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Cullen, B.R., “Human Immunodeficiency Virus as a Prototypic Complex Retrovirus”, Journal of Virology (1991); 65(3): 1053-1056. cited by applicant . Koldej, R.M., et al., “Comparison of Insulators and Promoters for Expression of the Wiskott-Aldrich Syndrome Protein Using Lentiviral Vectors” Human Gene Therapy Clinical Development (2013); 24: 77-85. cited by applicant . Kutner et al., “Production, concentration and titration of pseudotyped HIV-1-based lentiviral vectors”, Nature Protocols (2009); 4: 495-505. cited by applicant . Imren, S. et al., “High-level beta-globin expression and preferred intragenic integration after lentiviral transduction of human cord blood stem cells”, J Clin Invest (2004); 114(7): 953-962. cited by applicant . Giannoni, F., et al., “Allelic Exclusion and Peripheral Reconstitution by TCR Transgenic T Cells Arising From Transduced Human Hematopoietic Stem/Progenitor Cells.” Molecular Therapy (2013); 21(5): 1044-1054. cited by applicant . Human Gene Therapy (2013); 24(10): 824-839. cited by applicant . Cribbs, A.P., et al., “Simplified production and concentration of lentiviral vectors to achieve high transduction in primary human T cells.” BMC Biotechnology (2013); 13(1): 98. cited by applicant .

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Holt, L. et al., “Domain antibodies: proteins for therapy”, Trends in Biotechnology (2003); 21(11): 484-490. cited by applicant . De Felipe, Pablo, and Ryan, Martin D. “Targeting of proteins derived from self-processing polyproteins containing multiple signal sequences.” Traffic (2004); 5.8: 616-626. cited by applicant . Lee, H. C. et al., “Remission in models of type 1 diabetes by gene therapy using a single-chain insulin analogue”, Nature (2000); 408(6811): 483-488. cited by applicant . Liu, Lin, et al., “Adoptive T-cell therapy of B-cell malignancies: Conventional and physiological chimeric antigen receptors.” Cancer Letters (2012); 316(1): 1-5. cited by applicant . Nature Biotechnology (2007); 25.12: 1477-1482. cited by applicant . Desjarlais, John R., and Berg, Jeremy M. “Use of a zinc-finger consensus sequence framework and specificity rules to design specific DNA binding proteins.” Proceedings of the National Academy of Sciences (1993); 90.6: 2256-2260. cited by applicant . Journal of Medicinal Chemistry (1994); 37.9: 1233-1251. cited by applicant . Journal of Experimental Medicine (1999); 190.9: 1319-1328. cited by applicant . Proceedings of the National Academy of Sciences USA (1993); 90.15: 6909-6913. cited by applicant . Blood (2013); 122(21): 1659. cited by applicant . Kozak, M., “Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes”, Cell (1986); 44(2): 283-292. cited by applicant .

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