ライフサイエンスコーパス: pig

1 P663L) and without the substitution (control pigs).

2 nimal model for JUNV infection is the guinea pig.

3 er next-day recovery in PEG-20k resuscitated pigs.

4 tigations on the reproductive performance of pigs.

5 to predict farrowing outcomes in commercial pigs.

6 signal of the tracer in the pancreas of mini pigs.

7 gut microbiome is not yet well understood in pigs.

8 ficiently blocks FXIIa in mice, rabbits, and pigs.

9 her in the Montanera pigs than in the Pienso pigs.

10 Zealand White rabbits and 14 Hartley guinea pigs.

11 (p < 0.01) birth weights than high responder pigs.

12 apical membranes, like tissues from control pigs.

13 shown to infect and cause virus shedding in pigs.

14 a controlled feeding experiment with guinea pigs.

15 iates these intercollicular nuclei in guinea pigs.

16 ds disrupted mucociliary transport in EDA-KO pigs.

17 r potentials to be transmitted from birds to pigs.

18 with boar taint, an off-odour in entire male pigs.

19 enced the physiological responses in nursery pigs.

20 signal was detected in the pancreas of mini pigs.

21 thin all cellular zones in growing miniature pigs.

22 s such as SNU (100%) and NIH (76%) miniature pigs.

23 UFA in the Montanera pigs than in the Pienso pigs.

24 pectively dampen HRV in hypercholesterolemic pigs.

25 d often lethal hemorrhagic fever in domestic pigs.

26 ot influenced by increasing removals of wild pigs.

27 h was normalized in metformin-treated guinea pigs.

28 fic HF183/BFDrev and CPQ_056, swine-specific Pig-2-Bac, and cattle-specific Bac3qPCR assays.

29 10 baboons, 12 rhesus monkeys, 20 Yorkshire pigs, 20 Sprague-Dawley rats, 10 New Zealand White rabbi

30 Seven anesthetized pigs 28.7 kg (SD, 2.1 kg).

31 res including poultry (3% vs 28%; P = .003), pig (4% vs 25%; P = .04), feed grain (13% vs 34%; P = .0

32 Nine studies were performed in 6 pigs; 5 studies were done in the native state and 4 afte

33 ts to remove wild pigs averaged $50 per wild pig (6.8 effort hours per wild pig) for removing the fir

34 electivity over the human functional homolog PIG-A.

35 and composition in biceps femoris of Iberian pigs according to the rearing system (Montanera vs Piens

36 measuring pig DC responses, and potentially pig affect and welfare, under field conditions.

37 cesarean-derived, colostrum-deprived (CDCD) pigs allocated to the following 5 inoculation groups of

38 stage-specific regulation, and revealed that pig and human islet cells share characteristic features

39 ern Cook Islands (SCIs) register evidence of pig and/or human occupation on a virgin landscape at thi

40 recently reported using genetically modified pigs and a clinically applicable drug treatment regimen.

41 timulate efficient glucose disposal in rats, pigs and dogs during constant intravenous infusion and e

42 The assay was specific to cattle, pigs and fish, having been tested against 14 non-target

43 opharyngeal and oesophageal tumours in mice, pigs and fresh human biospecimens when delivered topical

44 In adult pigs and goats, SSCT with allogeneic donor stem cells le

45 fied in the comparison between heat-tolerant pigs and heat-susceptible pigs under heat stress.

46 ompatibilities between the immune systems of pigs and humans as well as by the risk of transmitting p

47 e and improve host intestinal health in both pigs and humans exposed to Trichuris.

48 the Nipah virus (NiV) outbreak in Malaysia, pigs and humans were infected.

49 s but decreased across development in guinea pigs and members of the Mus genus, animals that navigate

50 echanisms related to heat stress response in pigs and provide potential biomarkers for future investi

51 e that is currently spreading among domestic pigs and wild boar (Sus scrofa) in large areas of Eurasi

52 petition binding assays at the human, guinea pig, and mouse H(2) receptors (co-)expressed in HEK293(T

53 To date, mouse, hamster, ferret, guinea pig, and non-human primates have been investigated.

54 , including nonhuman primates, bats, horses, pigs, and rodents, but are not associated with disease.

