ライフサイエンスコーパス: ovine

1 and genital mucosal surfaces of bovines and ovines.

2 enotype data generated using the caprine and ovine 50K SNP BeadChips from Barki goats and sheep that

3 These findings indicate that ovine AANAT is dual-phosphorylated.

4 -3 binding was also observed using humanized ovine AANAT, which has a different C-terminal sequence (

5 recently emerged as the predominant cause of ovine abortion in the United States.

6 ampylobacter infection is a leading cause of ovine abortion worldwide.

7 cter infection is one of the major causes of ovine abortions worldwide.

8 nthase inhibition shows potential benefit in ovine acute lung injury by reducing nitrosative stress i

9 , as well as with those of the stramenopilan ovine agent Pythium insidiosum.

10 fter the onset of hypoxia was analysed using ovine Agilent 15.5k array and validated with qPCR and im

11 emical properties of complex I prepared from ovine and bovine mitochondria and that ovine complex I r

12 hich specifically amplified small amounts of ovine and caprine BSE agent which had been mixed into a

13 The motif is strongly conserved across the ovine and caprine lentiviruses, implying a critical func

14 ompare the fatty acid and terpene profile of ovine and caprine milk from animals raised under a semi-

15 was detected in the majority of the examined ovine and caprine milk samples suggesting that its prese

16 st-partum variation of polyamine content, in ovine and caprine milk, from indigenous Greek breeds.

17 PadA was able to activate bovine, ovine and caprine Plg, but not human Plg.

18 ed-tube method allowing us to detect bovine, ovine and caprine species and authenticate Greek PDO Fet

19 dMT markers can be detected in vivo in adult ovine and human valves.

20 overed from human, poultry, bovine, porcine, ovine, and canine sources by multilocus sequence typing

21 f 0.74, 0.82, and 0.66 ng mL(-1) for bovine, ovine, and caprine IgGs, respectively, which are lower t

22 d into the arterial system of a pre-clinical ovine animal model, where they endothelialized within on

23 sels (A-TEVs) into the arterial system of an ovine animal model.

24 e the safety and effectiveness of polyclonal ovine anti-TNF fragment antigen binding (Fab) fragments

25 In the present study, an ovine antibody-based platform for passive immunotherapy

26 Screening of these proteins against ovine antisera identified eight immunogenic proteins tha

27 tigation of the neutralizing activity of the ovine antisera in vitro revealed that it neutralized EBO

28 h limiting dilutions (endpoint titration) of ovine AS isolates.

29 a 2-dimensional model and optical mapping of ovine atrial scar-related AF.

30 s when reconstituted onto DNA containing the ovine beta-lactoglobulin gene.

31 NA, encompassing the chicken beta-globin and ovine beta-lactoglobulin genes, respectively, we mapped

32 ent of mitochondrial density and activity in ovine biceps femoris skeletal muscle during the perinata

33 g mouse model, resulting in 96% knockdown of ovine BLG in milk.

34 uct was expressed in the mammary gland of an ovine BLG-expressing mouse model, resulting in 96% knock

35 -ray structure of the unliganded form of the ovine BMPR-II ECD as a guide.

36 Mesenchymal stem cells were isolated from ovine bone marrow and characterized by their morphology

37 hate (beta-Ca3(PO4)2 scaffold implanted into ovine bone.

38 es of D-spacings was previously reported for ovine bone; however, this report demonstrates that the e

39 eutzfeldt-Jakob disease (vCJD), experimental ovine bovine spongiform encephalopathy (BSE), and natura

40 eir ability to react with recombinant mouse, ovine, bovine, or human PrP dimers.

41 iated virus that infects neural cells in the ovine brain was injected into the subventricular zone (S

42 d at similar levels in fetal, lamb and adult ovine brain.

43 er/lower-quality milks from non-autochthones ovine breeds compromises the quality of the final produc

44 a blinded series of brain samples, in which ovine BSE and distinct isolates of scrapie are mixed at

45 ood can become infectious at early stages of ovine BSE infection and that the PrP(d) immunohistochemi

46 at leads to its rapid intracellular decay in ovine but not in Culicoides cells and to the attenuation

47 found that NS3 protein turnover may vary in ovine but not in Culicoides cells due to a single amino

48 ally occurring large animal (canine, feline, ovine, caprine, and bovine) models been so essential for

49 Although T(3) is known to abrogate ovine cardiomyocyte proliferation stimulated by insulin-

50 feration of near-term serum-stimulated fetal ovine cardiomyocytes in vitro.

