ライフサイエンスコーパス: tilt angle

1 of self-assembled structures via control of tilt angle.

2 deuterium order parameters, and cholesterol tilt angle.

3 , and the surfactant protein B peptide helix tilt angle.

4 rom homeotropic alignment to an intermediate tilt angle.

5 al age, appendiceal base location, and cecal tilt angle.

6 onds to hydrophobic mismatch by changing its tilt angle.

7 M, with molecules characterized by a smaller tilt angle.

8 ctral power decreased progressively with the tilt angle.

9 ncreased directly and significantly with the tilt angle.

10 eter and the increase in the average helical tilt angle.

11 coiling, and skewing patterns with substrate tilt angle.

12 hastic load profile and solar module optimal tilt angle.

13 ility depends directly on the Earth's dipole tilt angle.

14 ext] to [Formula: see text], with increasing tilt angle.

15 factors associated with the ON head vertical tilt angle.

16 good proxy measure for the vertical ON head tilt angle.

17 e DOPC lipid, by lowering of the hydrocarbon tilt angles.

18 w-frequency cross-spectra, decreased at high tilt angles.

19 qually in expiration and inspiration at high tilt angles.

20 ut there is a decided preference for smaller tilt angles.

21 s negligible or significantly reduced across tilt angles.

22 xcessive beam broadening occurring at higher tilt angles.

23 adiation, and (iii) steeper-than-usual panel tilt angles.

24 tein particles in different orientations and tilted angles.

25 ects of temperature on area per chain Ac and tilt angle 0, the area expansivity alpha A is quite smal

26 20 degrees, resulting in a mean value of the tilt angle 23 degrees < or = theta(0) < or = 37 degrees.

27 ns safety trade-offs by limiting the maximum tilt angle achievable before loss of stability.

28 The sterol possessed a tilt angle alpha(0) = 24 degrees +/- 1 degrees in 22:6-2

29 olubility chi(NMR)(chol) = 17 +/- 2 mol% and tilt angle alpha(0) = 25 +/- 1 degrees in 20:4-20:4PC we

30 m(-1)) porphyrin modes indicates the average tilt angle (alpha) of the porphyrin ring with respect to

31 -helices and their orientation is given by a tilt angle and an azimuthal rotation angle around the ma

32 The chain tilt angle and an estimate of the methylene electron den

33 stribution was used to recover the mean heme tilt angle and angular distribution about the mean, whic

34 The modulation scheme utilizes the tilt angle and axial ratio (AR) of a wireless signal to

35 Whether the agreement is better at the known tilt angle and axis of the microscope or its inverse ind

36 e identification of the known values for the tilt angle and axis, can be used as targets for rapidly

37 ns is determined for all possible choices of tilt angle and axis.

38 Furthermore, this work indicates that the tilt angle and conformation of transmembrane portions of

39 Analysis of the tilt angle and film thickness data shows a significant m

40 lying basis for the relationship of vertical tilt angle and glaucoma severity should be further explo

41 Remarkably, the tilt angle and one of the two rotation angles are identi

42 er model is then constructed using the helix tilt angle and several interhelical distances previously

43 Large BMO tilt angle and thin PCT are characteristics of highly my

44 The algorithm can also be used to refine the tilt angles and further improve the 3D reconstruction.

45 per lipid, the bilayer height, and the chain tilt angles and has important consequences for other bil

46 ane orientations with small non-zero average tilt angles and moderate to high dynamic averaging in bi

47 der samples can be analyzed to yield precise tilt angles and rotation angles of the helices.

48 radient (created by visual gradient and bike tilt angle) and actual workload (pedalling resistance) c

49 application of total horizontal derivative, tilt angle, and a combination of filters in ternary imag

50 orm in hydrogen bond geometry, peptide plane tilt angle, and backbone torsion angles.

51 performed to design optimum device geometry, tilt angle, and cell throughput that is more than 20 tim

52 ereas the dipole variability, average dipole tilt angle, and frequency of polarity reversals increase

53 ral joint alignment (bisect offset, patellar tilt angle, and Insall-Salvati ratio), trochlear morphol

54 trained by the predicted membrane height and tilt angle, and model scoring accounting for the energy

55 ior helices (the pitch, the hole radius, the tilt angle, and the number of turns) yield the largest f

56 ., the ratio of perceived tilt to equivalent tilt angle, and the ratio of perceived translation to eq

57 placements of lipids and nanoparticle, chain tilt angle, and the surfactant protein B peptide helix t

58 evals from rover wheel turns, suspension and tilt angles, and overlapping images.

