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Curr Protoc Nucleic Acid Chem ; Chapter 4: Unit 4.1, 2001 May.
Article in English | MEDLINE | ID: mdl-18428848

ABSTRACT

The advent of rapid and efficient methods of oligonucleotide synthesis has allowed the design of modified oligonucleotides that are complementary to specific nucleotide sequences in mRNA targets. Such modified oligonucleotides can be used to disrupt the flow of genetic information from transcribed mRNAs to proteins. This antisense strategy has been used to develop therapeutic oligonucleotides against cancer and various infectious diseases in humans. This overview reports recent advances in the application of oligonucleotides as drug candidates, describes the relationship between oligonucleotide modifications and their therapeutic profiles, and provides general guidelines for enhancing oligonucleotide drug properties.


Subject(s)
Drug Design , Oligonucleotides/therapeutic use , Base Pairing , Deoxyribonucleases/metabolism , Gene Expression , History, 20th Century , Oligonucleotides/chemistry , Oligonucleotides/history
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