ライフサイエンスコーパス: calorimetry

1 X-ray diffraction and differential scanning calorimetry.

2 t capacity measured by differential scanning calorimetry.

3 le 10 nm Kd measured by isothermal titration calorimetry.

4 e were monitored using pressure perturbation calorimetry.

5 myosin was observed by differential scanning calorimetry.

6 cal/cellular assays and isothermal titration calorimetry.

7 diture was measured with the use of indirect calorimetry.

8 stability measured by differential scanning calorimetry.

9 ions were determined by isothermal titration calorimetry.

10 tibody binding by using isothermal titration calorimetry.

11 anges were monitored by isothermal titration calorimetry.

12 exchange (HDX), molecular dynamics (MD), and calorimetry.

13 d from ellipsometry and isothermal titration calorimetry.

14 ray crystallography and isothermal titration calorimetry.

15 X-ray diffraction and differential scanning calorimetry.

16 e plasmon resonance and isothermal titration calorimetry.

17 analysis and modulated differential scanning calorimetry.

18 ray crystallography and isothermal titration calorimetry.

19 ter being determined by isothermal titration calorimetry.

20 easurement by room-temperature acid solution calorimetry.

21 co-crystallization and isothermal titration calorimetry.

22 shift perturbation and isothermal titration calorimetry.

23 s, GaAl12(7+) and GeAl12(8+), using solution calorimetry.

24 roism spectroscopy and differential scanning calorimetry.

25 muM) were determined by isothermal titration calorimetry.

26 ined by high-temperature oxide melt solution calorimetry.

27 ion crystallography and isothermal titration calorimetry.

28 obalamin in vitro using isothermal titration calorimetry.

29 he value measured using isothermal titration calorimetry.

30 on chromatography, and differential scanning calorimetry.

31 f 2 mum determined with isothermal titration calorimetry.

32 e mass spectrometry and isothermal titration calorimetry.

33 labeled palmitate and in mice using indirect calorimetry.

34 d thermal behaviour by differential scanning calorimetry.

35 pendent metabolism as determined by indirect calorimetry.

36 as further confirmed by isothermal titration calorimetry.

37 oth Hscen2 and Crcen by isothermal titration calorimetry.

38 est and cold stress was measured by indirect calorimetry.

39 obility shift assay and isothermal titration calorimetry.

40 xes by a combination of isothermal titration calorimetry, (1)H, NOESY, and ROESY NMR, and ion mobilit

41 mputer simulations, and isothermal titration calorimetry, a screening of ganglioside analogues togeth

42 of magnitude superior in sensitivity to a.c. calorimetry, allowing entropy measurements with only 10(

43 d for 36 hours in the laboratory by indirect calorimetry along with detailed cognitive and clinical a

44 However, isothermal titration calorimetry analyses of SiaP from two H. haemolyticus st

45 uld not be obtained by differential scanning calorimetry analyses.

46 e plasmon resonance and isothermal titration calorimetry analyses.

47 Differential scanning calorimetry analysis revealed that polymorph alpha irrev

48 Indirect calorimetry analysis showed that Cc1(-/-) mice develop h

49 Based on scanning calorimetry analysis, the melting of the gel phases form

50 characterization from differential scanning calorimetry and (1)H NMR and UV-vis-NIR spectroscopies i

51 tabilization of the B2 structure measured by calorimetry and accounts for the increased glass-forming

52 of dehydration effect has been observed from calorimetry and changes in chemical shifts from nuclear

53 MC values determined by isothermal titration calorimetry and confirm the conclusions with the aid of

54 teins are commonly measured using isothermal calorimetry and differential scanning calorimetry provid

55 lts, the present study aims (i) to show that calorimetry and EINS using the Bicout and Zaccai model e

56 However, isothermal titration calorimetry and enzyme kinetics experiments showed that

57 have been estimated primarily from indirect calorimetry and from nitrogen balance studies.

58 nteraction, as shown by isothermal titration calorimetry and gel filtration of recombinant subunits.

59 ffinities obtained from isothermal titration calorimetry and intrinsic fluorescence spectroscopy sugg

60 typic behavior in vivo Differential scanning calorimetry and limited trypsinolysis studies revealed a

61 sing this long-standing incongruity, we used calorimetry and magnetic resonance to probe interactions

62 linking experiments via isothermal titration calorimetry and mitochondrial import assays.

