ライフサイエンスコーパス: bovine

1 while utilizing 10 times less DNA in the Tc bovine.

2 of the bone points are made from cervids and bovines.

3 31.27%, P = 0.49), residual graft material (bovine = 20.47%, porcine = 19.52%, P = 0.82) and connect

4 for mean percentage of vital bone formation (bovine = 36.21%, porcine = 31.27%, P = 0.49), residual g

5 .52%, P = 0.82) and connective tissue/other (bovine = 43.32%, porcine = 49.21%, P = 0.19).

6 erwent AWR using either porcine ADM(PADM) or bovine ADM(BADM) from 2005 to 2019.

7 Analysis of freshly isolated bovine adrenal vesicles shows that the size and internal

8 Bovine alphaherpesvirus 1 (BoHV-1) is an important patho

9 ro co-culture model, comprising immortalised bovine alveolar type II (BATII) epithelial cells and bov

10 The structures of the bovine and human BBSome reveal that a conformational cha

11 arity in the regulatory circuitry underlying bovine and human EGA compared to mouse.

12 al resistant (AMR) S. enterica isolates from bovine and human hosts in New York and Washington states

13 e of large-scale transposition in genomes of bovine and human isolates at different times.

14 enes (e.g., virulence genes) associated with bovine and human isolates.

15 nN) as an EC mitogen and survival factor for bovine and human microvascular EC, with an additivity wi

16 to degradation by four different nucleases, bovine and human serum, and human urine.

17 form of CAPG (91% sequence identity between bovine and human) was produced and bovine endometrial ep

18 ketoprofen by equine SA to binding of it by bovine and leporine SAs.

19 ototheca zopfii GT-II (but not GT-I) invaded bovine and murine mammary epithelial cells (MECs) and in

20 nic solvent extractions for the detection of bovine and non-dairy milks based on lipids fingerprint b

21 Comparison of eight isolates of bovine and ovine origin at three key time-points (2 h, 4

22 nd non-pathogenic M. haemolytica isolates of bovine and ovine origin.

23 y, is extracted from bone and skin of mainly bovine and porcine origins.

24 egies that may help to prevent the spread of bovine and zoonotic TB.

25 vaccines, passive countermeasures (e.g., Tc bovine), and as a means to produce more potent DNA-launc

26 We show for the first time that isolated bovine antibody knob domains can function as autonomous

27 olation of small, cysteine-rich domains from bovine antibody ultralong complementarity-determining re

28 g milks from a variety of mammals, including bovine, Asian buffalo, African lion, and goat.

29 m 1999 to 2016 from either human clinical or bovine-associated sources in NYS were characterized usin

30 icroscopy (cryo-EM) structures of the native bovine BBSome in inactive and active states at 3.1 and 3

31 Bovine BCMs 3 to 7 and human BCMs 3 to 9 were searched.

32 Bovine BCMs 3, 4, 6 and 7 were found in the undigested f

33 he digestive conditions of premature infant, bovine BCMs still occurred in fortified PDHM; the human

34 Here we report cryo-EM structures of bovine bestrophin-2 (bBest2) bound and unbound by Ca(2+)

35 Recently, a role for bovine beta-casein A1 has been proposed.

36 iscomfort due to either lactose or differing bovine beta-casein types.

37 Bovine beta-lactoglobulin (BLG), the main whey protein,

38 Ticks were fed on bovine blood containing 10-fold dilutions of the pathoge

39 on (ABR) and orthodontic tooth movement into bovine bone (BB) regenerated sites.

40 d 23 adjacent to the fenestration defects on bovine bone blocks.

41 trometry (HPLC/MS) was used to differentiate bovine bone gelatin from gelatin derived from bovine ski

42 bdivided into test and control groups: Test: bovine bone graft associated with porcine collagen and c

43 gen and collagen membrane was used; control: bovine bone graft associated with porcine collagen was u

44 beta-TCP), biphasic calcium phosphate (BCP), bovine bone mineral (BBM) or blood clot.

45 Deproteinized bovine bone mineral (DBBM) has been extensively studied

46 the extra-oral approach, where deproteinized bovine bone mineral (DBBM) particles were placed contral

47 yo-EM structures of the intact V-ATPase from bovine brain with all the subunits including the subunit

48 ve proteomic distances between three Spanish bovine breeds (Asturiana de los Valles, AV; Retinta, RE;

49 Others - using bovine CA (bCA), untagged NBCe1-A, and protocols keeping

50 ed for 24 hours with and without recombinant bovine CAPG (rbCAPG).

