Transduction with Lentiviral vectors has been shown to be the most efficient method for the
stable delivery of nucleic acid sequences into mammalian cells. Lentiviral vectors have been …

Lentiviral gene transfer represents a versatile and powerful method for genetic transduction
of many cell lines and primary cells including “hard-to-transfect” cells. As a consequence of …

Lentiviral vectors are proving to be effective agents for the direct delivery and sustained
expression of a transgene in several tissues, including brain, retina, muscle and liver …

The capacity to efficiently transduce nondividing cells, shuttle large genetic payloads, and
maintain stable long-term transgene expression are attributes that have brought lentiviral …

This review summarises an emerging viral vector system for use in human gene therapy-
lentiviral vectors. Lentiviral vectors have several advantages over existing viral vectors. They …

Lentiviral gene transfer technologies exploit the natural efficiency of viral transduction to
integrate exogenous genes into mammalian cells. This provides a simple research tool for …

Gene transfer vectors based on retroviruses including oncogenic retroviruses and
lentiviruses provide effective means for the delivery, integration and expression of …

Lentiviral vectors are tools for gene transfer derived from lentiviruses. From their first
application to now they have been strongly developed in design, in biosafety and in their …

The use of lentiviral vectors for transgene delivery in vitro and in vivo for applications in
neuroscience, hematology, developmental biology, stem cell biology, and transgenesis has …

Transgenic animals are of outstanding relevance for medical sciences, because they can be
used to model human diseases and to develop gene therapy strategies. A recent …