63 Using NMR spectroscopy, isothermal titration calorimetry and molecular dynamics simulations, we demon

64 have evaluated, through isothermal titration calorimetry and molecular-dynamics simulation, the effec

65 Isothermal titration calorimetry and NMR experiments indicate that key residu

66 Isothermal titration calorimetry and NMR indicate a 100 fold enhanced affini

67 Here, we employ isothermal titration calorimetry and NMR spectroscopy to characterize MeCP2 b

68 Here, using isothermal titration calorimetry and NMR spectroscopy, we report that acidic

69 ary structure profile, differential scanning calorimetry and oscillatory dynamic rheology were used t

70 We used solution calorimetry and periodic DFT calculations to analyze the

71 Using a combination of isothermal titration calorimetry and quantum and molecular dynamics calculati

72 f, was investigated by differential scanning calorimetry and related to nuclear magnetic resonance pr

73 an in-depth analysis by optical microscopy, calorimetry and small angle X-ray scattering studies.

74 Isothermal titration calorimetry and surface plasmon resonance measurements r

75 Using mutagenesis, NMR, isothermal calorimetry and surface plasmon resonance we demonstrate

76 results to those using isothermal titration calorimetry and surface plasmon resonance.

77 thermal analysis using differential scanning calorimetry and thermogravimetry.

78 nance spectroscopy, and isothermal titration calorimetry and to exhibit lethality in cells partially

79 her characterized using isothermal titration calorimetry and upconversion emission measurements.

80 d by pressure-gradient differential scanning calorimetry and variable pressure powder X-ray diffracti

81 is was confirmed using differential scanning calorimetry and X-ray diffraction methods.

82 e validated in vitro by isothermal titration calorimetry and yeast two- and three-hybrid assays.

83 ycerides), lipid oxidation (LOx; by indirect calorimetry), and ketogenesis (from circulating beta-hyd

84 electric spectroscopies, neutron scattering, calorimetry, and ab initio calculations.

85 y expenditure was measured by using indirect calorimetry, and an accelerometer was also used to deter

86 nance, electron microscopy, digital scanning calorimetry, and high resolution X-ray diffraction with

87 CL5 using solution NMR, isothermal titration calorimetry, and molecular dynamics simulations.

88 of UV-vis spectroscopy, isothermal titration calorimetry, and multidimensional NMR reveals that suita

89 luorescence anisotropy, isothermal titration calorimetry, and NMR titrations indicated that covalent

90 ) by molecular docking, isothermal titration calorimetry, and photoaffinity labeling.

91 orescence polarization, isothermal titration calorimetry, and quartz crystal microbalance) for interp

92 her with the results of isothermal titration calorimetry, and radio-ligand uptake and fluorescent tra

93 nolamine (POPE), using differential scanning calorimetry, and sequential (2)H and (31)P solid-state n

94 using CD spectroscopy, isothermal titration calorimetry, and small-angle X-ray scattering, we show t

95 ation of coarse-grained modeling, isothermal calorimetry, and structural analysis, that decreasing th

96 unds was studied using differential scanning calorimetry, and the energies of formation were calculat

97 In this study, using a calorimetry approach, we identified the first LD motif (

98 Isothermal titration calorimetry assays also revealed that recombinant CAR DB

99 ion during analysis by differential scanning calorimetry at heating and cooling rates of 10 and 1 deg

100 scitation, datasets comprising hemodynamics, calorimetry, blood gases, cytokines, and cardiac and ren

101 id metabolism was assessed by using indirect calorimetry, blood sampling, and microdialysis.

