ライフサイエンスコーパス: crab

1 basis of the existence of CRAB criteria (AL-CRAB).

2 s, Gecarcoidea natalis (Christmas Island red crab).

3 predator cues (Carcinus maenas, common shore crab).

4 h includes spiders, scorpions, and horseshoe crabs).

5 etected with 16 clusters of clonally related CRAB.

6 tion on visual processing available for this crab.

7 y each hemiellipsoid body in an adult hermit crab.

8 imilar sizes to those found in the horseshoe crab.

9 ors: Bay shrimp, English sole, and Dungeness crab.

10 were developed to detect numerous species of crab.

11 erotonin than is aggressiveness in the shore crab.

12 observed in the visually guided behaviors of crabs.

13 o effect on the functional response of large crabs.

14 upstream reach containing only killifish and crabs.

15 tae permits comparison with extant horseshoe crabs.

16 decomposition rates fourfold compared to the crabs.

17 n the appendages of two species of horseshoe crabs.

18 Among the 1,255 patients, 100 (8%) had AL-CRAB, 476 (38%) had AL-PCMM, and 679 (54%) had AL only.

19 We describe CRAB - a fully integrated text mining tool designed to s

20 arisons between these taxa and the horseshoe crab, a chelicerate from the sister group to arachnids.

21 ime PCR assay was developed for detection of crab, a crustacean allergen, in food products.

22 ntly, over the 3-year duration of the study, crab abundance declined at those sites invaded by the cr

23 The effects of crab activity level on the functional response were depe

24 of waterborne chemical cues known to reduce crab activity level.

25 genomes are similar to that of the horseshoe crab, although both of the solifuges possess a region of

26 On multivariate analysis, pooled AL-CRAB and AL-PCMM retained negative prognostic value inde

27 Because the outcomes of AL-CRAB and AL-PCMM were similar, they were pooled for univ

28 ves of Chelicerata, which includes horseshoe crabs and arachnids.

29 n mollusks, and arthropods such as horseshoe crabs and beetles, indicating that this pathway has been

30 a second pool of MMHg, compared to sediment, crabs and fish.

31 Recent records show that 22 species of crabs and lobsters have been reported from the Southern

32 16,000 records of Recent Southern Hemisphere crabs and lobsters.

33 vestigated two emerging diseases of juvenile crabs and oysters from the UK using massively parallel s

34 Several obligate associate crabs and shrimps species may co-occur and interact with

35 -dependent effects of rocky shore consumers (crabs and snails) on community recovery under both high

36 larity between the Middle Triassic horseshoe crabs and their recent analogues documents anatomical co

37 this influence of serotonin is conserved in crabs and whether these behaviours are sensitive to huma

38 Invertebrates (shrimp, oyster, crab) and other nearshore species comprised the majority

39 artitioning the direct impacts of predators (crabs) and grazers (snails) on community recovery across

40 ognosis, similar to that of patients with AL-CRAB, and should therefore be considered together as AL

41 ere 20% d(-1) for polychaetes, 10% d(-1) for crabs, and 6% d(-1) for fish after acquisition of Cs fro

42 ples consisting of 86 fishes, 65 shrimps, 59 crabs, and 68 oysters were collected and analyzed weekly

43 articular marine calcifiers such as oysters, crabs, and corals.

44 1), 14% d(-1), and 5% d(-1) for polychaetes, crabs, and fish, respectively.

45 cuds, sideswimmers), and Decapoda (lobsters, crabs, and shrimps).

46 ers in males are plesiomorphic for horseshoe crabs, and the bulbous claspers in Tachypleus and Limulu

47 mplanted into the pericardial region of live crabs, and the resulting dialysates were desalted, conce

48 of engineered tree holes for refuge by tree crabs, and the use of two behaviour patterns in this spe

49 ts of fruit industry, five dessert and seven crab apple varieties grown in Eastern Europe (Latvia).

50 l) when compared to seed oils recovered from crab apples (130.55-202.54 mg/100g oil).

51 mal refuge, by the herbivorous mangrove tree crab Aratus pisonii.

