ライフサイエンスコーパス: paralyze

1 nhancement if the flagella rotary motion was paralyzed.

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

3 remainder of the cells twitch feebly or are paralyzed.

4 ype with approximately 30% of flies becoming paralyzed.

5 flagella that either beat very slowly or are paralyzed.

6 cation and control to people who are totally paralyzed.

7 plantation, whereas control animals remained paralyzed.

8 etrical responses even after their eyes were paralyzed.

9 rmal lungs were anesthetized, intubated, and paralyzed.

10 is (AFM) that have left hundreds of children paralyzed.

11 28% of these patients were pharmacologically paralyzed.

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

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

14 ts, animals lacking both Cl(-) extruders are 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 NRA in decerebrate cats, most of which were paralyzed and artificially ventilated.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

48 een identified that readily explains how PZQ paralyzes and damages schistosomes.

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 The animals were anesthetized, paralyzed, and mechanically ventilated in pressure-contr

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

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

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

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

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

60 Sheep were anesthetized, paralyzed, and mechanically ventilated.

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

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

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

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

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

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

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

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

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

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

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

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

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

74 Five anesthetized, paralyzed, and ventilated pigs.

75 Anesthetized, paralyzed, and ventilated sheep.

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

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

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

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

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

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

82 Paralyzed animals transplanted with EBD cells partially

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

84 ective thick filament assembly, resulting in paralyzed animals.

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

86 ts of the nervous system leading to severely paralyzed animals.

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

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

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

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

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

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

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

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

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

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

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

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

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

100 zed to tether the snail to its prey, rapidly paralyzed by neuroexcitatory peptides [2,3].

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

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

103 ross distinct V2 stripes in anesthetized and paralyzed capuchin monkeys (N = 3 animals, 6 hemispheres

104 se anesthetized, artificially ventilated and paralyzed cats.

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

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

107 ate host produce a water-soluble factor that paralyzes cercariae, the life cycle stage infecting huma

108 ty of detecting wild poliovirus excretion in paralyzed children.

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

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

111 embly usually result in motility-impaired or paralyzed cilia, which in humans causes disease.

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

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

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

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

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

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

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

119 Eighteen anesthetized and paralyzed dogs.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

137 Animals were anesthetized and paralyzed for imaging stability.

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

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

140 The paralyzed growth plate showed disruptions to column orga

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

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

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

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

145 h respiratory depression and in those with a paralyzed hemidiaphragm confirmed that the controller ca

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

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

148 to protect themselves and their provisions, paralyzed honeybees, against mold fungi.

149 complex mixture of bioactive molecules that paralyze host defenses.

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

151 king growing hosts and parasitoids attacking paralyzed hosts.

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

153 hich brain-controlled interfaces are used by paralyzed human subjects to control computer cursors or

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

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

156 nic electrocorticography (ECoG) implant in a paralyzed individual, which allowed stable monitoring of

157 o precise interaction with objects, enabling paralyzed individuals to perform many tasks of daily liv

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

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

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

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

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

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

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

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

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

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

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

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

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

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

172 graded control of muscle contraction in his paralyzed limb.

173 etween the contralesional hemisphere and the paralyzed limb.

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

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

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

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

178 y to control assistive devices and reanimate paralyzed limbs.

179 This mutant toxin shows enhanced efficacy in paralyzing local muscles at the injection site and lower

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

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

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

183 Paralyzed LRs exhibited marked atrophy compared with fun

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

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

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

187 n pentobarbital anesthetized, ventilated and paralyzed male rats.

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

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

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

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

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

193 In paralyzed mice significant damage was observed in the ou

194 However, F-wave latencies were increased in paralyzed mice, which suggests that neuropathy may exist

195 d the gastrocnemius muscle were unchanged in paralyzed mice.

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

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

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

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

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

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

202 Paralyzed motors of cells carrying a motA point mutation

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

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

205 Paralyzed muscles can be reanimated following spinal cor

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

207 on of new neuromuscular junctions within the paralyzed muscles.

208 One paralyzed mutant recovered in our screen contains an all

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

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

211 es of human infection but succumb to chronic paralyzing myositis and skeletal muscle vasculitis, not

212 % vs n = 22, 56% in controls; p < 0.001) and paralyzed (n = 34, 77% vs n = 3, 14% in controls; p < 0.

213 Its hyphae can paralyze nematodes within a few minutes of contact, but

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

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

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

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

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

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

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

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

222 s that can record the intended movement of a paralyzed part of the body, a computer algorithm that de

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

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

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

226 hich not only can restore communications for paralyzed patients but also have the potential to transf

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

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

229 Paralyzed patients received either TOF monitoring with a

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

231 Twenty-five consecutive sedated and paralyzed patients with acute respiratory distress syndr

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

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

234 In a subgroup of seven paralyzed patients, we also measured ventilation-perfusi

235 st function, most commonly motor function in paralyzed patients.

236 elopment of neural prosthetics for assisting paralyzed patients.

237 lopment of motor-cortical neuroprostheses in paralyzed patients.

238 tegy aimed at restoring mobility in severely paralyzed patients.

239 l signals for neural prosthetics that assist paralyzed patients.

240 e movements are promising aids for assisting paralyzed patients.

241 velop into clinically viable systems to help paralyzed people.

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

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

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

245 Ten anesthetized and paralyzed preoperative infants with HLHS were evaluated

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

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

248 synergistically to modify channel gating and paralyze prey.

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

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

251 Twenty-seven anesthetized and paralyzed rabbits.

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

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

254 ased from sciatic nerves in anesthetized and paralyzed rats.

255 We show that this compound paralyzes schistosome cercariae and prevents infection a

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

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

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

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

260 nerve (C7) from the nonparalyzed side to the paralyzed side results in increase of 17.7 in Fugl-Meyer

261 ns from the contralesional hemisphere to the paralyzed side.

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

263 After paralyzing spinal cord injury the adult nervous system h

264 uromodulation that restored locomotion after paralyzing spinal cord injury.

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

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

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

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

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

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

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

272 This paralyzes the capacity of neutrophils and macrophages to

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

274 Rather than paralyzing the CTL response, these epitope modifications

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

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

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

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

279 that disrupt neuromuscular communication to paralyze their prey.

280 d metabolic state to CD8(+) T cells, thereby paralyzing their effector functions.

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

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

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

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

285 rform a laparoscopic procedure or a recently paralyzed user of a powered wheelchair must learn to ope

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

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

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

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

290 Paralyzed, ventilated rats were hemorrhaged (18 mL blood

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

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

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

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

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

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

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

298 lectrical activity in nerves and muscles and paralyzing would-be predators.

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

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