Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Berch E. Henry"'
Publikováno v:
Laboratory Medicine. 29:484-489
DNA tests have many advantages over traditional serologic methods. They are more powerful and applicable in a greater variety of specimens. Since DNA testing began being used in forensic testing in the past decade, techniques have developed rapidly.
Publikováno v:
Journal of forensic sciences. 38(1)
Restriction fragment length polymorphism (RFLP) profile results were obtained from deoxyribonucleic acid (DNA) isolated from human bloodstains that had been subjected to cyanoacrylate ester (“superglue”) fuming, argon ion laser light and alternat
Publikováno v:
Virology. 107:415-423
A new DNA polymerase (DNA nucleotidyl transferase) can be found in Raji cells following superinfeetion by Epstein-Barr virus (EBV). This polymerase is not present prior to infection and can be selectively extracted from infected cells. The polymerase
Publikováno v:
Virology. 101:335-362
Permissive primary hamster embryo cells (HEF) were morphologically transformed in vitro by uv-irradiated standard equine herpesivrus type 1 (EHV-1). Cell lines (LSEH) were established and were shown to exhibit growth and biological properties typical
Publikováno v:
Journal of General Virology. 47:343-353
Summary High multiplicity, undiluted passage of equine herpesvirus type 1 (EHV-1) in L-M cells resulted in the rapid production of virus particles whose genome was genetically less complex, contained more reiterated DNA sequences and exhibited a grea
Publikováno v:
Virology. 109:106-119
Equine cytomegalovirus (equine herpesvirus type 2; ECMV) exhibited cultural characteristics typical of the cytomegalovirus group. Ninety-six to one hundred twenty hours were required to reach a maximum titer of 1 × 10 7 PFU/ml in infected cells, fro
Autor:
Sally S. Atherton, Steven A. Dauenhauer, Robin A. Robinson, Gary S. Hayward, Dennis J. O'Callaghan, Berch E. Henry
Publikováno v:
Virology. 115:97-114
The molecular structure of the genome of equine herpesvirus type 1 (EHV-1) was determined by restriction endonuclease mapping studies. Primary restriction enzyme digestion of purified EHV-1 DNA, either unlabeled, 32P04 labeled, or [3H]TdR labeled, ga
Publikováno v:
Journal of virology. 37(1)
After Epstein-Barr virus superinfection of the human lymphoblastoid cell line Raji, a Burkitt lymphoma-derived line that contains Epstein-Barr virus genomes in an episomal form, at least 40 polypeptides could be resolved by polyacrylamide gel electro
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 80(4)
Epstein-Barr virus (EBV) DNA was analyzed for the presence of autonomous replicating sequences (designated ars) in a eukaryotic system consisting of a uracil auxotroph of Saccharomyces cerevisiae, YNN27, and a pBR322 hybrid plasmid, YIp5, containing
Publikováno v:
Virology. 92(2)
Defective interfering (DI) particles of equine herpesvirus type 1(EHV-1) were purposely generated in an in vitro system of L-M cells by repeated high-multiplicity, serial, undiluted passage. Quantitation of infectious virus revealed a definite cyclic