戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 erase and butyrylcholinesterase using enzyme kinetic analysis.
2 sembly process as constraints for subsequent kinetic analysis.
3 etamide are rationalized by detailed in situ kinetic analysis.
4 y extent, and can provide valuable real-time kinetic analysis.
5  dynamics simulation, electrophysiology, and kinetic analysis.
6 lecular dynamic simulations (BOMD) and micro-kinetic analysis.
7 mproved precatalyst (thtAuBr3) to facilitate kinetic analysis.
8 mplified methods by comparing them with full kinetic analysis.
9 rebellum was used as the reference region in kinetic analysis.
10  series of XAS spectra and opens the door to kinetic analysis.
11 g regional nerve density with PET and tracer kinetic analysis.
12 -resolved absorption spectroscopy and global kinetic analysis.
13 cular interactions, making them suitable for kinetic analysis.
14 ion was overturned on the basis of extensive kinetic analysis.
15 ry excretion during a 24-h period and from a kinetic analysis.
16 nce of the present intact cell-based binding kinetics analysis.
17                                              Kinetic analysis allowed investigation of the reaction m
18                                        Rapid kinetics analysis also shows that ring resetting of a se
19                                  Preliminary kinetic analysis and density functional calculations sup
20                             A combination of kinetic analysis and DFT calculations reveals the comple
21                                              Kinetic analysis and DFT calculations suggest that the C
22                             Pre-steady-state kinetic analysis and elucidation of the crystal structur
23 echanism-based inhibitors that allow precise kinetic analysis and faithfully mimic the transition sta
24                                  To simplify kinetic analysis and handling, a variant PCM-F was gener
25                                 Quantitative kinetic analysis and immunochemistry studies suggest tha
26            Mechanistic investigation through kinetic analysis and isotopic labeling studies indicates
27                            Reaction progress kinetic analysis and kinetic isotope effects suggest tha
28                                 Steady-state kinetic analysis and modeling independently support this
29                                          The kinetic analysis and molecular dynamics of the A25.C20 d
30                                      Through kinetic analysis and optimization, we report an improved
31 arious formats of assays for equilibrium and kinetic analysis and rapid determination of degradation
32                                              Kinetic analysis and reaction profile fitting of both th
33       SCADS combines microscopy, single-cell kinetic analysis, and population/cluster analysis to dis
34 with that obtained from conventional Biacore kinetic analysis, and the stoichiometries for the result
35                   By using reaction progress kinetic analysis as an evaluation method for the obtaine
36 d enzymes were characterized by steady-state kinetic analysis at temperatures from 0 to 25 degrees C
37 8alpha and allowed discovery of a predictive kinetic analysis based on cooperativity to distinguish T
38                                              Kinetic analysis based on time-resolved fluorescence rev
39 pensive and simple alternative to do binding kinetics analysis between small molecules in solution an
40 cessfully demonstrate binding specificity in kinetic analysis biomechanics in peptide aptamers and GO
41 inhibitors that we have subjected to further kinetic analysis by comparing k(off) constants determine
42 ve tissue are not amenable to structural and kinetic analysis by conventional methods.