51 Treatment of hEECs with bovine CAPG increased expression of transcripts previous

52 activity supported by rabbit skeletal and by bovine cardiac myosin.

53 Six weeks after sensitization to bovine casein, mice received four, monthly IN immunizati

54 e that contains cross-reactive epitopes with bovine caseins.

55 period) on cellular metabolism in activated bovine CD4(+) T cells.

56 Previous studies in bovine cells demonstrated that deletions (leaderless [LL

57 diate for rat and human cells and lowest for bovine cells.

58 at late times during productive infection of bovine cells.

59 able to hydrolyze kappa-casein similarly to bovine chymosin.

60 hat observed in the cryo-EM structure of the bovine CLC-K channel, though the volume of the intracell

61 We evaluated the stability of AVX-470, a bovine colostral anti-tumor necrosis factor (TNF) polycl

62 Bovine colostral antibodies, purified from cow's milk pr

63 Results from a bovine corneal opacity and permeability test demonstrate

64 mic respiratory CoV infections of livestock: bovine coronavirus (BCoV) and porcine respiratory corona

65 OC43 apparently emerged from a bovine coronavirus (BCoV) spillover.

66 oductive and respiratory syndrome (PRRS) and bovine coronavirus viruses.

67 S-CoV-2 RNA as well as coronavirus recovery (bovine coronavirus) and fecal strength (pepper mild mott

68 erestingly, yeast, mouse liver, and isolated bovine cytochrome c oxidase were directly inhibited by t

69 Forty bovine dental discs (6 cm x4 cm) were pigmentated and ra

70 Bovine derived chymosin in rennet cannot coagulate camel

71 previously reported architectures of fly and bovine DHX36.

72 Bovine digital dermatitis (BDD), an infectious disease o

73 The structure of the bovine dimer also demonstrates that the structures of di

74 s is associated with the RNAs present in the bovine embryo prior to EGA.

75 diting efficiency at three different loci in bovine embryos and decreased levels of mosaicism relativ

76 ced genome editing reagents into single-cell bovine embryos to compare the effect of Cas9 mRNA and pr

77 of H3K9me3, 5mC, and 5hmC in preimplantation bovine embryos.

78 We find that bovine endometrial and skin fibroblasts are more resista

79 y between bovine and human) was produced and bovine endometrial epithelial (bEECs) and stromal (bESCs

80 characterization of aqueous solutions of the bovine eye lens protein beta(H) crystallin from dilute c

81 associated with corresponding reductions in bovine fecal prevalence of ciprofloxacin-resistant E. co

82 Intramammary administration of two doses of bovine fetal AT-MSCs in healthy cows did not induce chan

83 ramammarily with a 2.5 x 10(7)-suspension of bovine fetal AT-MSCs on experimental days 1 and 10.

84 for different glycan types was studied using bovine fetuin, asialofetuin, IgG, ribonuclease B, and al

85 specifically and dose dependently adhered to bovine fibrinogen.

86 First, we showed that the treatment of bovine fibroblasts with UNC0638 did mitigate the levels

87 ibute to the somatosensory flavor profile of bovine fluid milk products were investigated.

88 rmatitis (BDD), an infectious disease of the bovine foot with a predominant treponemal etiology, is a

89 lizing antibodies in a transchromosomic (Tc) bovine for use as a passive immunoprophylactic.

90 A recombinant bovine form of CAPG (91% sequence identity between bovin

91 issue culture infective dose (TCID(50)) of D/bovine/France/5920/2014 (D/OK-like).

92 Bovine full-depth articular cartilage explants were load

93 s and cultural concerns, because porcine and bovine gelatins are prohibited in Halal, Kosher and Hind

94 Origin of bovine gelatins in different test samples were predicted

95 ene constructs at a specific location of the bovine genome and contribute to the next generation of e

96 ing three loci (POLLED, H11, and ZFX) in the bovine genome and saw a significantly higher rate of mut

97 date the increasing amount and complexity of bovine genomics data, BGD continues to advance its pract

98 o survey the XO and PAO activities in human, bovine, goat and camel milk samples, and it can be readi

99 ect (CSD) when combined with a deproteinized bovine graft (DBG) material.

100 directly affects the function of luteinized bovine granulosa cells (LGCs), a model for large-luteal

101 For this, bovine granulosa cells from smaller follicles were cultu

102 cipher the cellular and EV-coupled miRNAs of bovine granulosa cells in response to HS.