51 l proliferation and T(3) signalling in fetal ovine cardiomyocytes, with the sensitivity to TR blockad

52 Similar to ovine cathelicidin SMAP-29, putatively mature fowlicidin

53 Infection of primary ovine cells with an ORFV024 deletion mutant virus result

54 , claudin-1, claudin-5 or ZO-1 expression in ovine cerebral cortices.

55 investigate the single-channel behaviour of ovine CFTR and the impact of the most common CF mutation

56 , the F508del mutation had reduced impact on ovine CFTR channel gating in contrast to its marked effe

57 y and efficacy, ATP more strongly stimulated ovine CFTR channel gating.

58 TR modulator phloxine B failed to potentiate ovine CFTR Cl(-) currents.

59 Like human CFTR, ovine CFTR formed a weakly inwardly rectifying Cl(-) cha

60 We conclude that ovine CFTR forms a regulated Cl(-) channel with enhanced

61 re-sensitive folding defect, which disrupted ovine CFTR protein processing and reduced membrane stabi

62 However, for three reasons, ovine CFTR was noticeably more active than human CFTR.

63 gment to bovine chromosome 12 on caprine and ovine chromosomes 12 and 10, respectively, providing, mo

64 sent an early marker of LV dysfunction in an ovine chronic MR model.

65 The L-BSE agent differs from both ovine classic BSE or CH1641 scrapie maintaining its spec

66 ell as splenotropism, clearly differing from ovine classic BSE or from scrapie strain CH1641.

67 n the subunit composition of subcomplexes of ovine complex I as compared with bovine, suggesting diff

68 from ovine and bovine mitochondria and that ovine complex I represents a suitable alternative target

69 the bovine enzyme, remains tightly bound to ovine complex I.

70 essed in the trophectoderm of the elongating ovine conceptus after day 12 of pregnancy.

71 of SLC7A1 mRNA, the arginine transporter in ovine conceptus trophectoderm (Tr).

72 ction of arginine transporter SLC7A1 mRNA in ovine conceptus trophectoderm.

73 and differentiation in the periimplantation ovine conceptus.

74 was found to be a poor inhibitor of purified ovine COX-1 and a relatively weak inhibitor of purified

75 COX-1 selectivity, the crystal structures of ovine COX-1 in complexes with an enantiomeric pair of th

76 RE's in the proximal promoter regions of the ovine cry1 and mt1 genes, and confirmed their functional

77 se type-2, and >100-fold selectivity against ovine cyclooxygenase-1 and human cyclooxygnease-2.

78 5-hLO, platelet 12-hLO, epithelial 15-hLO-2, ovine cyclooxygenase-1, and human cyclooxygenase-2.

79 a protein (GIF) that binds and inhibits the ovine cytokines granulocyte-macrophage colony-stimulatin

80 is present 2 years following ovariectomy in ovine dermal samples.

81 munoreactive cells were spread widely in the ovine diencephalon and overlapped with the known distrib

82 Contagious ovine digital dermatitis (CODD) is an important foot dis

83 y poor in interferon (IFN)-competent primary ovine endothelial cells compared to replication of BTV8L

84 erent C-terminal sequence (Gly-Cys) than the ovine enzyme (Asp-Arg), indicating that that characteris

85 hat that characteristic is not unique to the ovine enzyme.

86 testinal (GI) tracts of six species (bovine, ovine, equine, porcine, chicken, and deer) and from two

87 peared hyperintense in both freshly prepared ovine eyes and living rat eyes using T2-weighted MRI.

88 The expression of TRalpha1 and TRbeta1 in ovine fetal myocardium increases with age, although TRal

89 roliferation of beta cells isolated from the ovine fetal pancreas is sensitive to physiological conce

90 tric-oxide synthase 3) protein expression in ovine fetoplacental artery endothelial cells (oFPAEC).

91 Studies in ovine fetus and placenta have pointed to an interaction

92 These results demonstrated that the infected ovine fetus is able to initiate an innate and adaptive i

93 lood-brain barrier permeability in premature ovine fetuses and the incidence of intraventricular hemo

94 before the development of immunocompetency, ovine fetuses at 35 days of gestation were inoculated in

95 To address these questions, ovine fetuses at 35 days of gestation were inoculated in

96 und guidance we applied steroids directly to ovine fetuses at d62 and d82 of gestation, and examined

97 was directly administered to developing male ovine fetuses to model excess prenatal androgenic overex

98 tion (TJ) proteins in the cerebral cortex of ovine fetuses with and without exposure to in utero brai

99 ormations have been previously reproduced in ovine fetuses.

