ライフサイエンスコーパス: diagonal

1 wo levels of landing orientation (forward or diagonal).

2 rosspeaks that are otherwise obscured by the diagonal.

3 ty is biased due to partial overlap with the diagonal.

4 rum has 4 peaks, 2 on the diagonal and 2 off-diagonal.

5 with a sharp switch across the phase diagram diagonal.

6 rgent SDS, we show here the application of a diagonal 2D (D2D) SDS/PAGE assay to identify KSPs in com

7 Suppression of the diagonal allows the accurate identification of cross-pea

8 ic programming algorithm, which includes off-diagonal anchors that result from map coordinate errors

9 rational echo spectrum has 4 peaks, 2 on the diagonal and 2 off-diagonal.

10 stingly, the channel with two wt subunits at diagonal and adjacent configurations showed the same pH

11 two forms could be estimated from the NOESY diagonal and cross peak intensities.

12 show that a combination of amide I' and II' diagonal and cross peaks can effectively distinguish bet

13 eta-sheets, interference effects between the diagonal and cross-peaks arising from the sheets, combin

14 ncy blue-shift and intensity decrease of the diagonal and cross-peaks of the sheet's two IR active mo

15 otect receptors from cross-links at both the diagonal and lateral interfaces.

16 el G-quadruplex structure that featured both diagonal and lateral TTA loops.

17 ious orientations (horizontal, vertical, and diagonal) and a steady flow rate of Q = 1.5 mL/min was a

18 the electronic excitations along the nodal (diagonal) and antinodal (parallel to the Cu-O bonds) dir

19 ise-trait phenotypic correlations (rP, below diagonal) and pairwise-trait genetic correlations (rG, a

20 esponses in the triangle between the ansate, diagonal, and coronal sulcus were identified in all anim

21 ts confirmed that the polarization tensor is diagonal, and matrix elements were determined with high

22 es, including different variants of lateral, diagonal, and propeller loops, and six different loop se

23 ficant overrepresentation of microtubules at diagonal angles with respect to the cell axis, which coi

24 ne (CBr2Cl2) shows previously unobserved off-diagonal anharmonic coupling between thermally populated

25 ion systems approaches, in what is termed a "diagonal approach."

26 s not interact in a specific manner with the diagonal aromatic residue.

27 either interdigitated or non-interdigitated diagonal arrangements.

28 the presence of Ce(2)O(3) dimers, which form diagonal arrays that have specific orientations of 0, 24

29 is around horizontal or vertical rather than diagonal axes.

30 n two strands symmetrically disposed about a diagonal axis.

31 immunopositive neurons in the medial septal/diagonal band (MS/DB) and nucleus basalis of Meynert (NB

32 urons freshly dissociated from medial septum/diagonal band (MS/DB) exhibit relatively slow kinetics o

33 was substantially blunted for medial septum/diagonal band (MS/DB) neurons in brain slices on PD 11-1

34 properties of I(h) currents in medial septum/diagonal band (MS/DB) neurons.

35 In the medial septum/diagonal band (MS/DB), no effect of treatment with Prema

36 ve lesions of medial septal/vertical limb of diagonal band (MS/VDB) cholinergic neurons produced by 1

37 The medial septum-diagonal band (MSDB) complex, via the septohippocampal p

38 input, the medial septum and nucleus of the diagonal band (MSDB).

39 munofluorescence in the vertical limb of the diagonal band (VLDB) revealed enhanced optical density f

40 ptum that was concentrated in the horizontal diagonal band and areas of the posterior septum includin

41 ere observed in BFCNs from the medial septum diagonal band and horizontal diagonal band, but not the

42 The medial septal diagonal band area (MS/DB), made up of GABAergic and cho

43 ergic innervation from the medial septum and diagonal band complex contributes to temporal coordinati

44 ergic projections from the medial septum and diagonal band complex exclusively innervate GABAergic in

45 oriens layer of CA1, the medial septum, the diagonal band complex, the substantia innominata, and th

46 antia innominata, lateral preoptic area, and diagonal band nuclei of the basal forebrain; central, me

47 expression in the medial septum (MS) and the diagonal band of Broca (DBB), moderate levels in the pre

48 nergic input from the horizontal limb of the diagonal band of Broca (HDB) and expresses both muscarin

49 ucleus (MCPO) and the horizontal limb of the diagonal band of Broca (HDB) of the basal forebrain comp

50 The medial septum and diagonal band of Broca (MS-DBB) has an essential role fo

51 ippocampus arises from the medial septum and diagonal band of Broca (MS-DBB), and we investigated how

52 posure on neurons in the mouse medial septum/diagonal band of Broca (MS/DB), focusing on the choliner

53 ensely and abut neurons in the medial septum/diagonal band of Broca (MS/DB).

