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1 eniently expressed as a fraction of the cell sedimentation velocity.
2  other mRNAs by sedimentation equilibrium or sedimentation velocity.
3 ced tubulin spiral formation, as measured by sedimentation velocity.
4 attering, N-terminal protein sequencing, and sedimentation velocity.
5  this heterogeneity was further confirmed by sedimentation velocity.
6 analytical size exclusion chromatography and sedimentation velocity.
7 ROPRO were compared with those determined by sedimentation velocity.
8  cells also exhibited the largest amyloplast sedimentation velocities.
9 added U4 RNA that is associated with U6 RNA (sedimentation velocity 16 S) was significantly higher in
10                                              Sedimentation velocity analyses indicated that dimeric P
11            Size-exclusion chromatography and sedimentation velocity analyses indicated that the bulk
12                                              Sedimentation velocity analyses of detergent-solubilized
13                           Gel filtration and sedimentation velocity analyses of in vitro synthesized
14            Size exclusion chromatography and sedimentation velocity analyses of the cytosolic fractio
15 gomeric state and shape of A3G, we conducted sedimentation velocity analyses of the pure enzyme under
16            Size exclusion chromatography and sedimentation velocity analyses revealed that FANCJ-WT e
17      Importantly, intrinsic fluorescence and sedimentation velocity analyses show that GroES is capab
18 bient temperature as shown by native gel and sedimentation velocity analyses.
19                                              Sedimentation velocity analysis indicated single sedimen
20                                              Sedimentation velocity analysis is a powerful tool for t
21 tion chromatography and fluorescence-adapted sedimentation velocity analysis of cell lysates, we coll
22 e and IQ sequence is demonstrated further by sedimentation velocity analysis of complexes of Mlc1p wi
23                                 A method for sedimentation velocity analysis of polyribosomes is pres
24                                              Sedimentation velocity analysis of translin indicates th
25 Analytical gel filtration chromatography and sedimentation velocity analysis revealed that a(NT(104-3
26 ed receptor by sedimentation equilibrium and sedimentation velocity analysis reveals a monodisperse p
27 roscopy, molecular dynamics simulations, and sedimentation velocity analysis reveals differences in t
28                                              Sedimentation velocity analysis showed that the polysacc
29                                              Sedimentation velocity analysis shows that the reconstit
30   By circular dichroism, gel filtration, and sedimentation velocity analysis, we determined that each
31 cies, and the overall capability of boundary sedimentation velocity analysis.
32 ble for BH3 peptide binding, as confirmed by sedimentation velocity analysis.
33 ange high-pressure liquid chromatography and sedimentation velocity analysis.
34  IPOD and JUNQ patterns of aggregation using sedimentation velocity analysis.
35 ity interactions using fluorescence detected sedimentation velocity analytical ultracentrifugation (F
36                                              Sedimentation velocity analytical ultracentrifugation (S
37  as circular dichroism (CD) spectroscopy and sedimentation velocity analytical ultracentrifugation (s
38                                              Sedimentation velocity analytical ultracentrifugation (S
39                                              Sedimentation velocity analytical ultracentrifugation (S
40 ural characterization of the RAM linker with sedimentation velocity analytical ultracentrifugation an
41                                              Sedimentation velocity analytical ultracentrifugation co
42                                              Sedimentation velocity analytical ultracentrifugation eq
43 the past, both sedimentation equilibrium and sedimentation velocity analytical ultracentrifugation ha
44                                              Sedimentation velocity analytical ultracentrifugation is
45 he size-distribution analysis of polymers by sedimentation velocity analytical ultracentrifugation is
46                                              Sedimentation velocity analytical ultracentrifugation is
47                                              Sedimentation velocity analytical ultracentrifugation sh
48 raction of Myo5a and Rab3A was determined by sedimentation velocity analytical ultracentrifugation us
49                                              Sedimentation velocity analytical ultracentrifugation wi
50  and DeltaTM-FAAH by chemical cross-linking, sedimentation velocity analytical ultracentrifugation, a
51                     These techniques include sedimentation velocity analytical ultracentrifugation, f
52                Sedimentation equilibrium and sedimentation velocity analytical ultracentrifugation, t
53 gen deuterium exchange mass spectrometry and sedimentation velocity analytical ultracentrifugation, w
54  purified proteins and their interactions is sedimentation velocity analytical ultracentrifugation.
