ライフサイエンスコーパス: mollusc

1 e with a monophyletic Aplacophora (worm-like molluscs).

2 lone, Haliotis rufescens, a marine gastropod mollusc.

3 polypropionate natural product found in this mollusc.

4 atella vulgata is an underutilized gastropod mollusc.

5 d be recorded in well-preserved taxa such as molluscs.

6 ifferentiate tropomyosins in crustaceans and molluscs.

7 of the molecular evolution of NOS enzymes in molluscs.

8 mals - birds - and one quite far -cephalopod molluscs.

9 bly represents a plesiomorphic condition for molluscs.

10 s the second K2p subunit to be identified in molluscs.

11 nterpretations for primitive segmentation in molluscs.

12 e is efficiently degraded by crustaceans and molluscs.

13 quences have not been characterized in other molluscs.

14 role in the D quadrant organizer cell 3D in molluscs.

15 have only been documented in equal-cleaving molluscs.

16 lpha-reductase genes have been identified in molluscs.

17 olfactory memories in terrestrial pulmonate molluscs.

18 brafish, and in adult stages of annelids and molluscs.

19 nsport proteins found in many arthropods and molluscs.

20 velopment in another major systematic group, molluscs.

21 to the diversification of other crown-group molluscs.

22 e AstC signaling system in Aplysia and other molluscs.

23 ike PKS (AFPK) was identified in sacoglossan molluscs.

24 died in arthropods, but minimally studied in molluscs.

25 gut in chordates, echinoderms, annelids and molluscs.

26 natural products from gastropod and bivalve molluscs.

27 ng example of nervous system segmentation in molluscs.

28 9 in common spider, and up to 132 in bivalve molluscs.

29 cent work assigns such fossils to stem-group molluscs.

30 nto question its purported relationship with molluscs.

31 also observed in the mantle tissues of other molluscs.

32 ies are manifest in the movement patterns of molluscs.

33 close to the common ancestor of annelids and molluscs.

34 -allergic patients according to tolerance to molluscs.

35 oth vertebrates and invertebrates, including molluscs.

36 comparisons of developmental processes among molluscs.

37 in olfactory systems of mammals, insects and molluscs.

38 s of lophotrochozoans (a group that includes molluscs) [7] and, possibly, with the Mab-5 genes of nem

39 ovide molecular support for the monophyly of molluscs, a group long recognized by morphologists.

40 n both simulated and real data, we show that MOLLUSC accurately estimates all parameters.

41 nts with anaphylaxis to crustaceans (14 with mollusc allergy and 17 with mollusc tolerance) were stud

42 s with crustacean anaphylaxis, patients with mollusc allergy and mollusc tolerance show a different p

43 Patients with mollusc allergy presented more frequently SPTs positive

44 Patients with mollusc allergy reacted more frequently to tropomyosin i

45 os of 4.3 and 10.9 for the identification of mollusc allergy.

46 tion of the larval shell after settlement in molluscs allows use of this geochemical proxy to assess

47 nervous systems, such as those of gastropod molluscs, allows behaviors to be dissected at the level

48 Phylogenetic analysis revealed that mollusc alpha-CA evolution was affected by lineage and s

49 oan that has been interpreted as a primitive mollusc and as a polychaete annelid worm.

50 he results show that the hemocyanin from the mollusc and that from the arthropod have distinct tertia

51 e close relationship of the lophophorates to molluscs and annelids (Lophotrochozoa).

52 Furthermore, the latest common ancestor of molluscs and annelids was also indirectly developing.

53 cestral to 15 invertebrate groups, including molluscs and annelids-most lineages specify cell fates c

54 es assemblies of other difficult-to-sequence molluscs and arthropods, including millimeter-sized orga

55 It further supports the conjecture that molluscs and brachiopods are descended from an ancestral

56 s and higher sIgE titres in response to both molluscs and crustaceans.

57 y presented more frequently SPTs positive to molluscs and higher sIgE titres in response to both moll

58 trategies used by cooperative hemoglobins in molluscs and mammals to control ligand affinity by modul

59 utualism, and as phylogenetically distant as molluscs and mammals.

60 central role in several behaviors in marine molluscs and other species.