54 ns in the medial septum/vertical limb of the diagonal band of Broca (MS/VDB) and cholinergic neurons

55 The medial septum and diagonal band of Broca (MSDB) are major afferents to the

56 and cholinergic neurons in the medial septum-diagonal band of Broca (MSDB) have been associated with

57 electrical stimulation in the medial septum diagonal band of broca (MSDB) on neuronal activity in th

58 c and GABAergic nucleus of the medial septum/diagonal band of Broca (MSDB) which projects to the hipp

59 ide a dense innervation to the medial septum-diagonal band of Broca (MSDB), a sleep-associated brain

60 Models of path integration use medial septum/diagonal band of Broca (MSDB)-dependent MEC grid-cell fi

61 ne acetyltransferase neurons in the vertical diagonal band of Broca (vChATs) degenerate in the early

62 ing GABA receptors in the anterior thalamus, diagonal band of Broca and RSC.

63 tic protein oChIEF-tdTomato in medial septum/diagonal band of Broca cholinergic neurons using Cre rec

64 The medial septum/diagonal band of Broca complex (MSDB) is a key structure

65 cetylcholine, derived from the medial septum/diagonal band of Broca complex, has been accorded an imp

66 r glutamatergic neurons in the medial septum/diagonal band of Broca does not affect modulation of fir

67 mol injections into the anterior thalamus or diagonal band of Broca provide substantial protection, s

68 neurons in the medial BF (medial septum and diagonal band of Broca) of macaque monkeys encodes a uni

69 lamus, preoptic area, septum, nucleus of the diagonal band of Broca, and main olfactory bulb.

70 nuclei, vertical and horizontal limbs of the diagonal band of Broca, and SUM.

71 ucleus, vertical and horizontal limbs of the diagonal band of Broca, and the nucleus basalis of Meyne

72 ential input from the septum, nucleus of the diagonal band of Broca, preoptic area, hypothalamus, ros

73 tical and horizontal limbs of the nucleus of diagonal band of Broca, supramammillary nuclei (SUM), an

74 in the olfactory bulb, cerebral cortex, the diagonal band of Broca, the medial septal nucleus, retic

75 nuclei, nucleus accumbens, caudate putamen, diagonal band, amygdala, hypothalamus, zona incerta, tha

76 ppocampal regions including the tenia tecta, diagonal band, and retromammillary nucleus, but also bro

77 e medial septum diagonal band and horizontal diagonal band, but not the nucleus basalis.

78 across its different regions (medial septum, diagonal band, magnocellular preoptic area, and substant

79 al and medial preoptic areas, nucleus of the diagonal band, nucleus accumbens shell, inferior collicu

80 mygdaloid nuclei, the horizontal limb of the diagonal band, the paraventricular hypothalamic nucleus,

81 derate input from the horizontal limb of the diagonal band, whereas the entorhinal cortex receives ma

82 e hypothalamus, and the vertical limb of the diagonal band.

83 and the vertical and horizontal limbs of the diagonal band.

84 medial septum (MS), vertical and horizontal diagonal bands of Broca (VDB and HDB), perifornical late

85 species are strongly 2D, with dominant "off-diagonal" beta(zyy) components.

86 disubstituted species are dominated by 'off-diagonal' beta(zyy) components.

87 anization of the previous array, although no diagonal bias was observed in these cells.

88 (MHC)-bound peptide, employing the canonical diagonal binding mode utilized by most TCRs.

89 example, always turn left into the arm with diagonal black stripes on the walls and gravel glued to

90 aged over a large cell population, revealing diagonal blocks called Topological Associating Domains (

91 ors inside restricted regions to account for diagonal blocks.

92 rior descending artery (n = 5) or the second diagonal branch (n = 2).

93 rval, 1.19-2.59), additional bypass graft to diagonal branch (odds ratio, 1.92; 95% confidence interv

94 is or with an additional bypass graft to the diagonal branch had increased risk for IMA failure.

95 gs) underwent thoracotomy and occlusion of a diagonal branch of the left anterior descending coronary

96 he left anterior descending artery or second diagonal branch, and akinesis of the infarcted segment w

97 ed by the left anterior descending artery, a diagonal branch, or a ramus intermedius with diagonal di

98 scending artery between the first and second diagonal branch.

