ライフサイエンスコーパス: be probed by

1 for calix[5]arene derivatives 1a.H and 1b.H was probed by (1)H NMR spectroscopy and single-crystal X

2 ssociation behavior of 1 in various solvents was probed by (1)H NMR.

3 Kinetics and electronic effects were probed by (1)H NMR spectroscopy in CDCl(3).

4 new reaction is described, and the mechanism is probed by (11)B NMR experiments.

5 charge delocalization in these carbocations was probed by (13)C NMR chemical shifts and substantiate

6 NDOR, while the axial Fe-CN and Fe-S bonding is probed by 13C ENDOR of the cyanide ligand and 1Hbeta

7 pulse, and the subsequent structural changes are probed by 150 ps or 1 micros X-ray pulses at 14 lase

8 r interactions with crown ether compounds to be probed by (19)F NMR spectroscopy.

9 es in membrane-associated macromolecules can be probed by (19)F NMR.

10 /II-helix-2, peripheral interactions in NmHO are probed by 2D (1)H NMR to reveal unique structural fe

11 structure of the [Cu4I4P4] cluster cores has been probed by (31)P and (65)Cu solid-state NMR analysis

12 apidly increasing or decreasing the [Ca(2+)] were probed by 5-iodoacetamidofluorescein covalently bou

13 s within the arrowhead and hexad motifs have been probed by a combination of Brownian dynamics and un

14 hough the mechanisms of these reactions have been probed by a number of techniques such as NMR, fluor

15 F)-sensitized TiO(2) nanoparticles (NPs) has been probed by a single-molecule photon-stamping techniq

16 nd released into the optical cavity where it is probed by a near-infrared diode laser operating at ap

17 s are manufactured such that each transcript is probed by a set of sequences with a wide affinity ran

18 nduced unfolding of proteins in cell lysates is probed by a short pulse of proteolysis, and the effec

19 ue character of the N2 entity in Li2Ca3[N2]3 is probed by a variety of complementary techniques, incl

20 The interaction of CRP with specific DNA was probed by a protein footprinting technique using che

21 Topology was probed by accessibility of introduced cysteines to a

22 This can be probed by adding a renewal phase to standard conditio

23 ons of GrpE side-chains to GrpE-DnaK binding were probed by alanine-scanning mutagenesis.

24 These grand cycle variations are probed by alpha - Omega dynamo model with meridional

25 ynamics of PKA holoenzymes Ialpha and IIbeta were probed by amide hydrogen-deuterium exchange coupled

26 The degree of active site perturbation was probed by amino acid nucleophiles, supporting the vi

27 Sensitivity to water activity can also be probed by an in vivo selection using the antibacteria

28 The nature of the NH(3)-BH(3) interaction is probed by an energy decomposition scheme based on the

29 Two Bacillus subtilis lysogenic libraries were probed by an antibody specific for a previously des

30 cond-to-millisecond dynamics of the leadzyme are probed by analysis of the power dependence of (13)C

31 Potential transition movement was probed by analysis of the denaturant, ionic strength

32 binding site in a variety of DNA polymerases was probed by analyzing incorporation of dideoxy and acy

33 O-Ti bonding at the TiO2/Si interface, which was probed by angle-resolved X-ray photoelectron spectro

34 tness of the method as a structure predictor is probed by applying it to a set of proteins of unknown

35 The function of myosin II was probed by applying inhibitors either globally or loc

36 es of the oculomotor corollary discharge can be probed by asking subjects to localize stimuli that ar

37 eins during adaptation to temperature stress were probed by auxotrophic complementation of yeast with

38 d charge separation and charge recombination are probed by both steady-state and time-resolved fluore

39 The photochemical events of the triads are probed by both steady-state and time-resolved techni

40 The structure and bonding of 4 was probed by both experimental and computational method

41 ity of the CBPQT(2(*+)) subsetMV(*+) complex was probed by both isothermal titration calorimetry (ITC

