ライフサイエンスコーパス: gyration

1 ation enhancements (PREs), and the radius of gyration.

2 wed that it exhibited an increased radius of gyration.

3 angle scattering intensity and the radius of gyration.

4 ected by a quick alteration of its radius of gyration.

5 n distinguished by their respective radii of gyration.

6 responding to structures with large radii of gyration.

7 ations, tertiary interactions, and radius of gyration.

8 mean-square deviation, for a given radius of gyration.

9 act of residual momentum during intermittent gyration.

10 to increase the surface charge and radius of gyration.

11 nsions far smaller than their bulk radius of gyration.

12 resulting in cortical thickening and reduced gyration.

13 wer fractal dimension, and smaller radius of gyration.

14 complex brain phenotype involving simplified gyration.

15 es that are less than 40 nm in the radius of gyration.

16 ler exponent parameters and larger radius of gyrations.

17 biology underlying the formation of cortical gyrations.

18 The radius of gyration, 34-35 A, is unchanged from 0-6 M guanidinium c

19 ng with the macromolecule size (diameters of gyration: 8-22 nm).

20 tures were compact with an average radius of gyration 9% greater than the native state.

21 n of 1 M TMAO leads to a decreased radius of gyration, a greater number of protein-protein hydrogen b

22 er with complex bilateral occipital cortical gyration abnormalities.

23 nformation, which has an increased radius of gyration, an increased maximum dimension, and a reduced

24 an be determined to be parallel by radius of gyration analysis.

25 otein adopts a global shape with a radius of gyration and a maximum linear dimension of 21.3 and 70 A

26 a wide range of responses, from isolation to gyration and circulation, and verify our findings by rea

27 encephaly, which is characterized by reduced gyration and cortical thickening; however, the phenotype

28 rs are measured, e.g., the protein radius of gyration and eccentricity, the deviation of the protein

29 chemical shifts, (2) the peptide's radius of gyration and end-to-end distance, (3) the rates of pepti

30 FRET-estimated radii of gyration and hydrodynamic radii estimated by fluorescenc

31 h classic power-law scaling of the radius of gyration and hydrodynamic radius with weight-average mol

32 ensemble-averaged estimates of the radius of gyration and hydrodynamic radius, respectively.

33 correlation between the electron's radius of gyration and its optical absorption maximum, and extrapo

34 The cross-sectional radii of gyration and linear mass density describing the rod-like

35 e same pH range indicated that the radius of gyration and maximum linear dimension of gelsolin molecu

36 The exponent upsilon relating the radius of gyration and molecular weight (R(g) proportional, varian

37 Band-like calcification with simplified gyration and polymicrogyria (BLC-PMG) is a rare autosoma

38 caling exponent (0.22) between the radius-of-gyration and Q-length that is substantially below expect

39 However, acyl-PAF increases the radius of gyration and root-mean-square deviation of PAFR, resulti

40 e fraction of native contacts, the radius of gyration and so on.

41 ong correlation exists between the radius of gyration and the DME for low energy structures.

42 -linear relationship between their radius of gyration and the extent to which they activate Hsp90.

43 molar mass dependence of both the radius of gyration and the hydrodynamic radius.

44 cative of a monomeric state with a radius of gyration and the maximum dimension of 9.1 A and approxim

45 oteins, random coil scaling of the radius of gyration and the presence of significant amounts of loca

46 order characterized by a paucity of cortical gyration and thickening of the cortical gray matter, lea

47 the extrapolated Io scattering and radius of gyration and was supported by NMR spectrum and nuclease

48 5 +/- 2.2 microM (obtained from the radii of gyration), and 6.8 +/- 1.5 microM (obtained from the for

49 (Root Mean Square Deviation), Rg (Radius of Gyration), and HB (Hydrogen Bonding), revealed the stabi

50 agenesis of corpus callosum, and simplified gyration), and severe encephalopathy with seizures.

51 coefficient, hydrodynamic radius, radius of gyration, and activation energy of diffusion were calcul

52 ed in terms of the hydrophobicity, radius of gyration, and charge of the allowed substitutions and ma

53 arison of the intrinsic viscosity, radius of gyration, and elution time of the synthesized cyclic pol

54 Further, the radius of gyration, and hence the global conformation of Taq polym

55 than average surface areas, smaller radii of gyration, and higher C(alpha) densities.

