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1 ding to a 3'-(dT)(20)-18 bp DNA substrate by sedimentation equilibrium.
2 gin-1 associates as a dimer when analyzed by sedimentation equilibrium.
3 ight scattering, sedimentation velocity, and sedimentation equilibrium.
4 r interference or absorbance measurements at sedimentation equilibrium.
5 f a dimerizing system in chemical as well as sedimentation equilibrium.
6 nce profiles acquired during the approach to sedimentation equilibrium.
7 ized by isothermal titration calorimetry and sedimentation equilibrium.
8 association of the peptides were measured by sedimentation equilibrium.
9 ansmembrane helices during the time-scale of sedimentation equilibrium.
10 7 +/- 4) kDa, a value confirmed by low-speed sedimentation equilibrium.
11 tistically different from values acquired by sedimentation equilibrium.
12 nd compared to values measured previously by sedimentation equilibrium.
13 detection, fluorescence quench titration, or sedimentation equilibrium.
14 l electrophoresis, isoelectric focusing, and sedimentation equilibrium.
15  with the equilibrium constant determined by sedimentation equilibrium.
16  the application to expedite the approach to sedimentation equilibrium.
17 his hypothesis was examined rigorously using sedimentation equilibrium.
18 n moiety in the protein/detergent complex by sedimentation equilibrium; (2) measurement of the appare
19 ed by disassociation constants determined by sedimentation equilibrium: 6.62 x 10(-6) M (rbetaA3), 0.
20 an be verified by sedimentation velocity and sedimentation equilibrium after correction for bound det
21                                              Sedimentation equilibrium analyses confirmed that Purbet
22                                              Sedimentation equilibrium analyses of con-G show that Ca
23 acentrifugation, sedimentation velocity, and sedimentation equilibrium analyses of the native dirigen
24 g of about 13 tubulin units as determined by sedimentation equilibrium analyses.
25                                              Sedimentation equilibrium analysis also indicates that d
26                                              Sedimentation equilibrium analysis by analytical ultrace
27                                              Sedimentation equilibrium analysis demonstrates that sel
28                                              Sedimentation equilibrium analysis in 0.1 M potassium ph
29 ree paramyxovirus F proteins was analyzed by sedimentation equilibrium analysis in detergent and buff
30                                              Sedimentation equilibrium analysis indicated that ClpA p
31                                              Sedimentation equilibrium analysis indicates an alpha 4
32 r organization in solution, we carried out a sedimentation equilibrium analysis of arrestin at both c
33  of this protein in solution, we carried out sedimentation equilibrium analysis of ATIC over a broad
34                                              Sedimentation equilibrium analysis of the recombinant hu
35                                              Sedimentation equilibrium analysis of TM domains contain
36                                              Sedimentation equilibrium analysis revealed that CsA beh
37 nce chemical shift perturbation mapping, and sedimentation equilibrium analysis show that KIX binds a
38                                              Sedimentation equilibrium analysis shows that Ms-Lon ass
39                                              Sedimentation equilibrium analysis shows that Tax and th
40 applied a method described previously, using sedimentation equilibrium analysis to calculate the cont
41 esidue long N-terminal fragment was shown by sedimentation equilibrium analysis to form a dimer with
42                                              Sedimentation equilibrium analysis using purified protei
43                                              Sedimentation equilibrium analysis was also used to esta
44                                              Sedimentation equilibrium analysis was used to compare t
45                                              Sedimentation equilibrium analysis yielded a weight-aver
46 on protein, a novel dye-label technique, and sedimentation equilibrium analysis, we directly and conc
47                                      Through sedimentation equilibrium analysis, we show that the enz
48         Using both protein cross-linking and sedimentation equilibrium analysis, we showed that the A
49                        This was confirmed by sedimentation equilibrium analysis, which also revealed
50 a single predominant oligomeric species, and sedimentation equilibrium analysis-derived mass values i
51 n, high affinity heterodimers were formed in sedimentation equilibrium analysis.
52 examined as determined by gel permeation and sedimentation equilibrium analysis.
53 e reliability of the results obtained from a sedimentation equilibrium analysis.
54 igands in self-association was studied using sedimentation equilibrium analysis.
