ライフサイエンスコーパス: mollusk

1 o the underlying memory trace in this marine mollusk.

2 ng-term memory in this behaviorally advanced mollusk.

3 ntly described xenopsins in larval eyes of a mollusk.

4 eostasis, and complete development of marine mollusks.

5 establishes the dorsal-ventral axis in some mollusks.

6 s and 140 species of extinct Cenozoic marine mollusks.

7 , but most of these treatments also kill the mollusks.

8 been isolated from amphibian (frog) skin and mollusks.

9 production of marine organisms, particularly mollusks.

10 pecific sELISA to protect people allergic to mollusks.

11 ks in chordates, crustaceans, and cephalopod mollusks.

12 f origin for numerous taxa such as gastropod mollusks.

13 -gated sodium channel (FaNaC) from gastropod mollusks.

14 orescence (WDXRF) in pressed pellets bivalve mollusks.

15 systems and can accumulate in the tissues of mollusks.

16 r assumed as a proxy of Vtg in other bivalve mollusks.

17 h formed by chitons, a class of rock-grazing mollusks.

18 al summary, MP content was 0 - 10.5 MPs/g in mollusks, 0.1 - 8.6 MPs/g in crustaceans, 0 - 2.9 MPs/g

19 In the marine mollusk abalone, sperm secrete enormous quantities of tw

20 We discovered that a mollusk acetylcholine binding protein (AChBP), as a stru

21 In the present study, the homopentameric mollusk ACh binding protein (AChBP), used as a surrogate

22 The gamma2-PTC subunit was homologous to the mollusk AChBP (acetylcholine binding protein) but was no

23 ecialized sulfide-carrying hemoglobin from a mollusk adapted to life in a sulfide-rich environment.

24 evolve rapidly in many organisms, including mollusks, algae, and primates.

25 Crustacean and mollusk allergies have different manifestations includin

26 o acids into an endogenous neuropeptide from mollusks (ALSGDAFLRF-NH(2)) with weak antimicrobial acti

27 e acetylcholine-binding protein (AChBP) from mollusks, an established structural and functional surro

28 ed aculiferan sclerites, suggesting that the mollusk ancestor was densely covered with hollow chitino

29 dentified a broad FaNaC family that includes mollusk and annelid channels gated by FMRFa, FVRIamides,

30 his revealed only one pdf homolog in several mollusk and annelid species; two in Onychophora, Priapul

31 es achieved are the fastest movements of any mollusk and exceed previous estimates by over an order o

32 on and pre-concentration of pb(2+) ions from mollusk and fish samples were performed by nanocomposite

33 limits of the assay were 0.1 ppm for heated mollusks and 0.1-0.5 ppm for raw mollusks, depending on

34 Among spiral cleaving embryos (e.g. mollusks and annelids), it has long been known that one

35 ciliates) and metazoa (predominantly pelagic mollusks and cnidarians) were the most common sinking pa

36 Shellfish are classified into mollusks and crustaceans, the latter belonging to the cl

37 us dimeric assemblies with similar ones from mollusks and echinoderms suggests plausible pH-dependent

38 hozoa with three main clades: Tetraneuralia (mollusks and entoprocts), Lophophorata (brachiopods, pho

39 cognitive abilities (vertebrates, cephalopod mollusks and euarthropods) are distinct from all others

40 hat the genomes of Herpesvirales that infect mollusks and fish encode CLCC1 genes acquired from host

41 ore in depth studies of cellular immunity in mollusks and non-model invertebrates and set the ground

42 s on reproduction and population dynamics of mollusks and other marine organisms.

43 owever, several scaffold families present in mollusks and other protostomes are absent in vertebrates

44 he analysis of smoked meat and fish, bivalve mollusks and processed cereal-based food for infants.

