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1  of A. marginale and the related pathogen A. ovis.
2 distinct A. marginale strains, and Anaplasma ovis.
3                            Persistence of A. ovis 17 to 21 months following experimental infection wa
4 f A. marginale, 5.04 x 10(3) copies/ul of A. ovis, 4.58 x 10(3) copies/ul of A. phagocytophilum, and
5 discovery that eipA is essential in Brucella ovis, a naturally rough species that harbors mutations i
6                                  Helcococcus ovis, a recently described organism cultured from sheep,
7 ing ibex Capra sibirica and sprinting argali Ovis ammon-responded to predation risk from shared preda
8 enic (T. lestoquardi) and non-pathogenic (T. ovis), amongst a cohort of naive sheep in Oman.
9 nd MSP3 of Anaplasma marginale and Anaplasma ovis, Anaplasma phagocytophilum MSP2 (p44), Ehrlichia ch
10 ucella species diverged from their common B. ovis ancestor in the past 86,000 to 296,000 years, which
11 B. suis are pathogenic to humans, whereas B. ovis and B. neotomae are nonpathogenic to humans and B.
12  naturally occurring rough species, Brucella ovis and Brucella canis, has confused interpretation.
13        There were similar findings in 6 wild Ovis and Capra genera.
14 ide mass fingerprinting show exploitation of Ovis and Capra, while cementum analysis of intact teeth
15 responses to Epstein-Barr virus and Brucella ovis and Lactobacillus lactis antigens which contain the
16 -reactive epitopes with antigens found in A. ovis and some Ehrlichia spp.
17  = A. marginale, 5.04 x 10(6) copies/ul = A. ovis, and 4.58 x 10(3) copies/ul = A. phagocytophilum, a
18 and phenotypically distinct A. marginale, A. ovis, and A. centrale strains.
19                      Anaplasma marginale, A. ovis, and A. phagocytophilum are the causative agents of
20 nsis, Brucella suis-Brucella canis, Brucella ovis, and Brucella ceti.
21  characterization of complex I purified from Ovis aries (ovine) heart mitochondria.
22 ge panel of tissues, and conservation in the Ovis aries genome.
23                                     Mouflon (Ovis aries musimon) became extinct from mainland Europe
24 c genes in several breeds of domestic sheep (Ovis aries) and the wild Mouflon (Ovis orientalis musimo
25                                       Sheep (Ovis aries) are a major source of meat, milk, and fiber
26 he origins and prehistory of domestic sheep (Ovis aries) are incompletely understood; to address this
27 armots (Marmota flaviventer) and Soay sheep (Ovis aries) as a proof-of-concept showing that new insig
28 es underlying phenotypic variation in sheep (Ovis aries) may facilitate our efforts towards further i
29 a nearly complete atomic structure of ovine (Ovis aries) mitochondrial complex I at 3.9 A resolution,
30 fitness components, in 3400 wild Soay sheep (Ovis aries) monitored between 1989 and 2012.
31 ture and an interaction with domestic sheep (Ovis aries) on the altitude use and activity budgets of
32 ns in an unmanaged population of Soay sheep (Ovis aries) on the island of Hirta, St. Kilda, northwest
33 n contrast, overexpression of Cdk5 in sheep (Ovis aries) only produces brown patches on a white backg
34 ormation in a wild population of Soay sheep (Ovis aries) to investigate the genetic architecture of i
35 sequences and genes annotation of the sheep (Ovis aries) Y chromosome are still absent.
36 dyadic formation in fetal and newborn sheep (Ovis aries), and the regulation of this process by fetal
37 opathies (TSEs), including scrapie in sheep (Ovis aries), are fatal neurodegenerative diseases caused
38          In a wild population of Soay sheep (Ovis aries), phenotypic and genetic associations between
39 uus caballus), soybean (Glycine max), sheep (Ovis aries), poultry (Meleagris meleagris), pork (Sus sc
40 ruminal contents of cow (Bos Taurus), sheep (Ovis aries), reindeer (Rangifer tarandus) and red deer (
41  in the related species, domestic sheep (DS; Ovis aries), under both natural and experimental conditi
42 rst epigenetic clock for domesticated sheep (Ovis aries), which can predict chronological age with a
43 r studying the demographic history of sheep (Ovis aries).
44 ttrition in a precocial large mammal, sheep (Ovis aries).
45 otoxin, in comparison to domestic sheep (DS, Ovis aries).
46  of two different ruminant species, one from Ovis aries, designated ovine (O), and the other from Bos
47 s, domestic animals (Canis lupus familiaris, Ovis aries, Gallus gallus, Bos taurus, Felis catus, and
48                     Samples from Bos taurus, Ovis aries, Sus scrofa domestica, Equus caballus, Orycto
49 a (pronghorn), and the bovids Bos taurus and Ovis aries.
