ライフサイエンスコーパス: horse

1 uld potentially compromise the health of the horse.

2 , with mortality reaching up to 95% in naive horses.

3 e about relevant allergens in dogs, cats and horses.

4 1 vaccine as well as a prophylactic agent in horses.

5 sis and function in skeletal muscle of young horses.

6 s and represent the last remaining true wild horses.

7 indication for hepatic impairment in 7 of 11 horses.

8 i that causes upper respiratory infection in horses.

9 e energy metabolism and better immunity than horses.

10 preading outbreaks of respiratory disease in horses.

11 mber of the Flaviviridae family that infects horses.

12 past 100 million years and the radiation of horses.

13 construct, given the near extinction of wild horses.

14 ableness, which may have been key for taming horses.

15 the predominance of this haplotype in modern horses.

16 virus replication and disease progression in horses.

17 activation reported for both humans [9] and horses [10, 11].

18 wild horse assemblies (3 M bp) and Mongolian horse (2 M bp) were also sequenced and de novo assembled

19 he COPSAC2000 birth cohort data: (1) dog/cat/horse, (2) timothy grass/birch, (3) molds, (4) house dus

20 Severely asthmatic horses (6 horses/group) were treated with fluticasone, s

21 e samples of fresh beef (76 extractions) and horse (62 extractions) using Naive Bayes classification.

22 efense has reportedly been used against both horses [7] and humans [8].

23 us) specific primers that amplify fragments (horse; 85 bp, soybean; 100 bp, sheep; 119 bp, poultry; 1

24 nce of the corresponding allele in Icelandic horses (9(th)-11(th) century) strongly suggests that amb

25 presents most of the isolates recovered from horses, a smaller MLST and MLSA defined sub-population s

26 Other horses acted quickly, consistently detoured in the same

27 represent an essential part of the Yakutian horse adaptive genetic toolkit.

28 es in mice, suggesting that it could protect horses against EHV-1 infection.

29 orse (PH; Equus ferus przewalskii), the only horses alive today not successfully domesticated by huma

30 Thus horses, an animal far-removed from the primate lineage,

31 es with different composition percentages of horse and beef meat.

32 The separation of both horse and beef myoglobins was achieved in only seven min

33 Human hunting of horse and camel in Canada, coupled with mammoth, mastodo

34 in evidence for prehistoric human hunting of horse and camel in North America occurs at the Wally's B

35 n (HA) cleavage, and infection and growth in horse and dog tracheal explant cultures.

36 omesticated horses and the wild Przewalski's horse and found genetic structure within Eurasia in the

37 se of myoglobin from four meats: beef, pork, horse and lamb.

38 In the 'odd-toed' jerboa (Dipus sagitta) and horse and the 'even-toed' camel, extensive cell death sc

39 , which was hitherto represented only by the horse and the domestic donkey.

40 with an especially high frequency in gaited horses and breeds used for harness racing [2].

41 Comparison of sequences of viruses from horses and dogs revealed mutations that may be linked to

42 V affects draft, thoroughbred, and companion horses and donkeys in Africa, Asia, and Europe.

43 ted with acute and chronic EHCV infection in horses and further justifies it as a large animal model

44 r from its reservoir host, pteropid bats, to horses and further on to humans, and the severe clinical

45 ding is the most fundamental use of domestic horses and has had a huge influence on the development o

46 paramyxovirus that causes deadly illness in horses and humans.

47 he Americas and that is capable of infecting horses and humans.

48 es the major route of cortisol metabolism in horses and is up-regulated in adipose tissue in obesity

49 Here, the butchered remains of seven horses and one camel are associated with 29 nondiagnosti

50 virus outbreaks in Australia, all involving horses and some involving transmission to humans, have b

51 The evolutionary origins of Yakutian horses and the genetic basis of their adaptations remain

52 d these genomes with genomes of domesticated horses and the wild Przewalski's horse and found genetic

53 trition developed during my experiences with horses and then Angus cattle and entry into an animal sc

54 omplete genomes of nine present-day Yakutian horses and two ancient specimens dating from the early 1

55 Infected WBCs can also function as 'Trojan horses' and carry viruses into immune-sheltered spaces,

56 equences for a male wild horse (Przewalski's horse) and a male domestic horse (Mongolian horse), with

57 also obtained with heat-inactivated pus (24 horses) and blood (23 horses) spotted onto Whatman FTA c

58 ween the two periods for both large (cattle, horse, and camel) and small livestock (sheep and goat).

