ライフサイエンスコーパス: squid

1 superconducting quantum interference device (SQUID).

2 superconducting quantum interference device (SQUID).

3 ure to HHP for lowering the allergenicity of squid.

4 alopods, such as the octopus, cuttlefish and squid.

5 fresh squid fit for consumption and spoiled squid.

6 and survival of injured, but not uninjured, squid.

7 cilitate foraging opportunities for Humboldt squid.

8 oral sequences [7, 8] earlier than uninjured squid.

9 pharmaceuticals) including shrimp, crab, and squid.

10 s and snails but none in oyster, octopus and squid.

11 nents and their roles in colonization of the squid.

12 arly phases of bacterial colonization of the squid.

13 um interference of currents in an atomtronic SQUID.

14 mbda(max)) at 528 nm in bovine and 554 nm in squid.

15 p techniques for the genetic manipulation of squid.

16 on between neuronal trigger and color in the squid.

17 tro and to establish symbiosis with juvenile squid.

18 ium Vibrio fischeri and the Hawaiian bobtail squid.

19 superconducting quantum interference device (SQUID)(4).

20 t mainly feed on crustaceans; large fish and squid; a mixture of crustaceans, small fish and squid; o

21 Large squid abandoned seasonal coastal-shelf habitats in 2010

22 Squid-adaptive binK alleles promoted colonization and im

23 Site-directed mutagenesis of squid ADAR2a showed that its increased affinity and edit

24 efects in their ability to colonize juvenile squid, although the impact of the loss of SypB or SypI w

25 this sensitization during encounters between squid and a natural fish predator.

26 hic species, its purpose in pelagic species (squid and certain fish and crustaceans) is poorly unders

27 The robust sucker ring teeth (SRT) from squid and cuttlefish are one notable exception of thermo

28 Coleoid cephalopods (octopus, squid and cuttlefish) are active, resourceful predators

29 interesting SQUID physics with an atomtronic SQUID and especially, macroscopic quantum phenomena with

30 ave grown ever more reliant on nutrient-poor squid and invertebrates as teleost fish have declined in

31 en rise to descendants as different as giant squid and microscopic pea clams.

32 Juvenile squid and octopods hatch from the egg already swimming i

33 If made genetically tractable, squid and other cephalopods offer a wealth of biological

34 simulate the microgravity environment, host squid and symbiosis-competent bacteria were incubated to

35 Other systems, for example, hydra, squid and the honeybee, are valuable alternative models

36 red habitat and trophic interactions between squid and white sharks, in which future ecosystem studie

37 cally stimulating the optic lobe of the oval squids and observing their body pattern changes, surpris

38 observed in superconducting devices such as SQUIDs and qubits is still a major unsolved puzzle.

39 insically influences the phase difference in SQUIDs and qubits.

40 lected from specialized cells in the skin of squids and related cephalopods.

41 uperconducting quantum interference devices (SQUIDs) and qubits are feasible.

42 ctroelectrochemistry, magnetic measurements (SQUID), and structural and morphological investigations

43 f the visual system of cephalopods (octopus, squid, and cuttlefish) that have a single unfiltered pho

44 excised single neurons from marine worm and squid, and then exterior to intact, optically opaque mar

45 n the neural tissues of coleoids (octopuses, squids, and cuttlefishes), with a greater fraction of no

46 ariables, our analyses suggest that Humboldt squid are indirectly affected by OMZ shoaling through ef

47 However, only in loliginid squids are they and the subwavelength photonic structure

48 ephalopods), namely octopus, cuttlefish, and squid, are widely considered to be the most cognitively

49 link with a frequency-tunable high impedance SQUID array resonator.

50 Seminal studies using squid as a model led to breakthroughs in neurobiology.

51 pite their anatomical advantages, the use of squid as a model receded over the past several decades a

52 one hour later further ingested raw tuna and squid as an evening meal at a bar.

53 ng squid oriented toward and pursued injured squid at greater distances than uninjured squid, regardl

54 pplement the decreased amount of provisioned squid available during this time.

55 gly, mutant FUS-induced impairment of FAT in squid axoplasm and of axonal outgrowth in mammalian prim

56 Vesicle motility assays in isolated squid axoplasm further demonstrated that both mutant mer

57 Experiments presented here using isolated squid axoplasm reveal inhibition of FAT as a common toxi

58 s impaired anterograde and retrograde FAT in squid axoplasm, whereas FUS WT had no effect.