42 gments exploring two binding site subpockets was probed by calculating relative binding affinities fo

43 bstrate selectivity on sequence optimization is probed by carrying out independent calculations for c

44 The MTOX active site was probed by characterization of various substrate anal

45 ethods, and the size of its binding site has been probed by chemical shift perturbations in NMR titra

46 properties of the hIAPP aggregates and could be probed by chiral sum frequency generation (SFG) spect

47 Chromatin organization can be probed by Chromosomal Capture (5C) data, from which t

48 The effect of labeling on protein structure is probed by circular dichroism.

49 Protein folding kinetics has recently been probed by clever experiments using circular permuta

50 These MHC-II/MHC-II interactions have been probed by co-immunoprecipitation analysis of the MH

51 imultaneously, both catabolism and anabolism were probed by coincubation with BODIPY-FL labeled LacCe

52 e effects of active-site polarity and volume were probed by combinations of active-site mutations.

53 slightly earlier epoch (z approximately 1.6) was probed by combining the spectra of 24 massive quiesc

54 nce intensity of metal chalcogenide aerogels was probed by comparison of CdSe aerogels prepared from

55 Interactions with the N-terminus were probed by comparisons between proteins with a proto

56 water, benzoquinone and phosphoric acid has been probed by computing the energetics using several co

57 The topology of the simulated chromosomes is probed by computing the distribution of their knot in

58 active index changes, the solution viscosity is probed by continuously monitoring solution conductivi

59 nt of SAM formation for all three conditions was probed by cyclic voltammetry for surfaces functional

60 , the formation of [MS subsetm-CBPQT](4(+*)) was probed by cyclic voltammetry, demonstrating that the

61 This conclusion is probed by density functional theory (DFT) calculation

62 to this loop, with the phosphodianion of OMP was probed by determining the kinetic parameters k(cat)

63 The state of the myoplasmic water was probed by determining the osmotic coefficient of par

64 ingle bonds by steric and electronic effects is probed by DFT calculations of sterically crowded bicy

65 Here, such an interaction was probed by differential scanning calorimetry (DSC) an

66 DNA accessibility is probed by digesting nuclei with a gradient of DNase I

67 This idea was probed by disrupting the hydrogen-bonding network in

68 tal functions of the 21 C. elegans skr genes were probed by dsRNA-mediated gene inactivation (RNAi).

69 ence of the assignment of protonation states was probed by either assigning "standard" protonation st

70 strong electron-donating properties of MTTFP were probed by electrochemical measurement and demonstra

71 with the substrate, myo-inositol (MI), have been probed by electron paramagnetic resonance (EPR) and

72 -lyase (EAL) from Salmonella typhimurium has been probed by electron paramagnetic resonance (EPR) spe

73 xide reductase (DMSOR) with (CH(3))(3)NO has been probed by electron paramagnetic resonance (EPR), el

74 r electron hopping between the PDI molecules was probed by electron paramagnetic resonance (EPR) and

75 The effect of the cross-strand interaction was probed by electron paramagnetic resonance and electr

76 m exchange in the cAPK type IIbeta R-subunit was probed by electrospray mass spectrometry.

77 Receptor function was probed by enzymic removal of FcgammaRIIIb from the c

78 The O2 reactivity of the Cu(I) site was probed by EPR and stopped-flow absorption spectrosco

79 e ligands on the surface of Au nanoparticles was probed by EPR spectroscopy.

80 on the cyclooxygenase active site structure was probed by examination of cyclooxygenase inhibitor ki

81 olding less than His18-Fe-His26 coordination is probed by examining the double histidine mutant H26QH

82 es and chromophoric dissolved organic matter was probed by examining the dependence of the initial H(

83 The nature of the NO/cysteine interaction was probed by examining the effects of redox active reag

84 Mechanistic underpinnings of this tolerance were probed by examining four ion channel conductances c

85 fer of electrons to Au nanoparticles has now been probed by exciting TiO(2) nanoparticles under stead

86 The nature of the bonding in 4(*) and 5 was probed by experimental and theoretical methods.

87 he nature of the bonding in isomeric 3 and 4 was probed by experimental and theoretical methods.

