Babiss et al., “Regulation of N-myc gene expression: Use of an adenoviral vector to demonstrate posttranscriptional control”, Mol. Cell. Biol. 10(12): 6700-6708, Dec. 1990.* |
Bojocchi et al. Nature Genetics 3: 229, 1993.* |
Bajocchi et al., Direct in vivo gene transfer to ependymal cells in the central nervous system using recombinant adenovirus vectors, Nature Genetics vol. 3, pp. 229-234, (1993). |
Breakfield et al., Herpes Simplex Virus for Gene Delivery to Neurons, New Biologist ((3):203-218, 1991. |
Stramm et al., B-Glurcuronidase Mediated Pathway Essential for Retinal Pigment Epithelial Degradation of Glycosaminoglycans, Experimental Eye Research 50(5):521-32, 1990. |
Le Gal La Salle et al., An Adenovirus Vector for Gene Transfer into Neurons and Glia in the Brian, Science 259:988-90, 1993. |
Stratford-Perricaude et al., Feasibility of adenovirus-mediated gene transfer in vivo, Bone Marrow Transp. 9(Sup 1):151-52, 1992. |
Bookstein et al., Suppression of Tomorigenicity of Human Prostate Carcinoma Cells by Replacing a Mutated RB Gene, Science 247:712-715, 1990. |
Wills et al., Adenovirus Vectors for Gene Therapy of Cancer, J. Cell Biochem. Supp. 17E-17F:204, 5216, 1993. |
Maneval et al., Tumor Suppressor Gene Therapy of Cancer: Adenoviral Mediated Gene Transfer of p53 and Retinoblastoma cDNA into Human Tumor Cell Lines, J. Cell Biochem. Supp. 18C:204, N524, 1994. |
Huang et al., Suppression of the Neoplastic Phenotype by Replacement of the RB Gene in Human Cancer Cells, Science, 242:1563-66, 1988. |
Friedmann, Gene Therapy of Cancer Through Restoration of Tumor-Suppressor Functions, Cancer 70:1810-1817, 1992. |
Stratford-Perricaude et al., Gene Transfer into Animals: the promise of adenovirus, Human Gene Transfer 219:51-61, 1991. |