56 of data, including particle mass, radius of gyration, and hydrodynamic radius during longitudinal as

57 The total writhe, radius of gyration, and ordered elements of the diagonalized inert

58 sured values of the heat capacity, radius of gyration, and percentage of peptides that form the vario

59 ing deposition, fractal dimension, radius of gyration, and permeability decreased with increasing spe

60 with increased fractal dimension, radius of gyration, and permeability.

61 ratio of the hydrodynamic radius, radius of gyration, and the intrinsic viscosity of semi-flexible k

62 of the solvation free energy, the radius of gyration, and the mainchain rms difference from the nati

63 the Kramers theorem for calculating radii of gyration, and the other featuring the metric of maximum

64 ollective variables of handedness, radius of gyration, and three others based on the peptide torsion

65 on at 40 degrees C: oligomers with radius of gyration approximately 10 nm and fractal submicrometer p

66 and significant differences in the radii of gyration are also observed.

67 he fraction of native contacts and radius of gyration are often used; however, there is an issue rega

68 es of the proton gyrofrequency (frequency of gyration around the field line) from the 17th up to the

69 mpanied by a clear increase in the radius of gyration as the solution pH was shifted from 6.5 to 3.4.

70 TMEM161B as a regulator of cerebral cortical gyration, as involved in primary ciliary structure, as a

71 maging was almost identical, with simplified gyration associated with a non-thickened cortex, severe

72 The radii of gyration at infinite contrast were determined to be 3.65

73 TP induces a significantly smaller radius of gyration at pH=7 with a transition midpoint at approxima

74 H2O mixtures was performed and gave radii of gyration at the calculated match points for the calcium

75 sit fractal dimension, and deposit radius of gyration, at different vertical positions, were conducte

76 reduction of the polymer size, the radius of gyration being instead determined by shape anisotropy.

77 e formation of nanodiamonds with a radius of gyration between 12 and 35 nm consistent with 32-90 nm d

78 he difference in the square of the radius of gyration between the D and N states.

79 rocess about 50 % of the change in radius of gyration between the unfolded protein and the native sta

80 eeding, hard braking, entropy, and radius of gyration) between groups.

81 ty of a loop or an increase of the radius of gyration by < 1%.

82 on with structure suggest that the radius of gyration can be a misleading reaction coordinate for unf

83 hains in the micelle (e.g., blocks' radii of gyration, chain radii of gyration, monomer concentration

84 erve a dimeric form of SecA with a radius of gyration comparable to that previously observed for SecA

85 ttraction induced by polymers with radius of gyrations comparable to the NP diameter.

86 otein structure, as measured by its radii of gyration, compared to the crystal structure, in agreemen

87 By imposing radius of gyration constraint during mode selection, it was possib

88 ctual disability, simplification of cerebral gyration, corpus callosum hypoplasia, and dysmorphic fac

89 sive neutralization of the H4, its radius of gyration decreases linearly with the tail charge q, the

90 leads to a twofold increase in the radius of gyration derived from the small-angle neutron scattering

91 197,600+/-13,700 and the apparent radius of gyration determined by X-ray scattering was 2.80+/-0.05

92 ast to H2O-buffered solutions, the radius of gyration did not increase significantly in D2O-buffered

93 The radii of gyration, distance distribution functions, and Kratky pl

94 Variants associated with PMG or atypical gyration encoded regions of the phosphatase or C2 domain

95 dimensions of IDRs, including the radius of gyration, end-to-end distance, polymer-scaling exponent

96 disorder termed Microcephaly with simplified gyration, Epilepsy and permanent neonatal Diabetes Syndr

97 ic sequence-independent behavior of radii of gyration for denatured proteins.

98 asures of internal loops as well as radii of gyration for known RNAs.

99 d toroid genomes revealed declining radii of gyration for neutrophil chromosomes.

100 The larger radius of gyration for the ATP-bound relative to the ADP-bound for

101 relaxation times of writhe and the radius of gyration for the same molecules.

102 ation functions for the writhe and radius of gyration for the supercoiled molecules.

103 ox model, providing a value of the radius of gyration for titin-II (63 +/- 1 nm) in agreement with st

104 ate with a corresponding change in radius of gyration from 17 to 32 A.

105 minus, as implied by a decrease of radius of gyration from 18.5 A to 16.2 A.

106 of a polypeptide chain with fixed radius of gyration from a dilute (ideal) solution to a solution co

107 nterfere with the determination of radius of gyration from the SAXS experiments.