88 tness landscape, whose genetic structure can be probed by experiments.

89 Its functional integrity can be probed by exposing CLL cells to ionizing radiation (I

90 ted on the N-terminal and C-terminal domains was probed by expressing this domain as an independent p

91 he molecular level, an L-2 cell cDNA library was probed by expression screening and solution hybridiz

92 The reaction being probed by FCS and PCH is suggested to be a rapid e

93 chamber, and the RNA conformational changes are probed by fluorescence resonance energy transfer (FR

94 omplementary non-modified DNA or RNA decamer was probed by fluorescence and circular-dichroism spectr

95 echanism of action of the selected compounds was probed by fluorescence and competition studies, whic

96 The dual-modified particle was probed by fluorescence resonance energy transfer (FR

97 ach by which some evoked neuronal events can be probed by functional MRI (fMRI) signal with temporal

98 nu 4 antisymmetric stretch fundamental of C7 are probed by gated detection of diode laser absorption.

99 The native state of alpha-synuclein was probed by gel filtration coupled with native gradien

100 onal properties of the folding intermediates were probed by H/D exchange pulsed labeling, which showe

101 tum state populations and M(J) distributions are probed by high-resolution polarization-modulated inf

102 The fold within lipid bilayers has been probed by high field and dynamic nuclear polarizati

103 ystokinin-A receptor, CCK(A)-R(329-357), has been probed by high-resolution NMR and extensive compute

104 nreacted graphitic regions of graphene oxide was probed by high resolution X-ray absorption near edge

105 The vicinity of receptor-bound C2 groups was probed by homology modeling based on recent X-ray st

106 ormational dynamics during thermal unfolding were probed by hydrogen/deuterium (H/D) exchange-in expe

107 When infected cells were probed by immunofluorescence laser confocal microsc

108 The linkage between G(s)alpha and Syk was probed by immunoprecipitations revealing association

109 perties of this unique high-valent state may be probed by in situ spectroscopy.

110 catabolism in primary rat cerebella neurons was probed by incubation with tetramethylrhodamine-label

111 d in a cavity of PREP that, to date, has not been probed by inhibitors.

112 The mechanism of umpolung amide synthesis was probed by interrogating potential sources for the ox

113 MP binding on the stability of the R subunit was probed by intrinsic fluorescence and circular dichro

114 The unique tryptophan motif was probed by intrinsic tryptophan fluorescence, which d

115 spatial extent of electronic wave functions is probed by investigating the dependence of these energ

116 Several types of Au sites are probed by IR of CO adsorption during the ligand remo

117 Sterne, was probed by isotopic feeding experiments in iron-defic

118 The GNP microarrays could be probed by lectins labeled with fluorescein as well as

119 study, the topology of the glycine receptor was probed by limited proteolysis coupled to mass spectr

120 The protein side of the ligase-DNA interface was probed by limited proteolysis of ligase with trypsin

121 Conformations of Hop and Hop mutants were probed by limited proteolysis.

122 hol dehydrogenation by a PNP-Ru(II) catalyst was probed by low-temperature NMR experiments.

123 the formation of three-coordinate complexes were probed by low-temperature 31P NMR spectroscopy; the

124 cyclic AMP-dependent protein kinase A (PKA) were probed by MALDI-TOF mass spectrometry.