43  of multiple assembly pathways, and show how kinetic analysis can be used to distinguish different as
44 f Ki, Kd, IC50, and/or EC50, a more thorough kinetic analysis can provide useful information for the
45                                    An enzyme kinetic analysis comparing ERBB2(YVMA) to wild type usin
46                Site-directed mutagenesis and kinetic analysis confirm the critical catalytic role pla
47                                              Kinetic analysis confirmed the existence of an intermedi
48                             The steady-state kinetic analysis coupled with the normal (13)(V/K) kinet
49 mentary biophysical, structure-function, and kinetic analysis define the features that facilitate the
50                                  Binding and kinetic analysis demonstrate that the MUG-K68N substitut
51                                      Further kinetic analysis demonstrated first-order kinetics with
52 -fluoro-2-deoxyglucose ((18)FDG) ligand with kinetic analysis demonstrated increased mean lung parenc
53                                  Preliminary kinetic analysis demonstrated that BPND values obtained
54               This massively parallel enzyme kinetics analysis detailed the specificity of ADAMTS13 a
55 ks and guides users through the key steps of kinetic analysis: determination of constraints to be pla
56                                          The kinetic analysis enabled by the platform provided a rapi
57              Surface plasmon resonance-based kinetic analysis enabled the selection of mini-Abs with
58                                              Kinetic analysis establishes that the reaction rate is d
59                                 Steady state kinetic analysis establishes the enzyme is specific for
60                                          The kinetic analysis exhibited discontinuities in the Arrhen
61    Molecular modeling studies in tandem with kinetic analysis exhibited that these hybrids target bot
62 spectroscopy/steady-state isotopic transient kinetic analysis) experiments demonstrates that the rate
63                                              Kinetic analysis for different E2 concentrations shows t
64                                              Kinetic analysis for different E2 concentrations shows t
65                                            A kinetic analysis for TVBN, SSP, hardness, adhesiveness a
66    PL titrations, thermochemical cycles, and kinetic analysis (for the mcb compounds) provided self-c
67                                              Kinetic analysis further indicated that PPTases possess
68                                              Kinetic analysis further shows that W32 oxidation likely
69                                              Kinetic analysis further shows the antioxidant reactivit
70  via a Makosza-like interfacial process, and kinetic analysis has shown that the reaction possesses a
71                              In steady-state kinetic analysis, hpol eta preferred to incorporate dATP
72                                 Modeling and kinetic analysis identified Pz-1 as a type II tyrosine k
73                                              Kinetics analysis identifies that the slow solid-state s
74 ce temperature and Z-value commonly used for kinetic analysis in food microbiology.
75                                              Kinetic analysis indicated an overall 5,000-fold and 1,1
76  occupies the active site cavity of G9a, and kinetic analysis indicates competitive inhibition of G9a
77  in general acid-base chemistry, whereas our kinetic analysis indicates that thioredoxin is likely to
78                                              Kinetic analysis indicates that, in LB medium supplement
79  LTA4 concentrations during the steady-state kinetics analysis, indicating poor lipid substrate bindi
80 al evidence (spectroscopic characterization, kinetic analysis, intermolecular reactivity, and radical
81 his noninvasive dual-window acquisition with kinetic analysis is recommended.
82 rovide good fits to the data, so blood-based kinetic analysis is recommended.
83                                              Kinetic analysis, labeling, competition, and nonlinear e
84 sion estimates is not affected by the tracer kinetic analysis method used.
85 ecently reported variable-time normalization kinetic analysis method was used to delineate the comple
86 pressure IR (HPIR) and the reaction progress kinetic analysis methodology suggested two steps in the
87                                 Furthermore, kinetic analysis monitoring FVIIIa inactivation by APC v
88                                              Kinetic analysis of (11)C-GSK215083 uptake in the human
89                                 Steady-state kinetic analysis of 20 G. max ATP sulfurylase point muta
90                     The 2-tissue-compartment kinetic analysis of a 90-min dynamic scan with arterial
91  study, we present the first biochemical and kinetic analysis of a peptidoglycan O-acetyltransferase
92      Herein we report the first steady-state kinetic analysis of a PKS DH domain employing LC-MS/MS a
93     Here, we identify and provide a detailed kinetic analysis of a transcription cycle analogous to a
94 ractions, and the results were compared with kinetic analysis of active site mutants.