108 s that involves a 10A reduction in radius of gyration (from 56 to 46 A) and a 35 A shortening of the

109 he penultimate residue has a small radius of gyration (glycine, alanine, serine, threonine, proline,

110 l hypoplasia in 3 children, abnormalities of gyration in 2, brainstem hypoplasia in 2, isolated fourt

111 ving force of the reduction in the radius of gyration in that phase.

112 ength scale reduces to the analyte radius of gyration in the limiting cases of spherically symmetric

113 hydrodynamic radius to the static radius of gyration indicates that the proteins obey Gaussian stati

114 heir second virial coefficient and radius of gyration indicating an influence of P(A) on polymer-solv

115 Pressurized gyration is a new method of combining rotation and contr

116 o hold for coupling polymers whose radius of gyration is comparable to size of the chelated particle.

117 rol of the polarization of this core and its gyration is key to the utilization of vortices in techno

118 A molecule, with a radius of gyration larger than the nanochannel width, that straddl

119 the protein's single-chain average radius of gyration <Rg>.

120 perimentally obtained datasets, of which the gyration method is much less computationally demanding.

121 ent the mass value in the modified radius-of-gyration metric.

122 ., blocks' radii of gyration, chain radii of gyration, monomer concentration profiles).

123 y the fact that the molar mass and radius of gyration obtained by HDC with multiangle static light sc

124 f human alpha-LA, based on measured radii of gyration obtained from nuclear magnetic resonance experi

125 An ultrafast increase of myoglobin radius of gyration occurs within 1 picosecond and is followed by a

126 tron scattering (SANS) provides the radii of gyration of 1.2-1.8 nm.

127 to form a spherical micelle with a radius of gyration of 14.2 A and that the larger micelles are more

128 mers contained 22 dimers and had a radius of gyration of 14.8 nm.

129 precursor species with an initial radius of gyration of 16.1 +/- 5.9 A and average mass of a dimer t

130 protein periodically expanded to a radius of gyration of 18 to 20 A.

131 is a non-spherical protein with a radius of gyration of 3.4 nm.

132 ystem of particles with an average radius of gyration of 30.3 +/- 0.6 A and a maximum linear dimensio

133 gle x-ray scattering studies report radii of gyration of 38.3 A for Taq, 30.7 A for Klentaq, and 30.5

134 ight gene 5 protein dimers, with a radius of gyration of 45 A and an overall maximum dimension of 120

135 o form an annular structure with a radius of gyration of 7.0 +/- 1.0 nm when placed in serum.

136 omposed of blobs, inside which the radius of gyration of a polymer segment is a power-law function of

137 derive a relationship between the radius of gyration of a structure and its hydrodynamic ratio, whic

138 average hydrodynamic radius and a radius of gyration of about 17 nanometers at a very low critical a

139 Guinier analysis indicates a radius of gyration of about 35 A.

140 The radius of gyration of alpha-crystallin on its own and when mixed w

141 1 and the D181A mutant each have a radius of gyration of approximately 26 A, and the effect of Mg2+ o

142 light scattering revealed that the radius of gyration of bacterial EPS with addition of CaCl2 was 20

143 While the radii of gyration of both were the same at 4.05 nm and both had o

144 g studies were used to measure the radius of gyration of bovine lens alpha-crystallin when complexed

145 reported length dependence for the radii of gyration of chemically denatured proteins containing 50-

146 cently proposed expression for the radius of gyration of circular polymers into the Zimm model.

147 The radius of gyration of CR2 SCR 1-15 was determined to be 11.5 nm by

148 iron release from the N-lobe, the radius of gyration of cross-section, Rc, increases from 16.9+/-0.2

149 scattering was used to measure the radius of gyration of cytochrome c after initiation of folding by

150 On saturation with cGMP, the radius of gyration of Delta(1-52)PKG-I beta increases from 29.4 +/

151 Radii of gyration of denatured proteins vary with chain length an

152 composite BSA@ZIF to determine the radius of gyration of encapsulated BSA through Guinier, Kratky, an

153 The radius of gyration of FH was determined to be 11.1-11.3 nm by both

154 calculation of the distribution of radii of gyration of four different unfolded proteins published b

155 s as small as 20 bases that have a radius of gyration of only 3 nm.

