ライフサイエンスコーパス: paralyze

1 remainder of the cells twitch feebly or are paralyzed.

2 ype with approximately 30% of flies becoming paralyzed.

3 flagella that either beat very slowly or are paralyzed.

4 cation and control to people who are totally paralyzed.

5 plantation, whereas control animals remained paralyzed.

6 etrical responses even after their eyes were paralyzed.

7 rmal lungs were anesthetized, intubated, and paralyzed.

8 n early adulthood and the mice do not become paralyzed.

9 28% of these patients were pharmacologically paralyzed.

10 The swine were anesthetized, intubated, and paralyzed.

11 ing only the DPY-30 domain in RSP2 were also paralyzed.

12 ts, animals lacking both Cl(-) extruders are paralyzed.

13 nhancement if the flagella rotary motion was paralyzed.

14 t day 7 and by day 9 animals were completely paralyzed.

15 cally ventilated, 16% were pharmacologically paralyzed, 18% required vasoactive infusions, 36% were n

16 ,000 times more mutant virus was required to paralyze 50% of inoculated mice, compared to that with w

17 Patients were paralyzed 66 +/- 12 (SEM) hrs, with recovery of the four

18 tage characterized by the assembly of short, paralyzed, 9+0 ciliary axonemes that lack central pair M

19 model was altered to simulate the effects of paralyzing a muscle, the subjects simply increased the r

20 d new users are now presented with an almost paralyzing abundance of choices.

21 unctionally replace those cells destroyed in paralyzed adult rats.

22 onitors the sensitivity of C. elegans to the paralyzing affects of an acetylcholinesterase inhibitor,

23 y the infant, despite excluding periods when paralyzing agents were used.

24 re we show that, without using anesthetic or paralyzing agents, fluorescence imaging with one-nanomet

25 e flagella in Chlamydomonas ndk5 mutant were paralyzed, albeit only deficient in three RS subunits.

26 6 complex cells in area 17 of cats that were paralyzed and anesthetized with propofol and N2O.

27 measurements were performed on anesthetized, paralyzed and artificially ventilated adult male Sprague

28 ve pressure in 15 decerebrated, vagotomized, paralyzed and artificially ventilated cats.

29 NRA in decerebrate cats, most of which were paralyzed and artificially ventilated.

30 ) can be used to determine if a diaphragm is paralyzed and confirm our predictions that a chronically

31 l mutants develop slowly, and the adults are paralyzed and dumpy.

32 Nova1/Nova2 double knockout mice are paralyzed and fail to cluster AChRs at the NMJ, and bree

33 In TMEV infection, only Wld mice were paralyzed and had increased inflammation, virus antigen-

34 Zebrafish nsf mutants are paralyzed and have impaired response to light, reflectin

35 and in eight alpha-chloralose anesthetized, paralyzed and mechanically ventilated beagle dogs, we ha

36 n two groups (n=10 in each) of anesthetized, paralyzed and mechanically ventilated dogs.

37 oups (n = 10 in each group) of anesthetized, paralyzed and mechanically ventilated dogs.

38 Experiments were conducted using both paralyzed and non-paralyzed decerebrate cats, in which r

39 ultrasonography could distinguish between a paralyzed and normally functioning diaphragm.

40 ay roles in guiding nerve terminal growth in paralyzed and partially denervated muscles; however, the

41 diameter; 3.6-mm outer diameter); they were paralyzed and placed on a mechanical ventilator.

42 All were sedated and paralyzed and received positive-pressure ventilation.

43 vae resulting from morpholino injection were paralyzed and their "muscle" cells lacked myofibrils.

44 were recorded in pentobarbital anesthetized, paralyzed and ventilated male rats.

45 In anesthetized, paralyzed and ventilated rats, moderate AIH-induced pLTF

46 L2-L3) in sodium pentobarbital anesthetized, paralyzed and ventilated rats.

47 ts 2-3 in sodium pentobarbital anesthetized, paralyzed and ventilated rats.

