1 nt of C-H metalation has been supported by a
kinetic study.
2 n PET dosimetry, biodistribution, and tissue
kinetics study.
3 ance, high-resolution mass spectrometry, and
kinetic studies.
4 ntrinsic PDI fluorescence is appropriate for
kinetic studies.
5 s, when feasible, are therefore preferred in
kinetic studies.
6 , time and reagents and is also suitable for
kinetic studies.
7 sonances but were not suitable for multishot
kinetic studies.
8 02), which was confirmed by in situ (1)H NMR
kinetic studies.
9 howed mixed inhibition of AChE in the enzyme
kinetic studies.
10 type of information that can be gained from
kinetic studies.
11 competitive mode of inhibition determined by
kinetic studies.
12 N, but this stabilization is not revealed by
kinetic studies.
13 tructural, spectroscopic, thermodynamic, and
kinetic studies.
14 A mechanism proposal is given based on
kinetic studies.
15 (PPh(2))] as well as from stoichiometric and
kinetic studies.
16 topic labeling, intermediate validation, and
kinetic studies.
17 10 nm spatial resolution of SECM imaging and
kinetic studies.
18 model, and thus generalizable beyond enzyme
kinetics studies.
19 eduction of the Schiff base intermediate and
kinetics studies.
20 hese computational findings are validated by
kinetic studies across a range of hydroamination reactio
21 Detailed experimental, spectroscopic, and
kinetic studies along with kinetic modeling of the catal
22 Kinetic studies also demonstrate the requirement for sus
23 The
kinetic studies also establish that there are considerab
24 Furthermore,
kinetic studies also help in understanding AR allosteris
25 Kinetic studies also revealed that designed reversible i
26 PRMT6 was confirmed by mass spectrometry and
kinetic studies and by a cocrystal structure.
27 ith molecular dynamics simulations, in vitro
kinetic studies and chemical derivatization experiments,
28 Detailed
kinetic studies and computational investigations have be
29 Kinetic studies and density functional theory calculatio
30 Kinetic studies and deuterium-labeling experiments, as w
31 enzyme present in the cell, enabling enzyme
kinetic studies and emphasizing the application of the p
32 Rapid
kinetic studies and EPR measurements of rapid freeze-que
33 sed binding assay suitable for both detailed
kinetic studies and high throughput competition binding
34 The mechanism is fully consistent with
kinetic studies and isotopic labeling experiments, and t
35 Kinetic studies and linear free-energy relationships rev
36 that of cDC1 and cDC2 in both reconstitution
kinetic studies and parabiotic mice.
37 euterium labeling experiments, KIE and other
kinetic studies,
and by examining the reactivity of XylN
38 , rapid injection NMR spectroscopy (RI-NMR),
kinetic studies,
and computational analysis has enabled
39 Combined catalyst characterization,
kinetic studies,
and isotopic labeling experiments unvei
40 -activity relationships, electrochemical and
kinetic studies,
and pressurized sample infusion high-re
41 en we summarize the key findings of reaction
kinetic studies,
and provide some mechanistic details em
42 ics/molecular mechanics (QM/MM) simulations,
kinetic studies,
and the results of site-directed mutage
43 atus including bone mineral density, calcium
kinetics studies,
and markers of bone remodeling.
44 Kinetic studies are a suitable tool to disclose the role
45 Associated
kinetic studies are discussed and compared with a struct
46 versus kinetic control of the reactions, and
kinetic studies are in excellent agreement with the calc
47 of a broader scope of nucleophiles and some
kinetic studies are presented.
48 Kinetic studies,
as a function of 1,4-cyclohexadiene con
49 Kinetic studies at 22 degrees C and pH 7.1 showed that t
50 te buffer and orange and tomato juices) in a
kinetic study at pH 3.5.
51 Our
kinetics studies at 4 degrees C complement the canonical
52 the underlying molecular mechanisms through
kinetic studies,
binding free energy calculations, and m
53 state, the most relevant state suggested by
kinetic studies,
both with (2.45 A) and without (3.10 A)
54 Kinetic studies by (1)H NMR revealed that ruthenium benz
55 Through detailed
kinetic studies by absorption spectroscopy, scanning ele
56 Kinetic studies carried out with TEMPO-H(D) reveal secon
57 ies were analyzed using flow cytometry, cell
kinetic studies,
co-culture with CD4 T cells, and cytoki
58 Kinetic studies combined with simulation reveal a large
59 amylase activity and as an easy method to do
kinetic studies compared to other available methods.