52 Horseshoe crabs are classic "living fossils", supposedly slowly ev

53 local thermal conditions at the vents, these crabs are not restricted by the physiological limits tha

54 The living horseshoe crabs are remnants of a much larger diversity of aquatic

55 However, some animals, including fiddler crabs, are sensitive to the polarization of light across

56 terest following the "discovery" of lithodid crabs around Antarctica has centred on a hypothesis that

57 ignals from commercial food products listing crab as an ingredient than from those containing other c

58 efold density decreases among juvenile stone crabs as habitat increased (i.e. weak habitat imitation)

59 rks, and epibenthic invertebrates (Dungeness crab) because they consume species known to be sensitive

60 sheries worldwide, difficulties in observing crabs' behaviour over their annual cycles, and the timin

61 ments and various estuarine organisms (green crab, blue mussel, killifish, eider) to investigate meth

62 on the functional response were dependent on crab body size.

63 True crabs (Brachyura) are the most successful group of decap

64 y poor fossil record of a different group of crabs (Brachyura), and examination of relatively few Rec

65 We find that the timing of the annual crab breeding migration is closely related to the amount

66 We found that crabs build separate appetitive and aversive memories th

67 Warming increased mortality rates of crabs, but had no effect on their moulting rates.

68 The aim of this work was to separate a snow crab by-products hydrolysate by electrodialysis with ult

69 Recently, a snow crab by-products hydrolysate has demonstrated antibacter

70 This indicates that replacement of native crabs by invasive crayfish likely alters the structure a

71 Key inclusion criteria were presence of CRAB (C=calcium elevation; R=renal impairment; A=anaemia

72 Adult blue crab Callinectes sapidus exhibit behavioral and ecologic

73 pericardial organs of a model organism blue crab Callinectes sapidus were detected from the MALDI MS

74 rtality was primarily attributed to the blue crab Callinectes sapidus, whilst the mud crab Panopeus h

75 5'-RACE) to clone from Y-organs of the blue crab (Callinectes sapidus) a cDNA encoding a putative PM

76 The metabolomic profile of blue crab (Callinectes sapidus) captured in the Acquatina lag

77 investigated in 11 finfish species and blue crabs (Callinectes sapidus) in the Passaic River estuary

78 egulation, the full-length cDNAs of the blue crab, Callinectes sapidus EcR1 and RXR1 were isolated fr

79 Crabs can escape directly away from a visual threat wher

80 ceptors, the gastropyloric receptor 2 in the crab Cancer borealis and the coxobasal chordotonal organ

81 The pyloric network frequency in the crab Cancer borealis is correlated with the preferred fr

82 The crab Cancer borealis undergoes large daily fluctuations

83 of the stomatogastric nervous system of the crab Cancer borealis, projection neurons convey sensory,

84 In stomatogastric ganglia of the crab Cancer borealis, the duty cycle of the bursting pac

85 solated stomatogastric ganglion (STG) of the crab Cancer borealis, we showed previously that pyrokini

86 tified neurons in the pyloric network of the crab Cancer borealis.

87 in the stomatogastric nervous system of the crab Cancer borealis.

88 neuron of the stomatogastric ganglion of the crab Cancer borealis.

89 ircuit of the stomatogastric ganglion of the crab Cancer borealis.

90 in the stomatogastric ganglion (STG) of the crab Cancer borealis.

91 n several decapod crustaceans, including the crab Cancer productus, but whether these peptides serve

92 Multiple motor neurons of the crab (Cancer borealis) cardiac ganglion have highly cons

93 using the gastric mill (chewing) CPG in the crab (Cancer borealis) stomatogastric ganglion, where st

94 We are exploring this issue in the crab (Cancer borealis) stomatogastric nervous system by

95 systems with slow muscle dynamics, as in the crab (Cancer borealis) stomatogastric system used here.

96 Edible crab (Cancer pagurus) is one of the most important crust

97 and absence of waterborne cues from feeding crabs (Cancer productus).

98 of the stomatogastric ganglion (STG) of the crab, Cancer borealis, are remarkably invariant between

99 s were then used for in vivo MD in the Jonah crab, Cancer borealis, during a feeding study, with mass

100 work function in the cardiac ganglion of the crab, Cancer borealis.

101 mple neuropeptides from the hemolymph of the crab, Cancer borealis.

102 in the stomatogastric ganglion (STG) of the crab, Cancer borealis.