156 s of 0:1, 1:1, and 5:1, the average radii of gyration of particles on quartz were 5.7 +/- 0.3, 4.6 +/

157 late well with reported changes in radius of gyration of S1 associated with different states of the b

158 The radius of gyration of the capsular polysaccharides ranged between

159 cal filaments through the external medium or gyration of the cell body in response to the rotation of

160 was found to increase the average radius of gyration of the chains by 20-40%, with the expansion fac

161 t dynamic variation is the overall radius of gyration of the chromatin region, followed by domain reo

162 .1-11.3 nm by both methods, and the radii of gyration of the cross-section were 4.4 nm and 1.7 nm.

163 D/caspase-2 signaling is critical for normal gyration of the developing human neocortex and for norma

164 ual to 1.5, where R(g,N)(b) is the radius of gyration of the folded beta-hairpin in the bulk.

165 ation about the molecular mass and radius of gyration of the individual complexes can be obtained.

166 is enhanced for systems where the radius of gyration of the linear polymer is greater than the radiu

167 SAXS measurements determined the radius of gyration of the native protein to be 25.0 +/- 0.3 A, whi

168 were inversely correlated with the radius of gyration of the protein in the plane of the bilayer.

169 he higher temperature and that the radius of gyration of the protein is temperature and redox state i

170 ct measurable parameters, including radii of gyration of the proteins and chemical shifts, residual d

171 , and the molecular weight and the radius of gyration of the proteins can be determined.

172 in the monodisperse region with a radius of gyration of the rod cross-section (Rt) of approximately

173 eight-average molecular weight, the radii of gyration of the starch polysaccharide chains, and the di

174 The radii of gyration of the subpopulation of unfolded molecules for

175 These techniques identified gyration of the three p-phenylene rotators on the millis

176 The distribution of the radius of gyration of the transition states shows that these struc

177 The radius of gyration of the uncrowded protein was estimated to be 30

178 robing shows that TMAO reduces the radius of gyration of the unfolded ensemble to the same endpoint a

179 ntally measurable root mean-square radius of gyration of the unfolded protein.

180 Second, the radius of gyration of the unfolded RNA decreases from 76 to 64 A a

181 The sedimentation coefficients and radius of gyration of TT30 were unaffected by citrate or phosphate

182 expanded form (by about 25% in the radius of gyration) of the native conformation.

183 icant changes were detected on the radius of gyration or maximum interatomic distance.

184 capsular PS molecular mass and the radius of gyration provided strong evidence against a simple linea

185 We found that a gyration quantification method and a Bayesian statistics

186 kinetic study include the squared radius of gyration R(2)(g), the fraction of native contacts within

187 cule's diffusion coefficient D and radius of gyration R(g) and is concentration insensitive, providin

188 Its Guinier X-ray radius of gyration R(G) is 5.18 nm and its neutron R(G) is 5.03 nm

189 The Guinier X-ray radius of gyration R(G) likewise increased with concentration in 1

190 For CR2 SCR 1-2, its radius of gyration R(G) of 2.12(+/-0.05) nm, its maximum length of

191 The Guinier radius of gyration R(G) of 3.1-3.3 nm and the R(G)/R(O) ratio of 2

192 The Guinier radius of gyration R(G) of 4.3 nm for SCR-1/5 and those of 4.7 nm

193 ntation coefficient of 3.1 S and a radius of gyration R(G) of 6.9 nm.

194 The Guinier X-ray radius of gyration R(G) of 6.9(+/-0.1)nm showed that IgD is more e

195 The radius of gyration R(G) of CR2-Ig was determined to be 5.39(+/-0.1

196 The radius of gyration R(G) of rCrry was determined to be 4.9-5.0 nm,

197 The radius of gyration R(G) of sCR1 of 13.4(+/-1.1) nm is not much gre

198 X-ray scattering of dp6-dp36 gave radii of gyration R(G) that ranged from 1.33 nm to 3.12 nm and ma

199 owed that the dimer and trimer have radii of gyration R(G) values of 7.5 nm and 10.3 nm, respectively

200 btained by calculating the squared radius of gyration R(g)(2), the root-mean-squared pair separation

201 , respectively, and cross-sectional radii of gyration R(XS) values of 1.3 nm and 1.5 nm, respectively

202 d, and the experimentally observed radius of gyration (R g) is coincidental to that calculated by the

203 eavy water revealed that the X-ray radius of gyration (R(g) ) is 5.2-5.4 nm, after allowing for radia

204 ated that FHR5 was dimeric, with a radius of gyration (R(g) ) of 5.5 +/- 0.2 nm and a maximum protein

205 ge of characterized denatured-state radii of gyration (R(G)) and by reexamining proteins that reporte