103 ed patients completed the study, 17 from the bovine group and 21 from the porcine group.

104 The LPO activities ranked as bovine > goat > camel > human in the four types of milk

105 to be present in multiple animal hosts, and bovines have been identified as its natural reservoir.

106 Bovines have been proposed to be the primary host, and t

107 ignificantly faster (5-10 times) than in the bovine heart enzyme.

108 he basis of studies with CytcO isolated from bovine heart mitochondria, it was suggested that in mito

109 is of an artificially oxidized CL extract of bovine heart.

110 roteins (e.g., horseradish peroxidase (HRP), bovine hemoglobin, immunoglobulin G, and glucose oxidase

111 hways of oxidation and glucose metabolism in bovine hepatocytes exposed to increasing concentrations

112 orticosteroid dexamethasone (DEX) stimulates bovine herpesvirus 1 (BoHV-1) and herpes simplex virus 1

113 Alphaherpesvirinae subfamily members such as bovine herpesvirus 1 (BoHV-1) and herpes simplex virus 1

114 incidence of reproductive failure.IMPORTANCE Bovine herpesvirus 1 (BoHV-1) is the most frequently dia

115 An important site for bovine herpesvirus 1 (BoHV-1) latency is sensory neurons

116 ssion following stressful stimuli.IMPORTANCE Bovine herpesvirus 1 (BoHV-1), an important bovine patho

117 in vitro system were able to infect a naive bovine host.

118 ing on genetically susceptible and resistant bovine hosts and their corresponding proteomes.

119 tion with RSV or with a chimeric recombinant bovine/human parainfluenza virus type 3 (rB/HPIV3) vecto

120 Bovine IgG1 antibodies, the primary component of AVX-470

121 This infliximab-bovine IgG1 chimera (bovinized infliximab) retained the

122 sequences from these regions, including the bovine IgG1 hinge region and a predicted disulfide bondi

123 In contrast, bovine IgG2 and human IgG1 antibodies were cleaved rapid

124 is known about the role of serotonin in the bovine immune system.

125 cription unit 1 (IEtu1) promoter that drives bovine infected cell protein 0 (bICP0) and bICP4 express

126 o viral transcriptional regulatory proteins, bovine infected cell protein 0 (bICP0) and bICP4.

127 portantly, the JH analog methoprene, but not bovine insulin (to restore IIS) and amino acids (to rest

128 Here, we studied the structure of native bovine IRBP in complex with a monoclonal antibody (mAb5)

129 Notably, bovine isolates contained significantly more transposase

130 ore, a trained panel evaluated the effect of bovine lactoferrin (LF) on NG bitterness using time-inte

131 The removal of cationic proteins from bovine lactoserum markedly reduced its capacity to induc

132 e protozoan parasite genus Theileria infects bovine leukocytes and induces their uncontrolled prolife

133 Beta-lactoglobulin (BLG) is a bovine lipocalin in milk with an innate defense function

134 luated using standard reference materials of bovine liver and bovine muscle.

135 eaction and the decomposition of H(2)O(2) by bovine liver catalase.

136 Bovine lung tissue homogenate was selected as a surrogat

137 sphorylation of DRP1 on Ser616 and Ser637 in bovine luteal cells.

138 Bovine luteal LDs are distinct from LDs in other bovine

139 Bovine luteal tissue contained abundant lipid droplets,

140 e that were non-essential for persistence in bovine lymph nodes.

141 Bovine lysozyme (BvLz) is a potent broad-spectrum antimi

142 heating were characterised and compared for bovine masseter (fibre type I) and cutaneous trunci (fib

143 Staphylococcus aureus are a common cause of bovine mastitis and can result in both clinical (CM) or

144 ction of E. coli are of great importance for bovine mastitis control and milk quality monitoring.

145 Bovine mastitis is the most economically important infec

146 ntibiotics are effective in the treatment of bovine mastitis, they do not address the regeneration of

147 ostics tools to identify S. aureus CC during bovine mastitis.

148 zopfii is an alga increasingly isolated from bovine mastitis.

149 for on-site detection and field diagnosis of bovine mastitis.

150 ed intramammary therapy for the treatment of bovine mastitis.

151 promising for on-site pathogen detection of bovine mastitis.

152 st genetic with the heritability of 0.776 in bovine MDM and 0.8 in mouse peritoneal macrophages.