99 left anterior descending artery, additional diagonal branches, and atrial biopsy for CSC culture wer

100 n in a dot plot, tend to agglomerate along a diagonal but can also be disrupted by gaps or shifted aw

101 This enzyme-based diagonal capillary electrophoresis assay appears to be g

102 Diagonal capillary electrophoresis is a form of two-dime

103 Diagonal capillary electrophoresis is a two-dimensional

104 Here, we demonstrate diagonal capillary electrophoresis-mass spectrometry for

105 Adjacent (row, column, and off-diagonal) cells with the greatest similarity in baseline

106 pts a novel (3+1) basket conformation with a diagonal central loop.

107 aturation, as did the control peptide with a diagonal Cha...Nle interaction, indicating different dri

108 we implemented ubiquitin combined fractional diagonal chromatography (COFRADIC) for proteome-wide ubi

109 lysates using N-terminal COmbined FRActional DIagonal Chromatography (COFRADIC).

110 By means of N-terminal combined fractional diagonal chromatography, the physiological substrates of

111 We report acquisition of diagonal-compensated protein structural restraints from

112 al long-range order due to non-vanishing off-diagonal components of the single-particle density matri

113 vic movement were significantly later in the diagonal condition.

114 hin what in d.c. transport would be the zero diagonal conductivity of an integer quantum-Hall-effect

115 The diagonal conjugate was at least 15 mm longer than the ob

116 The distance between diagonals connecting 2 points was measured.

117 nts (C11 and C44) and a hardening in the off-diagonal constant (C12) at ~8 GPa where significant elas

118 ch larger than that for spherical cells with diagonal contraction.

119 timulus pair alternated between the opposing diagonal corners of the approximately 1 cm(2) stimulatio

120 The diagonal-couplet lateral sequence gait was accomplished

121 and climbs waterfalls with a salamander-like diagonal-couplets lateral sequence gait and has evolved

122 sing Marcus-Hush theory reveals that its off diagonal coupling element, H(ab), is large enough, relat

123 Fore-hindlimb coupling favored a more stable diagonal coupling.

124 he variables are independent with the use of diagonal covariance matrices.

125 own parameters associated with a general non-diagonal covariance matrix, we generalize the mixture of

126 otonics lattices possessing both on- and off-diagonal deterministic disorders for realizing localized

127 ngly, the nematic director orients along the diagonal direction of the CuO(2) square lattice, in shar

128 fect; thresholds are higher for motion along diagonal directions than for motion along cardinal direc

129 les were found to form linear arrays in both diagonal directions, while planar tiles showed significa

130 nt ranged from - 1.08 to 0.21%/ppm along the diagonal directions.

131 ssifiers modelled by support vector machine, diagonal discriminant analysis, linear discriminant anal

132 e .632+ bootstrap have the smallest bias for diagonal discriminant analysis, nearest neighbor and cla

133 e to the size of small bacteria, matches the diagonal distance of the lattice.

134 tterfly type motions that modulate the Re-Re diagonal distance.

135 In contrast, PDF peaks measured across the diagonal distances of the molecular square deviate signi

136 icative of configurational broadening of the diagonal distances.

137 diagonal branch, or a ramus intermedius with diagonal distribution in all but one case.

138 The conserved diagonal docking mode observed in structures of T-cell r

139 The conserved diagonal docking of TCRs could thus orient each CDR loop

140 tions and that these interactions impose the diagonal docking of TCRs on MHC.

141 on diffraction revealed an in-plane oriented diagonal double-stripe antiferromagnetic spin structure.

142 a perpendicular spin component, keeping the diagonal double-stripe order.

143 rupted by gaps or shifted away from the main diagonal due to mismatches between the contig and the re

144 transfer integrals, often referred to as off-diagonal dynamic disorder, which causes transient locali

145 d the frequency and clinical significance of diagonal earlobe crease (DELC) in cognitively impaired p

146 2 pairwise correlations (after excluding 144 diagonal edges).

147 We have observed an elastic softening in the diagonal elastic constants (C11 and C44) and a hardening

148 and 1.5-cm spacing, application of energy to diagonal electrode pairs increased coagulation.