61 nctions of As1-4 and their homologs in other molluscs and point to a pivotal role of these neurons in

62 The culture of both molluscs and seaweed is increasingly recognized for its

63 The potential for molluscs and seaweed to support global nutritional secur

64 Shell mass decreased with latitude in molluscs and shell inorganic content decreased with lati

65 also reveal the unintended declines in both molluscs and shorebirds following a conservation-motivat

66 rsistence of TiO(2) and Ag NPs in standards, molluscs and surimi.

67 acts, long-distance transportation of marine molluscs and systematic use of heat shatter in stone too

68 This contrasts with data from molluscs and the molecular mechanism suggested for anoth

69 f an endogenous growth factor of a gastropod mollusc, and provides direct evidence of gain of resista

70 that Su(H) from a wide array of arthropods, molluscs, and annelids includes motifs that directly bin

71 We focused on molluscs, and chose Pacific oyster Magallana gigas as ex

72 lyses placed Xenoturbella within the bivalve molluscs, and eggs and larvae resembling those of bivalv

73 rompted comparison with various annelids and molluscs, and has been used as a template to reconstruct

74 Cephalopod molluscs, and in particular Octopus vulgaris, are well k

75 proxy for 807 species including vertebrates, molluscs, and insects.

76 sion-feeding crustaceans, substrate-scraping molluscs, and morphologically exotic priapulids with com

77 Fossil tetrapods, fish, molluscs, and plants of the Zhongning Formation are asso

78 tor (AstC-R) represents the first example in molluscs, and provides an important basis for further st

79 g their release from experimentally infected molluscs, and refer to this novel route of parasite tran

80 include Rap v 2, an allergenic paramyosin in molluscs, and Sal s 4 and Pan h 4, allergenic fish tropo

81 In the case of the equal-cleaving molluscs, animal-vegetal inductive interactions between

82 ncluding vertebrate, ascidian, hemichordate, mollusc, annelid and arthropod, but not in RNAs from sev

83 is common in protostome animals (arthropods, molluscs, annelids etc.), but a break has also been repo

84 bsent from other lophotrochozoans, including molluscs, annelids, and nemerteans, supporting a groupin

85 Many lophotrochozoans (i.e., molluscs, annelids, nemerteans, and polyclad flatworms)

86 Four species of bivalve molluscs (Anomalocardia brasiliana, Iphigenia brasiliana

87 (NOS)-containing cells in the opisthobranch mollusc Aplysia californica was studied by using NADPH-d

88 l cell (MCC) in the cerebral ganglion of the mollusc Aplysia californica.

89 tify the AstC signaling system in the marine mollusc Aplysia californica.

90 ess this issue in the feeding network of the mollusc Aplysia In this system, there are two stimulatio

91 re we report that noxious stimulation of the mollusc Aplysia produces transcription-dependent, long-t

92 in the negative biasing that is seen in the mollusc Aplysia when there is a transition from egestive

93 In the hermaphroditic mollusc Aplysia, after learning that food is inedible, m

94 integration in the feeding circuitry of the mollusc Aplysia.

95 orskali Chiaje (sea cucumber), the gastropod molluscs Aplysia fasciata Poiret and Aplysia punctata Cu

96 In the marine mollusc, Aplysia californica, feeding-induced transition

97 of the central nervous system of the marine mollusc, Aplysia californica.

98 alcium carbonate structures, such as shelled molluscs, appear restricted to the shallower province.

99 Data from mollusc archives are especially important because of the

100 Molluscs are a highly speciose phylum that exhibits an a

101 ies were resilient to climate change because molluscs are better adapted to high temperatures than ot

102 Bivalve molluscs are descendants of an early-Cambrian lineage su

103 Cephalopod molluscs are renowned for their unique central nervous s

104 Cephalopod molluscs are the most neurally and behaviorally complex

105 Molluscs are undoubtedly special - their extraordinary e

106 While many of these non-native molluscs are valuable as commercial breeding products an

107 y, proposals have been made to adopt bivalve molluscs as bioindicators of MP pollution.

108 with nemerteans, phoronids and brachiopods, molluscs as sister to that assemblage, and the placement

109 a lens crystallin in at least two classes of molluscs as well as elephant shrews.

110 as a model for studying cellular adhesion in molluscs at the molecular level.

