De novo Induction of Genetically Engineered Brain Tumors in Mice Using Plasmid DNA

SM Wiesner, SA Decker, JD Larson, K Ericson… - Cancer research, 2009 - AACR
Spontaneous mouse models of cancer show promise to more accurately recapitulate human
disease and predict clinical efficacy. Transgenic mice or viral vectors have been required to …

The hyperactive Sleeping Beauty transposase SB100X improves the genetic modification of T cells to express a chimeric antigen receptor

Z Jin, S Maiti, H Huls, H Singh, S Olivares, L Mátés… - Gene therapy, 2011 - nature.com
Sleeping Beauty (SB 3) transposon and transposase constitute a DNA plasmid system used
for therapeutic human cell genetic engineering. Here we report a comparison of SB100X, a …

Preferential delivery of the Sleeping Beauty transposon system to livers of mice by hydrodynamic injection

JB Bell, KM Podetz-Pedersen, EL Aronovich… - Nature protocols, 2007 - nature.com
Nonviral, DNA-mediated gene transfer is an alternative to viral delivery systems for
expressing new genes in cells and tissues. The Sleeping Beauty (SB) transposon system …

Chromosomal mobilization and reintegration of Sleeping Beauty and PiggyBac transposons

Q Liang, J Kong, J Stalker, A Bradley - genesis, 2009 - Wiley Online Library
Abstract The Sleeping Beauty and PiggyBac DNA transposon systems have recently been
developed as tools for insertional mutagenesis. We have compared the chromosomal …

Emerging potential of transposons for gene therapy and generation of induced pluripotent stem cells

T VandenDriessche, Z Ivics, Z Izsvák… - Blood, The Journal of …, 2009 - ashpublications.org
Effective gene therapy requires robust delivery of the desired genes into the relevant target
cells, long-term gene expression, and minimal risks of secondary effects. The development …

[HTML][HTML] DNA transposon-based gene vehicles-scenes from an evolutionary drive

KA Skipper, PR Andersen, N Sharma… - Journal of biomedical …, 2013 - Springer
DNA transposons are primitive genetic elements which have colonized living organisms
from plants to bacteria and mammals. Through evolution such parasitic elements have …

Translating Sleeping Beauty transposition into cellular therapies: Victories and challenges

Z Izsvák, PB Hackett, LJN Cooper, Z Ivics - Bioessays, 2010 - Wiley Online Library
Recent results confirm that long‐term expression of therapeutic transgenes can be achieved
by using a transposon‐based system in primary stem cells and in vivo. Transposable …

High efficiency site‐specific genetic engineering of the mosquito genome

DD Nimmo, L Alphey, JM Meredith… - Insect Molecular …, 2006 - Wiley Online Library
Current techniques for the genetic engineering of insect genomes utilize transposable
genetic elements, which are inefficient, have limited carrying capacity and give rise to …

[HTML][HTML] Helper-independent Sleeping Beauty transposon–transposase vectors for efficient nonviral gene delivery and persistent gene expression in vivo

JG Mikkelsen, SR Yant, L Meuse, Z Huang, H Xu… - Molecular Therapy, 2003 - cell.com
Transposon-based vectors represent promising new tools for chromosomal transgene
insertion and establishment of persistent gene expression in vivo. Here, we report the …

Phenotypic correction and long-term expression of factor VIII in hemophilic mice by immunotolerization and nonviral gene transfer using the Sleeping Beauty …

JR Ohlfest, JL Frandsen, S Fritz, PD Lobitz… - Blood, 2005 - ashpublications.org
Hemophilia A is a lead candidate for treatment by gene therapy because small increments in
the missing secreted protein product, coagulation factor VIII (FVIII), would result in …