59 onnected with a vertical arm at a 45 degrees tilted angle, and a rectangular shape is incorporated in

60 ned nearly parallel to the membrane surface (tilt angle approximately 77 degrees ) and is characteriz

61 Only with such a large tilt angle are the hydrophilic residues aligned to the c

62 ons, minor groove widths, buckle, twist, and tilt angles are observed between bound and unbound kappa

63 When the tilting angles are arbitrary, the grain boundaries form

64 ne residues, thereby decreasing the roll and tilt angles at the ApA step by approximately 8 degrees a

65 OA, as well as a lower valgus (tibial medial tilt) angle at address for those classified to be at hig

66 ng various patterns or slide off at designed tilting angles at specified positions on a superhydropho

67 icular to the monolayer, the predicted final tilt angles average 54 degrees approximately 62 degrees

68 Data analysis yielded the helix tilt angle beta=31.6(+/-6.2) degrees and the rotational

69 together with the known changes in the helix tilt angle between high and low pH, push the imidazole a

70 lly as a conformational change affecting the tilt angle between the heme plane and the proximal histi

71 imer conformations in which the stacking and tilt angles between planar iCy3 monomers are varied.

72 be the pore size, pore angle, mesh rotation, tilt angle (branch droop) and layering (branch overlap).

73 ly during expiration than inspiration at low tilt angles, but occurred equally in expiration and insp

74 nd unique biological object from a series of tilted angles, but it is challenging to image a single p

75 al segment N-terminal to G34 to increase its tilt angle by 3 degrees , and the G34-I35 torsion angles

76 tion, the transmembrane helices increase the tilt angle by 6 degrees and the average pore diameter en

77 omogeneous suspension of cells at a specific tilt angle by taking advantage of the gradual change in

78 d continuation, total horizontal derivative, Tilt angle, Centre for Exploration Targeting (CET) analy

79 516W mutations that reverse dimerization and tilt angle changes induced by the W515K and W515L mutati

80 phatidylglycerol (POPG), as expected, with a tilt angle close to 90 degrees .

81 intercalation site, such bases would have a tilt angle closer to that of A-DNA (20 degrees) than to

82 omain of the active W515K mutant has a helix tilt angle closer to the bilayer normal than that of the

83 Mediolateral and anteroposterior tilt angle, degree of perforation, and dwell time were h

84 initio transport calculations shows that the tilt-angle dependence of the electrical conductance is a

85 Analysis of the tilt-angle dependency of the intensities associated with

86 The tilt angle difference between the monomer and pentamer i

87 Conversely, peptides exhibiting larger tilt angles display more narrow distributions of tilt an

88 he peptide bundle, the width of the bundle's tilt angle distribution should be sigma < or = 20 degree

89 Fibril tilt-angle distribution was investigated by combining th

90 we show for the first time that the pyrazine tilt angle does not play a role in determining the stren

91 same packing area, the value of the overall tilt angle does not seem to be sensitive to whether the

92 cy towards water and oils with extremely low tilt angles due to the smooth liquid-liquid contact betw

93 s cryo-EM practitioners to define an optimal tilt angle during data acquisition.

94 ncorporates angular refinement to reduce the tilt angle error.

95 offers low contact angle hysteresis and low tilt angle for water droplet shedding.

96 PS with low contact angle hysteresis and low tilt angle for water shedding by coating the equal-volum

97 es electrostatic repulsion, yielding optimum tilt angles for packing of approximately 40-60 degrees a

98 The calculated tilt angles for PGLa are in excellent agreement with rec

99 arrays with uniform, continuous and extreme tilt angles for real-time manipulation are reported.

100 s of density in the map are used to estimate tilt angles for the seven helices.

101 nalysis on data collected at different stage tilt angles for three-dimensional reconstruction and str

102 C-POPC-DMPC) led to an increase in the helix tilt angle from 10 degrees to 30 degrees with respect to

103 induced a decrease in the average acyl chain tilt angle from 35 degrees to 28 degrees.

