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1 d after provocation (unilateral cooling, one calf).
2 losis and pregnancy or being observed with a calf.
3 laque of FDH on her left posterior thigh and calf.
4 PIV-3 causes respiratory infections in young calves.
5 not been in direct contact with pigs or veal calves.
6  of ORF2 does not reactivate from latency in calves.
7 essed in cells isolated from PT32-challenged calves.
8 The rate of false negatives varied among the calves.
9 d, peaking at 21 days, in PT21/28-challenged calves.
10 e performed in lymph nodes of MCF-developing calves.
11 onmental areas used for feeding and watering calves.
12 stently induces reactivation from latency in calves.
13 d in trigeminal ganglia of latently infected calves.
14 hat in small intestinal tissue from the same calves.
15 6 h after DEX treatment of latently infected calves.
16 identified in the microbiota of pre-ruminant calves.
17  infected calves than in those of uninfected calves.
18 ssed in sensory neurons of latently infected calves.
19 dding, diarrhea, and dehydration in neonatal calves.
20 tently infected calves but not in uninfected calves.
21  infected nasal discharge from the treatment calves.
22 atenin-positive neurons in latently infected calves.
23 borns with diminished transfer to subsequent calves.
24 of latently infected, but not mock-infected, calves.
25  Charcot-Marie-Tooth 1A thigh -0.3 pu [0.1], calf -0.7 pu [0.1]).
26 sitis thigh -1.5 percentage units [pu; 0.2], calf -1.1 pu [0.2]; Charcot-Marie-Tooth 1A thigh -0.3 pu
27 , the alphaIIb lower leg is bent between the calf-1 and calf-2 domains and the beta3 Integrin-Epiderm
28 nd cell biological interactions suggest that CALF-1 couples intracellular traffic to functional matur
29  sEGFR and alpha5-integrin and a role of the calf-1 domain in cell adhesion.
30 59 N-glycan at the beta3-I-EGF3 and alphaIIb-calf-1 domain interface, and the beta3-N654 N-glycan at
31 e that the carboxy terminus of sEGFR and the calf-1 domain of alpha5-integrin share a region of seque
32 lfide "clamp" between the alphaIIb thigh and calf-1 domains.
33                           Acute induction of calf-1 mobilizes preexisting UNC-2 for delivery to synap
34                                           In calf-1 mutants, UNC-2 is retained in the endoplasmic ret
35 lative to TG prepared from latently infected calves, 11 cellular genes were induced more than 10-fold
36 s oxytetracycline with highest level in veal calves (1718 ng mL(-1)) vs. young bulls (2.8 ng mL(-1)).
37 ; Charcot-Marie-Tooth 1A thigh 1.0 ms [0.3], calf 2.0 ms [0.3]) and MTR reduced compared with control
38 nt role for the region that links the distal calf-2 and beta-tail domains to their respective transme
39 N-glycan at the beta3-beta-tail and alphaIIb-calf-2 domain interface positively regulate the activati
40 IIb lower leg is bent between the calf-1 and calf-2 domains and the beta3 Integrin-Epidermal Growth F
41 l ester groups within the pores also protect CALF-25 from decomposition by water vapor, with crystall
42 m tetraethyl-1,3,6,8-pyrenetetraphosphonate (CALF-25), which contains a new phosphonate monoester lig
43 clusion body myositis thigh 4.0 ms [SE 0.5], calf 3.5 ms [0.6]; Charcot-Marie-Tooth 1A thigh 1.0 ms [
44 dola, cheeses made from raw ewes' milk using calf (A) and kid (B) rennets were compared to those prod
45 ion of diarrhoea and dehydration in neonatal calves, a clinical model of cryptosporidiosis that close
46                    The URT of Holstein dairy calves aged 3 to 35 days revealed to host a highly diver
47 imal (17/48 35% vs. 12/49, 24%, P = 0.27) or calf alone (11/56, 20%, P = 0.08).
48                                  Forearm and calf alpha1-adrenergic vasoconstriction were unimpaired
49   In trigeminal ganglia of latently infected calves, an sncRNA that migrated between nucleotides 20 a
50 d an array with whole-volume coverage of the calf and a phosphorus signal-to-noise ratio of more than
51  on survival and reproduction, and find that calf and fetus survival appear more readily affected tha
52 l and proximal muscles and remained lower in calf and gluteus muscles 4 weeks later.