100 ormations have been previously reproduced in ovine fetuses; however, no studies have established the

101 Ovine footrot is a highly prevalent bacterial disease ca

102 Dichelobacter nodosus causes ovine footrot, a disease that leads to severe economic l

103 proximal promoter between -172/-1 bp of the ovine FSHB gene are required for gonadotrope expression

104 ssary for gonadotrope-specific expression of ovine FSHB in vivo.

105 quately recognize regulatory elements on the ovine FSHB promoter associated with gonadotrope-specific

106 ntify sequences between -1866/-750 bp of the ovine FSHB promoter that are also required for tissue/ce

107 e element between -750 bp and -232 bp of the ovine FSHB promoter.

108 ontained -2871 bp, -750 bp or -232 bp of the ovine FSHB promoter.

109 e are required for gonadotrope expression of ovine FSHB.

110 We identified 1,971 ovine genes differentially expressed in JSRV-infected lu

111 s of VEGF and NO metabolite (NOx) throughout ovine gestation and to determine if there was an effect

112 o critical to the GIF protein for binding to ovine GM-CSF (ovGM-CSF).

113 welfare, the recent increase in diagnoses of ovine haemonchosis caused by the nematode Haemonchus con

114 l intravenous boluses of a (P)RR antagonist, ovine handle region peptide (HRP) (1, 5, and 25 mg at 90

115 (MVO2) were determined in control (n=5) and ovine heart failure (n=5).

116 ate effect of varying restraint levels in an ovine heart failure model.

117 ventricular restraint were then evaluated in ovine heart failure with (n=3) and without (n=3) restrai

118 s mitral annular strains in a normal beating ovine heart preparation.

119 increased AML strains in the normal beating ovine heart.

120 ation of complex I purified from Ovis aries (ovine) heart mitochondria.

121 In healthy, beating ovine hearts, annuloplasty rings (COS, RSA, PHY, ETL, an

122 Two variants of an organism resembling the ovine hemoplasma, Mycoplasma ovis, were detected by PCR

123 Ovine herpesvirus 2 (OvHV-2) is a gammaherpesvirus in th

124 Entry of ovine herpesvirus 2 (OvHV-2), the causative agent of she

125 e three deceased rhebok were coinfected with ovine herpesvirus-2, and two animals additionally had a

126 is an obligate inhabitant of the bovine and ovine host, the formation of a biofilm may be crucial to

127 Recombinant ovine IFNT (roIFNT) induced the IFN-stimulated genes (IS

128 A pool of intact ovine immunoglobulin G, herein termed EBOTAb, was prepar

129 In response to the 2014 outbreak, an ovine immunoglobulin therapy was developed, termed EBOTA

130 ocardial tissue during acute fibrillation in ovine isolated left atria.

131 representative pathogenic and non-pathogenic ovine isolates over ten time-points by enumeration of ti

132 creased proliferative capacity by pathogenic ovine isolates was observed.

133 A1 and OmpA2, are associated with bovine and ovine isolates, respectively.

134 Two natural models of ovine IUGR are those of hyperthermic exposure during pre

135 triction and postnatal obesity on the UPR in ovine juvenile offspring.

136 and biological properties of QQ171 and RQ171 ovine L-BSE prions were investigated in transgenic mice

137 In both mouse lines, ovine L-BSE transmitted similarly to cattle-derived L-BS

138 never-smokers and in the airways of a novel, ovine large animal model.Methods: Mucociliary parameters

139 oited a validated finite element model of an ovine left ventricle with an anteroapical infarct to exa

140 Like human immunodeficiency virus (HIV), ovine lentivirus (OvLV) is macrophage-tropic and causes

141 transmission of Visna/maedi virus (VMV), an ovine lentivirus, is thought to be via the respiratory t

142 ith saline (0.9% NaCl; n = 6) or recombinant ovine leptin (0.5-1.0 mg kg(-1) day(-1); n = 6) for 5 da

143 were cultured in the presence of recombinant ovine LGALS15.

144 ing to study the transcriptional response of ovine lung tissue to infection by JSRV.

145 ed the infection of specific segments of the ovine lung.

