ライフサイエンスコーパス: torsion

1 ethod in the diagnosis of partial testicular torsion.

2 T mutant embryos that shows left-handed body torsion.

3 radiologically mimicing traumatic testicular torsion.

4 cause misdiagnoses, such as inflammation or torsion.

5 greater omentum leading to secondary omental torsion.

6 rther insights of layered materials by using torsion.

7 nal wall leading to these lesions suggesting torsion.

8 al treatment, required in case of testicular torsion.

9 ized on the basis of differences in backbone torsion.

10 bnormal muscle contractions and cause embryo torsion.

11 . On Whitehead torsion. 8. A few lines on L2-torsion.

12 urgery to either treat pattern strabismus or torsion.

13 al features, binocular alignment, and fundus torsion.

14 mus developed after transposition to address torsion.

15 portional limit under pure shear stresses of torsion.

16 coming increasingly popular among studies on torsion.

17 ers are efficiently retained irrespective of torsion.

18 iac muscle twitch relaxation and ventricular torsion.

19 ch is accompanied by an increase in backbone torsion.

20 motions including contraction, bending, and torsion.

21 n group were recoverable after four hours of torsion.

22 xamination was performed after four hours of torsion.

23 tions include induced vertical deviation and torsion.

24 ontractions that prevent the accumulation of torsion.

25 the early diagnosis of incomplete testicular torsion.

26 C) in the diagnosis of incomplete testicular torsion.

27 s are coupled with a worsening in strain and torsion.

28 tho or para position could slow down the tau torsion.

29 ted and 2 patients with bilateral testicular torsion.

30 andatory to prevent threatening mass pedicle torsion.

31 wo patients (38%) had a diagnosis of adnexal torsion.

32 alization of the graft insured against graft-torsion (0%) despite a transperitoneal approach to graft

33 igher torsion indices (adjusted estimate for torsion, 0.33+/-0.04 degrees (SE)/decade; P<0.001).

34 ection) (34 of 114 responses [29.8%]), globe torsion (20 [17.5%]) leading primarily to inadvertent op

35 ratio (1.3+/-0.5 versus 1.4+/-0.5; P=0.66), torsion (7.6+/-1.7 versus 8.0 degrees +/-2.1 degrees ; P

36 f communication was highest in acute scrotal torsion (70.6%) and ectopic pregnancy (65.4%) and lowest

37 ison and other determinants. 7. On Whitehead torsion. 8. A few lines on L2-torsion.

38 In the case of pure torsion, a competition between MAP tau tensile and MT be

39 were held near parity and only the geometric torsion about a xylyl- or phenylthiophene bridge was var

40 operating reversibly by a coupled tension-to-torsion actuation mechanism.

41 e during replication elongation to dissipate torsion ahead of the forks.

42 d four different dsDNA substrates containing torsion-ally constrained or relaxed strands.

43 olydiacetylenes can be strongly modulated by torsions along the polymer chains.

44 able secondary structure with abnormally low torsion and bending elastic constants that prevails afte

45 MRI measurements revealed reductions in LV torsion and circumferential strain, as well reduced circ

46 We present a case of wandering spleen with torsion and complete infarction that occurred in a 32-ye

47 mmon however acute presentation with omental torsion and infarction is an unusual entity.

48 ondition which if uncorrected, can result in torsion and infarction.

49 n with peritoneal fold is necessary to avoid torsion and related graft loss.

50 uences IVS and LV geometry, which impairs LV torsion and segmental LS and CS, more for the IVS than f

51 ierarchical nanotwinned structure during pre-torsion and subsequent tensile deformation.

52 and ductility retention, and how sequential torsion and tension lead to the observed hierarchical na

53 Simultaneous application of torsion and tension on MT bundles is shown to accelerate

54 hlear nerve palsy by the direction of ocular torsion and the change in the degree of vertical deviati

55 tely diagnosed from the nature of the ocular torsion and the vertical deviation, along with the prese

56 mponents of the ocular tilt reaction, ocular torsion and tilt of subjective visual vertical, seem to

57 ening and early diastolic strain rate and LV torsion and torsional recoil rate were determined using

58 ositions strongly modulates polymer backbone torsion and, therefore, intramolecular pi-conjugation an

59 dynamics simulations showed that low-energy torsions and displacements of the peptides enabled the a

60 hstand mechanical forces, including tension, torsion, and compression.