95 Here, we report the cloning, expression, and kinetic analysis of ASNA from Leishmania donovani.
96                                   A detailed kinetic analysis of cardiac myosin has shown that the dr
97                                              Kinetic analysis of channel gating revealed that AITC ac
98  pattern was confirmed through synthesis and kinetic analysis of cleavage of a set of optimized pepti
99                           Intriguingly, cell kinetic analysis of clonal isolates derived from single
100           Here, the authors show an operando kinetic analysis of CO2 hydrogenation over a palladium c
101                            Reaction progress kinetic analysis of data obtained through in situ FTIR s
102                                              Kinetic analysis of DNA cleavage suggests flexible tethe
103                       These proteins allowed kinetic analysis of DNA recognition and structural analy
104                                This detailed kinetic analysis of Drosophila myosin carrying the R759E
105                                              Kinetic analysis of extraction was performed.
106                                              Kinetic analysis of five different AD-causing mutations
107                                              Kinetic analysis of fluorescence signals indicate that P
108                             Here we report a kinetic analysis of fluorescent guanine nucleotides bind
109                             In contrast, the kinetic analysis of GDP-ManPP was only possible with thr
110                        This allowed detailed kinetic analysis of global and stoichiometric phosphoryl
111                                              Kinetic analysis of GoxA revealed allosteric cooperativi
112                                    Moreover, kinetic analysis of human carbonic anhydrase refolding s
113 sing these techniques, we describe the first kinetic analysis of LD growth and secretion at peak lact
114                                              Kinetic analysis of lipid and content transfer showed th
115      A general differential approach for the kinetic analysis of living polymerizations with fast pro
116               Most interestingly, results of kinetic analysis of LPS bioactivity, using modified limu
117 ssay was developed that allowed steady-state kinetic analysis of LsrK to be undertaken with the subst
118                                              Kinetic analysis of M. tuberculosis growth in the lungs
119                                              Kinetic analysis of miniature EPSCs revealed quantal rel
120                      A detailed steady-state kinetic analysis of MtNadD suggests that ATP must first
121                                 Steady-state kinetic analysis of multiple point mutants of the lipid-
122 s likely to be bendable in one direction and kinetic analysis of mutant DNA sequences with biolayer i
123 e subject of controversy; we report that the kinetic analysis of ndSQR is consistent with glutathione
124                                              Kinetic analysis of NF-kappaB levels following loss of s
125                                              Kinetic analysis of NiCl(CCl2CCl3)(CNAr(Mes2))2 decompos
126                    Here we report a detailed kinetic analysis of nucleotide incorporation and exonucl
127                                              Kinetic analysis of peptide substrate phosphorylation an
128                                              Kinetic analysis of peptide-membrane interactions genera
129                                              Kinetic analysis of percentage and yield of preplasma an
130 -dependent Stokes and anti-Stokes SERS, with kinetic analysis of photocatalytic reactions in an Ag na
131 ar approach can be potentially developed for kinetic analysis of protein-small molecule binding by ot
132 ation by multiple catalytic inhibitors using kinetic analysis of purified BRAF(V600E) and RAF(WT) enz
133                                              Kinetic analysis of purified oligo-ulvans incubated with
134                We describe a novel method of kinetic analysis of radioligand binding to neuroreceptor
135                                       Enzyme kinetic analysis of recombinant AtXTH31 confirmed this p
136                                              Kinetic analysis of ribozymes with systematically altere
137              Here we develop Single Molecule Kinetic Analysis of RNA Transient Structure (SiM-KARTS)
138                                              Kinetic analysis of single-channel recordings made with
139                     The x-ray structures and kinetic analysis of site-directed mutants are consistent
140                                              Kinetic analysis of specific peptide generation reveals
141                         It provides accurate kinetic analysis of strand assimilation in high-throughp
142                 We report a pre-steady-state kinetic analysis of structural rearrangements of the DNA
143                                              Kinetic analysis of sugar translocation obtained from si
144 s article, we complement our two-dimensional kinetic analysis of TCR-pMHC-CD8 interaction with concur
145                                              Kinetic analysis of the activation reaction according to
146  presents a detailed computational study and kinetic analysis of the aminolysis of dithioates, dithio
147                   Steady-state and transient kinetic analysis of the ATPase cycle shows that the ADP
148  presents a detailed computational study and kinetic analysis of the aza-Michael addition of primary
149               Here, by means of a systematic kinetic analysis of the Bi-Te system reacting to Bi2Te3,
150                          We have performed a kinetic analysis of the blocking mechanism of the protot
151 le quantitative results were obtained from a kinetic analysis of the changes in FRET.
