1 %), as evident from the Fe(CN)6(3-/4-) redox
kinetic study.
2 nt of C-H metalation has been supported by a
kinetic study.
3 n PET dosimetry, biodistribution, and tissue
kinetics study.
4 02), which was confirmed by in situ (1)H NMR
kinetic studies.
5 howed mixed inhibition of AChE in the enzyme
kinetic studies.
6 type of information that can be gained from
kinetic studies.
7 competitive mode of inhibition determined by
kinetic studies.
8 ted by structural (single crystal X-ray) and
kinetic studies.
9 termining step of the catalysis according to
kinetic studies.
10 terized, is discounted as an intermediate by
kinetic studies.
11 s, when feasible, are therefore preferred in
kinetic studies.
12 , time and reagents and is also suitable for
kinetic studies.
13 sonances but were not suitable for multishot
kinetic studies.
14 ntrinsic PDI fluorescence is appropriate for
kinetic studies.
15 eduction of the Schiff base intermediate and
kinetics studies.
16 ypsin fold uncovered by structural and rapid
kinetics studies.
17 model, and thus generalizable beyond enzyme
kinetics studies.
18 hese computational findings are validated by
kinetic studies across a range of hydroamination reactio
19 Detailed experimental, spectroscopic, and
kinetic studies along with kinetic modeling of the catal
20 The
kinetic studies also establish that there are considerab
21 Furthermore,
kinetic studies also help in understanding AR allosteris
22 Kinetic studies also revealed that designed reversible i
23 We document, by
kinetic studies and by determination of three X-ray stru
24 Detailed
kinetic studies and computational investigations have be
25 Kinetic studies and density functional theory calculatio
26 Kinetic studies and deuterium-labeling experiments, as w
27 identical withN bond cleavage as assessed by
kinetic studies and experimentally derived activation pa
28 sed binding assay suitable for both detailed
kinetic studies and high throughput competition binding
29 Furthermore,
kinetic studies and in situ spectroscopic investigations
30 The mechanism is fully consistent with
kinetic studies and isotopic labeling experiments, and t
31 Kinetic studies and linear free-energy relationships rev
32 he mechanism of this PRC2 inhibition through
kinetic studies and photo-cross-linking.
33 with the previous steady-state and transient
kinetic studies and show that the individual nonprocessi
34 ed by X-ray diffraction and in solution with
kinetic studies and spectrophotometric titrations.
35 Based on
kinetic study and surface characterization, PDS is propo
36 euterium labeling experiments, KIE and other
kinetic studies,
and by examining the reactivity of XylN
37 , rapid injection NMR spectroscopy (RI-NMR),
kinetic studies,
and computational analysis has enabled
38 en we summarize the key findings of reaction
kinetic studies,
and provide some mechanistic details em
39 atus including bone mineral density, calcium
kinetics studies,
and markers of bone remodeling.
40 Kinetic studies are a suitable tool to disclose the role
41 versus kinetic control of the reactions, and
kinetic studies are in excellent agreement with the calc
42 Kinetic studies are needed to fully explain magnesium ho
43 of a broader scope of nucleophiles and some
kinetic studies are presented.
44 Kinetic studies,
as a function of 1,4-cyclohexadiene con
45 ing temporal connections are missed, even in
kinetic studies,
as transcription factor (TF) binding wi
46 te buffer and orange and tomato juices) in a
kinetic study at pH 3.5.
47 Our
kinetics studies at 4 degrees C complement the canonical
48 In both
kinetic studies,
blood and breath samples were collected
49 state, the most relevant state suggested by
kinetic studies,
both with (2.45 A) and without (3.10 A)
50 Kinetic studies by (1)H NMR revealed that ruthenium benz
51 Through detailed
kinetic studies by absorption spectroscopy, scanning ele
52 eviously unexplored model membrane for these
kinetic studies,
can be used for monitoring interfacial
53 Kinetic studies combined with simulation reveal a large
54 Kinetic studies conducted under both catalytic and stoic
55 ng maleic anhydride as dienophile as well as
kinetic studies confirm the calculations.
56 Rapid
kinetic studies confirmed that limiting rate constants f
57 Kinetic studies confirmed that the Leishmania GMPR catal
58 hizosaccharomyces pombe, LC-MS analyses, and
kinetic studies confirmed their monofunctionality.
