ライフサイエンスコーパス: torso

1 K in the PG phenocopies the loss of PTTH and Torso.

2 t way that sound interacts with the head and torso.

3 o the independent movements of the limbs and torso.

4 the head, and misorientation of hairs on the torso.

5 eration of peripheral nerve terminals in the torso.

6 rm in 2D using movements of the shoulder and torso.

7 dels of the swine ventricular epicardium and torso.

8 st with 256 ECG electrodes was fitted to the torso.

9 e usually located on the face, arm, or upper torso.

10 918) phosphotyrosine (pY) signaling sites on Torso.

11 ifically required for its down-regulation by Torso.

12 targets is required to mediate the effect of torso.

13 igher angular velocity in the knee, hip, and torso.

14 oned medium specifically by cells expressing Torso.

15 d activation of the receptor tyrosine kinase Torso.

16 in complex with the ligand-binding region of Torso.

17 contacts were focussed above the occupant's torso.

18 ic,LBNP reduced blood volume in all regions (torso: 22 +/- 8%; heart: 18 +/- 6%; spleen: 15 +/- 8%).

19 Most primary melanomas were on the torso (44%).

20 53%), face (29%), tail (12%), leg (12%), and torso (6%).

21 lumes to LBNP relative to heat stress alone (torso: 73 +/- 1%; heart: 72 +/- 2%; spleen: 74 +/- 3%, a

22 er when compared to LBNP while normothermic (torso: 73 +/- 2%; heart: 72 +/- 3%; spleen: 72 +/- 5%, a

23 in rash, predominantly on the face and upper torso (86% with any grade; 18% with grade 3), and a comp

24 romotes PGC fate by mediating degradation of Torso, a receptor tyrosine kinase (RTK) and major determ

25 Here we demonstrate that Torso, a receptor tyrosine kinase that regulates embryon

26 rotein containing the dimerization domain of Torso acted as a potent amplifier of Wg signaling but co

27 in Drosophila, the receptor tyrosine kinase Torso activates both STAT and Ras during the early phase

28 PTTH, through its receptor Torso, acts on two light sensors--the Bolwig's organ and

29 5% confidence interval: 0.43, 0.71) for head/torso air bags and 0.89 (95% confidence interval: 0.79,

30 Risk was reduced when cars with head/torso air bags were struck by cars/minivans (significant

31 fused to the cytosolic domain of Drosophila Torso (alpha(Tor)) or the mouse fibroblast growth factor

32 major implications of the O. bambolii lower torso anatomy and how O. bambolii informs scenarios of h

33 ting that it participates in the pathways of Torso and DFGF-R1 receptor tyrosine kinases.

34 ad no head injury (74) or head combined with torso and extremity injuries (30).

35 ox reduced contamination deposition on HCPs' torso and face predoffing; the use of an aerosol box del

36 ding and local feature analysis in the head, torso and leg regions.

37 ow-up, whereas the corresponding IRR for the torso and legs was 1.16 (95% confidence interval: 0.91,

38 d tetraplegic patients alike perceived their torso and limbs as elongated relative to their body widt

39 (1) plastic bag or plastic wrap covering the torso and limbs with the head uncovered or covered with

40 HCWs touched their own torso and mask in 32% and 29% of the visits, respectivel

41 requires other maternal regulators, such as Torso and Nanos, suggesting that integration of maternal

42 rdiovascular structure of the human head and torso and of a mouse lung based on three-dimensional ima

43 e measured the GVS-evoked tilts of the head, torso and pelvis.

44 Relative changes in torso and regional blood volumes were determined by gamm

45 work extends previous studies of Csw during Torso and Sevenless RTK signaling to include an in-depth

46 This pattern depends upon torso and tailless activity, but is not affected in huck

47 phantom simulating 201Tl uptake in the upper torso and the SIMSET Monte Carlo code, noise-free projec

48 repressing zygotic target genes of both the torso and Toll pathways in the embryo.

49 Both Torso and Torso's presumed ligand, Trunk, are expressed

50 sion during 1999-2001 were computed for head/torso and torso-only side air bags in cars from model ye

51 Like the latter, the molecules have a torso and two arms.

52 arly head orientation and adjustments of the torso and un-stimulated paws.