55 It is unknown whether anti-TKO pig antibodies are present in IVIg.

56 Anti-pig antibodies in IVIg could be harmful in clinical xeno

57 Pigs appear uniquely susceptible to both avian and human

58 Pigs are less able to resist and/or eliminate secondary

59 says, we show that cells from the engineered pigs are resistant to human humoral rejection, cell-medi

60 Next, to investigate the guinea pig as a model for evaluating vaccine efficacy during pr

61 ific to the genome of Sus scrofa domesticus (pig) as a target and incorporated internal controls.

62 mice and by house dust mite (HDM) in guinea pigs, as well as investigating the action of IRL201104 o

63 w oxygen levels has not been demonstrated in pig ASCs.

64 Finally, the costs to remove wild pigs averaged $50 per wild pig (6.8 effort hours per wil

65 her species used in research-including rats, pigs, bears, and marmosets-as well as in humans, providi

66 (FoI, the average rate at which susceptible pigs become infected) across geographical settings will

67 Changes in pig behaviours are a useful aid in detecting early signs

68 commercial settings, automatic detection of pig behaviours through visual imaging remains a challeng

69 In AcGGM-fed pigs, both target populations differentially express AcG

70 hts into the phylogeny of Chinese indigenous pig breeds and benefit gene mining efforts to improve ma

71 ibution of SLA-1 alleles among the different pig breeds, including the breed specific alleles.

72 syltransferase gene-knockout (GTKO), and TKO pigs by flow cytometry.

73 wed those of dogs, sheep, goats, cattle, and pigs by ~2,500-10,000 years.

74 for the discrimination of individual Iberian pig carcasses into the four official quality categories

75 initial introduction of domesticated guinea pigs (Cavia porcellus) beyond South America into the Car

76 ence of naturally-existing antibodies to TKO pig cells in OWMs complicates the transplantation of TKO

77 s have minimal or no natural antibody to TKO pig cells.

78 In pigs challenged by gavage with HEWP, clinical signs were

79 he nasal cavity of inoculated pigs, with all pigs clearing HS069Deltacap by 5 days postchallenge.

80 We measured SFOAEs while perfusing guinea pig cochleas from apex to base with salicylate or KCl so

81 Increased removals of wild pigs coincided with periods of cold weather.

82 -regulated) were identified in heat-tolerant pigs compared to themselves during the thermoneutral per

83 Finally, Mtb-infected guinea pigs cough in a manner dependent on SL-1 synthesis.

84 s human nociceptive neurons and makes guinea pigs cough.

85 and largely irreversible, whereas, in guinea pigs, counts of immunostained synaptic puncta can recove

86 Examples of pig CoVs include porcine epidemic diarrhea virus (PEDV),

87 In 2011, a state-wide wild pig damage management program involving federal, state,

88 hus offers a practical approach to measuring pig DC responses, and potentially pig affect and welfare

89 hts are summarized here that informed recent pig design and therapeutic choices, which together appea

90 All pigs developed acute forms of acute swine fever (ASF).

91 RESTV-infected pigs developed severe cyanosis, tachypnea, and acute int

92 uscle of 51 Apulo-Calabrese and 52 crossbred pigs differing in growth performances.

93 to the following 5 inoculation groups of 10 pigs each: (i) negative control, (ii) Mycoplasma floccul

94 ETV2-null pig embryos lacked hematoendothelial lineages and were e

95 All pigs except for 1 (DCD-SCS-group) survived 4 days.

96 The engineered pigs exhibit normal physiology, fertility and germline t

97 Female wild pigs exhibited a constant rate of depredation regardless

98 The proximal colon of T. suis-infected pigs exhibited general inflammation around day 21 after

99 eeks postinoculation, 75% of pregnant guinea pigs experienced stillbirths or spontaneous abortions mi

100 POON was developed and tested in nonsurvival pig experiments.

101 known that pig offspring born from pregnant pigs exposed to elevated ambient temperatures during ges

102 Consequently, EDA-KO pigs failed to eradicate a bacterial challenge in lung r

103 tides onto coronary stents implanted in farm pigs favors their peaceful integration within the corona

104 The pigs fed with low or standard protein diets had differen

105 Relative to CON, pigs fed with LP had lower feed intake (FI) and body wei

106 n undesirable characteristic for poultry and pig feeding and represents a challenge for breeding prog

107 When the pig feeding regime was disrupted, we automatically detec

108 ing a broad range of hosts including humans, pigs, ferrets, dogs, cats, hamsters, and at least 2 gene

109 1) pandemic 2009 (pdm09) viruses detected in pigs following numerous reverse zoonosis events since th

110 The extensive genome engineering of pigs for greater compatibility with the human immune sys

111 intestinal mucus collected from fully-grown pigs for studying colloidal transport of sub-micron size

112 $50 per wild pig (6.8 effort hours per wild pig) for removing the first 99% of the animals.