48 Infants and children who were sedated and paralyzed and were receiving mechanical ventilation thro

49 in which Pseudomonas aeruginosa PAO1 rapidly paralyzes and kills the nematode Caenorhabditis elegans.

50 In urethane-anesthetized, paralyzed, and artificially ventilated cats, we observed

51 cted, anesthetized, vagotomized, pancuronium paralyzed, and artificially ventilated male Sprague-Dawl

52 L2-L3) in sodium pentobarbital anesthetized, paralyzed, and artificially ventilated rats.

53 ducted on adult cats that were decerebrated, paralyzed, and artificially ventilated.

54 Ten anesthetized, paralyzed, and mechanically ventilated mongrel dogs (19-

55 Twenty anesthetized, paralyzed, and mechanically ventilated mongrel dogs.

56 apnea, was investigated in 18 anesthetized, paralyzed, and mechanically ventilated newborn piglets.

57 All animals were anesthetized, paralyzed, and mechanically ventilated throughout the ex

58 gs were anesthetized in the supine position, paralyzed, and mechanically ventilated with 50% O(2) at

59 Sheep were anesthetized, paralyzed, and mechanically ventilated.

60 anesthetized with pentobarbital, intubated, paralyzed, and mechanically ventilated.

61 within 6 hours of surgery and while sedated, paralyzed, and mechanically ventilated.

62 s) were anesthetized with ketamine, sedated, paralyzed, and mechanically ventilated.

63 Pigs were tracheally intubated, sedated, paralyzed, and mechanically ventilated.

64 fulminant hepatic failure who were sedated, paralyzed, and mechanically ventilated; 16 age-, gender-

65 Viral RNA level, percent paralyzed, and percent mortality were linearly correlate

66 Juvenile pigs (12 kg) were anesthetized, paralyzed, and placed on a motion platform that oscillat

67 eter placement, rabbits were tracheotomized, paralyzed, and placed on the conventional ventilator.

68 tive end-expiratory pressures of < 5 cm H2O, paralyzed, and sedated) were examined (n = 12), the corr

69 -pons in urethane-anesthetized, vagotomized, paralyzed, and servo-ventilated adult Sprague Dawley rat

70 omozygous brec mutants are embryonic lethal, paralyzed, and show no detectable synaptic transmission

71 were recorded in pentobarbital anesthetized, paralyzed, and ventilated male rats.

72 were recorded in pentobarbital anesthetized, paralyzed, and ventilated male rats.

73 Five anesthetized, paralyzed, and ventilated pigs.

74 Anesthetized, paralyzed, and ventilated sheep.

75 Injured animals, which were anesthetized, paralyzed, and ventilated with 100% oxygen and not treat

76 Four groups of anesthetized, paralyzed, and ventilated young Yorkshire pigs, weighing

77 mins; 20 hrs later, all rats were intubated, paralyzed, and ventilated.

78 assive deviation of the eye in anesthetized, paralyzed animals can profoundly affect the auditory res

79 Within the brain stems and brains of three paralyzed animals examined late in infection (days 5 and

80 consistent with the behavior recorded in non-paralyzed animals from the muscles innervated by those n

81 Paralyzed animals transplanted with EBD cells partially

82 activity patterns of most nerves recorded in paralyzed animals were consistent with the behavior reco

83 ective thick filament assembly, resulting in paralyzed animals.

84 ion of the laryngeal and pharyngeal areas in paralyzed animals.

85 In urethane/chloralose-anesthetized, paralyzed, artificially ventilated rats, microinjection

86 hway, even though these animals are strongly paralyzed as a result of functional (nondevelopmental) d

87 iatic nerve, TDP-43 transgenic mice remained paralyzed at the injured limb unlike control mice, which

88 lyzed mouse embryos and in pharmacologically paralyzed avian and rat embryos.

89 of organophosphorous compounds which cause a paralyzing axonal degeneration and recently mutations in

90 with organophosphate compounds that cause a paralyzing axonal degeneration in humans and has been sh

91 s might restore voluntary control to muscles paralyzed below a spinal lesion.