103 hree of the four extant species of horseshoe crabs-Carcinoscorpius rotundicauda, Limulus polyphemus a

104 crofibers (1-5 mm in length) ingested by the crab Carcinus maenas and the consequences for the crab's

105 a community comprised of the predator (shore crab Carcinus maenas), various grazing detritivores (amp

106 ics may be ingested and inhaled by the shore crab Carcinus maenas, although the biological consequenc

107 e coxobasal chordotonal organ (CBCTO) in the crab Carcinus maenas.

108 distinct introductions of the European green crab (Carcinus maenas) along the coast of eastern North

109 Here, we test the hypothesis that the shore crab (Carcinus maenas) can take up microplastics through

110 tions using behavioural bioassays with shore crabs (Carcinus maenas) as a model system.

111 eir shells in response to a long-established crab, Carcinus maenas.

112 sites coincident with the invasion of green crabs (Carcinusmaenas) into intertidal Sesarma burrows.

113 he samples were mussel tissue, squid muscle, crab claw meat, whale meat, cod muscle, Greenland halibu

114 d we identify PHABULOSA (PHB), REVOLUTA, and CRABS CLAW (CRC) as potential downstream targets of SEUS

115 Other YABBY proteins (e.g. CRABS CLAW [CRC] and YABBY3 [YAB3]) can substitute for I

116 The paralogous loci encode maize CRABS CLAW co-orthologs in the YABBY family of transcrip

117 ed to explain scaling in organs from fiddler crab claws to human brains.

118 the hemiellipsoid bodies of the land hermit crab Coenobita clypeatus resolve microglomerular synapti

119 oid body in the terrestrial Caribbean hermit crab, Coenobita clypeatus, and compare this organization

120 in assemblages between mesocosms containing crabs compared to mesocosms without crabs, decreasing cr

121 fine-structural organization of the fiddler crab compound eye in relation to visual processing and v

122 Although the fiddler crab compound eye is of the apposition type, typical for

123 existing MM on the basis of the existence of CRAB criteria (AL-CRAB).

124 butable to clonal expansion of plasma cells (CRAB criteria) also have multiple myeloma (MM).

125 Coral-dwelling gall crabs (Cryptochiridae) are obligate symbionts of stony c

126 ckness and apertural area in the presence of crab cues, indicating among-habitat variation in defence

127 wth (scope for growth) from 0.59 to -0.31 kJ crab d(-1) in crabs fed with 1% plastic.

128 ntaining crabs compared to mesocosms without crabs, decreasing crab size had no detectable effect on

129 However, for adult stone crabs, density remained stable across treatments, demons

130 Highly active insects and crabs depend on visual motion information for detecting

131 or divisions of the body of living horseshoe crabs differ in the loss of the outer and inner ramus, r

132 habitats with and without abundant predatory crabs differed in constitutive and inducible aspects of

133 nome browsers for three species (brown kiwi, crab-eating macaque and Malayan flying lemur); eight upd

134 cted nonhuman primate cell cultures and then crab-eating macaques with either simian hemorrhagic feve

135 -limiting disease in experimentally infected crab-eating macaques, while simian hemorrhagic fever vir

136 of balancing selection on at least one case (Crab-eating monkey retrocopy 6, or CER6) in both species

137 nes at four molting stages of Chinese mitten crab (Eriocheir sinensis).

138 guppies (Poecilia reticulata) and omnivorous crabs (Eudaniela garmani).

139 ally timed behaviors in these two species of crabs evidently differed.

140 t of this find on our understanding of early crab evolution.

141 fish had low MC concentrations, whereas Blue Crabs exhibited high levels of MC in both muscle and vis

142 p to constrain the antiquity of this cryptic crab family.

143 ion to existing requirements of attributable CRAB features (hypercalcaemia, renal failure, anaemia, a

144 sociated with near inevitable development of CRAB features in patients who would otherwise be regarde

145 riteria for the presence of myeloma-defining CRAB features, and the histological and monoclonal prote

146 growth) from 0.59 to -0.31 kJ crab d(-1) in crabs fed with 1% plastic.

147 Despite concerns over the sustainability of crab fisheries worldwide, difficulties in observing crab

148 were retained within the body tissues of the crabs for up to 14 days following ingestion and up to 21

149 to evaluate the food safety of the red king crab from Norwegian waters and obtain information on pos

150 Here we report a new fossil horseshoe crab from the mid-Silurian Lagerstatte in Herefordshire,

151 iassic (ca. 244 million years old) horseshoe crab from Yunnan Province, SW China.

