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1 in to globally map miRNA interactions in the cow.
2 potent serum antibody responses in all four cows.
3 w infections in the healthy mammary gland of cows.
4 of 44 milk traits in 1,246 Canadian Holstein cows.
5 itis is a widely spread disease of lactating cows.
6 certified organic or conventional grass-fed cows.
7 nstitute the main pathology afflicting dairy cows.
8 ry of Georgia after they were exposed to ill cows.
9 teric methane emission in lactating Holstein cows.
10 ere also about 30% less for the 3NOP-treated cows.
11 the blood of humans, horses, dogs, cats, and cows.
12 ria from clinical mastitic milk samples from cows.
13 rains to proliferate in the genital tract of cows.
14 lk from Friesian, Jersey and FriesianxJersey cows.
15 p; 119 bp, poultry; 183 bp, pork; 212 bp and cow; 271 bp) of the mitochondrial cyt b, lectin, 12S rRN
16 was applied to goat (69.03+/-6.23mg GAE/L), cow (49.00+/-10.77mg GAE/L), sheep (167.6+/-58.77mg GAE/
20 ve significantly more bioavailable GABA than cow and human milks and are able to activate GABArho rec
21 probe sequences that specifically recognise cow and pig components, against the backdrop of myostati
23 el included the daily life events of a dairy cow and reflects several current dairy management proces
25 the remodelled pulmonary arterioles of rats, cows and humans susceptible to hypoxia-induced pulmonary
28 all bowel was obtained from deceased humans, cows, and sheep supported with a continuous-flow LVAD (n
29 submucosa of the jejunum of human patients, cows, and sheep supported with a continuous-flow LVAD.
30 lude horses, rodents, bats, colobus monkeys, cows, and, most recently, catsharks, shedding new light
32 generated from three individual multiparous cows at 13 time points over the first three months of la
34 n. gambiae s.s. feeding on human compared to cow blood, whereas the more zoophilic An. arabiensis had
36 Meleagris meleagris), pork (Sus scrofa), and cow (Bos taurus) specific primers that amplify fragments
39 methane emissions from high-producing dairy cows by 30% and increased body weight gain without negat
41 es bat (Chiroptera), horse (Perissodactyla), cow (Cetartiodactyla), and dog (Carnivora), and extracte
43 usion of antibiotics in the mammary gland of cows consumes 11 tons/year of medically relevant antimic
49 xes and cheeses, allows for an estimation of cow DNA in a dynamic range varying from 0.1-5% to 1-25%.
53 in these environments can be a primary goal (cow dung mixing) or an unintended consequence (anaerobic
54 onments, including mixing arsenic waste with cow dung, landfills, anaerobic digesters, and pond sedim
55 hough extinction of these last remaining sea cows during early years of the Pacific maritime fur trad
57 f drops in the number of calvings among beef cows during the Bluetongue epizootic of 2007 and 2008, b
58 ms regulating bovine milk synthesis in dairy cows fed high forage rations with different basal forage
59 milk and cream made from milk obtained from cows fed indoors, and by early or late grazing, in alpin
62 inal cells from four soy formula-fed and six cow formula-fed girls from the Infant Feeding and Early
64 s in methylation between soy formula-fed and cow formula-fed infants at three CpGs in the gene prolin
66 l, archaeal, and fungal communities of dairy cows from 2 weeks to the middle of first lactation (>2 y
70 hemistry, for rapid identification of DNA of cow, goat, sheep and buffalo in dairy products, and for
75 A monoclonal antibody isolated from this cow harboured an ultralong HCDR3 of 60 amino acids and n
76 ritical role in the milk production of dairy cows; however, the mechanisms regulating bovine milk syn
78 nowledge of mammary gland immune protection, cows immunized either intramuscularly or intramammarily
79 ethodology enabled the detection of DNA from cow in mixes of milk and cheeses with a limit of detecti
81 was developed on 201 samples collected from cows in early and late lactation, and was successively u
82 used to predict TA on samples collected from cows in early lactation and in samples with high somatic
85 predicting enteric CH4 emissions from dairy cows in North America (NA), Europe (EU), and Australia a
86 te to which plant compounds of concern dairy cows in the Netherlands are exposed, a ranking filter mo
87 exposure to an orthopoxvirus was detected in cows in the patients' herd and in captured rodents and s
88 The demand for dairy products from grass-fed cows is driven, in part, by their more desirable fatty a
89 respiratory and gastrointestinal disease in cows, is the type member of the Bocaparvovirus genus of
90 e highest homology with a GBS strain causing cow mastitis and that the 1992 ST-1 strain differed from
94 s of 36 samples from different categories of cow milk (brands, batches, and fat percentages) with exp
