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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                                     We found molluscan AFPK diversification correlated with shell los
14 rm appears to be a sub-family related to the molluscan alphabeta-domain MTs.
15 , Crassostrea virginica showed the canonical molluscan alphabeta-domain structure.
16                  In recent years, studies of molluscan and crustacean feeding circuits have greatly e
17                                          The molluscan archive is dominated by extremophile taxa, inc
18  the end-Cretaceous mass extinction based on molluscan assemblages at four well-studied sites.
19 ies argue against a concerted phase shift of molluscan assemblages from one well-defined regime to an
20 uctuations at far-flung sites indicates that molluscan assemblages shifted to differently structured
21    K-means cluster analysis identified three molluscan assemblages, corresponding to sand-associated
22                               Moreover, four molluscan AstCs with variations of sequences from Aplysi
23  predicted gene regulatory network (GRN) for molluscan biomineralization using Antarctic clam (Latern
24                         Crayfish burrows and molluscan body fossils, abundant below and above the PET
25 o new papers provide important insights into molluscan body plan disparity.
26  retained many plesiomorphic features of the molluscan body plan.
27                                              Molluscan brains are composed of morphologically consist
28 rvival to OsHV-1 through selection using the Molluscan Broodstock Program oysters.
29 r resistance to OsHV-1, 71 families from the Molluscan Broodstock Program, a US West Coast Pacific oy
30 acid sequence resembles previously described molluscan buccalin precursors, this indicates that LDA i
31 lade, which contains lancelet, nematode, and molluscan carotenoid oxygenase sequences.
32  effects of conoCAP-a and CCAP indicate that molluscan CCAP-like peptides have functions that differ
33                                              Molluscan CCAP-like peptides sequences, while homologous
34 anization is analogous to recently predicted molluscan CCAP-like preprohormones, and suggests a mecha
35 putatively encoding an integrin subunit from molluscan cells, and establishes the Bge cell line as a
36 ilations of extant species in 30 pantropical molluscan clades show that the IWP accounts for 71% of t
37 aking innovations in tropical marine Neogene molluscan clades that arose uniquely in either (but not
38  have received little attention, such as the molluscan class Bivalvia.
39 lly characterized in the medically-important molluscan Class Gastropoda.
40 uctural morphogenesis of shells from 3 major molluscan classes: A bivalve Unio pictorum, a cephalopod
41                                The impact on molluscan communities may have been low because detrimen
42 ty nor composition of the Gulf Coastal Plain molluscan communities.
43     This record of benthic foraminiferal and molluscan community change from continental shelf depths
44 e plesiomorphic (an ancestral trait) for the molluscan crown.
45          However, statistical analysis of 73 molluscan data sets from estuaries and lagoons reveals s
46                                              Molluscan data sets from open shelf settings (n = 34) al
47 ever, statistical meta-analysis of 85 marine molluscan data sets indicates that, although sensitive t
48 stic estimates of the ecological fidelity of molluscan death assemblages tend to be erroneously pessi
49 k concerning the molecular regulation of the molluscan defence response provides a new framework for
50  However, limited genomic resources spanning molluscan diversity has prevented use of a phylogenomic
51 tion that culminated with the final shift to molluscan dominance in the Late Jurassic.
52           Although the Late Permian shift to molluscan dominance was a pronounced ecological change,
53 pods, lending support to the contention that molluscan endocrinology differs from the well-characteri
54 ich animal phylum, but the pathways of early molluscan evolution have long been controversial(1-5).
55                                              Molluscan evolution in toto is characterized by plastici
56 tionships and improve understanding of early molluscan evolution, we carefully curated a high-quality
57                                              Molluscan eyes exhibit an enormous range of morphologica
58 aphy (u-CT) for investigating the anatomy of molluscan eyes in three species of the family Solarielli
59 -Cretaceous mass extinction differ among the molluscan faunas of the North American Gulf Coast, north
60                   Here, we show that, in the molluscan feeding system, both modified and unmodified p
61                    We briefly review work on molluscan feeding, maintenance of postural control in ca
62 ertebrate colon, lung, kidney, and tongue, a molluscan FMRFamide-gated channel (FaNaC), and the nemat
63                        We analysed coral and molluscan fossil assemblages from reefs near Bocas del T
64 complexity in cephalopods, where the typical molluscan ganglia become highly developed and fuse into
65                                     However, molluscan gene sequence data suggest the presence of tro
66        Morphologically-defined mammalian and molluscan genera (herein "morphogenera") are significant
67 ocene-Recent history of body sizes within 82 molluscan genera show little support for the expectation
68                       The flexibility of the molluscan genome likely explains both historic challenge
69 lyzed in a sea star genus (Patiriella) and a molluscan genus (Littorina), each with diverse modes of
70 rt the clade Aculifera, containing the three molluscan groups with spicules but without true shells,
71                                     Familiar molluscan groups-gastropods, bivalves, and cephalopods-e
72 data, represent for the first time all major molluscan groups.
73                    This represents the first molluscan hemocyanin to be completely sequenced.
74                                        Their molluscan heritage, innovative nervous system, and speci
75 ater similarity to fish insulins than to the molluscan hormone and are unique in that posttranslation
76 nge of definitive mammalian and intermediate molluscan hosts.
77 idative burst during host defenses and under molluscan hypoxia, we propose that these intermediates i
78                           For three repeated molluscan innovations, 28-71% of instantiations are repr
79 ent hosts: a mammalian definitive host and a molluscan intermediate host.