55 on of nanoparticles and macromolecules using sedimentation velocity analytical ultracentrifugation.
56 ell as a weaker Nank self-association, using sedimentation velocity analytical ultracentrifugation.
57 d AMPA receptors using fluorescence-detected sedimentation velocity analytical ultracentrifugation.
58 n of long-standing interest in the theory of sedimentation velocity analytical ultracentrifugation.
59 -linking, size-exclusion chromatography, and sedimentation-velocity analytical ultracentrifugation we
60            However, BPI can enhance both the sedimentation velocity and apparent size of LPS aggregat
61                               In analyses by sedimentation velocity and by cross-linking, both protei
62 odextrin DE17 causing a greater reduction in sedimentation velocity and compressibility of sediment f
63 ional AUC data obtained from analytical band sedimentation velocity and density gradient sedimentatio
64 oncentrations of salt (up to 13.4 M NaBr) by sedimentation velocity and diffusion experiments, becaus
65                               For both IRPs, sedimentation velocity and dynamic light-scattering expe
66 protein complexes have been characterised by sedimentation velocity and EMSA using native and mutant
67                                              Sedimentation velocity and equilibrium analyses were use
68 or a range of solution conditions using both sedimentation velocity and equilibrium approaches.
69 t ratio (f/f(0)) of 1.28 calculated from the sedimentation velocity and equilibrium data is close to
70                                              Sedimentation velocity and equilibrium experiments and s
71                                              Sedimentation velocity and equilibrium experiments have
72                                Additionally, sedimentation velocity and equilibrium experiments indic
73 ced, allowing the global analysis of several sedimentation velocity and equilibrium experiments.
74 ar dichroism, analytical ultracentrifugation sedimentation velocity and equilibrium methods, and sequ
75                                              Sedimentation velocity and equilibrium results establish
76                                              Sedimentation velocity and equilibrium studies conducted
77                                              Sedimentation velocity and equilibrium studies revealed
78 -B dimerization was examined by carrying out sedimentation velocity and equilibrium studies under hig
79 re (5-35 degrees C; pH 8.3) using analytical sedimentation velocity and equilibrium techniques, and f
80                                              Sedimentation velocity and equilibrium ultracentrifugati
81 ow micromolar monomer concentration range by sedimentation velocity and equilibrium ultracentrifugati
82 uring detergent environments was assessed by sedimentation velocity and equilibrium.