59 nhibited anterograde transport when added to squid axoplasm.

60 exposure of PAD inhibited anterograde FAT in squid axoplasm.

61 Here we report the development of a SQUID-based flux noise spectrometer and measurements of

62 ch may provide a means to reduce the size of SQUID-based superconducting electronics.

63 is a feasible technological alternative for squid-based surimi production improving its yield and ge

64 Structure of the squid bathorhodopsin is characterized by formation of a

65 d were found to be very similar to those for squid bathorhodopsin.

66 Similar to the squid beak, we have developed nanocomposites where the d

67 nhanced mechanical gradient character of the squid beak, we herein report a nanocomposite that mimics

68 Using stable isotope ratios measured in squid beaks recovered from diet samples of wandering alb

69 Once targeted, injured squid began defensive behavioral sequences [7, 8] earlie

70 Hydro-acoustic data, reveal that squid biomass in this study area nearly doubled between

71 As in mammals, injury in squid can cause persistent SA in peripheral afferents.

72 Cephalopods, such as octopus and squid, can change their coloration in an instant, and ev

73 interactions between sqADAR2 and RNA because squid cells have a approximately 3-fold higher ionic str

74 Concurrently, using an annotated squid chromatophore proteome together with microscopy, w

75 y, we revealed that eptA promotes successful squid colonization by V. fischeri, supporting its potent

76 ts that were reproducibly depleted following squid colonization represented 380 genes, including 37 t

77 defect for a DeltalapD mutant in initiating squid colonization, indicating a role for the Lap system

78 ocalization, and role in the early stages of squid colonization.

79 Magnetic susceptibility measurements (SQUID) confirm the paramagnetic scaffold with repeating

80 ice, fish, insects, and the Hawaiian bobtail squid, continue to provide critical insight into how hos

81 ifferent seafood organisms: oysters, prawns, squid, crabs, and sardines.

82 Analogous to a conventional SQUID, currents flowing through two junctions in an atom

83 Cephalopods (squid, cuttlefish and octopuses) have a unique set of bi

84 ementing previous X-ray crystallographic and SQUID data for solid material, the electronic structure

85 measured low-frequency flux noise spectra in SQUID devices if one takes as a source of fluctuations t

86 h with extensive validation to show that the squid Doryteuthis pealeii recodes proteins by RNA editin

87 e demonstrate efficient gene knockout in the squid Doryteuthis pealeii using CRISPR-Cas9.

88 n-producing injury reduced predation risk in squid (Doryteuthis pealeii).

89 tion of behavioral and neuronal responses in squid, Doryteuthis pealei [5, 6].

90 Previous studies have inferred that jumbo squid Dosidicus gigas support growth during maturation t

91 Humboldt (jumbo) squid (Dosidicus gigas) are highly migratory predators a

92 ates were evaluated and compared to those of squid (Dosidicus gigas) muscle proteins (SM).

93 structural modifications in beta-chitin from squid (Dosidicus gigas, d'Orbigny, 1835) pens and their

94 hicles to study the behavior of the Humboldt squid, Dosidicus gigas, in its natural deep-sea habitat.

95 superconducting quantum interference device (SQUID) down to temperatures of 2 K and in fields up to 7

96 Squid dynamically tune the intensity and colors of iride

97 Previously, we isolated a squid editing enzyme (sqADAR2) that shows a unique struc

98 Knocking out TDO in squid embryos efficiently eliminated pigmentation.

99 microgravity on the interactions between the squid Euprymna scolopes and its beneficial symbiont Vibr

100 Here, we used the symbiosis between the host squid Euprymna scolopes and its luminescent bacterium Vi

101 ral binary light-organ symbiosis between the squid Euprymna scolopes and its luminous bacterial partn

102 namic stability of the mutualism between the squid Euprymna scolopes and its specific, bioluminescent

103 n important defense molecule secreted by the squid Euprymna scolopes and sensed by the bacterial symb

104 Efficient symbiotic colonization of the squid Euprymna scolopes by the bacterium Vibrio fischeri

105 The Hawaiian squid Euprymna scolopes forms a natural symbiosis with V

106 dence that a galaxin protein, EsGal1, of the squid Euprymna scolopes participates in both: (i) select

107 an symbiosis between Vibrio fischeri and the squid Euprymna scolopes.

