ライフサイエンスコーパス: sheep

1 pecies (Zebrafish, Fly, C. elegans, Rat, and Sheep).

2 w and oxygen consumption rates in IUGR fetal sheep.

3 uptake was significantly lower in IUGR fetal sheep.

4 (but not 25(OH)D2) concentrations than dark sheep.

5 sativa ssp. falcata subjected to grazing by sheep.

6 is sufficient to cause scrapie in recipient sheep.

7 the known cortical degeneration in CLN5(-/-) sheep.

8 nel activity in uterine arteries of pregnant sheep.

9 in NREM sleep delta power seen in unaffected sheep.

10 lar adaptations in chronically anaemic fetal sheep.

11 decline with age in mice, rats, horses, and sheep.

12 onic hypoxia that are different from lowland sheep.

13 ied as fat-tail, thin-tail and fat-rump hair sheep.

14 Sleep homeostasis has not been studied in sheep.

15 term health effects in a cohort of 13 cloned sheep.

16 acavirus that is carried asymptomatically by sheep.

17 , as has been shown for classical scrapie in sheep.

18 encephalographies of Batten disease affected sheep.

19 oencephalography study has been performed in sheep.

20 oxide (NO) and vascular dysfunction in uni-x sheep.

21 colon, a rat esophagus, and small airways in sheep.

22 conceived sheep, and our healthy aged cloned sheep.

23 Scrapie is a prion (PrP(Sc)) disease of sheep.

24 rom presymptomatic HD transgenic and control sheep.

25 ased significantly in HD compared to control sheep.

26 ies and parasite-specific IgG in female Soay sheep.

27 ) signaling in osteocytes was not studied in sheep.

28 i-MAP antibody responses in paratuberculosis sheep.

29 ne strains, albeit at a lesser level than in sheep.

30 fy fragments (horse; 85 bp, soybean; 100 bp, sheep; 119 bp, poultry; 183 bp, pork; 212 bp and cow; 27

31 for 30 min in chronically catheterized fetal sheep (125 +/- 3 days), with or without ketamine (3 mg k

32 -6.23mg GAE/L), cow (49.00+/-10.77mg GAE/L), sheep (167.6+/-58.77mg GAE/L) and human milk (82.45+/-12

33 conception effects on offspring LTL in Soay sheep, a primitive breed experiencing strong sperm compe

34 nsistent with the recent expansion of clone "sheep abortion." These results identify a key virulence

35 Uterine arteries of pregnant sheep acclimatized to long-term high-altitude hypoxia we

36 Immune signatures of sheep acutely-infected with Fasciola hepatica, an import

37 or rapid identification of DNA of cow, goat, sheep and buffalo in dairy products, and for quantificat

38 tions of three or six different serotypes in sheep and cattle, the two natural hosts of BTV.

39 ssed in mammalian cells was used to immunize sheep and elicited a robust immune response and produced

40 ttle, horse, and camel) and small livestock (sheep and goat).

41 Since RPV vaccine protects sheep and goats from PPRV, it is important to determine

42 ants (PPR) is a highly infectious disease of sheep and goats that is caused by PPR virus, a member of

43 um and liver tissue of 5 year old transgenic sheep and matched controls by gas chromatography-mass sp

44 ay contribute to early abnormalities seen in sheep and patients and warrant further study.

45 Plasma separated from deer, sheep and pig blood, obtained from abattoirs, was hydrol

46 ng dryland stress adaptation in the fat-tail sheep and showcase the indigenous stocks as appropriate

47 ong virus neutralizing antibody responses in sheep and was DIVA (differentiating naturally infected f

48 r fetus is a venereal pathogen of cattle and sheep, and an opportunistic human pathogen.

49 rom various species, including cow, buffalo, sheep, and goat.

50 Ruminants, such as cows, sheep, and goats, predominantly ferment in their rumen p

51 irus (IDV), was identified in swine, cattle, sheep, and goats.

52 ilar to that observed in naturally conceived sheep, and our healthy aged cloned sheep.

53 lth parameters to groups of 5-and 6-year-old sheep, and published reference ranges.

