1 Docked structures were consistent with
calorimetric analyses against bacterial beta-lactamases.
2 anistic studies by mutational and isothermal
calorimetric analyses allowed the design of RelA-mutants
3 Bioinformatic and
calorimetric analyses indicate that DnaA-box sequences i
4 However,
calorimetric analyses indicate very different thermodyna
5 onance spectroscopy and isothermal titration
calorimetric analyses of 10 of the inclusion complexes a
6 utant cycles (DMCs) coupled with kinetic and
calorimetric analyses of cognate Im9 and non-cognate Im2
7 Kinetic and
calorimetric analyses of site-specific replacement varia
8 Isothermal titration
calorimetric analyses of the purified YiiP and binding c
9 Isothermal titration
calorimetric analyses of the wild-type protein reveal th
10 and flap regions, and differential scanning
calorimetric analyses show that the mutation lowers the
11 Complementary, differential scanning
calorimetric analyses suggest that the two domains of VP
12 entation velocity method in combination with
calorimetric analyses, we studied initial binding events
13 Here we report a
calorimetric analysis for the binding of a broad panel o
14 Calorimetric analysis of ARF7PB1 site-directed mutants d
15 Calorimetric analysis of several active site variants co
16 Isothermal titration
calorimetric analysis of the binding of (G202A)G alpha(i
17 Isothermal titration
calorimetric analysis of the comparative binding of Dyn2
18 Calorimetric analysis of the effect of active site mutat
19 Our isothermal titration
calorimetric analysis of the interaction between the GAB
20 Calorimetric analysis revealed that the enthalpy, rather
21 Calorimetric analysis showed that although these CBMs de
22 Calorimetric analysis shows that binding can occur first
23 crease in body weight or insulin resistance;
calorimetric analysis suggested an accelerated metabolis
24 Here we show by crystallographic, NMR, and
calorimetric analysis that the phosphotyrosine binding (
25 To examine these features, we used
calorimetric analysis to probe a possible ligand binding
26 supported both by molecular dynamics and by
calorimetric analysis.
27 Calorimetric and biochemical titrations indicate that th
28 The aim of this study was to assess
calorimetric and dielectric properties in combination, a
29 the (AATT)2 sequence was investigated using
calorimetric and equilibrium constant measurements.
30 dely useful and complementary alternative to
calorimetric and fluorescence measurements.
31 st this hypothesis, we used a combination of
calorimetric and fluorescence techniques.
32 Calorimetric and fluorescence titrations yielded binding
33 ermosensor, employing diverse spectroscopic,
calorimetric and hydrodynamic measurements.
34 and caspase 9 activities were measured with
calorimetric and luminescent assays in retinal extracts
35 That allowed prediction of the
calorimetric and mechanical glass transition temperature
36 Isothermal titration
calorimetric and molecular modeling data conformed to th
37 standing the binding mechanism, we performed
calorimetric and NMR titrations of several hnRNP A1 subd
38 comparison of simulated crystallinities with
calorimetric and optical measurements strongly suggests
39 arious DNA recognition sequences using micro-
calorimetric and optical methods.
40 The
calorimetric and quartz crystal microbalance data indica
41 n defect-free P3HT, as elucidated by various
calorimetric and scattering experiments, allow the devel
42 Calorimetric and spectroscopic characterizations of defe
43 Site-directed mutagenesis coupled with
calorimetric and spectroscopic data has been used to cha
44 Calorimetric and spectroscopic investigations of these t
45 ic bisquinolinium ligands, were monitored by
calorimetric and spectroscopic methods and by gel electr
46 ixtures that are inaccessible by traditional
calorimetric and spectroscopic methods.
47 d non-native forms of TNF-alpha by employing
calorimetric and spectroscopic methods.
48 In this study, we use
calorimetric and spectroscopic observables to detect, re
49 In the present work, we apply
calorimetric and spectroscopic techniques to a series of
50 Here we report results from
calorimetric and stress relaxation experiments using a 2
51 For Ac-(Gly-4(R)Hyp-4(R)Hyp)(10)-NH(2), the
calorimetric and the van't Hoff transition enthalpy Delt
52 We have made these measurements using
calorimetric and ultraviolet hypochromicity methods, as
53 was investigated by 1H NMR spectroscopy and
calorimetric and voltammetric techniques.