152 ecifically individual activity level, on the crab functional response to mussel (Brachidontes exustus

153 its exoskeleton is shed, the blackback land crab Gecarcinus lateralis relies on an unconventional ty

154 t, or a true gall) shows that species within crab genera tend to inhabit the same pit shape.

155 , preys on mussels (Mytlius edulis), but the crab has not yet invaded northern New England.

156 omatogastric nervous systems of lobsters and crabs have led to numerous insights into the cellular an

157 vading from outside Antarctica, the lithodid crabs have likely persisted, and even radiated, on or ne

158 n New England (USA) the invasive Asian shore crab, Hemigrapsus sanguineus, preys on mussels (Mytlius

159 Land hermit crabs hollow out the shells in which they live.

160 usively inside epithelial cell nuclei of its crab host.

161 exploitation and the integration of the blue crab in human diet of European countries as an healthy a

162 This will help to control the spread of CRAB in the Middle East and in hospitals accommodating t

163 red to the physiological resilience of shore crabs in maintaining osmoregulatory and respiratory func

164 r shrimp-like prey, when visually exposed to crabs in the first hours of day one, they later prefer c

165 ional intervention in the Australian fiddler crab, including why the ally tended to be larger than bo

166 s ingesting Fukushima sediment, up to 55% in crabs ingesting polychaetes, and about 80% in fish inges

167 n structure and aggregation to the horseshoe crab innate immune protein tachylectin 5A.

168 In an adult hermit crab, intrinsic neurons and one class of efferent neuron

169 clude there is no evidence for a modern-day "crab invasion".

170 The Crab is a complex system consisting of a central pulsar,

171 Hence, red king crab is a safe food.

172 The lobula plate of this crab is a small elongated neuropil.

173 Early evolution of crabs is still very incompletely known.

174 ns from a bright celestial X-ray source, the Crab, is reported here for the first time in the hard X-

175 a jet that can be directly compared with the Crab jet through well-defined physical scaling laws.

176 rection, mimicking the kink behaviour of the Crab jet.

177 d by these vents are dominated by a new yeti crab (Kiwa n.

178 sibly dominated by a new species of anomuran crab, Kiwa n. sp. (abundance >700 individuals m(-2)), fo

179 ant populations of a new species of anomuran crab, Kiwa tyleri, occur at hydrothermal vent fields on

180 Here, we report a fossil crab larva, 150 mya, documented with up-to-date imaging

181 It is only the second find of any fossil crab larva, but the first complete one, the first megalo

182 gy, being indistinguishable from many extant crab larvae.

183 at the costovertebral junction producing a "crab-like" configuration of the thorax.

184 In the horseshoe crab Limulus polyphemus, enhanced phosphorylation of an

185 known chelicerates, including the horseshoe crab Limulus polyphemus.

186 f the sea cucumber Thyone, and the horseshoe crab Limulus.

187 wers the acrosomal reaction of the horseshoe crab (Limulus polyphemus) sperm.

188 struction of myosin filaments from horseshoe crab (Limulus) muscle.

189 Among the likely first arrivals are king crabs (Lithodidae), which were discovered recently on th

190 But in the case of land crabs, little water is available to provide a temporary

191 owth rates in the presence of crabs, whereas crabs lost mass in the presence of crayfish.

192 ailed high-speed video analysis reveals that crabs measure distance by integrating strides, rather th

193 ctica has centred on a hypothesis that these crabs might be poised to invade the Antarctic shelf if t

194 Eastern Channel crabs migrated further than western Channel crabs, while

195 vealed that the consumption of cooked edible crab muscle should be promoted, whereas brown meat inges

196 ry by the Chandra X-ray observatory that the Crab nebula's jet periodically changes direction provide

197 es of (36)ArH(+) at several positions in the Crab Nebula, a supernova remnant known to contain both m

198 Its detection in the Crab Nebula, the product of such a supernova event, conf

199 g and energetic pulsar powers the well-known Crab Nebula.