95 L; 1.7 mug vitamin D/100 mL) or nonfortified cow milk (CM) (0.02 mg Fe/100 mL; no vitamin D) for 20 w
97 ncow milk contains less protein and fat than cow milk and may not have the same effect on height.We s
98 fficiently digested compared to caseins from cow milk and peptide profiles from goat milk were distin
99 lex matrices such as milk (whole and skimmed cow milk and semi-skimmed goat milk) and yogurt (an unsw
101 ultaneous quantification of 15 mycotoxins in cow milk by liquid chromatography-mass spectrometry, is
102 detection of five common adulterants in raw cow milk by using attenuated total reflectance (ATR) mid
104 on analysis was conducted to explore whether cow milk consumption mediated the association between no
105 lower height in childhood and assess whether cow milk consumption mediates the relation between nonco
108 tract to enhance the shelf life of anhydrous cow milk fat was evaluated by measuring Free Fatty Acids
109 cts of seasonal variations and processing on cow milk fat, raw milk collected in six individual month
114 g of bottle-fed infants with high volumes of cow milk in late infancy may have a persisting effect on
115 lting curves of amplicons and percentages of cow milk in milk mixes and cheeses, allows for an estima
116 n determining the geographical origin of raw cow milk in Peninsular Malaysia had been investigated in
122 5) of 1:1, 2:1, and 1:2 (12)C-/(13)C-labeled cow milk samples showed that 95.7%, 94.3%, and 93.2% of
124 e libraries obtained from two mixed goat and cow milk samples, one buffalo mozzarella cheese, one goa
126 Thermal stability of beetroot betalains in cow milk was determined during heating at 70-90 degrees
132 , >/=600 mL formula milk/d (FMhigh), <600 mL cow milk/d (CMlow), and >/=600 mL cow milk/d (CMhigh).
133 ming 3 cups noncow milk/d relative to 3 cups cow milk/d was 1.5 cm (95% CI: 0.8, 2.0 cm).Noncow milk
134 LA in several varieties of milk (raw and UHT cows' milk as well as human milk) and infant formulation
135 ither a casein hydrolysate or a conventional cows' milk formula supplemented with 20% of the casein h
139 re invited for clinical evaluation including cows' milk-specific IgE antibodies (IgE), skin prick tes
140 ncentrations of different types of goat- and cow-milk fermented products and evaluate the influence o
141 idation potential of iron fortified goat and cow milks and casein phosphopeptides obtained from each
148 polar lipids was conducted with 19 Holstein cows over the entire milking season using liquid chromat
149 tially expressed between metritis and normal cows (p </= 0.05, fold regulation >/=2 magnitudes).
150 tion systems, only a limited fraction of all cow pats end up on pastures, offering limited scope for
151 Defatted cowpea flour was prepared from cow pea beans and the protein isolate was prepared (CPI)
153 n cows with metritis and normal uterus (four cows per group), integrate miRNAs to their target genes,
154 d wheat bread and sponge cake fortified with cow protein isolates that had been denatured and glycate
157 nococcus albus 8, a common inhabitant of the cow rumen, alludes to a bacterium well-endowed with gene
158 t, by which the betaHBA concentration in the cow's blood and milk samples was determined via fluoresc
159 nce interval (CI): 0.88, 1.03) and intake of cow's milk (<2 cups/day vs. 2 cups/day: aOR = 0.95 (95%
162 tive foods identified by food challenge were cow's milk (64%), wheat (28%), egg (21%) and legumes (7%
168 the frequent ingestion of baked hen's egg or cow's milk accelerates the resolution of hen's egg or co
169 into the diet of children with hen's egg or cow's milk allergies respectively leads to a larger prop
171 and fifty-four infants up to 18 months, with cow's milk allergy (CMA) and/or atopic dermatitis (AD) w
179 mparator; and resolution of the hen's egg or cow's milk allergy as determined by food challenge as th
190 ; children aged 0-18 years with hen's egg or cow's milk allergy; baked hen's egg or cow's milk interv
196 loped celiac disease had increased titers of cow's milk antibodies before the appearance of anti-TG2A
201 the asthma-protective effect of unprocessed cow's milk consumption in a birth cohort and to determin
203 ysis using alpha-casein as the biomarker for cow's milk detection, to be used directly in final rinse
204 Every fifth product contained quantities of cow's milk exceeding an amount where approximately 10% o
210 gg or cow's milk allergy; baked hen's egg or cow's milk intervention with or without a comparator; an
211 ether the introduction of baked hen's egg or cow's milk into the diet of children with hen's egg or c
213 s to cow's milk were very likely to tolerate cow's milk one year after diagnosis, whereas only half o
215 83% of the patients who avoided chicken egg, cow's milk or wheat were advised by their doctors to do
216 mended as 'cow's milk-free' were bought, and cow's milk protein levels were measured using ELISA.