59 ing this, we studied whether the degradation
kinetics study correlates with pH-sensitive variations i
60 The
kinetics' study could elucidate how the polyphenols work
61 Finally,
kinetic studies demonstrate that assembly of the ring te
62 li CFT073 relative to Amp/Amx, and time-kill
kinetic studies demonstrate that Ent-Amp/Amx kill this s
63 Kinetic studies demonstrate that neutrophil infiltration
64 Kinetic studies demonstrate that the B(Ac)2 mechanistic
65 Kinetic studies demonstrate that this substitution resul
66 Mechanistically, in vitro
kinetics studies demonstrate that Grp94 recognizes on-pa
67 Preloaded and
kinetic studies demonstrated adsorption of [Cu-CA] compl
68 Kinetic studies demonstrated that dynasore reduced the n
69 Kinetic studies demonstrated that ketotifen reversed the
70 Kinetic studies demonstrated that the reaction is first-
71 Kinetics studies determine a large kinetic isotope effec
72 Kinetic studies employing the modeling software AmyloFit
73 was studied by a suite of methods, including
kinetic studies,
EPR spectroscopy, and computational met
74 Steady-state
kinetic studies establish that the enzyme is capable of
75 Temperature-dependent
kinetic studies establish the energy requirements for th
76 with isotopic labeling, stoichiometric, and
kinetic studies established 1,2-alkene insertion as both
77 Finally,
kinetic studies examining the transfer of a fluorescent
78 Kinetic studies facilitated by photochemical radical gen
79 Numerous experimental methods, including
kinetic studies,
filtration tests, Hg poisoning experime
80 Kinetic studies for the 9 most active compounds indicate
81 A
kinetic study for adduct hydrolysis in 0.1 M aqueous HCl
82 A detailed
kinetic study for C(sp(3))-H amination of 1-azido-4-phen
83 here results from a detailed mechanistic and
kinetic study for trapping RSNOs by three distinct phosp
84 Our mutagenic and
kinetic studies further demonstrate that the side chain
85 Kinetic studies,
H/D exchange experiments, and kinetic i
86 ochemical, spectroscopic, computational, and
kinetic studies has been used to elucidate the key mecha
87 An electrochemical
kinetics study has revealed that water oxidation occurs
88 Structural and
kinetic studies have characterized a rapid, pre-catalyti
89 Previous ensemble transient
kinetic studies have estimated the average translocation
90 (1)H NMR-based
kinetic studies have revealed the latent mechanistic com
91 Previous
kinetic studies have shown that I1 is formed in a rapid
92 In contrast, results from
kinetic studies,
heparin pulldown experiments, and inhib
93 ehavior is observed, while for X = Cl or Br,
kinetic studies implicate product catalysis.
94 Kinetic studies in E. coli reveal that differential prot
95 sed with the object of avoiding the need for
kinetic studies in the method.
96 A time-resolved
kinetic study in acetonitrile and a theoretical investig
97 Kinetic studies indicate a bimolecular process, rate = k
98 Kinetic studies indicate cultured APCs release high amou
99 Structural and enzyme
kinetic studies indicate that dGTP binding to the first
100 Kinetic studies indicate that in contrast to 3CL(pro) fr
101 Initial stoichiometric and
kinetic studies indicate that the mechanism of this reac
102 An in silico modeling approach together with
kinetic studies indicate that the nonconsensus amino aci
103 Kinetics studies indicate that TCL is capable of inhibit
104 Herein we disclose that
kinetics studies indicate the reaction is first order bo
105 Michelis-Menten
kinetic studies indicated a noncompetitive mechanism of
106 Mass spectrometry and enzyme
kinetic studies indicated that AQs are noncovalent, reve
107 Kinetic studies indicated that formation of the Ir-carbe
108 Furthermore, enzyme
kinetic studies indicated that the Cel3A enzyme is signi
109 ions are important for the interpretation of
kinetic studies involving deuteration.
110 on detailed photophysical and isomerization
kinetic studies is provided that shed light into the rea
111 A
kinetic study is reported for the acid-catalyzed hydroly
112 Kinetic studies,
isotope labeling, and in situ high-reso
113 Combining both docking and saturation
kinetic studies led to the formulation of an enantiosele
114 Such single-molecule based
kinetic studies may be extended to various protein-polym
115 Results of
kinetic studies monitoring the incorporation of modified
116 Kinetic studies of a model enzyme, M8, showed that a dif
117 n environmental oxidant and model system for
kinetic studies of aromatic amine oxidation.