111 ttempts to understand the early evolution of molluscs become even more complex when considering the l

112 that declines in fishery species and endemic molluscs began well before commercial fishing in Lake Ta

113 n were investigated in bivalve and gastropod molluscs, brachiopods, and echinoids.

114 ties: coastal fishes, echinoderms, gastropod molluscs, brachyuran decapod crustaceans, polychaete ann

115 dinocysts, foraminifera, ostracods, corals, molluscs, bryozoans, echinoids, fishes, and marine mamma

116 r invertebrate taxa (echinoderms and bivalve molluscs) but not to vertebrates, which significantly de

117 mferential disposition of sclerites in early molluscs, but does closely resemble the armature of cert

118 hilic stage' characterized by chemosynthetic molluscs, but instead the bones were colonized by microb

119 ely interpreted as the most primitive extant molluscs, but Lower Palaeozoic fossils of the former lac

120 sing role of ERK1/2 in Owenia is shared with molluscs, but not with autonomous annelids.

121 Limited evidence placed Xenoturbella with molluscs, but the tissues can be contaminated with prey.

122 s are known to occur in pacemaker neurons in molluscs, but there have been no studies reporting on wh

123 Intensification in the exploitation of molluscs by humans indicates demographic growth in these

124 ochondrial genome of the pulmonate gastropod mollusc Cepaea nemoralis has been determined.

125 hts into ancestral character states of major mollusc clades.

126 ed with feeding was examined in the pteropod mollusc Clione limacina by using wholemount immunohistoc

127 ase-containing cells in the pelagic pteropod mollusc Clione limacina were studied using nicotinamide

128 and to accelerate heart contractions in the mollusc Clione limacina.

129 ls prey capture reactions in the carnivorous mollusc Clione limacina.

130 yr BP) that coincide with markedly increased mollusc collection and accumulation of shell middens, in

131 cs diverged before the origin of the shelled molluscs (Conchifera) or lost their shells secondarily.

132 evels and, consequently, the risk of bivalve mollusc consumption in humans.

133 d second cleavage divisions in the gastropod mollusc Crepidula fornicata.

134 introduced ranges, using 26 host species of molluscs, crustaceans, fishes, birds, mammals, amphibian

135 by 38% in our study areas, yielding fish and mollusc declines.

136 Observations and experiments on living molluscs demonstrate that those inhabiting acidic settin

137 ple in the hypobranchial gland of the marine mollusc, Dicathais orbita, using DIOS-MSI.

138 Molluscs display a rich diversity of body plans ranging

139 ether the shell-less, vermiform aplacophoran molluscs diverged before the origin of the shelled mollu

140 Genomic searches have revealed that molluscs do not possess many of the steroidogenic enzyme

141 Early in its life cycle, the marine mollusc Elysia chlorotica Gould forms an intracellular e

142 ird mechanism of asymmetric inheritance in a mollusc embryo.

143 Equally cleaving mollusc embryos establish the D quadrant via cell-cell i

144 in mammals, 20-30Hz in insects, 0.5-1.5Hz in molluscs), engaging the reciprocal dendrodendritic synap

145 Intricate biomineralization processes in molluscs engineer hierarchical structures with meso-, na

146 e remarkable fact that normal development in molluscs, especially snails, can flip between two chiral

147 alyzed together with the largest data set of molluscs ever assembled, clearly illustrate that monopla

148 onstitute a framework for further studies of mollusc evolution, development and anatomy.

149 These unusual molluscs evolved over 400 million years ago from slow-mo

150 SI using the biosynthetic organs of a marine mollusc for proof of principle.

151 specific differentiation of crustaceans and molluscs for food labelling very difficult.

152 lation between lake temperature and fish and mollusc fossils over the last approximately 500 y indica

153 squamiferum, a recently discovered gastropod mollusc from the Kairei Indian hydrothermal vent field,

154 acrofossils (primarily new data from benthic molluscs) from a highly expanded Cretaceous-Paleogene su

155 ing a database of 2497 marine vertebrate and mollusc genera.

156 During an investigation of published mollusc genomes and transcriptomes, we serendipitously i

157 Only those mollusc groups, which are tolerant of both hypoxia and h

158 d AFPKs widely distributed in arthropods and molluscs (>6300 newly described AFPK sequences).