54 l/mol) have been measured in acetonitrile by
calorimetric and/or equilibrium methods.
55 Complementary adsorption,
calorimetric,
and infrared studies of the probe adsorbat
56 lished through a combination of biochemical,
calorimetric,
and spectroscopic techniques.
57 In recognition of this need, a
calorimetric-
and NMR-based approach for obtaining the r
58 The mystery surrounding this
calorimetric anomaly is epitomized by four decades long
59 A
calorimetric approach was used to characterize PPARgamma
60 Furthermore, using a new
calorimetric assay to accurately determine the temperatu
61 Calorimetric assessment of binding thermodynamics for he
62 energy expenditure, as measured by indirect
calorimetric assessment.
63 Calorimetric binding analysis indicated that Asp49 and A
64 Calorimetric binding analysis of residues in the c-di-GM
65 the basis of a thermostability shift assay,
calorimetric binding data, and biochemical assays which
66 -Fc complex and conduct isothermal titration
calorimetric binding studies.
67 In this report, a paper-based micro-
calorimetric biochemical detection method is presented.
68 this work, we introduce a wearable hot-film/
calorimetric breath sensing system composed of a hot-fil
69 Indirect
calorimetric canopy tests showed significant reductions
70 g structural data with observed spectral and
calorimetric changes, we now show that NusA binding dest
71 binding competent protein concentration, for
calorimetric characterization of homotropic cooperative
72 Calorimetric characterization of the association energet
73 Correlation of the
calorimetric,
circular dichroism, fluorescence, turbidit
74 The
calorimetric competition assay introduced here overcomes
75 phobic high-affinity ligands employing a new
calorimetric competition experiment is described.
76 Results from
calorimetric,
crystallographic, and theoretical analyses
77 t dielectric data and heating-rate-dependent
calorimetric data allow us to construct the relaxation m
78 Calorimetric data also shows that the membrane-proximal
79 Our fluorescence, absorbance, and
calorimetric data are consistent with loop migration/tra
80 The
calorimetric data confirm the presence of at least two e
81 Calorimetric data confirmed that YkoF binds two thiamin
82 Calorimetric data indicate that M-CSF cannot dimerize FM
83 g site in each monomer, crystallographic and
calorimetric data indicate that VcFadR has two.
84 By applying a statistical model to
calorimetric data obtained on solvent mixtures, we show
85 Previously published
calorimetric data of a closely related bacteriophage, P2
86 Crystallographic and
calorimetric data of wild-type and mutant SiaP showed th
87 Using
calorimetric data on surface energies for cobalt, iron,
88 n hydrophobic effect, in accord with earlier
calorimetric data on the membrane partition of other amp
89 s, which uses simulated annealing of complex
calorimetric data representing multiple coupled equilibr
90 Subtraction of buffer contributions to the
calorimetric data reveals that all three peptides have a
91 epresented by the Langmuir model; therefore,
calorimetric data should be used to extract thermodynami
92 Calorimetric data show that binding of pTppAp to RNase A
93 The (45)Ca binding and isothermal titration
calorimetric data show that myristoylation increases the
94 Calorimetric data show that this is due to proton-based
95 SbCOMT steady-state kinetic and
calorimetric data suggest a random bi-bi mechanism.
96 er a range of ionic strengths, combined with
calorimetric data, allowed separation of the electrostat
97 cture of this trapped complex, together with
calorimetric data, identifies sites of protein-protein i
98 For lipids lacking
calorimetric data, measurement of the critical micelle c
99 lent agreement with previous mutagenesis and
calorimetric data, providing the basis for further inves
100 Considering the
calorimetric data, substrate binding of SbHCT should occ
101 dues, coupled with available mutagenesis and
calorimetric data, suggest that subtle structural pertur
102 To aid interpretation of the
calorimetric data, the first crystal structure of a smal
103 ptide binding was recently proposed based on
calorimetric data.