146 We have directly cannulated the ovine lymphatic vessels to detail the in vivo innate and

147 immune specificity of OmpA among bovine and ovine M. haemolytica isolates, recombinant proteins repr

148 loped by comparing two RNA-seq datasets from ovine macrophages, identical except for RNA selection me

149 d fetal pituitary and testicular function in ovine male fetuses.

150 ine weeks after bioreactor implantation, the ovine mandibles were repaired with the autologous bony t

151 d a dry stack mixture of equine, bovine, and ovine manure.

152 n organs of female deer; (3) nine commercial ovine meat cuts contained similar Neu5Gc levels.

153 Here we analysed Ovine medium-density SNP array genotypes of 92 mouflon f

154 Human embryonic kidney (HEK) cells and ovine mesenchymal stem cells (oMSCs) were printed at tis

155 Pa) were injected into a clinically relevant ovine MI model to evaluate the associated salutary effec

156 produced from A: 100% whey; B: 90% whey+10% ovine milk and C: 90% whey+10% skimmed ovine milk and we

157 y+10% ovine milk and C: 90% whey+10% skimmed ovine milk and were evaluated.

158 Regarding fatty acid profile, ovine milk had a higher percentage of conjugated linolei

159 Ovine milk had better nutritional value in comparison to

160 er comprising samples manufactured with only ovine milk or milk admixtures.

161 s increases the antithrombotic properties of ovine milk PL.

162 AM-MS/MS) that fermentation of yoghurts from ovine milk using specific starter cultures altered the P

163 In ovine milk, the profile of the mean concentrations showe

164 lk that had an enriched terpene profile than ovine milk.

165 se and yoghurt made from spiked and incurred ovine milk.

166 terolateral infarcts were investigated in an ovine model (n>/=6 per group), with injection of saline

167 he impact of CF on lesion formation using an ovine model both endocardially and epicardially.

168 Biocompatibility was studied in vivo in an ovine model by implanting the scaffolds into femoral art

169 Here, we show that, in an ovine model of a variant late-infantile NCL, there is ab

170 onclusions: Endobronchial hMSC therapy in an ovine model of ARDS and ECMO can impair membrane oxygena

171 g CF human bronchial epithelial cells and an ovine model of CF-like airway disease.Methods: Losartan'

172 g 2D and real-time 3D echocardiography in an ovine model of chronic IMR, we evaluated the geometric i

173 insufficiency and ventricular function in an ovine model of chronic postoperative pulmonary insuffici

174 , and preserves biventricular function in an ovine model of chronic pulmonary insufficiency.

175 In humans and in an ovine model of combined smoke inhalation and burn injury

176 acute lung injury using our well-established ovine model of cutaneous burn and smoke inhalation.

177 Using an established late gestation ovine model of fetal development under chronic hypoxic c

178 Using an ovine model of granulomatous skin inflammation, we demon

179 small RNA sizes in the bovine leukemia virus ovine model of leukemia/lymphoma, we provide in vivo evi

180 In an ovine model of long-standing persistent AF we tested the

181 Using an ovine model of myocardial infarction, we aimed to determ

182 expansion, and preserves contractility in an ovine model of myocardial infarction.

183 e of sleep deficits in a naturally occurring ovine model of neuronal ceroid lipofuscinosis (NCL, Batt

184 Using an ovine model of polycystic ovary syndrome (PCOS), (pregna

185 he objective of this study was to develop an ovine model of septic acute lung injury and characterize

186 onine, with or without hydrocortisone, in an ovine model of septic shock did not markedly alter norep

187 renal structure and function over time in an ovine model of septic shock.

188 mmune response induced by AS01 in an outbred ovine model, 2) to develop a lymphatic cannulation model

189 steum-mediated bone regeneration in a common ovine model, it was shown that mechanistic models incorp

190 In an ovine model, tubular SIS-ECM TV bioprostheses demonstrat

191 In a chronic ovine model, we tested whether isolated mitral regurgita

192 growth, structure, and function in a growing ovine model.

193 somatosensory evoked potentials (SEPs) in an ovine model.

194 using irrigated RFA on the epicardium in an ovine model.

195 at late induction studies </=200 days in an ovine model.

196 scending coronary artery was performed in an ovine model.

197 y 75 gestation, using a clinically realistic ovine model.

198 R) implantation using the Melody valve in an ovine model.

199 system) that ameliorates functional MR in an ovine model.

200 nstruction research in a clinically relevant ovine model.

201 and also fully resorbed by 18 months in the ovine model.

202 stinal inflammation and mucosal injury in an ovine model.