125 ges in this transiently phosphorylated state were probed by MALDI-TOF-detected amide hydrogen/deuteri

126 Different levels of this pattern are probed by manufacturing silicon chips with terraces

127 This metal-ligand pi bond is probed by MCD and resonance Raman spectroscopies whic

128 defects in cholesteric liquid crystals that are probed by means of laser manipulation and three-dime

129 e and upper parts of the switch complex have been probed by means of targeted cross-linking and mutat

130 tion behavior of the mass-selected dications is probed by means of collision-induced dissociation exp

131 Catalyst and substrate substituent effects were probed by means of systematic physical organic tren

132 ed (Adx(o)) and reduced (Adx(r)) adrenodoxin were probed by measurement of (15)N relaxation parameter

133 n to lowering the order parameters, and have been probed by measuring three-bond scalar couplings.

134 Urea denaturation of the wild-type protein is probed by measuring intrinsic and extrinsic (binding

135 Residue-to-residue topology was probed by measuring 19F NMR relaxation rates for sit

136 The structure of the transition state was probed by measuring pairwise interaction energies us

137 xisting ordered and disordered lipid domains was probed by measuring the amount of LW Trp fluorescenc

138 Saccade preparation was probed by measuring the direction of saccades evoked

139 Phospholipid-receptor interactions were probed by measuring the level of rhodopsin activati

140 Longer-range interactions were probed by measuring the paramagnetic relaxation enh

141 helix packing at the periplasmic surface has been probed by metal-chelate mediated proteolysis.

142 d assay, and the primary chromatin structure is probed by micrococcal nuclease.

143 These potentials are probed by microelectrodes that are integrated into t

144 The allosteric mechanism was probed by microsecond MD simulations in explicit wat

145 diffusion into solvent-filled MOF-1 channels was probed by modeling time-dependent luminescence quenc

146 as a function of [Ca(2+)], and its structure was probed by molecular dynamics.

147 2 and CP, and the roles of specific residues were probed by molecular genetics.

148 nd extent of acyl chain unsaturation can now be probed by monitoring the conformer preferences using

149 from different stages of disease progression was probed by mRNA in situ hybridization and protein imm

150 Although protein properties can be probed by mutagenesis, this approach has been limited

151 tifies a putative dsRNA activation site that is probed by mutagenesis, thus providing structural insi

152 The function of these residues was probed by mutagenesis experiments, which confirmed t

153 n reduced thermodynamic stability of TRX(HE) was probed by mutagenesis on the basis of these structur

154 e role of W57 in the photophysics of GFP has been probed by mutating this residue to phenylalanine.

155 Possible mechanisms of catalysis were probed by mutating each of the four invariant resid

156 Its folding mechanism was probed by mutation at sites throughout the structure

157 nd a subsequent on-pathway intermediate, I1, was probed by mutational analysis of 20 branched aliphat

158 the homodimeric coiled-coil peptide GCN4-p1, was probed by mutational analysis.

159 of rare high-energy partially folded states were probed by native-state hydrogen-exchange NMR analys

160 rmation of this two-disulfide variant of LR5 is probed by NMR in the presence of calcium, only the C-

161 rmation of the cyclic aryl phosphoimidazoles was probed by NMR and ESI-MS techniques.

162 oop following the first transmembrane domain were probed by NMR spectroscopy.

163 ization, and intraplaque hemorrhage, can now be probed by novel imaging techniques.

164 The IgE and IgA paratopes were probed by nuclear magnetic resonance spectroscopy w

165 AF or AAF adduct in or near the active site was probed by nuclease and protease digestion analyses.

166 This can be probed by observing the lineshape of the OH-stretch m

167 In addition, the active site was probed by observing binding of BCA to a charged aryl

168 the coverage of the isotopic space that can be probed by obtaining the complete distribution of isot

169 Traditionally, gene function has been probed by often-laborious methods that either incre

170 ective interaction with chiral compounds has been probed by optical rotation measurements during expo

171 e mechanisms of ventricular arrhythmias (VA) were probed by optical mapping, whole-cell patch clamp t

172 l changes in the visible region (450-750 nm) were probed by optical multichannel detection, allowing

173 ortant for cell wall architecture but cannot be probed by other spectroscopic or diffraction techniqu

174 characterized and the reaction mechanism has been probed by oxidation of the monomeric species dGuo,

175 d oxygen reactivity in PutA(Hh) and PutA(Hp) was probed by oxidative stress studies in E. coli.