54 w that electroencephalography can be used in sheep, and that longitudinal recordings spanning many mo

55 near-term ( approximately 142 days) pregnant sheep, and were treated ex vivo with 21.0 or 10.5% O2 fo

56 ing tyrosine residues, Tyr-23 and Tyr-149 in sheep AQP0, to the corresponding residues in the high-pe

57 Our HD OVT73 sheep are a prodromal model and exhibit minimal patholog

58 African indigenous sheep are classified as fat-tail, thin-tail and fat-rump

59 Sheep are potential hosts for growing human organs throu

60 Goats and sheep are versatile domesticates that have been integrat

61 the basis for the production of gene-edited sheep as a host for interspecies organ generation.

62 he earliest events in myelopoiesis using the sheep as a model.

63 at can identify 80% of the presymptomatic HD sheep as transgenic, with 90% confidence.

64 ferred complete protection in all vaccinated sheep, as evidenced by prevention of viremia, fever and

65 rpesvirus 2 (OvHV-2), the causative agent of sheep associated-malignant catarrhal fever, which is one

66 oorly adapted animals with OvHV-2 results in sheep-associated malignant catarrhal fever, a fatal dise

67 the novel strains, while rplM was unique to sheep-associated strains.

68 Abs and systemically infused mAbs into fetal sheep at 126 days of gestation after exposure to brain i

69 and eight low-altitude (LA; 520 m) pregnant sheep at approximately 90% gestation.

70 ed against ISG15s from humans, mice, shrews, sheep, bats, and camels, which are mammalian species kno

71 pancreatic islets isolated from intact fetal sheep, beta cell proliferation in vitro was reduced by T

72 tivity and complement-dependent cytolysis of sheep blood erythrocytes.

73 solation and/or subcultures than they did on sheep blood or chocolate agar.

74 d by contaminated laboratory media made from sheep blood.

75 impaired for survival in guinea pig sera and sheep blood.

76 Injection of Ae1a into sheep blowflies (Lucilia cuprina) induced rapid but reve

77 screwworm fly and 2.3 Ma for the Australian sheep blowfly.

78 alyzed the DCX-expressing cells in the whole sheep brain of both sexes to search for an indicator of

79 s; 3) delineated 25 external and 28 internal sheep brain structures by segmenting both templates and

80 with previously computed T1W and T2W in vivo sheep brain templates and nlTPMs, provide a complete set

81 high-resolution 3D atlas of average in vivo sheep brains linked to a reference stereotaxic space.

82 ion average images (or templates) of in vivo sheep brains.

83 The two sheep breeds native to the Canary Islands display distin

84 Comparative analyses with 40 other sheep breeds showed that haplotypes associated with reco

85 l centuries has generated a number of native sheep breeds, which are presumably adapted to the divers

86 ith data from 330 individuals of 16 domestic sheep breeds.

87 ogression between resident mouflon and local sheep breeds.

88 art rate and plasma renin activity in intact sheep, but these responses were significantly attenuated

89 tisol concentrations were raised in pregnant sheep by infusion, proportionately more of the glucose t

90 plays a role in determining the body mass of sheep by Methylated DNA immunoprecipitation - sequencing

91 re the creation of pancreatogenesis-disabled sheep by oocyte microinjection of CRISPR/Cas9 targeting

92 ected in asymptomatic scrapie-infected donor sheep can transmit the disease.

93 Further, we infer that Soay and Sarda sheep carry introgressed mouflon alleles involved in bit

94 tica, common liver fluke, infects cattle and sheep causing disease and production losses costing appr

95 of CF, we have investigated the function of sheep CFTR.

96 lpha-lactalbumin and beta-lactoglobulin from sheep cheese sweet whey, an under-utilized by-product of

97 tionated in reasonable yield and purity from sheep cheese whey in one streamlined process.

98 report detailing the health status of cloned sheep concluded that the animals had aged normally.

99 enetic diversity in mouflon than in domestic sheep, consistent with past bottlenecks in mouflon.

100 We found immature-like neurons in the whole sheep cortex and in large populations of DCX-expressing

101 egg production than the susceptible Canaria Sheep (CS).

102 cheese manufacture generated by an emerging sheep dairy industry in New Zealand.

103 Our analyses of St Kilda Soay sheep data thus concurs with our cross-study review that

104 red contact networks to test whether bighorn sheep demographic states vary systematically in infectio

105 with age-matched controls, chronically obese sheep demonstrated greater total body fat (p < 0.001); L

106 ontrast, nonaborting experimentally infected sheep developed mainly antibodies to surface antigens (M

107 Importantly, CLN5(-/-) sheep did not show the increase in NREM sleep delta powe

108 ies in the mountain pasture prevailed in the sheep diet of the commercial flock.