59 2 gene for precise quantification of cattle, horse, and pig in processed meat products.

60 and enabled detection of 10% (w/w) of pork, horse, and turkey meat and 5% (w/w) of chicken meat in b

61 GT) concentrations were mildly elevated in 3 horses, and 1 horse displayed even highly elevated GGT l

62 frotheria than with the euungulates (cattle, horses, and allies) of superorder Laurasiatheria.

63 r outbreaks of viral encephalitis in humans, horses, and birds, with particularly virulent strains ca

64 cats, Bos d 5 from cow's milk, Equ c 1 from horses, and Mus m 1 from mice, all of them representing

65 s of GDF11/8 decline with age in mice, rats, horses, and sheep.

66 Both decreased contact between people and horses, and the concomitant increase in swine production

67 that have occurred during virus evolution in horses, and to investigate the role of HA in the equine

68 acterium radiobacter K84 secretes the Trojan Horse antibiotic agrocin 84 that is selectively transpor

69 chemical versatility than traditional Trojan horse antibodies and other proteins.

70 bly decreased by giving millions of doses of horse antitoxin to wounded soldiers.

71 This study presents a "Trojan-Horse" approach to combating these tumors by using a rec

72 The domestication of the horse approximately 5.5 kya and the emergence of mounted

73 roaches, since the canine virus emerged from horses approximately 15 years ago.

74 of the disease in humans vs dogs, cats, and horses are most often caused by similar, but sometimes s

75 Most domestic horses are non-dun, a more intensely pigmented phenotype

76 nonprimate hepaciviruses (NPHV) that infect horses are the closest relatives of HCV described to dat

77 ectricity overtook steam and trains overtook horses as a means of transportation, both around the yea

78 sed as a viral vector for the vaccination of horses as well as, potentially, for the vaccination of o

79 Portion of Y chromosome from wild horse assemblies (3 M bp) and Mongolian horse (2 M bp) w

80 Horses, asses, and zebras belong to a single genus, Equu

81 rogesterone-dependent gene expression in the horse at subphysiological concentrations and to maintain

82 for three different lipoxygenases, soybean, horse bean and wheat and compared to the values obtained

83 anaerobic reaction catalysed by soybean and horse bean lipoxygenases was observed with 2,6-di-tert-b

84 All infected horses became viremic after 1 or 2 wk and viremia could

85 Such "Trojan horse" bispecific antibodies have potential as broad ant

86 S. mitis survival in horse blood or in a mouse model of bacteremia was not si

87 th in human serum, human plasma, or sheep or horse blood.

88 ate northern European haplotypes, all modern horse breeds clustered together in a roughly 700-year-ol

89 and efficacious endogenous progestin in the horse but that the PR evolved with increased agonistic p

90 e the first Y chromosome genealogy of modern horses by screening 1.46 Mb of the male-specific region

91 d macrophages are believed to act as "Trojan horses" carrying infectious particles to be released on

92 uise of a food source, function as a 'Trojan Horse', carrying genes encoding an exotoxin into target

93 EAV preferentially infects subpopulations of horse CD14(+) monocytes expressing EqCXCL16 and that inf

94 Dun is a wild-type coat color in horses characterized by pigment dilution with a striking

95 sculi, and the bark-associated microbiota of horse chestnut (Aesculus hippocastanum) trees.

96 cessed samples manufactured from beef, pork, horse, chicken and turkey meat.

97 ly treated meat species, namely, beef, pork, horse, chicken, and turkey meat, to select and identify

98 sociated (LA) MRSA CC398 isolates from pigs, horses, chickens, and veal calves, and five methicillin-

99 whisky brands: Red Label, Black Label, White Horse, Chivas Regal (12years), Ballantine's Finest, Old

100 In other individual horses, chronic infections could be observed with the co

101 t-extensive genome dataset characterized for horses, comprising 21 new genomes.

102 Encapsulation of oxidized horse cytochrome c in 1-decanoyl-rac-glycerol/lauryldime

103 n the initial 140 microseconds of folding of horse cytochrome c.

