ライフサイエンスコーパス: jellyfish

1 no robust evidence for a global increase in jellyfish.

2 d by repetitive muscular contractions of the jellyfish.

3 ations coupled to the motion of a simplified jellyfish.

4 nd from a central body like tentacles from a jellyfish.

5 bout the evolution of body shape and size in jellyfish.

6 are expressed highly in the eye lens of this jellyfish.

7 ethal effects of post-2050 OA projections on jellyfish.

8 neuronal network model for the nerve nets of jellyfish.

9 te the associated vortex for swimming like a jellyfish.

10 for swimming similar to the motion of a Moon jellyfish.

11 t-2050 OA projections on the medusa stage of jellyfish.

12 allergenicity may be different for different jellyfish.

13 o refrain from consuming any food containing jellyfish.

14 nutes after ingestion of antipasto made with jellyfish.

15 ncluding sea anemones, corals, hydroids, and jellyfish.

16 ls activating bioluminescence in firefly and jellyfish.

17 ithm applied to freely swimming lampreys and jellyfish.

18 fish, herring (Clupea pallasii), shrimp, and jellyfish].

19 rted that cnidarian soft corals [21] and box jellyfish [22, 23] exhibit periods of quiescence, a pre-

20 dy focuses on medusae of Cassiopea andromeda jellyfish: a unique benthic jellyfish known to favor (su

21 l available long-term datasets on changes in jellyfish abundance across multiple coastal stations, us

22 Robust time-series of direct observations of jellyfish abundance are not available for many ecosystem

23 A perceived recent increase in global jellyfish abundance has been portrayed as a symptom of d

24 ction in fish abundance alongside increasing jellyfish abundance has led to hypotheses suggesting tha

25 an indirect ecological route to reconstruct jellyfish abundance in the Irish Sea: since zooplankton

26 leaving it difficult to determine changes in jellyfish abundance, the possible causes (e.g. climate c

27 ed to the perception of a global increase in jellyfish abundance.

28 plankton communities may provide proxies for jellyfish abundance.

29 rding of the activation speed confirmed that jellyfish actuate within this range, and flow visualizat

30 Here, we show that medusa jellyfish adopt the best strategy to achieve the most un

31 s were consistently associated with multiple jellyfish adults.

32 ve photoprotein originally obtained from the jellyfish Aequorea aequorea.

33 The green fluorescent protein (GFP) from the jellyfish Aequorea victoria and its fluorescent homologs

34 The luminescent system of the jellyfish Aequorea victoria consists of the photoprotein

35 The green fluorescent protein (GFP) from the jellyfish Aequorea Victoria forms an intrinsic chromopho

36 constructed gfph, a synthetic version of the jellyfish Aequorea victoria green fluorescent protein (g

37 The green fluorescent protein (GFP) of the jellyfish Aequorea Victoria has attracted widespread int

38 The green fluorescent protein (GFP) from the jellyfish Aequorea victoria has become a useful tool in

39 ent protein (GFP) from the Pacific Northwest jellyfish Aequorea victoria has generated intense intere

40 The green fluorescent protein (GFP) of the jellyfish Aequorea victoria has recently attracted great

41 The green-fluorescent protein (GFP) of the jellyfish Aequorea victoria has recently been used as a

42 the green fluorescent protein (GFP) from the jellyfish Aequorea victoria has vaulted from obscurity t

43 The green fluorescent protein (GFP) from the jellyfish Aequorea victoria is a versatile reporter prot

44 The Green Fluorescent Protein (GFP) from the jellyfish Aequorea victoria is a widely used marker for

45 ing green fluorescent protein (GFP) from the jellyfish Aequorea victoria, have revolutionized researc

46 the green fluorescent protein (GFP) from the jellyfish Aequorea victoria, which is a widely used gene

47 ing green fluorescent protein (GFP) from the jellyfish Aequorea victoria, with that of the Ob-tobamov

48 proteins involved in bioluminescence of the jellyfish Aequorea victoria--aequorin and green fluoresc

49 n fluorescent protein (GFP) derived from the jellyfish Aequorea victoria.

50 wild-type GFP isoforms isolated from native jellyfish Aequorea victoria.

51 sis of highly purified GFP obtained from the jellyfish Aequorea.

52 the green fluorescent protein (GFP) from the jellyfish Aequorea.

