ライフサイエンスコーパス: tilt angle

1 deuterium order parameters, and cholesterol tilt angle.

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

3 rom homeotropic alignment to an intermediate tilt angle.

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

5 onds to hydrophobic mismatch by changing its tilt angle.

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

7 ctral power decreased progressively with the tilt angle.

8 ncreased directly and significantly with the tilt angle.

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

10 factors associated with the ON head vertical tilt angle.

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

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

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

14 qually in expiration and inspiration at high tilt angles.

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

16 xcessive beam broadening occurring at higher tilt angles.

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

18 20 degrees, resulting in a mean value of the tilt angle 23 degrees < or = theta(0) < or = 37 degrees.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

56 516W mutations that reverse dimerization and tilt angle changes induced by the W515K and W515L mutati

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

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

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

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

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

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

63 The tilt angle difference between the monomer and pentamer i

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

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

66 Fibril tilt-angle distribution was investigated by combining th

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

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

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

70 ncorporates angular refinement to reduce the tilt angle error.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

88 However, the tilt angle increased systematically with increasing posi

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

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

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

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

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

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

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

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

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

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

99 The heme tilt angles measured experimentally are in close agreeme

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

171 Cecal tilt angles showed moderate correlation with appendiceal

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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