ライフサイエンスコーパス: torsion

1 C) in the diagnosis of incomplete testicular torsion.

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

3 ted and 2 patients with bilateral testicular torsion.

4 andatory to prevent threatening mass pedicle torsion.

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

6 radiologically mimicing traumatic testicular torsion.

7 cause misdiagnoses, such as inflammation or torsion.

8 greater omentum leading to secondary omental torsion.

9 chain, because it is repositioned by linker torsion.

10 nal wall leading to these lesions suggesting torsion.

11 al treatment, required in case of testicular torsion.

12 ized on the basis of differences in backbone torsion.

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

14 urgery to either treat pattern strabismus or torsion.

15 al features, binocular alignment, and fundus torsion.

16 mus developed after transposition to address torsion.

17 uperhelix that can be stabilized by positive torsion.

18 coming increasingly popular among studies on torsion.

19 ers are efficiently retained irrespective of torsion.

20 iac muscle twitch relaxation and ventricular torsion.

21 mensional Anti-de Sitter (AdS) geometry with torsion.

22 ethod in the diagnosis of partial testicular torsion.

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

24 n group were recoverable after four hours of torsion.

25 tions include induced vertical deviation and torsion.

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

27 rther insights of layered materials by using torsion.

28 bnormal muscle contractions and cause embryo torsion.

29 portional limit under pure shear stresses of torsion.

30 motions including contraction, bending, and torsion.

31 quently deforms in compression, tension, and torsion.

32 xamination was performed after four hours of torsion.

33 ontractions that prevent the accumulation of torsion.

34 the early diagnosis of incomplete testicular torsion.

35 stry, isomerization, and drug-like molecular torsions.

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

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

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

39 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

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

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

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

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

44 Observed bands were assigned to donor torsion, acceptor wag, acceptor twist, intermolecular st

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

46 ed by the strategy of molecular conformation torsion adjustment ratio fluorescent signal.

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

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

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

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

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

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

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

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

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

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

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

58 geometry to gain control over the curvature, torsion and the number of helices, we have constructed 1

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

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

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

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

63 for a borderline tumour, 0.4% (0.1-0.7) for torsion, and 0.2% (<0.1-0.4) for cyst rupture.

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

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

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

67 rious tactile motions (shear, pinch, spread, torsion, and so on).

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

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

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

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

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

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

74 The torsion angle between the carbonyl and naphthalene is 26

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

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

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

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

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

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

81 hanical movement involving sterically driven torsion angle flipping of two residues that drive the mo

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

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

84 ted based on secondary chemical shifts using torsion angle likeliness obtained from shift (TALOS+) sh

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

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

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

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

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

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

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

92 Protein secondary structure and backbone torsion angle prediction can provide important informati

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

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

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

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

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

98 er reaction coordinate (i.e., the glycosidic torsion angle) is unable to resolve the intermediates.

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

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

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

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

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

104 Predictions of protein backbone torsion angles ( and psi) and secondary structure from s

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

106 ominated by thermal fluctuations of backbone torsion angles and H-bond lengths, not by transient heli

107 d to derive conformational models of linkage torsion angles and psi in solution, which were compared

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

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

110 lity, and reliability and to compare femoral torsion angles between the four different measurement me

111 red, which make it possible to determine the torsion angles between the peptide planes without assumi

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

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

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

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

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

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

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

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

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

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

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

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

124 ves consistent improvements in both backbone torsion angles prediction and secondary structure predic

125 In particular, after using our torsion angles refinement method OPUS-Refine as the post

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 Mean torsion angles were greater by 17.6 degrees for CT and 1

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

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

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

132 t their calculated energetics, modeled N-C3' torsion angles, and evaluated properties.

133 predictions of protein secondary structures, torsion angles, beta-turns and gamma-turns for a given p

134 or predicting secondary structures, backbone torsion angles, beta-turns and gamma-turns, respectively

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

136 s, the main chain hydrogen bond network, and torsion angles, which it uses to build models in an iter

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

138 is a valuable method for predicting protein torsion angles.

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

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

141 cessible surface area and the local backbone torsion angles.

