On the use of double FLP recognition targets (FRTs) in the LTR of retroviruses for the construction of high producer cell lines

Nucleic Acids Research

Volumn 24, Issue 9, 1996, Pages 1616-1624

  Karreman, Simone ^a   Hauser, Hansjörg ^a   Karreman, Christiaan ^a,b  

^a HELMHOLTZ CENTRE FOR INFECTION RESEARCH   (Germany)

^b INSTITUTE OF EPIDEMIOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

RECOMBINASE;

ANIMAL CELL; ARTICLE; CELL LINE; CONTROLLED STUDY; DNA RECOMBINATION; EXPRESSION VECTOR; GENE EXPRESSION; HAMSTER; LONG TERMINAL REPEAT; MARKER GENE; MOLECULAR CLONING; NONHUMAN; PRIORITY JOURNAL; RETROVIRUS; SACCHAROMYCES CEREVISIAE;

ANIMALS; BASE SEQUENCE; BINDING SITES; CELL LINE; CRICETINAE; DNA NUCLEOTIDYLTRANSFERASES; DNA, FUNGAL; DNA, RECOMBINANT; GENE TRANSFER TECHNIQUES; GENETIC VECTORS; KIDNEY; MOLECULAR SEQUENCE DATA; PROVIRUSES; RECOMBINATION, GENETIC; REPETITIVE SEQUENCES, NUCLEIC ACID; RETROVIRIDAE; SACCHAROMYCES CEREVISIAE; TRANSFECTION;

EID: 0029932546     PISSN: 03051048     EISSN: None     Source Type: Journal    
DOI: 10.1093/nar/24.9.1616     Document Type: Article

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