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1 sh) and invertebrate animals such as corals (Cnidaria).
2 ering functional cell biology experiments in Cnidaria.
3 hund-related CRE-like sequences in anthozoan Cnidaria.
4 ght to be restricted to a few species within Cnidaria.
5 mpting us to ask whether sleep is present in Cnidaria.
6 parasites, recently placed within the phylum Cnidaria.
7 firmly as sister taxon to Myxozoa within the Cnidaria.
8  member of the early branching animal phylum cnidaria.
9 s, an important model organism in the phylum Cnidaria.
10 than a medusa) is the ancestral body type in Cnidaria.
11 imply likely affinity within the Porifera or Cnidaria.
12 constitute the oldest eumetazoan phylum, the Cnidaria.
13  from early diverging phyla like Porifera or Cnidaria.
14 on-bilaterian animal, a member of the phylum Cnidaria.
15  a common form of gastrulation in the phylum Cnidaria.
16 e origin of coelenterazine within the phylum Cnidaria.
17 e recent common ancestor than either does to Cnidaria.
18 nary pathway from nervous to venom system in Cnidaria.
19           Porifera (45% of observations) and Cnidaria (40%) dominated the megafauna.
20   Here we show that sleep is also present in Cnidaria [6-8], an earlier-branching metazoan lineage.
21 hsous cadherins in Hydra, a member of phylum Cnidaria a sister group of bilaterian.
22                         These data show that Cnidaria, a diploblastic phylum ancestral to the triplob
23  in the clarification of relationships among Cnidaria, a key phylum of early-diverging animals.
24 wn to be sufficient for induction of axis in Cnidaria, a sister group to Bilateria, and is important
25 ondrial genomic data for the second class of Cnidaria allows us to reconstruct characteristic feature
26  have arisen at the divergence of sponge and cnidaria, an adaptation of the extracellular matrix in r
27  been described in Porifera, Ctenophora, and Cnidaria and are widespread among Bilateria, but our stu
28 tween the peptidergic neuronal properties of Cnidaria and Bilateria and those of Ctenophora, the most
29 thin Cnidaria, or prior to the divergence of Cnidaria and Bilateria.
30 ienced selection along the branch separating Cnidaria and Bilateria.
31 dgehog pathway in the common ancestor of the Cnidaria and Bilateria.
32 metry arose before the evolutionary split of Cnidaria and Bilateria.
33 st in all metazoan lineages except Placozoa, Cnidaria and Cephalochordata.
34                                              Cnidaria and Ctenophora are the first metazoan phyla to
35 evealed that the peptide-expressing cells of Cnidaria and Ctenophora express the vast majority of gen
36 as suggested trends of increasing jellyfish (Cnidaria and Ctenophora) biomass in several major ecosys
37 st and specific Endozoicomonas clades within Cnidaria and Porifera.
38     Since SLs are also present in Nematodes, Cnidaria and primitive chordates, this method could also
39 ry changes between species within the phylum Cnidaria and structures genomic and expression data to f
40 y signaling roles in patterning processes in cnidaria and, plausibly, in more complex metazoans as we
41 as a class within subphylum Medusozoa of the Cnidaria) and hexactinellid sponges evolved from demospo
42 ozoa) or have a sac-like gut (Ctenophora and Cnidaria) and that a through-gut originated within Bilat
43 latyhelminthes, Rotifera, Nematoda, Porifera/Cnidaria, and Chordata.
44 archaeal and bacterial phyla associated with Cnidaria, and highlights key bacteria hosted across host
45 7 different organisms ranging from humans to Cnidaria (anemone/coral).
46  reproduction in the coral Acropora palmata (Cnidaria, Anthozoa), we found that uniparental, meiotic
47 odern reefs, are classified as Scleractinia (Cnidaria, Anthozoa, and Hexacorallia) in reference to th
48                                     Although cnidaria are known to contain complex apoptotic signalin
49               Although animals of the phylum Cnidaria are not within the Bilateria, some representati
50 a anemone, Nematostella vectensis (Anthozoa, Cnidaria), are established during embryogenesis.
51 ast twice independently in Ctenophora and in Cnidaria + Bilateria.
52 zed metameric structures were present in the Cnidaria-Bilateria common ancestor over 600 million year
53 s of Medusozoa, one of the major lineages of Cnidaria, but are unreported for Anthozoa, which include
54                  Among the major lineages of Cnidaria, Ceriantharia ("tube anemones") remains one of
55 cific' Dicer partner, in the metazoan phylum Cnidaria, challenges the view that miRNAs evolved conver
56 f the soft coral Sarcophyton glaucum (phylum Cnidaria, class Anthozoa, subclass Octocorallia, order A
57 mt) DNA molecules of Hydra attenuata (phylum Cnidaria, class Hydrozoa, order Anthomedusae) has been d
58  member of the early diverging animal phylum Cnidaria, contains a gene encoding a Syk kinase.
59 n Bilateria and cnidocyte differentiation in Cnidaria - controls hair cell development in the sea ane
60       All known visual pigments in Neuralia (Cnidaria, Ctenophora, and Bilateria) are composed of an
61 ee in supporting the monophyly of Bilateria, Cnidaria, Ctenophora, and Metazoa.
62  eATP signaling in non-bilaterian metazoans (Cnidaria, Ctenophora, Placozoa, and Porifera).
63  reported in metazoan mtDNAs developed after Cnidaria diverged from the common ancestral line of all
64 g metazoan Nematostella vectensis (Anthozoa, Cnidaria) during embryonic and larval development.