152                                              Kinetic analysis of the cysteine:SufE sulfurtransferase
153                                              Kinetic analysis of the DNA unwinding and translocation
154                      We undertook a detailed kinetic analysis of the drug responses of K13 wild-type
155                 Critically, pre-steady-state kinetic analysis of the E3 rRNase(IDP)-Im3 complex demon
156                                      Further kinetic analysis of the ECEC path revealed that base inc
157                                              Kinetic analysis of the effect of B6 on co-polymerizatio
158 er indirect flight muscle S1, we performed a kinetic analysis of the effect of mutations in the conve
159                                              Kinetic analysis of the electrochemical response with ti
160 rode: (i) allows time-resolved detection and kinetic analysis of the electrode response (the underlyi
161                                              Kinetic analysis of the encapsulation-isomerization even
162                                              Kinetic analysis of the enzymatic activities toward 3-ox
163 he sliding clamp and clamp loader mechanism, kinetic analysis of the events following beta.gamma comp
164                                              Kinetic analysis of the formation of the 75 kDa iPLA2bet
165 tions with a comprehensive thermodynamic and kinetic analysis of the growth process, which explains t
166                                              Kinetic analysis of the HIV-1 Tat (transactivator of tra
167              Interestingly, the steady-state kinetic analysis of the initial rates determined at vary
168                                          The kinetic analysis of the ligations using model peptides s
169 e report here the first detailed biochemical kinetic analysis of the motor domain of the human beta-c
170                Site-directed mutagenesis and kinetic analysis of the mutant enzymes, in conjunction w
171                                 Steady-state kinetic analysis of the new mechanism is consistent with
172         By X-ray absorption spectroscopy and kinetic analysis of the oxygen evolution reaction, we sh
173                                              Kinetic analysis of the pancreas was performed using a 1
174   We present here the first complete in situ kinetic analysis of the PD-1/PD-ligands/B7-1 system.
175 da N protein (lambdaN) to initiate the first kinetic analysis of the proteolytic mechanism of this en
176                     This was corroborated by kinetic analysis of the purified enantiomers, which show
177                                      ITC and kinetic analysis of the R93A mutant also showed a comple
178                                              Kinetic analysis of the reaction between the respective
179               Steady state and time-resolved kinetic analysis of the reaction catalyzed by the bacter
180                                              Kinetic analysis of the reaction is presented showing a
181          Mechanistic studies through in situ kinetic analysis of the reaction reveal key differences
182                   Here we present a thorough kinetic analysis of the relationship between C-extein co
183 centration, with no need for model-dependent kinetic analysis of the signal used for detection or the
184                     Here, we report detailed kinetic analysis of the Steap4 cell surface metalloreduc
185 s in continuous assays, and pre-steady-state kinetic analysis of the target enzymes.
186                                  A transient kinetic analysis of the ternary complex formation aided
187                                              Kinetic analysis of these effects confirm this observati
188                                 Steady-state kinetic analysis of these substances demonstrates that t
189                                     To date, kinetic analysis of this complex process has been achiev
190                                          Our kinetic analysis of this response shows that cells have
191 ion by Trm10, we performed a biochemical and kinetic analysis of Trm10 and variants with alterations
192                   Here we present a thorough kinetic analysis of Trypanosoma brucei TryS in a newly d
193  The assay was used to conduct a comparative kinetic analysis of two LanM enzymes (HalM2 and ProcM) t
194                                              Kinetic analysis of wild-type UGDH and the inducible hex
195                                              Kinetic analysis of WT ADAMTS13 revealed approximately 2
196                             It is shown from kinetics analysis of both the enzyme catalytic responses
197   Here we demonstrate a quantitative binding kinetics analysis of drug-target interactions to investi
198                                              Kinetics analysis of SV release supports that the proxim
199 fied conserved transitions between them, and kinetic analysis paralleled these observations.