104 from unstained, frozen hydrated specimens at tilt angles from 0 degrees to 60 degrees.

105 The NEXAFS-derived phenylalanine tilt angles have been verified with sum frequency genera

106 CT appearance of tip embedding, increased tilt angle, higher-grade perforation, and longer dwell t

107 lations of Tb-MscL as a function of TM helix tilt angle in a dimyristoylphosphatidylcholine bilayer.

108 raction (GIXD), a strong change in molecular tilt angle in a monolayer of P2TP, depending on whether

109 The difference in tilt angle in C14 and C16 bilayer environments is also c

110 Preretrieval CT images were evaluated for tilt angle in mediolateral and anteroposterior direction

111 atistically significant correlation with the tilt angle in multivariate analyses (P = .044 for axial

112 Furthermore, by introducing a uniform tilt angle in the unit cells breaks the spatial symmetry

113 The Pf1 helix tilt angles in bilayers composed of two different lipids

114 be localized directly to changes in roll and tilt angles in the ApA base-pair step involved in intera

115 Due to the limited tilt angles in the electron microscope, the tomographic

116 However, the tilt angle increased systematically with increasing posi

117 atterns collected from a single crystal with tilt angle increment of 0.1-1 degrees and a total accumu

118 we exhibit a striking size dependence in the tilt angle interval for the vanishing of the [Formula: s

119 ceptors of the ionized PA headgroup, and the tilt angle is affected by the interactions of Tyr-7 and

120 der a positive mismatch; 4), the minimum-PMF tilt angle is generally located where there is the hydro

121 The chain tilt angle is measured to be 32.3 +/- 0.6 degrees near f

122 ine bond is unusually long and a substantial tilt angle is observed between the heme and imidazole pl

123 The tilt angle is readily visualized and has been found to b

124 The cecal tilt angle is useful for localizing the appendix in preg

125 n-heptane droplets to bounce and roll-off at tilt angles </= 2 degrees .

126 splay water contact angles >160 degrees with tilt angles <2 degrees .

127 hexadecane contact angles >150 degrees with tilt angles <5 degrees , whilst the superhydrophobic coa

128 The heme tilt angles measured experimentally are in close agreeme

129 strated only a moderate correlation with the tilt angle measurements and hence is not a good proxy me

130 Mean leaf tilt angle (MTA) and canopy height were found to be the

131 ximately the same PIP(2)-triggered change in tilt angle observed by EPR.

132 ecular dynamics simulations, which predict a tilt angle of 13.3 degrees (SA in POPC), 16.4 degrees (S

133 A tilt angle of 15 +/- 1 degrees was measured when equimol

134 the hydrophobic domain of each peptide has a tilt angle of 15 +/- 3 degrees in POPC, whereas in DMPC,

135 A tilt angle of 18 degrees was observed in 18:1-O-PC/DOPG

136 The data correspond to an average helix tilt angle of 25 degrees in PH75 vs 16 degrees in fd, Pf

137 hat the helices are oriented with an average tilt angle of 27 degrees from the bilayer normal.

138 elical conformation, with a computed average tilt angle of 28 +/- 6 degrees and azymuthal angles of 6

139 An average tilt angle of 33 degrees for the helices was found with

140 peptide in phospholipid bilayers revealed a tilt angle of 40 degrees and two possible rotation angle

141 -phosphatidyl-choline (POPC) bilayers with a tilt angle of 65 degrees +/- 15 degrees.

142 As the tilt angle of a helix is dominated by hydrophobic mismat

143 Moreover, the tilt angle of an assumed helical portion of the peptide

144 a transmembrane helix in M2 protein having a tilt angle of approximate 25 degrees, quantitatively sim

145 l configuration, crossing the bilayer with a tilt angle of approximately 11 degrees with respect to t

146 nsemble of all-trans-conformer chains with a tilt angle of approximately 14-18 degrees with respect t

147 residues 31-52) traverses the bilayer with a tilt angle of approximately 24 degrees .

148 The proposed orientation features a heme tilt angle of approximately 35-40 degrees with respect t

149 approximately 10 A from the cobalt and at a tilt angle of approximately 70 degrees to the normal of

150 d into the plane of the lipid bilayer with a tilt angle of approximately 80 degrees from the membrane

151 nd H2 ranges from 35 to 69 degrees , and the tilt angle of Cav182-136 is 27 +/- 6 degrees .