153 erred that the functional characteristics of bovine MDMs are associated with NO-based classification.

154 In the current study, the transcriptome of bovine MDMs was compared between two extreme phenotypes

155 derness or marbling, two major attributes of bovine meat-eating qualities for consumers' satisfaction

156 l microbiome and metabolome of infants fed a bovine MFGM supplemented experimental formula (EF) and c

157 odifications and antigenic response of these bovine milk allergens as induced by non-thermal treatmen

158 asma can be tailored to mitigate the risk of bovine milk allergens in the dairy processing and ingred

159 Bovine milk and human serum (25 muL) spiked with a mixtu

160 The masses of particles in a bovine milk extracellular vesicle (EV) preparation enric

161 Bovine milk fat globule membrane (MFGM) has shown many h

162 Bovine milk lipids can be replaced with cheaper indigeno

163 This is the case for bovine milk where addition of non-dairy milks such as ve

164 human colorectal carcinoma cell culture, raw bovine milk, and Ascaris suum nematode excretions), reco

165 ate and feeding influence the composition of bovine milk, which is further affected by thermal treatm

166 milks origins and to detect foreign milks in bovine milks.

167 e structure of the dimeric ATP synthase from bovine mitochondria determined in three rotational state

168 Production of NO(-) by bovine monocyte-derived macrophage (MDM) and mouse perit

169 scopy to track the conformational changes of bovine MRP1 (bMRP1) in real time.

170 Mineral contents in bovine muscle can affect meat quality, growth, health, a

171 dard reference materials of bovine liver and bovine muscle.

172 ts as they are typically derived from either bovine or porcine animals.

173 1 to receive ridge preservation using either bovine or porcine xenograft material.

174 TriNAG), aptamer, p-aminobenzamidine (pABA), bovine pancreatic ribonuclease A (RNaseA), and uridine-3

175 simulations using trypsin and its inhibitor bovine pancreatic trypsin inhibitor (BPTI) as a model sy

176 Serine protease inhibitors of the Kunitz-bovine pancreatic trypsin inhibitor (BPTI) family are ub

177 ic tail domains with their counterparts from bovine parainfluenza virus type 3 (BPIV3) F protein to d

178 ica, where it is associated with the disease bovine parasitic otitis.

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

180 Bovine pericardium (BP) is a vascular biomaterial used i

181 We established that bovine peripheral leukocytes express all known serotonin

182 Most importantly, bovine PL injection restored beta-cell proliferation and

183 IDVs emerge, evolve, spread, and maintain in bovine populations.

184 g TaqMan probe was developed to discriminate bovine, porcine and fish gelatin species in a single ass

185 we profile changes in open chromatin during bovine preimplantation development.

186 ces observed between the two variants of the bovine protein.

187 a formula containing extensively hydrolyzed bovine proteins (whey and/or casein) with use of any oth

188 lveolar type II (BATII) epithelial cells and bovine pulmonary arterial endothelial cells (BPAECs).

189 BGD now hosts both the newest bovine reference genome assembly, ARS-UCD1.2, as well as

190 tulathromycin use in calves at high risk of bovine respiratory disease (BRD) on antimicrobial resist

191 In this manuscript, we show that bovine respiratory syncytial virus (bRSV), which infects

192 ting early colonization and infection of the bovine respiratory tract.

193 the ideas derived from previous work in the bovine retina that R-type Ca(2+) channels are involved i

194 nts, evolutionary-more distant from template bovine RH1, and provided mechanistic insights into the r

195 colocalize the RSV N protein and p65 within bovine RSV (bRSV) IBs, which are granular, membraneless

196 In both human and bovine RSV-infected cells, we demonstrated that the p65

197 This study investigated the fluctuations of bovine rumen metaproteome utilizing three mid to late-la

198 genomes and gene annotation datasets for non-bovine ruminant species (goat and sheep), support for mu

199 aim was to describe the genetic variation of bovine S. aureus in Europa.

200 This report is the largest dataset of bovine seminal plasma proteins.

201 nd posttranslational modifications (PTMs) in bovine seminal plasma.

202 TROY/RKIP interaction was enhanced by fetal bovine serum (FBS) exposure, and TROY knockdown also led

203 e uniquely sensitive to a component in fetal bovine serum (FBS) identified as serum albumin.

204 ery of near-infrared fluorescent dye-labeled bovine serum albumin (800CW-BSA, used as a model agent).