55                                        A new sedimentation equilibrium analytical procedure shows the
56 analytical size-exclusion chromatography and sedimentation equilibrium analytical ultracentrifugation
57 he core of the protein were studied by using sedimentation equilibrium analytical ultracentrifugation
58                                              Sedimentation equilibrium analytical ultracentrifugation
59 e have used alanine-scanning mutagenesis and sedimentation equilibrium analytical ultracentrifugation
60                                              Sedimentation equilibrium analytical ultracentrifugation
61                                              Sedimentation equilibrium analytical ultracentrifugation
62 ducing single-alanine substitutions and used sedimentation equilibrium analytical ultracentrifugation
63                                 We have used sedimentation equilibrium analytical ultracentrifugation
64                                              Sedimentation equilibrium analytical ultracentrifugation
65                  Using SDS-PAGE analysis and sedimentation equilibrium analytical ultracentrifugation
66                                    Utilizing sedimentation equilibrium analytical ultracentrifugation
67 into stable monomers in solution as shown by sedimentation equilibrium and CD and formed an intrachai
68                                              Sedimentation equilibrium and chemical cross-linking exp
69                                              Sedimentation equilibrium and circular dichroism studies
70                                              Sedimentation equilibrium and cross-linking data demonst
71                                        Using sedimentation equilibrium and cross-linking methods, we
72  have been measured in the absence of DNA by sedimentation equilibrium and gel filtration chromatogra
73                                  As shown by sedimentation equilibrium and gel-filtration experiments
74 chemical and biophysical analyses, including sedimentation equilibrium and scanning transmission elec
75                                              Sedimentation equilibrium and sedimentation velocity ana
76                            In the past, both sedimentation equilibrium and sedimentation velocity ana
77 f the octylglucoside-solubilized receptor by sedimentation equilibrium and sedimentation velocity ana
78 cterized and compared using a combination of sedimentation equilibrium and sedimentation velocity in
79 d S3/S4 half-operator oligonucleotides using sedimentation equilibrium and sedimentation velocity mea
80 Using analytical ultracentrifugation in both sedimentation equilibrium and sedimentation velocity mod
81  have established that C-tau is a monomer by sedimentation equilibrium and sedimentation velocity ult
82                                     Based on sedimentation equilibrium and size exclusion chromatogra
83 tion constant (Ka) of 2-4 x 10(8) M-1, using sedimentation equilibrium and size exclusion chromatogra
84        Stoicheometric analyses, coupled with sedimentation equilibrium and size exclusion chromatogra
85                                              Sedimentation equilibrium and small-angle X-ray scatteri
86                The pH dependence of both the sedimentation equilibrium and the oxygen binding of the
87                                          The sedimentation equilibrium and velocity data indicate tha
88 single-headed myosin-She3p complex, based on sedimentation equilibrium and velocity data.
89                                              Sedimentation equilibrium and velocity runs revealed oli
90                                       Recent sedimentation equilibrium and velocity studies show that
91 ar UV CD spectroscopy, thermal denaturation, sedimentation equilibrium and velocity, and intrinsic fl
92                Affinities were determined by sedimentation equilibrium and/or surface plasmon detecti
93                    Dynamic light scattering, sedimentation equilibrium, and circular dichroism measur
94 echniques, including sedimentation velocity, sedimentation equilibrium, and dynamic light scattering
95 ircular dichroism, dynamic light scattering, sedimentation equilibrium, and fluorescence experiments
96 eport the results of sedimentation velocity, sedimentation equilibrium, and gel-filtration experiment
97               We have used NMR spectroscopy, sedimentation equilibrium, and intrinsic fluorescence to
98 n explored by analytical gel chromatography, sedimentation equilibrium, and oxygen binding experiment
99 he techniques of intensity light scattering, sedimentation equilibrium, and radiation inactivation we
100  forms a very stable trimer as determined by sedimentation equilibrium, and the concentration depende
101  assembly in these mutants were monitored by sedimentation equilibrium, and the conformational states
102 s, as measured by sedimentation velocity and sedimentation equilibrium, and the tryptic cleavage patt
103 now shown unambiguously by light scattering, sedimentation equilibrium, and titration calorimetry tha
104 chemical methods including light scattering, sedimentation equilibrium, and titration calorimetry, we
105 the "Smc2/4 complex," which upon analysis by sedimentation equilibrium appears to reversibly self-ass
106                                              Sedimentation equilibrium assays indicate that the Ig3 d
107 en measured under a variety of conditions by sedimentation equilibrium at pH 7.5 and 4 and 20 degrees
108 ll design for analytical ultracentrifugation-sedimentation equilibrium (AUC-SE), ideal for studying s
109 nfirmed by analytical ultracentrifugation to sedimentation equilibrium by which a 1:1 complex was obt
110 d on results from sedimentation velocity and sedimentation equilibrium centrifugation as well as anal
111  of the self-association state of hDlg using sedimentation equilibrium centrifugation, matrix-assiste
112 oresis, isoelectric focusing, and analytical sedimentation equilibrium centrifugation.
