ライフサイエンスコーパス: calorimetry

1 d NMCAM is shown using differential scanning calorimetry.

2 o-micelle transition by isothermal titration calorimetry.

3 )H NMR spectroscopy and isothermal titration calorimetry.

4 of nutrient intake, feces, and urine by bomb calorimetry.

5 cyclic voltammetry, and isothermal titration calorimetry.

6 ayer interferometry and isothermal titration calorimetry.

7 the respiratory quotient (RQ) using indirect calorimetry.

8 s were determined with differential scanning calorimetry.

9 omain spectroscopy and differential scanning calorimetry.

10 l sulfoxide (DMSO) and differential scanning calorimetry.

11 nM) was demonstrated by isothermal titration calorimetry.

12 3.0 muM, as measured by isothermal titration calorimetry.

13 imated by Rancimat and differential scanning calorimetry.

14 X-ray diffractions and differential scanning calorimetry.

15 were determined using differential scanning calorimetry.

16 ion crystallography and isothermal titration calorimetry.

17 d thermal behaviour by differential scanning calorimetry.

18 t capacity measured by differential scanning calorimetry.

19 obalamin in vitro using isothermal titration calorimetry.

20 he value measured using isothermal titration calorimetry.

21 on chromatography, and differential scanning calorimetry.

22 f 2 mum determined with isothermal titration calorimetry.

23 e mass spectrometry and isothermal titration calorimetry.

24 labeled palmitate and in mice using indirect calorimetry.

25 33 muM, as evaluated by isothermal titration calorimetry.

26 Substrate oxidation was measured by indirect calorimetry.

27 pendent metabolism as determined by indirect calorimetry.

28 as further confirmed by isothermal titration calorimetry.

29 oth Hscen2 and Crcen by isothermal titration calorimetry.

30 ath oxygen uptake was determined by indirect calorimetry.

31 X-ray diffraction and differential scanning calorimetry.

32 , and resting energy expenditure by indirect calorimetry.

33 atio and validated with isothermal titration calorimetry.

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

35 c force microscopy and differential scanning calorimetry along with UV-Vis absorption, steady-state f

36 ompare predictive equations against indirect calorimetry among critically ill patients at different p

37 ting energy expenditure measured by indirect calorimetry among the three phases.

38 Indirect calorimetry analyses revealed that the deletion of ALX d

39 Thermogravimetry and differential scanning calorimetry analyses reveals that the moisture content o

40 Isothermal titration calorimetry analyses suggested that saponins increased t

41 Isothermal titration calorimetry analysis confirmed high-affinity binding to

42 Differential scanning calorimetry analysis on the reversible isomeric transfor

43 measured by techniques including isothermal calorimetry analysis, fluorescence, and FRET quenching,

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

45 are investigated using differential scanning calorimetry and (2)H nuclear magnetic resonance spectros

46 re studied by means of differential scanning calorimetry and (31)P-NMR.

47 thologues, results from isothermal titration calorimetry and analytical ultracentrifugation experimen

48 man serum albumin using isothermal titration calorimetry and assess the structural integrity of the A

49 doubly-labeled water and whole-room indirect calorimetry and body composition as 3-compartment model

50 Using isothermal titration calorimetry and CBD-mimetic peptides, as well as CaM-aga

51 Isothermal titration calorimetry and CD experiments revealed that the interac

52 ly characterized using differential scanning calorimetry and circular dichroism.

53 Solution-phase isothermal titration calorimetry and density functional theory (DFT) calculat

54 nally, a combination of isothermal titration calorimetry and dynamic light scattering experiments sho

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

56 Using differential scanning calorimetry and Forster resonance energy transfer techni

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

58 Isothermal calorimetry and luminescence assay reveal that the desig

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

60 of RPRD1A and RPRD1B proteins in isothermal calorimetry and molecular modeling experiments.

