Rapid Detection of Classical Swine Fever Virus by a Portable Real-Time Reverse Transcriptase PCR Assay
Author:
Affiliation:
1. Plum Island Animal Disease Center, Agricultural Research Service, U.S. Department of Agriculture, Greenport, New York 11944
2. Tetracore Inc., Gaithersburg, Maryland 20878
Abstract
Publisher
American Society for Microbiology
Subject
Microbiology (medical)
Link
https://journals.asm.org/doi/pdf/10.1128/JCM.41.1.500-505.2003
Reference39 articles.
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2. Biront, P., J. Leumen, and J. Vandeputte. 1987. Inhibition of virus replication in the tonsils of pigs previously vaccinated with a Chinese strain vaccine and challenged oronasally with a virulent strain of classical swine fever virus. Vet. Microbiol.14:105-113.
3. Boye, M., S. Kamstrup, and K. Dalsgaard. 1991. Specific sequence amplification of bovine virus diarrhea virus (BVDV) and hog cholera virus and sequencing of BVDV nucleic acid. Vet. Microbiol.29:1-13.
4. Carbrey, E. A., W. C. Stewart, and S. H. Young. 1966. The changing picture of hog cholera: case studies. J. Am. Vet. Med. Assoc.149:1724.
5. Carbrey, E. A., W. C. Stewart, J. I. Kresse, and M. L. Snyder. 1976. Natural infection of pigs with bovine viral diarrhea virus and its differential diagnosis from hog cholera. J. Am. Vet. Med. Assoc.169:1217-1219.
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