ライフサイエンスコーパス: artiodactyl

1 evious difficulties in its identification in artiodactyls.

2 es revealed highest homology between the two artiodactyls.

3 ut no comparable assay has been described in artiodactyls.

4 cell receptors only in certain primates and artiodactyls.

5 nthracothere affinities with other Paleogene artiodactyls.

6 acean sister group and supports monophyly of artiodactyls.

7 pod dinosaurs during the Mesozoic and extant artiodactyl and perissodactyl mammals.

8 d differential selection pressure within the artiodactyl and primate lineage.

9 te), horse (perissodactyl), and a variety of artiodactyls and carnivores.

10 onstructed a database of viruses of domestic artiodactyls and examined the correlation between traits

11 losses of ancestral genes in carnivores and artiodactyls and gains of many new genes by gene duplica

12 present data on fast and slow carnivores and artiodactyls and on slow afrotherians and monotremes tha

13 sustained bursts of rapid evolution (in the artiodactyls and primates), during which the rate increa

14 e time of primates and rodents, primates and artiodactyls and the different great ape species by usin

15 sister group of carnivores, perissodactyls, artiodactyls, and cetaceans (e.g., 100% bootstrap value

16 ion rates in 48 nuclear genes from primates, artiodactyls, and rodents.

17 man counterparts, APOBEC3F and APOBEC3G, the artiodactyl APOBEC3F proteins are DNA cytosine deaminase

18 ver, unlike human APOBEC3F and APOBEC3G, the artiodactyl APOBEC3F proteins have an active N-terminal

19 we show that the Eocene south Asian raoellid artiodactyls are the sister group to whales.

20 tion in a comparative study of 46 species of artiodactyls belonging to seven of the eight extant taxo

21 t whales are related to even-toed ungulates (artiodactyls), but until now no artiodactyls were morpho

22 /spatially more consistent bending), and the artiodactyl calcaneus is even more simply loaded in bend

23 dents (mouse and rat), carnivores (dog), and artiodactyls (cattle) and then conducted phylogenetic an

24 Among artiodactyls, cattle but not pigs have diverse KIRs.

25 significant increase in publications on the artiodactyls-cattle and bird-poultry interface after 200

26 , double deaminase domain protein from three artiodactyls: cattle, pigs and sheep.

27 f the X, with gene content reflective of the artiodactyl common ancestor.

28 Sequencing of this region from other artiodactyls coupled with phylogenetic analysis has been

29 rted here is much more similar to the oldest artiodactyl, Diacodexis, in the derived condition of the

30 environment that descended from terrestrial artiodactyls, exhibit tremendous interspecific differenc

31 e deeply nested within the otherwise extinct artiodactyl family Anthracotheriidae, most precisely wit

32 is stops short of identifying any particular artiodactyl family as the cetacean sister group and supp

33 r were determined for representatives of the artiodactyl family Bovidae.

34 hese data provide a case for the power of an artiodactyl genome to contribute to the understanding of

35 In primates and artiodactyls, growth hormone exhibits accelerated rates

36 The recent identification of IgD in artiodactyls, however, suggests that IgD might be more w

37 ohyus is similar to whales, and unlike other artiodactyls, in the structure of its ears and premolars

38 In even-toed ungulates (artiodactyls, including cattle), limbs are adapted for r

39 ntributed to evolutionary diversification of artiodactyl limbs.

40 in the rodent lineage than in the primate or artiodactyl lineage, suggesting more intense purifying s

41 logical convergence, particularly within the artiodactyl lineage.

42 re family that has been variously considered artiodactyls or perissodactyls, but most recently placed

43 ning orders of placental mammals (cetaceans, artiodactyls, perissodactyls, carnivores, pangolins, bat

44 across species, with some (sub)orders (e.g., artiodactyls, perissodactyls, feliforms) exhibiting bifu

45 functional and variable KIRs in primates and artiodactyls predates placental reproduction.

46 the ankle with characteristics diagnostic of artiodactyls; R. balochistanensis has virtually complete

47 evolution, during the evolution of primates, artiodactyls, rodents, and elephants.

48 es encompassing the CFTR gene from two other artiodactyl species (cow and pig) for comparative sequen

49 lized to the placental surface epithelium of artiodactyl species.

50 and analysis of the sjTREC sequences in two artiodactyls suggested why previous attempts at cloning

51 The sjTREC in two artiodactyls, swine and sheep, was identified using forw

52 s that cetaceans are more closely related to artiodactyls than to any mesonychian.

53 mammalian orders (primates, carnivores, and artiodactyls), the species with the larger brains are mo

54 As with other artiodactyls, the giraffe shares the presence of a horiz

55 y change occurred during the transition from artiodactyls to whales and that raoellids were aquatic w

56 d ungulates (artiodactyls), but until now no artiodactyls were morphologically close to early whales.

57 ccurred during the evolution of primates and artiodactyls, when the rate of GH evolution apparently i

58 lian orders (primate, carnivore, rodent, and artiodactyls), which together contain a total of 20,457,