149 nnections, E has diagonal elements Q and off-diagonal elements (1-Q)/(n-1), where Q, the quality, is

150 Using all 400 K SNPs, 46% of the off-diagonal elements (OD) were between - 0.01 and 0.01.

151 In particular, the off-diagonal elements of the Fock matrix that is composed of

152 r this bias, it was suggested to discard the diagonal elements of the outer products of each data mat

153 intrinsically privileged connections, E has diagonal elements Q and off-diagonal elements (1-Q)/(n-1

154 s between morphologically equivalent stages (diagonal elements) than in the correlation between morph

155 between morphologically distinct stages (off-diagonal elements).

156 zero elements and instead allow non integer diagonal elements, which leads to retention of the full

157 differ by no more than the signs of the off-diagonal elements.

158 ce between classifiers, we show that the off-diagonal entries of their covariance matrix correspond t

159 Our measurements successfully highlight off-diagonal features of the 2D spectra and, in combination

160 t laser pulses reveals previously hidden off-diagonal features.

161 Separation of diagonal FF and coupling effects on the spectra are used

162 An 80[Formula: see text] diagonal field of view is achieved by on-axis optical co

163 growth between mesoderm and endoderm drives diagonal folding.

164 y, adding constraints via the elimination of diagonal folds in the quads decreases the number of degr

165 s made contact with the CD1d molecule with a diagonal footprint, typical of MHC-TCR interactions, whe

166 determine frequencies characteristic of the diagonal force field (FF) contributions at each position

167 e assume the covariance matrix takes a block diagonal form.

168 irwise-trait genetic correlations (rG, above diagonal) from 1, 15, and 100 DPH.

169 l polyacrylamide or agarose microplate array diagonal gel electrophoresis (MADGE) which is microplate

170 oproteins, this is the first report of a new diagonal gel electrophoresis method to isolate and ident

171 caspase-12 also was confirmed by whole-cell diagonal-gel analysis.

172 LAD stenosis and additional diagonal graft remained predictive of IMA failure in an

173 subjects were trained for >24 d to detect a diagonal grating pattern in one quadrant of the visual f

174 d into two subdomains and bisected by a long diagonal helix.

175 ies and will generate spots that fall on the diagonal in a reconstructed two-dimensional electrophero

176 the negative symmetric dissipation matrix is diagonal in a suitable basis.

177 rk upbeat, hemi-seesaw, torsional, or upbeat-diagonal in each of the others.

178 ents, clusters them with respect to the main diagonal in the dot plot using a weighted linear regress

179 ry and will generate spots that fall off the diagonal in the electropherogram.

180 ly, the MreB protein directed the helical or diagonal incorporation of new peptidoglycan into the wal

181 The diagonal interaction between Trp2 and Trp9, which have a

182 actions, and LPNs, mediating homolateral and diagonal interactions.

183 2, ... for H, A gives rise to a matrix whose diagonal is a sequence d=(d1, d2, ...) with the property

184 alpha-spectrin-deficient MEL cells, the mean diagonal length was 650 nm with a mean residency time of

185 indlimb-forelimb coordination, ensuring that diagonal limb pairs move synchronously while the ipsilat

186 ty (pL) and recurrences, maximum and average diagonal line (dlmax, dlmean) and the Multiscale time ir

187 at all the saturated FAMEs lie on a straight diagonal line bisecting the separation plane, while the

188 le were completely isolated as spots off the diagonal line in the second dimension of PAGE.

189 A nominally best 30-probe set Diagonal Linear Discriminant Analysis classifier was sel

190 model, as well as standard methods including Diagonal Linear Discriminant Analysis, k-Nearest Neighbo

191 the shrunken centroids classifier and other diagonal linear discriminant type of models.

192 cation, part of Fig. 6B was distorted (extra diagonal lines appeared).

193 a phenomenon technically referred to as off-diagonal long-range order due to non-vanishing off-diago

194 form an antiparallel basket structure with a diagonal loop across one end), the LambdaLambda isomer b

195 a isomer is prevented from binding under the diagonal loop by the rigidity of the loop.

196 Several lateral and diagonal loop conformations have been found to be simila

197 The crystal structures show that the diagonal loop in this quadruplex results in a large cavi

198 he LambdaLambda isomer fits neatly under the diagonal loop, whereas the DeltaDelta isomer is unable t

199 table mini-hairpin motif inserted within the diagonal loop.

200 tures have lateral loops, in contrast to the diagonal loops reported for the analogous quadruplex wit

201 cate that lateral T3 loops are favoured over diagonal loops, in accordance with the experimental stru

202 differing in the relative orientation of the diagonal loops.

