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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 graphic retinal features also found in other artiodactyls.
5 nthracothere affinities with other Paleogene artiodactyls.
6 acean sister group and supports monophyly of artiodactyls.
7 cetes are homologous to those of terrestrial artiodactyls.
8  diversity dynamics of endemic and immigrant artiodactyls.
9 alatal foramina in 61 species of terrestrial artiodactyls.
10  cell receptors only in certain primates and artiodactyls.
11 en vegetation cover and locomotor traits for artiodactyl and carnivoran communities.
12 pod dinosaurs during the Mesozoic and extant artiodactyl and perissodactyl mammals.
13 d differential selection pressure within the artiodactyl and primate lineage.
14 te), horse (perissodactyl), and a variety of artiodactyls and carnivores.
15 onstructed a database of viruses of domestic artiodactyls and examined the correlation between traits
16  losses of ancestral genes in carnivores and artiodactyls and gains of many new genes by gene duplica
17 e of lateral palatal foramina in terrestrial artiodactyls and non-filter-feeding whales (odontocetes
18 understanding of the retinal organization in artiodactyls and offers insights on the importance of vi
19 present data on fast and slow carnivores and artiodactyls and on slow afrotherians and monotremes tha
20  sustained bursts of rapid evolution (in the artiodactyls and primates), during which the rate increa
21 e time of primates and rodents, primates and artiodactyls and the different great ape species by usin
22 est evidence of previously-undescribed large artiodactyls and/or tapiroids, mutually supporting recen
23  sister group of carnivores, perissodactyls, artiodactyls, and cetaceans (e.g., 100% bootstrap value
24 ion rates in 48 nuclear genes from primates, artiodactyls, and rodents.
25 man counterparts, APOBEC3F and APOBEC3G, the artiodactyl APOBEC3F proteins are DNA cytosine deaminase
26 ver, unlike human APOBEC3F and APOBEC3G, the artiodactyl APOBEC3F proteins have an active N-terminal
27 we show that the Eocene south Asian raoellid artiodactyls are the sister group to whales.
28 tion in a comparative study of 46 species of artiodactyls belonging to seven of the eight extant taxo
29        We show that, in comparison to the 11 artiodactyl brains studied (from 11 species), the 5 ceta
30 ve competition between endemic and immigrant artiodactyls but rather suggest a passive or opportunist
31 t whales are related to even-toed ungulates (artiodactyls), but until now no artiodactyls were morpho
32 /spatially more consistent bending), and the artiodactyl calcaneus is even more simply loaded in bend
33 dents (mouse and rat), carnivores (dog), and artiodactyls (cattle) and then conducted phylogenetic an
34                                        Among artiodactyls, cattle but not pigs have diverse KIRs.
35  significant increase in publications on the artiodactyls-cattle and bird-poultry interface after 200
36 , double deaminase domain protein from three artiodactyls: cattle, pigs and sheep.
37 f the X, with gene content reflective of the artiodactyl common ancestor.
38         Sequencing of this region from other artiodactyls coupled with phylogenetic analysis has been
39 rted here is much more similar to the oldest artiodactyl, Diacodexis, in the derived condition of the
40  environment that descended from terrestrial artiodactyls, exhibit tremendous interspecific differenc
41 e deeply nested within the otherwise extinct artiodactyl family Anthracotheriidae, most precisely wit
42 is stops short of identifying any particular artiodactyl family as the cetacean sister group and supp
43 r were determined for representatives of the artiodactyl family Bovidae.
44  deltaviruses infected bats, rodents, and an artiodactyl from the Americas but were absent from geogr
45 hese data provide a case for the power of an artiodactyl genome to contribute to the understanding of
46                              In primates and artiodactyls, growth hormone exhibits accelerated rates
47          The recent identification of IgD in artiodactyls, however, suggests that IgD might be more w
48 nt use of the coastal habitat by these large artiodactyls in SW Iberia.
49 ohyus is similar to whales, and unlike other artiodactyls, in the structure of its ears and premolars
50  to infect a wide range of wild and domestic Artiodactyls including African buffalo, gazelle, saiga a
51                      In even-toed ungulates (artiodactyls, including cattle), limbs are adapted for r
52 ntributed to evolutionary diversification of artiodactyl limbs.
53 in the rodent lineage than in the primate or artiodactyl lineage, suggesting more intense purifying s
54 logical convergence, particularly within the artiodactyl lineage.
55  locomotor traits of both primary consumers (artiodactyls, n = 157 species) and secondary consumers (
56 re family that has been variously considered artiodactyls or perissodactyls, but most recently placed
57                               The absence of artiodactyls, perissodactyls, and euprimates at Albas le
58 ning orders of placental mammals (cetaceans, artiodactyls, perissodactyls, carnivores, pangolins, bat
59 across species, with some (sub)orders (e.g., artiodactyls, perissodactyls, feliforms) exhibiting bifu
60 functional and variable KIRs in primates and artiodactyls predates placental reproduction.
61 the ankle with characteristics diagnostic of artiodactyls; R. balochistanensis has virtually complete
62                     We show that the endemic artiodactyl radiation was mainly related to the Eocene t
63 evolution, during the evolution of primates, artiodactyls, rodents, and elephants.
64 -fermenting mammals (e.g., colobine monkeys, artiodactyl ruminants) the enzymes pancreatic ribonuclea
65 n the Iberian Peninsula the fossil record of artiodactyls spans over 53 million years.
66 es encompassing the CFTR gene from two other artiodactyl species (cow and pig) for comparative sequen
67 lized to the placental surface epithelium of artiodactyl species.
68            We find that even-hoofed mammals (artiodactyls, such as deer and boars) represent about ha
69  and analysis of the sjTREC sequences in two artiodactyls suggested why previous attempts at cloning
70                            The sjTREC in two artiodactyls, swine and sheep, was identified using forw
71 s that cetaceans are more closely related to artiodactyls than to any mesonychian.
72  mammalian orders (primates, carnivores, and artiodactyls), the species with the larger brains are mo
73                                As with other artiodactyls, the giraffe shares the presence of a horiz
74             In contrast to savannah-dwelling artiodactyls, the horizontal streak of the Nubian ibex a
75 n the species-rich group of endemic European artiodactyls to determine the drivers of the Grande Coup
76  we use the inner ear morphology of ruminant artiodactyls to test for a deep-time correlation between
77 y change occurred during the transition from artiodactyls to whales and that raoellids were aquatic w
78 Trampled Surface (TTS) and some of the large artiodactyl tracks in the Matalascanas Trampled Surface,
79 dual coronal sections of the brains of seven artiodactyl ungulates, the pyramidal layer of CA1 is fou
80 d ungulates (artiodactyls), but until now no artiodactyls were morphologically close to early whales.
81 ccurred during the evolution of primates and artiodactyls, when the rate of GH evolution apparently i
82 lian orders (primate, carnivore, rodent, and artiodactyls), which together contain a total of 20,457,