83 MutL and its binding to DNA using analytical sedimentation velocity and equilibrium.
84                    Global analysis combining sedimentation velocity and fluorescence anisotropy yield
85  the DnaB helicase have been performed using sedimentation velocity and fluorescence energy transfer
86                                Together with sedimentation velocity and fluorescence polarization ass
87                             Here, we combine sedimentation velocity and fluorescence titration studie
88                                 Furthermore, sedimentation velocity and gel filtration showed that NE
89                                              Sedimentation velocity and gel-filtration analysis showe
90                                              Sedimentation velocity and isothermal titration calorime
91                                              Sedimentation velocity and limited proteolysis experimen
92 c analysis by analytical ultracentrifugation sedimentation velocity and native mass spectrometry reve
93 complete CcO dimerization can be verified by sedimentation velocity and sedimentation equilibrium aft
94 and both are monomeric based on results from sedimentation velocity and sedimentation equilibrium cen
95                                 In contrast, sedimentation velocity and sedimentation equilibrium exp
96 o contains octamers and hexamers, using both sedimentation velocity and sedimentation equilibrium exp
97                             A combination of sedimentation velocity and sedimentation equilibrium in
98 e chloride buffer (pH 6.8, I = 0.10 M) using sedimentation velocity and sedimentation equilibrium in
99 he energetics of PR-B self-association using sedimentation velocity and sedimentation equilibrium met
100                                              Sedimentation velocity and sedimentation equilibrium stu
101 ric human kinesin constructs, as measured by sedimentation velocity and sedimentation equilibrium, an
102 of the catalytic cycle were characterized by sedimentation velocity and small-angle X-ray scattering
103 wo subsets of complexes that differ in their sedimentation velocity and their association with cytosk
104 ANT-ADP, have been examined using analytical sedimentation velocity and time-dependent fluorescence a
105                                          Our sedimentation velocity and transmission electron microsc
106                                              Sedimentation velocity and X-ray scattering indicated th
107 dependent conformational changes detected in sedimentation velocity and/or fluorescence anisotropy me
108                                              Sedimentation-velocity and coimmunoprecipitation experim
109                                 Differential sedimentation-velocity and gel electrophoresis reveal th
110                        Analyses with SEDFIT (sedimentation velocity) and MultiSig however revealed th
111 on column multiangle laser light scattering, sedimentation velocity, and circular dichroism (CD) were
112 ction by using small-angle x-ray scattering, sedimentation velocity, and computational modeling techn
113 re analyzed by electrophoretic shift assays, sedimentation velocity, and electron microscopy.
114 COS-1 cells as assessed by Western blotting, sedimentation velocity, and immunofluorescence microscop
115                              Gel filtration, sedimentation velocity, and immunoprecipitation experime
116 ES, intrinsic fluorescence, bis-ANS binding, sedimentation velocity, and limited proteolysis, we show
117              Analytical ultracentrifugation, sedimentation velocity, and sedimentation equilibrium an
118 ntitative fluorescence titration, analytical sedimentation velocity, and sedimentation equilibrium te
119 on, as measured by dynamic light scattering, sedimentation velocity, and sedimentation equilibrium.
120       Protein expression, disulfide bonding, sedimentation velocity, and subcellular localization of
121 ssayed by nonreducing Western blot analysis, sedimentation velocity, and subcellular localization.
122 o fill this gap, we report crystallographic, sedimentation-velocity, and kinetics data for human PYCR
123  the analysis of protein self-association by sedimentation velocity are developed, their statistical
124 , provided that the suspension viscosity and sedimentation velocity are scaled appropriately, and tha
125                                              Sedimentation velocity assays suggest that the expanded
126                Here, we use a combination of sedimentation velocity, atomic force microscopy and nucl
127               Analytical ultracentrifugation-sedimentation velocity (AUC-SV) is emerging as an import
128 urther insight was gained by analyzing EI by sedimentation velocity, by near UV CD spectroscopy, and
129 d by static and dynamic light scattering and sedimentation velocity, can be jointly described in a se
130                                 Furthermore, sedimentation velocity centrifugation and electron micro
131                                 Polyribosome sedimentation velocity centrifugation can be used to ide
132  crosslinked and mildly sheared chromatin to sedimentation velocity centrifugation followed by size-f
133 s determined to be approximately 0.81 MDa by sedimentation velocity combined with dynamic light scatt
134 R-measured spin lattice relaxation rates and sedimentation velocity compared to those of the wild-typ
135  of the HMM molecule as judged by its slower sedimentation velocity compared with that in EGTA.