113 luble CD4 molecule, as determined by ITC and sedimentation equilibrium centrifugation.
114 tracentrifugation data confirmed this, where sedimentation equilibrium curve fits gave a mean molecul
115                                              Sedimentation equilibrium curve fits gave a mean molecul
116                                              Sedimentation equilibrium data (obtained at 4.8-11.2 muM
117                       Global analysis of the sedimentation equilibrium data demonstrated that PR-B se
118                       Global analysis of the sedimentation equilibrium data has enabled us to determi
119                     SEDFIT-MSTAR analyses of sedimentation equilibrium data indicates a weight averag
120 tein concentrations, and good global fits to sedimentation equilibrium data require a positive value
121                                          Our sedimentation equilibrium data show that, in the presenc
122                                              Sedimentation equilibrium data showed that SCR-1/5 is mo
123                                              Sedimentation equilibrium data suggest at a minimum, a m
124 vely, in agreement with their sequences, and sedimentation equilibrium data supported these determina
125                            Global fitting of sedimentation equilibrium data under native solution con
126                                              Sedimentation equilibrium data were interpreted in terms
127 he recombinant protein by gel filtration and sedimentation equilibrium demonstrate a dimer-tetramer s
128 ons, static light scattering, and analytical sedimentation equilibrium, demonstrate that Ud NS1A ED f
129                                              Sedimentation equilibrium demonstrated that both echista
130                                              Sedimentation equilibrium-derived mass values for both f
131                                      Whereas sedimentation equilibrium distributions for phosphorylas
132 l allowance for thermodynamic nonideality in sedimentation equilibrium distributions reflecting solut
133                                  Analysis of sedimentation-equilibrium distributions obtained at 15 0
134                                              Sedimentation equilibrium, dynamic light scattering, ele
135 he approach to equilibrium in a short-column sedimentation equilibrium experiment followed by a high-
136 in after start of a conventional long-column sedimentation equilibrium experiment.
137 rization of C167PM has been characterized in sedimentation equilibrium experiments (K(d) approximatel
138 e prolonged stability needed in conventional sedimentation equilibrium experiments and it can increas
139                                 Results from sedimentation equilibrium experiments are consistent wit
140 ce optical data acquisition system, allowing sedimentation equilibrium experiments at loading concent
141                 To clarify this discrepancy, sedimentation equilibrium experiments by analytical ultr
142                                              Sedimentation equilibrium experiments by analytical ultr
143                                              Sedimentation equilibrium experiments confirm that the E
144                                              Sedimentation equilibrium experiments confirmed that the
145                                              Sedimentation equilibrium experiments demonstrated that
146                                              Sedimentation equilibrium experiments establish that the
147 ce the number of SCR domains compared to CR2 Sedimentation equilibrium experiments gave a mean molecu
148  sedimentation velocity and density gradient sedimentation equilibrium experiments in CsCl with UV de
149                Analytical gel filtration and sedimentation equilibrium experiments indicate that doub
150                                              Sedimentation equilibrium experiments indicate that thes
151                                              Sedimentation equilibrium experiments of pRB/Ad5 E1A and
152 iments and it can increase the efficiency of sedimentation equilibrium experiments of previously unch
153                                              Sedimentation equilibrium experiments on each subunit an
154                                              Sedimentation equilibrium experiments show that an alani
155      In contrast, sedimentation velocity and sedimentation equilibrium experiments show that full-len
156                                              Sedimentation equilibrium experiments show that single-c
157 dI is found to form a homodimer of 16.7 kDa; sedimentation equilibrium experiments show that the dime
158                                              Sedimentation equilibrium experiments show that the tetr
159                                              Sedimentation equilibrium experiments showed that a cons
160 slinking, size-exclusion chromatography, and sedimentation equilibrium experiments shows that the mos
161                                              Sedimentation equilibrium experiments suggest that bindi
162 6 E7 and Ad5 E1A oligomerization properties, sedimentation equilibrium experiments were performed wit
163                                              Sedimentation equilibrium experiments were then used to
164                                              Sedimentation equilibrium experiments with EcoRuvA showe
165       Their oligomerization was confirmed in sedimentation equilibrium experiments, which also establ
166 K(A) = 5.6 and 5.1 [M(-1)], respectively, in sedimentation equilibrium experiments.
167 nder nondenaturing conditions as measured by sedimentation equilibrium experiments.