102 These data include RMR (indirect calorimetry), body composition (dual-energy X-ray absorp

103 semble averages involved in traditional bulk calorimetry cannot probe the transient effects that the

104 m days 7-10, animals were housed in indirect calorimetry chambers after which soleus muscle and liver

105 was monitored by using differential scanning calorimetry, circular dichroism, and Fourier transform i

106 Finally, differential scanning calorimetry combined with cross-polarized optical micros

107 ure in conjunction with isothermal titration calorimetry confirm the mode of binding and show that ma

108 Calorimetry confirms binding of six molecules with high

109 X-ray crystallography, isothermal titration calorimetry, confocal fluorescence microscopy, and in vi

110 y thermogravimetry and differential scanning calorimetry coupled with mass spectrometric analysis of

111 mogravimetry (TG/DTG), differential scanning calorimetry coupled with optical microscope (DSC-thermom

112 an affinity constant of ~3.10(4)M(-1); these calorimetry data corroborating Scatchard analysis of dis

113 t temperature-dependent isothermal titration calorimetry data for binding of 11 tryptophan ligands to

114 The method is validated using calorimetry data for chicken egg lysozyme, mutated Prote

115 Isothermal titration calorimetry data indicated a sequential binding mechanis

116 structure together with isothermal titration calorimetry data on several related viral and cellular p

117 nce energy transfer and isothermal titration calorimetry data on which the trans clamping model was o

118 Permutation arrays and isothermal titration calorimetry data showed that the preferred binding motif

119 omparing the results to isothermal titration calorimetry data.

120 ligoG CF-5/20, however, isothermal titration calorimetry demonstrated a weak calcium-mediated interac

121 Indirect calorimetry demonstrated increased oxygen consumption, r

122 ies were determined by differential scanning calorimetry, density, impact sensitivity, heat of format

123 t with biological data, isothermal titration calorimetry determined that the dimer conformation of th

124 e Syt7 C2 domains using isothermal titration calorimetry, did not reveal major differences that could

125 Differential scanning calorimetry (DSC) & novel FT-IR analysis based on peak s

126 Here, we showed that differential scanning calorimetry (DSC) analysis of blood serum proteins could

127 metric analysis (TGA), differential scanning calorimetry (DSC) and Fourier transform-infrared spectro

128 haracterized by use of differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA)

129 Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) e

130 ents with conventional differential scanning calorimetry (DSC) and thermogravimetric analyzer (TGA).

131 In addition, differential scanning calorimetry (DSC) and time domain nuclear magnetic reson

132 Differential scanning calorimetry (DSC) characterization showed that the capsu

133 re consistent with the differential scanning calorimetry (DSC) data for the peaks corresponding to di

134 ering were compared to Differential Scanning Calorimetry (DSC) measurements as the gold standard meth

135 Differential scanning calorimetry (DSC) reveals that the longer polyyne rotaxa

136 lization studies using differential scanning calorimetry (DSC) showed increased inhibitory effects on

137 Spectroscopy (FT-IR), Differential Scanning Calorimetry (DSC), and Scanning Electron Microscopy (SEM

138 NMR spectroscopy, and differential scanning calorimetry (DSC), and the structure was confirmed by X-

139 tibility measurements, differential scanning calorimetry (DSC), crystal structure determination, UV-v

140 rized by MALDI-TOF MS, differential scanning calorimetry (DSC), fluorescence-quenching, infrared and

141 diffraction (XRD) with differential scanning calorimetry (DSC).

142 tal analysis (EA), and differential scanning calorimetry (DSC).

143 of starch depicted by differential scanning calorimetry (DSC).

144 ils was assessed using differential scanning calorimetry (DSC).

145 rther characterized by Differential Scanning Calorimetry (DSC).

146 of the respiratory quotient (RQ) by indirect calorimetry during the fasted to fed transition (e.g. mi

147 electron-spectroscopy, differential scanning calorimetry, dynamic mechanical analysis, and AC impedan

148 Solid state NMR, isothermal titration calorimetry, electrophysiology, antiviral assays, and mo

149 uch as NMR, UV-vis, and isothermal titration calorimetry, enables the disentanglement of such multipl

150 cant reductions in the differential scanning calorimetry endothermic peak enthalpies and loss of bire

151 RNA binding assays and isothermal titration calorimetry experiments establish that double-SPSP phosp

152 Differential scanning calorimetry experiments revealed that the mutation cause

153 Isothermal titration calorimetry experiments revealed tight binding to McpX(P

154 Isothermal titration calorimetry experiments show that only LtnA1 binds to th

155 f 30 with COX-2 were supported by isothermal calorimetry experiments showing a Ka of 6.10 +/- 1.10 x

156 are consistent with the isothermal titration calorimetry experiments showing two sites with different

157 Isothermal titration calorimetry experiments support this model by showing th

158 We show through isothermal titration calorimetry experiments that dsRBD2 of TRBP binds dsRNA

159 olation, as revealed by isothermal titration calorimetry experiments.

