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1 NA sites have a significant effect on search kinetics.
2 no-1,2,4-triazol-5-one following first-order kinetics.
3 tem can be applied to evaluate the enzymatic kinetics.
4 alysis framework to quantify the recruitment kinetics.
5 ication among parasites and influence growth kinetics.
6  and plasticity and synaptic vesicle release kinetics.
7  from low n to high n species with different kinetics.
8 ntial adsorption of oxygen atoms with facile kinetics.
9 rphology, viral RNA profile, and replication kinetics.
10 ve substitution, which together enable rapid kinetics.
11 ct the polymer with pH-dependent degradation kinetics.
12 uires atomic-level understanding of reaction kinetics.
13 ing, slower digestion and leucine absorption kinetics.
14 d to more accurately describe DO consumption kinetics.
15 hput analysis of grafted-from polymerization kinetics, accelerating reaction discovery, and optimizat
16                    By mapping visual pigment kinetics across the central retina, high fidelity IRD pr
17 ette Na(+) had no effect on the selectivity, kinetics, amplitude, rectification or reversal potential
18                                     Detailed kinetic analyses across different time scales, that is,
19         Reported here are thermochemical and kinetic analyses of a new pincer-ligated rhenium complex
20                      Results of steady-state kinetic analyses revealed that AsFMO exhibited negligibl
21                                    Enzymatic kinetic analyses revealed that EAEP generated uncompetit
22                                              Kinetic analyses revealed that Mg dissolution to Mg(2+)
23  expressed proteins, in vitro transcription, kinetic analyses, and in vivo cell viability assays, we
24                                        Using kinetic analyses, fluorescence binding, X-ray crystallog
25              Steady state isotopic transient kinetic analysis (SSITKA) of ammonia synthesis showed th
26 f the reactor and the benefits of performing kinetic analysis as a routine part of reaction optimizat
27                              Single-molecule kinetic analysis demonstrates that the IUTD enters from
28                            Observations from kinetic analysis in concert with in situ (19)F NMR monit
29                               Application to kinetic analysis of a wide variety of transformations (a
30     This report describes the first detailed kinetic analysis of the Banert cascade proceeding by bot
31                                              Kinetic analysis, in situ FTIR, and in situ XAS measurem
32 rived using an arterial input function-based kinetic analysis.
33  one species to another, as measured through kinetic analysis.
34                   At steady-state U release, kinetic and spectroscopic results suggest detachment of
35 This reveals multiple cellular mechanisms of kinetic and thermodynamic control that maintain the prop
36 he presence of the self-assembled capsule, a kinetic and thermodynamic modulation of the imine consti
37 ition defect is due to altered nsDNA binding kinetics and affinity for the bacterial chromosome.
38 rter enables whole-brain imaging with faster kinetics and brighter fluorescence than commonly used nu
39 led electron transfer result in sluggish OER kinetics and catalysts are required.
40 ined catalytic activity, albeit with altered kinetics and cooperativity.
41  each cell division modulates nuclear growth kinetics and dictates size scaling throughout early deve
42 e presence and absence of protons reveals ET kinetics and diffusion behavior similar to other small c
43 both sides of the lesion within 1 h; but the kinetics and distribution of modification around the DSB
44 ary alcohol follows clean pseudo-first-order kinetics and exhibits a sizable kinetic isotope effect.
45 nal cysteines (NCys) that proceeds with fast kinetics and exquisite selectivity, thereby enabling fac
46 gh seeded growth can accelerate the assembly kinetics and increase the optimal temperature by circa 4
47 aproline, features rapid amide isomerization kinetics and isoenergetic amide bond geometries influenc
48  viral interferon antagonists in shaping the kinetics and magnitude of the host response during virus
49 ence, with subcellular resolution, subsecond kinetics and nanomolar-to-submicromolar affinity.
50  is the first to measure mGlu(5) NAM binding kinetics and negative allosteric modulation of mGlu(5) r
51 c crowding nontrivially alters transcription kinetics and presents dynamic crowding within the bulk n
52 chromatin remodeling was found to define the kinetics and selectivity of gene activation in response
53 sequential infections and correlate antibody kinetics and sequence of infections with disease outcome
54 ipid compositions and quantified interaction kinetics and the affinity of HuNoV virus-like particles
55               PFA decay followed first-order kinetics and the inactivation of MNV was governed by the
56   Elevated pCO(2) was reported to affect the kinetics and thermodynamics of biochemical conversions b
57 aterial imparts significant influence on the kinetics and thermodynamics of electron transfer, and fr
58  residues reveals its contribution to enzyme kinetics and thermostability.