53 The bioluminescent jellyfish (Aequorea victoria) green fluorescent protein

54 erial xylanase, green fluorescent protein of jellyfish [Aequorea victoria], and human placental alkal

55 The green fluorescent protein (GFP) from the jellyfish, Aequorea victoria, has become a versatile rep

56 whether the weak increasing linear trend in jellyfish after 1970 is an actual shift in the baseline

57 ward swimming velocities of the model oblate jellyfish after two pulse cycles are comparable to those

58 We report a case of jellyfish allergy diagnosed via an oral food challenge.

59 The patient was diagnosed with a jellyfish allergy due to IgE mediated anaphylaxis after

60 tudy to detect specific allergens related to jellyfish allergy would be particularly useful to specif

61 the presence of an energetic pathway between jellyfish and a commercially important invertebrate spec

62 ient and DOM pathways, yet the links between jellyfish and bacterioplankton metabolism and community

63 Visibly fluorescent proteins (FPs) from jellyfish and corals have revolutionized many areas of m

64 Except for a negative association between jellyfish and crustacean zooplankton in the Black Sea, w

65 We extracted crude allergen from jellyfish and evaluated allergen specific IgE antibody l

66 germ cells (PGCs) of organisms as diverse as jellyfish and humans.

67 Cnidarians (corals, anemones, jellyfish and hydras) are a diverse group of animals of

68 e marine gastropod (Aplysia, a sea hare), in jellyfish and in the compound eyes of some arthropods; a

69 in Podocoryne metalloproteinase 1 (PMP1) of jellyfish and in toxins of sea anemone.

70 The association between the jellyfish and its reduced microbiome was close and tempo

71 del of the swimming-motor-net of a hydrozoan jellyfish and let it control a swimming jellyfish in a f

72 Stinging cells or nematocytes of jellyfish and other cnidarians represent one of the most

73 Jellyfish and sea anemones fire single-use, venom-covere

74 Cnidarians, including jellyfish and sea anemones, both detect and capture prey

75 deployment of accelerometers on free-ranging jellyfish and simulated the behavior observed in wild je

76 Medusozoans (jellyfish and siphonophores) exhibit diverse life cycles

77 he differences between the 3D reality of the jellyfish and the 2D simplification, as well as the rigi

78 ex dynamics between when the 2D model oblate jellyfish and the organism.

79 m Cnidaria, which includes anemones, corals, jellyfishes and hydras.

80 ancestor of diploblasts (corals, hydra, and jellyfish) and triploblasts (bilaterians).

81 m Cnidaria, which includes anemones, hydras, jellyfish, and corals.

82 bust cycles of toxic dinoflagellate blooms, jellyfish, and disease.

83 y primitive animals that, along with corals, jellyfish, and hydras, constitute the oldest eumetazoan

84 a group that includes corals, sea anemones, jellyfish, and hydroids, is supported by some phylogenet

85 and ancient phylum, encompassing corals and jellyfish, and occupy both the pelagic and benthic realm

86 cell type used by cnidarians (i.e., corals, jellyfish, and their kin) to immobilize prey.

87 isk-like structures, as well as more complex jellyfish- and flower-like structures.

88 of jellyfish-zooplankton dependencies using jellyfish- and zooplankton-abundance data obtained using

89 in many cnidarian species including corals, jellyfish, anemones, and giant clams.

90 At first glance, the trailing tentacles of a jellyfish appear to be randomly arranged.

91 l predatory mode is counterintuitive because jellyfish are described as inefficient swimmers that mus

92 d backward swimming motions of the idealized jellyfish are emergent properties determined by the resu

93 C transfer to higher trophic levels because jellyfish are not readily consumed by other predators.

94 ailable time-series data do not suggest that jellyfish are outcompeting, or have replaced, small pela

95 Jellyfish are radially symmetric organisms without a bra

96 darians (corals, sea anemones, hydroids, and jellyfish) are a basal taxon closely related to bilatera

97 in the germline and stem cell populations of jellyfish as well as humans.

98 ment in the genome is similar to that of the jellyfish Aurelia aurita.

