Generation of Recombinant Vaccinia Viruses

Author:

Earl Patricia L.1,Moss Bernard1,Wyatt Linda S.1,Carroll Miles W.2

Affiliation:

1. National Institute of Allergy and Infectious Diseases; Bethesda Maryland

2. Oxford BioMedica; Oxford United Kingdom

Publisher

John Wiley & Sons, Inc.

Reference23 articles.

1. TAP (transporter associated with antigen processing)-independent presentation of endogenously synthesized peptides is enhanced by endoplasmic reticulum insertion sequences located at the amino- but not carboxyl-terminus of the peptide;Bacik;J. Immunol.,1994

2. One hundred base pairs of 5′ flanking sequence of a vaccinia virus late gene are sufficient to temporally regulate late transcription;Bertholet;Proc. Natl. Acad. Sci.U.S.A.,1985

3. Selection of recombinant vaccinia viruses on the basis of plaque formation;Blasco;Gene,1995

4. E. coli β-glucuronidase (GUS) as a marker for recombinant vaccinia viruses;Carroll;BioTechniques,1995

5. Host range and cytopathogenicity of the highly attenuated MVA strain of vaccinia virus: Propagation and generation of recombinant viruses in a nonhuman mammalian cell line;Carroll;Virology,1997

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