45 ation of strength and stiffness exhibited by mollusks and produce a nacre-mimicking metal matrix comp

46 o reconstruct the trophic habits of floating mollusks and their sister species, revealing that prey p

47 in chaetae and shell fields in brachiopods, mollusks, and annelids provide molecular evidence suppor

48 NF-kappaB proteins have been identified in mollusks, and arthropods such as horseshoe crabs and bee

49 erved spectromicroscopically in echinoderms, mollusks, and cnidarians, phyla drawn from the 3 major c

50 ntal ecosystems (marine plankton, intertidal mollusks, and deciduous forest), and recover hidden line

51 rticle proposed that vertebrates, cephalopod mollusks, and euarthropods independently converged onto

52 only three lineages (vertebrates, cephalopod mollusks, and euarthropods) can be attributed to the piv

53 range of hosts, including crustaceans, fish, mollusks, and humans.

54 a, is a rich accumulation of pottery, marine mollusks, and nonhuman bones that represents first human

55 ent invasions by species such as crayfishes, mollusks, and plants.

56 food source, including pathogens, nematodes, mollusks, and vertebrates.

57 Both "protostome" animals (e.g., mollusks, annelids, and arthropods) and "deuterostomes"

58 ke values from existing data for arthropods, mollusks, annelids, and chordates (77 species total) and

59 eeply conserved mode of development found in mollusks, annelids, nemerteans, entoprocts, and some mar

60 hanisms of rejection responses in the marine mollusk Aplysia californica and compared these mechanism

61 on of an estrogen receptor ortholog from the mollusk Aplysia californica and the reconstruction, synt

62 % of an individual B2 neuron from the marine mollusk Aplysia californica are presented.

63 We used the marine mollusk Aplysia californica to investigate circadian mod

64 ained from the atrial gland of the gastropod mollusk Aplysia californica were chemically analyzed ind

65 experimentally advantageous preparation (the mollusk Aplysia californica).

66 al axons of identified neurons in the marine mollusk Aplysia californica, and in axons within the vag

67 t fly neuromuscular junction, as well as the mollusk Aplysia californica, have provided evidence for

68 examined two feeding behaviors in the marine mollusk Aplysia californica, one of which must precede t

69 sibly block ganglion cell activity in marine mollusk Aplysia californica, regardless the firing frequ

70 ractin, a 58-residue protein secreted by the mollusk Aplysia californica, stimulates sexually mature

71 In the marine mollusk Aplysia californica, waterborne protein pheromon

72 ls in the unmyelinated axons from the marine mollusk Aplysia californica.

73 contribute to feeding behavior in the marine mollusk Aplysia californica.

74 f intact peptidergic neurons from the marine mollusk Aplysia californica.

75 smission and neurite outgrowth in the marine mollusk Aplysia californica.

76 uction using sensory neurons from the marine mollusk Aplysia californica.

77 in the central nervous system of the marine mollusk Aplysia californica.

78 Withdrawal reflexes of the mollusk Aplysia exhibit sensitization, a simple form of

79 The gastropod mollusk Aplysia is an important model for cellular and m

80 suggested that meal satiation in the marine mollusk Aplysia is associated with stretch of the crop.

81 In the experimentally advantageous marine mollusk Aplysia, LTM for sensitization can be induced by

82 sms that control egg laying in the gastropod mollusk Aplysia, relatively little is known about the re

83 xt of memory for sensitization in the marine mollusk Aplysia.

84 in-related peptides (TKRPs) in a protostome, mollusk Aplysia.

85 Nicotinic agonist interactions with mollusk (Aplysia californica) acetylcholine binding prot

86 systems, including the hermaphrodite marine mollusk, Aplysia californica Moreover, different types o

87 Of 39 mollusk aragonite-associated protein sequences, 100% con

88 Brachiopods and mollusks are 2 shell-bearing phyla that diverged from a

89 The toxoglossate mollusks are a large group of venomous animals (>10,000

90 Mollusks are a major allergenic food under the food alle

91 Mollusks are a major component of animal biodiversity an

92 Vibrio includes serious human pathogens, and mollusks are a significant reservoir for species such as

93 how that delta(18)O signatures in freshwater mollusks are able to explain 95% of the variance of stre

94 Bivalve mollusks are consumed worldwide and can provide an adequ

95 Acetylcholine-binding proteins (AChBPs) from mollusks are suitable structural and functional surrogat

96 Mollusks are the second most diverse animal phylum, yet

97 re discovered in protostomian invertebrates (mollusks, arthropods).