200 When tested in a walking simulator, the crab Neohelice granulata immediately adjusts its running

201 ion of the lobula plate in a crustacean, the crab Neohelice granulata using a variety of histological

202 istochemical analysis, we identified, in the crab Neohelice granulata, HBs that resemble the calyxles

203 the first optic neuropil, the lamina of the crab Neohelice granulata, possesses a surprisingly high

204 The existence of WGD in the horseshoe crabs, noted for relative morphological stasis over geol

205 Western blots yielded two bands for the crab NR1-like subunit, at approximately 88 and approxima

206 described, highly processive duplex-specific crab nuclease.

207 loric, and pyloric dilator neurons from male crabs of the species Cancer borealis.

208 d wasps, and the tracking of conspecifics by crabs on intertidal mudflats.

209 After applying WGS to a CRAB outbreak that occurred during the study, we identif

210 alyzing a carbapenem-resistant A. baumannii (CRAB) outbreak.

211 nt platforms, exhibited high specificity for crab over other types of crustaceans, and yielded much h

212 wed no association with shrimp (P = 0.21) or crab (P = 0.48) consumption and a highly significant pos

213 uman antidepressant drugs; the striped shore crab, Pachygrapsus crassipes, was studied using anxiety

214 lue crab Callinectes sapidus, whilst the mud crab Panopeus herbstii had no effect on recruit mortalit

215 We tested the effects of crab (Panopeus herbstii) behavioural type, specifically

216 predator (toadfish--Opsanus tau), prey (mud crab--Panopeus herbstii) and resource (ribbed musse--Geu

217 Samples of claw and leg meat of 185 red king crabs (Paralithodes camtschaticus), collected from 23 po

218 ssurella latimarginata), and pinnotherid pea crab parasites for a sea urchin (Loxechinus albus).

219 tures presented here and the known horseshoe crab pentraxin sequences, suggest that adaptation and re

220 'Caribbean Creep' we exposed the non-native crab Petrolisthes armatus to different thermal treatment

221 In particular, semiterrestrial crabs possess a highly developed visual system and displ

222 of the type II functional response of small crabs, potentially through an increase in time spent for

223 the detection of pulsed gamma rays from the Crab pulsar at energies above 100 giga-electron volts (G

224 ast 22 years, the radio pulse profile of the Crab pulsar has shown a steady increase in the separatio

225 olarized gamma rays from the vicinity of the Crab pulsar using data from the spectrometer on the Inte

226 n, driven by the rotational slow down of the Crab pulsar, is explored.

227 ely the conditions for the parameters of the Crab pulsar.

228 aker neurons on the network frequency in the crab pyloric CPG.

229 ptic strength and short-term dynamics in the crab pyloric network by the neuropeptide proctolin.

230 three currents in identified neurons of the crab pyloric network.

231 ored this in the pacemaker PD neurons of the crab pyloric network.

232 ed further than western Channel crabs, while crabs released outside the Channel showed little or no m

233 ns were punctuated by a 7-month hiatus, when crabs remained stationary, coincident with the main peri

234 Like their aquatic counterparts, terrestrial crabs repeatedly shed their rigid exoskeleton during mou

235 reely available for non-profit use at http://crab.rutgers.edu/~dslun/gdbb.

236 Carcinus maenas and the consequences for the crab's energy budget.

237 The number of layers in the crab's lobula plate, the retinotopic connections receive

238 lar class of motion-sensitive neurons of the crab's lobula that project to the midbrain, the monostra

239 g objects conforms the visual ecology of the crab's mudflat world.

240 crospheres nor natural sediments altered the crab's response to osmotic stress regardless of plastic

241 t marsh die-off by releasing the herbivorous crab Sesarma reticulatum from predator control.

242 Cape Cod (USA) has released the herbivorous crab Sesarmareticulatum from predator control leading to

243 ichopsenius display the protective horseshoe-crab-shaped body form typical of many modern termitophil

244 ich possess specialized swollen or horseshoe-crab-shaped body plans.

245 hopseniini, display the protective horseshoe-crab-shaped body typical of many extant termitophiles.

246 The complex reveals a crab-shaped homodimeric TrkA structure, but a mechanism

247 efficient growth on both purified chitin and crab shell particles.

248 rman cockroach, Oriental cockroach, codfish, crab, shrimp, and cheese (all P </= 0.01).

249 s with a prevalence of assemblages involving crab-shrimp partnerships.

