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Human Gene Therapy|January 12, 2022
Genetic Modification of the AAV5 Capsid with Lysine Residues Results in a Lung-Tropic Liver-Detargeted Gene Transfer VectorKatie M Stiles, Esther Z Frenk, Stephen M Kaminsky, et al.
Human Gene Therapy|October 15, 2009
MyD88-dependent silencing of transgene expression during the innate and adaptive immune response to helper-dependent adenovirusMasataka Suzuki, Vincenzo Cerullo, Terry K Bertin, et al.
Human Gene Therapy|October 25, 2011
Prednisolone treatment does not interfere with 2'-O-methyl phosphorothioate antisense-mediated exon skipping in Duchenne muscular dystrophyIngrid E C Verhaart, Hans Heemskerk, Tatyana G Karnaoukh, et al.
Human Gene Therapy|January 11, 2012
Asymmetric siRNA: new strategy to improve specificity and reduce off-target gene expressionZhongping Yuan, Xilin Wu, Chao Liu, et al.
Human Gene Therapy|March 21, 2012
Zinc finger protein designed to target 2-long terminal repeat junctions interferes with human immunodeficiency virus integrationSupachai Sakkhachornphop, Carlos F Barbas, Rassamee Keawvichit, et al.
Human Gene Therapy|April 10, 2012
In vivo gene transfer strategies to achieve partial correction of von Willebrand diseaseLan Wang, Jonathan B Rosenberg, Bishnu P De, et al.
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