Rapid Genetic Engineering of Human Cytomegalovirus by Using a Lambda Phage Linear Recombination System: Demonstration that pp28 (UL99) Is Essential for Production of Infectious Virus

Journal of Virology

Volumn 78, Issue 1, 2004, Pages 539-543

  Britt, William J ^a,b,c,e   Jarvis, Michael ^d   Seo, Jun Young ^b   Drummond, Derek ^d   Nelson, Jay ^d  

^a University of Alabama at Birmingham   (United States)

^b University of Alabama at Birmingham   (United States)

^c UNIVERSITY OF ALABAMA SCHOOL OF MEDICINE   (United States)

^d OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^e NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN PP28; PROTEIN UL99; UNCLASSIFIED DRUG; VIRUS PROTEIN;

ARTICLE; ARTIFICIAL CHROMOSOME; BACTERIAL CHROMOSOME; BACTERIOPHAGE LAMBDA; CONTROLLED STUDY; CYTOMEGALOVIRUS; GENETIC CODE; GENETIC ENGINEERING; HUMAN; HUMAN CELL; MUTAGENESIS; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; VIRUS ASSEMBLY; VIRUS GENOME; VIRUS INFECTIVITY; VIRUS MORPHOGENESIS; VIRUS RECOMBINATION; VIRUS REPLICATION;

BACTERIOPHAGE LAMBDA; CELLS, CULTURED; CHROMOSOMES, ARTIFICIAL, BACTERIAL; CYTOMEGALOVIRUS; ESCHERICHIA COLI; FIBROBLASTS; GENETIC ENGINEERING; HUMANS; PHOSPHOPROTEINS; RECOMBINATION, GENETIC; TIME FACTORS; VIRAL PROTEINS; VIRION; VIRUS ASSEMBLY;

EID: 0346365287     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/JVI.78.1.539-543.2004     Document Type: Article

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