Royal Society of Chemistry, Chemical Communications, 41(56), p. 5496-5499, 2020
DOI: 10.1039/d0cc00444h
Full text: Unavailable
The combination of amide coupling with standard oligonucleotide synthesis enables assembly of reduced charge chimeric gapmer antisense oligonucleotides that trigger an efficient RNase H response while improving serum lifetime and cellular uptake.