160 dynamic simulations and isothermal titration calorimetry experiments.

161 ion in-shear and micro differential scanning calorimetry experiments.

162 , electrochemistry, and isothermal titration calorimetry experiments.

163 face plasmon resonance, isothermal titration calorimetry, fluorescence, and UV-visible spectroscopy)

164 parable sensitivity to differential scanning calorimetry for detecting HOS differences.

165 Differential scanning calorimetry for each ring showed that cyclization did no

166 Using calorimetry, functional assays, and complementary struct

167 An anomaly in differential scanning calorimetry has been reported in a number of metallic gl

168 So far it is the first time that chip calorimetry has been used to characterize and identify e

169 Isothermal titration calorimetry has been used to investigate both dye-dye an

170 Calorimetry has proven indispensable in this regard for

171 Isothermal titration calorimetry has the potential to directly quantify the t

172 re, in a series of neuroimaging and indirect calorimetry human studies, we examine the relative roles

173 stigation of binding by isothermal titration calorimetry illustrated significant differences in the a

174 ax) were determined with the use of indirect calorimetry in 305 healthy volunteers [150 men and 155 w

175 al.REE was measured with the use of indirect calorimetry in cancer patients before the initiation of

176 max during cycling (Body VO2 max , indirect calorimetry) in 10 endurance exercise-trained and 10 unt

177 Isothermal titration calorimetry indicated a stoichiometry of two oligosaccha

178 euglycemic clamp), lipid oxidation (indirect calorimetry), insulin secretion (2-h hyperglycemic clamp

179 nalysis, in particular differential scanning calorimetry, is commonly used to obtain structural infor

180 on analysis as well as differential scanning calorimetry, it is clear that the air-exposed reaction p

181 displacement assay and isothermal titration calorimetry, it was confirmed that fructose does indeed

182 Isothermal titration calorimetry (ITC) analyses demonstrated that the ligand-

183 m site of pre-snRNAs by isothermal titration calorimetry (ITC) and mutagenesis assays.

184 have been performed by isothermal titration calorimetry (ITC) and saturation transfer difference (ST

185 s were characterized by isothermal titration calorimetry (ITC) and shown to bind potently with K(D)s

186 lected and analyzed via isothermal titration calorimetry (ITC) and surface plasmon resonance (SPR), r

187 Isothermal titration calorimetry (ITC) directly measures heat evolved in a ch

188 Previously, isothermal titration calorimetry (ITC) experiments performed in different lab

189 te, consistent with the isothermal titration calorimetry (ITC) experiments.

190 Isothermal titration calorimetry (ITC) is a powerful and widely used method t

191 Isothermal titration calorimetry (ITC) is a powerful tool for acquiring both

192 lacement titrations and isothermal titration calorimetry (ITC) provided up to nanomolar binding affin

193 ht scattering (LLS) and isothermal titration calorimetry (ITC) studies revealed that the tailorable i

194 We have used NMR and isothermal titration calorimetry (ITC) to study the interactions of a broad-s

195 Isothermal titration calorimetry (ITC) using a histone H4 peptide showed that

196 given with emphasis on isothermal titration calorimetry (ITC), a method still underrepresented in su

197 tch sorption isotherms, isothermal titration calorimetry (ITC), and Cd K-edge EXAFS spectroscopy were

198 Using NMR, isothermal calorimetry (ITC), and small angle x-ray scattering (SAX

199 X-ray crystallography, isothermal titration calorimetry (ITC), and small-angle X-ray scattering (SAX

200 e, we report the use of isothermal titration calorimetry (ITC), electron microscopy and density funct

201 embrane binding through isothermal titration calorimetry (ITC), stopped-flow measurements, mutagenesi

202 shift assay (EMSA) and isothermal titration calorimetry (ITC), we found no significant difference in

203 cement assays (FID) and isothermal titration calorimetry (ITC), with binding preference to telomere R

204 complex solution using isothermal titration calorimetry (ITC).