176 PNP conformations are probed by peptide amide deuterium exchange (HDX) usi

177 er-dependent preferences of 3F4, the epitope was probed by peptide membrane array and antigen competi

178 ds under the basic permethylation conditions was probed by permethylating a library of short syntheti

179 PI-SceI amino acids, the PI-SceI-DNA complex was probed by photocross-linking and affinity cleavage m

180 Here, functional surfaces of insulin were probed by photocross-linking of an extensive set of

181 espectively, and their electronic structures were probed by photoelectron spectroscopy.

182 These surface states can be probed by photoemission and tunnelling experiments.

183 cation of the two binding domains on CcP has been probed by photoinduced interprotein electron transf

184 e binding sites on the full ectodomain LFA-1 were probed by photolabeling using photoactivatable isof

185 e characteristics of the excited states have been probed by picosecond time-resolved absorption (TRVI

186 Select gene and protein changes were probed by polymerase chain reaction (PCR) and immun

187 absence and presence of a model biomembrane was probed by pressure perturbation.

188 ies was performed, and the resultant samples were probed by protein immunoblot for the presence of ub

189 d the conformational states of these mutants were probed by proteolysis and accessibility of Cys178 t

190 ultrastructure into the full-length channel was probed by proteolytic mapping with immobilized tryps

191 t reaction of ethanolamine ammonia-lyase has been probed by pulsed electron nuclear double resonance

192 d on the fullerene cage and the guest H2 has been probed by pulsed ENDOR.

193 The environments of loop adenines were probed by quantitative fluorescence studies using s

194 e bicyclo[1.1.0]but-2-ylcarbinyl cations has been probed by quantum chemical calculations.

195 omere binding protein of Oxytricha nova have been probed by Raman spectroscopy, CD spectroscopy, and

196 to the 2'-deoxy-FAD-reconstituted enzyme has been probed by Raman spectroscopy.

197 himurium by hydroxyethylhydrazine (HEH) have been probed by rapid-mixing sampling techniques, and the

198 hamster prion protein (residues 90-232) have been probed by reaction with two tyrosine nitration reag

199 The nature of this intermediate was probed by reaction of bis(thiosemicarbazone) ligands

200 (BB)-carboryne fragment with small molecules was probed by reactions with electrophiles.

201 The nature of the intermediate has been probed by reactivity studies, and the synthetic uti

202 e (RT)-PCR was performed, and resultant cDNA was probed by real-time PCR for 36 candidate indicator g

203 of reduced bovine cytochrome c oxidase have been probed by reduction with both ferrocytochrome c and

204 icial groundwater media amended with acetate were probed by repeated injection of radiotracer over th

205 g helix in channel gating and ion permeation was probed by replacing them with amino acid residues of

206 emaker activity in juvenile rat brain slices were probed by replacing native channels blocked with th

207 RP-PEG) dissolved in benzene and toluene has been probed by resonance Raman dispersion spectroscopy.

208 Finally, the A. thaliana enzyme has been probed by resonance Raman spectroscopy.

209 I pre-tRNA(ile) from the bacterium Azoarcus was probed by ribonuclease T(1) and hydroxyl radical cle

210 Possible advantages of bifunctionality were probed by separating the domains on the cDNA level

211 So far this idea was probed by single-particle tracking of membrane compo

212 traction process and 2D-to-3D transformation were probed by single-crystal and powder X-ray diffracti

213 Conformations of PMCAox-CaM complexes were probed by single-molecule polarization modulation s

214 E211, and I50 in the GABA-AT mechanism have been probed by site-directed mutagenesis.

215 ) in yeast cytochrome c peroxidase (CcP) has been probed by site-directed mutagenesis.

