In this paper, we survey recent advances in the self-assembly processes of novel functional
platforms for nanomaterials and biomaterials applications. We provide an organized …

The translational therapies to promote interaction between cell and signal come with
stringent eligibility criteria. The chemically defined, hierarchically organized, and simpler yet …

Gene therapy, a medical approach that involves the correction or replacement of defective
and abnormal genes, plays an essential role in the treatment of complex and refractory …

Gene therapy offers the possibility to skip, repair, or silence faulty genes or to stimulate the
immune system to fight against disease by delivering therapeutic nucleic acids (NAs) to a …

Epstein Barr Virus (EBV) is one of the most common human herpesviruses. After primary
infection, it can persist in the host throughout their lifetime in a latent form, from which it can …

Therapeutic viral gene delivery is an emerging technology which aims to correct genetic
mutations by introducing new genetic information to cells either to correct a faulty gene or to …

Cytosolic delivery of bioactive agents has exhibited great potential to cure undruggable
targets and diseases. Because biological cell membranes are a natural barrier for living …

The Salmonella enterica bacteriophage P22 is one of the most promising models for the
development of virus-like particle (VLP) nanocages. It possesses an icosahedral T= 7 …

The intentional use of viruses for cancer therapy dates back over a century. As viruses are
inherently immunogenic and naturally optimized delivery vehicles, repurposing viruses for …

Cell penetrating peptides (CPPs) can be broadly defined as relatively short synthetic, protein
derived or chimeric peptides. Their most remarkable property is their ability to cross cell …