53 nants from the mother cows to their suckling calf and the uptake of soil by grazing cattle.
54 DS: Volunteer's legs were measured at ankle, calf and thigh following guidance from British nurses an
55 sound and surface EMG were recorded from the calf and tibialis anterior (TA) muscles.
56                                              Calf and vegetable (Cynara cardunculus) rennets were cov
57 h fever and vesiculobullous eruptions on the calves and backs of the hands.
58 y adventitial fibroblasts were isolated from calves and humans with severe PH (PH-Fibs) and from norm
59 scribed previously in studies of gnotobiotic calves and pigs experimentally infected with bovine FLUD
60 ough improved management between susceptible calves and shedding animals may be more effective than e
61 al recessive cardiomyopathy in Poll Hereford calves and Wa3 mice.
62 erent therapeutic protocols applied for veal calves and young bulls enrolled in this study.
63 of severe lower-respiratory tract disease in calves and young children, yet no human vaccine nor effi
64 kness cartilage during bovine growth (fetal, calf, and adult) and human adult aging (young and old);
65 lenged calves, NK cells from PT32-challenged calves, and CD8(+) and gammadelta T cells from both PT21
66 olates from pigs, horses, chickens, and veal calves, and five methicillin-susceptible Staphylococcus
67 a-agonist ractopamine administration in veal calves, and it investigates different strategies applied
68  collected from ERFX-treated and non-treated calves, and the aqueous NH4OH extracts were directly ana
69                           Cattle, especially calves, are the largest contributors, followed by chicke
70 on SvO2, and T2* were each quantified in the calf at 2-s temporal resolution, yielding a dynamic time
71 pillary density was seen within the ischemic calf at 4 weeks (P=0.004).
72 als, and the total bacterial load of newborn calves at day 3 was higher for animals that developed pn
73 ion analysis showed that increased odds of a calf being a BNP case were associated with its dam havin
74                          Decreased odds of a calf being a BNP case were associated with the calf havi
75                                 As controls, calf biopsies of nondiabetic and nonischemic patients un
76                                  Forearm and calf blood flow were evaluated by venous occlusion pleth
77 rm blood flow, forearm vascular conductance, calf blood flow, and calf vascular conductance were simi
78 rm blood flow, forearm vascular conductance, calf blood flow, and calf vascular conductance) were sig
79 rm blood flow, forearm vascular conductance, calf blood flow, and calf vascular conductance) were sig
80 g skills as well as a long and strong mother-calf bond.
81 disease in 20% of all captive Asian elephant calves born in zoos in the United States and Europe sinc
82 eminal ganglion neurons in latently infected calves but not in uninfected calves.
83 show that resistant strains readily colonize calves by contact with contaminated bedding and without
84  which there is a high level of challenge of calves by infected ticks, absence of clinical disease in
85 es that were divided in four groups: healthy calves, calves diagnosed with pneumonia, otitis or both
86 ibling controls 5.7 mm, 2.3 to 9.1, p=0.02), calf circumference (adjusted difference vs community con
87 sk Screening (2002), body weight, midarm and calf circumference, serum albumin, handgrip strength (HG
88 cking in tracheal epithelia of the treatment calves compared to control animals.
89 duced after viral boosting of BCG-vaccinated calves compared to those in BCG-only-vaccinated animals.
90                                   In the PAD calf compartment of human and mouse models, most VEGF165
91 ds of thromboprophylaxis, such as sequential calf compression devices and perioperative low molecular
92 oid dexamethasone (DEX) to latently infected calves consistently induces reactivation from latency.
93                            Latently infected calves consistently reactivate from latency following a
94     At 1 day postinoculation, a seronegative calf (contact animal) was added to each of the treatment
95 -prey ratios, progesterone concentrations or calf-cow ratios.
96 reases in the number of bulls harvested, and calf:cow ratios declined in the Northeastern population
97 P E. coli populations in pens with untreated calves (day 4; P < 0.005).
98 ctor, or a first unprovoked isolated distal (calf) deep vein thrombosis (DVT), has a low risk of recu
99 d the availability of smaller prey (i.e. elk calves, deer).
