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 bly represents a plesiomorphic condition for molluscs.

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

5 nterpretations for primitive segmentation in molluscs.

6 quences have not been characterized in other molluscs.

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

8 have only been documented in equal-cleaving molluscs.

9 olfactory memories in terrestrial pulmonate molluscs.

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

11 nsport proteins found in many arthropods and molluscs.

12 also observed in the mantle tissues of other molluscs.

13 velopment in another major systematic group, molluscs.

14 ies are manifest in the movement patterns of molluscs.

15 close to the common ancestor of annelids and molluscs.

16 -allergic patients according to tolerance to molluscs.

17 nto question its purported relationship with molluscs.

18 comparisons of developmental processes among molluscs.

19 in olfactory systems of mammals, insects and molluscs.

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

21 ifferentiate tropomyosins in crustaceans and molluscs.

22 of the molecular evolution of NOS enzymes in molluscs.

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

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

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

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

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

28 Patients with mollusc allergy presented more frequently SPTs positive

29 Patients with mollusc allergy reacted more frequently to tropomyosin i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

56 integration in the feeding circuitry of the mollusc Aplysia.

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

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

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

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

61 Cephalopod molluscs are the most neurally and behaviorally complex

62 Molluscs are undoubtedly special - their extraordinary e

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

85 Molluscs display a rich diversity of body plans ranging

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

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

88 ird mechanism of asymmetric inheritance in a mollusc embryo.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

119 Molluscs include Solenogastres, with their worm-like bod

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

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

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

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

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

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

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

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

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

129 The bivalve mollusc Lucina pectinata harbors sulfide-oxidizing chemo

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

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

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

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

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

135 The nudibranch molluscs Melibe leonina and Dendronotus iris exhibit hom

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

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

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

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

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

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

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

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

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

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

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

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

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

149 hurricanes on commercial landings of bivalve molluscs or shrimp.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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