203 The proposed CIN and diagonal LPN connections contribute to speed-dependent g

204 from 30 to 330 GHz simultaneously along with diagonal magnetoresistance as a function of the magnetic

205 Shubnikov-de Haas (SdH) oscillations of the diagonal magnetoresistance.

206 Block-diagonal matrices F are the simplest examples; wavelet t

207 t 1070 nm, estimated to correspond to an off-diagonal matrix coupling element of 310 cm(-)(1).

208 are non-stoquastic, i.e., have positive off-diagonal matrix elements in a given basis, are known to

209 Diagonal maxillary/mandibular quadrants were probed with

210 l left anterior descending artery and distal diagonal (mdLAD + dD).

211 ubstrate-parallel spindle alignment of quasi-diagonal metaphase spindles in anaphase.

212 )1/2 amino acids to dock in the conventional diagonal mode on the mimotope-DR52c complex, the interfa

213 parately; in other test problems, such block diagonal models rigorously provide upper and lower bound

214 ing algorithm for longer 454 reads that uses diagonal multiple seed-match criteria, customized q-gram

215 legans body wall muscle and in male-specific diagonal muscles.

216 lt suggests a competing relationship between diagonal nematic and charge-density-wave order in HgBa(2

217 kable feature is that the enhancement of the diagonal nematicity with decreasing temperature is suppr

218 through-space coupling is found between the diagonal nitroxide radicals at the conformationally cons

219 olecules that feature by far the largest off-diagonal octopolar first hyperpolarizability tensor comp

220 uent intrachromosomal interactions along the diagonal of a chromatin contact map, we propose a comput

221 equences with that property can arise as the diagonal of a normal operator with spectrum X.

222 erty: If s(d) not equal 0, then d is not the diagonal of any such operator A.

223 Near the diagonal of Cu-O bond direction (nodal direction), we fo

224 es and devices striving to advance along the diagonal of Ragone plots, providing enhanced energy and

225 ogonal switch from one diagonal to the other diagonal of the square [2 x 2] network leading to a very

226 rystals in the <1 1 0> orientation along the diagonal of the square holes strongly indicates that the

227 130, 144, and 161 nm and octahedra with body diagonals of 113, 126, and 143 nm have been prepared, al

228 Au-Ag cubes with body diagonals of 130, 144, and 161 nm and octahedra with bod

229 are more favorable for ATP binding than two diagonal ones.

230 te to any atomic masa [Formula: see text] of diagonal operators with respect to an orthonormal basis

231 or pointed poles became trapped in either a diagonal or a parallel orientation.

232 Valpha4 29Y, arranged to impose the familiar diagonal orientation of TCR on MHC.

233 ssel orientation under static stretching and diagonal orientation under cyclic stretching, supported

234 i) TCRs that bind self-pMHC in the canonical diagonal orientation, but where there are structural def

235 and, both receptors bind ligand with similar diagonal orientations.

236 In the solid state, dimerization of one diagonal pair of nitroxides leads to a pinched cone conf

237 but only 4.1 cm +/- 0.3 of ablation without diagonal pairs (7.5 minutes +/- 1.0, P < .03 for both).

238 +/- 0.3 of ablation for 2.0-cm spacing with diagonal pairs but only 4.1 cm +/- 0.3 of ablation witho

239 mixing time dependence of the cross-peak and diagonal-peak signals to a magnetization exchange model,

240 The 2 diagonal peaks are the 0-1 transitions of the water-like

241 On a picosecond time scale, additional off-diagonal peaks grow in.

242 Whereas the strong diagonal peaks in the 2D rephasing spectrum of the FMO c

243 asured in real time by the appearance of off-diagonal peaks in the two-dimensional vibrational echo s

244 ling, free of the interference of the strong diagonal peaks that typically dominate 2D-IR spectroscop

245 ures of coupling are often obscured by broad diagonal peaks, especially in the visible regime.

246 -2 transition frequencies give rise to 2 off-diagonal peaks.

247 sted in the 2D spectrum by the growth of off-diagonal peaks.

248 itude, and line shape of the cross-peaks and diagonal peaks.

249 procal phase shift due to their non-zero off-diagonal permittivity tensor elements, and also possess

250 ic perturbations, adaptation to unpracticed, diagonal, perturbations happened along the previously le

251 these included an arborised cell junction, a diagonal-plane junction and an osteochondral interface.

