Læknaneminn - 01.04.1994, Side 134

Læknaneminn - 01.04.1994, Side 134
12. Carter BJ. Adeno-associated virus vectors. Current Opinion in Biotechnology 1992; 3: 533-9. 13. Wu GY, Wu CH. Receptor-mediated in vitro gene transformation by a soluble DNA carrier system. J Biol Chem 1987; 262: 4429-32. 14. Curiel DT, Wagner E, Cotten M et al. High-efficiency gene transfer mediated by adenovirus coupled to DNA-polylysine complexes. Hum Gene Ther 1992; 3: 147-154. 15. Zenke M, Steinlein P, Wagner E et al. Receptor- mediated endocytosis of transferrin-polycation conjugates: an efficient way to introduce DNA into hematopoietic cells. Proc Natl Acad Sci USA 1990; 87: 3655-9. 16. Mannino RJ, Gould Fogerite S. Liposome-mediated gene transfer. Biotechniques 1988; 6: 682-90. 17. Acsadi G, Dickson G, Love DR et al. Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs. Nature 1991; 352: 815-8. 18. Chen CA, Okayama H. Calcium phosphate-mediated gene transfer: A highly efficient transfection system for stably transforming cells with plasmid DNA. Biotechniques 1988; 6: 632-8. 19. McNally MA, Lebkowski JS, Okarma TB et al. Optimizing electroporation parameters for a variety of human hematopoietic cell lines. Biotechniques 1988; 6: 882-6. 20. Yao SN, Wilson JM, Nabel EG et al. Expression of human factor IX in rat capillary endothelial cells: toward somatic gene therapy for hemophilia B. Proc Natl Acad Sci USA 1991; 88: 8101-5. 21. Karlsson S. Treatment of genetic defects in hematopoietic cell function by gene transfer. Blood 1991; 78: 2481-92. 22. Mulligan RC. The basic science of gene therapy. Science 1993; 260: 926-32. 23. Gupta S, Wilson JM, Chowdhury JR. Hepatocyte transplantation: development of new systems for liver repopulation and gene therapy. Semin Liver Dis. 1992; 12: 321-31. 24. Miller AD. Human gene therapy comes of age. Nature 1992; 357:455-60. 25. Wilson JM, Grossman M. Therapeutic strategies for familial hypercholesterolemia based on somatic gene transfer. Am J Cardiol 1993; 72: 59D-63D. 26. Friedmann T. Approaches to gene therapy of complex multigenic diseases: cancer as a model and implications for cardiovascular disease and diabetes. Ann Med. 1992;24:411-7. 27. Cheng J, Yee JK, Yeargin J et al. Suppression of acute lymphoblastic leukemia by the human wild-type p53 gene. Cancer Res 1992; 52: 222-6. 28. Golumbeck PT, Lazenby AJ, Levitsky HI et al. Treatment of established renal cancer by tumor cells engineered to secret interleukin-4. Science 1991; 254: 713-6. 29. Culver KW, Ram Z, Wallbridge S et al. In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors. Science 1992; 256: 1550-2. 30. Takamiya Y, Short P, Moolten FL et al. An experimental model of retrovirus gene therapy for malignant brain tumors. J Neurosurg 1993; 79: 104- 10. " 31. Chien KR. Molecular advances in cardiovascular biology. Science. 1993; 260: 916-7. 32. Rubin EM, Krauss RM, Spangler EA et al. Inhibition of early atherogenesis in transgenic mice by human apolipoprotein AI. Nature 1991; 353: 265-7. 33. Simons M, Edelman ER, DeKeyser JL et al. Antisense c-myb oligonucleotides inhibit intimal arterial smooth muscle cell accumulation in vivo. Nature 1992; 359: 67-70. 34. Jiao S, Gurevich V, Wolff JA. Long-term correction of rat model of Parkinson’s disease by gene therapy. Nature 1993;362:450-3. 35. Buchschacher GL, Jr. Molecular targets of gene transfer therapy forHIV infection. JAMA 1993; 269: 2880-6. 36. Lisziewicz J, Sun D, Smythe J et al. Inhibition of human immunodeficiency virus type 1 replication by regulated expression of a polymeric Tat activation response RNA decoy as a strategy for gene therapy in AIDS. Proc Nat Acad Sci USA 1993; 90(17): 8000- 4. 37. Buonocore L, Rose JK. Blockade of human immunodeficiency virus type 1 production in CD4+ T cells by an intracellular CD4 expressed under control of the viral long terminal repeat. Proc Nat Acad Sci USA 1993; 90(7): 2695-9. 38. Harrison GS, Long CJ, Curiel TJ et al. Inhibition of human immunodeficiency virus-1 production resulting from transduction with a retrovirus containing an HlV-regulated diphtheria toxin A chain gene. Hum Gene Ther 1992; 3(5): 461-9. 39. McCarthy M. Gene therapy for HIV infection [news]. Lancet 1993; 342: 799. 40. Temin-HM. Safety considerations in somatic gene therapy of human disease with retrovirus vectors. Hum Gene Ther 1990; 1: 111-23. 124 LÆKNANEMINN 1 1994 47. árg.
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