61 hanics from measures of deformation: strain, torsion, and dyssynchrony.

62 duced circumferential shortening, reduced LV torsion, and reduced ejection fraction.

63 Left ventricular ejection fraction, cardiac torsion, and strain were significantly lower in the pati

64 essed by left ventricular ejection fraction, torsion, and strain.

65 o which they are exposed (e.g., compression, torsion, and stretch).

66 tion to address pattern strabismus may cause torsion, and transposition to address torsion may cause

67 orsion angles, with a 15 degrees increase in torsion angle (148 degrees to 163 degrees ) observed to

68 ure features, including secondary structure, torsion angle and solvation, are predicted by single-seq

69 prediction of secondary structure, backbone torsion angle and solvent accessible surface area.

70 The torsion angle between the carbonyl and naphthalene is 26

71 In the 1,2-Me,Ph substitution motif the torsion angle C(Me)-C-C-C(i) determines the length of th

72 For example, a small change in one torsion angle can radically change the behavior of the w

73 , we show that internal friction arises when torsion angle changes are an important part of the foldi

74 tability by orienting and partially freezing torsion angle chi of the 6'F-bcT nucleoside.

75 by the change in stripe direction, while the torsion angle defined by each segment of three helices i

76 n addition, clustering analysis based on the torsion angle distribution can be performed to obtain th

77 a glycan search is complete, each glycosidic torsion angle distribution is displayed in terms of the

78 et process mixture density estimation of the torsion angle distributions and (ii) kernel density esti

79 predicted relative solvent accessibility and torsion angle information improves the accuracy of profi

80 -containing protein, is the insensitivity of torsion angle isomerization to solvent friction.

81 Backbone torsion angle measurements indicate that the basic struc

82 ence, which is partially validated by direct torsion angle measurements of selected loop residues, su

83 Using the correlation in torsion angle movements calculated from microseconds-lon

84 monolayer indicated that the global average torsion angle of a monolayer was gradually shifted.

85 Gradual and reversible tuning of the torsion angle of an amphiphilic chiral binaphthyl, from

86 adduct 1(*) in the crystalline state shows a torsion angle of approximately 90 degrees between the ph

87 estigated to obtain tolanophanes, fixing the torsion angle of the two phenyl rings.

88 impact of factors other than the intervening torsion angle on (3)J will be minimal, making these coup

89 on of a single geometric variable, such as a torsion angle or interresidue distance, can select for o

90 Boltzmann machine (DReRBM) since the protein torsion angle prediction is a sequence related problem.

91 ve resulted in 111 quantitative distance and torsion angle restraints (10 per residue) that describe

92 ophene rings results in a restriction on the torsion angle space available to these molecules when bo

93 t the constraint creates a closed surface in torsion angle space.

94 ns are functions of the intervening backbone torsion angle varphi.

95 ely, values that correlate with the backbone torsion angle varphi.

96 x vicinal J-couplings sensitive to the C2-N2 torsion angle were parametrized: (3)J(H2,NH), (3)J(H2,CO

97 mmodated by single-sequence based solvation, torsion angle, and secondary structure predictions.

98 e anti orientation about the pseudo-glycosyl torsion angle, which mimics precisely the mutagenic arra

99 We show that optimized torsion-angle normal modes reproduce protein conformatio

100 rthogonalizing the displacement vectors from torsion-angle normal-mode analysis and projecting them a

101 o our knowledge is a new method of optimized torsion-angle normal-mode analysis, in which the normal

102 long C(Me)-C(i) and C(Me)-C(o) distances for torsion angles >80 degrees do not allow a CH/pi interact

103 e integrate predicted solvent accessibility, torsion angles and evolutionary residue coupling informa

104 mpounds are almost planar (the corresponding torsion angles are below 7 degrees ).