65                                              Cnidaria (e.g. sea anemones and jellyfishes) is the sist
66  of the sea anemone Metridium senile (phylum Cnidaria) each contain a group I intron.
67  from homologous dehalogenases across phyla (Cnidaria, Echinodermata, and Chordata).
68 opment in eggs from diverse phyla, including Cnidaria, Echinodermata, and Chordata.
69 ng the early-branching non-bilaterian phylum Cnidaria, embryos of the sea anemone Nematostella vecten
70 on and apical budding characteristic of some Cnidaria, especially the extinct tabulates.
71 lished prior to the divergence of the phylum Cnidaria from the rest of the metazoans.
72 idence regarding the origins of luciferin in Cnidaria has implications for the evolution of biolumine
73 t sea anemone Nematostella vectensis (phylum Cnidaria) has emerged as a leading laboratory model orga
74 ropoda (insects, spiders, mites, scorpions), Cnidaria (Hydra, sea anemones), and Mollusca (oysters) b
75 ial DNA (mtDNA) molecule of Hydra oligactis (Cnidaria, Hydrozoa)--the first from the class Hydrozoa--
76 the well-known siphonophore belonging to the Cnidaria, Hydrozoa.
77 c chimeras of Hydractinia symbiolongicarpus (Cnidaria:Hydrozoa) and developed molecular markers to de
78 s within five families and two orders of the Cnidaria in the western Pacific.
79 ydroid Hydractinia symbiolongicarpus (Phylum Cnidaria) inbred for fusibility and here report results
80  Octocorals, a globally distributed class of Cnidaria, inhabit a wide range of environments, from col
81                                              Cnidaria is the sister taxon to bilaterian animals, and
82 ea anemone Nematostella vectensis (Anthozoa, Cnidaria) is a powerful model for characterizing the evo
83 ne, Metridium senile (class Anthozoa, phylum Cnidaria) is presented.
84 ge (phylum Porifera) and a jellyfish (phylum Cnidaria), making it safe to conclude that all animal gr
85                                   Myxozoans (Cnidaria: Myxozoa) are an extremely diversified group of
86 ary cells from all tissues of two species of Cnidaria: Nematostella vectensis and Pocillopora damicor
87                                           In Cnidaria, neurons are organized into a non-centralized r
88                             The soft corals (Cnidaria, Octocorallia), a diverse group of colonial mar
89 mbers of the early diverging metazoan phylum Cnidaria offer an exceptionally rich perspective into th
90 able to form symbioses with corals and other Cnidaria) on medium supplemented with glucose and amino
91 nor is it likely that Bilateria gave rise to Cnidaria or Ctenophora.
92 ct mechanosensory neurons diversified within Cnidaria, or prior to the divergence of Cnidaria and Bil
93  and arose at the divergence of Porifera and Cnidaria over 500 Mya.
94 > gene pair emerged in basal Ctenophores and Cnidaria phyla and is highly conserved across metazoans.
95 s of six bilaterians, three basal metazoans (Cnidaria, Placozoa, Porifera), two unicellular eukaryote
96 side this MPA, the coral Madracis myriaster (Cnidaria: Pocilloporidae) was found as the main reef bui
97 short peptides from early-branching lineages Cnidaria, Porifera and Ctenophora.
98 ce and features of SL addition in the phylum Cnidaria raise interesting questions regarding the evolu
99 volved in triploblasts after separation from Cnidaria, raising the possibility that cnidarian and sop
100                                   The phylum Cnidaria represents a close outgroup to Bilateria and in
101 ) molecule of the moon jelly Aurelia aurita (Cnidaria, Scyphozoa) - the first mtDNA sequence from the
102                                   The phylum Cnidaria (sea anemones, corals, hydras and jellyfish) is
103 been characterized in basal phyla, including Cnidaria (sea anemones, corals, hydras, and jellyfish),
104 rganism hydra (a member of the animal phylum Cnidaria) secrete neuropeptides with antibacterial activ
105                               As a member of Cnidaria, the body wall of hydra is structurally reduced
106                                           In Cnidaria, the frequency of appendage regeneration in the
107 proaches, we discovered that a member of the Cnidaria, the myxozoan Henneguya salminicola, has no mit
108 re we demonstrate, for the first time in the Cnidaria, the neuronal localization of nitric oxide synt
109                                       Within Cnidaria, the upside-down jellyfish Cassiopea spp. displ
110 lities, have been shown in taxa ranging from Cnidaria to Mammalia.
111 rior patterning and brain morphogenesis from Cnidaria to Mammals, and genetically underlie several hu
112 rpus, a member of the early-branching phylum Cnidaria, to provide insight into this question.
113 animals Placozoa are derived from medusozoan Cnidaria (we therefore place Placozoa as a class within
114  is limited to members of the ancient phylum Cnidaria, where it is used to accelerate water and enhan
115  closely related to Ctenophora than it is to Cnidaria, whereas LSU data alone do not refute either hy
116 ) is a leading model organism for the phylum Cnidaria, which includes anemones, corals, jellyfishes a
117 velopmental and genomic model for the phylum Cnidaria, which includes anemones, hydras, jellyfish, an
118 anemone Nematostella vectensis of the phylum Cnidaria, which is separated from bilaterians by ~600 mi
119 hed for a Pax-6 homolog and related genes in Cnidaria, which is the lowest phylum of animals that pos
120 suggests a single route to endoparasitism in Cnidaria, with larval stages of a common ancestor exploi

 
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