ライフサイエンスコーパス: mollusk

1 o the underlying memory trace in this marine mollusk.

2 ntly described xenopsins in larval eyes of a mollusk.

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

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

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

6 s and 140 species of extinct Cenozoic marine mollusks.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

31 % of an individual B2 neuron from the marine mollusk Aplysia californica are presented.

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

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

34 experimentally advantageous preparation (the mollusk Aplysia californica).

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

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

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

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

39 In the marine mollusk Aplysia californica, waterborne protein pheromon

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

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

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

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

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

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

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

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

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

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

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

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

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

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

54 Mollusk bioaccumulation factors were similar between HBC

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

97 Spines in mollusk seashells are classically interpreted as having

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

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

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

101 In mollusk shell nacre, complex mixtures and assemblies of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

117 in polymorph control of crystal formation in mollusk shells.

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

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

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

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

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

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

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

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

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

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

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

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

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

131 imilarities with tropomyosin and myosin from mollusks were detected.

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

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

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

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

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

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

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

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

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