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

62 Isothermal titration calorimetry and multiphoton microscopy showed that L9 an

63 For the latter, calorimetry and neutron data show that a disordered flui

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

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

66 es were measured using Differential Scanning Calorimetry and revealed that only dried pasta induced g

67 Differential Scanning Calorimetry and Scanning Electron Microscopy revealed th

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

69 affected its function, isothermal titration calorimetry and solid-state nuclear magnetic resonance s

70 Isothermal titration calorimetry and spectral data show that Cu(II) binds to

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

72 are available, such as differential scanning calorimetry and surface plasmon resonance, but these bio

73 nergy expenditure (REE) measured by indirect calorimetry and TEE by doubly labeled water.

74 The differential scanning calorimetry and the rapid visco analysis showed a signif

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

76 Differential scanning calorimetry and tryptophan fluorescence spectra indicate

77 Isothermal titration calorimetry and two-dimensional lineshape analysis of NM

78 rystallinity showed by differential scanning calorimetry and X-ray diffraction scattering, respective

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

80 iposome sedimentation, differential scanning calorimetry, and acyltransferase assays, we determined t

81 three orthogonal measurements - respiration, calorimetry, and biochemical assays - that Drosophila me

82 deuterium-exchange MS, isothermal titration calorimetry, and computational methods in conjunction wi

83 f dual-energy X-ray absorptiometry, indirect calorimetry, and ELISA.

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

85 chemistry, surface science, DFT, adsorption calorimetry, and in situ XRD and TEM to provide new insi

86 proline was measured by isothermal titration calorimetry, and involved more hydrogen bonding than hyd

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

88 y ((1)H and (31)P NMR), isothermal titration calorimetry, and optical spectroscopies (UV/vis absorpti

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

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

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

92 finity pulldown assays, isothermal titration calorimetry, and thermal denaturation CD spectroscopy, w

93 sing mass spectrometry, isothermal titration calorimetry, and x-ray crystallography that a purified G

94 Here, we report solution NMR-, isothermal calorimetry-, and X-ray crystallography-based analyses o

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

96 Magnetometry, neutron scattering, and calorimetry are used to explore the pressure dependence

97 Isothermal titration calorimetry assays also revealed that recombinant CAR DB

98 ty, flow cytometry, and isothermal titration calorimetry assays, we found that heparin-dependent modu

99 ting energy expenditure measured by indirect calorimetry at different phases.

100 es namely Rancimat and differential scanning calorimetry at selected temperatures in the range 50-110

101 re further supported by isothermal titration calorimetry binding assays as well as modeling studies.

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

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

104 ues have been employed, isothermal titration calorimetry, circular dichroism spectroscopy and intrins

105 Isothermal titration calorimetry, circular dichroism, and NMR studies of smal

106 g electron microscopy, differential scanning calorimetry, colour, textural and sensory evaluations of

107 ting energy expenditure measured by indirect calorimetry compared with predictive equations developed

108 Non-invasive and label-free calorimetry could become a disruptive technique to study

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

110 Isothermal calorimetry data analysis indicates that, unlike ubiquit

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

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

113 Isothermal titration calorimetry data indicated that the assembly is driven b

114 ssessment was based on differential scanning calorimetry data indicating that ADT exhibits endothermi

115 e plasmon resonance and isothermal titration calorimetry data, apparently at least two KN-93 molecule

116 omparing the results to isothermal titration calorimetry data.

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

118 rared spectroscopy and differential scanning calorimetry, demonstrating cross-linking of the polymer

119 measured by powerful and sensitive indirect calorimetry devices.

120 Isothermal titration calorimetry disclosed that the highest affinity peptides

121 Differential scanning calorimetry (DSC) analysis revealed glass-transition and

122 correlated with RS and differential scanning calorimetry (DSC) analysis showed consistency with this

123 re type II) muscles by Differential Scanning Calorimetry (DSC) and Fourier Transform InfraRed (FTIR)

124 ) phase transition via differential scanning calorimetry (DSC) and multiple (thermo) magnetization me

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

126 Differential scanning calorimetry (DSC) is increasingly used as evidence to su

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

128 Using the method of differential scanning calorimetry (DSC) the starch gelatinization temperature

129 rug interactions using differential scanning calorimetry (DSC), and Fourier transform infrared spectr