159 of faunal change during global warming, (c) molluscs had a threshold response to productivity change

160 s were derived, such as paired shells in the mollusc Halkieria.(3) Tommotiids are a key group of phos

161 We show that commercial molluscs have become an essential resource for the mollu

162 ell deletion experiments performed mainly in molluscs have demonstrated that one or two cells associa

163 Studies of the origin and radiation of the molluscs have yet to resolve many issues regarding their

164 Each eye of the mollusc Hermissenda consists of five photoreceptors, two

165 eural bases of CI, we exposed the nudibranch mollusc Hermissenda crassicornis to explicitly unpaired

166 bular stimuli cause short-term memory of the mollusc Hermissenda that lasts approximately 7 min.

167 ntified synapse in the nervous system of the mollusc Hermissenda, the influence of somatic calcium ac

168 Classical conditioning of the mollusc, Hermissenda crassicornis, is a model system use

169 are particularly prominent in the venoms of mollusc-hunting Conus species.

170 tly from the two known delta-conotoxins from mollusc-hunting Conus venoms.

171 erozygosity are reported for the prosobranch mollusc Hydrobia ulvae (Pennant) together with a method

172 alian developmental program are seen in some molluscs (i.e., cephalopods), the findings presented her

173 l experiments performed on the embryo of the mollusc Ilyanassa obsoleta demonstrate that the 3D macro

174 hat, in the unequally cleaving embryo of the mollusc Ilyanassa obsoleta, the MAPK pathway is activate

175 In the spiralian embryo of the mollusc Ilyanassa, the IoTis11 RNA is segregated into th

176 f red abalone (Haliotis rufescens), a marine mollusc important to fisheries and global aquaculture.

177 n of CpG motifs, i.e., yeast, nematodes, and molluscs in addition to bacteria and insects.

178 oring, control, and management of non-native molluscs in China is urgently needed.

179 xicity, and development in L. stagnalis, and molluscs in general.

180 To test this, the 4000-year history of molluscs in Great South Bay, a bar-built lagoon, was rec

181 t shared a common ancestor with other extant molluscs in the Cambrian period, roughly 550 million yea

182 l ecological shift to numerical dominance by molluscs in the Late Permian, before the major taxonomic

183 including brown trout, riverine insects and molluscs, in Chubu Sangaku National Park.

184 Molluscs include Solenogastres, with their worm-like bod

185 lopods are a diverse group of highly derived molluscs, including nautiluses, squids, octopuses and cu

186 e highly rearranged relative to other extant molluscs, indicating an intense, early burst of genome r

187 Suspension feeding bivalve molluscs interact with different types of microplastics

188 The python implementation of MOLLUSC is available at

189 iated with intersexuality in vertebrates and molluscs is often a serious threat to ecosystems.

190 An epidemic of leukemia among bivalve molluscs is spreading along the Atlantic coast of North

191 The eyes on the backs of molluscs known as chitons are shadow and motion detector

192 ed NaV and KCNQ genes of worms, insects, and molluscs lack the ankyrin-G binding motif.

193 hell damage and shell thickness in a bivalve mollusc (Laternula elliptica) from seven sites around An

194 i, a brachiopod Liothyrella uva, two bivalve molluscs, Laternula elliptica, Aequiyoldia eightsii, a g

195 scleritome must be reconciled with Wiwaxia's mollusc-like mouthparts and foot; together these point t

196 es from the annelid Capitella teleta and the molluscs Lottia gigantea and Patella vulgata.

197 The bivalve mollusc Lucina pectinata harbors sulfide-oxidizing chemo

198 siological approach, we demonstrate that the mollusc Lymnaea performs a sophisticated form of decisio

199 s and egg masses of the freshwater gastropod mollusc Lymnaea provide a microenvironment for developin

200 In the feeding system of the mollusc Lymnaea, one of the best-studied rhythmical netw

201 In the mollusc Lymnaea, this pathway involves the functional in

202 elliptica, Aequiyoldia eightsii, a gastropod mollusc Marseniopsis mollis and an echinoderm Cucumaria

203 el, we devise a maximum likelihood framework-MOLLUSC (Maximum Likelihood Estimation Of Lineage and Lo

204 ng that numerical dominance by more tolerant molluscs may have been driven by variably stressful envi

205 The nudibranch molluscs Melibe leonina and Dendronotus iris exhibit hom

206 In the nudibranch mollusc, Melibe leonina, swim interneuron 1 (Si1) is in

207 d in fish (tuna and plaice) but decreased in molluscs (mussel and octopus).