118 Here we report stopped-flow
kinetic studies of azide binding to human ferricytochrom
119 In
kinetic studies of BDE-47 metabolism by CYP2B6 and poole
120 Kinetic studies of benzylic and aryl C-H borylation cata
121 It permits
kinetic studies of biological processes with significant
122 Kinetic studies of calcium effects on the labeled alpha1
123 nded-beta2AR binding to arrestin and through
kinetic studies of cAMP turnover.
124 Kinetic studies of COM growth at varying inhibitor conce
125 In particular, we show how
kinetic studies of coupled folding and binding reactions
126 enzymatic activity through variable pressure
kinetic studies of electron transfer and turnover.
127 Previous
kinetic studies of EutT revealed the importance of a HX1
128 Here we report on
kinetic studies of H3K4 methylation by PRDM9 in vitro in
129 Here we discuss how
kinetic studies of individual reactions and cycles that
130 den Markov modeling (HMM) has revolutionized
kinetic studies of macromolecules.
131 confocal spectroscopy as a powerful tool in
kinetic studies of membrane-protein folding in membrane-
132 Through
kinetic studies of PP32, we find folding to be rate-limi
133 Kinetic studies of reactions with HBpin and PhSiH3 show
134 Kinetic studies of regulatory factor interactions at the
135 parallel pathways differs from results from
kinetic studies of repeat-proteins composed of sequence-
136 Spectroscopic and
kinetic studies of the NO reaction revealed a rapid, mul
137 Stopped flow
kinetic studies of the OAT reactions show a range of kin
138 Kinetic studies of the reaction indicated that it is fir
139 Fluorescence-based
kinetic studies of the reaction with beta-mercaptoethano
140 Kinetic studies of the two-step reaction revealed that t
141 Comprehensive
kinetic studies of the variants reveal that they fold vi
142 The conceptual framework for
kinetic studies of these systems is presented with a foc
143 Steady-state and single turnover
kinetic studies of these variants, combined with pulsed
144 change of aryl iodides, this report presents
kinetic studies of this process, giving first-order kine
145 he computational results are consistent with
kinetic studies of variant forms of P2O altered at resid
146 A comprehensive
kinetic study of Ac-SDKP and domain co-operation was per
147 A
kinetic study of beta-carotene degradation showed that t
148 Here, we report the
kinetic study of in situ phase transformation of In2O3 n
149 The
kinetic study of oxidation development and the consumer
150 We report the synthesis and
kinetic study of PEGylated, water-soluble aminyl radical
151 Moreover,
kinetic study of preassembled cube and tetrahedron demon
152 The method supports the
kinetic study of RNA-ligand systems, in particular at di
153 A
kinetic study of the gas-phase reactions of OH radicals
154 Here we present a
kinetic study of the HOR on representative catalytic sys
155 A time-resolved
kinetic study of the hydrogen atom transfer (HAT) reacti
156 A
kinetic study of the hydrogen atom transfer (HAT) reacti
157 A
kinetic study of the hydrogen atom transfer (HAT) reacti
158 A
kinetic study of the hydrogen atom transfer from activat
159 Through a
kinetic study of the hydrogen atom transfer processes pr
160 stimuli-responsive block enabled a detailed
kinetic study of the molecular mechanism of the enzymati
161 Recently, a
kinetic study of the nitrogenase Fe protein cycle involv
162 This work constitutes the first
kinetic study of the reactions of OH radicals with (Z)-3
163 e and extend its characterization to a rapid
kinetic study of the reductive half-reaction (the reacti
164 ructurally related guests, together with the
kinetic study of the template assembly and disassembly,
165 his phenomenon, we have conducted a detailed
kinetic study of wild-type IDH1 as well as the known 2HG
166 Kinetics studies of m4-1BB disclosed a very tight nanomo
167 t, versatile, and reliable method of HMM for
kinetics studies of macromolecules under thermodynamic e
168 This first rapid
kinetics study of MCR with its natural substrates descri
169 In this paper we report on a
kinetics study of the discharge process and its relation
170 Deuterium scrambling and
kinetic studies offer valuable facts for understanding t
171 We report
kinetic studies on Bloom (BLM) helicase and human telome
172 conducted steady-state and pre-steady-state
kinetic studies on LRRKtide and its analog LRRKtide(S).