59 parallel platform that measures the cleavage kinetics and time-resolved cleavage products for over 10
60  applied to characterize substrate transport kinetics and to test 294 top-marketed drugs for OATP2B1
61 plet-triplet annihilation pathway, where the kinetics and yield depend sensitively on the energies of
62                  Results from thermodynamic, kinetic, and computational analyses suggested that this
63     Yet, studies that address their dynamic, kinetic, and mechanistic role in target reactions are sc
64 , electrochemical redox, reaction mechanism, kinetics, and degradation.
65 lize, and be explained by simple mass action kinetics, and more likely to contain proteins with intri
66 ations of alpha-dicarbonyls, their formation kinetics, and presence of stabilizing residues in close
67 he complex, the association and dissociation kinetics, and the microviscosity, which governs translat
68                           Here, we present a kinetic approach complemented by a hydrodynamic theory f
69                   Here, we used quantitative kinetic approaches to determine the transient kinetics o
70  same cell revealed that PPP2R5A degradation kinetics are comparable to those of APOBEC3G with a half
71 edure requires that lipid-detergent exchange kinetics are in the fast exchange regime in order to fol
72 s obfuscated by labels, however, as reaction kinetics are inevitably perturbed.
73 and persistent mark of nucleus rupture whose kinetics are partially dictated by membrane resealing.
74 ion occurs in uls1Delta cells with wild-type kinetics, arguing that global histone depletion rather t
75 eveloping new therapeutics requires reliable kinetic assays and an analysis framework to extract kine
76   Genetic complementation studies and enzyme kinetics assays indicate that B. fragilis UroS is functi
77 RFA) on Cu(II) reduction and Cu(I) oxidation kinetics at pH 8.2.
78 olution transformation because they have few kinetic barriers apart from ionic diffusion.
79                  However, we also found that kinetic barriers can be encountered in these systems and
80 calization of charge give rise to additional kinetic barriers in NCA and nonmetallic LTMOs in general
81 n by enabling simulation of protein shedding kinetics based on tumor tissue-specific characteristics.
82 the SMA-PSI complexes display a heterogenous kinetic behavior.
83 eronuclear single-quantum coherence spectra, kinetics, biochemical assays, and MS analyses, we show t
84 study, we show that Ag potency regulates the kinetics but not the magnitude of NFAT1 activation in si
85 ere we quantified Mediator-controlled Pol II kinetics by coupling rapid subunit degradation with orth
86 kinetic limitation manifests not only as the kinetic capacity loss during discharge but as a subtle b
87 e because of expeditious synthesis/secretion kinetics (CCL3/4/5) and low activation thresholds (CCL1/
88  of the N(2) molecule pose thermodynamic and kinetic challenges for promoting reactivity.
89                                The metabolic kinetic changes revealed the alteration of metabolism an
90 other bacterial systems, and yields bursting kinetics characteristic of eukaryotic systems.
91                   Considering its favourable kinetic characteristics, the sensor can be used for moni
92                                              Kinetic characterization revealed that the MpBgl3 was hi
93 ress numerous viral genes spanning all three kinetic classes, and suppress productive infection.
94                    Furthermore, we find that kinetic constants of maintenance methylation are correla
95            Together, structure snapshots and kinetic constants provide glimpses of intermediate confo
96 ty for 6b, and a keto-enol tautomerism under kinetic control has been proposed as the source of diast
97 alculations in packing column demonstrated a kinetic control with highly viscous FIL/ILs, revealing h
98                                     PL decay kinetics corroborated by DFT calculations reveal a compl
99                                              Kinetic crystal growth theory is used to show that cryst
100 halcogenouronium species and comparison with kinetic data demonstrate the significance of 1,5-O...Ch
101            The combination of structural and kinetic data illustrates how different conformations of
102   The Upstream module outputs were fitted to kinetic data on cGMP activity and early membrane potenti
103 irmed the catalytic effect and the estimated kinetic data point out that the bulky diol at 1 mol L(-1
104 of initial rate determination for processing kinetic data sets, no simple and automated program exist
105 d the system parameters of the model to cell kinetics data without treatment and then validated the m
106 ial [O(2) ], QO2 ) dependency that slows VO2 kinetics, decreasing CP and VO2max , increasing the O(2)
107               This effect is attributed to a kinetic delay in which characteristic times for equilibr
108           Prospective monitoring of mutation kinetics demonstrated that TKI-resistant low-level mutat
109 h a polarity that is high, relative to their kinetic diameter.
