Transfection is a modern and powerful method used to insert foreign nucleic acids into
eukaryotic cells. The ability to modify host cells' genetic content enables the broad …

The transfer of foreign genes into eukaryotic cells, in particular mammalian cells, has been
essential to our understanding of the functional significance of genes and regulatory …

Genetically modified animals are state of the art in biomedical research as gene therapy is a
promising perspective in the attempt to cure hereditary diseases. Both approaches have in …

Gene therapy encompasses the transfer of exogenous genetic materials into the patient's
target cells to treat or prevent diseases. Nevertheless, the transfer of genetic material into …

Gene therapy is the process of introducing foreign genomic materials into host cells to elicit
a therapeutic benefit. Although initially the main focus of gene therapy was on special …

Development of an efficient method for introducing a therapeutic gene into target cells in
vivo is the key issue in treating genetic and acquired diseases by gene therapy. To this end …

The ability to make site-specific modifications to the human genome has been an objective
in medicine since the recognition of the gene as the basic unit of heredity. Thus, gene …

A practical manual of protocols for achieving expression of foreign genes in mammalian
cells. It includes some very new techniques such as PCR-based expression. The author …

Over the past few decades, gene therapy has gained immense importance in medical
research as a promising treatment strategy for diseases such as cancer, AIDS, Alzheimer's …

The structure of DNA was unraveled by Watson and Crick in 1953, and two decades later
Arber, Nathans and Smith discovered DNA restriction enzymes, which led to the rapid …