100 nalysis of hormonally induced milk from this calf demonstrated absence of BLG and a concurrent increa
101 fected ticks, absence of clinical disease in calves despite infection, and a high level of immunity i
102 ted during June to November 2010 for 56 case calves diagnosed with BNP between 17 March and 7 June of
103 were divided in four groups: healthy calves, calves diagnosed with pneumonia, otitis or both diseases
104         The rumen microbiota of pre-ruminant calves displayed a considerable compositional heterogene
105  We show that a 26-amino acid peptide in the calf domain of alpha5-integrin (residues 710-735) is 35%
106  we identified 697 patients with an isolated calf DVT and excluded 313 of these.
107 r diagnosis of a PE suspected at the time of calf DVT diagnosis were excluded.
108 th ultrasonographic detection of an isolated calf DVT from January 1, 2010, to December 31, 2013, at
109                                          The calf DVT involved an axial vein (anterior tibial, poster
110 ous doppler sonography for the evaluation of calf DVT may be limited by patient characteristics such
111 tic anticoagulation and those with a chronic calf DVT, a contraindication to anticoagulation, prior v
112 with central venous catheter-associated DVT, calf DVT, and unsuspected VTE.
113 ic and sonographically proven acute isolated calf DVT.
114 in 180 days of the diagnosis of the isolated calf DVT.
115 of proximal DVT or PE are low after isolated calf DVT.
116 nship between systolic blood pressure (SBP), calf electromyography (EMG), and resultant center of pre
117 in vivo validation, we produced a transgenic calf, engineered to express these tandem miRNAs.
118 re, during, and after near-maximal isometric calf exercise.
119                                              Calves exhibited similar microbial families and genera b
120 ed the increased alveolar cell thickening in calves experimentally infected with BRSV followed by H.
121     Three of the four CD4(+) T-cell-depleted calves failed to generate an antibody response to the no
122 terized the rumen microbiota of pre-ruminant calves fed milk replacer using two approaches, pyroseque
123 re determined in oat flakes (89.4mug/kg) and calf feed (129.3mug/kg).
124 position of milk replacers typically used in calf feeding.
125 cells from both PT21/28- and PT32-challenged calves following ex vivo restimulation with T3SPs.
126  fibre was placed in the skin of the lateral calf for graded infusions of noradrenaline (norepinephri
127 ta are reported for two muscles in the human calf, for each subject and over a wide range of exercise
128  daughters co-breed, the mortality hazard of calves from older-generation females is 1.7 times that o
129                                          All calves from one farm showed evidence of exposure, while
130 lder-generation females is 1.7 times that of calves from younger-generation females.
131                     Development of the dairy calf gastrointestinal tract (GIT) and its associated mic
132 garding the establishment of microbes in the calf GIT.
133 n therapeutic use of antimicrobials in dairy calves has an appreciable environmental microbiological
134 lf being a BNP case were associated with the calf having been kept outside (OR 0.11, p = 0.006).
135 characterized by distal lower limb weakness, calf hypertrophy and progressive decline in ambulation.
136 icrobiota and that oral supplementation with calf IAP (cIAP) rapidly restores the normal gut flora.
137 ined skin sodium content at the level of the calf in 99 patients with mild to moderate CKD (42 women;
138 was also associated with decreased odds of a calf in that herd being a BNP case (OR 0.97, p = 0.011).
139 ory tract infection, they were mild, and the calves in the treatment group did not differ from the co
140 ed while the core microbiome of pre-ruminant calves included 45 genera.
141 injection of botulinum toxin A (BTxA) in the calf induces paralysis and profound loss of ipsalateral
142 RSV followed by H. somni compared to that in calves infected with BRSV or H. somni alone.
143                            For both cows and calves, ingestion of contaminated soil, although often o
144 on that interleukin-1beta was upregulated in calves inoculated with the hha sepB mutant.
145 ration or the magnitude of fecal shedding in calves inoculated with these strains.
146 hedding in feces of weaned (n = 4 per group) calves inoculated with this mutant strain.
147             We measured reaction kinetics of calf intestinal alkaline phosphatase (CIAP) immobilized
148                                              Calf intestinal alkaline phosphatase (CIP) is examined i
149                                              Calf intestine phosphatase treatment shifted SIBLINGs fr
150  (BPV), identified in the 1960s in diarrheic calves, is the type member of the Bocaparvovirus genus o
151 expression in the trigeminal ganglia (TG) of calves latently infected with BHV-1 versus DEX-treated a
152  within 6 h after dexamethasone treatment of calves latently infected with BHV-1.