98 interacting tissues of a range of cephalopod mollusks, arthropods, and cubozoan cnidarians.

99 The hyperdiverse Kourou mollusk assemblage suggests stronger affinities between

100 as with other invertebrates, positioning the mollusk at a critical juncture in evolution of this gene

101 Mollusk bioaccumulation factors were similar between HBC

102 erent main taxa of protostome invertebrates (mollusk bivalves, crustacean amphipods, branchiopods, co

103 we present a global assessment of freshwater mollusk (bivalves & gastropods) isotope data from 25 riv

104 eraction during development between the soft mollusk body and its hard shell.

105 Here, we report foraminifer, metazoan (mollusks, bony fish, bryozoans, decapods, and sharks amo

106 Cephalopods are set apart from other mollusks by their advanced behavioral abilities and the

107 s, and the basic logarithmic coiling seen in mollusks can be simulated with few parameters.

108 matophores) in the skin,(6) these cephalopod mollusks can dynamically adjust their body patterns in r

109 a reliable immunoassay for detecting edible mollusks (cephalopods, gastropods, and bivalves) has not

110 nomes from four phyla (annelids, arthropods, mollusks, chordates), spanning 19 independent transition

111 The vestibular organs in the marine mollusk Clione, the statocysts, react to the external en

112 cloned by sequence identity from arthropods, mollusks, cnidarians, and nematodes.

113 Mollusks collected off the coasts of Asia were the most

114 rs are under accelerated human pressure, and mollusk communities are among its most sensitive, threat

115 tructural and functional responses of native mollusk communities were not yet compared.

116 ing species composition of native freshwater mollusk communities.

117 E (1-5), from the hypobranchial gland of the mollusk Conus geographus.

118 for negative effects of heatwaves on native mollusks, corals and anemone.

119 oduction (-39%)-across the taxonomic groups (mollusks, crustaceans and fish), ontogenetic stages and

120 Evidence was available on four phyla: mollusks, crustaceans, fish, and echinodermata.

121 an exemplary subset of tropical West African mollusks, currently separated from the Mediterranean by

122 for heated mollusks and 0.1-0.5 ppm for raw mollusks, depending on the mollusk species tested.

123 e tablet thickness decreases with age of the mollusk, despite roughly similar appearance of nacre at

124 ecies, and the central nervous system of the mollusk displayed the highest isomerase activity among t

125 that protostomes (arthropods, annelids, and mollusks) diverged from deuterostomes (echinoderms and c

126 a depsipeptide originally isolated from the mollusk Dolabella auricularia, permitted us to study its

127 et al. now reveal the crystal structures of mollusk egg coat protein, VERL, complexed with cognate s

128 hijacked by a third partner, the herbivorous mollusk Elysia rufescens, and employed similarly for def

129 Mollusks encompass enormous disparity, including familia

130 steroidogenesis and steroid-like hormones in mollusk endocrinology.

131 -level modelling and isotope geochemistry on mollusks establish that the inhabitants of these earlies

132 ortunities to interpret ammonites' and other mollusks' evolution.

133 Cephalopod mollusks evolved numerous anatomical novelties, includin

134 Chitons, a group of marine mollusks, evolved scaled armors that address similar cha

135 the two proteins from marine and fresh water mollusks exhibit the characteristic features of the extr

136 Shipworms are marine wood-boring bivalve mollusks (family Teredinidae) that harbor a community of

137 ra tuberculosa, is an economically important mollusk for the human population living on the Colombian

138 om a broad geographic distribution of marine mollusk fossils.

