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 o the independent movements of the limbs and torso.

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

4 dels of the swine ventricular epicardium and torso.

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

6 oned medium specifically by cells expressing Torso.

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

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

9 ifically required for its down-regulation by Torso.

10 targets is required to mediate the effect of torso.

11 d activation of the receptor tyrosine kinase Torso.

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

13 contacts were focussed above the occupant's torso.

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

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

16 53%), face (29%), tail (12%), leg (12%), and torso (6%).

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

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

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

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

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

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

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

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

25 5% confidence interval: 0.43, 0.71) for head/torso air bags and 0.89 (95% confidence interval: 0.79,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

48 - 7 y) received 2 dynamic PET studies of the torso area 2 h apart with 11C-L-deprenyl and deuterium-s

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

114 The torso location of IAF measurement was a significant pred

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

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

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

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

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

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

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

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

123 from these epicardial potentials in a human torso model.

124 from these epicardial potentials in a human torso model.

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

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

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

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

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

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

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

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

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

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

135 89 (95% confidence interval: 0.79, 1.01) for torso-only air bags.

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

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

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

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

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

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

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

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

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

145 Torso phantom data were acquired.

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

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

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

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

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

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

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

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

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

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

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

157 simulated in image quality measurements of a torso phantom.

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

159 the heart wall insert of an anthropomorphic torso phantom.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

197 ctive but acted synergistically to stimulate Torso signaling.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

240 visceral injury in patients with penetrating torso wounds.

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

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