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1 other extinct lineage within this hemipteran suborder.
2 ones fossil, which represents a new, extinct suborder.
3 nesis for this clinically relevant bacterial suborder.
4 tide level from anemones within the existing suborders.
5  toxins from Araneomorphae and Mygalomorphae suborders.
6  host suborder and the families within these suborders.
7 ooming movements (CCGs) shared by all rodent suborders.
8 classified in five modern families and three suborders.
9 entative of the two most species-rich beetle suborders.
10 sils have been placed within the four extant suborders [3-5].
11  sequence data supports the monophyly of two suborders, a sister-group relationship between Stenuroth
12 adiation of poxviruses according to the host suborder and the families within these suborders.
13 her than Devonian diversification for extant suborders and directly impacting inferences of terrestri
14                                Monophyly for suborder Annulipalpia sensu stricto also is widely ackno
15 umans, all primate species examined from the suborder Anthropoidea had amino acid substitutions at po
16 yet in a species that belongs to the primate Suborder Anthropoidea.
17        Sap-feeding insects in the hemipteran suborder Auchenorrhyncha show complex symbioses with at
18               Despite its prevalence in this suborder, both the evolutionary trajectory and proximate
19  tibial tympanal ears co-evolved, but in the suborder Caelifera, abdominal tympanal ears first evolve
20 the suborder Feliformia and some taxa in the suborder Caniformia across much of their evolutionary hi
21 in a large sample of nematode species of the suborder Cephalobina.
22                                          The suborder Corynebacterineae encompasses species like Cory
23 terium tuberculosis and other species in the suborder Corynebacterineae possess a distinctive outer m
24 lycolipids are found in many bacteria in the suborder Corynebacterineae, but methyl-branched acyltreh
25 obic mycolic acid-producing bacterium in the suborder Corynebacterineae; revisions within the Propion
26                                        nov., suborder Endeostigmata) and integrate this information i
27                                       In the suborder Ensifera, we infer that forewing-based stridula
28 es) of corals conventionally assigned to the suborder Faviina.
29 ora allometry that characterizes much of the suborder Feliformia and some taxa in the suborder Canifo
30 us, is a hystricognathous rodent, a distinct suborder from the Sciurognathi, such as rats and mice.
31 inifera have been placed within 1 clade, the Suborder Globigerinina.
32                          Among primates, the suborder Haplorhini is considered to have evolved a cons
33        The respective monophylies of the two suborders have been tacitly assumed, although microbat m
34 nd morphological results, we propose a third suborder (Helenmonae) within the Actiniaria to accommoda
35                 Harlequin bugs belong to the suborder Heteroptera, which contains a number of economi
36 d in species representative of both cetacean suborders in addition to hominids and elephants suggests
37  is widely acknowledged, as is monophyly for suborder Integripalpia sensu stricto.
38 er group of birds, seabirds, and a different suborder (Lari).
39 VE1 occurs specifically within the marsupial suborder Macropodiformes (present-day kangaroos, wallabi
40 such a way that flying foxes form one of the suborders most closely related to primates.
41 mparative purposes as representatives of the suborder Mysticeti.
42 e species belonging to the Corynebacterineae suborder, namely, Mycobacterium bovis BCG, Mycobacterium
43  the Southern Ocean (family Channichthyidae, suborder Notothenioidei) are unique among vertebrates in
44 Antarctic icefishes (family Channichthyidae, suborder Notothenioidei) constitute the only vertebrate
45  revealed that Antarctic fish of the teleost suborder Notothenioidei, including icefishes, diverged f
46                                   Icefishes (suborder Notothenioidei; family Channichthyidae) are the
47       Our analyses demonstrate that cetacean suborders occupy distinct areas of cranial morphospace,
48             Members of the Corynebacterineae suborder of Actinobacteria have a unique cell surface ar
49 allicolids are related to the Eimeriorina, a suborder of apicomplexan coccidians that include other n
50 on of a total of 27 sequenced genomes in the suborder of Corynebacterineae (18 from the Mycobacterium
51                       Songbirds - the oscine suborder of perching birds that constitute roughly half
52 tes of molecular change in the strepsirrhine suborder of primates and test whether body size or age a
53 utria, representatives of the Hystricognathi suborder of rodents.
54  about 18,700 described recent species, is a suborder of the Hemiptera, one of big five most diverse
55  that occurred near the origin of the modern suborders of cetaceans approximately 34 million years ag
56             Relationships among families and suborders of scleractinian corals are poorly understood
57  neurons in 11 species representing all four suborders of the nudibranch clade: Dendronotoidea (Trito
58  these animals are allied with the primitive suborder Pantolesta (currently placed in the order Cimol
59 cters to European merialine Paroxyclaenidae (suborder Pantolesta), their affinities clearly lie with
60 tides prevalent in blood cells of tunicates (suborders phlebobranchia and stolidobranchia).
61 ncluding 90% of the genera of the xenarthran suborder Phyllophaga (sloths).
62                                          The suborder Pleuronectoidei receives moderate support, and
63 ents of species from the mostly plant-eating suborder Polyphaga with those of the mainly predatory Ad
64 -diverging lineage of the megadiverse beetle suborder Polyphaga, marsh beetles (Scirtidae) are crucia
65                   Indeed, the largest beetle suborder, Polyphaga, mostly includes plant eaters among
66 tative species and subspecies of the primate suborders Prosimii (family Lemuridae) and Anthropoidea (
67 ies for numerous species of the Artiodactyla suborder Ruminantia to examine chromosomal evolution in
68     We searched for similar genes within the suborder Ruminantia where the placenta lacks an extended
69 l as traditional concepts of the insectivore suborder Soricomorpha.
70 es, aphids, and mealybugs are members of the suborder Sternorrhyncha and share a common property, nam
71 abolic collaboration between the sap-feeding suborders Sternorrhyncha and Auchenorrhynca.
72  in Mengenillidia are free-living but in the suborder Stylopidia they remain endoparasitic in the hos
73                             We establish the suborder Tetrophthalmi subordo nov., which bore four eye
74 s the origins of the Anthropoidea, a primate suborder that includes humans.
75 e, a member of the most derived lepidopteran suborder, the Ditrysia.
76 ogy and diversity of early Anthropoidea, the suborder to which humans belong.
77  approximates the ancestral condition of the suborder Vombatiformes.
78 oup as a member of the extant daddy-longlegs suborder, which in turn resulted in older estimated ages
79  as stem members of Strepsirrhini, a primate suborder whose crown clade includes lemurs, lorises and
80 roups corresponding to recognized Orders and Suborders, with <5% unsupported nodes.
81 hinolophoid family Nycteridae belongs to the suborder Yangochiroptera along with vespertilionoids, no
82 inolophidae and Megadermatidae belong to the suborder Yinpterochiroptera along with rhinopomatids and
83 ocation either evolved separately in the bat suborders Yinpterochiroptera and Yangochiroptera, or had
84 -read sequencing for two polar fishes in the suborder Zoarcoidei and leveraged additional published l