152 The average tilt angle of cholesterol with respect to bilayer normal

153 F19, F23 has improved the calculation of the tilt angle of membrane proteins for 90% of WALP peptides

154 (P < .0001), with an odds ratio of 33 with a tilt angle of more than 15 degrees in any direction (P <

155 nd -3 adopt perfect in-plane alignments, the tilt angle of phylloseptin-1 deviates by 8 degrees proba

156 MR in oriented DMPC bilayers yielded a helix tilt angle of tau = 14 degrees , a high order parameter

157 e material resulting from a variation in the tilt angle of the 1,2-bis(4-pyridyl)ethylene pillars.

158 that a change that substantially alters the tilt angle of the alkyl chain (and, therefore, the thick

159 ich provides the force required to alter the tilt angle of the body necessary to break the surface te

160 ches, we estimate a approximately 36 degrees tilt angle of the chromophore to the membrane normal.

161 s direction, the spinterface "size", and the tilt angle of the detector with respect to the surface.

162 rees and 61 degrees, respectively, while the tilt angle of the entire rotaxane is psi = 41 degrees an

163 The connector group determines the tilt angle of the Fc unit which in turn affects the pack

164 circular dichroism were used to measure the tilt angle of the helical segments in macroscopically al

165 gle is, to a large extent, determined by the tilt angle of the individual helices.

166 The data show that the tilt angle of the M2TMP helices depends on the membrane

167 s precise control of the contact spacing and tilt angle of the molecule.

168 arated-local-field experiments show that the tilt angle of the peptide is 80 +/- 5 degrees , in agree

169 hydrophobic thickness of the bilayer, on the tilt angle of the peptides was investigated using thicke

170 The mean tilt angle of the protein's zinc-substituted porphyrin w

171 Although the tilt angle of the ring decreases with decreasing surface

172 d to both the distance between rings and the tilt angle of the rings with respect to the microtubule

173 reases with decreasing surface coverage, the tilt angle of the rotaxane has a maximum at 144 A(2)/mol

174 The tilt angle of the TCR EC domain is both coupled to a rot

175 ate orthologs unresponsive to Vpu change the tilt angle of the TMD in the lipid bilayer without abrog

176 ipid bilayers, indicating that the change in tilt angle of the trans-membrane helix is a principal co

177 t in DOPC/DOPE mixed lipid bilayers reveal a tilt angle of the transmembrane domain with respect to t

178 processing in general, for which the optimal tilt angle of the tube is typically 45 degrees .

179 Switching the tilt angle of this bundle is essentially equivalent to s

180 old surface, ellipsometry and PM IRRAS yield tilt angles of 29 +/- 4 degrees (monolayers of type A) a

181 Tilt angles of 30 degrees and 21 degrees are observed in

182 ture (NEXAFS) spectroscopy yielded molecular tilt angles of 33-43 degrees .

183 a-helices of TMDs two and five oriented with tilt angles of 34 degrees and 32 degrees, respectively,

184 s of the same particle field recorded at two tilt angles of a single tilt-axis specimen holder togeth

185 Regardless of gestational age, cecal tilt angles of at least 90 degrees were predictive of a

186 l properties, we examined the helix lengths, tilt angles of individual helices and the entire bundle,

187 ane contact angles exceeding 155 degrees and tilt angles of less than 4 degrees .

188 +) ring, which is reflected in the segmental tilt angles of the mpTTF and DNP units.

189 nal data points for evaluating the segmental tilt angles of the two halves of the peptide, we substit

190 s the number of conformers is increased, the tilt angles of WALP23 ensemble structures become larger

191 ft-handed tilt of TM3 relative to TM2 with a tilting angle of 44 +/- 2 degrees between TM2 (V1-Q14) a

192 setup was further utilized to determine the tilting angle of the microtubules buried in agarose gel

193 helices, and shifted the lateral and radial tilting angles of TM2 toward a closed-channel conformati

194 firming the observed dependence of the helix tilt angle on bilayer thickness.

195 and mean deviation were correlated with the tilt angle (P = .002, P = .011, and P = .013, respective

196 pth, lateral trochlear inclination, patellar tilt angle, patellar height ratio, distance between pate

197 gamma, are more informative than an average tilt angle [phi].