113 Estimating pig force-of-infection (FoI, the average rate at which s

114 demanding conditions, e.g., occlusion of one pig from another.

115 pared with 23 free-ranging wild boars and 22 pigs from different breeds, taking into account sex, mas

116 omplete mitogenomes of archaeological guinea pigs from sites in Peru, Bolivia, Colombia, the Caribbea

117 s directed a concerted effort to remove wild pigs from the county until the last wild pig (of 376 tot

118 MS-based method has been developed to detect pig gelatin and egg white in experimental five-year aged

119 While pigs generally developed severe respiratory disease due

120 i.m.-immunized pigs generated a high titer of neutralizing Abs but poor

121 Here we show that male mice, pigs, goats, and cattle harboring knockout alleles of th

122 Heat stress adversely affects pig growth and reproduction performance by reducing feed

123 t a collection of cultured bacteria from the pig gut, including 110 species across 40 families and ni

124 A mixed model indicated that Apulo-Calabrese pigs had higher a* (P-value < 0.0001), chroma (P-value <

125 Fetuses from ET pigs had reduced (P = 0.032) M. longissimus fibre number

126 and the cellular/molecular integrity of mini pig hard tissues, then demonstrated that the results of

127 Until today, the virulence of RESTV for pigs has remained elusive, with unclear pathogenicity in

128 Consistent survival of life-supporting pig heart xenograft recipients beyond 90 days was recent

129 IVIg commercial preparations contained anti-pig IgG that bound to WT and GTKO pRBCs, but not to TKO

130 We measured anti-pig IgM/IgG binding, and complement-dependent cytotoxici

131 ere significant increases in both baboon and pig IL-6 in the baboon serum, especially in baboons that

132 In prime:boost guinea pig immunizations, when formulated with the MF59-like ad

133 d during prechallenge and after challenge of pigs immunized with the naturally attenuated isolate OUR

134 press nine human transgenes that enhance the pigs' immunological compatibility and blood-coagulation

135 ssociated with a fall in HRV in Ossabaw mini-pigs, implying aggravated autonomic imbalance.

136 ic NWAs, enhancing viral infection in guinea pigs.IMPORTANCE JUNV is one of five known NWAs that caus

137 A01354299/2017 [sw/OH/2017]) isolated from a pig in the agricultural fair outbreak to replicate in fe

138 Its 2008 emergence in pigs in the Philippines raised concerns about food safet

139 with HEWP, clinical signs were noted in 5/6 pigs including diarrhoea, emesis, and skin rash.

140 50)) produced a clinical disease in domestic pigs indistinguishable from that induced by the same dos

141 f piglets without anaesthesia/analgesia, the pig industry is searching for a mode of action for the v

142 med an in vivo study of transmission between pigs infected with an H3.2010.1 H3N2 IAV and aerosol con

143 ed therapeutic protection in mice and guinea pigs infected with MARV.

144 ation and acute inflammation in the lungs of pigs infected with the Malaysian NiV strain.

145 We propose that the pig influenza model will be useful for testing candidate

146 -expression network of plaque-induced genes (PIGs) involving the complement system, oxidative stress,

147 Our knowledge about the gut microbiota of pigs is still scarce, despite the importance of these an

148 In an Ascaris suum infection model in pigs, it was found that, although 2-MPC levels were much

149 rticles in adult human ileal mucus and adult pig jejunal and ileal mucus revealed no significant diff

150 x. two times lower than the viscosity of the pig jejunal mucus (P < 0.05).

151 first deduce from the in vivo experiments in pigs key digestive parameters such as gastric pH, stomac

152 imal marker genes [TPM threshold =15]), with pig kidney cells (LLC-PK1) close behind (39%).

153 igh perfusate PO2 during continuous HMP in a pig kidney ischemia-reperfusion autotransplant model.