110 r graphene electrodes displayed only a small kinetic difference with respect to SLG, suggesting that
111 his problem in mouse retina by analysing the kinetic differences between rod flash responses and rece
112 ptoRaf and optoAKT differ in their signaling kinetics during regeneration, showing a gated versus gra
113 l reflection (TIR)-we elucidate the freezing kinetics during the solidification of a droplet while it
114 y based on Dynamic FBA (DFBA), called Linear Kinetics-Dynamic Flux Balance Analysis (LK-DFBA), to sat
115  the apparent first-cycle capacity loss is a kinetic effect linked to limited Li mobility at x > 0.88
116 lved photoelectron spectroscopy, whereby the kinetic energy and angle of photoelectrons emitted from
117 ion, as predicted by solutions to the master kinetic equation.
118 nts an improvement in efficiency for typical kinetic experimentation in batch as well.
119 In particular, via a synergy between NMR and kinetic experiments, we demonstrate the presence of a mi
120       This new method allowed calculation of kinetic features of these metabolites, thus enabling a d
121         Most reactions followed second-order kinetics, first order in amine and first order in electr
122  ), critical power (CP) and speed of the VO2 kinetics following exercise onset.
123                     Quantifying the exchange kinetics for analytes relative to the exchange kinetics
124  The real-time data sets revealed extraction kinetics for VOCs present in these samples.
125                       They have rapid twitch kinetics (full width at half-maximal stress: 11 +/- 1 ms
126 could also open undamaged DNA, suggesting a 'kinetic gating' mechanism whereby lesion discrimination
127 ts with ECG and EGC, but not in line with FQ kinetics, highlighted possible interferences of starch-f
128 VT and HVT-DeltavNr-13 showed similar growth kinetics; however, at early time points, HVT-DeltavNr-13
129        Connections between thermodynamic and kinetic hydricity are discussed, and opportunities for u
130                                              Kinetic hydricity represents the rate of hydride transfe
131 o promote the transgene expression level and kinetics in both adherent and suspension cells.
132  ratio correlated with different contraction kinetics in knockout versus wild-type; (2) Aberrant acti
133 is pilot study demonstrated DPSMA uptake and kinetics in localized renal masses.
134 ms to monitor bacterial concentration, decay kinetics in the presence of various antibiotics (ciprofl
135                                 Inactivation kinetics in TLF and on dry SS followed the Weibull model
136 pigallocatechin (EGC) exhibited slow binding kinetics (in the order of minutes), epicatechin gallate
137 urfactant formation as well as autocatalytic kinetics; indeed, no selection is observed when all reac
138  antibacterial potential and the degradation kinetics indicated first-order reactions.
139                                       Enzyme kinetics indicated that this RdRp efficiently incorporat
140 is, DeepFRET consequently outputs the common kinetic information metrics.
141 ll provide researchers with lots of valuable kinetic information regarding oxidizability as a functio
142 on the assigned kinetic model and to dissect kinetic interaction parameters from single-molecule FRET
143 this has shown that RdRp nucleotide addition kinetics is stochastically interrupted by rare pauses of
144                Observations of a significant kinetic isotope effect (k(H) /k(D) =5.7) for the reactio
145 -80 degrees C); thus, the hydrogen/deuterium kinetic isotope effect (KIE) = 6, consistent with H-atom
146  RMCF analysis predicts that the H/D primary kinetic isotope effect can serve as a probe for these me
147 nt work, quantum mechanical computations and kinetic isotope effect experiments demonstrate that the
148 l of mechanistic techniques, including (13)C kinetic isotope effect experiments, deuterated labeling
149                        A primary (13)C/(12)C kinetic isotope effect of 1.022(4) was measured at 23 de
150                                  Hammett and kinetic isotope effect studies, in combination with comp
151 -first-order kinetics and exhibits a sizable kinetic isotope effect.