168 amers, using both sedimentation velocity and sedimentation equilibrium experiments.
169 tion using cross-linking and mutagenesis and sedimentation equilibrium experiments.
170 molecular mass of 31.9 kDa, as determined by sedimentation equilibrium experiments.
171                                       Global sedimentation equilibrium fits indicated that a monomer-
172 ive site by means of sedimentation velocity, sedimentation equilibrium, fluorescence solute quenching
173                           The suitability of sedimentation equilibrium for characterizing the self-as
174 his investigation indicates the potential of sedimentation equilibrium for the quantitative character
175 al offsets from interference optical data of sedimentation equilibrium gradients.
176                                        Using sedimentation equilibrium in C14 betaine micelles, we di
177                                              Sedimentation equilibrium in the analytical centrifuge r
178 lation) have been studied using short-column sedimentation equilibrium in the analytical ultracentrif
179                                              Sedimentation equilibrium in the analytical ultracentrif
180 t average molar mass (M(w)) determined using sedimentation equilibrium in the analytical ultracentrif
181 I = 0.10 M) using sedimentation velocity and sedimentation equilibrium in the analytical ultracentrif
182 tail analytical solutions of expressions for sedimentation equilibrium in the analytical ultracentrif
183  A combination of sedimentation velocity and sedimentation equilibrium in the analytical ultracentrif
184 0 Da as determined by neutron scattering and sedimentation equilibrium, in good agreement with the se
185                                              Sedimentation equilibrium indicated a weight average mol
186  conformation is remarkably changed, and the sedimentation equilibrium indicates that the protein is
187                                              Sedimentation equilibrium is a powerful tool for the cha
188          Characterizing membrane proteins by sedimentation equilibrium is challenging because deterge
189 timate for SCF-sKit interaction, obtained by sedimentation equilibrium, is about 17 nm at 25 degrees
190 e assembly process have been dissected using sedimentation equilibrium measurements and DNaseI footpr
191                                              Sedimentation equilibrium measurements and scanning tran
192  of dynamin II by analytical ultracentrifuge sedimentation equilibrium measurements at high ionic str
193                                              Sedimentation equilibrium measurements confirmed the pen
194                                              Sedimentation equilibrium measurements in the analytical
195                                              Sedimentation equilibrium measurements indicate that PKR
196                                              Sedimentation equilibrium measurements indicated that a
197                                              Sedimentation equilibrium measurements of LC8 at pH 7 re
198                                              Sedimentation equilibrium measurements reveal that 11 of
199                                Additionally, sedimentation equilibrium measurements reveal that coupl
200                                              Sedimentation equilibrium measurements reveal that pPKRm
201                                              Sedimentation equilibrium measurements show that the agg
202                                              Sedimentation equilibrium measurements show these protei
203                                              Sedimentation equilibrium measurements showed recombinan
204                                              Sedimentation equilibrium measurements showed the reduce
205                                              Sedimentation equilibrium measurements to determine the
206                                         From sedimentation equilibrium measurements, we determined th
207        The aggregation numbers determined by sedimentation equilibrium methods match those measured b
208 association using sedimentation velocity and sedimentation equilibrium methods.
209                                              Sedimentation equilibrium of a homogeneous 4.5 S populat
210 polysomes were separated from other mRNAs by sedimentation equilibrium or sedimentation velocity.
211 ants, SN228 and SR228, was also evaluated by sedimentation equilibrium over this same temperature ran
212 reduce the systematic errors in the measured sedimentation equilibrium profiles by more than an order
213 ading concentrations are calculated from the sedimentation equilibrium profiles.
214 the monomer-monomer interface is stabilized, sedimentation equilibrium results demonstrated that the
215                                              Sedimentation equilibrium results further suggest that t
216                                              Sedimentation equilibrium results show that the associat
217 usion (F) proteins interact as trimers using sedimentation equilibrium (SE) analysis.
218                                              Sedimentation equilibrium (SE) analytical ultracentrifug
219                       The current study uses sedimentation equilibrium (SE), circular dichroism (CD),
220  and large molar mass profiles, confirmed by sedimentation equilibrium "SEDFIT MSTAR" analysis.