206 ure to accurately extract both the radius of gyration (R(g)) and end-to-end distance (R(ee)) from SAX

207 The radius of gyration (R(g)) and maximum dimensions (D(max)) of the M

208 mpaction during which the observed radius of gyration (R(g)) decreases from 75 angstroms to 55 angstr

209 RNA was expanded, with an average radius of gyration (R(g)) of 53 +/- 1 A.

210 a relatively compact shape with a radius of gyration (R(G)) of approximately 37.4 A and a maximal di

211 s an elongated conformation with a radius of gyration (R(g)) of approximately 52 A and a maximal dime

212 s resemble prolate ellipsoids with radius of gyration (R(g)) of approximately 75 and approximately 30

213 In 30 min, the average radii of gyration (R(g)) of particles on quartz grew from around

214 used to follow the decrease in the radius of gyration (R(g)) of the Azoarcus and Tetrahymena ribozyme

215 Our simulations predict that the radius of gyration (R(g)) of the dendrimer changes little with pH

216 causes a dramatic decrease in the radius of gyration (R(g)) of the PC2 EF-hand by small angle x-ray

217 that PIWF1 and PIWF4 have different radii of gyration (R(G)) values of 3.1 nm and 6.7 nm, respectivel

218 matic response in variation of the radius of gyration (R(g)) with the temperature (T) occurs, however

219 tively, but similar cross-sectional radii of gyration (R(XS)) values of 1.5 nm and 1.9 nm, respective

220 light scattering, to determine the radius of gyration, R(g), and hydrodynamic radius, R(H), of isolat

221 ttering (SAXS) experiment yields a radius of gyration, R(g), of 19.1 A, consistent with the value pre

222 aled increases in the native state radius of gyration, R(g), of 2.2% to 4.1%, at pH 5.5 and below, co

223 m unfolding experiments showed the radius of gyration, R(g), of native Cyt c to swell approximately 1

224 roperties-including an appropriate radius of gyration, R(g)-that facilitate this assembly process.

225 independent of FITC-dextran and Ficoll size (gyration radii [RG] 40-300 A).

226 Gyration radii of trivially knotted loops were found to

227 heat, contact maps, simulation trajectories, gyration radii, RMSDs from native state, fraction of nat

228 of crystal was further validated with least gyration radius (209 +/- 1.81 nm(2)), accessible surface

229 density and by angular light scattering for gyration radius and fractal dimension.

230 Analysis of energy and mobility profiles, gyration radius of peptide, and radial distribution func

231 that for an equivalent sphere defined by the gyration radius of the aggregate.

232 remarkable conclusion that, by adjusting the gyration radius of the bodies, one can always simultaneo

233 bility density distributions as functions of gyration radius were generated for loops of up to N = 3,

234 Probability of a trivial knot, average gyration radius, and probability density distributions a

235 The apparent cross-sectional radius of gyration (Rc) of TnI increased by about 9% when regulato

236 e is introduced that increases the radius of gyration relative to the native state and generates a la

237 small but significant increase in radius of gyration relative to wild-type.

238 ons in the hydrodynamic volume and radius of gyration, respectively, after photoinduced deprotection

239 The radii of gyration RG from Guinier analyses were similar at 6.11-6

240 n scattering showed that the x-ray radius of gyration Rg increased with salt concentration, whereas t

241 ier analyses showed that the X-ray radius of gyration RG of CEA was 8.0 nm.

242 ng measurements of HS dp6-dp24 gave radii of gyration RG values from 1.03 to 2.82 nm, cross-sectional

243 Scattering showed that the x-ray radius of gyration Rg was unchanged with concentration in 50-250 m

244 n are observed as monitored by the radius of gyration Rg, and by far and near UV CD (circular dichroi

245 geneous systems, quantified by the radius of gyration (RG ), can be measured by small-angle X-ray sca

246 ces the PYP signaling state, whose radius of gyration (Rg = 16.6 A) is significantly larger than that

247 creases (1-2 angstrom) in both its radius of gyration (Rg) and its Stokes radius (Rs), and the increa

248 The average radius of gyration (Rg) calculated from FRET data on freely diffus

249 Upon addition of 0.122 M NaCl, the radius of gyration (Rg) decreased substantially, which indicates t

250 n increasing free Ca2+ levels, the radius of gyration (Rg) increased nearly 12 A, from 31.1+/-0.3 to

251 e results show that apo-IRP1 has a radius of gyration (Rg) of 33.6+/-0.3A, and a Dmax of 118+/-2A.