153  viral gene expression in sensory neurons of calves latently infected with BoHV-1, culminating in vir
154                                              Calves latently infected with the LR rescued virus but n
155                               In contrast to calves latently infected with wild-type (wt) BHV-1 or th
156 erification of these biomarkers in boars and calves leads to the assumption that gene expression biom
157                                              Calf lens alpha-crystallin binds GRIFIN with relatively
158  detection of lipids in rat liver and bovine calf lens, using MALDI Fourier transform ion cyclotron r
159 ntities were successfully imaged from bovine calf lens, with clear and distinct distribution patterns
160  with Charcot-Marie-Tooth disease 1A, and at calf level (2.6%, 1.3-4.0, p=0.002) and thigh level (3.3
161 gnificantly during the 12-month follow-up at calf level (mean absolute change 1.2%, 95% CI 0.5-1.9, p
162  rumen microbial communities of pre-ruminant calves maintained a stable function and metabolic potent
163 isms suggests that the rumen of pre-ruminant calves may not be rudimentary.
164 combined to create a localized assessment of calf metabolism using phosphorus measurements and vascul
165 fety and clinical efficacy evaluation in the calf model for cryptosporidiosis.
166 ion showed elevated expression of miR-143 in calf models of PAH and in samples from PAH patients.
167 = .001), thigh muscle (r = 0.903; P , .001), calf muscle (r = 0.825; P = .003), and abdominal viscera
168 nces may be attributable to smaller baseline calf muscle area among women with PAD.
169 s in calf skeletal muscle, including smaller calf muscle area, increased calf muscle fat content, imp
170 l adjustment for baseline sex differences in calf muscle area.
171 BF/mean arterial blood pressure), as well as calf muscle blood flow (CalfBF, (1)(3)(3)xenon) and calf
172 nctional decline and more adverse changes in calf muscle characteristics over time.
173                 Computed tomography-assessed calf muscle characteristics were measured biannually.
174                                              Calf muscle characteristics were measured with computed
175               No significant associations of calf muscle characteristics with 6-minute walk outcomes
176 was associated with faster annual decline in calf muscle density (brisk/striding pace -0.32 g/cm(3),
177            This study analyzed whether lower calf muscle density and poorer upper and lower extremity
178 nd women with lower extremity PAD have lower calf muscle density and reduced lower extremity strength
179            These data demonstrate that lower calf muscle density and weaker plantar flexion strength,
180                                        Lower calf muscle density was associated with higher all-cause
181 eline, participants underwent measurement of calf muscle density with computed tomography in addition
182 er functional decline and greater decline in calf muscle density, respectively, in patients with PAD.
183   This result suggests that a more excursive calf muscle facilitates climbing with a bipedally adapte
184 ncluding smaller calf muscle area, increased calf muscle fat content, impaired leg strength, and impa
185 med hypokalemic periodic paralysis underwent calf muscle imaging.
186 400 or 800 islets were transplanted into the calf muscle of WAG/Rij rats (6-8 wk old).
187 ective, reliable clinical tool for measuring calf muscle perfusion in patients with CLI.
188 orrelate of treadmill exercise time, whereas calf muscle perfusion was the best correlate of 6-min wa
189 re is evidence that exercise strengthens the calf muscle pump and improves ankle ROM, few studies hav
190  Patients with venous leg ulcers (VLUs) have calf muscle pump dysfunction, which is associated with r
191 le joint mobility may lead to improvement in calf muscle pump function and subsequent healing.
192 complications is likely a dysfunction of the calf muscle pump, which includes veins and their valves,
193             T1rho- and T2-weighted images of calf muscle were acquired using a modified 3D-SPGR seque
194 ness caused by thixotropic properties of the calf muscle.
195 y promote progenitor cell homing to ischemic calf muscle.
196 g of creatine changes in the exercised human calf muscle.
197  on reversing pathophysiological findings in calf muscle.
198             Muscle length and tension in the calf muscles (gastrocnemius and soleus) are unlikely to
199 round, helping to fulfil one function of the calf muscles and Achilles tendon.
200 stent with the thixotropic properties of the calf muscles causing the observed changes in ankle stiff
201                 The passive stiffness of the calf muscles contributes to standing balance, although t
202 ation of IMCL and EMCL content in individual calf muscles in obese vs. normal healthy human subjects.