154 suggest that it would be ethical to offer a pig kidney transplant to selected patients who have a li

155 The optimal dose of Mirococept in pig kidney was 80 mg.

156 Using pMRI, we found that in pig kidney, ATP was rapidly generated in presence of oxy

157 The median survival of TKO pig kidneys (4 days) in baboons was significantly shorte

158 Pig kidneys (n = 5) were procured after 30 minutes of wa

159 OWMs complicates the transplantation of TKO pig kidneys in OWMs.

160 To mimic DCD, pig kidneys underwent 0, 30, or 60 min of warm ischemia,

161 EDA-KO pigs lacked SMGs throughout the airways.

162 It was initially identified in pig leukocytes with a broad-spectrum antibacterial and a

163 CI: 0.15, 0.68; P = .002), and ownership of pig livestock, which was a binary variable (beta coeffic

164 Pig LT was performed with livers from heart-beating dono

165 s of SadP are shown to predominantly bind to pig lung globotriaosylceramide (Gb3).

166 and tracheal samples (to establish the true pig M. hyopneumoniae status) were collected at 7- to 14-

167 a production in pure bacteria culture and in pig manure while simultaneously inhibiting methane and o

168 In laboratory headspace experiments on pig manure, we used proton-transfer-reaction mass spectr

169 The young pig may, therefore, be a useful large animal model for t

170 itional warthog genetic traits into domestic pigs may be one way to assist in combating the devastati

171 In BCG-vaccinated mice and guinea pigs, metformin enhances immunogenicity and protective e

172 dels, including a clinically highly relevant pig model of HF.

173 model is the first lentiviral vector induced pig model of high-grade spinal cord glioma and may poten

174 called "aerosolized fomites." In the guinea pig model of influenza virus transmission, we show that

175 omprehensive platform studying MR to MS in a pig model tightly related to human MS criteria.

176 red in vivo protein digestion in a miniature pig model with the dynamic in vitro system DiDGI(R), usi

177 neurons in vitro or induce cough in a guinea pig model.

178 with moderate to high affinity (human/guinea pig/mouse K(d): 24/28/94 nM).

179 blished data on individual PL classes in the pig muscle are inconsistent.

180 Female recipient pigs (n = 12) were randomized to undergo left lung trans

181 Female pigs (n = 12, Cross of Land Race, Duroc, and Yorkshire ~

182 rkers of vaccine responsiveness, a cohort of pigs (n = 120) were vaccinated and pigs representing the

183 Female, Danish slaughter pigs (n = 22, ~ 60 kg).

184 Pigs (n = 255) were assayed for aggressiveness (tendency

185 light stimulation in retinas of adult guinea pigs of either sex.

186 P8v2 to boost the breadth elicited in guinea pigs of FP-directed responses induced by immunogens cont

187 ild pigs from the county until the last wild pig (of 376 total) was successfully removed in 2016.

188 It is known that pig offspring born from pregnant pigs exposed to elevate

189 Following euthanasia of the pigs on d60, placental and fetal morphometry and biochem

190 A single subpial AAV9 injection in adult pigs or non-human primates using a newly designed device

191 edge gap, we investigated fetal and neonatal pig pancreas at multiple, crucial developmental stages u

192 However, little is known about pig pancreas development.

193 olated from the subcutaneous fat of domestic pigs (pASCs) and examine the effect of hypoxia on their

194 ine release and airway contraction in guinea pig PCLS.

195 roduction because of its negative effects on pig performance and, notably, to some humans with inflam

196 syltransferase gene-knockout (GTKO), and TKO pig peripheral blood mononuclear cells (PBMCs) using ser

197 at exposure during early-mid gestation, when pig placentae grow heavily, on placental and fetal devel

198 ures between d40 to d60 of gestation reduced pig placental efficiency, resulting in compensatory grow

199 an swine fever (ASF) poses a major threat to pig populations and food security worldwide.

200 ransmission of antigenic variants in Chilean pig populations.

201 li (ETEC) cause acute secretory diarrhoea in pigs, posing a great economic loss to the swine industry

202 lement-dependent lysis of IVIg against these pig pRBCs was measured by hemolytic assay.