252 genomes in Cluster I is barely detectable by diagonal plot analysis.

253 C-H...pi and hydrophobic interactions in the diagonal position of a beta-hairpin peptide through comp

254 nity periodontal index (CPI), and two random diagonal quadrants (1 and 3, 2 and 4).

255 int: 1) full-mouth (MB-B-DB/MB-B-DL); 2) two diagonal quadrants (six sites/MB-B-DB/MB-B-DL); 3) two r

256 Two diagonal quadrants protocol may be effective in identify

257 Two diagonal quadrants showed better accuracy; RT had the wo

258 ne or more rhenium atoms, with both edge and diagonal Re-Re interactions appearing prominently in PDF

259 t the HO parameter breaks local vertical and diagonal reflection symmetries at the uranium sites, res

260 alysis of peak patterns appearing in the off-diagonal region of the 2D-IR spectrum allows separation

261 d over a retention plane rather than along a diagonal, resulting in an orthogonal separation.

262 For the case of SH3, suppression of the diagonal results in facilitated identification of unambi

263 e structure of the FIM turns out to be block-diagonal, revealing hidden parameter dependencies and se

264 are-lattice cagelike structure reinforced by diagonal ridges.

265 th PTMs from MS/MS spectra: match scores and diagonal scores, as well as two spectral identification

266 ptimal molecular ordering for maximizing the diagonal second-order nonlinearity.

267 rent focal CNAs using the correlation matrix diagonal segmentation (CMDS) algorithm, which identified

268 Our approach, correlation matrix diagonal segmentation (CMDS), identifies RCNAs based on

269 matically reduces aliasing noise from strong diagonal signals, enabling the identification of weak NO

270 aks with intensities 100x less than those of diagonal signals.

271 couplings and observe dynamics, but the off-diagonal spectral signatures of coupling are often obscu

272 ale structure with LR asymmetry as parallel, diagonal stripes evenly spaced throughout the culture.

273 ntries in the matrix potentially belong to a diagonal structure, ii) cluster these entries into indiv

274 ory to show that the latter matrix has block-diagonal structure.

275 e, ii) cluster these entries into individual diagonal structures and iii) determine the neurons compo

276 ved, fully automated method which determines diagonal structures in the intersection matrix by a robu

277 Repeated SSEs are reflected in the matrix as diagonal structures of high overlap values.

278 owever, leaves the task of identifying these diagonal structures to visual inspection rather than to

279 ct anatomical guidelines, we report that the diagonal sulcus was present in 25% left and 20% right ch

280 use homonuclear (1)H-(1)H correlations with diagonal suppression and nonuniform sampling (NUS).

281 In addition, the diagonal suppression produces a spectrum with low dynami

282 similar topology characterized by a central, diagonal TCR binding mode that maximizes interactions wi

283 counted for with non-zero values for the off-diagonal terms of the Onsager matrix, at variance with c

284 organic semiconductors with substantial off-diagonal thermal disorder.

285 ke subunits are adjacent to (N1/N1/N2/N2) or diagonal to (N1/N2/N1/N2) one another-remains unclear.

286 h subunits of like conformations (e.g., A/C) diagonal to one another.

287 Its location is nearly diagonal to the helical axis of the template-primer.

288 one, involving an orthogonal switch from one diagonal to the other diagonal of the square [2 x 2] net

289 Although the vanishing of the gap along the diagonal to the square Cu-O bond directions is robust, t

290 on doping, long-lived excitations along the diagonals to the Cu-O bonds, and an energy gap at the Br

291 We report the dependence of the diagonal-to-cross-peak ratio on concentration, light int

292 The cleavage is thus represented by a diagonal trajectory across a free energy surface, that i

293 y ratio data from all samples and adopting a diagonal transformation strategy, CMDS substantially red

294 Folding of the peptide with a diagonal Trp...Lys interaction was found to be enthalpic

295 alpically driven, whereas the peptide with a diagonal Trp...Nle interaction displayed cold denaturati

296 , dynamical control over site-energy and off-diagonal tunnelling disorder has been lacking.

297 perty, known as kinetic stability, we used a diagonal two-dimensional sodium dodecyl sulfate-polyacry

298 subjects using achromatic Gabor stimuli in 4 diagonal visual field locations at 10 degrees eccentrici

299 nce matrix in the former is restricted to be diagonal while in the latter there is barely any restric

300 uses a channel with repeated ridges that are diagonal with respect to the direction of cell flow.