104 heme-undecapeptide derived from the protein horse cytochrome c.

105 birch and ragweed pollen, midge larvae, and horse dander; food allergens from peanut, cow's milk, an

106 These horses descend from a founding population of 12 wild-cau

107 st possible hacking attacks including Trojan horse, detector blinding, phase randomisation and photon

108 and behaviorally distinct from domesticated horses (DHs, Equus caballus).

109 ions were mildly elevated in 3 horses, and 1 horse displayed even highly elevated GGT levels.

110 tes, macrophages, and plasma cells with some horses displaying subclinical signs of hepatitis.

111 un and non-dun1 alleles are found in ancient horse DNA, demonstrating that this polymorphism predates

112 s horses, we find that contemporary Yakutian horses do not descend from the native horses that popula

113 determine hemoglobin in the blood of humans, horses, dogs, cats, and cows.

114 However, the genetics underlying horse domestication are difficult to reconstruct, given

115 emonstrating that this polymorphism predates horse domestication.

116 plasmosis is a disease of Equidae, including horses, donkeys, mules, and zebras, caused by either of

117 domesticated by humans, and herded, domestic horse (E. f. caballus) living in adjacent natural grassl

118 ule blood cells' in the lamprey, frog, fowl, horse, elephant and man.

119 constitute a perplexing group of Pleistocene horses endemic to North America.

120 thesized DHP is a biopotent progestin in the horse ends decades of speculation, explaining how equine

121 The method merges the use of horse (Equus caballus), soybean (Glycine max), sheep (Ov

122 Therefore we tested whether domestic horses (Equus caballus) could discriminate between facia

123 in equine blood and at high frequency among horses exhibiting cutaneous lesions.

124 included B cells could operate like 'Trojan horses': expression and function of the nonautoreactive

125 Zebras are members of the horse family.

126 Horses (family Equidae) are a classic example of adaptiv

127 rval: 0.41, 0.89; P for trend < 0.01) and to horse farming (>/=20 years: hazard ratio = 0.64, 95% con

128 sociation between lung cancer and cattle and horse farming.

129 or 2 wk and viremia could be detected in two horses for several weeks followed by a delayed seroconve

130 We tested twenty-six horses for their ability to detour around symmetric and

131 Genotyping the position in 4396 modern horses from 141 breeds revealed that nowadays the mutate

132 cific region of the Y chromosome (MSY) in 52 horses from 21 breeds.

133 number of insertions and relocations in the horse genome.

134 We therefore sequenced two ancient horse genomes from Taymyr, Russia (at 7.4- and 24.3-fold

135 ormation confirms the distinctiveness of the horse genomovar and indicates the presence of potentiall

136 The Oriental horse group consisted of two major subclades: the Origin

137 Severely asthmatic horses (6 horses/group) were treated with fluticasone, salmeterol,

138 ure functional stenosis severity over a work-horse guidewire and is used as a more feasible alternati

139 ly, the causative mutation for gaitedness in horses has been linked to a substitution causing a prema

140 cumentation of swine influenza, influenza in horses has been well documented for hundreds of years, a

141 emely low Y chromosome sequence diversity in horses has prevented the reconstruction of stallion gene

142 (e.g. ambling or pacing), so-called 'gaited' horses, have been highly valued by humans, especially fo

143 e secondary functions of cyt c obtained from horse heart (mammalian) and Saccharomyces cerevisiae (ye

144 nformational changes in oxidized and reduced horse heart cyt-c bound to CL-containing lipid bilayers.

145 was used to monitor the mild denaturation of horse heart myoglobin by acetonitrile, and the results s

146 up-regulated in adipose tissue in obesity in horses, humans and mice.

147 h viruses are associated with CNS disease in horses, humans, and mouse infection models.

148 We produced purified equine antisera from horses hyperimmunized with EBOV virus-like particles, an

149 duction of purified equine IgG obtained from horses immunized with plasmid DNA followed by boosting w

150 being the well known recording in 1878 of a horse in motion and the 1887 photograph of a supersonic

151 ividual spoken nouns in one language (e.g., "horse" in English) accurately predict the response patte

152 e most directly related to ongoing growth of horses independent of muscle group, and training further

153 lentivirus, using antibody escape data from horses infected with equine infectious anemia virus.