205 Meanwhile, the introduction of bovine serum albumin (BSA) and antibody (Ab) enhanced th

206 gregation behavior of two model proteins- i) bovine serum albumin (BSA) and ii) beta-galactosidase (b

207 izopus sp.) hydrolyzed iron oxide-associated bovine serum albumin (BSA) and the factors that affected

208 PTL approach with a 4-plex labeled sample of bovine serum albumin (BSA) and yeast lysates mixed at di

209 9, 1.25 mug/mL) after passive adsorption and bovine serum albumin (BSA) as a blocking agent generated

210 e pi (hGSTP), human serum albumin (HSA), and bovine serum albumin (BSA) as model target proteins.

211 linkages of insulin, alpha-lactalbumin, and bovine serum albumin (BSA) as well as the free C34-BSA w

212 the quinazolinone core allowed reduction of bovine serum albumin (BSA) binding (63c, 63d).

213 iffness of protein-based hydrogels made from bovine serum albumin (BSA) by using polyelectrolytes suc

214 del protein Fluorescein isothiocynate (FITC) Bovine Serum Albumin (BSA) conjugate incorporated in the

215 SERS data were collected from a solution of bovine serum albumin (BSA) digested by trypsin as an enz

216 The results of HS-SPME/GC indicated that bovine serum albumin (BSA) had the highest affinity towa

217 lex labeling of a yeast proteome spiked with bovine serum albumin (BSA) over a 10-fold dynamic range.

218 cture play important roles in the ability of bovine serum albumin (BSA) to form stable nanostructures

219 By culture media modifications, bovine serum albumin (BSA) was identified as blocking in

220 yanidin-3-glucoside (CYG) through binding to bovine serum albumin (BSA) was investigated at pH 3.0 us

221 ation of patients, antibodies against native bovine serum albumin (BSA) were detected.

222 In this report, a stepwise unfolding of bovine serum albumin (BSA) with guanidine hydrochloride

223 pitcher-plant leaves at different rates with bovine serum albumin (BSA), a molecular substitute for d

224 research on albumin hydrogels has focused on bovine serum albumin (BSA), leaving human serum albumin

225 en holes in the bilayer were backfilled with bovine serum albumin (BSA).

226 temperature (T(d)) and heat-set gelation of bovine serum albumin (BSA).

227 loped the biomimetic nanoparticles (cationic bovine serum albumin (CBSA) conjugated siS100A4 and exos

228 3 kDa); however, ion mobility resolution for bovine serum albumin (MW ~ 68 kDa) is less than ~20, whi

229 ized to demonstrate protein binding by using bovine serum albumin and detection of antibody-antigen i

230 LMG-bovine serum albumin and rabbit anti-sheep IgG were immo

231 ion of the pressure effect was performed for bovine serum albumin and thyroglobulin that required gra

232 Using sulforhodamine b, zidovudine, and bovine serum albumin as model hydrophilic drugs, we foun

233 ecoveries of the enrichment step from spiked bovine serum albumin digests were >80% for the commercia

234 ects of Centella asiatica phenolics (CAP) on bovine serum albumin glycoxidation in a BSA-glucose mode

235 s of cortisol solutions in a complex matrix (bovine serum albumin in phosphate buffered saline) is al

236 a detection limit of ~110 fg/mL biotinylated bovine serum albumin in serum.

237 retreatment of the particle supernatant with bovine serum albumin mitigates the negative effects of f

238 A bovine serum albumin pretreatment protocol was developed

239 The plasmonic construct consists of a bovine serum albumin scaffold with approximately 210 IRD

240 e validated using IDA in intact and digested bovine serum albumin solutions using the TCN (98 and 100

241 o detect miRNA-21 in human serum albumin and bovine serum albumin was almost identical to that in PBS

242 ples, mid-IR spectra of Escherichia coli and bovine serum albumin were recorded.

243 of the minor (lactoferrin, lactoperoxidase, bovine serum albumin) and major (alpha-lactalbumin, beta

244 ng compounds (sucrose, dopamine, starch, and bovine serum albumin), resulting in negligible cross-rea

245 sor with four reference molecules (dopamine, bovine serum albumin, glucose and elongated peptide) was

246 gh selectivity 1:400 horse radish peroxidase/bovine serum albumin, sensitivity to 100 attomoles, reco

247 A mass balance model based on bovine serum albumin-water (D(BSA/w)) and liposome-water

248 n poorly defined albumin supplements such as bovine serum albumin.

