ライフサイエンスコーパス: bovine

1 ver agents (methylene blue, MB, in PBS) into bovine AC.

2 iously shown that in vitro transduction with bovine adeno-associated viral (BAAV) vectors restores co

3 ta-miR-23a was an adipogenic miRNA mediating bovine adipogenesis in skeletal muscle.

4 Bovine anaplasmosis caused by the intraerythrocytic rick

5 Anaplasma marginale causes bovine anaplasmosis, a debilitating and potentially fata

6 y receptors regulate T-cell responses during bovine anaplasmosis.

7 ited approximately 1.3% of their genome from bovine ancestors after nearly continuous admixture over

8 perties of acid and sweet whey obtained from bovine and camel fresh milk was examined.

9 s (Cys, His, and Lys) and selected proteins (bovine and human hemoglobin and beta-lactoglobulin-A) we

10 Evolutionary divergence between bovine and human TLR5 was also apparent in relation to r

11 the purity of gelatin batches with regard to bovine and porcine constituents.

12 ic marker peptides of TG (five markers), and bovine and porcine fibrinogen (six markers each).

13 nase (TG) from Streptomyces mobaraensis, and bovine and porcine fibrinogen/thrombin in restructured m

14 echnical TG mixture (Activa, Ajinomoto), and bovine and porcine plasmapowder FG (PPFG; Sonac B.V.).

15 blood in meat, using a concentration of 0.6% bovine and porcine PPFG.

16 cial edible gelatins are often produced from bovine and porcine skin and bone and consist mainly of p

17 ctice, and the theoretical justification for bovine and porcine target selection.

18 a significant resource for understanding of bovine and species-conserved miRNA regulation, and demon

19 Healthy bovine annulus fibrosus cells, however, demonstrated a p

20 izing the structure of the HCDR3, similar to bovine antibodies, to aid in recognition of a cluster of

21 GF-induced VEGFR2 and Akt phosphorylation in bovine aortic endothelial cells, while PTP1B siRNA incre

22 (ERM) recognises the fraudulent addition of bovine (B) milk in water buffalo (WB) milk/dairy product

23 ive characterisation of genetic variation in bovine beta-defensin genes and functional analysis suppo

24 Species-specific peptides from bovine beta-lactoglobulin and alphaS1 casein were identi

25 biomarkers that would allow the detection of bovine blood products and processed animal proteins usin

26 s disease and human brucellosis) and animal (bovine brucellosis and foot-and-mouth disease) infection

27 This study examined the effects of bovine carbonic anhydrase (BCA) and CO2-rich gas streams

28 construct and substituted it for the VELC of bovine cardiac myosin subfragment 1.

29 present the crystal structure of OM bound to bovine cardiac myosin, which shows that OM stabilizes th

30 Bovine cartilage explants were cultured with IL-1alpha t

31 ng a therapeutically active dose of KAFAK to bovine cartilage explants, suppressing pro-inflammatory

32 , neutral pH (6.8), damage-free structure of bovine CcO (bCcO) in the carbon monoxide (CO)-bound stat

33 on the entire, as well as core, structure of bovine CcO in a lipid-solvent environment.

34 ced higher levels of CXCL8 when expressed in bovine cells and reciprocal results were found for human

35 that spanned a conserved syntenic segment to bovine chromosome 12 on caprine and ovine chromosomes 12

36 n of common regions of interest on different bovine chromosomes and mirroring the evolutionary dynami

37 included many other SBTs from plants but not bovine chymotrypsin or bacterial subtilisin A.

38 Here we determined the structure of a bovine CLC channel (CLC-K) using cryo-electron microscop

39 DBA/1 mice were immunised with bovine collagen type II and treated orally with specific

40 We assessed the efficacy of antiadhesin bovine colostral IgG (bIgG) antibodies against ETEC chal

41 d product taken alone or in combination with bovine colostrum (a natural source of growth factors), w

42 Bovine colostrum is potentially valuable source of essen

43 he analysis of the composition of the FAs in bovine colostrum.

