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1 atory, systemic, and reproductive disease of 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  almost exclusively in strains cultured from equids.
7 tion and disease in experimentally immunized equids.
8 a browser, unlike the grazing diet of modern equids.
9 l redundancy compared to the donor faeces of equids.
10 , sex chromosome regulation and evolution in equids.
11 ment and lifestyle on the gut microbiomes of equids.
12 rations, with shared benefits for humans and equids.
13 n and 31 ancient donkeys, as well as 15 wild equids.
14                                 Gomphothere, equid and camelid delta(13)C records show a broad variab
15 t causes a severe and often fatal disease in equids and humans.
16      In sum, EqHBV naturally infects diverse equids and mimics HBV infection patterns.
17 replication during acute disease in infected equids and serve as resilient reservoirs of virus infect
18 upporting a broad host range for EqHBV among equids and suggesting that horses might be suitable for
19 ls denoted by the selective culling of adult equids and the recovery of tanged and hafted projectile
20 l a trophic cascade involving cougars, feral equids and vegetation.
21 nts of 30 populations of hindgut fermenters (equids) and ruminants across biomes.
22 e species of middle to late Pleistocene NWSL equid, and demonstrate that it falls outside of crown gr
23 es have been identified only in primates and equids, and are expressed in placenta.
24 complete reproductive isolation, and promote equids as a fundamental model for understanding the inte
25  products contribute to molecular studies of equid biology and advance research on X-linked condition
26 resolution record of continental climate and equid body size change shows a directional size decrease
27 aracterized the Prdm9 gene in all species of equids by analyzing sequence variation of the ZF domains
28                      Persistent infection of equids by equine infectious anemia virus (EIAV) is typic
29 cument intentional breeding of highly valued equids called kungas for use in diplomacy, ceremony, and
30 clinical symptoms in experimentally infected equids coincided with rapid widespread seeding of viral
31 e extinct 'New World stilt-legged', or NWSL, equids constitute a perplexing group of Pleistocene hors
32 cant amounts of C(4) grasses were present in equid diets beginning at 9.9 Ma and in rhinocerotid diet
33 n and replication in experimentally infected equids during acute disease episodes and during asymptom
34 sands of humans and hundreds of thousands of equids during the past century.
35  notably the suid Notochoerus, the hipparion equid Eurygnathohippus, the giraffid Sivatherium, and th
36                     Our results suggest that equids, even those that are introduced or feral, are abl
37 ndrial and partial nuclear genomes from NWSL equids from across their geographic range.
38  in humans, we screened 2,917 specimens from equids from five continents for HBV.
39 nthropogenic forces can dramatically reshape equid gastrointestinal microbiomes, which has broader im
40 mental rock engravings of camels, ibex, wild equids, gazelles, and aurochs.
41 lanocortin 1 receptor (MC1R) - targeting the equid genome.
42        We discovered a distinct HBV species (Equid HBV, EqHBV) in 3.2% of donkeys and zebras by PCR a
43                           Antibodies against Equid HCV were codetected in 26.5% of donkeys seropositi
44                                              Equid herpesvirus (EHV) 1 and -4 are common viral pathog
45                                              Equid herpesvirus 1 (EHV-1) is a viral pathogen of horse
46 ly protective against the diseases caused by equid herpesvirus 1 (EHV-1), especially the neurologic f
47 that a single-nucleotide polymorphism in the equid herpesvirus type 1 DNA polymerase gene is associat
48 , we report that the nonneurovirulent strain equid herpesvirus type 1 strain NY03 caused lethal neuro
49 of EHV-1 and EHV-4, and did not detect other equid herpesviruses such as EHV-2, EHV-3, EHV-5, or seve
50 er-dependent fauna (for example, crocodiles, equids, hippopotamids and proboscideans)(2-6), sustained
51                                              Equids host homologs of hepatitis C virus (HCV).
52 erent vertebrates, including birds, rodents, equids, humans, and nonhuman primates.