60 Kinetic studies conducted under both catalytic and stoic
61 Rapid
kinetic studies confirmed that limiting rate constants f
62 Kinetic studies confirmed that the Leishmania GMPR catal
63 ing this, we studied whether the degradation
kinetics study correlates with pH-sensitive variations i
64 A combination of mutagenesis and
kinetic studies corroborate such a role.
65 The
kinetics' study could elucidate how the polyphenols work
66 Finally,
kinetic studies demonstrate that assembly of the ring te
67 Kinetic studies demonstrate that neutrophil infiltration
68 Preloaded and
kinetic studies demonstrated adsorption of [Cu-CA] compl
69 Kinetic studies demonstrated that dynasore reduced the n
70 Kinetic studies demonstrated that papaverine inhibited i
71 Kinetic studies demonstrated that the reaction is first-
72 Kinetics studies determine a large kinetic isotope effec
73 Kinetic studies determined the concentration dependence
74 Kinetic studies employing the modeling software AmyloFit
75 was studied by a suite of methods, including
kinetic studies,
EPR spectroscopy, and computational met
76 Steady-state
kinetic studies establish that the enzyme is capable of
77 Temperature-dependent
kinetic studies establish the energy requirements for th
78 with isotopic labeling, stoichiometric, and
kinetic studies established 1,2-alkene insertion as both
79 -active ligand, chemical and electrochemical
kinetic studies examined how complex geometry and charge
80 Kinetic studies facilitated by photochemical radical gen
81 A detailed
kinetic study for C(sp(3))-H amination of 1-azido-4-phen
82 ition experiments, gram-scale synthesis, and
kinetic studies further highlight the importance and ver
83 s estimations from ensemble pre-steady state
kinetic studies,
further confirming the catalytic origin
84 trates by UV-vis and (1) H NMR spectroscopic
kinetic studies,
H/D isotopic labelling, and X-ray cryst
85 ochemical, spectroscopic, computational, and
kinetic studies has been used to elucidate the key mecha
86 Control experiments, deuterium labeling, and
kinetic studies have been carried out for preliminary un
87 riments, deuterium labeling experiments, and
kinetic studies have been performed.
88 Previous ensemble transient
kinetic studies have estimated the average translocation
89 (1)H NMR-based
kinetic studies have revealed the latent mechanistic com
90 Ion uptake
kinetics studies have been invaluable in uncovering dist
91 In contrast, results from
kinetic studies,
heparin pulldown experiments, and inhib
92 Kinetic studies highlight that pore heterogeneity facili
93 Kinetic studies in E. coli reveal that differential prot
94 Kinetic studies,
including product and substrate inhibit
95 Kinetic studies indicate cultured APCs release high amou
96 Ligand-binding and
kinetic studies indicate severely reduced affinity for f
97 Kinetic studies indicate that amide reduction obeys an u
98 Kinetic studies indicate that in contrast to 3CL(pro) fr
99 Kinetic studies indicate that rapid export from the ER r
100 Initial stoichiometric and
kinetic studies indicate that the mechanism of this reac
101 An in silico modeling approach together with
kinetic studies indicate that the nonconsensus amino aci
102 Kinetic studies indicate that the oxidation of 5-formyl-
103 Kinetic studies indicated that formation of the Ir-carbe
104 Kinetic studies indicated that sustained EW RV replicati
105 Furthermore, enzyme
kinetic studies indicated that the Cel3A enzyme is signi
106 The
kinetic study indicates that the reaction is elusive in
107 An inhibition
kinetics study indicates that fucoxanthin is showing mix
108 tional docking, validated by mutagenesis and
kinetic studies,
indicates that AK-42 binds to an extrac
109 ions are important for the interpretation of
kinetic studies involving deuteration.
110 OF was subject to steady-state and transient
kinetic studies involving H/D and (13)C/(12)C exchange,
111 ative agreement of the obtained results with
kinetic studies is demonstrated.
112 on detailed photophysical and isomerization
kinetic studies is provided that shed light into the rea
113 This
kinetic study is carried out by recording simultaneous c
114 ray structures of Cu-alkyl intermediates and
kinetic studies)
is put forth illustrating that the init
115 Kinetic studies,
isotope labeling, and in situ high-reso
116 dy describing the reaction mechanism through
kinetic studies,
isotope-labeling experiments, (19)F NMR
117 Systematic experimental and
kinetic studies led to a mechanistic hypothesis that fac
118 Such single-molecule based
kinetic studies may be extended to various protein-polym
119 Results of
kinetic studies monitoring the incorporation of modified
120 In
kinetic studies,
OEC photoassembly shows a significant l
121 iurethane DMA are employed as model DMAs for
kinetic studies of 2-step enzymolysis by 2 esterases, ps
122 Comparative
kinetic studies of a series of new ruthenium complexes p
123 n environmental oxidant and model system for
kinetic studies of aromatic amine oxidation.