44 al cells (HMVEC) and vasodilatory actions on bovine coronary arteries and reciprocally regulated plat

45 In this study, we demonstrate that Tc bovine-derived Venezuelan equine encephalitis virus (VEE

46 with immediate implant and collagen-enriched bovine-derived xenograft blocks without a surgical flap

47 The major differences between human and bovine E. coli O157 isolates were due to the relative ab

48 lastomeres comprising entire preimplantation bovine embryos (n = 23) following in vitro fertilization

49 x of hydrogen peroxide through 1-mm discs of bovine enamel was measured at steady-state conditions, a

50 e the crystal structures of the picornavirus bovine enterovirus 2 (BEV2) and the cytoplasmic polyhedr

51 of the distantly related a subunit from the bovine F-type ATP synthase revealed a conserved pattern

52 Bovine fertility remains a critical issue underpinning t

53 (5)G substitution in both alleles of CD18 in bovine fetal fibroblast cells.

54 Bovine fetal fibroblasts, expressing miR-449b through a

55 ns bovine ribonuclease B, human transferrin, bovine fetuin and human alpha1-acid glycoprotein, the co

56 first optimized our automated protocol using bovine fetuin as a standard glycoprotein, and then asses

57 used bovine RNase B, human transferrin, and bovine fetuin as models to demonstrate the feasibility o

58 liver, kidney, and brain of control and LOS bovine fetuses and found that different tissues within L

59 SOX9-bound chromatin regions from murine and bovine foetal testes with sequencing of RNA samples from

60 IgE reactivity to meat extract and bovine gamma globulin (BGG) was assessed by immunoblotti

61 We report an update of the Bovine Genome Database (BGD).

62 ne data warehousing system, to integrate the bovine genome, annotation, QTL, SNP and expression data

63 spective lipid compositions of the MFGM from bovine, goat and sheep milks.

64 hoton and light sheet microscopy in cultured bovine hair follicles and plucked human hairs.

65 Here we inferred bovine haplotypes in the genomes of 76 Mongolian yaks us

66 address these issues, transchromosomic (Tc) bovines have been created, which can produce potent neut

67 Bovine hemolysate was purified by size exclusion chromat

68 The latency-related (LR) RNA encoded by bovine herpesvirus 1 (BoHV-1) is abundantly expressed in

69 Bovine herpesvirus 1 (BoHV-1) is an important pathogen o

70 ction following stressful stimuli.IMPORTANCE Bovine herpesvirus 1 (BoHV-1) is an important viral path

71 ion cycle.IMPORTANCE The lifelong latency of bovine herpesvirus 1 (BoHV-1) requires that significant

72 Bovine herpesvirus 1 (BoHV-1), an important bovine patho

73 Collagen was extracted from raw bovine hide and hydrolyzed by one of three enzymes - Alc

74 tween lymphostatin and immune cells from the bovine host are ill defined.

75 s, primarily associated with either human or bovine hosts.

76 A live attenuated chimeric bovine/human parainfluenza virus type 3 (rB/HPIV3) was d

77 atory adventitial fibroblasts from human and bovine hypertensive pulmonary arterial walls (PH-Fibs) t

78 iption unit 1 (IEtu1) promoter, which drives bovine ICP0 (bICP0) and bICP4 expression, is stimulated

79 Surprisingly, bovine immunodeficiency virus (BIV) Vif, but not HIV-1 V

80 (4-mm diameter, 2-mm depth) were prepared in bovine incisors and restored using Bond Force (BF), Scot

81 lecule probes and degradants of heat-treated bovine insulin as case studies.

82 Unlike USP porcine heparin, bovine intestinal heparin (BIH) has a low anticoagulant

83 viously characterized isolates from cases of bovine intramammary infection in the United States and t

84 on and predicted that only a small subset of bovine isolates have the potential to cause diseases in

85 focused on valve performance in the Contegra bovine jugular vein conduit.

86 real time PCR in BoHV-1 infected Madin-darby bovine kidney cells.

