ライフサイエンスコーパス: molluscan

1 d in terms of a homology model, based on the molluscan acetylcholine binding protein crystal structur

2 ith the structure of the binding site in the molluscan acetylcholine binding protein, a soluble prote

3 We identified a homologue of the molluscan acetylcholine-binding protein (AChBP) in the m

4 the benzodiazepine-binding site based on the molluscan acetylcholine-binding protein structure.

5 dy, based on the structure of the homologous molluscan acetylcholine-binding protein, predicted that

6 hR, and the crystal structure of the related molluscan ACh binding protein, much has been learned abo

7 family of receptors, which also includes the molluscan ACh-binding protein (AChBP), a soluble protein

8 aromatic residue (Tyr or Trp) in nAChRs and molluscan AChBPs, which has been implicated directly in

9 hBP) is 21-30% identical with those of known molluscan AChBPs.

10 ifs as well as unique PGY repeats found in a molluscan adhesive protein.

11 e concerning the long debate about the crown molluscan affinities of sachitids.

12 Their development pattern suggests a molluscan affinity.

13 rm appears to be a sub-family related to the molluscan alphabeta-domain MTs.

14 , Crassostrea virginica showed the canonical molluscan alphabeta-domain structure.

15 In recent years, studies of molluscan and crustacean feeding circuits have greatly e

16 The molluscan archive is dominated by extremophile taxa, inc

17 the end-Cretaceous mass extinction based on molluscan assemblages at four well-studied sites.

18 ies argue against a concerted phase shift of molluscan assemblages from one well-defined regime to an

19 uctuations at far-flung sites indicates that molluscan assemblages shifted to differently structured

20 K-means cluster analysis identified three molluscan assemblages, corresponding to sand-associated

21 Crayfish burrows and molluscan body fossils, abundant below and above the PET

22 o new papers provide important insights into molluscan body plan disparity.

23 retained many plesiomorphic features of the molluscan body plan.

24 acid sequence resembles previously described molluscan buccalin precursors, this indicates that LDA i

25 lade, which contains lancelet, nematode, and molluscan carotenoid oxygenase sequences.

26 effects of conoCAP-a and CCAP indicate that molluscan CCAP-like peptides have functions that differ

27 Molluscan CCAP-like peptides sequences, while homologous

28 anization is analogous to recently predicted molluscan CCAP-like preprohormones, and suggests a mecha

29 putatively encoding an integrin subunit from molluscan cells, and establishes the Bge cell line as a

30 have received little attention, such as the molluscan class Bivalvia.

31 lly characterized in the medically-important molluscan Class Gastropoda.

32 This record of benthic foraminiferal and molluscan community change from continental shelf depths

33 e plesiomorphic (an ancestral trait) for the molluscan crown.

34 However, statistical analysis of 73 molluscan data sets from estuaries and lagoons reveals s

35 Molluscan data sets from open shelf settings (n = 34) al

36 ever, statistical meta-analysis of 85 marine molluscan data sets indicates that, although sensitive t

37 stic estimates of the ecological fidelity of molluscan death assemblages tend to be erroneously pessi

38 k concerning the molecular regulation of the molluscan defence response provides a new framework for

39 However, limited genomic resources spanning molluscan diversity has prevented use of a phylogenomic

40 tion that culminated with the final shift to molluscan dominance in the Late Jurassic.

41 Although the Late Permian shift to molluscan dominance was a pronounced ecological change,

42 -Cretaceous mass extinction differ among the molluscan faunas of the North American Gulf Coast, north

43 Here, we show that, in the molluscan feeding system, both modified and unmodified p

44 We briefly review work on molluscan feeding, maintenance of postural control in ca

45 ertebrate colon, lung, kidney, and tongue, a molluscan FMRFamide-gated channel (FaNaC), and the nemat

46 We analysed coral and molluscan fossil assemblages from reefs near Bocas del T

47 complexity in cephalopods, where the typical molluscan ganglia become highly developed and fuse into

48 However, molluscan gene sequence data suggest the presence of tro

49 Morphologically-defined mammalian and molluscan genera (herein "morphogenera") are significant

50 ocene-Recent history of body sizes within 82 molluscan genera show little support for the expectation

51 lyzed in a sea star genus (Patiriella) and a molluscan genus (Littorina), each with diverse modes of

52 rt the clade Aculifera, containing the three molluscan groups with spicules but without true shells,

53 data, represent for the first time all major molluscan groups.

