Results 111 to 120 of about 977 (160)
circRNA_8521 promotes Senecavirus A infection by sponging miRNA-324 to regulate LC3A. [PDF]
Yang X +9 more
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Development and diagnostic applications of a group-specific caliciviridae cDNA hybridization probe cloned from San Miguel sea lion virus, type 5, a calicivirus of ocean origin [PDF]
Poet, Steven E.
core +1 more source
A comprehensive and single-use foot-and-mouth disease sero-surveillance prototype employing rationally designed multiple viral antigens. [PDF]
Hossain A +4 more
europepmc +1 more source
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Journal of the American Veterinary Medical Association, 1976
SUMMARY Vesicular exanthema of swine (ves) was first recognized in 1932. At that time, eradication measures and, later, quarantine procedures were instituted and extension of the disease to surrounding farms appeared to have been prevented. Between 1932 and 1936, however, seemingly unrelated epizootics continued among swine herds being fed raw garbage.
A W, Smith, T G, Akers
openaire +2 more sources
SUMMARY Vesicular exanthema of swine (ves) was first recognized in 1932. At that time, eradication measures and, later, quarantine procedures were instituted and extension of the disease to surrounding farms appeared to have been prevented. Between 1932 and 1936, however, seemingly unrelated epizootics continued among swine herds being fed raw garbage.
A W, Smith, T G, Akers
openaire +2 more sources
Biochemical and biophysical properties of vesicular exanthema of swine virus
Virology, 1971Abstract Vesicular exanthema of swine virus (VESV) was purified and some of its biochemical and biophysical properties measured. VESV grew in the presence of 2 μg/ml actinomycin D, was ether resistant, and was not stabilized by cations. Its sedimentation rate was approximately 207 S, and its composition was approximately 20% RNA and 80% protein.
A S, Oglesby, F L, Schaffer, S H, Madin
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Archiv f�r die gesamte Virusforschung, 1967
A plaque assay method, using 1.05% methyl cellulose overlay, was developed for vesicular exanthema of swine virus (VESV) types A48, H54, I55, and K54. The validity of this plaque method as an assay system was upheld by the well correlated dose response, and the specificity of plaque formation was demonstrated by the fact that a specific antiserum could
Yuan Chung Zee +2 more
openaire +2 more sources
A plaque assay method, using 1.05% methyl cellulose overlay, was developed for vesicular exanthema of swine virus (VESV) types A48, H54, I55, and K54. The validity of this plaque method as an assay system was upheld by the well correlated dose response, and the specificity of plaque formation was demonstrated by the fact that a specific antiserum could
Yuan Chung Zee +2 more
openaire +2 more sources
Nature, 1973
BETWEEN 1932 and 1954 there were repeated outbreaks of vesicular exanthema of swine (VES) in Californian swine herds, but since 1956 no cases have occurred in the United States and this has been attributed to a federal law which prohibited the feeding of raw garbage to swine1.
A W, Smith +3 more
openaire +2 more sources
BETWEEN 1932 and 1954 there were repeated outbreaks of vesicular exanthema of swine (VES) in Californian swine herds, but since 1956 no cases have occurred in the United States and this has been attributed to a federal law which prohibited the feeding of raw garbage to swine1.
A W, Smith +3 more
openaire +2 more sources