136  partial boundary modeling (PBM) to simplify sedimentation velocity data analysis by excluding specie
137                  Static light scattering and sedimentation velocity data are consistent with the form
138                                              Sedimentation velocity data coupled with time-derivative
139                                              Sedimentation velocity data fit a model where PKR monome
140                                  Analysis of sedimentation velocity data for a 15 muM solution of ERK
141  partial specific volume and molar mass from sedimentation velocity data for cases where the anisotro
142     In this work we show how the analysis of sedimentation velocity data from the AUC equipped with a
143      Time-derivative approaches to analyzing sedimentation velocity data have proven to be highly suc
144                      Kinetic analysis of the sedimentation velocity data indicated that holoBirA dime
145                   Consistent with this idea, sedimentation velocity data reveal that the apo- and Mg(
146 tation coefficient distribution, g(s*), from sedimentation velocity data that was developed by Walter
147            A method for fitting experimental sedimentation velocity data to finite-element solutions
148                              We analyzed the sedimentation velocity data using the van Holde-Weischet
149 , a method of globally analyzing multisignal sedimentation velocity data was introduced by Schuck and
150                            Direct fitting of sedimentation velocity data with numerical solutions of
151                 For the detailed analysis of sedimentation velocity data, the consideration of radial
152 ared with other current methods of analyzing sedimentation velocity data.
153 xtures is demonstrated via MWL evaluation of sedimentation velocity data.
154 apsid proteins are lost from the RTC and its sedimentation velocity decreases further.
155 er an external field and move with different sedimentation velocities dictated by their Svedberg coef
156 ing nonlinear least-squares curve-fitting of sedimentation velocity distributions to the Lamm equatio
157 a combination of native gel electrophoresis, sedimentation velocity, electron microscopy, and a recen
158 sphatidylcholine, PCPS) were evaluated using sedimentation velocity/equilibrium methods in the analyt
159                                              Sedimentation velocity/equilibrium studies revealed a tr
160 ed mass of the 3.3 S fragment estimated from sedimentation velocity/equilibrium studies; while the co
161 riment followed by a high-speed short-column sedimentation velocity experiment can result in sediment
162 ance analysis can increase the capacity of a sedimentation velocity experiment in ultracentrifugation
163                                              Sedimentation velocity experiments also show that additi
164                                              Sedimentation velocity experiments at low speeds and ele
165                                   1H NMR and sedimentation velocity experiments carried out with thei
166                                              Sedimentation velocity experiments confirm the presence
167                                              Sedimentation velocity experiments confirm the transient
168                                              Sedimentation velocity experiments confirmed that dimeri
169                                              Sedimentation velocity experiments confirmed the presenc
170                 Dynamic light scattering and sedimentation velocity experiments demonstrated that HMG
171                                              Sedimentation velocity experiments demonstrated that the
172                                              Sedimentation velocity experiments demonstrated the pres
173                                              Sedimentation velocity experiments determined that the M
174                                              Sedimentation velocity experiments gave a sedimentation
175                     To test this hypothesis, sedimentation velocity experiments in the analytical ult
176                                   Results of sedimentation velocity experiments in the presence of sa
177                                              Sedimentation velocity experiments indicate that ELP[V5G
178     In agreement with the crystal structure, sedimentation velocity experiments indicate that L7D2 is
179 y, protease sensitivity, gel filtration, and sedimentation velocity experiments indicate that Nup2p i
180                                              Sedimentation velocity experiments indicate that the bif
181               Analytical ultracentrifugation sedimentation velocity experiments indicate that these S
182        Results of laser light scattering and sedimentation velocity experiments indicated that Purbet
183                                              Sedimentation velocity experiments of titrated stoichiom
184                                              Sedimentation velocity experiments reveal that Ms-Lon mo
185            Size-exclusion chromatography and sedimentation velocity experiments revealed that the Aal
186                                              Sedimentation velocity experiments show that apo-SOD1 di
187                                              Sedimentation velocity experiments show that the deliver
188                For C3d, X-ray scattering and sedimentation velocity experiments showed that it exists
189                Size-distribution analyses in sedimentation velocity experiments showed that monomeric
190                                              Sedimentation velocity experiments showed that this dime
191 eous protein was adenylated as isolated, and sedimentation velocity experiments suggested that the en
192 ment of the spinning rotor during high-speed sedimentation velocity experiments up to 60,000rpm.