109 rrhagic fever virus, Erve virus, and Nairobi sheep disease virus were tested against ISG15s from huma

110 s after 8 months using 31 female merino land sheep divided into four groups: control, ovariectomy, ov

111 or double-muscled (DM) phenotype in cattle, sheep, dog and human.

112 virus in interferon (IFN)-competent primary sheep endothelial cells and immortalized cell lines.

113 antagonize the protective function of FH in sheep erythrocyte hemolytic assays and increase cell-sur

114 ay, we showed that the hybrid protein causes sheep erythrocyte lysis.

115 1119G-CFH had virtually no CA on (self-like) sheep erythrocytes (ES) but retained DAA.

116 We have shown that aborting sheep exhibited a strong antibody response to surface (M

117 In pregnant sheep, experimental models with a small, defective place

118 nt density in uterine arteries from pregnant sheep exposed to high-altitude hypoxia (3801 m, PaO2: 60

119 hypoxia both ex vivo and in vivo in pregnant sheep exposed to long-term high-altitude hypoxia.

120 l tissue from a cohort of 5-y-old OVT73-line sheep expressing a human CAG-expansion HTT cDNA transgen

121 reas within the Welsh agricultural sector is sheep farming, contributing around pound230 million to t

122 Two dairies, a beef cattle feedlot, and a sheep feedlot were chosen for repeated diurnal and seaso

123 eration and mass observed in the hypothyroid sheep fetus and may have consequences for pancreatic fun

124 Hypothyroidism in the sheep fetus resulted in an asymmetric pattern of organ g

125 inding has been replicated in normally grown sheep fetuses following a 7-day noradrenaline (norepinep

126 cell proliferation and mass were examined in sheep fetuses following removal of the thyroid gland in

127 s those of milk and cheese from a commercial sheep flock managed under extensive mountain grazing in

128 CODD lesions (n = 58) and healthy sheep foot tissues (n = 56) were analyzed by PCR for the

129 c hypoxic chambers able to maintain pregnant sheep for prolonged periods of gestation under controlle

130 monstrate neural recordings in freely moving sheep for up to 190 d.

131 ndividuals from five populations of fat-tail sheep from a desert environment in Egypt.

132 ough understanding of body size variation in sheep from an epigenetic perspective.

133 57 isolates from host reservoirs (cattle and sheep) from Scotland and to compare genetic variation of

134 Why do distantly related mammals like sheep, giant pandas, and fur seals produce bleats that a

135 Sheep given E. coli developed septic shock, oliguria, in

136 ceptible natural target species of the virus-sheep, goats and cattle.

137 Cattle, sheep, goats, and camels are particularly susceptible to

138 Southwest Asia in the eighth millennium BC, sheep, goats, pigs and cattle have been remarkably succe

139 ndance and trophic level during manipulative sheep grazing are not well understood.

140 and trophic level in response to continuous sheep grazing in steppe grasslands.

141 Insect abundance decreased as sheep grazing intensities increased, with a significant

142 gs highlight the importance of more flexible sheep grazing management and will be useful for developi

143 te that continuous years of heavy- and over- sheep grazing should be eliminated.

144 Poor vegetation conditions caused by heavy sheep grazing were detrimental to the existence of Acrid

145 ididae and Cicadellidae, were susceptible to sheep grazing, but Formicidae was tolerant.

146 y influenced by age, and that light coloured sheep had higher 25(OH)D3 (but not 25(OH)D2) concentrati

147 Over the last decade, TSE in sheep has emerged as a relevant model for assessing the

148 sted the hypothesis that high-altitude fetal sheep have evolved cardiovascular compensatory mechanism

149 Sheep have large brains with human-like anatomy, making

150 orphism in a sample of PrP(Sc) isolated from sheep heterozygous for their PrP(C) proteins.