154 However, intrahepatic RNA inoculation of a horse initiated infection, yielding high RNA titers in t

155 ins and ions) which act as a kind of 'Trojan-horse' internalization by cells.

156 The strategy was to herd horses into a pool containing electric eels, provoking t

157 The lifestyle of S. equi within the horse is defined by short-term acute disease, strangles,

158 Here we show that pigment dilution in Dun horses is due to radially asymmetric deposition of pigme

159 The donkey, like the horse, is a promising model for exploring karyotypic ins

160 Characterization of a subset of horse isolates by multilocus sequence analysis (MLSA) an

161 08 Lancefield group C (n = 96) or L (n = 12) horse isolates recovered in the United States and in thr

162 he Original Arabian lineage and the Turkoman horse lineage.

163 rotein from sardine (Sardina pilchardus) and horse mackerel (Trachurus mediterraneus) was hydrolysed

164 teins in frozen (-10 degrees C for 3 months) horse mackerel (Trachurus trachurus) was evaluated.

165 h samples from six different species, namely horse mackerel (Trachurus trachurus), European anchovy (

166 ) only in the samples of larger blue fish as horse mackerel and chub mackerel.

167 gy was validated in trout, hake and Atlantic horse mackerel and was used to study the shelf life of f

168 blages including Atlantic mackerel, Atlantic horse mackerel, European pilchard and European anchovy f

169 -NA activity increased slightly in sardines, horse mackerels and chub mackerel during frozen/thawed s

170 ications related to Human, Arctic fox, Yakut horse, Mammoth, Polar bear, and Minke whale were chosen.

171 andinavia) at this time implies that ambling horses may have spread from Iceland and maybe also the B

172 eef meat samples spiked with only 0.5% (w/w) horse meat (levels established by the European Commissio

173 screening protocol to distinguish beef from horse meat based upon comparison of triglyceride signatu

174 s (0.50mg/0.50g, w/w; approximately 0.1%) of horse meat can be detected and quantified in minced raw

175 ents that allows to determine the content of horse meat in its mixture with beef has been proposed.

176 ng the scandal of the presence of undeclared horse meat in various processed beef products across the

177 Evidence we found indicates that the Trojan-horse mechanism really exists.

178 erium Bacillus nematocida B16 uses a "Trojan horse" mechanism to kill Caenorhabditis elegans.

179 The so-called "Trojan-horse" mechanism, in which nanoparticles are internalize

180 This 'Trojan Horse' mechanism of exotoxin delivery into predator cell

181 the first long-read sequence assembly of the horse MHC class II region with rigorous manual gene anno

182 ificial Chromosome (BAC) clones spanning the horse MHC class II region.

183 nstruct a reliable reference sequence of the horse MHC region.

184 rse (Przewalski's horse) and a male domestic horse (Mongolian horse), with about 93-fold and 91-fold

185 Some horses moved slowly but were more accurate in choosing t

186 e estimated the de novo mutation rate of the horse MSY and showed that various modern horse Y chromos

187 has been developed to detect the presence of horse myoglobin in raw meat samples.

188 tles (Paussus) are the quintessential Trojan horses of the insect world.

189 r, we show that lactose can act as a "Trojan horse" on bi-functionalized QDs to help intracellular de

190 nt of the mitochondrial DNA D-loop region of horse onto the surface of magnetic microcarriers.

191 tion seems to be able to cause infections in horses, other animals and humans, indicating that transm

192 pig parasitic nematode Ascaris suum and the horse parasite Parascaris univalens.

193 icrocin C and related antibiotics are Trojan-horse peptide-adenylates.

194 olving the representatives bat (Chiroptera), horse (Perissodactyla), cow (Cetartiodactyla), and dog (

195 vestigated fecal microbiomes of Przewalski's horse (PH; Equus ferus przewalskii), the only horses ali

196 Przewalski's horses (PHs, Equus ferus ssp. przewalskii) were discover

197 Bovine, horse, pig, chicken, and turkey muscle digests were clea

198 onsequence of long-term residency within the horse post-acute disease.

