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Human Gene Therapy|March 21, 2006
Efficacy of gene therapy for Wiskott-Aldrich syndrome using a WAS promoter/cDNA-containing lentiviral vector and nonlethal irradiationLoïc Dupré, Francesco Marangoni, Samantha Scaramuzza, et al.
Human Gene Therapy|June 1, 1992
Gene transfer in vivo with DNA-liposome complexes: safety and acute toxicity in miceM J Stewart, G E Plautz, L Del Buono, et al.
Human Gene Therapy|December 16, 1998
Enhancer and promoter chimeras in plasmids designed for intramuscular injection: a comparative in vivo and in vitro studyK M Barnhart, J Hartikka, M Manthorpe, et al.
Human Gene Therapy|December 16, 1998
The treatment of malignant mesothelioma with a gene modified cancer cell line: a phase I studyP Schwarzenberger, L Harrison, A Weinacker, et al.
Human Gene Therapy|December 21, 2007
Impact of retroviral vector components stoichiometry on packaging cell lines: effects on productivity and vector qualityManuel J T Carrondo, Otto-Wilhelm Merten, Matthias Haury, et al.
Human Gene Therapy|December 13, 2007
Quantification and characterization of autotransduction in retroviral vector producer cellsEva Maria Brandtner, Petra Kodajova, Elzbieta Knapp, et al.
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