130 chromatography (SEC), differential scanning calorimetry (DSC), and hydrogen-deuterium exchange mass

131 ion mass spectrometry, differential scanning calorimetry (DSC), grazing-incidence wide-angle X-ray sc

132 sing light microscopy, differential scanning calorimetry (DSC), in vitro digestion, textural profile

133 were examined by using differential scanning calorimetry (DSC), polarised light microscopy and X-ray

134 d (FTIR) spectroscopy, differential scanning calorimetry (DSC), polarized optical microscopy, ion chr

135 ly and dynamically, by differential scanning calorimetry (DSC), water activity (a(w)) assessment and

136 nt and extractability, differential scanning calorimetry (DSC), X-ray diffraction (XRD), sensory prop

137 microscopy (SEM), and differential scanning calorimetry (DSC).

138 pectroscopy (FTIR) and Differential Scanning calorimetry (DSC).

139 been measured by using differential scanning calorimetry (DSC).

140 diffraction (XRD) and differential scanning calorimetry (DSC).

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

142 rther characterized by Differential Scanning Calorimetry (DSC).

143 ion (SHG) imaging with differential scanning calorimetry (DSC).

144 mAb) was measured with differential scanning calorimetry (DSC).

145 ric Analysis (TGA) and Differential Scanning Calorimetry (DSC).

146 icantly with more subtle changes in indirect calorimetry due to walking with different shoe inclinati

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

148 ircular dichroism, and differential scanning calorimetry, enable studies on protein unfolding and pro

149 Using a calibrated, transient calorimetry experiment we directly measure the temperatu

150 Isothermal titration calorimetry experiments further revealed that PSHCP also

151 Extensive isothermal titration calorimetry experiments reveal that the lectin was sensi

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

153 Finally, isothermal titration calorimetry experiments showed distinct entropic signatu

154 Thanks to isothermal titration calorimetry experiments, we show that this compound bind

155 , electrochemistry, and isothermal titration calorimetry experiments.

156 oss of binding shown by isothermal titration calorimetry, explaining the specificity of the riboswitc

157 significantly with large changes in indirect calorimetry from walking on different grades showing tha

158 Using calorimetry, functional assays, and complementary struct

159 PE polymer chains and differential scanning calorimetry gives the crystallinity.

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

161 Calorimetry has been widely used in metabolic studies, b

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

163 ody temperature, physical activity, indirect calorimetry, heart rate, and brain activity.

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

165 as potential predictors of mREE by indirect calorimetry (IC) in 122 SMAI children consecutively enro

166 ured by DXA and REE was assessed by indirect calorimetry in 201 healthy participants.

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

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

169 g a combination of room temperature solution calorimetry in dimethyl sulfoxide (DMSO) and differentia

170 ting energy expenditure measured by indirect calorimetry in late phase (1,878 +/- 517 kcal) was signi

171 nditure was measured by indirect respiration calorimetry in wild-type (WT) and heterozygous R163C (HE

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

173 er-transform infrared, differential scanning calorimetry, intrinsic fluorescence, and hydrogen-deuter

174 This example shows that fast scanning calorimetry is an important tool for establishing a comp

175 ty of AMPs to the bacterial cell envelope by calorimetry is difficult because of an overlapping of th

176 The power of fast scanning calorimetry is illustrated by considering two polymer:fu

177 ict resting energy expenditure when indirect calorimetry is not available.

178 The method, based on isothermal titration calorimetry, is the first universal, reporter-free, cont

179 86R GCAP1 detectable by isothermal titration calorimetry (ITC) also became less sensitive to Ca(2+),

180 ored successfully using isothermal titration calorimetry (ITC) analysis.