199 Horse prions produced in vitro by protein misfolding cyc

200 arrier to EqPrP(C) conversion, the resulting horse prions unexpectedly failed to cause disease upon f

201 g cyclic amplification of mouse prions using horse PrP(C) also failed to infect TgEq but retained tro

202 ed quality genomes sequences for a male wild horse (Przewalski's horse) and a male domestic horse (Mo

203 cted by treatment with anti-IgY labeled with horse radish peroxidase (Anti-IgY-HRP).

204 e arrays, the detection limits obtained from horse radish peroxidase (HRP) and bisphenol A assays wer

205 , the nanoparticles were functionalized with horse radish peroxidase (HRP) based on aminopropyl triet

206 Horse radish peroxidase (HRP) is one of the most common

207 , bovine serum albumin, primary antibody and Horse Radish Peroxidase (HRP) tagged secondary antibody

208 been utilized for covalent immobilization of horse radish peroxidase (HRP), via glutaraldehyde (Glu),

209 Here, we show that wheat germ agglutinin horse radish peroxidase (WGA-HRP) chemically conjugated

210 carried out using isoeugenol polymerised by horse radish peroxidase in aqueous solution.

211 In comparison with the natural horse radish peroxidase, WC NR exhibits excellent robust

212 solved fluorescence, Alexa-fluorophores, and horse radish peroxidase-based bead assays, enabling mult

213 ern animals and found that human, camel, and horse receptors sensitized cells to MERS-CoV infection m

214 Human, camel, and horse receptors were potent and nearly equally effective

215 ifferent concentrations through hemolysis of horse red blood cells.

216 Here, we examine historic horse remains for the DMRT3 SNP, tracking the origin of

217 mite, insect and mould allergens in dogs and horses, respectively.

218 NA from pus and blood samples from 25 and 17 horses, respectively.

219 ttlers selected for this comfortable mode of horse riding soon after arrival.

220 other primates) has now expanded to include horses, rodents, bats, colobus monkeys, cows, and, most

221 highly homologous with those on the domestic horse's chromosome 5.

222 tsonian translocation event through the wild horse's chromosomes 23 and 24, which contained sequences

223 f mammalian species, including humans, pigs, horses, seals, and mink.

224 This effect was not a Trojan horse: sensitization of cells was dependent on the forma

225 s a near-universal contaminant of commercial horse sera for cell culture.

226 ous solutions and in complex samples such as horse serum and cell culture media.

227 In a DMEM medium with 6% horse serum, the TSR was increased by 19% after a pressu

228 ally sterilized brain-heart infusion with 2% horse serum.

229 The remaining horses shifted from a faster, directionally consistent r

230 ormation at approximately 12 Ma, generating 'horse-shoe' slab geometries.

231 n other mammals, the corresponding region in horse shows extraordinary copy number variation and diff

232 nsmitted by biting midges and causes African horse sickness in equids, with mortality reaching up to

233 African horse sickness virus (AHSV) is a lethal arbovirus of equ

234 African horse sickness virus (AHSV), an orbivirus in the Reoviri

235 African horse sickness virus is transmitted by biting midges and

236 fic, and cost-effective detection method for horse, soybean, sheep, poultry, pork and cow species in

237 nimal species, supporting the existence of a horse specific genomovar.

238 ar and indicates the presence of potentially horse-specific virulence factors.

239 ctra were classified as authentic, and 16/16 horse spectra as non-authentic.

240 The H/L heterogeneity ratio of the horse spleen apoferritin (HS-ApoFt) shell was found to b

241 Here, we report NECD behavior from horse spleen ferritin, a approximately 490 kDa protein c

242 Although horse spleen holoferritin (HS-HoloFt) has been widely st

243 We observed a similar metallocluster in horse spleen L-ferritin, indicating that it represents a

244 These results indicate that horses spontaneously discriminate between photographs of

245 at-inactivated pus (24 horses) and blood (23 horses) spotted onto Whatman FTA cards.

246 Such a Trojan horse strategy can also extend activity of specific Gram

247 r-specific therapeutics can provide a Trojan-horse strategy of neutralizing CTCs to attenuate metasta

248 so interacted with the identity of the model horse, suggesting that individual differences in facial

249 Nevertheless, Yakutian horses survive all year round in the open air due to str

250 on of the "Brett character" (stable, manure, horse sweat and phenolic notes) due to 4-ethylphenols wa

251 o either Perissodactyla (the clade including horses, tapirs and rhinos, which is a member of the supe

252 y claimed, but instead crown Perissodactyla (horses, tapirs, and rhinoceroses).