104 The results are benchmarked against solution
calorimetric data.
105 Here, a
calorimetric demonstration that this striking variation
106 We introduce the
calorimetric descriptor "metabolic capacity" and show th
107 monstrate the feasibility of integrating the
calorimetric detection method with paper based microflui
108 Calorimetric detection of biochemical reactions is demon
109 lpy arrays enable label-free, solution-based
calorimetric detection of molecular interactions in a 96
110 The
calorimetric detection results of DNA concentrations fro
111 We present here a
calorimetric determination of the field-temperature phas
112 acuum gap between the planar surfaces of the
calorimetric device and a reverse-biased photodiode is r
113 ens of nanometres-solid-state cooling of the
calorimetric device can be accomplished via a combinatio
114 Microfabricated
calorimetric devices are promising, although they have y
115 ling small samples and attaching them to the
calorimetric devices have been developed.
116 correlation of inhibitor chemistry with the
calorimetric dissection of thermodynamics.
117 Differential scanning
calorimetric (
DSC) analysis of the ADC indicated that th
118 (PI-5P)) mixed vesicles were investigated by
calorimetric (
DSC) Fourier transform infrared spectrosco
119 Spectroscopic experiments agreed well with
calorimetric (
DSC).
120 mprehensive global thermodynamic analysis of
calorimetric (
DSC, ITC) and spectroscopic (CD) data obta
121 eaks corresponding to dissociation of water (
calorimetric effect of 536Jg(-1) for beta-cyclodextrin a
122 accurate estimation of 30h gigahertz for the
calorimetric energy resolution.
123 ing with increased unfolding temperature and
calorimetric enthalpy as compared to pH 7.4.
124 A 50% decrease in
calorimetric enthalpy is observed, which may result from
125 folding was estimated from the dependence of
calorimetric enthalpy on T(m).
126 erence is that for gp120-B the van't Hoff to
calorimetric enthalpy ratio (DeltaH(vH)/DeltaH) is 0.95
127 mperature was lowered by 6 degrees C and the
calorimetric enthalpy reduced by 50% following removal o
128 iction, a significant decrease in stability,
calorimetric enthalpy, and folding time was observed for
129 roximately 2 degrees C) and no change in the
calorimetric enthalpy.
130 The
calorimetric entropy of the olivine-spinel transition in
131 These structures, complemented by
calorimetric equilibrium binding studies of MtDnaA DBD i
132 Here, we present direct
calorimetric evidence that no such enthalpic effects exi
133 , which is confirmed by isothermal titration
calorimetric experiment carried out in solution.
134 Global regression analysis of
calorimetric experiments at various concentrations and t
135 Temperature-dependent
calorimetric experiments give a DeltaC(p) for ligand bin
136 Biosensor and
calorimetric experiments indicate that the binding affin
137 on agree with results obtained from separate
calorimetric experiments on the Ca(2+)-ATPase derived fr
138 The results of isothermal-titration-
calorimetric experiments show that both lipophilic bisph
139 We performed spectroscopic and
calorimetric experiments to explore the folding kinetics
140 denaturation data from differential scanning
calorimetric experiments, and temperature and denaturant
141 The structure, combined with
calorimetric experiments, suggests distinct roles of thr
142 rotein was subjected to isothermal titration
calorimetric experiments.
143 t upon binding, determined from the scanning
calorimetric experiments.
144 tive volume, and chemical calibration of the
calorimetric factor used to convert the measured electri
145 ation calorimeters require validation of the
calorimetric factor with chemical reactions with accurat
146 stent with the previous isothermal titration
calorimetric finding that their interactions are entropy
147 approach to the fabrication of micromachined
calorimetric gas sensors for combustible gases.
148 A combined
calorimetric gas- and spore-based biosensor array is pre
149 The occurrence of water's
calorimetric glass transition of low-density amorphous i
150 ous ice at ambient pressure shows a distinct
calorimetric glass transitions at 116 K and present evid
151 The
calorimetric glucose detection demonstrates a measuremen
152 M NaCl causes low-temperature shifts in the
calorimetric HDL transitions of up to -14 degrees C.