152                       Derivation of apparent kinetic isotope effects (AKIEs) for the reaction with oz
153                   Large intramolecular (13)C kinetic isotope effects (KIEs) for the di-pai-methane re
154 titutions showed varied effects on transport kinetics (K(m) and V(max)) and substrate specificity.
155 tentiometry (OCP) to measure enzyme turnover kinetics, k(turn).
156                                          The kinetic limitation manifests not only as the kinetic cap
157     (7)Li NMR measurements indicate that the kinetic limitation reflects limited Li transport at x >
158 behavior of breast cancer cells via reaction kinetics may help unravel the mechanisms that underlie m
159                                    Real-time kinetic measurements from a single well were used to det
160                               Concordance of kinetic measures with tumor-to-blood ratios provides a c
161 units and other factors modify the intrinsic kinetic mechanism to result in new molecular and cellula
162 N-oxide (CNO) has been widely used, sluggish kinetics, metabolic liabilities and potential off-target
163 ons of each FRET level based on the assigned kinetic model and to dissect kinetic interaction paramet
164                      We developed a detailed kinetic model of the fatty acid synthase (FAS) of Escher
165 ed relatively noise-free input functions for kinetic modeling approaches.
166 uses erroneous parameter estimates in tracer kinetic modeling in brain PET studies.
167                                 Quantitative kinetic modeling shows that only a fraction of RNApII bi
168                                         Full kinetic modeling to quantify tau load was investigated.
169 h-speed atomic force microscopy (HS-AFM) and kinetic modeling which allowed us to determine that sept
170 ombining molecular dynamics simulations with kinetic modeling, we quantify cavitation rates on biolog
171 n, allowing further analysis by fitting with kinetic models.
172                                              Kinetic, molecular docking, and site-directed mutagenesi
173  from stochastic switching due to the random kinetic motion of discrete defects in the nanometer-size
174 the most widely employed tool to measure the kinetics of actin polymerization and the interaction bet
175 nal Ba(2+) than in Ca(2+); voltage-dependent kinetics of activation, inactivation, and deactivation;
176 flow (19)F NMR spectroscopic analysis of the kinetics of alkene difluorocyclopropanation and competin
177 imaging flow cytometry (iFCM) to explore the kinetics of allograft sEV release and the extent to whic
178                                          The kinetics of antibody-antigen association are enhanced wh
179 on on the chemically-controlled dissociation kinetics of antibody-antigen pairs by the use of water-m
180 studied the effect of glycans on the binding kinetics of antiviral drugs to the influenza neuraminida
181                                          The kinetics of bleb formation, its dependence on POM121, an
182 cking either phot2 or chup1 and analyzed the kinetics of both the onset and recovery of NPQ under equ
183 rapies, cancer stage specific prognosis, the kinetics of cancer recurrence, as well as the limited da
184 strategies for improving the specificity and kinetics of Cas9 as a genome engineering tool and may in
185 cell tracking could be used to determine the kinetics of cell trafficking and arrest during the earli
186 nimal models that recapitulate the long-term kinetics of clinical disease, which would provide insigh
187 eptide 1 (CSP1) failed to modulate the onset kinetics of competence development in vivo The competenc
188                         Small changes in the kinetics of dendritic excitatory currents amplify when r
189  in natural environments, thermodynamics and kinetics of divalent mercury Hg(II) chemical speciation
190 anslocating DNA can be exploited to tune the kinetics of DNA translocation.
191 nd the effect of the imposed DeltaPsi on the kinetics of efflux was also studied in right-side-out me
192  that GluA3 largely determines the ultrafast kinetics of endbulb synapses glutamatergic currents by p
193 d postnatal GBS acquisition, we assessed the kinetics of GBS GI colonization, progression to invasive
194  experimental observation and transformation kinetics of GBs in an elemental metal have remained elus
195                                          The kinetics of glucocorticoid-induced eosinopenia and bone
196 species-specific differences in the rate and kinetics of glucose consumption and glycolysis throughou
197 o the SAR1 GTP-binding pocket and alters the kinetics of GTP exchange.