87 Bovine lactoperoxidase (LPO) and lactoferrin (LF) are su

88 c virus type 1 and 2 (HTLV-1 and HTLV-2) and bovine leukaemia virus (BLV).

89 isfactory results for 69 veterinary drugs in bovine liver and 68 compounds in bovine muscle and kidne

90 extended to the characterization of PCs in a bovine liver extract via a shotgun strategy.

91 ter is sensitivity, and we measure this in a bovine liver homogenate reference sample for 20 drugs re

92 An in vitro bovine liver model perfused with autologous blood via th

93 rials (NIST 1567a Wheat Flour and NIST 1577b Bovine Liver).

94 for the determination of veterinary drugs in bovine liver, kidney and muscle was developed.

95 ples of bovine muscle and only ivermectin in bovine liver.

96 irty-two ablations were performed in ex vivo bovine livers (eight per group) and 28 in the livers of

97 s of drug resistance and epidemiology of the bovine lungworm and related nematodes.

98 of M. bovis with its natural host cell, the bovine macrophage.

99 peron impairs the replication of M. bovis in bovine macrophages.

100 saccharide isolated from the cell envelop of bovine mastitis Streptococcus dysgalactiae 2023 is repor

101 vely composed of intrinsically (15)N-labeled bovine meat (30 g protein), cooked at 55 degrees C for 5

102 rescence detection in commercial porcine and bovine meat.

103 hylococcal species that can be isolated from bovine milk and are difficult to differentiate.

104 Temperature sensitivity of bovine milk beta-lactoglobulin (BLG) was assessed in the

105 Pasteurization did not affect the bovine milk content of nicotinamide riboside, whereas UH

106 this study were to characterize isolates of bovine milk origin from a collection that had previously

107 and heating) on protein glycation degrees in bovine milk products.

108 eptide sequences identified within camel and bovine milk protein hydrolysates generated under the sam

109 IV) inhibitory peptides during hydrolysis of bovine milk protein isolate (MPI) with Neutrase 0.8L, yi

110 ivity for peptide bond cleavage of camel and bovine milk proteins as well as dissimilarities in their

111 immunoreactivity and allergenicity of stable bovine milk proteins, using an improved digestibility mo

112 iry cows; however, the mechanisms regulating bovine milk synthesis in dairy cows fed high forage rati

113 in breast milk and also in various types of bovine milk, as tranquilizers are occasionally administe

114 min monophosphate and thiamin diphosphate in bovine milk.

115 el milks were higher than those of fermented bovine milk.

116 Lactobacillus spp., compared with fermented bovine milk.

117 m DSM2468 were employed to ferment camel and bovine milks separately.

118 he interaction of trehalose derivatives with bovine mincle has been probed with a series of synthetic

119 protons in bacterial A-type CcOs, studies of bovine mitochondrial CcO have led to suggestions that it

120 g and adult cortex of rat, mouse, carnivore, bovine, monkey, and human as determined with antibody- a

121 y, we determined the molecular structures of bovine MRP1 in two conformations: an apo form at 3.5 A w

122 source to monitor and perform RF ablation in bovine muscle and human artery samples in vitro and in r

123 ry drugs in bovine liver and 68 compounds in bovine muscle and kidney.

124 ctin and ivermectin were found in samples of bovine muscle and only ivermectin in bovine liver.

125 FMDV) in micro-dissected compartments of the bovine nasopharynx by microarray.

126 era with replacement of the human NTD by the bovine NTD resembled human PrP(c) The requirement for an

127 y, catabolic and pro-angiogenic phenotype in bovine nucleus pulposus and cartilage endplate cells at

128 modeling also extends to hamster, human, and bovine oocytes.

129 mples yielded collagen and blood proteins of bovine origin (Bos genus) and a large sequence coverage

130 phoresis for typing of S. aureus isolates of bovine origin.

131 ble on antibiotic-resistant Campylobacter of bovine origin.