53 so-like were active when co-transfected with Torso and when presented to Torso-expressing cells in co

54 iving hominoids are distinguished by upright torsos and versatile locomotion.

55 ever, genetic studies have demonstrated that Torso, and by extension other RTKs, can activate Raf and

56 of the PTTH receptor tyrosine kinase (RTK), TORSO, and of ERK phosphorylation, a key component of PT

57 n was presented intact or with the limbs and torso apart in visual space and either unoccluded or occ

58 - 7 y) received 2 dynamic PET studies of the torso area 2 h apart with 11C-L-deprenyl and deuterium-s

59 utcome and the location of imaging along the torso as the independent variable, using random intercep

60 of dpERK in mutants with different levels of Torso as well as the dynamics of the wild-type dpERK pat

61 te to mediate dimerization and activation of Torso at the ends of the Drosophila embryo.

62 Activation of Torso at the poles of the embryo triggers restricted exp

63 tial sessions of 3-dimensional PET/CT of the torso beginning approximately 15 min after (18)F-NaF inj

64 who underwent clinically indicated CT of the torso between April 1, 2007, and May 13, 2007.

65 formance computing simulations using a human torso/biventricular biophysically-detailed model were co

66 ta (REBOA) has been used clinically to limit torso bleeding and restore central perfusion.

67 on) normalizes regional blood volumes in the torso, but does not mitigate the reduction in central bl

68 The activation of Torso by PTTH stimulates extracellular signal-regulated

69 jective perception of tactile stimuli on the torso changes as people turn their heads in different di

70 rams from a 252-electrode-vest placed on the torso combined with computed tomography-scan-based biatr

71 an tattoo age = 6 years, IQR = 5] on the arm/torso completed an outdoor group fitness session.

72 c projector acting on the mathematic cardiac torso computer phantom.

73 l musculature anchored to a relatively rigid torso consisting of numerous short vertebrae, and contro

74 Quantifying breast-torso coordination and movement complexity across the ga

75 ower extremities integrated with multiphasic torso CT for trauma between May 2005 and September 2009

76 assess whether vibration-induced changes in torso cutaneous information contribute to whole-body pos

77 rors and measurement noise were added to the torso data, which were then used to noninvasively recons

78 rors and measurement noise were added to the torso data, which were then used to noninvasively recons

79 rors and measurement noise were added to the torso data, which were then used to noninvasively recons

80 ork is to identify the resting stance of the torso, defined as the position of the C7 vertebral body

81 nts, embryos derived from mothers expressing torso(Deg) in the germline display aberrant spreading of

82 location of tactile stimuli presented on the torso depend on the orientation of our heads with respec

83 sruption of D-Rap1 expression decreased both Torso-dependent ERK activation and the ERK-dependent exp

84 binds to the tyrosine-phosphorylated 150-kDa torso-DER chimeric receptor.

85 By contrast, high levels of Torso develop the signal intensity and duration of a non

86 Here we show that ligand-induced Torso dimerization results from the sequential and negat

87 to assays of downstream signaling activity, Torso dimerization was detected using bimolecular fluore

88 l specimen preparation; isolated lung, upper torso, direct right ventricle contrast injection, and wh

89 We propose that Torso does not affect the ability of Bcd to bind DNA, bu

90 (limbs), curved boundaries, and parts of the torso drove the large majority of neurons.

91 ent of a large organ (liver dome) within the torso due to respiration, change in intensity in small t

92 abusive trauma based on body region bruised (torso, ear, neck, frenulum, angle of jaw, cheeks [fleshy

93 ion of the primary other than extremities or torso; earlier year of diagnosis; and previous cancer.

94 n be readily identified with high-resolution torso ECG mapping.

95 aneous arrays of epicardial electrograms and torso ECGs were recorded during LAD occlusion and reperf

96 sting that mutual antagonism between Gcl and Torso ensures the controlled release of germ-plasm under

97 l electrograms computed using individualized torso/epicardial surface geometries extracted from compu

98 initiates metamorphosis by activation of the Torso/ERK pathway.

99 of tube potential on WED was negligible for torso examinations (Cohen d < 0.05).

100 We find that Torso expressed at high levels in cultured Drosophila ce

101 transfected with Torso and when presented to Torso-expressing cells in conditioned medium.

