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Fabio Cannata

Showing results (1-10 of 5) with videos related to

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Biochimie|May 8, 2008
Targeting DNA with triplex-forming oligonucleotides to modify gene sequencePhilippe Simon, Fabio Cannata, Jean-Paul Concordet, et al.
Nucleic Acids Research|September 5, 2006
Targeting chromosomal sites with locked nucleic acid-modified triplex-forming oligonucleotides: study of efficiency dependence on DNA nuclear environmentErika Brunet, Maddalena Corgnali, Fabio Cannata, et al.
Nucleic Acids Research|May 3, 2008
Sequence-specific DNA cleavage mediated by bipyridine polyamide conjugatesPhilippe Simon, Fabio Cannata, Loïc Perrouault, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 5, 2008
Triplex-forming oligonucleotide-orthophenanthroline conjugates for efficient targeted genome modificationFabio Cannata, Erika Brunet, Loïc Perrouault, et al.
Journal of Medicinal Chemistry|January 6, 2006
Substituted 2-thioxoimidazolidin-4-ones and imidazolidine-2,4-diones as fatty acid amide hydrolase inhibitors templatesGiulio G Muccioli, Nicola Fazio, Gerhard K E Scriba, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Biochimie|May 8, 2008
Targeting DNA with triplex-forming oligonucleotides to modify gene sequencePhilippe Simon, Fabio Cannata, Jean-Paul Concordet, et al.
Nucleic Acids Research|September 5, 2006
Targeting chromosomal sites with locked nucleic acid-modified triplex-forming oligonucleotides: study of efficiency dependence on DNA nuclear environmentErika Brunet, Maddalena Corgnali, Fabio Cannata, et al.
Nucleic Acids Research|May 3, 2008
Sequence-specific DNA cleavage mediated by bipyridine polyamide conjugatesPhilippe Simon, Fabio Cannata, Loïc Perrouault, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 5, 2008
Triplex-forming oligonucleotide-orthophenanthroline conjugates for efficient targeted genome modificationFabio Cannata, Erika Brunet, Loïc Perrouault, et al.
Journal of Medicinal Chemistry|January 6, 2006
Substituted 2-thioxoimidazolidin-4-ones and imidazolidine-2,4-diones as fatty acid amide hydrolase inhibitors templatesGiulio G Muccioli, Nicola Fazio, Gerhard K E Scriba, et al.
Pageof 1