132 or without human donor milk and avoidance of bovine-origin formula, or milk fortifier, on the risk of

133 ith their own mother's milk and avoidance of bovine-origin products might reduce the risk of necrotis

134 For babies who received no compared with any bovine-origin products within 14 days of birth, the abso

135 We illustrate them using bovine pancreatic trypsin inhibitor and present a new, d

136 s of diverse papillomavirus types, including bovine papillomavirus (BPV) and human papillomavirus 16

137 nt involving a conserved tyrosine (Y) in the bovine papillomavirus 1 (BPV-1) E2 protein at amino acid

138 Here we have discovered that the bovine papillomavirus 1 (BPV-1) transcription and replic

139 elicase ChlR1 is required for loading of the bovine papillomavirus E2 protein onto chromatin during D

140 The dimeric 44-residue E5 protein of bovine papillomavirus is the smallest known naturally oc

141 comparisons at the strain (HBoV) and genus (bovine parvovirus and HBoV) levels identified difference

142 Bovine herpesvirus 1 (BoHV-1), an important bovine pathogen, establishes lifelong latency in sensory

143 Furthermore, undeclared bovine peptides were observed in commercial injection ma

144 alve is a self-expanding, nitinol valve with bovine pericardial leaflets that is placed using a trans

145 file, self-expanding nitinol valve made from bovine pericardial tissue that is 14-F compatible with a

146 Despite bovine pericardium (BP) being the primary biomaterial us

147 plotype analysis, we found evidence that the bovine PLAG1 mutation (Q) with major effects on body siz

148 nstrate that a highly enriched population of bovine plasmacytoid dendritic cells (DCs) produced IFN i

149 vergent pathogens, demonstrating that the Tc bovine platform could be beneficial in areas where multi

150 ccessfully developed a transchromosomic (Tc) bovine platform technology that can produce fully human

151 By using a transchromosomic (Tc) bovine platform, it is theoretically possible to produce

152 fication of all the studied gelatin sources (bovine, porcine, and fish) were achieved by hierarchical

153 (n=127) raw meat from three animal species (bovine, porcine, poultry).

154 enetic reprogramming and apoptotic status of bovine preimplantation cloned embryos.

155 lementation (study fortifier adding 1.8 g of bovine protein/100 mL of breast milk [n = 15]) or indivi

156 ned to either a lower-protein (adding 1 g of bovine protein/100 mL of breast milk through a commercia

157 compared to single (free or nanoformulated) bovine proteins.

158 ered phosphorylation of a tyrosine (Y102) in bovine PV (BPV) E2.

159 nd infant formula, dissolved in a mixture of bovine red blood cells and Aedes physiological saline, w

160 Bovine respiratory disease (BRD) is the most common infe

161 BHV-1 is a major viral pathogen of Bovine Respiratory Disease (BRD), the leading cause of e

162 cattle experimentally challenged with either bovine respiratory syncytial virus, infectious bovine rh

163 Here we report that bovine Rh, regenerated instead with a six-carbon-ring re

164 vine respiratory syncytial virus, infectious bovine rhinotracheitis, bovine viral diarrhea virus, Man

165 of recently described scramblases including bovine rhodopsin and fungal TMEM16 proteins.

166 A comprehensive survey of bovine rhodopsin structures shows that the helical rearr

167 xhibited more Schiff base deprotonation than bovine rhodopsin, which could arise from the approximate

168 etics of photointermediates of the human and bovine rhodopsins in their native membranes revealed a c

169 ein structure on the kinetics, the human and bovine rhodopsins were inserted into 1-palmitoyl-2-oleoy

170 tivation kinetics observed between human and bovine rhodopsins.

171 tion of the well-characterized glycoproteins bovine ribonuclease B, human transferrin, bovine fetuin

172 Human calmodulin and bovine ribonuclease S (RNase S) were screened against th

173 We used bovine RNase B, human transferrin, and bovine fetuin as

174 is to evaluate the hydraulic conductance of bovine root dentin after irradiation with a 980-nm diode

175 ger to evaluate the efficacy of a live, oral bovine rotavirus pentavalent vaccine (BRV-PV, Serum Inst

176 nicity in seropositive cattle pre-exposed to bovine RSV, a virus closely related to hRSV.