102 esented with an eczematous dermatitis on her torso, extremities, and buttocks and who subsequently de

103 he head and torso in the anterior direction (torso flexion) while the hips shifted in the posterior d

104 ss tumor size and central pelvic spread) and torso fluorodeoxyglucose PET/CT (to assess lymphadenopat

105 nd require MRI or computed tomography of the torso for diagnosis.

106 0)) subcutaneous adipose tissue added to the torso for five fat distributions.

107 ar to large hylobatids in certain aspects of torso form.

108 own-regulation of Bcd-Gal4 activity requires torso function but does not depend on endogenous bcd act

109 ated from >250 body surface ECGs using heart-torso geometry obtained from computed tomographic images

110 during a series of repeated movements of the torso, head, and facial muscles as outlined by the US Oc

111 imulated two-sphere geometry and a realistic torso-heart geometry.

112 Noncompressible torso hemorrhage (NCTH) is a major cause of potentially

113 everity of limb amputation, head injury, and torso hemorrhage.

114 saving maneuver for the management of lethal torso hemorrhage.

115 onse to a lethal sepsis syndrome after lower torso I/R injury.

116 head (i.e., a direct mechanism) or with the torso (i.e., an indirect mechanism) presumably causes tr

117 lic rod was attached along the length of the torso in 109 patients (56 women, 53 men; age range, 21-7

118 th six vibrating actuators positioned on the torso in contact with the skin over the left and right e

119 fectors and target genes of Toll and the RTK Torso in krz maternal mutants reveals that Krz limits th

120 chnology designed to protect the head and/or torso in side-impact collisions, are becoming increasing

121 muscles induced shifts of both the head and torso in the anterior direction (torso flexion) while th

122 of gait cycles was spent with the breast and torso in-phase (> 90%) compared to no bra running (~ 66%

123 of the prothoracicotropic hormone receptor, torso, in the ring gland of developing larvae leaves the

124 ys, nor did Fas2 inhibit the FGF receptor or Torso, indicating specificity in the inhibitory role of

125 n of stab wounds in young people, overtaking torso injuries as most common pattern of injury by the e

126 able hemorrhage (e.g. those with penetrating torso injuries), even if they are hypoperfusing.

127 Our results suggest that Torso interacts with both Trunk and Torso-like, which co

128 e likely to have axillary and upper anterior torso involvement, whereas men were more likely to have

129 In larvae, torso is expressed specifically in the prothoracic gland

130 Phylogenic analysis indicates that Torso is found outside arthropods, including human paras

131 cerations, as well as selected extremity and torso lacerations (not on hands, feet, or joints).

132 Separate IRRs for head/neck tumors and torso/leg tumors were compared (IRR ratios) to further a

133 Trunk, the embryonic Torso ligand, is related to PTTH, and ectopic expression

134 cation of Trunk, Torso-like or another known Torso ligand, Prothoracicotropic Hormone.

135 he localized expression of the maternal gene Torso-like (Tsl).

136 ar to those present in the embryo, Trunk and Torso-like alone were ineffective but acted synergistica

137 Unexpectedly, the terminal pathway gene torso-like is required for Bcd-dependent transcription.

138 ctivated by individual application of Trunk, Torso-like or another known Torso ligand, Prothoracicotr

139 A second hormone peak activates Torso-like signal in SwCs, which stimulates the Torso re

140 Trunk and Torso-like were active when co-transfected with Torso an

141 Trunk and Torso-like were also taken up from conditioned medium sp

142 est that Torso interacts with both Trunk and Torso-like, which cooperate to mediate dimerization and

143 Polar activation of Torso requires Torso-like, which is expressed by follicle cells adjacen

144 The torso location of IAF measurement was a significant pred

145 e internal jugular and subclavian of a human torso mannequin using the long-axis and short-axis views

146 ace an ultrasound-guided catheter on a human torso mannequin.

147 s have investigated the effect of changes in torso mass and total body mass on peak knee contact forc

148 data based on an extended mathematic cardiac torso (MCAT) phantom and with noise levels typical of cl

149 We investigated the sensitivity of torso measures, recorded simultaneously with epicardial

150 Elements of the torso mesh corresponding to the locations of the placeme

151 patient to construct the first active heart-torso model from clinical MRIs.