153 ts by approximately -18 degrees C in the two
calorimetric HDL transitions without altering their natu
154 by magnetic nanoparticles is estimated from
calorimetric heating measurements.
155 he results demonstrated high accuracy of the
calorimetric immunoassay when compared with gold standar
156 In this study, we employ
calorimetric [
isothermal titration calorimetry (ITC) and
157 Calorimetric (
ITC) data also show that the overall entha
158 on resonance (SPR), and isothermal titration
calorimetric (
ITC) experiments with DB613, which has a c
159 also evaluated based on isothermal titration
calorimetric (
ITC) studies.
160 Also studied by
calorimetric,
kinetic, and in one case variable-temperat
161 fications in the DSC profiles might serve as
calorimetric markers when no monoclonal proteins can be
162 ers (T(m), DeltaH) as determined from direct
calorimetric means should be identical to those determin
163 Using direct
calorimetric measurement of heats of formation, MAPbI3 i
164 Isothermal titration
calorimetric measurements also showed an enthalpic contr
165 t reaction enthalpies in good agreement with
calorimetric measurements and isotherms.
166 tion are obtained from differential scanning
calorimetric measurements and thermal gravimetric analys
167 Systematic
calorimetric measurements are shown to provide a framewo
168 ined in spectroscopic, crystallographic, and
calorimetric measurements during early stages of insulin
169 ted Z-scores agree with estimates made using
calorimetric measurements for a few RNA molecules.
170 Instead,
calorimetric measurements have shown that the amorphous
171 Solution
calorimetric measurements in hexane show that the enthal
172 Calorimetric measurements indicate that RNase Sa has a h
173 Results of the
calorimetric measurements indicate that strong effector
174 asurements on crystals of d-ribose and other
calorimetric measurements make it possible to calculate
175 Direct
calorimetric measurements of a solid state passive switc
176 Calorimetric measurements of ATP binding to wild-type an
177 Calorimetric measurements of Ca and Li adsorption energi
178 Direct
calorimetric measurements of cognate telomeric ssDNA bin
179 Direct
calorimetric measurements of folding of a model host pep
180 ium oxide surfaces, determined from previous
calorimetric measurements of metal adsorption energies,
181 is absent in liposomes and not detectable in
calorimetric measurements on liposome suspensions.
182 Differential scanning
calorimetric measurements on POPE/POPC liposomes with in
183 Here we report magnetic and
calorimetric measurements on YbRh2Si2, down to temperatu
184 Calorimetric measurements quantitatively confirm the ent
185 The
calorimetric measurements reveal that the bcc superlatti
186 duces the affinity for desmosomal cadherins,
calorimetric measurements show no significant effects of
187 Calorimetric measurements show that the change in enthal
188 Direct HCl solution
calorimetric measurements show the compounds with n > 7
189 Differential scanning
calorimetric measurements showed that s3 gains thermal s
190 Isothermal titration
calorimetric measurements suggest these complexes to be
191 has a ligand titration profile in isothermal
calorimetric measurements that clearly shows that one nu
192 emonstrate through mobility shift assays and
calorimetric measurements that the SU(VAR)3-9 HOMOLOG 5
193 etic isotope effect measurements, isothermal
calorimetric measurements, and (31)P NMR spectroscopic t
194 In the present work, vibration spectroscopy,
calorimetric measurements, and density functional theory
195 istochemistry of intestinal mucosa, indirect
calorimetric measurements, whole-body composition, and e
196 for ferric ion binding were determined from
calorimetric measurements.
197 ort it by molecular dynamics simulations and
calorimetric measurements.
198 have developed a nanoparticle-based scanning
calorimetric method for the highly sensitive detections
199 This
calorimetric methodology provides a much more accurate a
200 Calorimetric methods are often used to determine enthalp
201 Considering that
calorimetric methods cannot distinguish between energeti
202 Calorimetric methods have been used to determine equilib
203 ed forms of Fet3p by using spectroscopic and
calorimetric methods in vitro (pH 7).