221 nzyme have been obtained by using analytical sedimentation equilibrium, sedimentation velocity studie
222                          Further analysis by sedimentation equilibrium showed that degludec exhibited
223                                              Sedimentation equilibrium shows the IDE mutants exhibit
224                                        Using sedimentation equilibrium, spontaneously inactivated HTb
225                 Here, we report results from sedimentation equilibrium studies and two different subu
226            Gel permeation chromatography and sedimentation equilibrium studies confirm that the Fe(3+
227 nergy scale and free energy differences from sedimentation equilibrium studies for point mutants of t
228            Gel filtration chromatography and sedimentation equilibrium studies indicate that these an
229                                              Sedimentation equilibrium studies indicate that these HR
230                                              Sedimentation equilibrium studies indicated that 8% of t
231                                     However, sedimentation equilibrium studies indicated that the ina
232                                              Sedimentation equilibrium studies of CR2 SCR 1-2 gave mo
233                                              Sedimentation equilibrium studies of dilute solutions of
234                                              Sedimentation equilibrium studies of translin with an FI
235                                     Further, sedimentation equilibrium studies reveal that reconstitu
236                                              Sedimentation equilibrium studies reveal that under non-
237                                 In addition, sedimentation equilibrium studies revealed that HL had a
238                                              Sedimentation equilibrium studies show that scRPA is a s
239                            Moreover, NMR and sedimentation equilibrium studies show that the activati
240                                              Sedimentation equilibrium studies show that the equilibr
241                                              Sedimentation equilibrium studies show that the Escheric
242                                              Sedimentation equilibrium studies show that the Escheric
243                                              Sedimentation equilibrium studies show that the regulato
244                                              Sedimentation equilibrium studies showed that in the abs
245                                              Sedimentation equilibrium studies showed very little ass
246                       We now show by NMR and sedimentation equilibrium studies that a mutant protease
247                   Sedimentation velocity and sedimentation equilibrium studies were performed.
248                                              Sedimentation equilibrium studies with purified proteins
249                                           By sedimentation equilibrium studies, we have found that pr
250 ly monomeric at 5 degrees C as determined by sedimentation equilibrium studies.
251 on calorimetry, biomolecular interaction, or sedimentation equilibrium studies.
252 ording to results from mass spectrometry and sedimentation equilibrium studies.
253 , using isothermal titration calorimetry and sedimentation equilibrium techniques.
254 tion, analytical sedimentation velocity, and sedimentation equilibrium techniques.
255 d CaM were determined by CD spectrometry and sedimentation equilibrium: their affinities were Cys(-)-
256 tions, isothermal titration calorimetry, and sedimentation equilibrium to determine whether scRPA can
257                                     However, sedimentation equilibrium ultracentrifugation data showe
258 However, a thermodynamic investigation using sedimentation equilibrium ultracentrifugation in deterge
259                        In the present study, sedimentation equilibrium ultracentrifugation is employe
260                                              Sedimentation equilibrium ultracentrifugation showed tha
261                                              Sedimentation equilibrium ultracentrifugation shows that
262            Size-exclusion chromatography and sedimentation equilibrium ultracentrifugation studies sh
263 Clostridium thermoaceticum was determined by sedimentation equilibrium ultracentrifugation to be 300,
264 mples of enzyme were subjected to analytical sedimentation equilibrium ultracentrifugation to obtain
265 -domain interactions were investigated using sedimentation equilibrium ultracentrifugation, cross-lin
266  apoBCCP and apoBCCP87 were determined using sedimentation equilibrium ultracentrifugation.
267  hybrid peptides were studied in micelles by sedimentation equilibrium ultracentrifugation.
268                                  Analysis by sedimentation equilibrium unequivocally identified the o
269 ein-surfactant complexes are investigated by sedimentation equilibrium via analytical ultracentrifuga
270                         The Mr determined by sedimentation equilibrium was 197,600+/-13,700 and the a
271  techniques, and additional studies in which sedimentation equilibrium was used show that the binding
272                                           By sedimentation equilibrium we determined that the main pl
273                                        Using sedimentation equilibrium, we show that yeast cTBP forms
274 ere a systematic study of K(a) determined by sedimentation equilibrium, which showed that it varied b
275                                              Sedimentation equilibrium yielded a molecular mass of 96

 
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