92 roduced earlier disease, and spinal cords of paralyzed bigenic mice showed YFP fluorescent inclusion-

93 During these attacks, the person is paralyzed, but fully conscious and aware of their surrou

94 migrated into the spinal cord parenchyma in paralyzed, but not uninjured, animals.

95 transgenic mouse model of ALS, which becomes paralyzed by 5-6 mo, where MN cell bodies are fluorescen

96 which restore function to the hemidiaphragm paralyzed by an ipsilateral spinal cord hemisection.

97 es recovery of the ipsilateral hemidiaphragm paralyzed by C2 spinal cord hemisection.

98 icroarray analysis of spinal cords from rats paralyzed by experimental autoimmune encephalomyelitis (

99 , the lambs were mechanically ventilated and paralyzed by using 1 mg/kg vecuronium bromide followed b

100 gulators LasR and RhlR, rapidly and lethally paralyzes C. elegans.

101 s duration were induced in the anesthetized, paralyzed cat (n = 7) ventilated with either room air or

102 se anesthetized, artificially ventilated and paralyzed cats.

103 n the primary visual cortex of anesthetized, paralyzed cats.

104 pe with nearly equal fractions of motile and paralyzed cells.

105 ns that are capable of restoring motility to paralyzed central pair or radial spoke defective strains

106 ty of detecting wild poliovirus excretion in paralyzed children.

107 pheres on the plasma membrane of immobilized paralyzed Chlamydomonas flagella.

108 ic blastulae covered on one side with short, paralyzed cilia, and on the other with normal, beating c

109 In paralyzed control mice, the SC had increased cellular in

110 ade and adjusting drug doses in continuously paralyzed critically ill medical patients results in low

111 were conducted using both paralyzed and non-paralyzed decerebrate cats, in which recordings were obt

112 In the paralyzed, decerebrate, vagotomized and ventilated cat,

113 d confirm our predictions that a chronically paralyzed diaphragm is atrophic and does not thicken dur

114 We predicted that a paralyzed diaphragm would be atrophic and not shorten, t

115 ne (OPV), proven to reduce the burden of the paralyzing disease.

116 Eighteen anesthetized and paralyzed dogs.

117 Macaque monkeys were anesthetized and paralyzed during single cell recording from the LGN whil

118 n granule exocytosis, as demonstrated by the paralyzing effect of pretreating CD4(+)CD28(null) T cell

119 heromone, as well as hypersensitivity to its paralyzing effects.

120 pidly developed the clinical signs of severe paralyzing encephalomyelitis but were eventually able to

121 fy axonal loss in spinal cord lesions from 5 paralyzed (Expanded Disability Status Scale score > or =

122 Neurophysiological data obtained with paralyzed eyes suggest that this coarse-to-fine sequence

123 ete embryogenesis and hatch, but they die as paralyzed first-stage larvae.

124 n extensive period of AChR-less development, paralyzed fish displayed a remarkable level of recovery,

125 imaging and morpholino depletion of axonemal Paralyzed Flagella 16 indicated that flagella-based forc

126 An RSP2 mutant had paralyzed flagella defective in RSP2 and multiple subuni

127 insertional mutant null for IFT46 has short, paralyzed flagella lacking dynein arms and with central

128 gomonas wittichii RW1, and a nonmotile (with paralyzed flagella) Escherichia coli K12 MG1655 Deltamot

129 Mutant cells have paralyzed flagella, and the C1 microtubule of the centra

130 Mutant cells have paralyzed flagella, and the entire central apparatus is

131 together with CK1-depleted axonemes from the paralyzed flagellar mutant pf17, which is defective in r

132 IC138 is hyperphosphorylated in paralyzed flagellar mutants lacking radial spoke and cen

133 icrotubule sliding in axonemes isolated from paralyzed flagellar mutants lacking radial spokes.

134 pared the wild type with flagellum-minus and paralyzed-flagellum mutants.

135 Animals were anesthetized and paralyzed for imaging stability.

136 ed peripheral nerves, associated muscles are paralyzed for weeks.