250 may be expected on epibenthic invertebrates (crabs, shrimps, benthic grazers, benthic detritivores, b

251 pared to mesocosms without crabs, decreasing crab size had no detectable effect on the amphipod or al

252 Regardless of the presence of crabs, snails from high-risk (HR) habitats developed rot

253 ationary, coincident with the main period of crab spawning and egg incubation.

254 nous (Eriphia verrucosa) and to a commercial crab species (Cancer pagurus).

255 Mangrove-related fish and crab species account for 32% of the small-scale fisherie

256 mpetition with a functionally similar native crab species on the population densities, growth rates a

257 Two key crab species were manipulated to test predator identity

258 istinguished the lipid profiles of the three crab species.

259 he actin-based acrosomal bundle of horseshoe crab sperm.

260 f a sodium channel activation inhibitor from crab spider venom.

261 method was able to detect several species of crab spiked into complex food matrices at levels ranging

262 circuits, such as the pyloric circuit of the crab stomatogastric ganglion (STG), exhibit robust neura

263 he unambiguously identifiable neurons in the crab stomatogastric ganglion to investigate the precise

264 A recent study has shown that, in the crab stomatogastric ganglion, this feedback is also subj

265 In the pyloric circuit of the crab stomatogastric ganglion, we pharmacologically isola

266 commissural neuron 1 (MCN1) in the isolated crab stomatogastric ganglion.

267 tworks from gastric mill (GM) neurons of the crab stomatogastric ganglion.

268 driven by the projection neuron MCN1 in the crab stomatogastric ganglion.

269 Here, using the crab stomatogastric nervous system, we show that sensori

270 riven, gastric mill (chewing) circuit in the crab stomatogastric nervous system.

271 s that regulate the gastric mill CPG, in the crab stomatogastric nervous system.

272 ibacterial protein of the Japanese horseshoe crab Tachypleus tridentatus, showed properties identical

273 From the release of 128 mature female edible crabs tagged with electronic data storage tags (DSTs), w

274 We used Neohelice crabs, taking advantage of two well-described appetitive

275 e did not significantly affect the number of crabs that emigrated, the presence of a predator decreas

276 In chronic 4 week feeding studies, crabs that ingested food containing microfibers (0.3-1.0

277 Cryptochiridae are small, fragile, symbiotic crabs that live in domiciles in modern corals.

278 al. (2015) found a community of Kiwa (Yeti) crabs that separated themselves along this gradient with

279 fense for "living fossils" such as horseshoe crabs, the role of the coagulation system in immunity in

280 lity in patients with AL amyloidosis without CRAB to produce two additional groups: AL only (</= 10%

281 he first hours of day one, they later prefer crabs to shrimps.

282 While on foraging excursions, fiddler crabs track their burrow location despite having no visu

283 After being frightened, crabs tried to escape but slipped as they did so.

284 The presence of native crabs triggered significant dietary niche constriction w

285 pulations in wild populations of the fiddler crab Uca stenodactylus, we provide evidence that these a

286 mmatidium in the compound eye of the fiddler crab, Uca vomeris, at both the light- and the electron-m

287 tudied gastric mill pattern generator of the crab, we show that modest temperature increase can aboli

288 the apposition type, typical for Brachyuran crabs, we identify a number of novel, functionally relev

289 hal mRNA in the two PD neurons from the same crab were similar, suggesting that the regulation of som

290 Crabs were collected at the wreck location and 4 nmi nor

291 "invasion hypothesis" suggests that decapod crabs were driven out of Antarctica 40-15 million years

292 Crabs were individually exposed to acute doses of the se

293 Fiddler crabs were passively translated to a position such that

294 arbapenem-resistant Acinetobacter baumannii (CRAB) were determined in hospitals in the states of the

295 different areas, and between male and female crabs, were found.

296 ned positive growth rates in the presence of crabs, whereas crabs lost mass in the presence of crayfi

297 ctor C, a serine protease found in horseshoe crabs, which is critical for antibacterial responses.

298 crabs migrated further than western Channel crabs, while crabs released outside the Channel showed l

299 the effects on osmoregulation, we challenged crabs with reduced salinity after microplastic exposure.

300 demonstrate that previous reluctance to tag crabs with relatively high-cost DSTs for fear of loss fo