139 d the occupancy histories of Cenozoic marine mollusks from New Zealand.

140 ain how the neurosecretory system of aquatic mollusks generates their diversity of shell structures a

141 ively softer microarchitectural units as the mollusk grazes on and erodes rock.

142 an enzyme enriched in the foot muscle of the mollusk H. pomatia, exhibits deaminase activity on adeno

143 associated protein of the nacre layer of the mollusk Haliotis rufescens and possesses a 36-amino acid

144 t years, the demand and exploitation of this mollusk have increased, putting it at risk to the point

145 Brachiopods and bivalve mollusks have also convergently evolved a bivalved shell

146 m the hypobranchial glands of various marine mollusks have been sources for dye compounds such as 6-6

147 Mollusks have developed a broad diversity of shelled str

148 gic cerebral giant cells (CGCs) of gastropod mollusks have important extrinsic modulatory actions on

149 from Seymour Island, comprised dominantly of mollusks, have been published over the last 30 years, bu

150 f 958 living genera and subgenera of bivalve mollusks having a fossil record occur in the Pliocene or

151 the membrane potential of B5 neurons of the mollusk Helisoma trivolvis, initially increasing their f

152 Mollusk hemocyanins, such as Concholepas concholepas (CC

153 age response, we investigated the effects of mollusks hemocyanins with varying structural and immunol

154 A fatigue-resistant mollusk hinge could in spire the development of new mate

155 We have found that in the mollusk Ilyanassa, Nanos messenger RNA and protein are s

156 In the spiralian embryo of the mollusk Ilyanassa, we find that the Dpp ortholog (IoDpp)

157 in lampreys and a somatic diversification of mollusk immune genes.

158 Magallana) gigas, is the most farmed bivalve mollusk in the world and is becoming a model species for

159 antly longer geologic ranges than the marine mollusks in general, but have ranges similar to those of

160 Mollusks in particular were commonly studied as both fac

161 e the well-known increase of deposit-feeding mollusks in postextinction assemblages and increases in

162 d burrowing fauna (polychaete worms, bivalve mollusks) increased from N to S with declining coral ske

163 s of neuropeptide modulation in crustaceans, mollusks, insects, and nematodes, with a particular emph

164 HTO in two algae and a mollusk is shown to exchange rapidly with seawater HTO.

165 ibitors of steroidogenesis, exert effects on mollusks is controversial.

166 the existing literature on the morphology of mollusks is descriptive.

167 at the development of chiral shells in these mollusks is different and that, unlike snails, ammonites

168 ion (as in arthropods) or Ca(2+)-binding (in mollusks, lacking phosphorylation), and another in verte

169 sults also reveal an enhanced sensitivity of mollusk larvae, but suggest that an enhanced sensitivity

170 pepod Calanus pacificus and pelagic pteropod mollusk Limacina helicina to ocean temperatures and pH b

171 ide diversities in three genera of gastropod mollusks (Littorina, Crepidula, and Hydrobia), each with

172 the central nervous system of the gastropod mollusk Lymnaea stagnalis produces a soluble protein tha

173 We found that in neurons of the mollusk Lymnaea stagnalis, two different RXR antagonists

174 vertebrate circuit generating feeding in the mollusk Lymnaea stagnalis, we identified three independe

175 lly verified or published cleavage data from mollusks, mammals and insects, and amino acid motifs rep

176 w years up to 200 years, this translation of mollusk metabolic properties into long term stream water

177 mutase was purified to homogeneity from the mollusk Mytilus edulis.

178 nges in the metabolic profile of the bivalve mollusk Mytilus galloprovincialis upon storage at 0 degr

179 nt in several invertebrate groups, including mollusks, nematodes, insects, and crustaceans (referred

180 se elements from HPAMPD into another related mollusk nucleoside adenosine deaminase, Aplysia ADGF.