105 For aromatic compounds these torsion angles are close to 0 degrees , but in five- and

106 l compounds have twisted configurations with torsion angles between the pyrene unit and the 2,3-diaza

107 This behavior is related to the torsion angles between the two ligands.

108 d that in the complex the glycosidic linkage torsion angles between the two reducing-end mannoses are

109 appropriately discretized/coarse-grained MD torsion angles data in a polypeptide is given by the cau

110 ructure.org, is a database of the glycosidic torsion angles derived from the glycan structures in the

111 contact number and the error distribution of torsion angles extracted from sequence fragments are use

112 contact number and the error distribution of torsion angles extracted from sequence fragments) are us

113 ts, scanning through backbone and side chain torsion angles for a model peptidomimetic.

114 of bond lengths and valence angles with XRD torsion angles held constant.

115 crystal structures revealed tether-specific torsion angles in the solid state.

116 such as predicted solvent accessibility and torsion angles into the profile-profile alignment is a u

117 htly puckered (quasi-boat conformation, with torsion angles of 5.9 degrees for C4N and 4.8 degrees fo

118 he 12-helical conformation; average backbone torsion angles of beta-residues and helical parameters a

119 to as a glycan, can be characterized by the torsion angles of glycosidic linkages between relatively

120 trated by the effect of modifications to the torsion angles of I, L, D, N.

121 nfirm the highly mobile nature of the chi(4) torsion angles of lysine side chains seen in the MD simu

122 s were observed for the beta, gamma, and chi torsion angles of the S-cdG nucleoside.

123 chain shapes is more important than that of torsion angles or of overall structural similarities in

124 the carbonyl of hyp distorts the main-chain torsion angles that typically accompany a C(gamma)-endo

125 ased minimization of backbone and side-chain torsion angles to design low-energy interfaces between t

126 Universally, for torsion angles up to 80 degrees CH/pi bonds were found,

127 ng compounds and in open-chain compounds the torsion angles vary considerably.

128 Conformational restrictions of flexible torsion angles were used to guide the identification of

129 Without constraints (e.g., imposed torsion angles), the theoretical and experimental data a

130 nd geometrical features, analyze bending and torsion angles, and determine distinct knowledge-based p

131 assignments reveal a difference in the helix torsion angles, as predicted by TALOS+, for the key resi

132 nformative features to guide its alignments: torsion angles, backbone Calpha atom positions, secondar

133 rmolecular contacts, backbone and side-chain torsion angles, relaxation measurements, and calculation

134 delta)-H/C(gamma)-O and C(beta)-H/C(gamma)-O torsion angles, with a 15 degrees increase in torsion an

135 , partial unfolding, bending, and side-chain torsion angles.

136 veraging, with essentially uncoupled phi/psi torsion angles.

137 nts including dipolar couplings and backbone torsion angles.

138 ituent effects which tune the intramolecular torsion angles.

139 is a valuable method for predicting protein torsion angles.

140 ep learning architectures to predict protein torsion angles.

141 thynylphenylene rotators can explore various torsion angles; this allows the BEPEB fluorophore dynami

142 tion methods (e.g, tension, compression, and torsion) are used on bulk samples of SMAs to determine t

143 mechanical behavior of MT bundles under pure torsion as well as a combination of torsional and tensil

144 bond lengths, bond angles, and peptide bond torsions, as well as ignoring molecular interactions to

145 uent tension tests performed parallel to the torsion axis.

146 (B=0.01; P=0.03) in women only and lower LV torsion (B=0.005; P=0.03) and lower LV ejection fraction

147 The molecular torsion balance concept was applied to a new conformatio

148 A new variant of the Wilcox molecular torsion balance featuring a naphthyl-alkyl side arm was

149 combined with an optical microprotractor and torsion balance using highly birefringent microspheres t

150 A molecular torsion balance was designed to study and measure OH-pi

151 he dibenzodiazocine hinge of the traditional torsion balance, the (ortho-tolyl)amide unit offers rest

152 mational equilibrium of the Wilcox molecular torsion balance.

