A main challenge in realizing the full potential of nucleic acid therapeutics is efficient delivery of them into targeted tissues and cells. N-acetylgalactosamine (GalNAc) is a well-defined liver-targeted moiety benefiting from its high affinity with asialoglycoprotein receptor (ASGPR). By conjugating it directly to the oligonucleotides or decorating it to a certain delivery system as a targeting moiety, GalNAc has achieved compelling successes in the development of nucleic acid therapeutics in recent years. Several oligonucleotide modalities are undergoing pivotal clinical studies, followed by a blooming pipeline in the preclinical stage. This review covers the progress of GalNAc-decorated oligonucleotide drugs, including siRNAs, anti-miRs...
AbstractTherapeutic gene silencing promises significant progress in pharmacotherapy, including consi...
International audienceOligonucleotide-based agents have the potential to treat or cure almost any di...
The development of oligonucleotide conjugates for in vivo targeting is one of the most exciting area...
A main challenge in realizing the full potential of nucleic acid therapeutics is efficient delivery ...
RNA interference has become increasingly used for genetic therapy following the rapid development of...
Conjugation of small interfering RNA (siRNA) to an asialoglycoprotein receptor ligand derived from N...
Asialoglycoprotein receptor (ASGPR) mediated delivery of triantennary <i>N</i>-acetylgalactosamine (...
Nucleic Acid Therapeutics (NATs) are establishing a leading role for the management and treatment of...
RNA interference has become increasingly used for genetic therapy following the rapid development of...
While the promise of oligonucleotide therapeutics, such as (chemically modified) ASO (antisense olig...
With the development of new anticancer medicines, novel modalities are being explored for cancer tre...
The discovery of RNAi and the subsequent demonstration that synthetic short interfering RNA (siRNA) ...
Advances in medicinal chemistry have produced new chemical classes of antisense oligonucleotides (AS...
Non-coding RNA (ncRNA) therapeutics are based on short oligonucleotides, both naturally occurring an...
Conjugation of small interfering RNA (siRNA) to an asialoglycoprotein receptor ligand derived from <...
AbstractTherapeutic gene silencing promises significant progress in pharmacotherapy, including consi...
International audienceOligonucleotide-based agents have the potential to treat or cure almost any di...
The development of oligonucleotide conjugates for in vivo targeting is one of the most exciting area...
A main challenge in realizing the full potential of nucleic acid therapeutics is efficient delivery ...
RNA interference has become increasingly used for genetic therapy following the rapid development of...
Conjugation of small interfering RNA (siRNA) to an asialoglycoprotein receptor ligand derived from N...
Asialoglycoprotein receptor (ASGPR) mediated delivery of triantennary <i>N</i>-acetylgalactosamine (...
Nucleic Acid Therapeutics (NATs) are establishing a leading role for the management and treatment of...
RNA interference has become increasingly used for genetic therapy following the rapid development of...
While the promise of oligonucleotide therapeutics, such as (chemically modified) ASO (antisense olig...
With the development of new anticancer medicines, novel modalities are being explored for cancer tre...
The discovery of RNAi and the subsequent demonstration that synthetic short interfering RNA (siRNA) ...
Advances in medicinal chemistry have produced new chemical classes of antisense oligonucleotides (AS...
Non-coding RNA (ncRNA) therapeutics are based on short oligonucleotides, both naturally occurring an...
Conjugation of small interfering RNA (siRNA) to an asialoglycoprotein receptor ligand derived from <...
AbstractTherapeutic gene silencing promises significant progress in pharmacotherapy, including consi...
International audienceOligonucleotide-based agents have the potential to treat or cure almost any di...
The development of oligonucleotide conjugates for in vivo targeting is one of the most exciting area...