151 used bluetongue virus (BTV) and its natural sheep host to reveal a previously uncharacterized mechan

152 Mouflon x sheep hybrids are larger-bodied than mouflon, potentiall

153 In uterine arteries of pregnant sheep, hypoxia significantly inhibited BKCa channel curr

154 eographically distinct genepools of fat-tail sheep in Africa that differ from the European genepool,

155 r amino acids decreased in presymptomatic HD sheep, including branched chain amino acids (isoleucine,

156 asurements in 13 aged (7-9 years old) cloned sheep, including four derived from the cell line that ga

157 Hypothyroidism in fetal sheep induced by removal of the thyroid gland caused asy

158 natal exposure to excess testosterone (T) in sheep induces adverse reproductive and metabolic program

159 4 different breeds representative of the UK sheep industry were studied: Welsh Mountain, Scottish Bl

160 mean, we find extensive spread with 203,000 sheep infected given virus introduction to the south of

161 Brains from adult and newborn sheep (injected with BrdU and analyzed at different surv

162 that growth retardation in hypothyroid fetal sheep is associated with reductions in pancreatic beta c

163 The coat colour polymorphism in Soay sheep is controlled by a single locus, suggesting vitami

164 In isolated fetal sheep islets studied in vitro, thyroid hormones inhibite

165 sites (SBI typing) revealed that cattle and sheep isolates had statistically indistinguishable raref

166 occur after fetal uninephrectomy (uni-x) in sheep, leading to a 30% nephron deficit.

167 ned through imaging of tissue taken from the sheep left ventricle using serial block face scanning el

168 mited by external constraint in 5 additional sheep (left ventricular constraint).

169 METHOD AND In 7 sheep, left ventricular endocardial and transmural mappi

170 To test the hypothesis that sheep live weight (LW) could be used to improve enteric

171 rce of periostin and VCAM-1 was the inflamed sheep liver tissue.

172 In vehicle-treated sheep, mean arterial pressure progressively declined fro

173 In 5-year-old female uni-x and sham sheep, mean arterial pressure, glomerular filtration rat

174 ve quantification of buffalo meat mixed with sheep meat was done by quantitative label-free mass spec

175 ffalo meat spiked at a minimum 0.5% level in sheep meat with high confidence.

176 t mixes containing cattle, water buffalo and sheep meat.

177 0s and 1990s showed that while some species (sheep, mice, and cats) are readily susceptible to TSEs,

178 e validated this hypothesis in primary fetal sheep microglia cultures re-exposed to LPS in presence o

179 and Th17 cells draining the inflamed skin of sheep migrated toward the CCR7 ligand CCL21, suggesting

180 mit were 1.43 and 4.77mg/ml respectively for sheep milk and, 2.25 and 7.5mg/ml respectively for goat

181 ice cream (10% w/w sheep milk cream; 10% w/w sheep milk cream, L. casei 01, 6logCFU/mL; 10% w/w inuli

182 , probiotic and synbiotic ice cream (10% w/w sheep milk cream; 10% w/w sheep milk cream, L. casei 01,

183 actobacillus casei 01 and inulin addition on sheep milk ice cream during storage (-18 degrees C, 150d

184 of salted or unsalted Jameed from fermented sheep milk product.

185 and preconcentration of SPI from aqueous and sheep milk samples, and an off-line MISPE method followe

186 atment for selective determination of SPI in sheep milk samples.

187 mpositions of the MFGM from bovine, goat and sheep milks.

188 Osteoporosis induction in a sheep model by steroid administration combined with ovar

189 Towards the development of a sheep model of CF, we have investigated the function of

190 port in these mice, and mucus transport in a sheep model of CF.

191 in the beta-ENaC mouse model as well as the sheep model of CF.

192 ative study of metabolites in our transgenic sheep model of HD (OVT73).

193 ences indicate a metabolic disruption in the sheep model of HD and could provide insight into the pre

194 The current study reproduced the sheep model of osteoporosis to study the RANKL/OPG ratio

195 We used a preterm fetal sheep model that reproduces key features of brain injury

196 We used a preterm fetal sheep model using both sexes that reproduces the spectru

197 The sheep model was first used in the fields of animal repro

198 All of these observations in sheep models with placental insufficiency are consistent

199 Sheep monocytes were divided into three populations, sim

200 ased and included woolly rhinoceros and wild sheep (mouflon), characteristic of a steppe environment.

201 In the current efficacy study, a group of sheep (n = 5) was vaccinated subcutaneously with the gly

202 urrent assemblies of the dog, CF 3.1 and the sheep, OA 3.1, genomes contain 264 and 598 FLIs, respect

203 In 5 fetal sheep of 109 to 111 days of gestation (term, 147 days),

204 With their large brains and long lives, sheep offer significant advantages for translational stu

205 s) collected from an unmanaged population of sheep on St Kilda, where individual age and parentage ar

206 so shows sleep homeostatic EEG correlates in sheep, opening up new opportunities for studying sleep i

207 eedles, to detection of BTV in the recipient sheep or cattle, was substantially longer than has previ

208 n in growth in human serum, human plasma, or sheep or horse blood.