152 A biophysically detailed heart-torso model was generated from patient MRIs.

153 trial model is placed into a newly developed torso model which considers the presence of the lungs, l

154 from these epicardial potentials in a human torso model.

155 from these epicardial potentials in a human torso model.

156 line for constructing patient-specific heart-torso models from clinical magnetic resonance images (MR

157 was applied to enhance the extended cardiac-torso models with patient-specific iodine-time profiles

158 o avatars who either mimicked their head and torso movements at a 1 or 3 second time delay or did not

159 permutation entropy in their left ankle and torso movements, but not in right ankle or wrist movemen

160 TCE is also sufficient to confer on maternal torso mRNA all three aspects of nos mRNA regulation: tra

161 poly(A) tail elongation of bicoid, Toll, and torso mRNAs upon egg activation.

162 Gaze with the informant's torso obscured (only the head was shown) produced no per

163 rconducting electromagnets that surround the torso of the experimental animal and a computer control

164 xtant monkeys and differing from the broader torsos of extant apes.

165 in reducing nearside driver deaths, whereas torso-only air bags appear less protective.

166 Protective effects associated with torso-only air bags were observed in single-vehicle cras

167 89 (95% confidence interval: 0.79, 1.01) for torso-only air bags.

168 g 1999-2001 were computed for head/torso and torso-only side air bags in cars from model years 1997-2

169 our results showed no significant changes in torso-only-exposed rats.

170 day separated by 2-6 wk, including brain and torso or pelvis scans.

171 genetic interactions with other RTKs (e.g., torso) or with components of the canonical Ras/MAP kinas

172 my was penetrating injury to the head, neck, torso, or extremities proximal to the elbow or knee (odd

173 sults revealed that one dynamic cue, lateral torso oscillation (sway) and one postural cue, shoulder

174 bjects who had suffered bone fracture in the torso (p < 0.0005).

175 epidermal growth factor receptor (EGFR) and Torso pathways, are hyperactivated in maternal Rho1 muta

176 ake in skeletal muscles and image quality of torso PET and compare stress myocardial perfusion imagin

177 Cardiac (18)F-FDG uptake on torso PET scans is unrelated to myocardial perfusion sta

178 y Application (VIDA) and 4D Extended Cardiac Torso Phantom (XCAT) were extended to provide radiation

179 MA/International Electrotechnical Commission torso phantom as well as a large 35-cm-diameter phantom

180 nd Molecular Imaging Clinical Trials Network torso phantom combined with a 20-cm-diameter cylindrical

181 Torso phantom data were acquired.

182 Twenty mathematical cardiac torso phantom models of the normal heart with different

183 ed to compare the CT numbers of standardized torso phantom regions across study sites, and multivaria

184 Image-quality measurements with the torso phantom show that very high quality images can be

185 A three-dimensional mathematical cardiac-torso phantom that realistically models the attenuation

186 We used the 2-dimensional mathematic cardiac torso phantom to simulate 2 patient anatomies: a large m

187 An anthropomorphic torso phantom was used to simulate tracer uptake in the

188 ean effective doses estimated for the pelvic-torso phantom were 15.9 mSv (CT urography) and 7.8 mSv (

189 We applied it to an anthropomorphic torso phantom with a cardiac insert, using a SPECT syste

190 The image-quality torso phantom with hot or cold spheres was also measured

191 The mathematical cardiac torso phantom, developed to study LV myocardium perfusio

192 d single- and dual-radionuclide studies of a torso phantom.

193 simulated in image quality measurements of a torso phantom.

194 es and with dose measured on a Lucite pelvic-torso phantom.

195 the heart wall insert of an anthropomorphic torso phantom.

196 After an evaluation of lesion torso phantoms to characterize quantitative accuracy, hu

197 Four renal compartments inserted into torso phantoms were filled with saline to simulate the u

198 population of 24 mathematic anthropomorphic torso phantoms, which realistically modeled a wide range

199 oscopic nephrectomy were examined by using a torso phased-array coil at 1.5 T.

200 Nipple and torso position was recorded.

201 IGF 11778 pelvis and lumbar region based on torso preparations and supplemented by other O. bambolii

202 mechanism, downregulation of Bcd activity by Torso, prevents activation near the anterior tip.