198 nuclear pore complex blockade to monitor the kinetics of HIV-1 nuclear import and define the biochemi
199          Circular dichroism measurements and kinetics of inhibition indicated that the most active C-
200                              The aggregation kinetics of insulin were not significantly affected in t
201 plenishment of vitamin B-12 stores, from the kinetics of its plasma appearance in a 2-compartment mod
202 ch is attributed to genomic position and the kinetics of lineage commitment.
203                                   We use the kinetics of loop closure involving closely spaced (131-1
204          Thus, understanding the fundamental kinetics of MOF-based molecular catalysis of electrochem
205              In this study, the inactivation kinetics of murine norovirus (MNV) by PFA, in phosphate
206 dulate the potency, selectivity, and binding kinetics of Na(V) channel ligands.
207              Analysis of the specificity and kinetics of neutralizing antibodies (nAbs) elicited by S
208 g peanut protein, although variations in the kinetics of passage were observed between individuals an
209 on in diversifying both antigenicity and the kinetics of peptide display.
210         In this work we directly compare the kinetics of photoreduction of six different heme protein
211  effector functions, which should affect the kinetics of plasma-virus decline.
212  the nanoscale can significantly enhance the kinetics of radical-mediated oxidation reactions-polluta
213 radiation, the block can be released and the kinetics of re-equilibration to the native conformationa
214 e subtle control over the thermodynamics and kinetics of reactions.
215 inetic approaches to determine the transient kinetics of recognition and repair of alkylated DNA by A
216 form, DropMap, to measure simultaneously the kinetics of secretion and other cellular characteristics
217                             By measuring the kinetics of spread at early time points, we were able to
218 brium potential landscape topography and the kinetics of state switching.
219                     The binding affinity and kinetics of target engagement are fundamental to establi
220 we investigated the urease-bound aggregation kinetics of the Au and Ag NPs which has not been explore
221                                 However, the kinetics of the channelrhodopsin-2 (ChR2) used for cell-
222                                          The kinetics of the first emission phase was mainly correlat
223                          Our analyses of the kinetics of the forward and reverse reactions of photool
224  an effective way to improve selectivity and kinetics of the oxygen reduction reaction (ORR).
225 netics for analytes relative to the exchange kinetics of the standards results in greater accuracy an
226 ew new methods for future elucidation of the kinetics of their turnover in humans.
227 entions because of the specific transmission kinetics of this virus.
228                   We measure the association kinetics of unlabeled L-Tym by detecting its influence o
229 at a mineralized surface zone influences the kinetics of water evaporation and the surface temperatur
230                    Further, the differential kinetics on this dimerization mechanism underlie an intr
231 t, O(2) limitation may differentially impact kinetic or thermodynamic versus physicochemical C protec
232 NRA over denitrification is not explained by kinetics or thermodynamics.
233  secondary oxidative process was run and the kinetic parameters (rate constant, activation energy, an
234                   The thermal sensitivity of kinetic parameters allows us to predict responses of bot
235 ly investigate the temperature effect on the kinetic parameters and rate constants representing lipid
236            The fundamental thermodynamic and kinetic parameters obtained here will advance our fundam
237   Here, we review previously reported enzyme kinetic parameters of cellular and viral DNA and RNA pol
238 ic MOFs should also consider other important kinetic parameters such as the rate of proton-associated
239 ences, and (iii) the estimation of bias-free kinetic parameters.
240 sport in Li(4+) (x) Ti(5)O(12) is enabled by kinetic pathways comprising distorted Li polyhedra in me
241                                 However, the kinetic pathways, following which such development occur
242  assays and an analysis framework to extract kinetic pharmacological parameters.
243 (NMR) spectroscopy to determine the reaction kinetic profile.
244 hotransfer and phosphorelay networks, T-cell kinetic proofreading, and ERK signalling.
245 nhuman primates and humans, showed excellent kinetic properties as a PET radioligand.
246                           We analyze how the kinetic properties of the reversible binding interaction
247                        Analysis of biomarker kinetics (PSP, routine markers) was performed on 90 pati
248 M/Fe(3)O(4)-40 following pseudo-second-order kinetics (R(2) > 0.97) and equilibrium isotherm data fit
249 ution to Mg(2+) followed mostly a zero-order kinetic rate law for both Mg anode materials, and the ra
250  organic ligands are separated to reduce the kinetic reaction rates for better control over the cryst
251  The proposed biosensor and method of native kinetic registration can be used to develop new criteria
252  an additional stereogenic center, effective kinetic resolution can be achieved.