137 days after fertilization and they are almost paralyzed four days after fertilization.

138 nteractions between escape and swimming in a paralyzed goldfish preparation in which we can activate

139 The paralyzed growth plate showed disruptions to column orga

140 lear output in both ears in anesthetized and paralyzed guinea pigs to explore possible differences in

141 sional neural activity leading to control of paralyzed hand grasping function through a brain-compute

142 n be used to drive grasping functions of the paralyzed hand through a brain-computer interface.

143 In 6 anesthetized, paralyzed healthy adult sheep, we compared effects of ga

144 ral paralysis, t(di) and delta t(di) for the paralyzed hemidiaphragm were significantly less than tho

145 a daily exercise program of actively moving paralyzed hindlimbs through the motions of walking.

146 complex mixture of bioactive molecules that paralyze host defenses.

147 epresents a strategy used by B. anthracis to paralyze host innate immunity.

148 king growing hosts and parasitoids attacking paralyzed hosts.

149 mation to restore coordinated arm actions in paralyzed human beings.

150 entral nervous system, is an animal model of paralyzing human disease, multiple sclerosis.

151 erface (BMI), particularly as a means to aid paralyzed humans in communication.

152 etic systems that aim to restore movement to paralyzed individuals.

153 can be used for real-time device control in paralyzed individuals.

154 of individual V1 neurons in anesthetized and paralyzed infant monkeys as a function of the relative,

155 volumes in 50 critically ill, intubated, and paralyzed infants (mean age [SEM]), 19.9 [4.6] mo) with

156 bly, allowing the virus to transcriptionally paralyze infected M phi responses while allowing basal t

157 - and gamma-secretase, respectively, thereby paralyzing inhibitory signaling; 2) shedding of soluble

158 Animals were anesthetized, paralyzed, intubated, and mechanically ventilated.

159 Animals were anesthetized, paralyzed, intubated, and ventilated.

160 of the central nervous system (CNS) leads to paralyzing, invariably lethal encephalomyelitis.

161 s, the pheromone arrests embryo development, paralyzes J2 larva, and inhibits exit of dauer larvae.

162 arrests development shortly thereafter as a paralyzed L1 larva, presumably as a consequence of neuro

163 l4 completely and virtually instantaneously "paralyzed" laboratory and clinical strains of serovar Ty

164 logical studies showed severe denervation in paralyzed limb muscles, suggesting either motor neuron o

165 Replacing the function of a missing or paralyzed limb with a prosthetic device that acts and fe

166 graded control of muscle contraction in his paralyzed limb.

167 etween the contralesional hemisphere and the paralyzed limb.

168 anced and more natural fine motor control of paralyzed limbs by BCI-FES neuroprosthetics.

169 cord injury, and none recovered function in paralyzed limbs.

170 y to control assistive devices and reanimate paralyzed limbs.

171 ause the lowest MUNE values were detected in paralyzed limbs.

172 restore voluntary control of a patients' own paralyzed limbs.

173 The paralyzed LR exhibited a significantly (P < 0.002) large

174 The behavior of the paralyzed LR inflection was consistent with LR pulley an

175 , but in LR palsy only the inflection of the paralyzed LR-0.17 mm further posterior per degree of abd

176 Paralyzed LRs exhibited marked atrophy compared with fun

177 tive tyrosine phosphatase termed YopH, which paralyzes lymphocytes and macrophages by dephosphorylati

178 primary visual cortex (V1) of anesthetized, paralyzed macaque monkeys.

179 he superficial layers of V1 in anesthetized, paralyzed macaque monkeys.

180 n pentobarbital anesthetized, ventilated and paralyzed male rats.

181 motor neurons was evaluated in anesthetized, paralyzed, mechanically ventilated adult rats (n = 108).

