Small-interfering RNA (siRNA) is a synthetic double-stranded RNA that consists of approximately 21 nucleotides (nts). It induces degradation of target mRNAs in a sequence-specific manner by the RNA interference (RNAi) mechanism. Thus, siRNAs offer a potential strategy for silencing mutated or defective genes that cause a variety of human diseases. The main obstacles of harnessing siRNAs as drugs are their inefficient delivery to cells and off-target effect making clinical applications very challenging. To address these issues, researchers have studied a variety of nanocarrier systems for siRNA delivery. This study presents the design, fabrication, and full characterization of innovative polyethyleneimine (PEI)-decorated polycationic 34.2 ± ...
RNA interference (RNAi) is a promising strategy to inhibit the expression of pathologically relevant...
The efficient delivery of sufficient amounts of nucleic acids into target cells is critical for succ...
Gene therapy is a promising strategy for treatment of genetically caused diseases. Successful gene d...
The discovery of RNA interference (RNAi) as a naturally occurring mechanism for gene knockdown has a...
Genetic diseases are illnesses caused by abnormalities in genes or chromosomes, including hemophilia...
Gene therapy using siRNA molecules is nowadays considered as a promising approach. For successful th...
The development of functional nanocarriers that can enhance the cellular delivery of a variety of nu...
RNA interference (RNAi) is an emerging technology in which the introduction of double-stranded RNA (...
The present study describes hybrid nanoparticles, built by alternate deposition of siRNA and modifie...
International audienceThe present study describes hybrid nanoparticles, built by alternate depositio...
RNA interference (RNAi) is a highly specific gene-silencing mechanism triggered by small interfering...
A low toxicity and efficient delivery system is needed to deliver small interfering RNAs (siRNA) in ...
A low cytotoxicity and high efficiency delivery system with the advantages of low cost and facile fa...
Regulation of gene expression using small interfering RNA (siRNA) is a promising strategy for resear...
RNA interference (RNAi) is a post-transcriptional gene silencing mechanism that occurs naturally wit...
RNA interference (RNAi) is a promising strategy to inhibit the expression of pathologically relevant...
The efficient delivery of sufficient amounts of nucleic acids into target cells is critical for succ...
Gene therapy is a promising strategy for treatment of genetically caused diseases. Successful gene d...
The discovery of RNA interference (RNAi) as a naturally occurring mechanism for gene knockdown has a...
Genetic diseases are illnesses caused by abnormalities in genes or chromosomes, including hemophilia...
Gene therapy using siRNA molecules is nowadays considered as a promising approach. For successful th...
The development of functional nanocarriers that can enhance the cellular delivery of a variety of nu...
RNA interference (RNAi) is an emerging technology in which the introduction of double-stranded RNA (...
The present study describes hybrid nanoparticles, built by alternate deposition of siRNA and modifie...
International audienceThe present study describes hybrid nanoparticles, built by alternate depositio...
RNA interference (RNAi) is a highly specific gene-silencing mechanism triggered by small interfering...
A low toxicity and efficient delivery system is needed to deliver small interfering RNAs (siRNA) in ...
A low cytotoxicity and high efficiency delivery system with the advantages of low cost and facile fa...
Regulation of gene expression using small interfering RNA (siRNA) is a promising strategy for resear...
RNA interference (RNAi) is a post-transcriptional gene silencing mechanism that occurs naturally wit...
RNA interference (RNAi) is a promising strategy to inhibit the expression of pathologically relevant...
The efficient delivery of sufficient amounts of nucleic acids into target cells is critical for succ...
Gene therapy is a promising strategy for treatment of genetically caused diseases. Successful gene d...