198 increases the optical bandgap, while Pb-I-Pb tilting angles play a secondary role.

199 oscope images recorded at different specimen tilt angles provides a powerful approach for evaluating

200 le cluster around the expected tilt axis and tilt angle, provides confidence in a structure determine

201 fast alignment at a low SNR (SNR=0.003) with tilt angle range +/-60( ) or +/-40( ).

202 We experimentally show uniform tilt angles ranging from 0 degrees to 57 degrees , and d

203 to half the change in eye position, giving a tilt angle ratio (TAR) of 0.5.

204 eye position was evaluated by computing the tilt angle ratio (TAR), the ratio of change in VOR axis

205 of the TpoR TM helix by increasing the helix tilt angle relative to the membrane bilayer normal, whic

206 hly variable in its orientation by attaining tilt angles relative to the membrane normal that range f

207 g geometries exhibit significantly different tilt angles relative to the plane of the membrane, presu

208 within < 10 min at 70 degrees and 60 degrees tilt angles, respectively.

209 of colloidal zeolite LTA superball (ZAS) by tilted-angle sedimentation forms macroscopic films with

210 Cecal tilt angles showed moderate correlation with appendiceal

211 te correlation between the ovality index and tilt angle (Spearman rho = 0.351; P < .001).

212 work, we introduce a unique configuration of tilted-angle standing surface acoustic waves (taSSAW), w

213 Our method uses tilted-angle standing surface acoustic waves.

214 The intrinsically small apparent tilt angles suggest that interactions of aromatic residu

215 l within a similar narrow range of twist and tilt angles, suggesting that Gbeta1gamma2 may bind to Ga

216 er is used, the resulting helix orientation (tilt angle (tau) of 5.6 +/- 3.2 degrees and rotation ang

217 rse guest residues adopt a range of apparent tilt angles that span 5 degrees -35 degrees in lipid bil

218 layers that is consistent with a decrease in tilt angle theta and with little change in water spacing

219 loidal interactions, by tuning the preferred tilt angle (theta(e)).

220 troduce the SuperBiHelix method in which the tilt angles (theta, varphi) are optimized simultaneously

221 It is found that the average tilt angle, theta, between the pVIII alpha-helix and the

222 performed to assess the ability of the cecal tilt angle to help differentiate between a high and low

223 e low-temperature lipid gel phase versus the tilt angle to the magnetic field.

224 The water molecule and the square ice have tilted angles towards the silicene nanodot plane at ~ 70

225 mean force (PMFs) as a function of TM helix tilt angle under various mismatch conditions.

226 imaging condition to measure TiO6 octahedral tilt angles, unit-cell-by-unit-cell, in perovskite-based

227 iffraction amplitudes to 8 A resolution with tilt angles up to 30 degrees.

228 urface area and, combined with steeper panel tilt angles, up to 50% of the winter deficit in electric

229 The median (IQR) tilt angle was 3.5 (1.2-11.2) degrees.

230 gle-shot fast spin-echo MR images, the cecal tilt angle was calculated as the angle between the imagi

231 The vertical tilt angle was measured on high-resolution cross-section

232 The values of maximum tilt angles were similar, with possible implication of c

233 nverse cosine function of the magnetic field tilt angles, which demonstrates the two-dimensional natu

234 ilament sliding, cross-bridges cannot change tilt angle while attached nor reach other target zones w

235 rection of the pressure gradient increase in tilt angle while those on the opposite side form gauche-

236 evidenced by a larger area per molecule and tilt angle with concomitant thinning of the monolayer.

237 ew method for measuring the ON head vertical tilt angle with high-resolution SDOCT imaging.

238 to insert in the bilayer and estimate their tilt angle with respect to the bilayer normal.

239 and the calculated hydrophobic thickness or tilt angle with respect to the bilayer normal.

240 ed of lateral motion of actin bundles, their tilt angle with respect to the direction of retrograde f

241 The average tilt angle with respect to the surface normal for the va

242 The correlation between the vertical tilt angle with the ovality index and the potential asso

243 l fragments having 20 degrees and 31 degrees tilt angles with respect to the membrane normal.

244 ins in Ste2p assume different structures and tilt angles within a membrane multilayer.