203 nd the uterine cavity, in swine and pregnant ovine models in vivo.

204 etofore have not typically been pursued with ovine models of developmental insults.

205 In ovine models of mucus clearance (tracheal mucus velocity

206 and compared its expression pattern in adult ovine, mouse, and human hypothalamic tissues.

207 We have confirmed that the ovine Nectin-4 protein, when overexpressed in epithelial

208 ng interest in the influence of vitamin D on ovine non-skeletal health.

209 ant species, one from Ovis aries, designated ovine (O), and the other from Bos taurus, designated bov

210 e of naturally or preclinical prion-diseased ovine or cervids.

211 Comparison of eight isolates of bovine and ovine origin at three key time-points (2 h, 48 h and 72

212 ogenic M. haemolytica isolates of bovine and ovine origin.

213 Both the bovine and ovine orthologs displayed fusogenic activity by conferri

214 Ovine (ov) ISG15 has three additional amino acids within

215 We isolated, mapped and fully sequenced the ovine (ov) TKDP-1 gene.

216 resent a nearly complete atomic structure of ovine (Ovis aries) mitochondrial complex I at 3.9 A reso

217 tion rates were determined in isolated fetal ovine pancreatic islets in vitro.

218 promote beta cell proliferation in the fetal ovine pancreatic islets, and that growth retardation in

219 enomic analysis of a wild-type strain of the ovine pathogen Chlamydia abortus and its nitrosoguanidin

220 Characterized ovine peripheral blood endothelial progenitor cells were

221 TGF)-beta1.Method and Results- Characterized ovine peripheral blood EPCs were seeded onto poly (glyco

222 )] designed to match the surface antigens on ovine peripheral blood-derived EPCs.

223 In ovine PGHS-1 crystallized in the absence of an NSAID, th

224 Ovine polyclonal antibodies were raised using an immunog

225 An ovine polyclonal antibody therapy has been developed aga

226 tion was performed in eggs, poultry, bovine, ovine, porcine and rabbit tissue and exceptionally low L

227 opurinol on fetal cardiovascular function in ovine pregnancy in late gestation.

228 ed ARQ sheep with variation elsewhere in the ovine prion gene.

229 Variation in the ovine prion protein amino acid sequence influences scrap

230 icrosecond folding and unfolding kinetics of ovine prion proteins (ovPrP) were measured under various

231 onventional mice has shown some diversity in ovine prion strains.

232 lies in the absence or presence of exogenous ovine prions.

233 Known as ovine progressive pneumonia virus (OPPV) in the U.S., an

234 locked only by a very high dose of unlabeled ovine prolactin.

235 ce, Tg mice overexpressing human, bovine, or ovine PrP did not develop prion disease after inoculatio

236 Cytosolic ovine PrP expressed in Drosophila was not overtly detrim

237 While cytosolic ovine PrP expressed in Drosophila was predominantly dete

238 enerated Drosophila transgenic for cytosolic ovine PrP in order to investigate its toxic potential in

239 ighly conserved (190)HTVTTTT(196) segment of ovine PrP led to spontaneous prion formation in the RK13

240 ctivity was also detected in brain tissue of ovine PrP mice inoculated with limiting dilutions (endpo

241 tedly, HMM PrPres was found in the spleen of ovine PrP transgenic mice infected with L-BSE from RQ171

242 to contain prion infectivity by bioassays in ovine PrP transgenic mice.

243 be found in RQ171 sheep and in the spleen of ovine PrP transgenic mice.

244 and MovS6 cell lines, which both express the ovine PrP VRQ allele, to assess to what extent natural a

245 scribe a new chemical category that inhibits ovine PrP(Sc) accumulation in primary sheep microglia an

246 transgenic mice expressing either bovine or ovine PrP.

247 in PT cell cultures, and is rhythmic in the ovine PT with a nadir in the early night.

248 retrovirus (JSRV) is the etiologic agent of ovine pulmonary adenocarcinoma (OPA), a neoplastic lung

249 retrovirus (JSRV) is the causative agent of ovine pulmonary adenocarcinoma (OPA), a transmissible lu

250 del for human lung adenocarcinoma.IMPORTANCE Ovine pulmonary adenocarcinoma is a chronic respiratory

251 retrovirus (JSRV) is the causative agent of ovine pulmonary adenocarcinoma, a contagious lung cancer

252 ent of a transmissible lung cancer in sheep, ovine pulmonary adenocarcinoma.