205 y PXCE and Kd = 17 +/- 2 nM using isothermal calorimetry (ITC).

206 erties obtained through isothermal titration calorimetry (ITC).

207 e, size measurement and isothermal titration calorimetry (ITC).

208 ore S-S reduction using isothermal titration calorimetry (ITC).

209 eraction as measured by isothermal titration calorimetry (ITC).

210 getics are monitored by isothermal titration calorimetry (ITC).

211 molecular modelling and isothermal titration calorimetry (ITC).

212 and hGal-7 measured by isothermal titration calorimetry (ITC).

213 Using isothermal titration calorimetry, mass spectrometry, and differential scannin

214 Isothermal titration calorimetry measurements and mutagenesis analysis confir

215 anking the core 15-bp site, where isothermal calorimetry measurements reveal that affinity is augment

216 solution (19)F NMR and isothermal titration calorimetry measurements suggest interactions between hy

217 In differential scanning calorimetry measurements, only maples from Stradivari vi

218 face plasmon resonance, isothermal titration calorimetry, microscale thermophoresis and bio-layer int

219 In addition, we have used NMR spectroscopy, calorimetry, mutagenesis, and molecular docking to provi

220 lytical gel filtration, isothermal titration calorimetry, NMR spectroscopy, and small-angle X-ray sca

221 further investigated by isothermal titration calorimetry, NMR spectroscopy, and X-ray crystallography

222 ase solubility studies, Isothermal Titration Calorimetry, Nuclear Magnetic Resonance spectroscopy and

223 Isothermal titration calorimetry of a gallium(III) derivative of NP4 demonstr

224 ities were studied with isothermal titration calorimetry, of which seven compounds had binding affini

225 Using scanning calorimetry on a bacterial virus (phage lambda) as an ex

226 Isothermal titration calorimetry performed at cyanobacterial cytosol or meani

227 Analysis, Photovisual Differential Scanning Calorimetry, Polarized Light Thermomicroscopy, and Powde

228 lusion chromatography, differential scanning calorimetry, polarized optical microscopy, and atomic fo

229 pressure perturbation differential scanning calorimetry (PPC) that studies a system on the whole by

230 Calorimetry provided evidence for existence of beta-gluc

231 bit autoprocessing, and isothermal titration calorimetry provided the thermodynamics of the binding.

232 hermal calorimetry and differential scanning calorimetry providing a measurement that averages over s

233 re consistent with the differential scanning calorimetry results as well as the differential suscepti

234 Isothermal titration calorimetry results revealed that the gating brake and C

235 Indirect calorimetry revealed lipid oxidation as the primary ener

236 Differential scanning calorimetry revealed reduced thermal stability of collag

237 Isothermal titration calorimetry revealed that NTF2 prevents sumoylation by r

238 Furthermore, isothermal titration calorimetry revealed that the CBM48 domain of PTST2, whi

239 Isothermal titration calorimetry showed a direct interaction between calcium

240 th these observations, differential scanning calorimetry showed an approximately 10 degrees C decreas

241 Isothermal titration calorimetry showed strong and weak constant increments i

242 Indirect calorimetry showed that Cyp2e1-null-mice fed FF exhibite

243 sing x-ray diffraction/differential scanning calorimetry showed that mannitol predominantly retained

244 y, cyclic voltammetry, differential scanning calorimetry, single-crystal X-ray diffraction, transient

245 e examined FPV039 using isothermal titration calorimetry, small-angle X-ray scattering, and X-ray cry

246 We used bomb calorimetry, stepwise isothermal thermogravimetric analy

247 The differential scanning calorimetry studies demonstrated that the samples contai

248 strate binding, whereas isothermal titration calorimetry studies revealed binding affinities in the l

249 Calorimetry studies show that CT can crystallize more ea

250 tional and experimental isothermal titration calorimetry studies that unequivocally show Pdx favors b

251 In isothermal titration calorimetry studies, the dimer bound 2 eq of HIP-CoA wit

252 ts were complemented by isothermal titration calorimetry studies.