108 on and growth within the light organs of the squid Euprymna scolopes.

109 rio fischeri during colonization of its host squid Euprymna scolopes.

110 ote colonization of its eukaryotic host, the squid Euprymna scolopes.

111 eri to form a symbiotic association with the squid Euprymna scolopes.

112 model V. fischeri host, the Hawaiian bobtail squid Euprymna scolopes.

113 t organ in the mantle cavity of the sepiolid squid Euprymna scolopes.

114 tive accessory nidamental gland (ANG) of the squid Euprymna scolopes.

115 onospecific symbiont of the Hawaiian bobtail squid, Euprymna scolopes, and the establishment of this

116 Female Hawaiian bobtail squid, Euprymna scolopes, have an accessory nidamental g

117 iotic relationship with the Hawaiian bobtail squid, Euprymna scolopes, where the squid provides a hom

118 iotic relationship with the Hawaiian bobtail squid, Euprymna scolopes, whose light organ it colonizes

119 iosis within the light organ of the Hawaiian squid, Euprymna scolopes.

120 gest the enormous eyes of giant and colossal squid evolved to see the bioluminescence induced by the

121 Thus, while squid exhibit peripheral alterations in afferent neurons

122 Second, RNA-Seq analysis of squid exposed to modeled microgravity conditions exhibit

123 array was able to discriminate between fresh squid fit for consumption and spoiled squid.

124 uperconducting Quantum interference Devices (SQUIDs) for measurement of the magnetic field vector, hi

125 rn provide camouflage that helps protect the squid from night-time predators.

126 superconducting quantum interfering device (SQUID), FT Raman, and X-ray crystallographic analysis, a

127 superconducting quantum interference device (SQUID), FT Raman, X-ray crystallographic etc.) and densi

128 resents a critical advancement toward making squid genetically tractable.

129 The squid giant axon and synapse, for example, laid the foun

130 lity assays performed with axoplasm from the squid giant axon showed a requirement for a Rab GTPase i

131 ll sites) are edited more extensively in the squid giant axon than in its cell bodies.

132 In addition, working with the squid giant axon, Cole and Moore noted that strong hyper

133 he falling phase of action potentials in the squid giant axon, the diversity of voltage-gated potassi

134 nd Huxley model and for eliciting a spike in squid giant axons, the preparation for which the model w

135 By applying rapid voltage steps to squid giant axons, we previously identified three compon

136 nd, more recently, in axoplasm isolated from squid giant axons.

137 n of this pathway in axoplasms isolated from squid giant axons.

138 lyzed before and after colonization of 1,500 squid hatchlings.

139 d their possible role in colonization of the squid have not previously been determined.

140 Squids have used their tunable iridescence for camouflag

141 The protein structure analysis of squid Hc showed that while HHP treatment decreased the a

142 t decrease in the allergenicity (P< 0.05) of squid Hc.

143 dary, tertiary, and quaternary structures of squid hemocyanin (Hc) were characterised, and the relati

144 etween the bacterium Vibrio fischeri and its squid host, which can be observed directly and in real t

145 The Japanese firefly squid Hotaru-ika (Watasenia scintillans) produces intens

146 culate that it can cooperate with endogenous squid Hsp(c)70 to mediate binding and/or disaggregation

147 ble mechanism by which D. gigas, and related squids, illuminate these patterns to create visual signa

148 bass, resulting in decreased survival of the squid in a 30-minute trial featuring free interaction be

149 onic system for the shelf-life assessment of squid in cold storage.

150 r of the ongoing range expansion of Humboldt squid in the northeastern Pacific Ocean.

151 companied by a collapse of this fishery, and squid in the region showed major changes in the distribu

152 ween white sharks Carcharodon carcharias and squids in the eastern North Pacific Ocean.

153 interactions between white sharks and large squids in the waters of Guadalupe Island, Mexico.

154 uperconducting quantum interference devices (SQUIDs) incorporating topological insulator weak links.

155 rconducting quantum interference devices (rf SQUIDs) inside a superconducting cavity.