216 dase from the yeast Hansenula polymorpha has been probed by site-directed mutagenesis.

217 n the active site of enoyl-CoA hydratase has been probed by site-directed mutagenesis.

218 osing of periplasmic or cytoplasmic cavities was probed by site-directed alkylation.

219 The role of the acid/base residue was probed by site-directed mutagenesis and steady-state

220 mmediate environment on rsTagRFP chromophore was probed by site-directed mutagenesis.

221 site(s) indicated by the structural analysis were probed by site-directed mutagenesis of three key as

222 (R177, K214, H215, M251, and D286) in Xyl3B were probed by site-directed mutagenesis.

223 tial interactions between ubiquitin and PLP2 were probed by site-directed mutagenesis.

224 The refolding kinetics are probed by small-angle x-ray scattering, circular dic

225 Crystalline structure was probed by small angle x-ray scattering of bulk meibu

226 helical geometry of membrane-associated HAfp is probed by solid-state NMR.

227 t Leu7 of the membrane-associated constructs was probed by solid-state nuclear magnetic resonance and

228 y but poorly understood protein interactions was probed by solution NMR using the catalytically compe

229 plexes with the nucleocapsid protein p7 (NC) were probed by solvent-accessibility reagents and electr

230 SX-PCR mtDNA was probed by Southern blot analysis.

231 f the silicon oxide units in these compounds is probed by spectroscopic methods, complementary comput

232 The dispersions were probed by steady-state and time-resolved spectrosco

233 alpha-amine group of the agonists have also been probed by studying the environment of the non-disul

234 athogenicity of diabetes insipidus mutations were probed by studying their effects on the properties

235 Additional hydrophobic clusters were probed by substitutions at residues I2, I61, and L1

236 of WRSs, their emission line spectra, cannot be probed by such studies.

237 ct of turn nucleation on Abeta self-assembly was probed by systematically replacing amino acid pairs

238 ionization, and their unimolecular chemistry is probed by tandem mass spectrometry experiments at var

239 interacting with the 2'-phosphate of NADP(+) were probed by targeted mutagenesis, indicating that Thr

240 thin these structures by photoexcitation and are probed by terahertz (THz) electromagnetic pulses.

241 ns in the transmembrane regions of subunit c was probed by testing the inhibitory effects of Ag(+) or

242 as well as the cation radicals AA*+ and SA*+ are probed by the combination of X-ray crystallographic

243 vironment of membrane associated peptide can be probed by the submonolayer surface sensitive sum freq

244 ragments of nucleosomal calf thymus DNA have been probed by the method of Raman difference spectrosco

245 current emission from the magnetic insulator is probed by the inverse spin Hall effect, which demonst

246 ption of the hydrophobic core of the protein was probed by the change in FRET efficiency between eith

247 onds to the hydroxyl group of the substrate, was probed by the mutation Y38F.

248 e electronic environment inside the channels was probed by the Xe chemical shift.

249 histidine (H55) and proximal histidine (H89) were probed by the creation of site-specific mutations H

250 c requirements at the aminopiperidine region were probed by the synthesis of analogues that substitut

251 These effects were probed by the use of nonpolar shape analogues of th

252 gATP-dependent priming of cracked PC12 cells were probed by their altered accessibility to various in

253 ual anti-van't Hoff/Le Bel oxygen, which has been probed by theoretical calculations, can be describe

254 This observation, which has also been probed by theoretical calculations, supports the hy

255 ause it provides strong constraints that can be probed by theoretically analyzing mathematical models

256 netic stability of the clathrates, which has been probed by thermal gravimetric analysis.