153 By using synthetic molecular torsion balances and a simple explicit solvation model,

154 A new series of molecular torsion balances were designed to measure the strength o

155 Here, molecular torsion balances were used to compare cohesive alkyl and

156 ested by simulation is the crossing of local torsion barriers.

157 Negative torsion behind the polymerase induces DNA strand separat

158 As a result, much smaller torsions between the NN and thiophene units ( approximat

159 Omental cyst and omental torsion both are uncommon but important causes of acute

160 tional strategy employs conjoined rigid body/torsion/Cartesian simulated annealing, and incorporates

161 V) magnitude and rates of LV wall strain and torsion compared with wild-type (WT) mice.

162 It is further shown that high-pressure torsion could prompt atoms to possess lower five-fold sy

163 allows for changes in ligand rigid-body and torsion degrees of freedom.

164 cant improvement compared with placebo in LV torsion (Deltatheta: sildenafil, -3.89 +/- 3.11 degrees

165 ra possess similar resistance to bending and torsion despite their different morphologies.

166 nts were identified by the review, 5 in whom torsion developed because of transposition to address pa

167 earning methods to improve the prediction of torsion (dihedral) angles of proteins.

168 Ocular torsion does not correlate with and thus cannot account

169 By finely designing the curvature and torsion, double-stranded DNA knots were accessed by hybr

170 A new device for the assessment of dynamic torsion during ocular counter roll response using after-

171 , and probably contributes to noncommutative torsion during the VOR.

172 Adult onset primary torsion dystonia (AOPTD) is a poorly penetrant autosomal

173 DYT1 early-onset generalized torsion dystonia (DYT1 dystonia) is an inherited movemen

174 lope, with a mutant form causing early onset torsion dystonia (DYT1).

175 Early-onset torsion dystonia (EOTD) is a neurological disorder chara

176 Only three genes for primary torsion dystonia (PTD), TOR1A (DYT1), THAP1 (DYT6) and C

177 Only three genes for primary torsion dystonia (PTD), TOR1A (DYT1), THAP1 (DYT6) and C

178 Early-onset torsion dystonia is the most severe heritable form of dy

179 P1 gene were recently shown to underlie DYT6 torsion dystonia.

180 mouse models of early-onset DYT1 generalized torsion dystonia; however, the relationship between the

181 secondary structure with an anomalously low torsion elastic constant commonly prevails.

182 Extravaginal testicular torsion (ETT), also called prenatal or perinatal, occurs

183 y, shear viscosities measured in high-strain torsion experiments are 15 times smaller than normal vis

184 ere we present results from laboratory-based torsion experiments on olivine aggregates with and witho

185 isalignment) and pulley heterotopy or static torsion (for "A" patterns) likely do not play a major ro

186 f this long sought-after regime as a planar, torsion-free backbone conformation that is surprisingly

187 Our results indicate that positive torsion generated by elongating RNAPII causes transient

188 om these experiments, we establish bounds on torsion gravity and possible long-range spin-spin forces

189 ological examination, all left testes in the torsion group were recoverable after four hours of torsi

190 In the torsion group, minimum ADC values for left testicles wer

191 testes, indicating reversible damage in the torsion group.

192 Exciting developments on ocular torsion have been described recently, and new ways to ac

193 and new ways to access and interpret ocular torsion have been devised as well.

194 Understanding the impact that polymer torsions have upon the properties of polydiacetylenes ne

195 es, such as testicular rupture, dislocation, torsion, hematoma, spermatic cord injury or contusion, a

196 Torsion, however, is greater in hypertension independent

197 Torsion, however, was greater at older ages (0.14 degree

198 We find that the superposition of torsion in a rotational DAC (RDAC) offers drastic enhanc

199 t it will affect both pattern strabismus and torsion in contradictory ways.

200 Positive torsion in front of the polymerase induces supercoiling

201 the fundamental mechanisms of high-pressure torsion in metallic glasses, but also leads to higher st

202 eased global longitudinal strain and greater torsion in multivariable models (all P<0.001).