173 These transient
kinetic studies on mouse cardiac myosins provide strong
174 Performing
kinetic studies on protein ligand interactions provides
175 tigations on the supramolecular heterodimer,
kinetic studies on the catalytic cycle, and a thorough a
176 Kinetic studies on the cyclopropanation show an inductio
177 arbonates by nucleophiles, we have performed
kinetic studies on the hydrolysis of carbonates using nu
178 Kinetic studies on the improved catalyst, 4-(H)2BPin, es
179 Previous
kinetic studies on the mitochondrial MDH did not yield a
180 reaction has been clarified on the basis of
kinetic studies on the overall catalytic reaction as wel
181 Kinetic studies on the reactions of iron complexes suppo
182 We report spectroscopic and
kinetic studies on the role of the individual reaction c
183 A time-resolved
kinetic study on the effect of trifluoroacetic acid (TFA
184 A
kinetic study on the hydrogen atom transfer (HAT) reacti
185 A time-resolved
kinetic study on the reactions of the cumyloxyl radical
186 Detailed
kinetic studies point to a mechanism for HER catalysis t
187 The results of an electrochemical
kinetics study point to a mechanism in which surface oxi
188 The results of an electrochemical
kinetics study point to a single-site mechanism for wate
189 Such
kinetic studies provide a general protocol for distingui
190 Structures and
kinetic studies provide an explanation for the lower aff
191 Kinetics studies provide mechanistic insight regarding t
192 Previous
kinetic studies provided evidence for the formation of a
193 Kinetic studies provided little support for resistance b
194 Temperature dependent
kinetic studies reinforce the novel finding that hydroge
195 Kinetic studies reveal an inverse relationship between t
196 Kinetic studies reveal first-order rate dependence on Fe
197 Kinetic studies reveal that the anaerobic burst and stea
198 Furthermore,
kinetic studies reveal that the presence of an engineere
199 Kinetic studies reveal that the propagating species emer
200 Kinetic studies reveal that the rate exhibits a first-or
201 Kinetic studies reveal that the rate-determining step in
202 Kinetic studies reveal that the rhodium complex acts as
203 The
kinetic studies reveal that the templating Fm7dG slows p
204 Kinetic studies revealed a first-order reaction rate.
205 Kinetic studies revealed effects of CBFbeta on both meta
206 Kinetic studies revealed that a representative SIRT2 inh
207 Kinetic studies revealed that CBFbeta increases the rate
208 Kinetic studies revealed that the formation of monohydro
209 In-depth fast
kinetic studies revealed that the gain in UAG reading by
210 Kinetic studies revealed that the homogeneous counterpar
211 The
kinetic studies revealed that the new compounds exhibite
212 Kinetic studies revealed that the rates of the polymer t
213 Further
kinetic studies revealed that this compound behaves as a
214 Kinetic studies revealed two possible expressions for th
215 Kinetic studies revealed two representative pathways for
216 Further enzyme
kinetic study revealed that both types of compounds inhi
217 Michaelis-Menten
kinetics studies revealed a classic noncompetitive mecha
218 er, Fe(III), and Cu(II) products; however, a
kinetic study reveals a one-electron rate-determining pr
219 Kinetic studies show that AKR1B15.1 is predominantly a r
220 Kinetic studies show that ethoxycarbonylnitrene reacts w
221 Kinetic studies show that inhibition of doxorubicin tran
222 Kinetic studies show that initial damage caused by apica
223 Kinetic studies show that M. jannaschii DHNA possesses a
224 Kinetic studies show that NS5806 decreases the rate of d
225 nation of spectroscopic, thermochemical, and
kinetic studies show that only those proton donors that
226 Direct measurement in single turnover
kinetic studies show that pyrophosphate release is faste
227 ing C-H bonds in the supporting ligands, and
kinetic studies show that the Fe/Co heterobimetallic spe
228 Dye displacement
kinetic studies show that the ligand is a much more rapi
229 Stopped-flow
kinetic studies show that the oxidative transformation o
230 Kinetic studies show that the rate of the initially rapi
231 Detailed
kinetic studies show that the translocation speed is slo
232 Kinetic studies show that these compounds not only trigg
233 Kinetic studies show that these enzymes are more efficie
234 Kinetic studies show that this intermediate is not itsel
235 Inactivation
kinetic studies show that TPA-RC has higher inactivation
236 Real-time
kinetics studies show that the polarization build-up rat
237 Kinetic studies showed a high extraction rate of phenoli
238 Transient
kinetic studies showed that cYY binding resulted in a lo
239 Previous
kinetic studies showed that IkappaBalpha accelerates NF-
240 Kinetic studies showed that ring strain increases nucleo
241 Kinetic studies showed that substrate affinities of the
242 Kinetic studies showed that the amination of aryl chlori
243 Kinetic studies showed that the conversion of 3a or 3b t
244 Kinetic studies showed that the phosphoantigens were rel
245 Pre-steady-state
kinetic studies showed that the substitutions at arginin
246 Kinetic studies showed that two of the compounds decompo
247 using the tetrahydrofuran-water system, this
kinetic study showed that Ni-MOF-74 forms within 12 hour
248 etate, pyruvate and D- and L-2HG support the
kinetic studies showing competition with 2OG.