156 owing through two junctions in an atomtronic SQUID interfere due to the phase difference from rotatio

157 Loss of a larger amount of energy in squid is attributed to the presence of a flexible bindin

158 e, magnetic monopole flux noise amplified by SQUID is audible to humans.

159 n which the light organ of Euprymna scolopes squid is colonized exclusively by Vibrio fischeri bacter

160 The squid is the only organism known to produce light using

161 Dosidicus gigas (jumbo or Humboldt squid) is a semelparous, major predator of the eastern P

162 sels from among 16,000 industrial longliner, squid jigger, and trawler fishing vessels.

163 graphy of V. fischeri populations within the squid light organ impacts the physiology of this symbiot

164 RNA by 30- or 100-fold in vertebrate-like or squid-like conditions, respectively.

165 We found that squid-like salt conditions severely impair the binding a

166 Properties of gelatin films from splendid squid (Loligo formosana) skin bleached with hydrogen per

167 SQUID magnetic measurements on the isomeric iron imides,

168 Through an extensive set of SQUID magnetic measurements, X-ray absorption spectrosco

169 transition above 80 K as inferred by the dc SQUID magnetic susceptibility measurement.

170 IR, UV-vis, and EPR spectroscopy as well as SQUID magnetization and single-crystal X-ray crystallogr

171 The ac SQUID magnetization data, at zero field and between freq

172 RD analyses, temperature and field-dependent SQUID magnetization methods, as well as (57)Fe Mossbauer

173 y UV/vis/NIR and EPR spectroscopy as well as SQUID magnetization studies.

174 th for a dinuclear complex (DeltaT = 22 K by SQUID magnetometer in "settle" mode) and show a remarkab

175 imaging with EDX analysis, XPS analysis, and SQUID magnetometry analysis of catalytic solutions.

176 th CASSCF-SO calculations and confirmed with SQUID magnetometry and EPR spectroscopy, showing easy-ax

177 Squid magnetometry and EPR studies yield data that are c

178 exchange coupling, Aex, is determined using SQUID magnetometry and ferromagnetic resonance (FMR), di

179 Variable-temperature SQUID magnetometry and IR, NIR, and EPR spectroscopies o

180 ition properties have been characterized via SQUID magnetometry and Raman spectroscopy.

181 Furthermore, SQUID magnetometry from 5 to 300 K of solid [(+)-NDI-Del

182 SQUID magnetometry indicates hysteresis below 6 K, while

183 SQUID magnetometry measurements indicate that 5 is a mac

184 ly prepared diradical 1 are characterized by SQUID magnetometry of polycrystalline powders, in polyst

185 SQUID magnetometry reveals that 1 has an effective barri

186 (V) but single-crystal X-ray diffraction and SQUID magnetometry suggest a Np(III) -U(VI) assignment.

187 SQUID magnetometry suggests that the iron containing sam

188 scopy, photoelectron spectroscopy (XPS), and SQUID magnetometry to gain information on its morphologi

189 EPR spectroscopy, SQUID magnetometry, and DFT calculations thoroughly char

190 , EPR, electronic absorption spectroscopies, SQUID magnetometry, and X-ray crystallography.

191 haracterized by X-ray crystallography, while SQUID magnetometry, EPR spectroscopy, and UV-vis-NIR spe

192 -ray diffraction analysis, (57)Fe Mossbauer, SQUID magnetometry, mass spectrometry, and combustion an

193 SQUID magnetometry, Mossbauer spectroscopy, and DFT calc

194 ies, as investigated by variable-temperature SQUID magnetometry, reveal weak intramolecular antiferro

195 onic properties of 1-4 have been assessed by SQUID magnetometry, while a DFT analysis of complexes 1

196 haracterized using (1)H NMR spectroscopy and SQUID magnetometry, while all species were structurally

197 been confirmed by X-ray crystallography and SQUID magnetometry.

198 ffording an S = 2 spin state as confirmed by SQUID magnetometry.

199 e of macroscopic ferromagnetism was found in SQUID magnetometry.

200 ic circular dichroism (MCD) spectroscopy and SQUID magnetometry.

201 of thermally active ASI systems by means of SQUID magnetometry.