253 suggested a closer relationship to caballine horses than to Asiatic asses.

254 In this study, we detected EHCV in 2 horses that developed post-transfusion hepatitis.

255 ts were obtained among blood samples from 20 horses that did not exhibit clinical signs of EZL.

256 kutian horses do not descend from the native horses that populated the region until the mid-Holocene,

257 In horses, the CXCL16 gene is located on equine chromosome

258 in themselves, but also an important Trojan horse to drive improved cancer control and care.

259 equine influenza virus was transmitted from horses to dogs in Florida and subsequently spread throug

260 through the transfer of a single virus from horses to dogs.

261 ated the transmission of H3N8 influenza from horses to dogs.

262 To model susceptibility of horses to prions, we produced transgenic (Tg) mice expre

263 cross fecal sources ranged from 1.3 +/- 0.1 (horse) to 6.3 +/- 0.4 (cattle wastewater) gene copies at

264 are apparently resistant (rabbits, dogs, and horses) to the same agent.

265 uld serve as a cell-based vector, or "Trojan Horse," to selectively deliver a protoxin to disseminate

266 trachea, although EIV was more infectious in horse trachea than CIV.

267 ood-brain barrier (BBB) by "molecular Trojan horse" transcytosis is feasible, we synthesized several

268 tally transmit EHCV to 4 young adult Arabian horses, two 1-month-old foals (1 Arabian and 1 Arabian-p

269 Here we report that horses use the head orientation of a conspecific to loca

270 ferent organs and tissues of 1 NPHV-positive horse using quantitative real-time polymerase chain reac

271 n profile of normal SDFTs from young and old horses using label-free relative quantification to ident

272 pism to explore the relevance of HCV-related horse viruses as a model for HCV infection.

273 (Electrophorus electricus) by "fishing with horses" [von Humboldt A (1807) Ann Phys 25:34-43].

274 profile of injured SDFTs from young and old horses was also assessed.

275 ncy of the ambling allele in early Icelandic horses, we believe that Norse settlers selected for this

276 27 domesticated, and three wild Przewalski's horses, we find that contemporary Yakutian horses do not

277 ng equine behaviour and cognition can inform horse welfare and management.

278 rhinitis/asthma sensitised to dog, cat, and horse were recruited.

279 (th) century) strongly suggests that ambling horses were brought from the British Isles to Iceland by

280 Following establishment of infection, the horses were euthanized and the endometrial surfaces were

281 Horses were i.v. injected with NPHV containing plasma.

282 Horses were more likely to approach photographic stimuli

283 Importantly, after a primary NPHV infection, horses were protected against rechallenge with the homol

284 We found that approximately 31.4% of 433 horses were seropositive for antibodies (Abs) against NP

285 Plasma and serum from these horses were used to experimentally transmit EHCV to 4 yo

286 e community of bacteria compared to domestic horses, which is likely partly explained by different pl

287 ask may reflect distinct cognitive styles in horses, which vary among individuals, and could be linke

288 to attack by pressing themselves against the horses while discharging.

289 PHV infection could be cleared in individual horses with a simultaneous emergence of nonstructural (N

290 ir ability to incapacitate fish, humans, and horses with hundreds of volts of electricity.

291 re taken, along with blood from a further 20 horses with no cutaneous EZL lesions.

292 Twenty-nine horses with signs of EZL from different climatic regions

293 Among the 29 horses with suspected cases of EZL, H. capsulatum var. f

294 Therefore, horses with the ability to perform comfortable gaits (e.

295 cute and chronic stages of NPHV infection in horses with viral RNA detectable predominantly within th

296 horse) and a male domestic horse (Mongolian horse), with about 93-fold and 91-fold coverage, respect

297 High seropositivity is found in horses worldwide with approximately 3% viremic.

298 t frequently diagnosed infectious disease of horses worldwide, is caused by Streptococcus equi.

299 the horse MSY and showed that various modern horse Y chromosome lineages split much later than the do

300 Twenty-four Quarter Horse yearlings were randomly assigned to either submaxi