181 structures, competitive isothermal titration calorimetry (ITC) and NMR, hydrogen-deuterium exchange (

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

183 srB-type receptors, and isothermal titration calorimetry (ITC) assays showed that binding of AI-2 occ

184 Isothermal titration calorimetry (ITC) binding studies with a range of anions

185 mon resonance (SPR) and isothermal titration calorimetry (ITC) can provide quantitative binding therm

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

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

188 c methods as well as by isothermal titration calorimetry (ITC) in acetonitrile at 20 degrees C.

189 Isothermal titration calorimetry (ITC) is a powerful method to determine CMCs

190 Isothermal titration calorimetry (ITC) is conventionally used to acquire ther

191 ve been quantified with isothermal titration calorimetry (ITC) measurements and analysis, providing t

192 Isothermal titration calorimetry (ITC) measurements indicated negative cooper

193 From the isothermal titration calorimetry (ITC) results, we propose that the bacterial

194 f both human CAMKKs and isothermal titration calorimetry (ITC) revealed that binding to some of these

195 we describe the use of isothermal titration calorimetry (ITC) to establish proton involvement in pro

196 ed NMR spectroscopy and isothermal titration calorimetry (ITC) to investigate the cooperativity of Ca

197 Herein, we add isothermal titration calorimetry (ITC) to our arsenal of techniques for chara

198 on of NMR spectroscopy, isothermal titration calorimetry (ITC), and computational methods.

199 zed by crystallography, isothermal titration calorimetry (ITC), and molecular dynamics (MD) simulatio

200 breakdown of STC using isothermal titration calorimetry (ITC), dynamic light scattering and cryogeni

201 nce spectroscopy (NMR), Isothermal Titration Calorimetry (ITC), Microscale Thermophoresis (MST), and

202 uated in solution using isothermal titration calorimetry (ITC), native nano-electrospray ionization m

203 posomes were studied by isothermal titration calorimetry (ITC), tryptophan (Trp) fluorescence, and mi

204 ere characterized using isothermal titration calorimetry (ITC), turbidity, and zeta-potential measure

205 By crystallography and isothermal titration calorimetry (ITC), we studied a series of d-Phe/d-DiPhe-

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

207 ing temperatures, using isothermal titration calorimetry (ITC).

208 ifference (STD)-NMR and isothermal titration calorimetry (ITC).

209 ) and, as a comparison, isothermal titration calorimetry (ITC).

210 molecular modelling and isothermal titration calorimetry (ITC).

211 d TTR stabilizers using isothermal titration calorimetry (ITC).

212 Differential scanning calorimetry, limited proteolysis and small-angle X-ray s

213 example, we demonstrate on-chip single-cell calorimetry measurement with metabolic heat rates rangin

214 Differential scanning calorimetry measurements on flours indicated two peaks a

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

216 ce with dissipation and isothermal titration calorimetry measurements reveal the mechanism of these c

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

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

219 Using calorimetry measurements, we establish a robust thermody

220 d confirmed by in vitro isothermal titration calorimetry measurements-specific mutations ablated preQ

221 The calorimetry method, however, provides new insight into c

222 Room temperature calorimetry methods were developed to describe the energ

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

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

225 erforming high-resolution real-time infrared calorimetry on the convection system as it is first driv

226 UV circular dichroism, differential scanning calorimetry, or size exclusion chromatography.

227 Isothermal titration calorimetry performed at cyanobacterial cytosol or meani

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

229 Differential scanning calorimetry, polarizing optical microscopy and X-ray dif

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

231 isation were measured by a standardised 36 h calorimetry protocol; body composition was determined us

232 g cysteine labeling and isothermal titration calorimetry provide evidence for allosteric coupling of

233 Using calorimetry, Raman spectroscopy, and solubility experime

234 n RMR), armband accelerometers, and indirect calorimetry, respectively.