99 quency of appendage regeneration in the moon jellyfish Aurelia was increased by feeding with the amin

100 We present the genome of the moon jellyfish Aurelia, a genome from a cnidarian with a medu

101 rate, contrary to prevailing views, that the jellyfish (Aurelia aurita) is one of the most energetica

102 vel tool for genome polishing called JASPER (Jellyfish-based Assembly Sequence Polisher for Error Red

103 ably the best electrophysiologically studied jellyfish because of its system of giant axons and uniqu

104 Vertebrates do not look like jellyfish because the bones of their skeletons are lever

105 hat current-oriented swimming contributes to jellyfish being able to form aggregations of hundreds to

106 on in the Black Sea, we found no evidence of jellyfish biomass being related to the biomass of small

107 ould become more important with increases in jellyfish blooms in some regions.

108 Jellyfish blooms occur in many estuarine and coastal reg

109 ncrease, given the potential damage posed by jellyfish blooms to fisheries, tourism, and other human

110 t also contributes to improve predictions of jellyfish blooms' magnitude and movements in coastal wat

111 obial structure and function associated with jellyfish blooms, and a large detour of C toward bacteri

112 gical structure of food webs associated with jellyfish blooms.

113 ribed anaphylaxis caused by the ingestion of jellyfish, but the allergens in jellyfish have not been

114 their share of the common resource, and that jellyfish can account for up to 30% of the combined fish

115 Our results show that jellyfish can actively swim countercurrent in response t

116 Evidence of scavenging on jellyfish carcasses by the Norway lobster (Nephrops norv

117 t proliferate in the sea anemone Aiptasia or jellyfish Cassiopea but can proliferate in the juvenile

118 In this study, we show that the upside-down jellyfish Cassiopea sp. plays a significant role with re

119 Within Cnidaria, the upside-down jellyfish Cassiopea spp. displays a quantifiable pulsing

120 The upside-down jellyfish Cassiopea xamachana sleeps, and this behavior

121 potential for adaptation of the upside-down jellyfish Cassiopea xamachana to increased temperature v

122 be an anaerobic fermenter associated to some jellyfish cells, whereas the Tenacibaculum-like as free-

123 ent evidence of curiosity-like behavior in a jellyfish, challenging the assumed link between centrali

124 The box jellyfish Chironex fleckeri produces extremely potent an

125 genes (jred, hcred, and mrfp1, isolated from jellyfish chromophore, coral Heteractis crispa, and cora

126 We report the draft genome of the hydrozoan jellyfish Clytia hemisphaerica and use multiple transcri

127 least since the divergence of Hydra and the jellyfish Clytia hemisphaerica more than 400 million yea

128 In hydrozoan cnidarians including the jellyfish Clytia hemisphaerica, MIH comprises neuropepti

129 scoffensis, and in neurosensory cells of the jellyfish Clytia hemisphaerica.

130 f studies has suggested trends of increasing jellyfish (Cnidaria and Ctenophora) biomass in several m

131 The nerve net of hydrozoan jellyfish comprises a condensed ring of electrically cou

132 g showed acid-soluble collagen fraction from jellyfish contained above 250kDa weighed protein that ma

133 age of cnidarians, negative impacts on adult jellyfish could severely impact the long-term survival o

134 Like Pax6, PaxB activates jellyfish crystallin and Drosophila rhodopsin rh6 promot

135 d by retionoid signaling in vertebrates, the jellyfish crystallin genes are candidate in vivo targets

136 ltage-gated Ca2+ channel from the scyphozoan jellyfish Cyanea capillata, one of the earliest existing

137 Stimulation with jellyfish-derived allergen showed expression of surface

138 Patient samples showed higher levels of jellyfish-derived allergen specific IgE than healthy con

139 ozoa) carcasses to simulate the transport of jellyfish detritus to the seafloor, hereby known as jell

140 Cnidarians (corals, sea anemones, and "jellyfish") diverged from other animals before the radia

141 As a k-mer counter, KAnalyze outperforms Jellyfish, DSK and a pipeline built on Perl and Linux ut

142 Rheological properties of jellyfish ECM (mesoglea) were measured in vivo at the ce

143 logy techniques: microbeads were injected in jellyfish ECM and their Brownian motion was recorded to

144 Current-oriented swimming may be achieved by jellyfish either directly detecting current shear across

145 onclude that body patterning in regenerating jellyfish emerges mainly from local interactions, trigge

146 n account for up to 30% of the combined fish-jellyfish energy consumption.

147 stinging cells unique to cnidarians (corals, jellyfish, etc).