124 Here we report stopped-flow
kinetic studies of azide binding to human ferricytochrom
125 Kinetic studies of benzylic and aryl C-H borylation cata
126 nded-beta2AR binding to arrestin and through
kinetic studies of cAMP turnover.
127 In particular, we show how
kinetic studies of coupled folding and binding reactions
128 Previous
kinetic studies of EutT revealed the importance of a HX1
129 Kinetic studies of exon alpha Pol beta revealed that it
130 Kinetic studies of FDHs provide key insights into their
131 into oxoA-induced mutagenesis, we conducted
kinetic studies of human DNA polymerases beta and eta re
132 Here we discuss how
kinetic studies of individual reactions and cycles that
133 Two examples of
kinetic studies of living cells under various doses of d
134 den Markov modeling (HMM) has revolutionized
kinetic studies of macromolecules.
135 confocal spectroscopy as a powerful tool in
kinetic studies of membrane-protein folding in membrane-
136 Parallel
kinetic studies of MutL activation of the UvrD helicase
137 Kinetic studies of regulatory factor interactions at the
138 Kinetic studies of single-step reactions suggest that fo
139 Here we present the structural and
kinetic studies of the human B3GNT2.
140 Spectroscopic and
kinetic studies of the NO reaction revealed a rapid, mul
141 Fluorescence-based
kinetic studies of the reaction with beta-mercaptoethano
142 Kinetic studies of the removal of 10 anionic PFASs at en
143 Kinetic studies of the two-step reaction revealed that t
144 Comprehensive
kinetic studies of the variants reveal that they fold vi
145 Kinetic studies of their thermal decomposition showed th
146 Kinetic studies of these transformations have also been
147 is notion was supported by the synthesis and
kinetic study of a putative off-cycle Pd complex.
148 A
kinetic study of beta-carotene degradation showed that t
149 ng employed as insightful surrogates for the
kinetic study of drug entry through bacterial cytoplasmi
150 Here, we report the
kinetic study of in situ phase transformation of In2O3 n
151 A
kinetic study of lactose digestion showed levels of hydr
152 The
kinetic study of oxidation development and the consumer
153 We report the synthesis and
kinetic study of PEGylated, water-soluble aminyl radical
154 Based on the
kinetic study of POBN-1-hydroxyethyl spin adduct (POBN-1
155 The method supports the
kinetic study of RNA-ligand systems, in particular at di
156 Here, we present an in-depth
kinetic study of the 1,2-addition of H(2) via an MLC pat
157 tivation parameters were determined from the
kinetic study of the Au(22) transformation.
158 A
kinetic study of the gas-phase reactions of OH radicals
159 Here we present a
kinetic study of the HOR on representative catalytic sys
160 A
kinetic study of the hydrogen atom transfer (HAT) reacti
161 A
kinetic study of the hydrogen atom transfer (HAT) reacti
162 A
kinetic study of the hydrogen-deuterium exchange reactio
163 Here we present a detailed
kinetic study of the multisite proton-coupled electron t
164 Recently, a
kinetic study of the nitrogenase Fe protein cycle involv
165 To this aim, a
kinetic study of the primary and secondary oxidative pro
166 ometallic studies along with a comprehensive
kinetic study of the reaction, including rate-driving fo
167 This work constitutes the first
kinetic study of the reactions of OH radicals with (Z)-3
168 e and extend its characterization to a rapid
kinetic study of the reductive half-reaction (the reacti
169 ructurally related guests, together with the
kinetic study of the template assembly and disassembly,
170 Kinetics studies of m4-1BB disclosed a very tight nanomo
171 t, versatile, and reliable method of HMM for
kinetics studies of macromolecules under thermodynamic e
172 ise because the air-quality models rely upon
kinetics studies of SO(2) oxidation conducted in dilute
173 Reaction
kinetics studies of the Bronsted acid-catalyzed dehydrat
174 is in real-time mass spectrometry (DART-MS),
kinetics studies of the ozonolysis of BaP in thin films
175 icular attention is given to mechanistic and
kinetics studies of vanadium-catalyzed reactions includi
176 Deuterium scrambling and
kinetic studies offer valuable facts for understanding t
177 Kinetic studies on methyl fluorination suggest that the
178 Kinetic studies on pyridine hydrogenation were conducted
179 tigations on the supramolecular heterodimer,
kinetic studies on the catalytic cycle, and a thorough a
180 arbonates by nucleophiles, we have performed
kinetic studies on the hydrolysis of carbonates using nu
181 Kinetic studies on the improved catalyst, 4-(H)2BPin, es
182 Previous
kinetic studies on the mitochondrial MDH did not yield a