203 ic sharing but were independent of width and torso proportions.

204 sed but all patients received neck and upper torso radiation.

205 limitations were in upper body strength and torso range of motion, and with respect to the ambient e

206 Ras/ERK signaling through activation of the Torso receptor by its ligand Trunk(3)-is critical for pr

207 tablishes a sharply localized pattern of the Torso receptor occupancy on the surface of the embryo.

208 In Drosophila embryos, the Torso receptor tyrosine kinase (RTK) activates the small

209 so-like signal in SwCs, which stimulates the Torso receptor tyrosine kinase (RTK) signaling pathway i

210 sophila embryo depends on signalling via the Torso receptor tyrosine kinase (RTK).

211 at has been implicated in signaling from the Torso receptor tyrosine kinase (RTK).

212 s is mediated by the local activation of the Torso receptor tyrosine kinase (Tor).

213 ontrolled by the localized activation of the Torso receptor tyrosine kinase [1-4].

214 cture, however, requires the activity of the Torso receptor tyrosine kinase cascade, which also repre

215 n parallel to activate Raf downstream of the Torso receptor tyrosine kinase in Drosophila.

216 l segment can play a positive role(s) in the Torso receptor tyrosine kinase pathway in vivo, and its

217 mbryonic terminal cells is controlled by the Torso receptor tyrosine kinase.

218 tic cell fate by specifically destroying the Torso Receptor Tyrosine Kinase.

219 g appears to be dependent on the activity of Torso receptor, suggesting this N-terminal segment can f

220 atic differentiation signals mediated by the Torso receptor-tyrosine kinase is important for germline

221 tion of the terminal patterning determinant, Torso receptor.

222 predominantly in the cytoplasm and show that Torso reduces the stability of Cic by controlling the ra

223 Polar activation of Torso requires Torso-like, which is expressed by follicl

224 te (hipbone) is from a primate with a narrow torso, resembling most extant monkeys and differing from

225 In addition to identifying additional torso response elements that mediate early blastoderm po

226 n the early Drosophila embryo, we found that Torso RTK signaling can increase the rate of Cic degrada

227 ere associated with a steady increase in the torso RTu dispersion as the shortest RTu interval moved

228 Both Torso and Torso's presumed ligand, Trunk, are expressed uniformly

229 act independent, scale-invariant features of torso shape from 3D scans of 43 male participants.

230 s into two distinct groups, particularly for torso shape.

231 lated, perfused canine hearts suspended in a torso-shaped electrolytic tank, we simultaneously record

232 e initiated by pacing a dog heart in a human torso-shaped tank.

233 The bottle was placed into a 36-cm-wide torso-shaped water phantom simulating the abdomen of a m

234 Highest DFs found on specific sites of the torso showed a significant correlation with DFs found in

235 Head/torso side air bags appear to be very effective in reduc

236 rane association permits transmission of the Torso signal by D-raf, but these D-raf molecules differ

237 CSW and RasGAP modulate the strength of the Torso signal, contributing to the establishment of preci

238 e that Tsl is not just a specialized cue for Torso signaling but also acts independently of PTTH/Tor

239 However, when Torso signaling is attenuated via mutation of Trunk or R

240 We provide evidence that the terminal torso signaling pathway protects the mis-specified telso

241 ifically dephosphorylates the negative pY918 Torso signaling site, thus identifying Torso to be a sub

242 tes with pY918 and is a negative effector of Torso signaling.

243 ctive but acted synergistically to stimulate Torso signaling.

244 We show that torso signalling permits terminal gap gene expression by

245 At low levels of Torso, similar to those present in the embryo, Trunk and

246 Electrocardiogram signals from 62 torso sites and multisite endocardial recordings were ob

247 i also lacks the complete reorganization for torso stiffness seen in extant great apes (i.e., living

248 s initiated by pacing a dog heart in a human torso tank.

249 mapping techniques (epicardium, non-invasive torso-tank and electrocardiographic imaging) is presente

250 d infarction was suspended in a human shaped torso-tank.