203 S reference spectrum and intracellular pH of calf muscles in the dominant limb of healthy, young, mal
204 hen reciprocal inhibition acted by TA on the calf muscles is more likely to be effective than the aut
205 d cross-sectional area (CSA) is preserved in calf muscles of patients with Becker muscular dystrophy
206 consistent with the data showing that in PAD calf muscles secrete mostly VEGF165b over total VEGF.
207 plitude of physiological tremor increased as calf muscles shortened in contrast to the stretch reflex
208                               The MTR in the calf muscles was significantly lower than controls in th
209                                              Calf muscles were scanned in 32 obese and 11 healthy sub
210 cent dye were done (15 ug/20 uL) in the left calf muscles, and in vivo fluorescent imaging performed
211 device that acts in parallel with the user's calf muscles, off-loading muscle force and thereby reduc
212 f generalized weakness, pseudohypertrophy of calf muscles, progressive joint contractures, severe sco
213 terest)=8x8x8 cm(3) (512 cm(3)) involving in calf muscles.
214 anical stiffness is partly determined by the calf muscles.
215          Cohorts of replacement dairy heifer calves (n = 42) with no prior exposure to F. hepatica, o
216 urgically isolated ileal segments in newborn calves (n = 5) were used to establish in vivo MAP infect
217 e analyzed the immune responses over time in calves naturally exposed to F. hepatica infection.
218 67 in CD4(+) T cells from PT21/28-challenged calves, NK cells from PT32-challenged calves, and CD8(+)
219 ealth) vaccination prior to the birth of the calf (odds ratio (OR) 40.78, p<0.001) and its herd of or
220    We found that challenging the skin of the calf of the hind paw or the cheek of previously sensitiz
221 followed by 10 injections into the thigh and calf of the index leg.
222 thasone (DEX) treatment of latently infected calves or rabbits consistently leads to reactivation fro
223 e scholars to suggest that the skin of fetal calves or sheep was used.
224 nvolving 31 whales and including eight adult-calf pairs.
225                     Here, colostrum-deprived calves persistently infected with HoBi-like pestivirus (
226          These were compared with 58 control calves randomly recruited from herds with no history of
227 phylum in the rumen microbiota of 42-day-old calves, representing 74.8% of the 16S sequences, followe
228 of house furniture foam as well as human and calf sera spiked with BDE 47 showed overall recovery of
229 hanically polished in the presence of bovine calf serum (BCS) in a hip simulator.
230 sformed foci when grown to confluence in 10% calf serum (CS).
231 endent and affected by the presence of fetal calf serum (FCS) in the growth medium.
232 um (minimum essential medium, MEM) and fetal calf serum (FCS) were probed by XANES and EXAFS.
233            The human serum (HS) and new-born calf serum (NCS) spiked with antigen-specific antibody w
234 total serum protein were confirmed when both calf serum and human serum were spiked with technical mi
235 somers in technical mixtures spiked to whole calf serum and human serum.
236    Response of cells to stimulation by fetal calf serum could be reproduced by the model, further sup
237 s well as the individual proteins from fetal calf serum that are associated with lipoplexes.
238 reproducibility, was studied using undiluted calf serum, and excellent recoveries in the range of 94.
239 500f gmL(-1) for the 3 proteins in undiluted calf serum.
240  media with or without pyruvate and 1% fetal calf serum.
241 microg mL(-1)) for IgY antibody in undiluted calf serum.
242 5 pg mL(-1) (25 fM) for IL-6 in 10 microL of calf serum.
243  junction (RAJ) tissues from three groups of calves showed no adherent O157 bacteria and similar proi
244 xtremity functional impairment, more adverse calf skeletal muscle characteristics, greater declines i
245  associated with pathophysiologic changes in calf skeletal muscle, including smaller calf muscle area
246 eight women; mean age, 62.6 years) underwent calf-station variable-FA MR, constant-FA MR, and FSD MR
247                Improvements in fecundity and calf survival are needed to reach a conservation objecti
248 gic diathesis and commonly known as bleeding calf syndrome) is a novel haemorrhagic disease of young
249 RS) missense mutations cause hereditary weak calf syndrome.
250 blasts from chronically hypoxic hypertensive calves (termed PH-Fibs) expressed a constitutive and per
251  the trigeminal ganglia of latently infected calves than in those of uninfected calves.
252 f a raised pigmented skin lesion on his left calf that proved to be melanoma with positive margins.