181 zed synapsin transcripts in the invertebrate mollusk Octopus vulgaris and present evidence of their e

182 nila clam Ruditapes philippinarum, a bivalve mollusk of high commercial interest with worldwide distr

183 Cone snails are gastropod mollusks of the genus Conus that live in tropical marine

184 Bivalve mollusks of the North Atlantic, most prominently the sof

185 B and tridachiahydropyrone C, isolated from mollusks of the order Sacoglossa, using a sequence of ph

186 e variability of these properties during the mollusk ontogeny, between both shells of bivalves or acr

187 ce of native annelids and chordates, but not mollusks or arthropods.

188 ate spiral shape often compared to shells of mollusks, particularly to the nautilus shell.

189 role of shell integrity and functionality on mollusk performance and survival, there are no studies,

190 c acid, was isolated from the cephalaspidean mollusk Philinopsis speciosa.

191 nimals otherwise as different as mammals and mollusks, polygamy rates and histograms of successful ma

192 Cuttlefish, a unique group of marine mollusks, produces an internal biomineralized shell, kno

193 utoclaved mollusk samples and all commercial mollusk products tested.

194 y potential effects atrazine maybe having on mollusk-prokaryote interactions, we used 16S rRNA gene a

195 rted protein class termed Conserved Anterior Mollusk Proteins (CAMPs).

196 This finding suggests that other mollusks release attractin-related pheromones to form an

197 ared radiation-assisted digestion method for mollusk sample analysis.

198 y of shallow water carbonates (e.g., corals, mollusks) sampled from a 337 m-long drill core; (2) mode

199 teamed, boiled, baked, fried, and autoclaved mollusk samples and all commercial mollusk products test

200 m (6.69+/-3.39 and 5.45+/-2.44% for fish and mollusk samples, respectively) were obtained.

201 etermination of Cd(II) and Pb(II) in bivalve mollusks samples with excellent results.

202 Spines in mollusk seashells are classically interpreted as having

203 e extracellular domain homologue secreted by mollusks, serves as a general structural surrogate for t

204 ry of the structure of a nacreous layer of a mollusk shell have shown reasonable success.

205 ch as protein-protein interaction within the mollusk shell matrix.

206 In mollusk shell nacre, complex mixtures and assemblies of

207 The formation of aragonite mineral in the mollusk shell or pearl nacre requires the participation

208 terminal sequence of an extracellular matrix mollusk shell protein, AP7, that exhibits partial homolo

209 Stalagmite, deep-sea coral, and mollusk shell samples yielded comparable signal intensit

210 AP7 is a nacre-associated protein of the mollusk shell that forms supramolecular assemblies that

211 used to investigate the prismatic layer of a mollusk shell, Pinctada fucata.

212 They are comprised largely of mollusk shells (e.g., Eastern oyster, Crassostrea virgin

213 Spider silk is extraordinarily strong, mollusk shells and bone are tough, and porcupine quills

214 As euendoliths, they penetrate limestone, mollusk shells and other carbonate substrates, where the

215 of a number of biological materials (namely mollusk shells and sponge spicules) are discussed here.

216 Mollusk shells are an ideal model system for understandi

217 Furthermore, biomineralization changes in mollusk shells can be used as a novel potential proxy to

218 years derived from oxygen isotopes in fossil mollusk shells from Peru.

219 ness and its disorder in nacre across entire mollusk shells from red and rainbow abalone (Haliotis ru

220 seasonal clumped isotope analyses of fossil mollusk shells from the North Sea are presented to test

221 his alternative, one needs to prove that the mollusk shells reflect the atmospheric carbon isotopic c

222 At the example of Pinctada margaritifera mollusk shells we identify and resolve ~ 50 nm interlame

223 In this study, 18 terrestrial mollusk shells with known collection dates from 1948 to

224 ites are large, circular to arcuate piles of mollusk shells with some reaching over three meters in e

225 sphoproteins (e.g. mammalian teeth and bone, mollusk shells, and sponge silica).

