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Acta Biologica Hungarica|February 27, 2008
Directed homologous recombination for genome engineering in Escherichia coliB Csörgö, G PósfaiGene|September 15, 1988
A simple method for locating methylated bases in DNA, as applied to detect asymmetric methylation by M.FokIAG Pósfai, W SzybalskiGene|October 1, 1984
High-copy-number derivatives of the plasmid cloning vector pBR322I Boros, G Pósfai, P VenetianerGene|October 1, 1984
The construction of a versatile plasmid vector that allows direct selection of fragments cloned into six unique sites of the cI gene of coliphage 434S Nikolnikov, G Pósfai, B SainGene|April 1, 1991
A novel gene-fusing vector: construction of a 5'-GGmCC-specific chimeric methyltransferase, M.BspRI/M.BsuRIS C Kim, G Pósfai, W SzybalskiGene|November 7, 1996
A broad-host-range in vivo pop-out and amplification system for generating large quantities of 50- to 100-kb genomic fragments for direct DNA sequencingJ Wild, Z Hradecná, G Pósfai, et al.Nucleic Acids Research|October 28, 1999
Markerless gene replacement in Escherichia coli stimulated by a double-strand break in the chromosomeG Pósfai, V Kolisnychenko, Z Bereczki, et al.Nucleic Acids Research|July 27, 2001
Role of DNA minor groove interactions in substrate recognition by the M.SinI and M.EcoRII DNA (cytosine-5) methyltransferasesA Kiss, G Pósfai, G Zsurka, et al.Nucleic Acids Research|April 11, 1989
Predictive motifs derived from cytosine methyltransferasesJ Pósfai, A S Bhagwat, G Pósfai, et al.Gene|December 22, 1998
Cre/loxP-mediated in vivo excision of large segments from yeast genome and their amplification based on the 2microm plasmid-derived systemY G Yoon, G Pósfai, W Szybalski, et al.Pageof 3