148 We show that jellyfish exhibit a unique mechanism of passive energy r

149 Radially symmetric animals, like jellyfish, face the additional challenge of having to re

150 ike other aquatic organisms, such as turtle, jellyfish, fish and frog et al., the diving beetle could

151 ces, cell migration and proliferation allows jellyfish fragments to regain shape and functionality ra

152 report the construction of a freely swimming jellyfish from chemically dissociated rat tissue and sil

153 e of nuclear activity among heavily stripped jellyfish galaxies may be due to ram pressure causing ga

154 we report that six out of a sample of seven 'jellyfish' galaxies-galaxies with long 'tentacles' of ma

155 enic mice, containing multiple copies of the jellyfish gene encoding the green fluorescent protein (G

156 MIHR mutant jellyfish generated using CRISPR-Cas9 editing had severe

157 Jellyfish genomes reveal a mosaic of conserved and diver

158 A sea nettle (a jellyfish) genomic library was constructed and two pax g

159 Upside-down jellyfish, genus Cassiopea (Peron and Lesueur, 1809), ar

160 ides the highest fluorescence signals of all jellyfish GFP or coral RFP derivatives, respectively.

161 ession in maize leaf cells than the original jellyfish GFP sequence.

162 novirus type-5 (Ad5) that expresses enhanced jellyfish green fluorescent protein (EGFP), AdEGFPuci, a

163 e of the yeast HDEL receptor (AtERD2) to the jellyfish green fluorescent protein (GFP) and transientl

164 ild-type Crx were fused to cDNA encoding the jellyfish green fluorescent protein (GFP) and were trans

165 formation, neurons were transfected with the jellyfish green fluorescent protein (GFP) gene.

166 o strains of transgenic mice, each bearing a jellyfish green fluorescent protein (GFP) reporter, were

167 FP-moe) by joining sequences that encode the jellyfish green fluorescent protein (GFP) to sequences t

168 vents in living yeast cells after fusing the jellyfish green fluorescent protein (GFP) to the C termi

169 To study p53 trafficking, the jellyfish green fluorescent protein (GFP) was fused to t

170 By fusion of MP with the jellyfish green fluorescent protein (GFP), we demonstrat

171 ted using transgenic C. elegans expressing a jellyfish green fluorescent protein (GFP)-tagged inducib

172 h the expression of the protein fused to the jellyfish green fluorescent protein (GFP).

173 The advent of jellyfish green fluorescent protein and its spectral var

174 Recent studies have identified jellyfish green fluorescent protein as an excellent repo

175 whereas altering the coding sequence of the jellyfish green fluorescent protein gene to conform to t

176 ased retroviral vector carrying the enhanced jellyfish green fluorescent protein inserted into the ne

177 e ecophysiological model that represents the jellyfish growth and degrowth in laboratory conditions a

178 This jellyfish has a high abundance in the Mediterranean Sea

179 ng Sea and the Black Sea, it is evident that jellyfish have increased their share of the common resou

180 ingestion of jellyfish, but the allergens in jellyfish have not been analyzed.

181 Cubomedusan jellyfish have three novel crystallin families (the J-cr

182 After ingesting 14g of boiled jellyfish, he experienced erythema, wheezing, nausea, an

183 f Symbiodiniaceae in sea anemone, coral, and jellyfish hosts) revealed that infection can occur witho

184 iverse origins (green fluorescent protein of jellyfish, human placental alkaline phosphatase [SEAP],

185 zoan jellyfish and let it control a swimming jellyfish in a fluid simulation.

186 ndance has led to hypotheses suggesting that jellyfish in these areas could be replacing small plankt

187 oft fragile marine species such as squid and jellyfish, including slow complex operations, unreliable

188 trics of the robot are comparable with other jellyfish-inspired robots that have utilized different a

189 r describes the development of a lightweight jellyfish-inspired swimming robot, which achieves a maxi

190 ines that porewater release by Cassiopea sp. jellyfish is due to suction pumping, and not the Bernoul

191 IgE-mediated food allergy caused by jellyfish is rare worldwide.

192 m Cnidaria (sea anemones, corals, hydras and jellyfish) is the likely sister group of the triploblast

193 Cnidaria (e.g. sea anemones and jellyfishes) is the sister group to well-studied Bilater

194 Zebrafish embryos homozygous for jellyfish (jef) mutations show craniofacial defects and

195 siopea andromeda jellyfish: a unique benthic jellyfish known to favor (sub-)tropical coastal regions

196 ourse of a year in a novel marine ecosystem (Jellyfish Lake, Palau), we show that DO declined through

197 ultifunctional saposin protein family in the jellyfish lens.