202 Superconducting quantum interference device (SQUID) magnetometry confirmed and quantitatively charact

203 superconducting quantum interference device (SQUID) magnetometry, double-coil mutual inductance, and

204 Additionally, squid maintained body condition during maturation regard

205 capacity of myofibrillar proteins from Jumbo squid mantle muscle along with the addition of isoascorb

206 The magnetic susceptibility was studied by SQUID measurements for TTT-NN and TPT-NN.

207 superconducting quantum interference device (SQUID) measurements for both, the open precursor 8 and t

208 Superconducting quantum interference device (SQUID) measurements reveal that the trisradical tricatio

209 superconducting quantum interference device (SQUID) measurements.

210 superconducting quantum interference device (SQUID) microscopy and secondary ion mass spectrometry (S

211 free exception (e.g., marine polychaetes and squids), minerals are thought to be indispensable for to

212 e of symbiotic initiation in the V. fischeri-squid model symbiosis, and more broadly it adds to a gro

213 This was confirmed by SQUID monitoring during H2 release from solid 2[K(DB18C6

214 is particularly common in coding regions of squid mRNAs.

215 ct of IA reduced (p < 0.05) the GFA of Jumbo squid muscle proteins.

216 Results demonstrate that washing squid muscle under the proposed acidic conditions is a f

217 The samples were mussel tissue, squid muscle, crab claw meat, whale meat, cod muscle, Gr

218 zyme, is expressed outside of the nucleus in squid neurons.

219 resistance to the high Cl(-) levels found in squid neurons.

220 A study in squid now suggests that nociceptive sensitization enhanc

221 the presence of evident scars made by large squids on the body of the white sharks, mainly on the he

222 uperconducting quantum interference devices (SQUIDs) on a transmission line.

223 superconducting quantum interference device (SQUID-on-tip)(8) to obtain tomographic images of the Lan

224 d A292T) in bovine and at site 111 (Y111) in squid opsins.

225 id; a mixture of crustaceans, small fish and squid; or carrion.

226 ack sea bass given access to freely swimming squid oriented toward and pursued injured squid at great

227 in single-junction diffraction patterns and SQUID oscillations are lifted and independent of chemica

228 The node-lifting of the SQUID oscillations is consistent with low-energy Andreev

229 At high temperatures, the SQUID oscillations revert to conventional behaviour, rul

230 Serial squid passaging of bacteria produced eight distinct muta

231 We show that in squid, patchy colloidal physics resulted from an evoluti

232 ing powder (CCP), shrimp shell powder (SSP), squid pen powder (SPP), alpha-chitin, and beta-chitin, T

233 f adding the cells of four lactobacilli to a squid pen powder (SPP)-containing medium on prodigiosin

234 Squid pen protein recovered from chitosan processing was

235 Squid pens were subjected to alkali hydrolysis to extrac

236 form a complex that crystallises inside the squid photophores, and that in the crystal one or more o

237 possibility of studying various interesting SQUID physics with an atomtronic SQUID and especially, m

238 We demonstrate that squid possess nociceptors that selectively encode noxiou

239 sult suggests that the repetitions in native squid proteins could have a genetic advantage for increa

240 bobtail squid, Euprymna scolopes, where the squid provides a home for the bacteria, and the bacteria

241 ed squid at greater distances than uninjured squid, regardless of previous anesthetic treatment.

242 udied despite the high biomass of fishes and squids residing at depths beyond the euphotic zone.

243 Ommochromes, the pigments found in squid retinas and chromatophores, are derivatives of try

244 y model is based on the crystal structure of squid rhodopsin (lambda(max) = 490 nm) and shows a maxim

245 rigger morphological changes in the juvenile squid's light organ that occur upon colonization.

246 rial biofilm formation on the surface of the squid's light organ.

247 neural basis of body patterning in the oval squid, Sepioteuthis lessoniana Most areas in the optic l

248 entrations of H(2)O(2) used for bleaching of squid skin prior to gelatin extraction directly affected

249 n from the dynamic color-changing ability of squid skin, we have developed a composite material with

250 delta(15)N) of five important Southern Ocean squid species in relation to indices of environmental co

251 s (bacterial photophores) from two divergent squid species.

252 Squid spoilage was monitored simultaneously by the color

253 ulation involves the translational repressor Squid (Sqd).