200  Kinetic experiments using reaction progress kinetic analysis protocols demonstrate that inhibition o
201                                              Kinetic analysis provided an activation energy (E(a)) of
202                                              Kinetic analysis provides evidence that the turnover lim
203 to parameters derived from full quantitative kinetic analysis (R(2) < 0.34).
204 es obtained from tail currents together with kinetics analysis reveal that the fast and slow gates of
205                                              Kinetic analysis revealed a larger turnover number for r
206                                              Kinetic analysis revealed apparent Km values of 20 and 9
207                              Biochemical and kinetic analysis revealed Lys(147) to be an intramolecul
208                                              Kinetic analysis revealed position 596 also plays a role
209 nalysis using Logan plots and full nonlinear kinetic analysis revealed significant inhibition for bot
210                                   A detailed kinetic analysis revealed that (E)-4-amino-3-methylbut-2
211                                       Enzyme kinetic analysis revealed that BA inhibited tyrosinase a
212                                 Steady-state kinetic analysis revealed that Dpo4 catalytic efficiency
213                                              Kinetic analysis revealed that most target mutation occu
214                             In contrast, our kinetic analysis revealed the presence of abundant CD25(
215                                              Kinetic analysis revealed the rate-limiting step of inac
216                                              Kinetic analysis reveals co-occupancy of the allosteric
217                             Our steady-state kinetic analysis reveals that A3A discriminates against
218                                          Our kinetic analysis reveals that aggregation proceeds via m
219                                              Kinetic analysis reveals that perovskite films with less
220                                       Simple kinetic analysis reveals that photo-oxidation of PhPyr b
221                                 Quantitative kinetic analysis reveals that the CP-mDia1 antagonism th
222               Furthermore, multiple-turnover kinetic analysis reveals that the rate-determining step
223                                 Steady-state kinetic analysis reveals that WRN improves hpol kappa-ca
224                          The force-dependent kinetics analysis reveals a mechanism that requires DNA
225  tunnel and LPA in the pocket, together with kinetic analysis, reveals that bile salts act as partial
226 -depth kinetic study using reaction progress kinetic analysis (RPKA) has been performed to probe the
227                               The results of kinetic analysis show that among the closely related adu
228                   EPR studies in tandem with kinetic analysis show that the 490 nm chromophore of 2 i
229                                              Kinetics analysis show that the HYH gene is indeed late
230                                     Overall, kinetic analysis showed an apparent zero-order model fit
231                                              Kinetic analysis showed brain uptake to be relatively hi
232                                              Kinetic analysis showed splicing rates with the selected
233                    Coimmunoprecipitation and kinetic analysis showed that E299V and wild-type isoform
234                                              Kinetic analysis showed that long-chain (C14-C18) substr
235                                    Our prior kinetic analysis showed that nonnucleoside inhibitors bi
236 hat NaOt-Bu was necessary for catalysis, but kinetic analysis showed that the base is not involved in
237                                              Kinetic analysis showed that the compounds function as r
238                                              Kinetic analysis showed that the predominant effect was
239                                              Kinetic analysis showed that these two domains contribut
240                                              Kinetic analysis showed that XXT5 has a 7-fold higher Km
241                                          The kinetic analysis showed the absorption efficiency was hi
242                                              Kinetic analysis shows a minor role for substrate bindin
243                               A steady-state kinetic analysis shows that interaction with SSB stimula
244 ctors are required for optimal activity, and kinetic analysis shows that MMCoA is incorporated first,