208 rustacean species, with partial detection in molluscs: mussels, scallops and snails but none in oyste

209 n component of the extrapallial fluid of the mollusc Mytilus edulis has been previously isolated and

210 In the bivalve mollusc Mytilus edulis shell thickening occurs from the

211 he chiton, Katharina, but unlike the bivalve mollusc, Mytilus.

212 rate neurons, the soma of many arthropod and mollusc neurons is placed at the end of a thin neurite.

213 obtain putative cMDH and mMDH cDNAs from the mollusc Nucella lapillus.

214 d psbO 3' flanking sequence in the algal and mollusc nuclear homologues and gene absence from the mit

215 8-13) We combine a new compilation of fossil mollusc occurrences, paleotemperature proxies, and bioge

216 s 1685 freshwater species of plants, fishes, molluscs, odonates, amphibians, crayfish and turtles alo

217 We have studied five species of bivalve molluscs of the family Thyasiridae (that is, thyasirids)

218 erial from a charismatic group of nudibranch molluscs of the genus Trinchesia from European waters to

219 Molluscs, one of the most disparate animal phyla, radiat

220 ave been allied with barnacles, echinoderms, molluscs or annelids.

221 been regarded as incertae sedis, related to molluscs or assigned to their own phylum.

222 hurricanes on commercial landings of bivalve molluscs or shrimp.

223 stem-group annelids, brachiopods, stem-group molluscs or stem-group aculiferans (Polyplacophora and A

224 ally occurs through ingestion of undercooked molluscs or vegetables contaminated by infective larvae.

225 provide important resolution of conchiferan mollusc phylogeny and offer new insights into ancestral

226 (NOS)-containing cells in the opisthobranch mollusc Pleurobranchaea californica was studied histoche

227 The central nervous systems of the marine molluscs Pleurobranchaea californica (Opisthobranchia: N

228 despread and I provide examples for insects, molluscs, polychaetes, vertebrates and flowering plants.

229 onsequently, the role of 5alpha-reductase in molluscs presents a mystery.

230 enetic autonomy and/or (ii) more likely, the mollusc provides the essential plastid proteins.

231 and the swim central pattern generator of a mollusc) provides an interpretation key to explain known

232 Bivalve molluscs quality depends mainly on the water quality, an

233 Therefore, in molluscs, rapid ATP-dependent signaling can be implicate

234 ed patterns of variability within individual mollusc records as well as within isochronous parts of s

235 In bivalve molluscs, related phenomena, marker-associated heterosis

236 s well as such groups as the brachiopods and molluscs) remains limited.

237 Organelles are sequestered in the mollusc's digestive epithelium, where they photosynthesi

238 Lower acclimation capacity was found in molluscs, sessile species, filter feeders and kelp assoc

239 The extensive use of mollusc shell as a versatile raw material is testament t

240 itat provide key insights into mechanisms of mollusc shell growth under future climate change conditi

241 o track the biological origin of prehistoric mollusc shell.

242 the first application of palaeoproteomics to mollusc shells (and indeed to any invertebrate calcified

243 Some mollusc shells are formed from an amorphous calcium carb

244 own matrix proteins previously isolated from mollusc shells but rather it highly resembles a heavy me

245 hat were obtained from fossil brachiopod and mollusc shells using the 'carbonate clumped isotope' met

246 f the samples from crossed lamellar zones of molluscs shells.

247 The anatomy of these molluscs shocked the zoological community for presenting

248 i.e., annelids, echiurans, vestimentiferans, molluscs, sipunculids, nemerteans, polyclad turbellarian

249 Molluscs (snails, octopuses, clams and their relatives)

250 Shell color shows broad variation within mollusc species and despite information on the genetic p

251 Many non-native mollusc species have been introduced both intentionally

252 For example, turnover of mollusc species in the US Gulf coastal plain was over 90

253 es, hyolith lophophorates, and helcionelloid mollusc species show dynamic and synchronous trends over

254 h-derived tropomyosin in 11 crustacean and 7 mollusc species, and to study the impact of heating on i

255 findings show that a total of 61 non-native mollusc species, spanning 15 orders, 23 families, and 41

256 placed them in their own phylum, chordates, molluscs (specifically cephalopods), or radiodont panart

257 e that extensive spatial mapping of multiple mollusc specimens using Laser Induced Breakdown Spectros

258 to identify p63/73 homologues in the marine mollusc Spisula solidissima.