142 TM domain, which yielded backbone (phi, psi) torsion angles.

143 and classify them according , psi, and omega torsion angles.

144 ep learning architectures to predict protein torsion angles.

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

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

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

148 at in 1-start fibres the DNA constrains more torsion (as writhe) than 2-start fibres with the same NR

149 Background Assessment of femoral torsion at preoperative hip imaging is commonly recommen

150 uent tension tests performed parallel to the torsion axis.

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

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

153 Torque sensors such as the torsion balance enabled the first determination of the g

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

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

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

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

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

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

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

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

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

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

164 pare MRI- and CT-based assessment of femoral torsion by using four commonly used measurement methods

165 bending (orally, aborally; inward, outward), torsion (clockwise, counter-clockwise), elongation, and

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

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

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

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

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

171 Ocular torsion does not correlate with and thus cannot account

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

173 challenges include controlling head tilt or torsion during imaging, estimating within-eye variabilit

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

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

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

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

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

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

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

181 e rotation cause excessive tissue damage; 2- torsion effects on the shaft and needle deflection at ti

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 the interactions in terms of a pseudo-scalar torsion field.

186 tible only by complex, nonphysical multibond torsions-form a unique subset of atropisomers that diffe

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

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

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

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

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

192 testes, indicating reversible damage in the torsion group.

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

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

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

196 Processing by high-pressure torsion (HPT), which was developed initially as a grain

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

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

199 ch the RNA synthesis leads to the buildup of torsion in DNA.

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

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

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

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

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

205 .59+/-0.36% (SE)/decade; P=0.08), and higher torsion indices (adjusted estimate for torsion, 0.33+/-0

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

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

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

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

210 50Zr50 metallic glasses during high-pressure torsion is investigated using molecular dynamics simulat

211 Ocular torsion is not infrequent in patients with intermittent

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

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

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

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

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

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

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

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

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

221 Torsion may therefore represent a compensatory mechanism

222 Conclusion MRI- and CT-based femoral torsion measurements showed high agreement and comparabl

223 CT and how different methods affect femoral torsion measurements.

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

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

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

227 Testicular torsion must be taken into consideration in differential

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

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

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

231 vertically oriented pectoral girdle, and low torsion of the femoral head relative to the condyles are

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

233 We hypothesized that PHA twisting led to torsion of the residual primordial common bulb, branchin

234 The most common causes of ASP are torsion of the testis (TT) or its appendages (TA) and ep

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

236 dence of spontaneous resolution of the mass, torsion or cyst rupture, or borderline or invasive malig

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

238 cceptor twist, intermolecular stretch, donor torsion overtone, and in-plane and out-of-plane libratio

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

240 Each torsion pattern has associated frequency histograms gene

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

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

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

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

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

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

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

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

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

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

251 The torsion profiling technique opens new dimensions for res

252 to von Helmholtz, knowledge of the amount of torsion provided by Listing's law, an extension of Donde

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

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

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

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

257 Preadjustment torsion ranged from 5 degrees excyclotropia to 40 degree

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

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

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

261 1% (23 of 27 patients) in acute and subacute torsion, respectively.

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

263 ing of ~50 zJ, from a nano-electromechanical torsion spring at the single molecule level.

264 stretching force and show that they exhibit torsion stiffening, in qualitative agreement with experi

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

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

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

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

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

270 derivatives, perhaps because of inter-arene torsions that emerge in theoretical geometry optimizatio

271 hm; for test cases with different numbers of torsions, the DGLRDPSO outperforms the LGA and LPSO in f

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

273 2.6 +/- 3.1; increased left ventricular [LV] torsion [theta], 18.4 +/- 4.6 degrees ; and increased ra

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

275 urons in monkey area V1 use knowledge of eye torsion to compensate the image tilt associated with spe

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 thologies in patients with acute and chronic torsion trauma of the knee joint.

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

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

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

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

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

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

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

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

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

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

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

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

291 Traumatic torsion was primarily suggested.

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

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

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

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

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

297 tics are directly affected by this molecular torsion, which can be explained using a simple circuit m

298 e docking problems with different numbers of torsions, which indicates that the proposed algorithm is

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 =