252 highly asymmetric structure with a radius of gyration (Rg) of 45 A and a maximum linear dimension (dm

253 The radius of gyration (Rg) of DnaK was determined as 37.5 +/- 1.0 ang

254 For the iron(III) only system, the radius of gyration (Rg) of heterogeneously formed precipitates gre

255 angle region it was found that the radius of gyration (Rg) of NCD281 is 3.60 +/- 0.075 nm, which is i

256 It was found that the radius of gyration (Rg) of S1.MgADP.AlF4 and of S1MgADP.Vi were si

257 We found that the radius of gyration (Rg) of TnI decreased by approximately 10% upon

258 njecture by showing that crambin's radius of gyration (Rg) remains constant below approximately 180 K

259 The radius of gyration (Rg) shows a cooperative transition with increa

260 tryptophan fluorescence and in the radius of gyration (Rg) which is reduced from 22 A in the fully un

261 e reported no such increase of the radius of gyration (Rg).

262 )app, molecular weights (Mapp), and radii of gyration (Rg)app in solutions containing mixed micelles

263 tering intensity (i.e., changes in radius of gyration, RG).

264 Conversely, the radius of gyration, Rg, determined from the SAXS data remains cons

265 The radius of gyration, Rg, of mFnFn3(9,10) derived from small-angle n

266 that FRET experiments overestimate radius of gyration, Rg, of the protein due to the application of G

267 reased to 20 microM, whereupon the radius of gyration, RG, values increased from 9 to 15 nm at [Zn]=2

268 inguished by measuring the squared radius of gyration Rg2 and the fraction of native contacts Q.

269 l and energetic properties such as radius of gyration, rms distance, solvent-accessible surface area,

270 om 1.03 to 2.82 nm, cross-sectional radii of gyration RXS values from 0.31 to 0.65 nm, and maximum le

271 The X-ray cross-sectional radius of gyration RXS was 2.1 nm, and is consistent with extended

272 PTerm455, and their cross-sectional radii of gyration RXS were also similar.

273 olecular weight (Mw) and z-average radius of gyration (Rz) were determined at intervals ranging from

274 The Mg(2+) dependence of the radius of gyration shows that globally the rRNA folds cooperativel

275 s suggested that the complex has a radius of gyration similar to that of the enzyme itself.

276 om-coil statistics and hence their radius of gyration simply scales with solvent quality (or concentr

277 Writhe, radius of gyration, slither motion, and branching probability were

278 ty, as shown by the combination of radius of gyration, solvent accessible surface area, secondary str

279 analyses of pairwise distances and radii of gyration suggest that the less frustrated energy landsca

280 The gyration tensors have just one independent component.

281 by the aspect ratio of the principal axes of gyration tensors.

282 term to prevent atomic overlap, a radius of gyration term (E(rgyr)) to avoid expansion at the protei

283 py that quantifies the diversity of radii of gyration that a protein can adopt in solution and does n

284 have end-to-end distances and mean radii of gyration that agree well with random-coil expectations i

285 mer chains, resulting in a polymer radius of gyration that grows with the nanoparticle volume fractio

286 m, and fluorescence to measure the radius of gyration, the average secondary structure content, and t

287 usly attribute apparent changes in radius of gyration to changes in the structure of SOD.

288 a similar time range show that the radius of gyration under native favoring conditions is comparable

289 eement with experiments for polymer radii of gyration up to 80% of the nanocrystal radius.

290 are reflected in a 13% increase in radius of gyration upon complex formation.

291 The radius of gyration values obtained by two different analyses of SA

292 in structural compactness was observed, with gyration values of 32.98 +/- 0.23 and 33.01 +/- 0.24 ang

293 revealed a dependence of the X-ray radius of gyration values on concentration that corresponded to th

294 The increase in the radius of gyration was associated with a single equilibrium unfold

295 Two distinct regimes of vortex gyration were detected depending on the vortex core posi

296 ngths of 14 nm, the cross-sectional radii of gyration were different at 1.70 nm for sFI and 1.57 nm f

297 requency, intrinsic viscosity, and radius of gyration were observed for all treated starches.

298 turing 3D structural properties is radius of gyration, which in this study is used to measure the spa

299 other methods found an increase in radius of gyration with denaturant concentration, but most small-a

300 ate decays of protein contrasts and radii of gyration with increasing temperature, which are shown to