ライフサイエンスコーパス: subgenera

1 ommon ancestor or independently in different subgenera.

2 e United States and has been divided into 12 subgenera.

3 rent genera of the same family or even among subgenera.

4 phological features used to delimit Cambarus subgenera.

5 ces for 19 Drosophila species from all three subgenera.

6 ve evolved independently in different poplar subgenera.

7 orts the idea of spitting the genus into two subgenera.

8 nding regions from taxa in the other Cuscuta subgenera.

9 type C retroviruses that belong to different subgenera.

10 t levels of these compounds among the tested subgenera.

11 g the reproduction of many Culex species and subgenera.

12 nize sequences from multiple Betacoronavirus subgenera.

13 persist longer than their low oncogenic risk subgenera 1 and 3 counterparts.

14 In the studied Sorbus subgenera, 101 polyphenolic compounds were identified cl

15 ence with hexon protein sequences from human subgenera A, B, C, D, F, bovine AV3, and mouse AV1 revea

16 human pathogenic species separated into two subgenera according to their development site inside the

17 otstocks and five scion cultivars from three subgenera (Amygdalus, Prunus and Cerasus) for genome-wid

18 eparation of the drosophilan and sophophoran subgenera and it seems likely that Sxl functions as a se

19 e structure of this interaction network: Bee subgenera and plant genera were arranged into distinct,

20 We did observe subgenera and species-group-specific variation in the ID

21 among coronavirids across vs within genera, subgenera, and species.

22 quitoes belonging to only three out of eight subgenera: Anopheles, Cellia and Nyssorhynchus.

23 The majority of the Cambarus subgenera are rejected as monophyletic, suggesting the m

24 x, which contains over 800 species across 28 subgenera, are commonly believed to exclusively lay egg

25 ficant differences in silent variation among subgenera arose over a relatively short period of time,

26 2 isolates revealed species belonging to the subgenera Aspergillus, Nidulantes, and Circumdanti.

27 icate that the genus Pinus L. split into two subgenera by the Late Cretaceous, although subgenus Stro

28 iral genomic RNA are not conserved among the subgenera Embecovirus and Sarbecovirus within the Betaco

29 An analysis of Late Maastrichtian bivalve subgenera from the North American Coastal Plain found no

30 l record, 308 of the 1,292 living genera and subgenera (herein termed "taxa") are not recorded as fos

31 should include three extant species and two subgenera, Homo (Homo) sapiens (humankind), Homo (Pan) t

32 is the sister group to all other Drosophila subgenera (including some named genera, previously consi

33 d in coronaviruses from different genera and subgenera, including SARS-CoV, MERS-CoV, multiple bat co

34 ave shown gonopod morphology used to delimit subgenera is also affected by convergent evolution.

35 We identified Fv1 in 3 of the 4 Mus subgenera; its absence from Coelomys and 1 of 3 species

36 n humans is caused by Leishmania spp. in the subgenera Leishmania and Viannia Species identification

37 s for 12 representative coronaviruses from 6 subgenera, most of which lack known receptors, and show

38 e NSP1 proteins from viruses in at least two subgenera of beta-CoVs associate with the open head conf

39 However, 906 of 958 living genera and subgenera of bivalve mollusks having a fossil record occ

40 ore host species with four or more different subgenera of coronaviruses than have been observed to da

41 es belonging to 23 species representing four subgenera of Cuscuta and ten species of autotrophic Conv

42 alpha4-type subunits in two widely diverged subgenera of Drosophila suggests that these subunit isof

43 is from eight species representing the three subgenera of Glossina: Austenina (=fusca group), Nemorhi

44 species, each representing one of the three subgenera of honey bees, namely the dwarf (Apis florea),

45 immigration, a global analysis of genera and subgenera of marine bivalves over the past 11 million ye

46 ymorphism in six pedigrees, representing two subgenera of Pinus and a distant member of the Pinaceae,

47 (sugar pine) genomic DNA is present in both subgenera of Pinus with at least 10(4) copies/genome.

48 ctured visitation patterns observed among 75 subgenera of pollen-collecting bees in the Great Basin/E

49 level, upending their conventional status as subgenera of the genus Anopheles.

50 major satellites of the nine species of the subgenera Pimelia s. str. and Amblyptera characterised i

51 NA gene also confirmed this relationship and subgenera separation.

52 We found that the clock network of both subgenera Sophophora and Drosophila consists of all late

53 The fruits of four Sorbus subgenera (Sorbus x arnoldiana 'Copper Glow', Sorbus hup

54 ent between the traditionally recognized two subgenera, suggesting different rates of concerted evolu

55 (six new), to overhaul genera (nine new) and subgenera (three new), and to display convergence in win

56 zes pseudotyped viruses from three different subgenera through the inhibition of membrane fusion, and

57 ifferent rates of concerted evolution in two subgenera which could be attributable to their different

58 proteins of betacoronaviruses from different subgenera, with emphasis on its function and role in pat