80 -driven, clonal expansion of larvae inside a molluscan intermediate host.
81 xistence of a nitrergic signalling system in molluscan larvae and juveniles.
82 eriality of organs in supposedly independent molluscan lineages, i.e., in chitons and the deep-sea li
83 agents are impeded by the organism's complex molluscan-mammalian life cycle, which limits experimenta
84 marine invertebrates and fish indicated that molluscan microbiomes were more similar to each other th
85 onstituent genes differs from those of other molluscan mitochondrial gene arrangements.
86                                    Using the molluscan model system Lymnaea, we investigate here whet
87 is has eluded investigators but now, using a molluscan model system, a cellular mechanism has been es
88 rank abundance and numerical abundance in 19 molluscan modes of life--each defined as a unique combin
89 dictory groupings across analyses for 10% of molluscan morphogenera and 37% of mammalian morphogenera
90                                    Two novel molluscan MT families are described.
91  off-state in both smooth muscle myosins and molluscan myosins.
92 lution, the relatively simple ganglion-based molluscan nervous system has been extensively transforme
93                 This research on this simple molluscan nervous system may lead to new therapeutic app
94 f the neuronal arborization of an identified molluscan neuron.
95                      When microinjected into molluscan neurons or rabbit cerebellar Purkinje cell den
96 ) expressed in Xenopus laevis oocytes and in molluscan neurons.
97 identified on the basis of similarity to the molluscan neuropeptide FMRF-amide.
98 we report on the characterization of a novel molluscan nitric oxide synthase (NOS)-related long non-c
99  the hyperpolarized voltage of -70 mV, where molluscan NMDA receptors open free of constitutive block
100                     Here we report the first molluscan NmU/PRXamide receptor from the slug, Deroceras
101 ation appears to exist about the ontogeny of molluscan NOS-containing neurons.
102                                We argue that molluscan or annelid cross, neither of which are present
103                                         This molluscan origin implies that all bivalve characters are
104                                              Molluscan pedal peptides (PPs) and arthropod orcokinins
105                                    The intra-molluscan phase provides a critical amplification step t
106 cellular dialysis of PIP2 on voltage-clamped molluscan photoreceptors and found a marked reduction in
107 C in the modulation of the light response in molluscan photoreceptors.
108  here that mitogenomics is a useful tool for molluscan phylogenetics, especially when using powerful
109                   Previous investigations of molluscan phylogeny, based primarily on nuclear ribosoma
110  of structural diversity underlying the many molluscan polyketides likely produced by the diverse AFP
111                   The total synthesis of the molluscan polypropionate (-)-crispatene is described.
112 red from the green alga Bryopsis sp. and its molluscan predator Elysia rufescens.
113  motifs, and predicted domain lengths of the molluscan protein, clearly identifies it as an integrin
114 ites or can be shell-less but with a typical molluscan radula and serially repeated gills.
115 or by direct binding of Ca(2+) to the ELC of molluscan RD.
116 rystal structures are available only for the molluscan RD.
117 e-type steroid androgens are not utilised in molluscan reproductive development.
118 w also determined the crystal structure of a molluscan (scallop) RD in the absence of Ca(2+).
119 rans, was assumed to be a relic of ancestral molluscan segmentation and was commonly accepted to supp
120  representing a significant knowledge gap in molluscan sensory biology.
121 l units, and comparison with other available molluscan sequences indicates that the multi-domain subu
122 ineralized composite during formation of the molluscan shell and pearl.
123                                The growth of molluscan shell crystals is usually thought to be initia
124           The molecular processes regulating molluscan shell production remain relatively uncharacter
125 a in marine environments, where seawater and molluscan shellfish are the primary vectors of V. vulnif
126 tuarine waters and occurs in high numbers in molluscan shellfish around the world, particularly in wa
127 aused by single or multiple strains found in molluscan shellfish, is unknown.
128                                              Molluscan shells are a classic model system to study for
129  diversity of forms and shows that, although molluscan shells are incrementally secreted at their ope
130 architectural constraint on the evolution of molluscan shells by defining a morphospace of possible s
131 dapted from available theoretical studies on molluscan shells, and apply the multiscale framework to
132             Nacre, a structure found in many molluscan shells, and bone are frequently used as exampl
133 the secretion of the prism and nacre of some molluscan shells; (4) the development of skeletal spicul
134                               Catch force in molluscan smooth muscle requires little, if any, energy
135 udinal ranges of 2838 eastern Pacific marine molluscan species, a subset of which figured in the orig
136 itial progeny of the M teloblast homologs in molluscan species, suggesting that it may be an ancestra
137  diversity of polyketides found in and among molluscan species.
138 onserved in helicid snails and less in other molluscan species.
139 ittle consideration and contains most (>95%) molluscan species.
140 isms underlying the development of the intra-molluscan stages remain poorly understood.
141    This "Serialia" concept may revolutionize molluscan systematics and may have important implication
142               Its occurrence in vertebrates, molluscan systems (i.e. Conus), and Drosophila and the a
143 te phyla; however, relationships among major molluscan taxa have long been a subject of controversy.
144 boundaries are shared among all the reported molluscan taxa, demonstrating a complete lack of conserv
145 e not evenly distributed among four regional molluscan time-series following the end-Cretaceous extin
146 ra (Tryblidia) to have several plesiomorphic molluscan traits.
147 iod, preceeding the differentiation of major molluscan types.
148 n of cleavage characters such as presence of molluscan vs. annelid cross for phylogenetic analyses is

 
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