53 ferent vertebrates including birds, rodents, equids, humans, and nonhuman primates.
54                 In placental tissue from the equid hybrids and the horse parent, the allelic expressi
55 ecline and demise of two Alaskan Pleistocene equids, I selected a large number of fossils from the la
56 re balanced view of the virus as a threat to equids in a diverse range of settings, thus leading to a
57 rse transport at Botai with wild Pleistocene equids in North America.
58 ing of 2-meter wells to groundwater by feral equids increased the density of water features, reduced
59 re we analyse (87)Sr/(86)Sr for 79 bovid and equid individuals representing 18 species from four loca
60 four copies for EHV-4, and 10 copies for the equid MC1R gene per reaction.
61 luding non-human primates, canines, felines, equids, ovids, suids, bovins, salmonids and murids.
62 he identification and precise demarcation of equid/Perissodactyl-specific features that for the first
63 ociated with sporadic outbreaks in human and equid populations in the Western Hemisphere.
64  as a mechanism to ensure its maintenance in equid populations.
65 ca through sporadic outbreaks into human and equid populations.
66 te from these data that rhinos diverged from equids prior to the occurrence of the mutations causing
67                                              Equids provide a unique opportunity for preclinical test
68  those of captive khulans (n = 12) and other equids-Przewalski's horse (n = 82) and domestic horse (n
69                          The timing of these equid regional extinctions and accompanying evolutionary
70  proximity to surface water was stronger for equids relative to ruminants, regardless of body size.
71 Osteological and biomolecular study of these equid remains demonstrates their successful reproduction
72 zoological analysis of identifiable domestic equid remains from two contexts associated with the init
73 y other members of the order Perissodactyla (equid, rhinoceros and tapir species).
74  another group contained the majority of the equid sequences identified.
75                            In analyses of 30 equid sera positive in an ELISA with whole cells, 24 (80
76                             Although dog and equid sera with antibodies to whole-cell B. burgdorferi
77 blood methylation data from three additional equid species (plains zebra, Grevy's zebras and Somali a
78 (MHC) class I genes isolated from a range of equid species and more distantly related members of the
79 ontained genes and alleles that are found in equid species and one group specific to the rhinoceros.
80       Here we match variation in striping of equid species and subspecies to geographic range overlap
81 ve figured centrally in that debate, because equid species dominated North American late Pleistocene
82 pha1, alpha2 and theta globin genes from six equid species have been determined to investigate relati
83                       Although multiple NWSL equid species have been named, our palaeogenomic and mor
84 horoughbreds and 42 samples from three other equid species that the T-allele was ancestral and there
85  the sequence and number of ZF domains among equid species, ranging from five domains in the Tibetan
86 evelop another clock that applies across all equid species.
87 m beyond the ranges reported for other known equid species.
88 asite that causes severe hemolytic anemia in equid species.
89                           In contrast, naive equids subjected to the low- or high-dose challenge deve
90                  Serum samples from dogs and equids suspected of having canine or equine borreliosis,
91 of climate produced from 16 serially sampled equid teeth spanning ~12,500 years of LRJ and Upper Pala
92 ckness virus (AHSV) is a lethal arbovirus of equids that is transmitted between hosts primarily by bi
93  an ancient mutation-conserved in all extant equids-that increases mitochondrial respiration while de
94 d from Parascaris and massively amplified in equids, to horse and donkey X chromosomes and three auto
95 d the genomes of one of these ~4500-year-old equids, together with an ~11,000-year-old Syrian wild as
96       These results reveal the challenges of equid translocation in early settlement of eastern North
97                     Morphometric analysis of equids uncovered in rich Early Bronze Age burials at Umm
98  sites, and, by mimicking flood disturbance, equid wells became nurseries for riparian trees.
99 tebrate richness and activity were higher at equid wells than at adjacent dry sites, and, by mimickin
100                                     Domestic equids were central to the initial colonization of the A
101  midges and causes African horse sickness in equids, with mortality reaching up to 95% in naive horse

 
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