253 l study was conducted including 174 Holstein calves that were divided in four groups: healthy calves,
254                             We show that for calves, the mother milk is the main uptake route of cont
255 C digestions of unfractionated histones from calf thymus and acid-extracted histones from HeLa, MCF-7
256  monostyryl derivativatives intercalate into calf thymus DNA (ct DNA), whereas photocyclization produ
257 ands regulate their ability to interact with calf thymus DNA (ctDNA) through an intercalative mode.
258             Interactions of the complex with calf thymus DNA (ctDNA) were conducted with a flow-cell
259 ost of the thymidine 5'-monophosphate (TMP), calf thymus DNA (CTDNA), and plasmid DNA (PLDNA) analyse
260 NA interactions results in high affinity for calf thymus DNA (Kapp approximately 5 x 10(7) M(-1)).
261 iologically reactive metabolite and binds to calf thymus DNA (pH 5.0 or 7.0) to form the N-(deoxyguan
262 vels of the alpha-anomer of dG (alpha-dG) in calf thymus DNA and in DNA isolated from mouse pancreati
263 nance (NMR) studies of the interactions with calf thymus DNA for the three molecules.
264 nsfer of the electronic excitation energy in calf thymus DNA is studied by time-resolved fluorescence
265 tandem MS confirmation of their formation in calf thymus DNA upon diazoacetate exposure, and the prep
266  of small fluorescent organic molecules with calf thymus DNA was developed using two-photon absorptio
267                                              Calf thymus DNA was selected for the investigation, sinc
268 t interact with plasmid (pBR322) DNA or with calf thymus DNA.
269 ouble-stranded nucleic acid homopolymers and calf thymus DNA.
270                      In vitro, histones from calf thymus or histones released by neutrophils undergoi
271 ld be demonstrated that, although 3 binds to calf-thymus DNA by intercalation, the biological effects
272 ng DPPH radical) and biocompatibility (using calf-thymus DNA) of curcumin-loaded mixed surfactant for
273 ry structure also results from the action of calf-thymus topoisomerase I (CT Topo I) on a native supe
274  species isolated from the faeces of newborn calves to grow on carbohydrates typical of a newborn rum
275 date genes could be verified in boars and in calves treated with anabolic substances.
276 his aspect of Koch's postulates, three dairy calves (treatment animals) held in individual pens were
277 scle blood flow (CalfBF, (1)(3)(3)xenon) and calf vascular conductance (CalfVC) were measured during
278 m vascular conductance, calf blood flow, and calf vascular conductance were similar between groups.
279 m vascular conductance, calf blood flow, and calf vascular conductance) were significantly lower in t
280 m vascular conductance, calf blood flow, and calf vascular conductance) were significantly lower in t
281                                We classified calf vein into into four main types.
282 ings as a complimentary approach to isolated calf vein thrombosis (DVT).
283 teal artery on the same side as the isolated calf vein thrombosis as well as on the opposite side.
284   Deep vein thrombosis (DVT) isolated to the calf veins (distal to the popliteal vein) is frequently
285 opliteal artery and the number of thrombosed calf veins was investigated.
286       Repeated balance perturbations through calf vibrations were used to study postural adaptation.
287                                          The calf was imaged at 3-T in young healthy control subjects
288 , the phylum-level composition of 14-day-old calves was distinctly different.
289 -and-mouth disease virus (FMDV) infection in calves was investigated by administering subset-specific
290 minant distal SMA initially manifesting with calf weakness, we identified by genetic linkage analysis
291 m the superficial and deeper zones of bovine calves were biomechanically characterized.
292                                              Calves were challenged either with a phage type 21/28 (P
293 Proton (hydrogen 1 [1H]) and 23Na MR of both calves were performed in 12 patients with HyperPP (mean
294                                              Calves were treated in pens where eGFP-labelled E. coli
295 resistant (cef(R)) E. coli and one-month old calves were used to study the selection effects of CFM a
296 cted with HoBi-like pestivirus (HoBi-like PI calves) were generated and sampled (serum, buffy coat, a
297 me) is a novel haemorrhagic disease of young calves which has emerged in a number of European countri
298 n of both genes at 7 days in PT32-challenged calves, while upregulation was delayed, peaking at 21 da
299   We found that adventitial fibroblasts from calves with severe hypoxia-induced PH and humans with id
300 ble following treatment of latently infected calves with the synthetic corticosteroid dexamethasone t

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