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1 phological features used to delimit Cambarus subgenera.
2 ces for 19 Drosophila species from all three subgenera.
3 orts the idea of spitting the genus into two subgenera.
4 nding regions from taxa in the other Cuscuta subgenera.
5 type C retroviruses that belong to different subgenera.
6 e United States and has been divided into 12 subgenera.
7 rent genera of the same family or even among subgenera.
8 ence with hexon protein sequences from human subgenera A, B, C, D, F, bovine AV3, and mouse AV1 revea
9  human pathogenic species separated into two subgenera according to their development site inside the
10 eparation of the drosophilan and sophophoran subgenera and it seems likely that Sxl functions as a se
11                               We did observe subgenera and species-group-specific variation in the ID
12                 The majority of the Cambarus subgenera are rejected as monophyletic, suggesting the m
13 ficant differences in silent variation among subgenera arose over a relatively short period of time,
14 icate that the genus Pinus L. split into two subgenera by the Late Cretaceous, although subgenus Stro
15    An analysis of Late Maastrichtian bivalve subgenera from the North American Coastal Plain found no
16 l record, 308 of the 1,292 living genera and subgenera (herein termed "taxa") are not recorded as fos
17  should include three extant species and two subgenera, Homo (Homo) sapiens (humankind), Homo (Pan) t
18  is the sister group to all other Drosophila subgenera (including some named genera, previously consi
19 ave shown gonopod morphology used to delimit subgenera is also affected by convergent evolution.
20          We identified Fv1 in 3 of the 4 Mus subgenera; its absence from Coelomys and 1 of 3 species
21 n humans is caused by Leishmania spp. in the subgenera Leishmania and Viannia Species identification
22        However, 906 of 958 living genera and subgenera of bivalve mollusks having a fossil record occ
23  alpha4-type subunits in two widely diverged subgenera of Drosophila suggests that these subunit isof
24 is from eight species representing the three subgenera of Glossina: Austenina (=fusca group), Nemorhi
25 immigration, a global analysis of genera and subgenera of marine bivalves over the past 11 million ye
26 ymorphism in six pedigrees, representing two subgenera of Pinus and a distant member of the Pinaceae,
27  (sugar pine) genomic DNA is present in both subgenera of Pinus with at least 10(4) copies/genome.
28  major satellites of the nine species of the subgenera Pimelia s. str. and Amblyptera characterised i
29      We found that the clock network of both subgenera Sophophora and Drosophila consists of all late
30 ent between the traditionally recognized two subgenera, suggesting different rates of concerted evolu
31 ifferent rates of concerted evolution in two subgenera which could be attributable to their different

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