204 We show using isothermal
calorimetric methods that NbSyn2 binds specifically to m
205 folding data obtained from spectroscopic and
calorimetric methods were combined into a unifying therm
206 ilar to values obtained by spectroscopic and
calorimetric methods with the additional confidence offe
207 iques, such as scattering, spectroscopic and
calorimetric methods, are not well adapted for their stu
208 red in acetonitrile by either equilibrium or
calorimetric methods.
209 ) with custom-fabricated picowatt-resolution
calorimetric microdevices, we created an experimental pl
210 use site-specific mutagenesis, coupled with
calorimetric,
NMR, and enzymological techniques, to defi
211 n a previously unidentified high-temperature
calorimetric peak.
212 The two
calorimetric peaks of the individual leaflets merged int
213 robust, highly sensitive and bio-compatible
calorimetric platform that features a resolution of ~270
214 are able to describe experimentally observed
calorimetric profiles and predict the anesthetic feature
215 on temperature of the main transition in the
calorimetric profiles and the shape similarity criterion
216 t common molecular markers contribute to the
calorimetric profiles of the different, secretory and no
217 ed that 4-MB exhibits a dual ratiometric and
calorimetric response toward peroxynitrite due to ONOO(-
218 In general for POMs, the combination of
calorimetric results and synthetic observations suggest
219 The
calorimetric results argue that, from a thermodynamics p
220 Based on the
calorimetric results for 12 peptides, it was found that
221 e plasmon resonance and isothermal titration
calorimetric results indicate that the compound binds wi
222 Below 30 degrees C the
calorimetric results show that apoA-I interaction with P
223 The computational and
calorimetric results were in excellent agreement.
224 bon binding to P450 2A6, as evidenced by the
calorimetric results.
225 ovel, custom-fabricated, picowatt-resolution
calorimetric scanning probes, we measured the thermal co
226 Using a combination of
calorimetric,
scattering, electron microscopic, and in s
227 s utilize electrochemical, optical, mass and
calorimetric sensing mechanisms to specifically identify
228 ed of a hot-film senor in the center and two
calorimetric sensors on two sides.
229 oach integrates microfabricated differential
calorimetric sensors with microfluidic titration.
230 ly by Mossbauer spectroscopy, is seen in the
calorimetric signal.
231 this connection, DeltaC(p) provides a useful
calorimetric signature for assessing the relative impact
232 d controversially for many years because its
calorimetric signature is very feeble.
233 The
calorimetric signature of the second glass transition is
234 We also report agglutination and
calorimetric solution-phase binding studies of mono- and
235 e and sensitive nanomechanical infrared (IR)
calorimetric spectrometer for use in the direct detectio
236 uption of spherical HDL in 0-15% PEG-8000 by
calorimetric,
spectroscopic, electron microscopic, and l
237 eous modeling of orthogonal observables from
calorimetric,
spectroscopic, hydrodynamic, biosensing, o
238 Calorimetric studies (ITC) show that the stronger bindin
239 the Rab11 GTPase using isothermal titration
calorimetric studies and mutational analysis.