50 ncluding Brucella abortus, B. melitensis, B. ovis, B. neotomae, marine mammal isolates (no species na
51           Rocky Mountain bighorn sheep rams (Ovis canadensis canadensis) routinely conduct intraspeci
52  in a metapopulation of desert bighorn sheep Ovis canadensis nelsoni in the Mojave Desert to investig
53 ponding variances from desert bighorn sheep (Ovis canadensis nelsoni), as a proxy for Caprinae sharin
54 ld mammalian host, the desert bighorn sheep (Ovis canadensis nelsoni).
55 rally endangered Sierra Nevada bighorn sheep Ovis canadensis sierrae across three spatial scales: pop
56 ine specialist, Sierra Nevada bighorn sheep (Ovis canadensis sierrae) using a 20-year study of GPS co
57    We performed this study in bighorn sheep (Ovis canadensis) (BHS), since they are highly susceptibl
58 annheimia haemolytica in bighorn sheep (BHS; Ovis canadensis) are more severe than those in the relat
59  MHC class II alleles of bighorn sheep (BHS, Ovis canadensis) are responsible for lower titer of anti
60 m a long-term study of hunted bighorn sheep (Ovis canadensis) at Ram Mountain, Canada.
61 nse to sport hunting of bighorn trophy rams (Ovis canadensis) body weight and horn size have declined
62  MHC and three MS loci in 235 bighorn sheep (Ovis canadensis) from 14 populations and found that both
63 ng populations of desert bighorn sheep (DBS; Ovis canadensis) in New Mexico, USA, plus bison (Bison b
64 g a wild population of desert bighorn sheep (Ovis canadensis) in the Chihuahuan desert of New Mexico,
65       We monitored 127 female bighorn sheep (Ovis canadensis) released in three populations from 2000
66 usative agent of pneumonia in bighorn sheep (Ovis canadensis), in a small number of older individuals
67 notyped in two populations of bighorn sheep (Ovis canadensis), with different demographic histories.
68 y trajectories in wild female bighorn sheep (Ovis canadensis).
69      Anaplasma phagocytophilum and Anaplasma ovis cause human infections.
70 ixed parasite infections, indicating that T. ovis confers heterologous protection against lethal T. l
71 sing an archival collection of Dall's sheep (Ovis dalli dalli), a capital breeder that depends on its
72 buting to regional declines in Dall's sheep (Ovis dalli), a poorly dispersing alpine specialist herbi
73 irculating leukocytes to infestation with P. ovis, during a 6 week period.
74 ne sera from animals infected with Anaplasma ovis, Ehrlichia risticii, and Ehrlichia ewingii reacted
75           Culture filtrates from selected M. ovis field isolates demonstrated hemolytic activity on b
76              These data indicate that the M. ovis field isolates examined produce one or more heat-la
77  of this study was, therefore, to examine M. ovis field isolates for the presence of the putative vir
78 nale rickettsemia, were identified in the A. ovis genome by Southern blot analysis, and expression of
79 ory System, however, Moraxella (Branhamella) ovis has been isolated with increasing frequency from ca
80 di indicated a competitive advantage over T. ovis in mixed infection.
81 ts which have recovered from acute Anaplasma ovis infection remain seropositive, although infected er
82 sights into the host systemic response to P. ovis infestation, including roles for the complement sys
83 sed upon DNA sequence analysis, a Mycoplasma ovis-like species was the most prevalent organism detect
84 th Ochrobactrum anthropi reveals that the B. ovis lineage is basal to the rest of the Brucella lineag
85 ive administration of oncolytic parapoxvirus ovis (ORFV) and vaccinia virus can reverse NK cell suppr
86 tic sheep (Ovis aries) and the wild Mouflon (Ovis orientalis musimon).
87 eat-labile exotoxins and may suggest that M. ovis plays a role in the pathogenesis of IBK.
88 ly mixed-infections of T. lestoquardi and T. ovis prevailed, and no further death occurred.
89 nditional depletion of eipA expression in B. ovis results in a cell chaining phenotype, providing evi
90 e skin with the ectoparasitic mite Psoroptes ovis results in the development of a rapid cutaneous inf
91 ihood (ML) analyses, with A. centrale and A. ovis sequences used as outgroups, provided strong bootst
92 cytes in sheep following infestation with P. ovis, this study has provided key insights into the infl
93 us, B. melitensis, B. suis, B. canis, and B. ovis-using whole-genome comparisons.
94  resembling the ovine hemoplasma, Mycoplasma ovis, were detected by PCR in blood samples from a veter