198 mable knits for developing robots based upon jellyfish like locomotion, and complex structures simila

199 The FdtA dimer assumes an almost jellyfish-like appearance with the sole alpha-helices re

200 sm, followed by Ostwald ripening to form the jellyfish-like morphology.

201 Uniform silica nanoparticles and jellyfish-like nanowires were synthesized by a chemical

202 he proposed programming method, we created a jellyfish-like robot, a spermatozoid-like undulating swi

203 Therefore, we developed a jellyfish-like robotic platform enabled by a synergy of

204 This study introduces a versatile jellyfish-like robotic platform with a wide range of fun

205 (PFD) is a heterohexameric chaperone with a jellyfish-like structure whose function is to deliver no

206 e protein (OMP) biogenesis, during which the jellyfish-like trimeric protein encapsulates partially f

207 unstable fluid flows to the canal system of jellyfish, loops suddenly form near the breakthrough whe

208 of the strain-stiffening characteristics of jellyfish, lung, and arterial tissues.

209 Jellyfish (medusae) are a distinctive life-cycle stage o

210 bers occurring gradually during aging of the jellyfish mesoglea and is enhanced by repetitive muscula

211 erformed with a shear rheometer on slices of jellyfish mesoglea.

212 rica as a transparent, genetically tractable jellyfish model for systems and evolutionary neuroscienc

213 compared to other cnidarians might make box jellyfish more vulnerable to OA.

214 rganisms include other invertebrates such as jellyfish, nematode, leech and lancelet as well as verte

215 Jellyfish nerve nets provide insight into the origins of

216 llowing for a comprehensive understanding of jellyfish neural control of locomotion.

217 Jellyfish neurons have been studied electrophysiological

218 , important in many biological applications, Jellyfish offers a much faster and more memory-efficient

219 ntly activate Gs-type G protein like the box jellyfish opsin from the same opsin group.

220 the third cytoplasmic loop of the Gs-coupled jellyfish opsin.

221 fluorescence comparable to that of FPs from jellyfish or coral.

222 Juvenile jellyfish, or ephyrae, break off from polyps swimming at

223 mall planktonic organisms, such as copepods, jellyfish, or protists.

224 abilities of Aurelia may have insulated this jellyfish over the 1985 regime shift when zooplankton co

225 Our data suggest that the ancestor of jellyfish PaxB, a PaxB-like protein, was the primordial

226 sediment plumes on the cosmopolitan deep-sea jellyfish Periphylla periphylla, combining insights gain

227 smitted from Ca2+-activated aequorin, in the jellyfish photophores.

228 Aequorin, a jellyfish photoprotein with Ca(2+)-dependent luminescenc

229 roteases in a sponge (phylum Porifera) and a jellyfish (phylum Cnidaria), making it safe to conclude

230 Shal channel subunit (jShalgamma1) from the jellyfish Polyorchis penicillatus that alters Shal curre

231 formal analysis of global temporal trends in jellyfish populations has been missing.

232 the proportion of increasing vs. decreasing jellyfish populations over all time periods examined.

233 oretell recurrent phases of rise and fall in jellyfish populations that society should be prepared to

234 her, the strongest nonrandom trend indicated jellyfish populations undergo larger, worldwide oscillat

235 Cnidaria (sea anemones, corals, hydras, and jellyfish), Porifera (sponges), and single-celled protis

236 Cnidarians such as sea anemones or jellyfish possess a nerve net, which lacks centralizatio

237 xB from Tripedalia cystophora, a cubomedusan jellyfish possessing complex eyes (ocelli), was characte

238 Voracious jellyfish predation impacts food webs by converting larg

239 tacean zooplankton is 2-30 times higher than jellyfish predation, depending on ecosystem.

240 ance in the Irish Sea: since zooplankton are jellyfish prey, historic variability in zooplankton comm

241 rhiza tuberculata is an important scyphozoan jellyfish producing population blooms in the Mediterrane

242 after eating a commercially available boiled jellyfish product (100g), he experienced nausea, wheezin

243 ed an oral food challenge of the same boiled jellyfish product bought at the same grocery store to th

244 s and had been eating commercially available jellyfish products twice yearly for the past 5-6 years.

245 e experienced environmental shifts favouring jellyfish proliferation.

