Results 231 to 240 of about 411,689 (282)
Preclinical toxicity analyses of lentiviral vectors expressing the HIV-1 LTR-specific designer-recombinase Brec1. [PDF]
Beschorner N +18 more
europepmc +1 more source
Continuous manufacturing of lentiviral vectors using a stable producer cell line in a fixed-bed bioreactor. [PDF]
Stibbs DJ +5 more
europepmc +1 more source
Use of Lentiviral Vectors in Vaccination
International audienceIntroduction: Lentiviral vectors have emerged as powerful vectors for vaccination, due to their high efficiency to transduce dendritic cells and to induce long-lasting humoral immunity, CD8 + T cells, and effective protection in ...
Laleh Majlessi, Pierre Charneau
exaly +2 more sources
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2005
We review the use of lentiviral vectors in current human gene therapy applications that involve genetic modification of nondividing tissues with integrated transgenes. Safety issues, including insertional mutagenesis and replication-competent retroviruses, are discussed.
Nils, Loewen, Eric M, Poeschla
openaire +2 more sources
We review the use of lentiviral vectors in current human gene therapy applications that involve genetic modification of nondividing tissues with integrated transgenes. Safety issues, including insertional mutagenesis and replication-competent retroviruses, are discussed.
Nils, Loewen, Eric M, Poeschla
openaire +2 more sources
2011
Lentiviral vectors have evolved over the last decade as powerful, reliable, and safe tools for stable gene transfer in a wide variety of mammalian cells. Contrary to other vectors derived from oncoretroviruses, they allow for stable gene delivery into most nondividing primary cells.
Giry-Laterrière M +2 more
openaire +3 more sources
Lentiviral vectors have evolved over the last decade as powerful, reliable, and safe tools for stable gene transfer in a wide variety of mammalian cells. Contrary to other vectors derived from oncoretroviruses, they allow for stable gene delivery into most nondividing primary cells.
Giry-Laterrière M +2 more
openaire +3 more sources
2002
After more than a decade of consternation over the lack of convincing efficacy data from the early gene therapy clinical trials, the recent reports of CAVAZZANA et al. (2000) and ABONOUR et al. (2000) have brought to gene therapists and their patients a new wave of optimism.
A, Larochelle, K W, Peng, S J, Russell
openaire +2 more sources
After more than a decade of consternation over the lack of convincing efficacy data from the early gene therapy clinical trials, the recent reports of CAVAZZANA et al. (2000) and ABONOUR et al. (2000) have brought to gene therapists and their patients a new wave of optimism.
A, Larochelle, K W, Peng, S J, Russell
openaire +2 more sources
2002
Advances in the nascent field of gene therapy have created a demand for gene transfer vehicles that are capable of safely and stably delivering genes to both dividing and nondividing cells. Retroviral vectors, by virtue of their ability to permanently integrate genes of interest into the target cell genome, have played a prominent role in much of the ...
M A, Curran, G P, Nolan
openaire +2 more sources
Advances in the nascent field of gene therapy have created a demand for gene transfer vehicles that are capable of safely and stably delivering genes to both dividing and nondividing cells. Retroviral vectors, by virtue of their ability to permanently integrate genes of interest into the target cell genome, have played a prominent role in much of the ...
M A, Curran, G P, Nolan
openaire +2 more sources
Immune Responses to Lentiviral Vectors
Current Gene Therapy, 2007Efficient delivery and sustained expression of a therapeutic gene into human tissues are the requisite to accomplish the high expectations of gene therapy. A major challenge has concerned development of gene transfer systems capable of efficient cell transduction and transgene expression without harm to the recipient.
FOLLENZI, Antonia +2 more
openaire +3 more sources
Production and Titration of Lentiviral Vectors
Current Protocols in Neuroscience, 2010AbstractLentiviral vectors have emerged over the last decade as powerful, reliable, and safe tools for stable gene transfer in a wide variety of mammalian cells. Unlike other vectors derived from oncoretroviruses, they allow for stable gene delivery into most nondividing primary cells, including neurons.
Barde, Isabelle +2 more
openaire +4 more sources