235 Differential scanning calorimetry results revealed enhanced thermal stability

236 Indirect calorimetry revealed lipid oxidation as the primary ener

237 Isothermal titration calorimetry revealed that Ca(2+)/CaM has higher affinity

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

239 Isothermal titration calorimetry, scanning electron microscopy, and Fourier t

240 tem (urea), stochastic differential scanning calorimetry (SDSC) was performed on trehalose dihydrate,

241 Isothermal titration calorimetry, sedimentation velocity, size-exclusion chro

242 ction time (OIT) using differential scanning calorimetry showed a good correlation with the accelerat

243 Intriguingly, isothermal calorimetry showed an approximate 1:1 MERS-CoV FP to Ca(

244 Differential scanning calorimetry showed endothermic (123 degrees C) and exoth

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

246 Isothermal titration calorimetry showed that these nucleobases had a modest b

247 llar DBS networks, and differential scanning calorimetry showed the DES nature of the liquid-like pha

248 ssays, native state MS, isothermal titration calorimetry, single-channel conductance measurements in

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

250 lysis, site-directed mutagenesis, isothermal calorimetry, small-angle X-ray scattering, and X-ray cry

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

252 The differential scanning calorimetry studies demonstrated that the samples contai

253 Additionally, isothermal titration calorimetry suggested that tannic acid modified the mole

254 fferential scanning and isothermal titration calorimetry, surface plasmon resonance spectroscopy, and

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

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

257 We confirmed by isothermal titration calorimetry that JMS-053 binds to human serum albumin.

258 Tv4AGT), and show using isothermal titration calorimetry that this protein binds HS.

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

260 Graphite calorimetry, the UK primary standard, has been employed

261 Docking and isothermal calorimetry titration confirmed interaction between lume

262 Isothermal calorimetry titrations indicate that this molecular reco

263 mon resonance, NMR, and isothermal titration calorimetry to characterize this presumed interaction.

264 y structure changes and isothermal titration calorimetry to investigate the impact of variants on ade

265 Recently, we established isothermal calorimetry to measure heat dissipation by living zebra-

266 id scrambling, we used differential scanning calorimetry to monitor the effect of gramicidin on the m

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

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

269 Differential scanning calorimetry together with the susceptibility to thermoly

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

271 ort study, 1-h REE (measured in a whole body calorimetry unit, WBCU) and body composition (BC, measur

272 Isothermal calorimetry was adopted for in situ quantification of th

273 Indirect calorimetry was also used to determine metabolic paramet

274 Isothermal titration calorimetry was also utilized to evaluate the binding ch

275 ting energy expenditure measured by indirect calorimetry was analyzed using intraclass correlation co

276 Nano isothermal titration calorimetry was applied to determine thermodynamic param

277 Indirect calorimetry was measured thrice during acute, late, and

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

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

280 ting energy expenditure measured by indirect calorimetry was used to assess accuracy.

281 m and fluorescence, and isothermal titration calorimetry was used to evaluate the interactions forces

282 ce at 9 mo postpartum (n = 43) by whole body calorimetry (WBC).

283 Using isothermal titration calorimetry, we also demonstrate direct binding of U4661

284 Using isothermal calorimetry, we characterized several metal-binding site

285 s, surface plasmon resonance, and isothermal calorimetry, we demonstrated the formation of a complex

286 Using isothermal titration calorimetry, we find that substitution of the FLVR argin

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

288 based assays along with isothermal titration calorimetry, we investigate KU-32, a derivative of the H

289 ng NMR spectroscopy and isothermal titration calorimetry, we map a region of the phosphoprotein, comp

290 namics simulations, and isothermal titration calorimetry, we show how the three structural elements a

291 Using isothermal titration calorimetry, we show that BK1.3 directly binds CCL8.

292 vitro kinase assays and isothermal titration calorimetry, we show that Lpg2603 is an active protein k

293 Fischer titration, and differential scanning calorimetry were also completed.

294 tion (4-compartment model) and RMR (indirect calorimetry) were measured after 4 wk of weight stabilit

295 pic titration studies, along with isothermal calorimetry, were used to show that binding of the singl

296 Here, fast scanning calorimetry, which allows measurement of device-relevant

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

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

299 ere, we demonstrate microfluidic single-cell calorimetry with 0.2-nW sensitivity, representing more t

300 using a combination of isothermal titration calorimetry, X-ray crystallography, NMR relaxation, and