ライフサイエンスコーパス: equid

1 almost exclusively in strains cultured from equids.

2 l nervous system (CNS) disease in humans and equids.

3 ent serotypes, causes devastating disease in equids.

4 s causing neurological disease in humans and equids.

5 , occasionally causing disease in humans and equids.

6 tion and disease in experimentally immunized equids.

7 a browser, unlike the grazing diet of modern equids.

8 atory, systemic, and reproductive disease of equids.

9 t causes a severe and often fatal disease in equids and humans.

10 replication during acute disease in infected equids and serve as resilient reservoirs of virus infect

11 e species of middle to late Pleistocene NWSL equid, and demonstrate that it falls outside of crown gr

12 es have been identified only in primates and equids, and are expressed in placenta.

13 complete reproductive isolation, and promote equids as a fundamental model for understanding the inte

14 resolution record of continental climate and equid body size change shows a directional size decrease

15 aracterized the Prdm9 gene in all species of equids by analyzing sequence variation of the ZF domains

16 Persistent infection of equids by equine infectious anemia virus (EIAV) is typic

17 clinical symptoms in experimentally infected equids coincided with rapid widespread seeding of viral

18 e extinct 'New World stilt-legged', or NWSL, equids constitute a perplexing group of Pleistocene hors

19 cant amounts of C(4) grasses were present in equid diets beginning at 9.9 Ma and in rhinocerotid diet

20 n and replication in experimentally infected equids during acute disease episodes and during asymptom

21 sands of humans and hundreds of thousands of equids during the past century.

22 notably the suid Notochoerus, the hipparion equid Eurygnathohippus, the giraffid Sivatherium, and th

23 ndrial and partial nuclear genomes from NWSL equids from across their geographic range.

24 nthropogenic forces can dramatically reshape equid gastrointestinal microbiomes, which has broader im

25 that a single-nucleotide polymorphism in the equid herpesvirus type 1 DNA polymerase gene is associat

26 , we report that the nonneurovirulent strain equid herpesvirus type 1 strain NY03 caused lethal neuro

27 erent vertebrates, including birds, rodents, equids, humans, and nonhuman primates.

28 ferent vertebrates including birds, rodents, equids, humans, and nonhuman primates.

29 In placental tissue from the equid hybrids and the horse parent, the allelic expressi

30 ecline and demise of two Alaskan Pleistocene equids, I selected a large number of fossils from the la

31 re balanced view of the virus as a threat to equids in a diverse range of settings, thus leading to a

32 luding non-human primates, canines, felines, equids, ovids, suids, bovins, salmonids and murids.

33 he identification and precise demarcation of equid/Perissodactyl-specific features that for the first

34 ociated with sporadic outbreaks in human and equid populations in the Western Hemisphere.

35 ca through sporadic outbreaks into human and equid populations.

36 as a mechanism to ensure its maintenance in equid populations.

37 te from these data that rhinos diverged from equids prior to the occurrence of the mutations causing

38 The timing of these equid regional extinctions and accompanying evolutionary

39 y other members of the order Perissodactyla (equid, rhinoceros and tapir species).

40 another group contained the majority of the equid sequences identified.

41 In analyses of 30 equid sera positive in an ELISA with whole cells, 24 (80

42 Although dog and equid sera with antibodies to whole-cell B. burgdorferi

43 (MHC) class I genes isolated from a range of equid species and more distantly related members of the

44 ontained genes and alleles that are found in equid species and one group specific to the rhinoceros.

45 Here we match variation in striping of equid species and subspecies to geographic range overlap

46 ve figured centrally in that debate, because equid species dominated North American late Pleistocene

47 pha1, alpha2 and theta globin genes from six equid species have been determined to investigate relati

48 Although multiple NWSL equid species have been named, our palaeogenomic and mor

49 horoughbreds and 42 samples from three other equid species that the T-allele was ancestral and there

50 the sequence and number of ZF domains among equid species, ranging from five domains in the Tibetan

51 In contrast, naive equids subjected to the low- or high-dose challenge deve

52 Serum samples from dogs and equids suspected of having canine or equine borreliosis,

53 ckness virus (AHSV) is a lethal arbovirus of equids that is transmitted between hosts primarily by bi

54 midges and causes African horse sickness in equids, with mortality reaching up to 95% in naive horse