182 halus), anesthetized with ketamine, sedated, paralyzed, mechanically ventilated for 11 days, and moni

183 in the anterior horn of the spinal cords of paralyzed mice exhibited a high degree of WNV infection,

184 tially regulated proteins in spinal cords of paralyzed mice expressing SOD1(G93A) may contribute to u

185 Pathological inspection revealed that the paralyzed mice had a dramatic degeneration of motor neur

186 In paralyzed mice significant damage was observed in the ou

187 Six adult anesthesized and paralyzed mongrel dogs (mean weight 24.3+/- 4.4 kg).

188 Six anesthetized, paralyzed mongrel dogs (mean weight, 24.7+/-3.8 kg).

189 nit recordings were made in anesthetized and paralyzed monkeys ranging in age between 6 days and 8 we

190 ording methods were used in anesthetized and paralyzed monkeys, and dichoptic sine-wave gratings were

191 In tissues of the central nervous systems of paralyzed moribund FVB/N mice, a major component of the

192 The abnormal/paralyzed motility is not due to an obvious deficiency o

193 human SOD1-YFP transgenics, developed lethal paralyzing motor symptoms at 9 months.

194 Paralyzed motors of cells carrying a motA point mutation

195 d in cn/cn embryos also occur in genetically paralyzed mouse embryos and in pharmacologically paralyz

196 e of irreversible neurological disability in paralyzed MS patients and indicate that reduced NAA as m

197 le is known about fascicle length changes in paralyzed muscles during locomotion.

198 on of new neuromuscular junctions within the paralyzed muscles.

199 One paralyzed mutant recovered in our screen contains an all

200 One paralyzed mutant recovered in our screen, D2, is an alle

201 ng the flagellar motor switch, we isolated a paralyzed mutant whose defect proved to be a 4-bp deleti

202 iously showed that anthrax lethal toxin (LT) paralyzes neutrophils, a major component of innate immun

203 nd that expression of PD-1 in TIDC tonically paralyzed NF-kappaB activation.

204 e brain with the goal to restore function in paralyzed or amputated patients.

205 compensatory sprouting of axon terminals in paralyzed or denervated muscles.

206 wild-type levels; all other deletions caused paralyzed or, more commonly, nonflagellate phenotype.

207 not as yet master the control of prosthetic, paralyzed, or otherwise disabled limbs.

208 s of these gad mutants reveals that they are paralyzed owing to defects in glutamatergic transmission

209 had no effect on UA mechanics in a group of paralyzed (pancuronium bromide) rats, despite similar el

210 ignals can be used to continuously monitor a paralyzed patient's preferences and motivation.

211 ssure transducer (invasive), or a relaxed or paralyzed patient.

212 NP) is a very versatile method for assisting paralyzed patients and patients with amputations.

213 ine interfaces are being developed to assist paralyzed patients by enabling them to operate machines

214 elopment of neural prosthetics for assisting paralyzed patients has focused on decoding intended hand

215 Paralyzed patients received either TOF monitoring with a

216 the visual cortex and to allow the brains of paralyzed patients to re-establish control of the extern

217 BMI control can be significantly improved in paralyzed patients with residual kinesthetic sense and p

218 s (ERPs) is of limited application value for paralyzed patients with severe oculomotor impairments.

219 lopment of motor-cortical neuroprostheses in paralyzed patients.

220 tegy aimed at restoring mobility in severely paralyzed patients.

221 l signals for neural prosthetics that assist paralyzed patients.

222 e movements are promising aids for assisting paralyzed patients.

223 velop into clinically viable systems to help paralyzed people.

224 discrete (non-rhythmic) hand movements in a paralyzed person.

225 erfaces have been proposed as a solution for paralyzed persons to communicate and interact with their

226 The sknac-knockdown embryos showed a paralyzed phenotype with little muscle contraction.

227 ns in each of them that produce the Mot- (or paralyzed) phenotype, in which flagella are assembled an

228 Ten anesthetized and paralyzed preoperative infants with HLHS were evaluated

229 d caused the worms to be hypercontracted and paralyzed, presumably as a result of excess extracellula

230 otoxin family to target the muscle nAChR and paralyze prey.

231 synergistically to modify channel gating and paralyze prey.