251 Anterior torso %TBSA increased with increasing body habitus (mean

252 more to organ shape and position within the torso than to organ mass, because many of the canine org

253 es of the early hominin Ardipithecus ramidus torso that are argued to have permitted both lordosis an

254 ci (typified by the receptor tyrosine kinase torso) that encode components of a signal transduction c

255 ade active epidermal growth factor (EGF) and Torso TKRs, leading to enhanced signaling and altered em

256 pY918 Torso signaling site, thus identifying Torso to be a substrate of CSW in the terminal pathway.

257 We propose that this may allow Torso to coordinate widely different functions from a si

258 ith parasagittal undulations of the tail and torso to effect gliding at non-vertical angles (minimum

259 activates the receptor tyrosine kinase (RTK) Torso to initiate metamorphosis through the release of e

260 ically detailed model of the human atria and torso to investigate the correlation between the morphol

261 protein for DRK binding, physically linking Torso to Ras activation.

262 zed activity of the receptor tyrosine kinase Torso (Tor) at each pole of the early embryo.

263 f serine/threonine kinase acts downstream of Torso (Tor) for specification of cell fates at the embry

264 n of the Drosophila receptor tyrosine kinase Torso (Tor) only at the termini of the embryo is achieve

265 ere, we analyze the function of D-raf in the Torso (Tor) pathway required to specify cellular fates a

266 Drosophila 14-3-3 gene leonardo (leo) in the Torso (Tor) receptor tyrosine kinase (RTK) pathway.

267 PK activity in signaling from the Drosophila Torso (Tor) receptor tyrosine kinase (RTK).

268 ly embryos, causes ectopic expression of the Torso (Tor) receptor tyrosine kinase-target gene tailles

269 ecome phosphorylated after activation of the Torso (Tor) receptor tyrosine kinase.

270 ing by wild-type and mutant forms of the RTK Torso (Tor) using a genetic approach in DROSOPHILA: Our

271 ndent upon the localized polar activation of Torso (Tor), a receptor tyrosine kinase that is uniforml

272 by a gain-of-function mutant Drosophila RTK Torso (Tor).

273 way mediated by the receptor tyrosine kinase Torso (Tor).

274 let-derived growth factor receptor-beta, and Torso (Tor).

275 Furthermore, we find that torso transiently regulates anterior repression of cauda

276 detector CT as a triage tool for penetrating torso trauma and the primacy of trajectory evaluation in

277 ents younger than 18 years treated for blunt torso trauma at the University of California, Davis Medi

278 - or 64-row multidetector CT for penetrating torso trauma below the diaphragm and had surgically conf

279 emodynamically stable victims of penetrating torso trauma continues to increase but remains less sing

280 l wounds and hypotensive patients with blunt torso trauma, immediate surgical intervention is justifi

281 le children treated in an ED following blunt torso trauma, the use of FAST compared with standard car

282 years; mean age, 28 years) with penetrating torso trauma.

283 peritoneal lavage was phased out in favor of torso ultrasound as a primary triage tool, and pelvic bi

284 The head-up/torso-up cardiopulmonary resuscitation bundle was feasib

285 No problems were observed with head-up/torso-up positioning (n = 1,489), but resuscitation rate

286 ected from six body locations, including the torso, upper and lower limbs, to determine which locatio

287 Craniodental morphology, tooth wear, torso vertebral morphology, and body size all suggest th

288 rdings were made of the fetal face and upper torso visualized by means of 4D full frontal or facial p

289 stributions in different organs of the upper torso was used for the investigation.

290 Vibrations around the torso were randomly applied at two locations simultaneou

291 th, mlc/NT-3 mice retract their limbs to the torso when lifted by the tail.

292 of vascular branching in the human head and torso, whereas locally or intermediately constrained ran

293 pustular rash, usually on the face and upper torso, which generally occurs in a dose-dependent manner

294 e expression of the receptor tyrosine kinase torso, which then promotes polyploidization and growth t

295 mplex interaction between the breast and the torso while running in different bra conditions.

296 en, with increasing IAF area moving down the torso with older ages.

297 visceral injury in patients with penetrating torso wounds.

298 l Measurement Unit (IMU) sensors on infants' torso, wrists, and ankles (N = 32: 10 term; 22 preterm).

299 em was incorporated into 58 extended cardiac-torso (XCAT) patient phantoms.

300 gnetic resonance imaging, location along the torso yields different IAF areas and distributions indep