249 Both DFT and
kinetic studies strongly point to a mechanism where the
250 These
kinetic studies suggest a biochemical explanation for th
251 Our structural, spectroscopic and
kinetic studies suggest that chemoselective organic tran
252 Kinetic studies suggest that the difference in cleavage
253 Density functional theory calculations and
kinetic studies suggest the reaction is catalyzed by tra
254 The
kinetics studies suggest that both Cys-RSE and Cys-DNIC
255 Kinetics studies suggest the bifurcation point to these
256 Kinetic studies suggested that linker exchange reactions
257 g density functional theory calculations and
kinetics studies,
support a conjugate addition pathway a
258 Kinetic studies,
temperature dependent photostationary s
259 through a combination of stoichiometric and
kinetic studies that a (PPh3)Ag-carboxylate is responsib
260 This hypothesis is supported by
kinetic studies that indicate almost instantaneous N-chl
261 We show through enzyme
kinetics studies that analogues of this chemotype are no
262 In
kinetic studies,
the reaction is second-order globally a
263 high-temperature and high-pressure chemical
kinetics studies,
the shock tube is the reactor of choic
264 Combined with the
kinetic study,
these data suggest a catalytic cycle invo
265 Optimisation of the method considered
kinetic studies to establish the incubation time to perf
266 nuclear magnetic resonance spectroscopy, and
kinetic studies to gain a better understanding of the fa
267 nuclear magnetic resonance spectroscopy and
kinetic studies to generate, observe, and characterize t
268 fore have carried out both computational and
kinetic studies to probe the reduction of Fe(IV)=O.
269 Detailed
kinetic studies,
together with the in situ spectroscopic
270 Our
kinetic studies unveil the existence of a delicate inter
271 Dissociation
kinetic studies using [(3)H]NMS further support that LY2
272 Quantitative
kinetic studies using artificial membranes confirm that
273 andem mass spectrometry analysis, and enzyme
kinetic studies using five different substrates confirme
274 Kinetic studies using in situ high pressure IR (HPIR) an
275 Kinetic studies using NMR and UV-vis spectroscopies conf
276 hesis, and on the basis of photochemical and
kinetic studies using UV/vis, CD, and (1)H NMR spectrosc
277 An in-depth
kinetic study using reaction progress kinetic analysis (
278 Kinetic studies utilizing surface plasmon resonance tech
279 Kinetic studies via UV-vis spectroscopy with this boron
280 The first
kinetic study was performed before participants started
281 geted metabolomics approaches, together with
kinetic studies,
was used to investigate biomarkers of W
282 luorescence resonance energy transfer (FRET)
kinetic studies,
we have investigated the search and bin
283 From physiological and
kinetic studies,
we identified 2-aminoacetophenone as a
284 Based on
kinetic studies,
we present a model suggesting that the
285 On the basis of mechanistic and
kinetic studies,
we propose a pathway in which rhodium p
286 Kinetic studies were carried out to unravel the mechanis
287 Enzyme
kinetic studies were carried out with Hoechst 33342 as f
288 fast affinity extraction for equilibrium and
kinetic studies were considered, and several approaches
289 Further cell-based and
kinetic studies were performed to substantiate our initi
290 Two identical
kinetic studies were performed, each with the use of a s
291 Kinetic studies were then employed to further clarify th
292 n modulates enzymatic activity, we performed
kinetic studies with both ADAM17 analogs and various TNF
293 In vitro
kinetic studies with purified NMT1A160T enzyme revealed
294 ally, the different options for carrying out
kinetic studies with temporal resolution such as rapid-s
295 Kinetic studies with wild-type IAPP and IAPP mutants dem
296 Kinetic study with extensive deuterium labeling experime
297 zed electrode and its application to fast ET
kinetic study with simple instrumentation should be usef
298 ) to a general heterogeneous electrochemical
kinetic study with ultramicroelectrodes (UMEs) even for
299 Kinetics studies with structurally varied aldehydes and
300 The results of
kinetic studies yield the values of hybridization and di