254 Here we describe thermoplastic processing of squid SRT via hot extrusion of fibres, demonstrating the

255 lymers), which is inspired by animals (e.g., squid, starfish, worms) that do not have hard internal s

256 superconducting quantum interference device (SQUID), steady-state and transient absorption spectrosco

257 ng the magnetic Compton scattering data with SQUID studies that measure the total magnetic moment sug

258 re based on a structural protein produced in squid suction cups that has a segmented copolymer struct

259 , robust changes far from sites of injury in squid suggest that persistently enhanced afferent activi

260 orted decades earlier, where a double-planar SQUID (Superconducting Quantum Interference Devices) gra

261 e lyophilized liposomes were incorporated in squid surimi gels at 10.5% concentration.

262 uid-surimi control (C), glucomannan-enriched squid-surimi (G) and glucomannan-spirulina enriched squi

263 urimi (G) and glucomannan-spirulina enriched squid-surimi (GS).

264 s of eight rats each received for 7weeks the squid-surimi control (C), glucomannan-enriched squid-sur

265 The effect of high-fat squid-surimi diets enriched in glucomannan or glucomanna

266 The squid symbiont Vibrio fischeri uses an elaborate TCS pho

267 ft genome sequence of Vibrio fischeri SR5, a squid symbiotic isolate from Sepiola robusta in the Medi

268 sulators(5,6), including Dy(2)Ti(2)O(7), the SQUID technique has been proposed for their direct detec

269 ocomotion and other spontaneous behaviors of squid that received distal injury to a single arm (with

270 , primarily due to a large increase in small squid that were not susceptible to the fishery.

271 mass concentration (0.3 mg g(-1) tissue) and squid the lowest (0.04 mg g(-1) tissue).

272 Juvenile squid thus appeared to respond to El Nino with an altern

273 uggesting increased levels of RNA editing in squids thus raise the question of the nature and effects

274 bacterial molecules that are produced by the squid to select V. fischeri from the ocean microbiota.

275 gella prompts its host, the Hawaiian bobtail squid, to prepare for its arrival.

276 currents may be realized with an atomtronic SQUID toward the goal of quantum metrology of rotation s

277 A new study describes editing of a gene in a squid using CRISPR.

278 MCD), electron paramagnetic resonance (EPR), SQUID, UV-vis absorption, and X-ray absorption spectrosc

279 d, more specifically, how one symbiosis, the squid-vibrio association, provides insight into the pers

280 Using the squid-vibrio model system, we provide a characterization

281 ed symbioses through the study of the binary squid-vibrio model.

282 (2013) reveal that first contact within the squid-vibrio symbiosis triggers profound molecular and c

283 our understanding of the early stages of the squid-vibrio symbiosis, and more generally inform the tr

284 mventing, host immune responses in the model squid-vibrio symbiosis.

285 /w) from the molecular distillation of crude squid visceral oil.

286 ed for vertebrate (bovine) and invertebrate (squid) visual photoreceptors shows that such a mechanism

287 ertebrate (bovine, monkey) and invertebrate (squid) visual pigments was carried out using a hybrid qu

288 etween vertebrate (bovine) and invertebrate (squid) visual pigments, the mechanism of molecular rearr

289 lta(15) N of potential prey (crustaceans vs. squid vs. fish and carrion), analysis of delta(15) N in

290 e and a bent oligophenylene loop ("molecular squid"), was obtained in an efficient, scalable synthesi

291 ium Vibrio fischeri and the Hawaiian bobtail squid, we characterized the bacterial transcriptional re

292 n the Guaymas Basin from 2010 to 2012, small squid were abundant and matured at an unusually small ma

293 rangements observed for 7-cis-rhodopsin from squid were found to be very similar to those for squid b

294 Although large squid were not found in the Guaymas Basin from 2010 to 2

295 Both small and large mature squid, were present in the Salsipuedes Basin during 2011

296 als, documented especially in cuttlefish and squid, where they are used both in camouflage and a rang

297 -like protein), possibly infested in the raw squid which he had ingested just before manifestation of

298 thin the light organ of the Hawaiian bobtail squid, which provides an opportunity to study how bacter

299 vidual showed new scars, confirming that the squid-white shark interaction likely occurs near Guadalu

300 ificantly delayed in its ability to colonize squid within the first 12 h, but eventually it establish