232 By contrast, in a subset of cats paralyzed prior to the third contraction, neither MAP no

233 VILI) in vivo, we subjected 12 anesthetized, paralyzed rabbits to high tidal volume ventilation (25 c

234 Twenty-seven anesthetized and paralyzed rabbits.

235 Anesthetized and paralyzed rats (n = 34) were studied.

236 e recorded in pentobarbital-anesthetized and paralyzed rats with dextran sulfate sodium-induced colit

237 ased from sciatic nerves in anesthetized and paralyzed rats.

238 ey transcripts, and restores motility in the paralyzed sfpq null mutants, indicating a non-nuclear pr

239 oric acid was instilled into the tracheas of paralyzed sheep receiving controlled mechanical ventilat

240 -negative effect in wild-type cells, causing paralyzed short flagella with hypophosphorylated, less a

241 These larvae are partially paralyzed, show a characteristically contracted abdomen,

242 ns from the contralesional hemisphere to the paralyzed side.

243 mechanical environment in embryonic duck by paralyzing skeletal muscles, and by blocking the ability

244 After paralyzing spinal cord injury the adult nervous system h

245 uromodulation that restored locomotion after paralyzing spinal cord injury.

246 Next, experiments with a paralyzed strain indicated that the stator-binding was m

247 pproaches to the development of decoders for paralyzed subjects unable to generate an output signal.

248 mise for the restoration of limb mobility in paralyzed subjects.

249 al motor prosthetic, which is used to assist paralyzed subjects.

250 mice may be a specific infectious trigger of paralyzing systemic necrotizing vasculitis most severely

251 We conclude that YopH not only paralyzes T cells acutely, but also ensures that the cel

252 lis we show that Nkx6.1 knockdown results in paralyzed tadpoles.

253 This paralyzes the capacity of neutrophils and macrophages to

254 The infusion abruptly paralyzes the millipede, which thereby is prevented from

255 Rather than paralyzing the CTL response, these epitope modifications

256 nctional loss and the severe side effects of paralyzing the immune system.

257 ovement because breakage can be prevented by paralyzing the mutant animals.

258 herefore, we propose that elevated [5HT](ex)"paralyzes" the translocation of SERT from intracellular

259 They are predators that paralyze their prey by injection of venom containing a p

260 that disrupt neuromuscular communication to paralyze their prey.

261 Seven adult cats were anesthetized and paralyzed to maximize imaging stability.

262 lesional hemisphere in response to MI of the paralyzed trained hand.

263 in subunit ACPM1 from the enzyme complex and paralyzed ubiquinone reductase activity.

264 c bacteria tumble, swim slowly, and are then paralyzed upon exposure to 390- to 530-nm light.

265 H and untreated rats were then anesthetized, paralyzed, vagotomized, and artificially ventilated.

266 All subjects were paralyzed (vecuronium bromide) and ventilated with room

267 before and after delayed sternal closure in paralyzed ventilated infants.

268 Paralyzed, ventilated dogs were studied at short and ext

269 were recorded in pentobarbital anesthetized, paralyzed, ventilated male rats (n=19).

270 Paralyzed, ventilated rats were hemorrhaged (18 mL blood

271 were performed on anesthetized, vagotomized, paralyzed, ventilated, and spinally injured (C2 hemisect

272 We addressed two questions: (1) Can paralyzed, ventilator-dependent patients use the sensati

273 singly, however, these rescued mice remained paralyzed, while electrophysiologic studies demonstrated

274 While paralyzed with 0.1 mg/kg/hr iv vecouronium bromide, all

275 luripotent cells to restore function in rats paralyzed with a virus-induced motor neuronopathy.

276 was placed on inverse ratio ventilation and paralyzed with cisatracurium.

277 resulted in disorganized actin filaments and paralyzed worms in wild-type background.

278 Knockdown of Hsp90alpha1 resulted in paralyzed zebrafish embryos with poorly organized myofib

279 electrophysiological recordings from awake, paralyzed zebrafish larvae that can produce behaviorally