240 Calorimetric studies demonstrate that this mutation faci
241 Calorimetric studies demonstrated these PDCs to be therm
242 ost promising stereoisomer (S)-16, X-ray and
calorimetric studies in PPARgamma revealed, at high liga
243 Calorimetric studies in which binding of 2',5'-ADP to CP
244 In fact,
calorimetric studies indicate that CD38-deficient animal
245 Calorimetric studies indicate that the increased stabili
246 +) should be purely enthalpic in accord with
calorimetric studies of a high-affinity consensus peptid
247 Isothermal titration
calorimetric studies of Co(2+) and Zn(2+) binding to EaC
248 Recent
calorimetric studies of interactions between small molec
249 Computational and
calorimetric studies of the anhydrous calcium phases, [C
250 Calorimetric studies of the binding of IscU mutants to t
251 Here we report isothermal titration
calorimetric studies of the effects of selectivity-modif
252 simulations of three cavitands, coupled with
calorimetric studies of their complexes with short-chain
253 Both structural and
calorimetric studies point to a structural role for the
254 Calorimetric studies reveal that NC destabilization is e
255 Calorimetric studies revealed that binding of f-ImPyIm,
256 es) = -52 +/- 5 cal mol(-1) K(-1).) Solution
calorimetric studies show that the enthalpy of formation
257 We further use structural and
calorimetric studies to demonstrate that the end product
258 ger-finger interactions are observed also in
calorimetric studies, in which the 160(+/-20)nM (zf1) an
259 Calorimetric studies, including a novel ITC compound dis
260 ompared through biochemical, structural, and
calorimetric studies, showing a complex interplay betwee
261 stallography, site-directed mutagenesis, and
calorimetric studies, we have characterized the interact
262 entropies relative to free energies in some
calorimetric studies.
263 as demonstrated by thermal-shift, AS-MS, and
calorimetric studies.
264 hermal denaturation and isothermal titration
calorimetric studies.
265 from the results of the isothermal titration
calorimetric studies.
266 ugh multiple cyclic mixed-gas adsorption and
calorimetric studies.
267 An isothermal titration
calorimetric study of the binding of substrates and inhi
268 Traditionally, a variety of
calorimetric techniques and in situ XRD at elevated temp
269 Calorimetric techniques have demonstrated that although
270 y, we use a combination of spectroscopic and
calorimetric techniques to detect and characterize kinet
271 DtxR(M10A,C102D) using crystallographic and
calorimetric techniques to gain insight into the possibl
272 We used a combination of spectroscopic and
calorimetric techniques to investigate the folding/unfol
273 We used a combination of optical and
calorimetric techniques to investigate the incorporation
274 This study applies NMR and
calorimetric techniques to map the binding site for Rem2
275 , we used a combination of spectroscopic and
calorimetric techniques to present a complete thermodyna
276 resting KatG was examined using optical and
calorimetric techniques to provide thermodynamic paramet
277 ining ionic liquids, measured directly using
calorimetric techniques, is presented in this paper.
278 othermal titration and differential scanning
calorimetric techniques.
279 (Tg-10 degrees C), previously determined by
calorimetric tests.
280 New endothermic peaks in the
calorimetric thermograms of treated milk revealed the fo
281 ule to bind cationic species was assessed by
calorimetric titration experiments and hyperpolarized (1
282 d by combination of isotherms from different
calorimetric titration experiments into a global analysi
283 Isothermal
calorimetric titration of LIGHT with either LTbetaR or L
284 Calorimetric titration shows that the RNA sequence 5'AGC
285 ty binding site of DtxR(E175K) obtained from
calorimetric titration with Ni(II) is K(a)=7.6+/-0.5x10(
286 he TSIL with U was carried out by isothermal
calorimetric titration, liquid-liquid extraction, (31)P
287 Calorimetric titrations in different buffers and pH cond
288 NMR and isothermal
calorimetric titrations of N-betaGRP with laminarihexaos
289 affinities for metal ion extracted from the
calorimetric titrations of the mutants DtxR(D6A,C102D) a
290 Calorimetric titrations of the syn isomer with bromide c
291 Calorimetric titrations result in one-to-one binding als
292 We have conducted isothermal
calorimetric titrations to investigate the halogen-bond
293 Calorimetric titrations using monomeric enzyme yielded a
294 showed no detectable change in Fe2+ and Hg2+
calorimetric titrations, indicating that Asp-157 is not
295 Here we report a combination of isothermal
calorimetric titrations, NMR spectroscopy, and extensive
296 ges observed in the SANS measurements, and a
calorimetric transition enthalpy of 60 +/- 3 kJ mol(-1)
297 The first
calorimetric transition reflects HDL fusion and dissocia
298 ils is located at temperatures far below the
calorimetric transition.
299 copy are marginally higher than those of the
calorimetric values.
300 , with good agreement between van't Hoff and
calorimetric values.