177 an respiratory syncytial virus (hRSV), hMPV, bovine RSV, and avian metapneumovirus (aMPV).

178 flavefaciens to degrade carbohydrates in the bovine rumen and provides a basis for constructing effic

179 ES cells cultured in media containing fetal bovine serum (FBS) and a glycogen synthase kinase-3 (GSK

180 n S. intermedius PC574 was cultured in fetal bovine serum (FBS) than when it was grown in the standar

181 This article reports the effects of fetal bovine serum (FBS), a physiologically relevant mixture o

182 onents, as discovered during growth in fetal bovine serum (FBS), elicit a robust increase in the amou

183 ic surface, in medium with and without fetal bovine serum (FBS).

184 edia containing human serum (group 1), fetal bovine serum (group 2), StemPro medium (group 3), protam

185 modification using electrospun amyloid like-bovine serum albumin (AL-BSA) nanofibers on QCM surfaces

186 Bovine serum albumin (BSA) adsorption was studied at dif

187 Bovine serum albumin (BSA) and dextran varying in molecu

188 capacity (PPC) using two different proteins [bovine serum albumin (BSA) and gelatin], molecular weigh

189 ility and biodegradability, albumins such as bovine serum albumin (BSA) and human serum albumin (HSA)

190 her physiologically relevant components like bovine serum albumin (BSA) and lipopolysaccharide.

191 The shells comprising alternate layers of bovine serum albumin (BSA) and tannic acid (TA) were tes

192 IR)-emitting gold nanoclusters (AuNCs) using bovine serum albumin (BSA) as a protecting agent.

193 vestigated the interaction of CA and MC with bovine serum albumin (BSA) at pH 3.5, 5.0, and 7.4 using

194 m and treated with palmitate (50 mumol/L) or bovine serum albumin (BSA) for 24 hr.

195 (C12E8) and dodecyl maltoside (DDM) protect bovine serum albumin (BSA) from unfolding in SDS.

196 t time, the mechanism of SA interaction with bovine serum albumin (BSA) has been investigated by mult

197 entrapment and in vitro release behaviour of bovine serum albumin (BSA) in chitosan-tripolyphosphate

198 alize the migration of fluorescently labeled bovine serum albumin (BSA) into the nanoslits; and fluor

199 ure-dependent adsorption and denaturation of bovine serum albumin (BSA) protein onto a silica-coated

200 d efficient way; LC-MS of a trypsin-digested bovine serum albumin (BSA) sample provided narrow peaks,

201 A biocompatible nanocomposite including bovine serum albumin (BSA) template Cu nanoclusters (CuN

202 It is demonstrated that the adsorption of bovine serum albumin (BSA) to aqueous gold colloids can

203 We illustrate a method that uses bovine serum albumin (BSA) to control the receptor-acces

204 determining the heat denaturation degree of bovine serum albumin (BSA) was assessed.

205 In this system, bovine serum albumin (BSA) was immobilized on gold grids

206 The interaction between Allura Red and bovine serum albumin (BSA) was studied in vitro at pH 7.

207 ) were immobilized via EDC-NHS chemistry and Bovine serum albumin (BSA) was used for blocking of the

208 adsorption followed by a post-treatment with bovine serum albumin (BSA) which served as the blocking

209 this study, we evaluated the interaction of bovine serum albumin (BSA) with AP and AS using surface

210 ns (Trypsin Inhibitor (TI); Ovalbumin (OVA); Bovine Serum Albumin (BSA)), we observe resolution of th

211 Compared to Y-tube compartments with bovine serum albumin (BSA), GDNF and NGF increased the m

212 eting proteins including chymotrypsin (chy), bovine serum albumin (BSA), lysozyme (lyz) and cytochrom

213 r both deposited gold film and adsorption of bovine serum albumin (BSA), respectively, on poly(methyl

214 Bovine serum albumin (BSA), whey protein isolate (WPI),

215 lass in a simulated biothreat scenario using bovine serum albumin (BSA).