253 IPMDH2 K232M mutant and isothermal titration calorimetry supports a key role of Lys-232 in the reacti

254 ctural properties using isothermal titration calorimetry, surface plasmon resonance, nuclear magnetic

255 On the whole, the micro-calorimetry technique provides a sensitive method to ass

256 Moreover, using SPR and isothermal calorimetry techniques, we establish for the first time

257 hroism, thermodynamics, optical tweezers and calorimetry techniques.

258 how quantitatively, through the novel use of calorimetry, terahertz (THz) spectroscopy and neutron sc

259 s thermogravimetry and differential scanning calorimetry (TG-DSC), evolved gas analysis (TG-DSC-FTIR)

260 lowing our previous observation by titration calorimetry that the ETS member PU.1 dimerizes sequentia

261 According to differential scanning calorimetry, the beta-Zn8Sb7 phase melts incongruently a

262 In isothermal titration calorimetry, the binding stoichiometry of 2 and 1 for gl

263 -protein interactions, such as biosensing or calorimetry, the high size resolution of complexes at pi

264 bility was measured by differential scanning calorimetry, the oil was found to be up to 5 times more

265 ture was measured by using portable indirect calorimetry throughout each experimental condition, and

266 Here, we use isothermal titration calorimetry to demonstrate that UHMK1 phosphorylation of

267 Here, we use isothermal titration calorimetry to determine the Na(+)/H(+) selectivity of t

268 f CEACAM homodimers and isothermal titration calorimetry to determine the thermodynamic parameters an

269 Using differential scanning calorimetry to monitor genome loss upon heating, we find

270 We further used isothermal titration calorimetry to show that ligand binding in rhodopsin is

271 Here, we have used titration calorimetry to study interactions of cellooligosaccharid

272 rential scanning fluorimetry, and isothermal calorimetry, to characterize various biophysical propert

273 nance spectroscopy and differential scanning calorimetry, together with dye leakage assays.

274 Isothermal titration calorimetry using recombinant full-length Plasmodium eno

275 Indirect calorimetry was also used to determine metabolic paramet

276 Nano isothermal titration calorimetry was applied to determine thermodynamic param

277 Isothermal titration calorimetry was applied to study the binding of purified

278 +) affinity measured by isothermal titration calorimetry was only significantly affected by half of t

279 two hours after colonic infusions, indirect calorimetry was performed and blood samples were collect

280 id profiles and insulin resistance, indirect calorimetry was performed and visceral white adipose tis

281 test these hypotheses, differential scanning calorimetry was performed on giant unilamellar vesicles

282 aracterized by elemental analysis, immersion calorimetry, water vapor adsorption, and Boehm titration

283 dynamic signature using isothermal titration calorimetry we discovered a better correlation between s

284 Using calorimetry, we also determined gel phase formation by P

285 canning fluorimetry and isothermal titration calorimetry, we characterized the MERS-CoV macro domain

286 Using isothermal titration calorimetry, we determined the dissociation constants an

287 the assistance of (1)H NMR spectroscopy and calorimetry, we found that 1 could trap a single molecul

288 Using isothermal titration calorimetry, we found that Munc18c, like Munc18a, binds

289 By fluorescence and isothermal titration calorimetry, we found that this affinity enhancement is

290 e NMR spectroscopy and differential scanning calorimetry, we investigate the folding landscape of the

291 sis, kinase assays, and isothermal titration calorimetry, we show that each PKR protein is properly f

292 Using isothermal titration calorimetry, we show that mJHBP specifically binds JH II

293 Optical microscopy and differential scanning calorimetry were employed to construct a partial phase d

294 Protein crystallography and calorimetry were used to characterize the binding of 1,2

295 , thermogravimetry and differential scanning calorimetry were used to study changes in structure of g

296 ucose tolerance, insulin tolerance, indirect calorimetry) were assessed.

297 y were monitored using differential scanning calorimetry whereas changes in volume were monitored usi

298 oduct 15 (hISG15) was probed with isothermal calorimetry, which suggests that the C-terminal domain o

299 ncrease in energy expenditure using indirect calorimetry, which was accompanied by increased expressi

300 , micro- and modulated differential scanning calorimetry, wide angle X-ray diffraction and infrared s