183 reaction has been clarified on the basis of
kinetic studies on the overall catalytic reaction as wel
184 Kinetic studies on the reactions of iron complexes suppo
185 We report spectroscopic and
kinetic studies on the role of the individual reaction c
186 This observation allows the application of
kinetic studies on the steric, electronic, and solvent e
187 Two different
kinetic studies on two rapidly evolving chemical reactio
188 A
kinetic study on the hydrogen atom transfer (HAT) reacti
189 Kinetic studies over a range of concentrations and tempe
190 Detailed
kinetic studies point to a mechanism for HER catalysis t
191 Kinetic studies point to the second protonation event as
192 Such
kinetic studies provide a general protocol for distingui
193 Kinetic studies provide evidence that the rate-determini
194 Michaelis-Menten enzyme
kinetic studies provide mechanistic details regarding th
195 Kinetics studies provide mechanistic insight regarding t
196 Previous
kinetic studies provided evidence for the formation of a
197 aive rats and mice were used for in vivo PET
kinetic studies,
radiometabolite studies, and dosimetry
198 Temperature dependent
kinetic studies reinforce the novel finding that hydroge
199 Kinetic studies reveal an inverse relationship between t
200 Kinetic studies reveal fast migration of NO(3) (-) in th
201 Kinetic studies reveal favorable binding of the probe wi
202 Kinetic studies reveal first-order rate dependence on Fe
203 Kinetic studies reveal that the anaerobic burst and stea
204 Kinetic studies reveal that the propagating species emer
205 Kinetic studies reveal that the rate exhibits a first-or
206 Kinetic studies reveal that the rate-determining step in
207 Kinetic studies reveal the presence of two distinct kine
208 Kinetic studies revealed a first-order reaction rate.
209 Kinetic studies revealed that a representative SIRT2 inh
210 Kinetic studies revealed that pyridine binding slows dow
211 Pre-steady-state and steady-state
kinetic studies revealed that RHA has little impact on t
212 Kinetic studies revealed that the formation of monohydro
213 In-depth fast
kinetic studies revealed that the gain in UAG reading by
214 The
kinetic studies revealed that the new compounds exhibite
215 Kinetic studies revealed that the rates of the polymer t
216 Kinetic studies revealed two representative pathways for
217 Further enzyme
kinetic study revealed that both types of compounds inhi
218 Enzyme
kinetics studies revealed that recifin A can specificall
219 er, Fe(III), and Cu(II) products; however, a
kinetic study reveals a one-electron rate-determining pr
220 A
kinetic study reveals a very fast reaction of TEMPO-H wi
221 Kinetic studies show that AKR1B15.1 is predominantly a r
222 Kinetic studies show that ethoxycarbonylnitrene reacts w
223 Kinetic studies show that initial damage caused by apica
224 nation of spectroscopic, thermochemical, and
kinetic studies show that only those proton donors that
225 Direct measurement in single turnover
kinetic studies show that pyrophosphate release is faste
226 ing C-H bonds in the supporting ligands, and
kinetic studies show that the Fe/Co heterobimetallic spe
227 Kinetic studies show that the rate of the initially rapi
228 Kinetic studies show that these compounds not only trigg
229 Kinetic studies show that these enzymes are more efficie
230 Inactivation
kinetic studies show that TPA-RC has higher inactivation
231 Steady-state
kinetics studies show that the dimers exhibit reasonably
232 Kinetic studies showed a high extraction rate of phenoli
233 Transient
kinetic studies showed that cYY binding resulted in a lo
234 The
kinetic studies showed that enzyme molecules with no net
235 Previous
kinetic studies showed that IkappaBalpha accelerates NF-
236 Kinetic studies showed that MB-gCs were mixed-type rever
237 Kinetic studies showed that membrane insertion occurs in
238 Kinetic studies showed that ring strain increases nucleo
239 Kinetic studies showed that substrate affinities of the
240 Kinetic studies showed that the conversion of 3a or 3b t
241 Kinetic studies showed that the coupling process occurs
242 Kinetic studies showed that the oxidation of Cr(III) to
243 Pre-steady-state
kinetic studies showed that the substitutions at arginin
244 In sharp contrast,
kinetic studies showed the binding of POT1 to an initial
245 using the tetrahydrofuran-water system, this
kinetic study showed that Ni-MOF-74 forms within 12 hour
246 Enzyme
kinetics studies showed that LDH activity with free NADH
247 Kinetics studies showed that the rapid rate of inhibitio
248 etate, pyruvate and D- and L-2HG support the
kinetic studies showing competition with 2OG.