259 Among these, bivalve molluscs such as mussels are filter-feeding and sessile,

260 alternative splicing of duplicated exon in a mollusc that produces a novel variant adaptive to stress

261 s (Nucella lapillus), a widespread predatory mollusc that structures biodiversity in temperate rocky

262 ese are the first linkage maps for a bivalve mollusc that use microsatellite DNA markers, which shoul

263 (Fe(3)O(4)) mineral in the tooth of a marine mollusc, the chiton Chaetopleura apiculata.

264 ess) and metabolic rate of a keystone marine mollusc, the sea hare Stylocheilus striatus, a specialis

265 In 3 equally cleaving molluscs, the chiton Chaetopleura, the limpet Tectura, a

266 yptophan (5-HTP), in two model opisthobranch molluscs, the nudibranch Tritonia diomedea and the anasp

267 lecular markers are difficult to develop for molluscs, the reasons for which are largely unknown.

268 unite two seemingly very different groups of mollusc: the Polyplacophora with multiple shells and the

269 bursatellin-type metabolites are produced by molluscs themselves rather than by their microbial symbi

270 on and, since the divergence of annelids and molluscs, there has been a shift in onset of MAPK activa

271 ence for de novo androgen steroidogenesis in molluscs, these findings suggest that novel substrates f

272 eviewed the impacts of introduced non-native molluscs to address these gaps.

273 y, and the contributions of these non-native molluscs to commercial breeding, the aquarium trade, and

274 t, or 'fingerprint', in species ranging from molluscs to mammals and from grasses to trees.

275 tate the entire Gulf Coastal Plain, allowing molluscs to rapidly recolonise vacated areas once harsh

276 aphylaxis, patients with mollusc allergy and mollusc tolerance show a different pattern of sensitizat

277 taceans (14 with mollusc allergy and 17 with mollusc tolerance) were studied using skin prick tests (

278 ly expressed in the main ciliary band of the mollusc Tritia (also known as Ilyanassa).

279 For the mollusc Tritonia diomedea to generate its escape swim mo

280 solated central nervous system of the marine mollusc Tritonia diomedea, brief stimulation (1 sec) of

281 n generator (CPG) for the escape swim of the mollusc Tritonia diomedea.

282 (STDN) was investigated in the opisthobranch mollusc Tritonia diomedea.

283 pattern generator (CPG) for swimming in the mollusc Tritonia diomedea.

284 In the mollusc, Tritonia diomedea, EPSCs evoked by ventral swim

285 We found that in the mollusc, Tritonia diomedea, subtle differences between a

286 , i.e., the almost imperceptible response of molluscs versus the marked turnover of foraminifera and

287 shift from abundant brachiopods to dominant molluscs was abrupt and largely driven by the catastroph

288 As reported from a mollusc, we find xenopsin coexpressed with rhabdomeric-o

289 To better resolve the relationships among molluscs, we generated transcriptome data for 15 species

290 ubulins and tektins from an echinoderm and a mollusc were studied systematically using detergent-free

291 The serotonergic systems in nudibranch molluscs were compared by mapping the locations of serot

292 y word Daniel Osorio explains why cephalopod molluscs were protected by a European Union directive on

293 In other molluscs, where a larval nervous system predates the dev

294 f endocrine disruption occurred in gastropod molluscs which led to the banning of tributyltin.

295 ibe, from this deposit, a complete vermiform mollusc, which we interpret as a plated aplacophoran.

296 orans, or chitons, are an important group of molluscs, which are argued to have retained many plesiom

297 variations occur in other related intertidal molluscs whose lineages are much older than Nucella, whi

298 to those from a platyhelminth, echiuran and mollusc with rather less to arthropod alpha-tubulins.

299 ticular from belemnites, an extinct group of molluscs with carbonate hard-parts.

300 a global database for fish, crustaceans and molluscs with raw, cooked and processed foods; to base t