54 This represents the first molluscan hemocyanin to be completely sequenced.

55 ater similarity to fish insulins than to the molluscan hormone and are unique in that posttranslation

56 nge of definitive mammalian and intermediate molluscan hosts.

57 For three repeated molluscan innovations, 28-71% of instantiations are repr

58 -driven, clonal expansion of larvae inside a molluscan intermediate host.

59 xistence of a nitrergic signalling system in molluscan larvae and juveniles.

60 eriality of organs in supposedly independent molluscan lineages, i.e., in chitons and the deep-sea li

61 agents are impeded by the organism's complex molluscan-mammalian life cycle, which limits experimenta

62 marine invertebrates and fish indicated that molluscan microbiomes were more similar to each other th

63 onstituent genes differs from those of other molluscan mitochondrial gene arrangements.

64 Using the molluscan model system Lymnaea, we investigate here whet

65 is has eluded investigators but now, using a molluscan model system, a cellular mechanism has been es

66 rank abundance and numerical abundance in 19 molluscan modes of life--each defined as a unique combin

67 dictory groupings across analyses for 10% of molluscan morphogenera and 37% of mammalian morphogenera

68 Two novel molluscan MT families are described.

69 off-state in both smooth muscle myosins and molluscan myosins.

70 This research on this simple molluscan nervous system may lead to new therapeutic app

71 f the neuronal arborization of an identified molluscan neuron.

72 When microinjected into molluscan neurons or rabbit cerebellar Purkinje cell den

73 ) expressed in Xenopus laevis oocytes and in molluscan neurons.

74 identified on the basis of similarity to the molluscan neuropeptide FMRF-amide.

75 the hyperpolarized voltage of -70 mV, where molluscan NMDA receptors open free of constitutive block

76 ation appears to exist about the ontogeny of molluscan NOS-containing neurons.

77 We argue that molluscan or annelid cross, neither of which are present

78 This molluscan origin implies that all bivalve characters are

79 Molluscan pedal peptides (PPs) and arthropod orcokinins

80 cellular dialysis of PIP2 on voltage-clamped molluscan photoreceptors and found a marked reduction in

81 C in the modulation of the light response in molluscan photoreceptors.

82 here that mitogenomics is a useful tool for molluscan phylogenetics, especially when using powerful

83 Previous investigations of molluscan phylogeny, based primarily on nuclear ribosoma

84 The total synthesis of the molluscan polypropionate (-)-crispatene is described.

85 motifs, and predicted domain lengths of the molluscan protein, clearly identifies it as an integrin

86 ites or can be shell-less but with a typical molluscan radula and serially repeated gills.

87 or by direct binding of Ca(2+) to the ELC of molluscan RD.

88 rystal structures are available only for the molluscan RD.

89 w also determined the crystal structure of a molluscan (scallop) RD in the absence of Ca(2+).

90 rans, was assumed to be a relic of ancestral molluscan segmentation and was commonly accepted to supp

91 l units, and comparison with other available molluscan sequences indicates that the multi-domain subu

92 ineralized composite during formation of the molluscan shell and pearl.

93 The growth of molluscan shell crystals is usually thought to be initia

94 a in marine environments, where seawater and molluscan shellfish are the primary vectors of V. vulnif

95 tuarine waters and occurs in high numbers in molluscan shellfish around the world, particularly in wa

96 aused by single or multiple strains found in molluscan shellfish, is unknown.

97 Nacre, a structure found in many molluscan shells, and bone are frequently used as exampl

98 the secretion of the prism and nacre of some molluscan shells; (4) the development of skeletal spicul

99 Catch force in molluscan smooth muscle requires little, if any, energy

100 udinal ranges of 2838 eastern Pacific marine molluscan species, a subset of which figured in the orig

101 itial progeny of the M teloblast homologs in molluscan species, suggesting that it may be an ancestra

102 ittle consideration and contains most (>95%) molluscan species.

103 onserved in helicid snails and less in other molluscan species.

104 This "Serialia" concept may revolutionize molluscan systematics and may have important implication

105 Its occurrence in vertebrates, molluscan systems (i.e. Conus), and Drosophila and the a

106 te phyla; however, relationships among major molluscan taxa have long been a subject of controversy.

107 boundaries are shared among all the reported molluscan taxa, demonstrating a complete lack of conserv

108 e not evenly distributed among four regional molluscan time-series following the end-Cretaceous extin

109 iod, preceeding the differentiation of major molluscan types.

110 n of cleavage characters such as presence of molluscan vs. annelid cross for phylogenetic analyses is