216 s) were prepared from inherent biocompatible bovine serum albumin (BSA).

217 adical polymerization from the model protein bovine serum albumin (BSA).

218 Bovine serum albumin (BSA)/curcumin binding and dye phot

219 ve activity of extracts was evaluated in the bovine serum albumin (BSA)/glucose system.

220 esented as densely immobilized conjugates of bovine serum albumin (DNP-BSA) or mobile in a supported

221 We encapsulated fluorescent-bovine serum albumin (FITC-BSA) inside the gel.

222 A simple post-adsorption of human serum:bovine serum albumin (HS:BSA) mixtures onto the folic ac

223 Methylated-bovine serum albumin (mBSA), but not vehicle challenge,

224 uantum clusters (AuQC@BSA) synthesized using bovine serum albumin and conjugated with acetylcholinest

225 onstrated via the covalent immobilization of bovine serum albumin antibody (anti-BSA) and fibrinogen

226 s of cytochrome c, ubiquitin, myoglobin, and bovine serum albumin formed by electrospray ionization a

227 ured on a test line comprised of the protein bovine serum albumin immobilized on nitrocellulose.

228 ue unaltered when the assay was processed in bovine serum albumin or human serum.

229 gg yolk and positive co-protein effects with bovine serum albumin, (S-)ovalbumin, egg white, whole eg

230 polypropylene glycol (PPG), angiotensin II, bovine serum albumin, and the "thermometer" compound p-m

231 the extent of supercharging was probed using bovine serum albumin, beta-lactoglobulin, and lysozyme,

232 t analysis of peptides from trypsin digested bovine serum albumin.

233 by E. coli cells and does not interact with bovine serum albumin.

234 phosphine-derivatized fluorophore-conjugated bovine serum albumin.

235 e and in combination of calcium alginate and bovine serum albumin.

236 ng selected the affinity interaction between bovine serum albumine (BSA) with anti-BSA antibody (AB)

237 valuated using Escherichia coli bacteria and bovine serum albumine (BSA).

238 erein alpha-MEM (supplemented with 10% fetal bovine serum and 1% antibiotic-antimycotic) was perfused

239 erein alpha-MEM (supplemented with 10% fetal bovine serum and 1% antibiotic-antimycotic) was perfused

240 leukocyte chemoattractant was isolated from bovine serum by an established four-step purification pr

241 rcity of bone marrow donors, and reliance on bovine serum during mesenchymal stem/stromal cell prolif

242 n, with sensitivities of 77%, 45%, and 9% in bovine serum samples from the United Kingdom (n = 126),

243 the H2O2 detection in the disinfected fetal bovine serum samples, and the recovery was obtained abou

244 n cultured in the presence of 10% FBS (fetal bovine serum), with a replication time of 1-3 weeks.

245 on of H2S spiked in whole human blood, fetal bovine serum, and E. coli.

246 ntibiotic/antimycotic solution and 10% fetal bovine serum, and incubated for 24 hours.

247 ity toward Cys-SeH in aqueous PBS buffer, in bovine serum, and on the silica gel surface that lead to

248 should be avoided because of the presence of bovine serum, but the tissue can be washed using balance

249 We find that cells cultured in adult bovine serum, which better reflects nutrients available

250 and is identical in aqueous buffer and fetal bovine serum.

251 fail to proliferate in the absence of fetal bovine serum.

252 as mouse-derived 3T3 feeder cells and fetal bovine serum.

253 nor fraction of EDA2 was also found in fetal bovine serum.