253 Twelve weeks of ovine "pure" MR caused LV remodeling with early changes

254 sferred bovine blastocysts into synchronized ovine recipients and allowed them to develop for 13 days

255 As the prion resistant model, we used ovine recPrP (OvPrP) carrying the protective polymorphis

256 T- and sialyl T-antigen varied in bovine and ovine reproductive tract mucins, and terminal N-acetylga

257 aware of any direct comparison of bovine and ovine responses to dietary PUFA.

258 ection chemical defaunation of the bovine or ovine rumen.

259 , at two time points (6 and 12 months) in an ovine scapula drillhole model using micro-CT, histology

260 Ovine scrapie and cervine chronic wasting disease show c

261 ng with implications for the transmission of ovine scrapie and very likely other prion diseases.

262 sess to what extent natural and experimental ovine scrapie can be detected ex vivo.

263 ignificantly, the toxic phenotype induced by ovine scrapie in cytosolic PrP transgenic Drosophila was

264 Biological strain typing of ovine scrapie isolates by serial passage in conventional

265 o discriminate field cases of mouse-passaged ovine scrapie isolates.

266 tosolic PrP transgenic Drosophila exposed to ovine scrapie showed a toxic phenotype absent from simil

267 Our data show that mouse-adapted ovine scrapie strains can be discriminated by their dist

268 ted with two principal Prnp(a) mouse-adapted ovine scrapie strains, namely, RML and ME7, in order to

269 ministration exerts beneficial effects in an ovine septic shock model.

270 a bovine serotype A1 isolate (rOmpA1) and an ovine serotype A2 isolate (rOmpA2) were overexpressed, p

271 e purification of polyclonal antibodies from ovine serum using the synthetic protein A absorbent MAbs

272 The ovine sexually dimorphic nucleus (oSDN) is characterized

273 preoptic area of the adult sheep contains an ovine sexually dimorphic nucleus (oSDN) that is larger a

274 l simulations and new experiments on ex vivo ovine skeletal muscle (n = 3).

275 Infestation of ovine skin with the ectoparasitic mite Psoroptes ovis re

276 s with similar designs were implanted in the ovine skull and at s.c. sites and retrieved after 12 and

277 ome-wide homozygosity mapping using Illumina Ovine SNP50 BeadChips on lambs descended from one carrie

278 of genomic variation by genotyping, with the Ovine SNP50K microarray, 394 individuals from five popul

279 Here, we first developed a set of 493 novel ovine SNPs of the male-specific region of Y chromosome (

280 We generated pharmacologic quantities of ovine-specific neutralizing anti-IL-6 mAbs and systemica

281 ilarly treated with five naturally occurring ovine STEC isolates or stx-negative E. coli.

282 om an M. avium subsp. paratuberculosis (Map) ovine strain (S-type) contained no identifiable glycopep

283 tains three amino acid specifying modules in ovine strains, compared to five modules in bovine strain

284 we present three architectures of mammalian (ovine) supercomplexes determined by cryo-electron micros

285 we investigated the surgical anatomy of the ovine sural nerve as a potential candidate for facial ne

286 The ovine sural nerve descended to the lower leg along the s

287 l anatomy and the number of fascicles of the ovine sural nerve were similar of those reported in huma

288 taining protein, Tck6, capable of modulating ovine T cell cytokine responses.

289 ffective in ameliorating functional MR in an ovine tachycardia model.

290 between changes in protein expression in an ovine tachypacing-induced HF model and ultrastructural r

291 tial competitive interaction between the two ovine Theileria spp., and a substantial reduction in the

292 In summary, the data suggest that ovine toxin A and B antibodies may be effective in the t

293 We employed a highly optimised ovine tracheal epithelial cell model to assess the colon

294 Genetic variation in the ovine transmembrane protein 154 gene (TMEM154) has been

295 GALS15 moderately increased proliferation of ovine trophectoderm (oTr) cells.

296 ostability of yeast ADP/ATP carrier AAC2 and ovine uncoupling protein UCP1 allow optimal conditions f

297 stimulate proliferation of pregnancy-derived ovine uterine artery endothelial cells (P-UAECs) through

298 e endometrial luminal epithelium (LE) of the ovine uterus in concert with blastocyst growth, elongati

299 ed for 46.49%, indicating the success in the ovine Y chromosome isolation and the high quality of the

300 e sequencing, assembly and annotation of the ovine Y chromosome, but also provide a validated approac

301 h a focus on isolation and sequencing of the ovine Y chromosome.