220 sis that the ingestion of baked hen's egg or cow's milk results in more patients outgrowing their hen
222 olute risk difference for the acquisition of cow's milk tolerance was 0.20 (95% CI, 0.05-0.35; P < .0
224 inant allergenic proteins from hen's egg and cow's milk were spotted on silicon chips coated with cop
225 ts without detectable specific antibodies to cow's milk were very likely to tolerate cow's milk one y
227 nut, (2) eosinophilic esophagitis related to cow's milk, and (3) delayed anaphylaxis to red meat.
231 f-reported lifetime prevalence of allergy to cow's milk, egg, wheat, soy, peanut, tree nuts, fish, an
232 valence of food-challenge-defined allergy to cow's milk, egg, wheat, soy, peanut, tree nuts, fish, an
233 ergoing open food challenges to hen's egg or cow's milk, either fresh or extensively heated into a mu
234 4 from dog, Fel d 4 from cats, Bos d 5 from cow's milk, Equ c 1 from horses, and Mus m 1 from mice,
236 s with objectively diagnosed food allergy to cow's milk, hen's egg, and/or wheat were recruited at an
237 year after diagnosis, 69% (22/32) tolerated cow's milk, including all children with non-IgE-associat
238 quential introduction of 6 allergenic foods: cow's milk, peanut, hard-boiled hen's egg, sesame, white
239 Se(VI) and some food samples including beer, cow's milk, red wine, mixed fruit juice, date, apple, or
240 of six allergenic foods (peanut, cooked egg, cow's milk, sesame, whitefish, and wheat; early-introduc
241 L of the ImmunoCAP system, whereas for total cow's milk, the silicon microarray was less sensitive.
242 ") of nine food items including chicken egg, cow's milk, wheat, soy bean, rice, buckwheat, peanut, se
243 ceeding an amount where approximately 10% of cow's milk-allergic children will show clinical relevant
246 extensively hydrolyzed formula compared with cow's milk-based formula would decrease the risk for cel
251 total/specific IgE; however, pHF-OS reduced cow's milk-specific IgG1 (P < 0.0001) and increased regu
256 t included sire(s) of bulls (SB), sire(s) of cows (SC), dam(s) of bulls (DB), and dam(s) of cows (DC)
257 r) for the Clinical Opiate Withdrawal Scale (COWS) score (taper mean, 5.19 [SE, .26]; post-taper mean
263 ignificantly higher in samples obtained from cows that received the isoflavone extract-supplemented d
265 real-time PCR to determine the impact of dry cow therapy without antibiotics on milk microbiome and b
266 H, high-quality) diets were fed to lactating cows to explore how forage quality affected the molecula
268 the transfer of contaminants from the mother cows to their suckling calf and the uptake of soil by gr
269 uberis mastitis in the United Kingdom, with cow-to-cow transmission of S. uberis potentially occurri
271 mastitis in the United Kingdom, with cow-to-cow transmission of S. uberis potentially occurring in t
273 verage, the body weight gain of 3NOP-treated cows was 80% greater than control cows during the 12-wk
274 provides information on the health stress in cows well before any external symptoms are observable.
276 tion, betaHBA in blood and milk samples from cows were successfully measured by this novel technology
278 ht correlation was found (R(2)>0.99) between cow whey percentages and mass spectrometry measurements
281 nt of vitamin B1 was observed between single cows, which ranged from 0.24mg/L up to 0.54mg/L of total
283 ing system, and pasture feeding conventional cows will remove differences previously reported for org
284 fect of supplementing a basal diet for dairy cows with "Soybean extract 40" (Biomedica, Prague, Czech
285 om the mammary tissue of 12 Chinese Holstein cows with 6 extremely high and 6 low phenotypic values f
287 ic and eicosapentaenoic acids were found for cows with a low proportion of BS genetics (0-24% and/or
290 ynomolgus monkeys were fed brain of (eleven) cows with bovine spongiform encephalopathy, and some wer
292 the right choice of the antibiotic to treat cows with mastitis could be determined based on the nake
293 ify differentially expressed serum miRNAs in cows with metritis and normal uterus (four cows per grou
294 nd bta-miR-10a were highly down-regulated in cows with metritis compared to cows with normal uterus.
297 profiles of peripheral blood lymphocytes in cows with S. aureus subclinical mastitis (SA group) and
299 is mastitis cases that occurred in different cows within the same herd and were attributed to a commo
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