          The CsCl sensitivity of this mutant is suppressed by recessi
106 perstructures: a superatomic relative of the CsCl lattice type and an unusual packing arrangement bas
107 ablished that the B8 phase transforms to the CsCl-type (B2) phase at core pressures and temperatures.
108 se is markedly enhanced for LiCl compared to CsCl.
109 repolarization and heightened sensitivity to CsCl at chamber and cellular levels.
110 were purified from Syn5-infected cells using CsCl centrifugation followed by sucrose gradient centrif
111             Cells were voltage clamped using CsCl filled electrodes, while action potentials and exci
112 negative-strand viral RNA was detected using CsCl-purified CVB3/TD virions, although no negative-stra
113 isera to known proteoglycans; purified using CsCl density gradient centrifugation, molecular sieve, a
114  the P(o) at depolarized potentials, whereas CsCl was more efficacious at hyperpolarized potentials.
115                    We further tested whether CsCl inhibition of repolarizing K+ currents, which are r
116 tanoyl phosphatidylserine (PS) bilayers with CsCl aqueous solutions, we show that the effects of lipi
117 by increased temperature in combination with CsCl or with NaCl plus an alpha subunit ligand, alpha-gl
118 either compositionally ordered crystals with CsCl and CuAu-I symmetries, or disordered, solid solutio
119                 In contrast to findings with CsCl, when organic ions were used in the pipette solutio
120 l layer V pyramidal cells were recorded with CsCl electrodes.
121  Ba(2+), and also reduced in recordings with CsCl-containing electrodes, suggesting a dual underlying
122                       I(K1) suppression with CsCl (5 mmol/L, n=3), BaCl(2) (3 micromol/L, n=3), and l

 
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