203 (ASFV) causes hemorrhagic fever in domestic pigs, presenting the biggest global threat to animal far

204 peripheral immune cells, and body weight in pigs provide both evidence and insight into potential bi

205 ted mainly in large-animal models, including pigs, rabbits, dogs, and nonhuman primates.

206 Pigs receiving cortisol showed strongly decreased adapti

207 een the sequence of the warthog and domestic pig RELA protein; a subunit of the NF-kappaB transcripti

208 ld, and averaged 122.8 effort hours per wild pig removed.

209 eosinophilic component is observed in young pigs rendered allergic to hen egg white protein (HEWP).

210 sequenced the whole genomes of 24 individual pigs representing 22 breeds distributed throughout China

211 cohort of pigs (n = 120) were vaccinated and pigs representing the high (n = 6; 90th percentile) and

212 the rostrum gyrus looks like a model of the pig rostrum at a scale of ~1:2.

213 The pig rostrum is packed with microvibrissae (~470 per hemi

214 The pig's cortical rostrum gyrus receives dense thalamic inn

215 The pig's rostrum has three major skin-folds.

216 omatosensory cortical gyrus representing the pig's rostrum.

217 +/- 48.7 ug/g protein), followed by cattle, pig, sheep, horse, cat and deer: >75% was conjugated.

218 uction of collagen degradation in an ex vivo pig-skin model.

219 In wild-type pigs, SMGs secrete mucus that emerges onto the airway su

220 enome-assembled genomes reveal prevalent and pig-specific species within Lactobacillus, Streptococcus

221 of WGS using Escherichia coli collected from pig surveillance performed between 2013 to 2017.

222 kers on cochlear inner hair cells, in guinea pigs surviving from 1 day to 6 months after a synaptopat

223 cicularis), rhesus macaque (Macaca mulatta), pig (Sus scrofa), and mouse (Mus musculus).

224 contest assessment strategy in the domestic pig (Sus scrofa).

225 ling from trapping) by applying them to wild pigs (Sus scrofa) across three habitats in South Carolin

226 Invasive wild pigs (Sus scrofa) are known to depredate nests, and have

227 In six mini-pigs, synthetic hydroxyapatite/tricalcium phosphate (HA/

228 white colobus), Macaca nemestrina (southern pig-tailed macaque), and Mandrillus leucophaeus (the dri

229 myelin contents were higher in the Montanera pigs than in the Pienso pigs.

230 ut lower levels of n-6 PUFA in the Montanera pigs than in the Pienso pigs.

231 dentified two new subpopulations of domestic pigs that encompass morphology-based criteria in China.

232 ex vivo porcine ureter segments and sedated pigs that, with respect to the administration of a place

233 estrain, and collect specimens directly from pigs thus providing an approach to emerging pathogen det

234 were significantly upregulated in miniature pig TMJ tissues relative to donor matched knee meniscus

235 the propensity of swine IAV to transmit from pig to ferret as a measure of risk to the human populati

236 spiratory droplet transmission from infected pigs to contact ferrets.

237 ages from 132 ETEC isolates from symptomatic pigs to determine their potential for spreading antibiot

238 hout the home ranges of 20 GPS-collared wild pigs to evaluate nest depredation relative to three peri

239 gans may be addressed in the future by using pigs to grow humanized organs with lower potential for i

240 e identify a modern reintroduction of guinea pigs to Puerto Rico, where local inhabitants use them fo

241 rate marked susceptibility of Hartley guinea pigs to uniformly lethal disease when challenged with as

242 ockade by tocilizumab (TCZ) has been used in pig-to-baboon organ xenotransplant models, but whether i

243 probable source of the earliest known guinea pigs transported, as part of the exotic pet trade, to bo

244 ween heat-tolerant pigs and heat-susceptible pigs under heat stress.

245 meters in heat-tolerant and heat-susceptible pigs under the effects of heat stress, respectively.

246 Hypercholesterolemic pigs underwent MI induction (90 min of ischemia) and wer

247 Male pigs underwent splenectomy followed by controlled hemorr

248 Here we showed TRPV4 expression in guinea-pig urothelium, suburothelium, and bladder smooth muscle

249 Our results revealed that wild pigs used bait sites most during evening and nocturnal p

250 ation on the later-life cognitive ability of pigs using a range of techniques.

251 te whether DC responses can be quantified in pigs using computer vision.