209 early stage CLN5(-/-) (homozygous, affected) sheep over 3 consecutive days, the second day being the

210 In contrast, overexpression of Cdk5 in sheep (Ovis aries) only produces brown patches on a whit

211 SNP information in a wild population of Soay sheep (Ovis aries) to investigate the genetic architectu

212 rse (Equus caballus), soybean (Glycine max), sheep (Ovis aries), poultry (Meleagris meleagris), pork

213 n and attrition in a precocial large mammal, sheep (Ovis aries).

214 mary causative agent of pneumonia in bighorn sheep (Ovis canadensis), in a small number of older indi

215 contributing to regional declines in Dall's sheep (Ovis dalli), a poorly dispersing alpine specialis

216 nsion and improved renal function in CKD-RDN sheep (p < 0.0001 for 2 and 5 months vs. pre-RDN).

217 ximately 1.5-fold in renal arteries of uni-x sheep (P<0.05).

218 cell fractions (RBCFs) separated from deer, sheep, pig, and cattle abattoir-sourced blood.

219 urrents (Isc) in tracheal mucosa from human, sheep, pig, ferret, and rabbit and in two types of cultu

220 enal blood flow were decreased less in uni-x sheep (PInteraction<0.01).

221 pneumoniae, an agent responsible for bighorn sheep pneumonia.

222 acticing open defecation within 50 m and the sheep population for Cryptosporidium, and with the villa

223 ne traits in the individually monitored Soay sheep population of St Kilda, using genomic inbreeding c

224 24 years of data collected from a wild Soay sheep population to quantify how an important environmen

225 bidirectional and affected most mouflon and sheep populations, being strongest in one Sardinian mouf

226 fective detection method for horse, soybean, sheep, poultry, pork and cow species in foodstuffs.

227 ince used the chronically instrumented fetal sheep preparation to investigate the fetal compensatory

228 at S-type strains, which are more adapted in sheep, produce a unique lipid.

229 Due to its significant impact on sheep production and welfare, the recent increase in dia

230 nous androgenic steroids applied to pregnant sheep programmes a PCOS-like phenotype in female offspri

231 ymorphisms at positions 136, 154, and 171 of sheep PrP(C) or PrP(Sc).

232 We characterized sleep in sheep, quantifying characteristic vigilance states and n

233 In hypertensive CKD sheep, RDN reduced blood pressure and improved basal ren

234 Two hours following induction of sepsis, 32 sheep received a 24-hour IV infusion of 1) placebo + pla

235 Sheep received a prime-boost vaccination regime comprisi

236 Pregnant sheep received intra-amniotic injections with 10(7) colo

237 Other sheep received only the ring devices without intramuscul

238 Chymotrypsin was used to digest sheep recombinant PrP to identify a set of characteristi

239 Sheep red blood cells (SRBCs) have long been used as a m

240 ptive introgression from mouflon to domestic sheep related to immunity mechanisms, but not in the opp

241 origin of these cells in the whole brain of sheep, relatively large-brained, long-living mammals.

242 Thirty-two sheep rendered septic with IV Escherichia coli and recei

243 s; second, highlighting the relevance of the sheep reservoir when considering farm based intervention

244 Genetic markers for sheep resistance to gastrointestinal parasites have long

245 The native envelope gene (env) of Jaagsiekte sheep retrovirus (JSRV) also acts as an oncogene.

246 The envelope protein (Env) of Jaagsiekte sheep retrovirus (JSRV) is an oncogene, but its mechanis

247 oBST2A impedes viral exit of the Jaagsiekte sheep retroviruses (JSRV), most probably by retaining vi

248 rican and western Asia fat-tail and European sheep, reveal at least two phylogeographically distinct

249 occupational exposure to C abortus-infected sheep revealed only sporadic immune responses to the ant

250 (156 readings) with MHA supplemented with 5% sheep's blood (BMHA), using mecA PCR as the reference st

251 vivo investigation of acoustical response of sheep's middle-ear ossicles.