193                                              Sedimentation velocity experiments using the g*(s) deriv
194                                              Sedimentation velocity experiments using the time deriva
195                         A method for fitting sedimentation velocity experiments using whole boundary
196                                              Sedimentation velocity experiments were also performed o
197                                              Sedimentation velocity experiments were employed to show
198 the determination of size-distributions from sedimentation velocity experiments were examined and dev
199                                              Sedimentation velocity experiments with gp59 protein and
200                                              Sedimentation velocity experiments yielded an estimate o
201 strated with double-sector and single-sector sedimentation velocity experiments, and with analytical
202 against noncognate tRNA was also observed in sedimentation velocity experiments, which showed that a
203 of 4.2 was calculated for the dimer based on sedimentation velocity experiments.
204 ecently described for the direct modeling of sedimentation velocity experiments.
205 tation and diffusion constants obtained from sedimentation velocity experiments.
206  and hydrodynamic properties determined from sedimentation velocity experiments.
207 ent in the analysis of boundary spreading in sedimentation velocity experiments.
208                                              Sedimentation-velocity experiments provided insight into
209                        Fluorescence detected sedimentation velocity (FDS-SV) has emerged as a powerfu
210                                      We used sedimentation velocity, fluorescence anisotropy, and sur
211      Our results suggest that using a single sedimentation velocity for all cloud droplets, as is don
212 mentation experiments showed a transition in sedimentation velocity from 7.2 to 4.2 S with a transiti
213 evealed similar results with a transition in sedimentation velocity from 7.9 to 4.4 S with a T(m) of
214                                              Sedimentation velocity gave a sedimentation coefficient
215 he shapes of the reaction boundaries and the sedimentation velocity gradients have been predicted by
216 sents practical limitations on the number of sedimentation velocity gradients that can be run simulta
217    Time resolved fluorescence anisotropy and sedimentation velocity has been used to study the rotati
218 dissociation of four subunits as detected by sedimentation velocity, high-performance ion-exchange ch
219 assessed easily by common techniques such as sedimentation velocity, HPLC, gel electrophoresis, and d
220 n altered resistance to Proteinase K, higher sedimentation velocities in gradient ultracentrifugation
221 d oligomers were studied with time-dependent sedimentation velocity in the analytical ultracentrifuge
222           Using dynamic light scattering and sedimentation velocity in the analytical ultracentrifuge
223 combination of sedimentation equilibrium and sedimentation velocity in the analytical ultracentrifuge
224                                              Sedimentation velocity in the analytical ultracentrifuge
225 ree hydrodynamic and microscopic techniques: sedimentation velocity in the analytical ultracentrifuge
226                                              Sedimentation velocity is a classical method for measuri
227                                              Sedimentation velocity measurements demonstrated that bo
228                                          Our sedimentation velocity measurements of the DnaB protein-
229                              Determined from sedimentation velocity measurements on the lipid-free pr
230                                              Sedimentation velocity measurements show that recombinan
231       Here, we describe methods to configure sedimentation velocity measurements using fluorescence d
232 leotides using sedimentation equilibrium and sedimentation velocity measurements.
233  using a novel hybrid fluorescence proximity/sedimentation velocity method in combination with calori
234 gation in both sedimentation equilibrium and sedimentation velocity modes, we studied the oligomeriza
235                                              Sedimentation velocities of protein-coated particles in
236               Nuclear-associated RTCs have a sedimentation velocity of 80S.
237 V RTCs isolated early after infection have a sedimentation velocity of approximately 560S.
238      We demonstrate that HMGN1 decreases the sedimentation velocity of nucleosomal arrays in low ioni
239                                          The sedimentation velocity of the RTC decreases during rever
240                                              Sedimentation velocity of varied ratios of LTbetaR to a
241                                              Sedimentation velocity provides the only direct evidence
242              Later, different species with a sedimentation velocity ranging from 350S to 100S appear.
243 eric structure, as measured by far UV-CD and sedimentation velocity, respectively.