245                                          Our kinetic analysis shows that NNI2 do not significantly bl
246                                   Our growth kinetic analysis shows that the calcined materials have
247           Dynamic images were processed with kinetic analysis software using a 1-tissue-compartment m
248                                 Results from kinetic analysis, stoichiometric reactions of isolated c
249                            The structure and kinetic analysis suggest that ATP sulfurylase overcomes
250                                              Kinetic analysis suggested a minor and variable contribu
251                                    Molecular kinetic analysis suggested that intravascular taste sens
252                                     In depth kinetic analysis suggested that loss of catalytic activi
253                                              Kinetic analysis suggests that binding of AM-8138 to the
254                                              Kinetic analysis suggests that hFACT decreases the lifet
255                                          The kinetic analysis suggests that prolyl cis --> trans isom
256     Molecular modeling studies combined with kinetic analysis supported favorable interaction with th
257                  The most successful binding kinetics analysis systems at this moment include surface
258      This prevents successful application of kinetic analysis techniques and causes semiquantitative
259 AUC) provides a better correlation with full kinetic analysis than does standard SUV.
260                           By using the micro-kinetic analysis, the CO oxidation following the tri-mol
261 irected mutagenesis followed by steady state kinetic analysis to ascertain their catalytic functions
262 e key microscopic steps by applying a global kinetic analysis to both the decrease in the concentrati
263 L-nucleotides and performed pre-steady-state kinetic analysis to determine the D-stereoselectivity me
264 ition of highly reproducible data and global kinetic analysis to determine the mechanistic influence
265 erial species were subjected to steady-state kinetic analysis to determine their specificities toward
266              We carried out pre-steady-state kinetic analysis to elucidate the kinetic mechanism of t
267 e performed a detailed non-linear regression kinetic analysis to simultaneously fit families of subst
268 we therefore extend contemporary statistical kinetic analysis to study collective transport phenomena
269           Here we used a combination of fine kinetic analysis under specific conditions (pH, PN conce
270                                              Kinetic analysis underscored the importance of motif 1a
271  to evaluate (18)F-AV-1451 binding with full kinetic analysis using a metabolite-corrected arterial i
272 -site affinity label, together with detailed kinetic analysis using a variety of well defined oligosa
273 isition times were tested comparatively to a kinetic analysis using MRTM2.
274                      Here, we demonstrate by kinetic analysis using physically tethered DNA substrate
275                                     In vitro kinetic analysis using purified protein demonstrated tha
276 uptake (BPND), was measured in subjects with kinetic analysis using the arterial input function both
277 ntration (VT) were measured in subjects with kinetic analysis using the arterial input function.
278 tal cortical subdivisions) was measured with kinetic analysis using the arterial input function.
279                       Ferricyanide reduction kinetic analysis (variation of ferricyanide absorption w
280 ding potential (BPND) obtained from the full kinetic analysis was compared with the SUVR and with non
281                                              Kinetic analysis was conducted to evaluate the dose-resp
282  residue impacts the L-glutaminase property, kinetic analysis was coupled with crystal structure dete
283      In this article, the reliability of the kinetic analysis was improved by obtaining steady-state
284                         Third, a preliminary kinetic analysis was performed using the radiometabolite
285                            Reaction progress kinetic analysis was performed, shedding light on a poss
286 egistered magnetic resonance images and full kinetic analysis was performed.
287  KIF3A and KIF3B stepping, a presteady-state kinetic analysis was pursued.
288 glucose uptake with (18)F-FDG PET and Patlak kinetic analysis was systematically assessed using the v
289                         A sigmoidal response kinetic analysis was used to calculate both the diffusio
290                                 Stopped flow kinetic analysis was used to confirm this prediction.
291                            Reaction progress kinetic analysis was used to obtain insight into the mec
292                              Using real-time kinetic analysis we show that mcm(5)-modified tRNA(Lys)
293                      From the structural and kinetic analysis, we can state that five residues at pos
294 ingle-molecule fluorescence measurements and kinetic analysis, we find that the reaction in solution
295 ents, chemical shift perturbation and enzyme kinetic analysis, we provide structural insights into th
296           Through the use of mutagenesis and kinetic analysis, we show that the active site of ssNAT
297                               The results of kinetic analysis were confirmed by chronocoulometry meth
298 rast, decreasing time-activity curves in the kinetic analysis were highly prognostic for shorter prog
299                Site-directed mutagenesis and kinetic analysis with substrate analogs revealed the rol
300 ction and to compare parameters derived from kinetic analysis with SUV ratio (SUVR) calculated over d

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top