254 Ralpha) positive progenitor cells from fetal bovine skeletal muscle and induced into adipocytes.

255 e, we report striking collective swimming of bovine sperm in dynamic clusters, enabled by the viscoel

256 However, since the bovine spongiform encephalopathy (BSE) crisis, their use

257 Chronic wasting disease (CWD) in cervids and bovine spongiform encephalopathy (BSE) in cattle are pri

258 ion diseases of cattle include the classical bovine spongiform encephalopathy (C-BSE) and the atypica

259 mals meals in feedstuffs in order to prevent Bovine Spongiform Encephalopathy infection and diffusion

260 y experimental challenge and the outbreak of bovine spongiform encephalopathy that occurred in the la

261 the human form of a prion disease of cattle, bovine spongiform encephalopathy-have been reported from

262 n ovine strains, compared to five modules in bovine strains (C-type).

263 inhibits mitogen-activated proliferation of bovine T cells and, to a lesser extent, proliferation of

264 hree stains, was used to develop microCT for bovine tail IVD using laboratory and synchrotron sources

265 l campaigns, there are sporadic outbreaks of bovine TB in regions declared TB free.

266 respective oligosaccharides were obtained by bovine testicular hyaluronidase digestion.

267 In bovine, the use of ART can induce a similar overgrowth c

268 files for alpha-Gal-containing analytes CTX, bovine thyroglobulin (Bos d TG), and human serum albumin

269 entified as a key inhibitory modification in bovine tissue approximately 50 years ago, and this regul

270 We previously purified TBCD from bovine tissues and showed that it tightly binds the smal

271 rmectin B1a in fat, kidney, liver and muscle bovine tissues using UHPLC-MS/MS.

272 , benzo[k]fluoranthene and benzo[a]pyrene in bovine tissues.

273 Building on our previous research that bovine TLR5 (bTLR5) is functional, we compared human and

274 (bTLR5) is functional, we compared human and bovine TLR5 activity and signalling in cognate cell line

275 achol demonstrated similar sensitivities for bovine tracheal force development and phosphorylation of

276 er, MBS85, was enriched in mouse, as well as bovine tracheal smooth muscle.

277 ation by electric field stimulation (EFS) in bovine tracheal smooth muscle.

278 sequencing (RNA-Seq) was used to explore the bovine transcriptome from the mammary tissue of 12 Chine

279 compared with those produced from commercial bovine trypsin (HB).

280 adgers (Meles meles) naturally infected with bovine tuberculosis (bTB) at Woodchester Park in Glouces

281 e largest molecular epidemiological study of Bovine Tuberculosis (bTB) in a sub-Saharan African count

282 Bovine tuberculosis (bTB) is a chronic disease of cattle

283 cant social and economic loss as a result of bovine tuberculosis (bTB) presents a continuous challeng

284 er is recognised as a wildlife reservoir for bovine tuberculosis (bTB); the control of which is compl

285 Bovine tuberculosis (TB) is a zoonotic disease caused by

286 species and the main wildlife reservoir for bovine tuberculosis infection in cattle.

287 tant reassessment, especially in areas where bovine tuberculosis is endemic and where people live in

288 burden of Mycobacterium bovis, the cause of bovine tuberculosis, might be underestimated in human be

289 roles for the cytokines IL-17A and IL-22 in bovine tuberculosis, where they show potential as both p

290 -studied wildlife systems such as rabies and bovine tuberculosis.

291 A chimeric bovine viral diarrhea virus construct containing an HEV

292 iridae(yellow fever virus, dengue virus, and bovine viral diarrhea virus) and a human coronavirus (OC

293 al virus, infectious bovine rhinotracheitis, bovine viral diarrhea virus, Mannheimia haemolytica or M

294 All beaches had detections of human and bovine viruses and pathogenic bacteria indicating influe

295 in four microbial categories (human viruses, bovine viruses, protozoa, and pathogenic bacteria).

296 s of acid camel whey, even if acid and sweet bovine whey exhibited the highest viscoelastic modulus a

297 Camel and bovine whey proteins were affected by a heat treatment o

298 acial properties of acid camel whey and acid bovine whey were preserved at air water interface even a

299 o natural samples extracted from a ruminant (bovine), which serve as common origins of trans fatty ac

300 In these studies, we have immunized these bovines with different VEEV immunogens and evaluated the