246 and experiments to match key determinants of jellyfish propulsion and feeding performance by quantita

247 d the cDNA encoding this 238-amino-acid (aa) jellyfish protein into an expression vector containing t

248 In addition, jellyfish release colloidal and dissolved organic matter

249 Here we report that jellyfish released substantial quantities of extremely l

250 owever, further clarification of the role of jellyfish requires higher-resolution spatial, temporal a

251 sition and their evolutionary age imply that jellyfish resemble some of the earliest neuron-bearing,

252 cells both express piwi-interacting RNAs in jellyfish revealing a conserved cnidarian feature, and e

253 we show that a weakly swimming organism, the jellyfish Rhizostoma octopus, can orientate its movement

254 usly missing metazoan phyla such as sponges, jellyfish, rotifers and flatworms.

255 Why are jellyfish round?

256 After modeling the jellyfish's muscle system and its bell in a hydrodynamic

257 A provocation test using jellyfish samples was not performed due to risk of anaph

258 port genome sequencing and assembly for true jellyfish Sanderia malayensis and Rhopilema esculentum.

259 nformatics software, including BiopLib, BWA, Jellyfish, SDSL, Dashing, SPAdes, and MUMmer.

260 ousekeeping proteins found in nematocysts of jellyfish, sea anemones and Hydra, but have lost the mos

261 The stinging organelles of jellyfish, sea anemones, and other cnidarians, known as

262 Jellyfish seem to respond when an ecosystem is over-fish

263 When co-expressed with the conserved jellyfish Shal homolog jShal1, jShalgamma1 dramatically

264 gh there has been a small linear increase in jellyfish since the 1970s, this trend was unsubstantiate

265 ing microrheological properties at different jellyfish sizes.

266 otheses using extended and published data of jellyfish, small pelagic fish and crustacean zooplankton

267 The Jellyfish software is written in C++ and is GPL licensed

268 Numerous jellyfish species harbor closely related endosymbiont ta

269 and regeneration in a genetically tractable jellyfish species.

270 receptors from hydroid filiform tentacles to jellyfish statocysts.

271 than PGA via a route different from that of jellyfish sting.

272 A 14-year-old boy had no history of jellyfish stings and had been eating commercially availa

273 -glutamic acid (PGA) which is a component of jellyfish stings was negative.

274 ions in noncardiac arrests, and treatment of jellyfish stings.

275 Chironex fleckeri (Australian box jellyfish) stings can cause acute cardiovascular collaps

276 nergy requirements of small pelagic fish and jellyfish stocks in the most recent years suggest that f

277 skin prick test for several kinds of edible jellyfish suggests that allergenicity may be different f

278 pports the jet propulsion by which hydrozoan jellyfish swim.

279 In jellyfish, swimming robustness emerges when marginal pac

280 roves the cost of transport by 48%, allowing jellyfish to achieve the large sizes required for suffic

281 ates eye development in animals ranging from jellyfish to Drosophila to humans.

282 sign have been found in animals ranging from jellyfish to humans, as well as in plants, yeast, and ba

283 p has been described in species ranging from jellyfish to humans.

284 d images and an ever-growing repertoire from jellyfish to sea anemones and corals.

285 into the evolutionary diversification of box jellyfish toxins from a structural and functional perspe

286 e major eye-lens proteins of the cubomedusan jellyfish (Tripedalia cystophora), shows similarity to v

287 brates, Drosophila melanogaster, and the box jellyfish, Tripedalia cystophora, a species previously i

288 ed by in situ field measurements of swimming jellyfish using a newly developed scuba-based laser velo

289 Here, we formed an RFB into the shape of a jellyfish, using two redox chemistries and architectures

290 We used biomimetic robotic jellyfish vehicles to elucidate that propulsive thrust e

291 ional fluid-structure interaction model of a jellyfish was developed to determine the resulting emerg

292 We measured that the ECM in adult jellyfish was locally stiffer than in juvenile ones.

293 orithm and associated implementation, called Jellyfish, which is fast and memory efficient.

294 that a 'soft' robot causes less stress to a jellyfish while handling compared to a traditional 'hard

295 The structure of the Skp trimer resembles a jellyfish with alpha-helical tentacles protruding from a

296 Jellyfish, with their tetraradial symmetry, offer a nove

297 and simulated the behavior observed in wild jellyfish within a high-resolution hydrodynamic model.

298 etermined the Bayesian ecological network of jellyfish-zooplankton dependencies using jellyfish- and