HIV-1 lentiviral vector can infect unseparated cells, can transfer longer fragment, can make objective gene have a long stabilized expression, and can not cause immune reaction of the host easily.

Empirical study of the lentiviral vectors expessing siRNA for survivin gene on tumor inhibition of A549 cells tumor-bearingnude mice;

Construction and identification of TAT-BACEsp-GFP triple fusion gene expressed from recombinant lentiviral vector;

Cloning of human CCR5Delta32 gene and construction of the recombinant lentiviral vector pLenti-CCR5Delta32;

Expressing profiles of transgenes in different cells and chicken tissues delivered by lentiviral vectors;

Methods NSCs cultured in vitro were transfected by lentiviral vectors expressing green fluorescent protein(GFP)to construct GFP-NSCs,then trans-seeded into lactide-co-glycolide(PLGA)scaffold and implanted into the injured site of T9 spinal cord in rat.

We transfected human neural stem cells using lentiviral vectors encoding glial cell line derived neurotrophic factor (GDNF) to study its expression level in vitro and to get a stable cell line expressing GDNF.

The appliance of lentivirus vector in cancer theray;

Study on infection of nondividing myeloma cells by lentivirus vector;

Extraction and gene transferring by lentivirus vector in CD34~+ cells from human cord blood;