257 The efficacy of ligand exchange was probed by thermogravimetric analysis (TGA) and FT-IR

258 The plate transmittance is probed by three discrete light emitting diodes (LEDs)

259 The unfolding was probed by three spectroscopic parameters: absorbance

260 ) and key residues within the EmrE dimer has been probed by through-space (13)C-(13)C correlation spe

261 NA/poly-L-lysine polyplex formation kinetics are probed by time-resolved multiangle laser light scatt

262 The Trp59-to-heme distance was probed by time-resolved Forster resonance energy tra

263 mbly kinetics for a norovirus capsid protein were probed by time-resolved small-angle X-ray scatterin

264 rescence dynamics in the PPESO3/HMIDC system were probed by time-resolved upconversion and the result

265 nt energy (ZPE) into the reaction coordinate was probed by trajectories in which initial ZPE in the C

266 vealed when stopped flow-triggered refolding is probed by tryptophan intensity: measurements on the Q

267 parate helices of transmembrane helix dimers were probed by ultrafast 2D vibrational photon echo spec

268 ing between paromomycin and ribostamycin can be probed by using an MS-MS protection assay.

269 eflective Si/SiO(2) interface allows them to be probed by using fluorescence-interference techniques.

270 The edge site chemistry of Co-OEC has been probed by using a dinuclear cobalt complex.

271 ) or corundum (alpha-Al(2)O(3)) surfaces has been probed by using an application of the long-period x

272 le of molecular motions in metal binding has been probed by using disulfide engineering to introduce

273 ties bound to triosephosphate isomerase have been probed by using solid- and solution-state NMR.

274 g to 2-, 3-, and 4-octarepeat sequences have been probed by using various spectroscopic techniques.

275 ing optical microscope, and energy transport is probed by using fluorescent nanospheres.

276 The effect of GlcNAc was probed by using a yeast strain expressing a single c

277 h their ethereal-solvated dimer counterparts was probed by using dynamic NMR (DNMR).

278 mechanism of protein-surfactant interaction was probed by using the surfactant as the anion in the o

279 Here, the role of Thr45 was probed by using the wild-type enzyme, its T45G varia

280 CHO cells stably expressing rbSGLT1 were probed by using atomic force microscopy tips carryi

281 sessment of native and denatured structures, were probed by using far-UV CD in the presence of variou

282 nion clusters of I-(D2O)n=4-6 and I-(H2O)4-6 were probed by using femtosecond photoelectron spectrosc

283 bound conformations of the two diastereomers were probed by using X-ray crystallography, 2-D NMR expe

284 of lithium perchlorate-diethyl ether (LPDE) was probed by utilizing the extraordinary spectral shift

285 radiazoles in chalcogen bonding interactions was probed by UV-vis, (1)H and (19)F NMR spectroscopy as

286 and resting on a rugged landscape, which has been probed by various theoretical studies.

287 led recombination processes in these devices were probed by various spectroscopic and dynamics measur

288 The electrochemical kinetics are probed by varying CO2 substrate and proton concentra

289 The osmosensory mechanism of ProP has been probed by varying the solvent within membrane vesic

290 water chemistry on the forces of interaction was probed by varying ionic strength (with 100 mM NaCl a

291 tors (1-3) to the zinc peptidase thermolysin was probed by varying the solvent composition.

292 ctural changes caused by photoexcitation are being probed by vibrational spectroscopy.

293 ransfer in sensitized solar cells has mostly been probed by visible-to-terahertz radiation, which is

294 pid and protein mobility within the membrane were probed by visualizing an artificial fluorescent lip

295 r of the rotators in the preceding complexes is probed by VT NMR.

296 The selected Fabs were probed by Western blot analysis against four antige

297 This equilibrium has been probed by X-ray crystallography, NMR spectroscopy,

298 n bond in hydrogen difluoromaleate monoanion is probed by X-ray crystallography and by the NMR method

299 osition to mimic biological membranes, which were probed by x-ray reflectivity and grazing incidence

300 tial medium, MEM) and fetal calf serum (FCS) were probed by XANES and EXAFS.