252 of a high-grade spinal cord glioma model in pigs using lentiviral gene transfer.

253 Food allergy was induced in young pigs using two protocols.

254 mmunization (SIM) by both routes in Babraham pigs, using the single cycle candidate influenza vaccine

255 We used a 24-week guinea pig vaccination-Mycobacterium tuberculosis (M.tb.) chall

256 ms in both expression and function in guinea pig ventricular cardiomyocytes.

257 diffusivity in the mucus obtained from adult pigs vs. 2-week old piglets showed better penetrability

258 Unlike domestic pigs, warthogs, which are wildlife hosts of the virus, d

259 nsplant model, the left kidney of a +/-40 kg pig was exposed to 30 minutes of warm ischemia prior to

260 ated probability of nest depredation by wild pigs was 0.3, equivalent to native species of nest preda

261 esponse to Mtb infection in untreated guinea pigs was associated with a marked increase in energy met

262 The true status of pigs was established by PCR testing on oral fluids sampl

263 idelity and time spent at bait sites by wild pigs was not influenced by increasing removals of wild p

264 ministration of (64)Cu-Macrin in rabbits and pigs, we detected heightened macrophage numbers in the i

265 Pigs were allocated as 'high play' or 'low play' based u

266 Fifteen pregnant pigs were allocated to thermoneutral (TN; 20 degrees C;

267 After prime and boost immunization, pigs were challenged with H1N1pdm09 virus.

268 A total of 1,028 pigs were characterized.

269 Pigs were cloned by transfer of chromatin from swine pri

270 Five pigs were excluded leaving n equals to 7 for each group.

271 The left kidneys of a +/-40 kg pigs were exposed to 30 minutes of warm ischemia and ran

272 The Apulo-Calabrese and crossbreed pigs were fed the same diet and slaughtered at 135 and 1

273 on would induce reproductive disease, guinea pigs were infected at mid-gestation and monitored daily

274 Ten 8-week-old pigs were intratracheally inoculated with M. hyopneumoni

275 A total of 12 pigs were randomized equally into a control and BTS plac

276 To test this hypothesis, guinea pigs were treated daily with the anti-diabetic drug metf

277 fficacy during pregnancy, nonpregnant guinea pigs were vaccinated with S19, 16MDeltavjbR + Quil-A, or

278 wing an adaption period, thirty-seven weaned pigs were weight matched (8.41 +/- 0.14 kg), housed indi

279 Therefore, we studied pigs, which have lungs like humans, and disrupted the ge

280 The pig whipworm Trichuris suis is important in swine produc

281 find that an uninfected, virus-immune guinea pig whose body is contaminated with influenza virus can

282 In the future, the pigs will also be genetically engineered to control the

283 Zooarchaeological remains of sheep and pig with minimal taphonomic modifications were analysed

284 s9 and transposon technologies, we show that pigs with all PERVs inactivated can also be genetically

285 SFVsRNA2 detected it in lymphoid tissue from pigs with ASF.

286 In pigs with chronic MI (6 weeks), in vivo monophasic actio

287 In addition, low responder pigs with high plasma interferon-gamma showed lower (p <

288 Following immunization of mice and guinea pigs with INO-4800 we measure antigen-specific T cell re

289 Feeding pigs with LP + BCAA impacted the phenylalanine and prote

290 response to ID-injected vaccines in mice and pigs with minimal local reaction at the injection site.

291 Enteroids were generated from pigs with MYO5B(P663L) and without the substitution (con

292 ingle intramuscular immunization of domestic pigs with OURT88/3 or BeninDeltaMGF followed by a challe

293 Pigs with play fighting interactions with many partners

294 1959) reported that treating pregnant guinea pigs with testosterone had enduring effects on the sex-r

295 logical parameters were observed in domestic pigs with the 2 amino acid substitution.

296 ingle intramuscular immunization of domestic pigs with the OURT88/3 isolate or BeninDeltaMGF virus, a

297 Feeding pigs with very-low protein (VLP) diets while supplemente

298 Triple-knockout (TKO) pigs (with added protective human transgenes) are likely

299 ntly colonize the nasal cavity of inoculated pigs, with all pigs clearing HS069Deltacap by 5 days pos

300 cheal (IT) inoculation of nonpregnant guinea pigs would replicate features of clinical disease in hum