226 ent biomineral lining the inner side of some mollusk shells, has alternating biogenic aragonite (calc

227 of-pearl, the iridescent inner layer of many mollusk shells, is a biomineral lamellar composite of ar

228 For example, nacre-the inner lining of some mollusk shells-encodes local environmental conditions th

229 hereas the sporophyte conchocelis bores into mollusk shells.

230 in polymorph control of crystal formation in mollusk shells.

231 rometer crystal dimensions, up to meter size mollusk shells.

232 We describe a shell-less, Cambrian stem mollusk, Shishania aculeata gen.

233 Nacre has been common in the shells of mollusks since the Ordovician (450 million years ago) an

234 ities for laboratory and field monitoring of mollusk species and provides key insights into endocrine

235 pread) is species-specific in at least eight mollusk species from completely different environments:

236 unosorbent assay (sELISA) detected 32 edible mollusk species in raw and heated without cross-reaction

237 1-0.5 ppm for raw mollusks, depending on the mollusk species tested.

238 environment, space, time, and invasive alien mollusk species, on structural and functional responses

239 w and heated without cross-reaction with non-mollusk species.

240 In this study, we developed a mollusk-specific sELISA to protect people allergic to mo

241 elid Capitella teleta, a sister clade to the mollusks, suggests that the dorsal-ventral axis is patte

242 e of an enzyme in the digestive gland of the mollusk that is able to biotransform laxaphycin B deriva

243 Cone snails are tropical marine mollusks that envenomate prey with a complex mixture of

244 and squid) are a group of soft-bodied marine mollusks that exhibit an array of interesting biological

245 communities are dominated by lucinid bivalve mollusks that live among the seagrass root system [4, 5]

246 Unlike mollusks, the barnacle shell comprises alternate layers

247 d sharp declines in the abundance of bivalve mollusks, the key phytoplankton consumers in this estuar

248 Paleozoic fossils trace crown mollusks to forms exhibiting a combination of biomineral

249 t causes lifelong infections in species from mollusks to humans.

250 We used the fossil record of seep mollusks to show that the living seep genera have signif

251 ntral nervous system of animals ranging from mollusks to vertebrates.

252 riety of systems (mammalian, crustacean, and mollusk) to demonstrate the unifying theme of state depe

253 cribe an interneuronal network in the marine mollusk Tritonia diomedea that is involved in producing

254 Here, in the marine mollusk Tritonia diomedea, we describe a detailed cellul

255 Here we demonstrate PPI in the marine mollusk Tritonia diomedea, which has a nervous system hi

256 swim central pattern generator (CPG) in the mollusk Tritonia diomedea.

257 Copper (Cu) isotope compositions in bivalve mollusks used in marine-monitoring networks is a promisi

258 ailed analysis of compound conditioning in a mollusk using discrete presentations of well-characteriz

259 etermination of Cd(II) and Pb(II) in bivalve mollusks using square wave anodic stripping voltammetry

260 being conotoxins RgIA and GeXIVA from marine mollusk venom, with an arginine content of >30%.

261 imilarities with tropomyosin and myosin from mollusks were detected.

262 m and M. trossulus than P. staminea when the mollusks were given to them either 1 species at a time o

263 al similar FMRFamide-like neuropeptides from mollusks were investigated by nuclear magnetic resonance

264 ood resources for lithodids--echinoderms and mollusks--were abundant on the upper slope (550-800 m) a

265 ested to lack actin-linked regulation is the mollusks, where contraction is regulated through the myo

266 Hence, the two soluble proteins from mollusks, which can be studied by a variety of physical

267 earlier extinction primarily affects benthic mollusks, while the boundary extinction primarily affect

268 (in addition to myosin-linked) regulation in mollusks would simplify our general picture of muscle re

269 onvertebrate organisms, including nematodes, mollusks, yeasts, and insects, cause polyclonal activati

270 argest archaeological growth rate dataset of mollusks yet.

271 pecially compared to those on post-Paleozoic mollusks, yet stratigraphically and geographically wides