International audienceGene therapy is a new and promising tool to treat many severe diseases and the silencing of proteins is the safest and the most efficient tool to treat diseases because it does not induce changes in human genome and avoids a huge problem encompassing insertional mutagenesis. Using small RNAs to switch on/off target proteins is limited due to existence of some barriers for them in the human body (blood RNAses, serum albumins, cell walls, etc). For therapeutic applications they need the efficient and non-toxic carrier which will deliver them into cell cytoplasm. Within the huge range of carriers available, dendrimers can be underlined as new promising efficient carriers. This review summarizes several findings in phospho...
Chemotherapy is the first choice in the treatment of cancer and is always preferred to other approac...
International audienceIrresponsiveness of triple negative breast cancer (TNBC) toward conventional t...
This study successfully evaluated gene delivery and transfection toward rat C6 glioma cell lines med...
International audienceGene therapy is a new and promising tool to treat many severe diseases and the...
International audienceDuring the past two decades, tremendous progress has been made in the dendrime...
Research concerning new targeting delivery systems for pharmacologically active molecules and geneti...
International audienceAmong the different types of dendrimers, those that incorporate phosphorus in ...
International audienceThis review concerns the use of dendrimers, especially of phosphorhydrazone de...
There are many types of dendrimers used as nanomolecules for gene delivery but there is still an ong...
International audienceGene delivery, one important cancer-therapy mode, still remains to be challeng...
International audienceThis paper examines a perspective to use newly engineered nanomaterials as eff...
Dendrimers are highly branched polymers with easily modifiable surfaces. This makes them promising s...
The lack of an appropriate intracellular delivery system for therapeutic nucleic acids (TNAs) is a m...
The delivery of nucleic acids to cells, in vitro and in vivo, is becoming a realistic approach for i...
Chemotherapy is the first choice in the treatment of cancer and is always preferred to other approac...
Chemotherapy is the first choice in the treatment of cancer and is always preferred to other approac...
International audienceIrresponsiveness of triple negative breast cancer (TNBC) toward conventional t...
This study successfully evaluated gene delivery and transfection toward rat C6 glioma cell lines med...
International audienceGene therapy is a new and promising tool to treat many severe diseases and the...
International audienceDuring the past two decades, tremendous progress has been made in the dendrime...
Research concerning new targeting delivery systems for pharmacologically active molecules and geneti...
International audienceAmong the different types of dendrimers, those that incorporate phosphorus in ...
International audienceThis review concerns the use of dendrimers, especially of phosphorhydrazone de...
There are many types of dendrimers used as nanomolecules for gene delivery but there is still an ong...
International audienceGene delivery, one important cancer-therapy mode, still remains to be challeng...
International audienceThis paper examines a perspective to use newly engineered nanomaterials as eff...
Dendrimers are highly branched polymers with easily modifiable surfaces. This makes them promising s...
The lack of an appropriate intracellular delivery system for therapeutic nucleic acids (TNAs) is a m...
The delivery of nucleic acids to cells, in vitro and in vivo, is becoming a realistic approach for i...
Chemotherapy is the first choice in the treatment of cancer and is always preferred to other approac...
Chemotherapy is the first choice in the treatment of cancer and is always preferred to other approac...
International audienceIrresponsiveness of triple negative breast cancer (TNBC) toward conventional t...
This study successfully evaluated gene delivery and transfection toward rat C6 glioma cell lines med...