203 sformations can be realized by high-pressure torsion in nanoscale Cu50Zr50 metallic glasses at room t

204 urate technique for the diagnosis of adnexal torsion in patients who have an adnexal mass with acute

205 coplastic model, predictions for bending and torsion in polycrystalline metals show excellent agreeme

206 vance of these determinants to the study of -torsion in topology.

207 When this application was used on key torsions in lactate dehydrogenase, it was found that the

208 .59+/-0.36% (SE)/decade; P=0.08), and higher torsion indices (adjusted estimate for torsion, 0.33+/-0

209 l strain, global circumferential strain, and torsion indices were analyzed using 3-dimensional echoca

210 achment at the cilium inflection point where torsion is at its maximum.

211 The phase dependence of cilia torsion is determined, and a bio-physical model of hardn

212 rcumferential myocardial shortening, whereas torsion is greater with older age.

213 aim of the present study was to evaluate how torsion is influenced by left ventricular (LV) remodelin

214 50Zr50 metallic glasses during high-pressure torsion is investigated using molecular dynamics simulat

215 uch a manner that a photophysically relevant torsion is limited to a range of angles generally associ

216 Ocular torsion is not infrequent in patients with intermittent

217 Although testicular torsion is the most frequent cause of acute scrotum, the

218 ly been avoided because the induced backbone torsion leads to poor pi-pi overlap and amorphous film m

219 e hydrocoele, inguinal hernia and testicular torsion; less common is epididymo-orchitis.

220 nterface for the management and usage of the torsion library, and we illustrate how the system helps

221 ulomotor demand, namely the resetting of eye torsion, likewise inevitably causing a loss of visual in

222 ger deviation or with the presence of ocular torsion may benefit from surgery of the cyclovertical mu

223 cause torsion, and transposition to address torsion may cause pattern strabismus.

224 Testicular torsion may concern boys even in the perinatal period.

225 transposition to treat pattern strabismus or torsion may have an adverse outcome if the surgeon is un

226 Torsion may therefore represent a compensatory mechanism

227 tistical potentials derived from bending and torsion measures of internal loops as well as radii of g

228 e were significantly higher in OHT patients (torsion: median 2.7 degrees /cm [Q1-Q3, 2.3-3.2] versus

229 observed friction domains using a cantilever torsion microscopy in conjunction with angle-resolved ph

230 Testicular torsion must be taken into consideration in differential

231 In particular, overstretching and torsion of axons can potentially damage the axonal cytos

232 der-compensatory because the brain tolerates torsion of binocular images that remain on the foveae.

233 Here we show that the combined tension and torsion of DNA in the presence of condensing agents dram

234 CT abdomen the findings of omental cysts and torsion of greater omentum with free fluid in abdomen we

235 ocete asymmetry involves curvature and axial torsion of the cranium, but no telescoping.

236 r has the highest resistances to bending and torsion of the crocodiles for its size and greater than

237 It exhibits torsion of the head relative to the base, a direct corre

238 esign relied on the assumptions that the tau torsion of the meta-amino-substituted BDI systems leads

239 ylenic C horizontal lineC bond twist and the torsion of the phenyl rings are important for quenching

240 Furthermore, we can show that the torsions of the different glycosidic linkages within the

241 However, the impact of torsion on nucleosome structure and stability is largely

242 The main outcome was a worsening of either torsion or pattern strabismus.

243 ric remodeling (P<0.01) and left ventricular torsion (P<0.01), and a decline in diastolic function (P

244 Each torsion pattern has associated frequency histograms gene

245 It is based on a hierarchical system of torsion patterns that cover a large part of druglike che

246 We present the concept behind the tree of torsion patterns, the design of an intuitive user interf

247 Here we use a torsion pendulum to study (3)He confined in an extremely

248 ic cavity incorporated into a high-precision torsion pendulum, and map the phase diagram between 0.1

249 Meanwhile, a higher torsion period leads to a greater degree of forced coope

250 flow at room temperature under high-pressure torsion permits the study of the shear transformation, i

251 ive-imaging approaches, we revealed that the torsion phenotype results from differential rolling and

252 to sensory neurons significantly rescued the torsion phenotype, axonal connectivity defects, and abno

253 ) calculations from our group found that the torsion potential about C-2-O-2 in protected glycopyrano

254 g to have the largest error; ii), side-chain torsion potentials, as illustrated by the effect of modi

255 lenes necessitates accurate estimates of the torsion potentials.