249 Kinetic study shows that the transglycosylation reaction
250 Enzyme
kinetics studies,
STD NMR, circular dichroism spectrosco
251 Both DFT and
kinetic studies strongly point to a mechanism where the
252 These
kinetic studies suggest a biochemical explanation for th
253 Our structural, spectroscopic and
kinetic studies suggest that chemoselective organic tran
254 Kinetic studies suggest that the difference in cleavage
255 Density functional theory calculations and
kinetic studies suggest the reaction is catalyzed by tra
256 Kinetics studies suggest the bifurcation point to these
257 unctional theory calculations, together with
kinetic studies,
suggest that the reaction proceeds by a
258 Previous
kinetic studies suggested that GTP binding to one Rag lo
259 Detailed
kinetic studies support the idea that the gating defect
260 e use of molecular probes and the results of
kinetic studies support the proposed mechanism and the r
261 Experimental
kinetics studies support the computations, showing that
262 g density functional theory calculations and
kinetics studies,
support a conjugate addition pathway a
263 Kinetic studies,
temperature dependent photostationary s
264 through a combination of stoichiometric and
kinetic studies that a (PPh3)Ag-carboxylate is responsib
265 This hypothesis is supported by
kinetic studies that indicate almost instantaneous N-chl
266 Here we present a
kinetic study that provides a quantitative basis for und
267 We show through enzyme
kinetics studies that analogues of this chemotype are no
268 In
kinetic studies,
the reaction is second-order globally a
269 high-temperature and high-pressure chemical
kinetics studies,
the shock tube is the reactor of choic
270 ndings are corroborated by subsequent enzyme
kinetic studies;
their atomic-resolution quality provide
271 nuclear magnetic resonance spectroscopy, and
kinetic studies to gain a better understanding of the fa
272 nuclear magnetic resonance spectroscopy and
kinetic studies to generate, observe, and characterize t
273 er with site-directed mutagenesis and enzyme
kinetic studies to identify residues within the UGT2B7 b
274 fore have carried out both computational and
kinetic studies to probe the reduction of Fe(IV)=O.
275 Our
kinetic studies unveil the existence of a delicate inter
276 Quantitative
kinetic studies using artificial membranes confirm that
277 andem mass spectrometry analysis, and enzyme
kinetic studies using five different substrates confirme
278 Kinetic studies using in situ high pressure IR (HPIR) an
279 Kinetic studies using NMR and UV-vis spectroscopies conf
280 hesis, and on the basis of photochemical and
kinetic studies using UV/vis, CD, and (1)H NMR spectrosc
281 cal reaction is confirmed by a high-pressure
kinetic study using infrared spectroscopy, indicating on
282 An in-depth
kinetic study using reaction progress kinetic analysis (
283 Kinetic studies utilizing surface plasmon resonance tech
284 Kinetic studies via UV-vis spectroscopy with this boron
285 geted metabolomics approaches, together with
kinetic studies,
was used to investigate biomarkers of W
286 From physiological and
kinetic studies,
we identified 2-aminoacetophenone as a
287 tial applications of the presented setup for
kinetic studies,
we monitored the conversion of p-nitrop
288 Based on
kinetic studies,
we present a model suggesting that the
289 The thermodynamic and
kinetic studies were carried out to understand the chara
290 Kinetic studies were carried out to unravel the mechanis
291 Enzyme
kinetic studies were carried out with Hoechst 33342 as f
292 e mechanistic detail of the crowding effect,
kinetic studies were conducted with varying concentratio
293 Kinetic studies were then employed to further clarify th
294 Kinetic studies with a series of collagen model peptides
295 Kinetic studies with a surrogate substrate and spectrosc
296 Kinetic studies with rabbit muscle and human liver glyco
297 Kinetic study with extensive deuterium labeling experime
298 zed electrode and its application to fast ET
kinetic study with simple instrumentation should be usef
299 ) to a general heterogeneous electrochemical
kinetic study with ultramicroelectrodes (UMEs) even for
300 The results of
kinetic studies yield the values of hybridization and di