253 rk unveils a genome-scale map of methylation kinetics, revealing highly variable and context-specific
254 s of alphabeta T cell subsets and refine the kinetic selection model of CD4(+) and CD8(+) T cell line
255 ub-angstrom precision leading to the optimal kinetic separation of all three xylene isomers at room t
256                           The polymerization kinetics show a second order rate law, first order in bo
257 denosyl radical were used to investigate the kinetic significance of the hydrogen atom abstraction.
258                                              Kinetic simulations at physiologically-relevant substrat
259                We present the first 3D fully kinetic simulations of laser driven sheath-based ion acc
260 ether a temporal-intensity voxel clustering (kinetic spatial filtering, or KSF) improved lesion detec
261 erized, with thermodynamic reversibility and kinetic stability also demonstrated.
262   We analyzed the steady-state abundance and kinetic stability of LMO2 and its partners via Halo prot
263 he approach may be broadly applicable to the kinetic stabilization and characterization of other weak
264 oredoxin, glutathione, and ascorbate) are in kinetic steady state rather than thermodynamic equilibri
265 st intriguingly, depending on the initiation kinetics, stochastic elongation can either enhance or su
266                                              Kinetic studies also demonstrate the requirement for sus
267                                        Rapid kinetic studies and EPR measurements of rapid freeze-que
268                                              Kinetic studies at 22 degrees C and pH 7.1 showed that t
269                                              Kinetic studies carried out with TEMPO-H(D) reveal secon
270 OF was subject to steady-state and transient kinetic studies involving H/D and (13)C/(12)C exchange,
271                                  Comparative kinetic studies of a series of new ruthenium complexes p
272                              Two examples of kinetic studies of living cells under various doses of d
273                                              Kinetic studies of these transformations have also been
274                                              Kinetic studies on methyl fluorination suggest that the
275                                              Kinetic studies point to the second protonation event as
276                                          The kinetic studies showed that enzyme molecules with no net
277                               To this aim, a kinetic study of the primary and secondary oxidative pro
278 ing crystallographic, spectroscopic and fast kinetics techniques.
279 ary scalar field [Formula: see text] and its kinetic term [Formula: see text], to explore non-minimal
280 exagonal-basket type; larger and with faster kinetics than in other models.
281 can have a pronounced effect on the observed kinetics that can manifest in significant run-to-run var
282 etween fluid instability and crystallization kinetics that determines the achievable feature sizes.
283 ence between folding in NDs and SUVs was the kinetics; the rate of folding was two- to threefold slow
284 Motivated by such observations, we propose a kinetic theory that addresses the nonadiabatic evolution
285                               We report here kinetic, thermodynamic, hydrodynamic and computational s
286           Effective application of signaling kinetics to developing new therapeutics requires reliabl
287  platform for measuring arrestin recruitment kinetics to GPCRs using a high quantum yield, geneticall
288  we use a general model based on biochemical kinetics to quantify the combined effects of water conte
289 ar FX activation and antithrombin inhibition kinetics to the FVIIa.sTF complex.
290 hybrid containing DHTKD1 displaying improved kinetics towards 2-oxoadipic acid.
291     ICEKAT allows users to interactively fit kinetic traces using convenient browser-based selection
292 ysis of initial rates from continuous enzyme kinetic traces.
293 and/or under conditions of slow exchange, as kinetic traps and nonequilibrium product distributions a
294 e reactions evolve with profoundly different kinetics, undergoing autoinhibition (TBAT) or quasi-stoc
295 ignificant role in mediating the association kinetics, undergoing conformational rearrangement upon i
296              The extent to which interaction kinetics vary for the same RNA element across the transc
297 r surface photovoltages to be created, which kinetics vary with the composite architecture and last b
298   Although using hydrogen-deuterium exchange kinetics with MS (HDX-MS) to interrogate the high-order
299 ET-MS to the study of heterogeneous chemical kinetics with the reaction of gas phase O(3) and aqueous
300 ipate that future studies of viral infection kinetics with this reporter system will enable basic inv

 
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