244 ependently consistent with K2 estimates from sedimentation velocity results for vinblastine and vinor
245 is capable of providing precise and accurate sedimentation velocity results that are consistent with
246                                     Previous sedimentation velocity results with vinblastine have bee
247 SDS-PAGE, size exclusion chromatography, and sedimentation velocity revealed two native high Mr disul
248                                              Sedimentation velocity reveals a distribution of species
249                 We demonstrate that a single sedimentation velocity run on an adenovirus sample can d
250 n and light scattering techniques, including sedimentation velocity, sedimentation equilibrium, and d
251               Here, we report the results of sedimentation velocity, sedimentation equilibrium, and g
252 ediate occupying the active site by means of sedimentation velocity, sedimentation equilibrium, fluor
253  combination of dynamic light scattering and sedimentation velocity showed that NTS1 was monomeric in
254                                              Sedimentation velocity shows that PYCR1 forms a concentr
255                                              Sedimentation velocity, size-exclusion chromatography an
256            Isothermal titration calorimetry, sedimentation velocity, size-exclusion chromatography co
257                                              Sedimentation velocity studies at neutral pH demonstrate
258 t micromolar concentrations of the receptor, sedimentation velocity studies demonstrate that PR-A und
259                                              Sedimentation velocity studies indicate that each polype
260                                              Sedimentation velocity studies of hormone-bound PR-B at
261                                    Moreover, sedimentation velocity studies of the ternary complex pr
262                                              Sedimentation velocity studies show that this repacking
263                     Fluorescence spectra and sedimentation velocity studies showed that melittin boun
264                               The results of sedimentation velocity studies were consistent with pred
265  using analytical sedimentation equilibrium, sedimentation velocity studies, and the rigorous fluores
266 e introduce a new analytical method based on sedimentation velocity (SV) analytical ultracentrifugati
267                                              Sedimentation velocity (SV) analytical ultracentrifugati
268                                              Sedimentation velocity (SV) analytical ultracentrifugati
269                                              Sedimentation velocity (SV) analytical ultracentrifugati
270                                 We performed sedimentation velocity (SV) analytical ultracentrifugati
271                                              Sedimentation velocity (SV) is a method based on first p
272 port small-angle X-ray scattering (SAXS) and sedimentation velocity (SV) studies on the enzyme-DNA co
273 l field to study ultra-weak binding, using a sedimentation velocity technique that allows us to deter
274 rates, has also been characterized using the sedimentation velocity technique.
275 by examining by dynamic light scattering and sedimentation velocity techniques the complexes formed w
276                        Here, we establish by sedimentation velocity that the ATDs of GluR6 and KA2 co
277 the dimeric and tetrameric enzyme species by sedimentation velocity, this procedure has been used to
278                           CAR-D1 is shown by sedimentation velocity to be monomeric at pH 3.0.
279 hysicochemical study described here, we used sedimentation velocity to compare vinorelbine- and vinfl
280 nt study, we have used fluorescence-detected sedimentation velocity to determine the effect of S-sulf
281                                   Similarly, sedimentation velocity ultracentrifugation experiments u
282 with a sedimentation coefficient of 4.8 S in sedimentation velocity ultracentrifugation experiments,
283                           Urea denaturation, sedimentation velocity ultracentrifugation, and electron
284 using a combination of methods that includes sedimentation velocity ultracentrifugation, electron mic
285 ological salt concentrations, as analyzed by sedimentation velocity ultracentrifugation.
286 s a monomer by sedimentation equilibrium and sedimentation velocity ultracentrifugation.
287  these monoclonal antibodies was analyzed by sedimentation velocity ultracentrifugation.
288             Using analytical gel filtration, sedimentation-velocity ultracentrifugation, and negative
289                                In this work, sedimentation velocity was employed to monitor the parti
290 hange MS, size-exclusion chromatography, and sedimentation velocity, we investigated how these diverg
291                                              Sedimentation velocities were converted to apparent aggr
292                                Complementary sedimentation velocity with deuterated water gives a pic

 
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