256 ure, ocular rotations, ocular alignment, and torsion preoperatively to postoperatively were compared.

257 The torsion profiling technique opens new dimensions for res

258 The systolic slope of the torsion-radial displacement loop relationship decreased

259 The slope of torsion-radial displacement loop, and its response to ex

260 Torsion, slope of the systolic limb of the torsion-radial displacement loop, and the untwist rate w

261 us 2.3 degrees /cm [Q1-Q3, 1.9-2.7]; P=0.03, torsion-radial displacement loop: 2.7 degrees /mm [Q1-Q3

262 Preadjustment torsion ranged from 5 degrees excyclotropia to 40 degree

263 Preoperative torsion ranged from 7 to 30 degrees excyclotropia (mean

264 equently observed, rare, and highly unlikely torsion ranges.

265 sses the Z --> E photoisomerization (the tau torsion) reaction, which is the major nonradiative decay

266 1% (23 of 27 patients) in acute and subacute torsion, respectively.

267 Torsion, slope of the systolic limb of the torsion-radia

268 otation angle, but the elastic and inelastic torsion stiffnesses are remarkably different.

269 , the metabolic indices were correlated with torsion, strain, N-terminal pro-B-type natriuretic pepti

270 emain few and unconvincing, but the cervical torsion test appears the most promising.

271 l strain, global circumferential strain, and torsion than men (all P<0.05).

272 A preferential amide torsion that improved the binding properties of the comp

273 ncies in children often caused by testicular torsion; the diagnosis is mostly clinical but must be su

274 2.6 +/- 3.1; increased left ventricular [LV] torsion [theta], 18.4 +/- 4.6 degrees ; and increased ra

275 creasing age were more likely to have higher torsion, though the association between advanced age and

276 After applying torsion to cylindrical twinning-induced plasticity steel

277 chandran-type" plots that relate D-B and B-A torsions to both electronic and exchange couplings.

278 Several groups have shown that DNA in the torsion-unconstrained B-form undergoes an "overstretchin

279 sible force-driven structural transitions of torsion-unconstrained DNA and the resulting three overst

280 de important insights into the structures of torsion-unconstrained DNA under large force.

281 es (peeled ssDNA, DNA bubble, and S-DNA) for torsion-unconstrained DNA under large tension.

282 e covalently closed to prohibit peeling) and torsion-unconstrained DNA.

283 Double-stranded DNA (dsDNA) unconstrained by torsion undergoes an overstretching transition at about

284 ariety of angular and linear motions such as torsion, unwinding, and sliding in addition to the previ

285 ly, a new method to measure objective ocular torsion using retinal arcade tilt as a reference has bee

286 LV torsion was decreased in patients with pulmonary hyperte

287 Torsion was defined as the difference between apical and

288 Reduced torsion was found to be exacerbated by steeper HAs.

289 er in hypertensive (-0.42%; P<0.01), whereas torsion was higher after adjustment for age and sex (0.1

290 association between advanced age and greater torsion was more pronounced in women than in men (both i

291 oad in both sexes, a significant increase of torsion was more pronounced in women.

292 , hematocele, and rupture were confirmed but torsion was not found.

293 Traumatic torsion was primarily suggested.

294 A testicular torsion was suspected, so the baby underwent an ultrasou

295 er some discussion of K-theory and Whitehead torsion, we indicate the relevance of these determinants

296 Myocardial shortening and torsion were assessed by tagged cardiac magnetic resonan

297 Features associated with adnexal torsion were identified by using univariate and recursiv

298 It has different etiology than intravaginal torsion, which appears later in life.

299 rols, OHT recipients were unable to increase torsion with exercise (OHT: 2.8 degrees /cm [2.7-3.2] ve

300 56.8], P = .03) were associated with adnexal torsion, with substantial interreader agreement (kappa =