252 erning solid matrices, cheeses produced from sheep's milk and animal feeds resulted the most contamin

253 re made using non-standard heat treatment of sheep's milk at 60 degrees C/5min.

254 possible to produce classical and probiotic sheep's milk yogurt by using a non-standard temperature

255 orphisms at positions 136, 154, and 171 of a sheep's normal cellular prion protein (PrP(C)).

256 The incubation period of sheep scrapie is strongly influenced by polymorphisms at

257 Previous experiments carried out in a sheep scrapie model demonstrated that the transfusion of

258 hat gave rise to Dolly, yet none of our aged sheep showed clinical signs of OA, and they had radiogra

259 CLN5(-/-) sheep showed comparable increases in time spent in NREM

260 In unaffected sheep, sleep deprivation led to increased EEG delta (0.5

261 was obtained from deceased humans, cows, and sheep supported with a continuous-flow LVAD (n=9 LVAD, n

262 of the jejunum of human patients, cows, and sheep supported with a continuous-flow LVAD.

263 MI created by coronary ligation in another 6 sheep (tethered plus MI), and left ventricular remodelin

264 ovine 50K SNP BeadChips from Barki goats and sheep that are indigenous to a hot arid environment in E

265 Heterozygous scrapie-infected sheep that produce two PrP variants associated with oppo

266 in D (25(OH)D) concentrations in female Soay sheep that were part of a long-term field study on St Ki

267 ural protein NS4 favors viral replication in sheep, the animal species most affected by bluetongue.

268 tor for BTV by favoring viral replication in sheep, the animal species most susceptible to bluetongue

269 In sheep, the BST2 gene is duplicated into two paralogs ter

270 ural conditions.IMPORTANCE In goats, like in sheep, there are PRNP polymorphisms that are associated

271 However, in contrast to the polymorphisms in sheep, they are more numerous in goats and may be restri

272 establish correlates of sleep homeostasis in sheep through a sleep deprivation experiment.

273 xamples of host species ranging from mice to sheep to humans, and parasites ranging from viruses to w

274 tissues were obtained from 2-year-old female sheep treated prenatally with T or oil (control) from da

275 In this study, using a sheep TSE model, we characterized the ability of differe

276 as sleep homeostasis is present in CLN5(-/-) sheep, underlying CLN5(-/-) disease processes prevent it

277 Thirteen sheep underwent baseline cardiac magnetic resonance imag

278 All sheep underwent electrophysiological and electroanatomic

279 Sheep underwent RDN (control-RDN, n = 8; CKD-RDN, n = 7)

280 These results show that the adult sheep, unlike rodents, is largely endowed with non-newly

281 Groups of sheep vaccinated with a cocktail of six different vaccin

282 We have created Csf1r-EGFP transgenic sheep via lentiviral transgenesis of a construct contain

283 or ARH/ARQ) scrapie-infected Rasa Aragonesa sheep was analyzed using this MRM method.

284 ain of heterozygous ARR/VRQ scrapie-infected sheep was compared with that of BSE-infected sheep with

285 ncus was measured while a cadaver and living sheep was exposed to the sinusoidal acoustical excitatio

286 quality methylation map of Chinese Mongolian sheep was obtained in this study.

287 y, despite BT having most clinical impact in sheep, we show that vaccination can have the greatest im

288 l myocytes from young and old Welsh Mountain sheep, we show the free Ca(2+) transient amplitude and r

289 Using data from experimentally raised sheep, we suggest that this (26)Mg enrichment up the tro

290 ontrol (CON) (n = 8) and IUGR (n = 13) fetal sheep were catheterized with aortic and femoral catheter

291 Six sham-operated sheep were control subjects.

292 Fifteen sheep were instrumented with a renal artery flow probe a

293 After the injury, sheep were randomized into two groups: 1) epinephrine, n

294 onary bypass, the papillary muscle tips in 6 sheep were retracted apically to replicate tethering, sh

295 Sheep were surgically instrumented with pulmonary and re

296 Sheep were treated with clonidine (1 mug/kg/hr) or salin

297 reatest impact on reducing BTv infections in sheep when administered to cattle, which has implication

298 sheep was compared with that of BSE-infected sheep with a similar genotype.

299 on, and the reflex response to hemorrhage in sheep with normotension (control) or with hypertensive c

300 ining beef, chicken, camel, rabbit, goat and sheep with varying percentage of pork (0%, 1%, 5%, 10%,