249 tide B spiked in a protein digest mixture of bovine serum albumin.

250 ver nanoparticles in ethanolic solutions and bovine serum albumin.

251 n controlled hydrolysis and precipitation of bovine serum albumin.

252 al RI containing small (glycerol) and large (bovine serum albumin; BSA) analyte molecules, indicating

253 critically important to prevent confounding bovine serum amine oxidase-induced cytotoxicity in mecha

254 re quickly oxidized by the copper-containing bovine serum amine oxidase.

255 ing biofilm formation required coating fetal bovine serum onto the poly(ether sulfone) microdialysis

256 ck-lactide) (mPEG-LA) were unstable in fetal bovine serum, human serum and synovial fluid, with varyi

257 The destabilizing factor in fetal bovine serum, identified as albumin, does not interfere

258 oteases relative to antibodies from human or bovine serum, making them of particular interest as oral

259 ith absorption and emission >700 nm in fetal bovine serum.

260 cell culture systems supplemented with fetal bovine serum.

261 d sulfates in complex urine samples of adult bovines, showing a slight matrix effect.

262 Adding purified bovine sialylated milk oligosaccharides (S-BMO) with str

263 ovine bone gelatin from gelatin derived from bovine skin.

264 Using LH-responsive bovine small luteal cells our results reveal that LH, fo

265 out to investigate the effects of sexing on bovine sperm function and early embryonic development.

266 rtificial insemination the use of sex-sorted bovine sperm results in reduced conception, the causes o

267 en though they were similarly exposed to the bovine spongiform encephalopathy (BSE) agent.

268 ese proteins is strongly regulated since the bovine spongiform encephalopathy (BSE) crisis.

269 Bovine spongiform encephalopathy (BSE) is a TSE that occ

270 Bovine Spongiform Encephalopathy (BSE) is the only anima

271 much lower degree of glycosylation (~60%) - bovine submaxillary mucin - a weaker but still demonstra

272 action (tECM) by urea extraction of juvenile bovine tendons, which is capable of enhancing transformi

273 ation of 105 veterinary drugs in homogenized bovine tissue in both negative and positive ionization m

274 ne luteal LDs are distinct from LDs in other bovine tissues, including follicular steroidogenic cells

275 Whole bovine tissues, isolated ovarian steroidogenic cells (gr

276 tion, we produced transgenic mice carrying a bovine tracheal AMP gene promoter-controlled PG-1 transg

277 r to better understand the spatial spread of bovine tuberculosis (bTB) in Wales, an All Wales Badgers

278 Bovine tuberculosis (bTB) is an economically important d

279 Bovine tuberculosis (BTB) testing in cattle requires a s

280 Bovine tuberculosis (bTB), a zoonosis mainly caused by M

281 outine surveillance in countries endemic for bovine tuberculosis (TB) and limited laboratory support

282 but are also involved in the epidemiology of bovine tuberculosis (TB) in cattle.

283 e the association between badger culling and bovine tuberculosis (TB) incidents in cattle herds in th

284 dapted surveillance and control measures for bovine tuberculosis in Wales.

285 related to the ecology and pathogenicity of bovine tuberculosis is scarce, especially in developing

286 n ridge preservation is accomplished using a bovine versus a porcine xenograft.

287 viral glycans and reduce the infectivity of bovine viral diarrhea and dengue viruses in cellular mod

288 hanism of miRNA dependency of the pestivirus bovine viral diarrhea virus (BVDV).

289 he glass transition temperature of camel and bovine whey powder (at 0.13, 0.23, and 0.33 of water act

290 tron spectroscopy results) in both camel and bovine whey powders regardless the pH (neutral (6.7) or

291 toglobulin was the most denatured protein in bovine whey powders regardless the pH value, while this

292 ity of lactose crystallization for camel and bovine whey powders.

293 Bovine whey protein was hydrolysed using cardosins A and

294 he glass transition temperature of camel and bovine whey protein's powders.

295 en challenged in vivo with the polybacterial bovine wound infection 'digital dermatitis', Zn/Cu-shell

296 tric outcomes and dimensional stability with bovine xenograft.

297 ated sequences as they are homologous to the bovine Y chromosome.

298 d-end reads that are properly aligned to the bovine Y sequence assembly accounted for 46.49%, indicat

299 Mycobacterium bovis (the causative agent of bovine/zoonotic tuberculosis, bTB) infection.

300 nal HR donor template or an HMEJ template in bovine zygotes.