AbstractHarnessing of a branched structure is a novel approach in the design of cell-penetrating peptides and it has provided highly efficient transfection reagents for intracellular delivery of nucleic acids. The new stearylated TP10 analogs, NickFects, condense plasmid DNA, splice correcting oligonucleotides and short interfering RNAs into stable nanoparticles with a size of 62–160nm. Such nanoparticles have a negative surface charge (−11 to −18mV) in serum containing medium and enable highly efficient gene expression, splice correction and gene silencing. One of the novel peptides, NickFect51 is capable of transfecting plasmid DNA into a large variety of cell lines, including refractory suspension and primary cells and in several cases e...
Doctor of PhilosophyDepartment of Biochemistry and Molecular BiophysicsJohn M. TomichSuccess for gen...
Despite the fact that non-viral nucleic acid delivery systems are generally considered to be less ef...
The successful applicability of gene therapy approaches will heavily rely on the development of effi...
AbstractHarnessing of a branched structure is a novel approach in the design of cell-penetrating pep...
AbstractCell-penetrating peptides with the ability to escape endosomes and reach the target are of g...
Establishment of multiple novel mechanisms and applications of cell-penetrating peptides (CPP) has b...
To overcome the low efficiency and cytotoxicity associated with most non-viral DNA delivery systems ...
Delivery of nucleic acid is a promising approach for genetic diseases/disorders. However, gene thera...
Gene therapy holds the promise of revolutionizing the way we treat diseases. By using recombinant DN...
Recent advances with techniques used for manipulating gene expression have brought us to an era wher...
The hydrophobic nature of cell membranes is one of the major obstacles in the therapeutic delivery o...
The sequencing of the human genome was expected to generate a veritable explosion of therapeutics ...
One of the greatest challenges for the development of genetic therapies is the efficient targeted de...
In order to enhance intracellular uptake and accumulation of therapeutic nucleic acids for improved ...
Regulation of biological processes through the use of genetic elements is a central part of biologic...
Doctor of PhilosophyDepartment of Biochemistry and Molecular BiophysicsJohn M. TomichSuccess for gen...
Despite the fact that non-viral nucleic acid delivery systems are generally considered to be less ef...
The successful applicability of gene therapy approaches will heavily rely on the development of effi...
AbstractHarnessing of a branched structure is a novel approach in the design of cell-penetrating pep...
AbstractCell-penetrating peptides with the ability to escape endosomes and reach the target are of g...
Establishment of multiple novel mechanisms and applications of cell-penetrating peptides (CPP) has b...
To overcome the low efficiency and cytotoxicity associated with most non-viral DNA delivery systems ...
Delivery of nucleic acid is a promising approach for genetic diseases/disorders. However, gene thera...
Gene therapy holds the promise of revolutionizing the way we treat diseases. By using recombinant DN...
Recent advances with techniques used for manipulating gene expression have brought us to an era wher...
The hydrophobic nature of cell membranes is one of the major obstacles in the therapeutic delivery o...
The sequencing of the human genome was expected to generate a veritable explosion of therapeutics ...
One of the greatest challenges for the development of genetic therapies is the efficient targeted de...
In order to enhance intracellular uptake and accumulation of therapeutic nucleic acids for improved ...
Regulation of biological processes through the use of genetic elements is a central part of biologic...
Doctor of PhilosophyDepartment of Biochemistry and Molecular BiophysicsJohn M. TomichSuccess for gen...
Despite the fact that non-viral nucleic acid delivery systems are generally considered to be less ef...
The successful applicability of gene therapy approaches will heavily rely on the development of effi...