Science 8 May 1992: Vol. 256. no. 5058, pp. 808 - 813 DOI: 10.1126/science.1589762

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Articles

Gene therapy in clinical medicine.

S M Selkirk (2004)
Postgrad. Med. J. 80, 560-570
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Gene Transfer of Human Hepatocyte Growth Factor into Rat Skin Wounds Mediated by Liposomes Coated with the Sendai Virus (Hemagglutinating Virus of Japan).

K. Nakanishi, M. Uenoyama, N. Tomita, R. Morishita, Y. Kaneda, T. Ogihara, K. Matsumoto, T. Nakamura, A. Maruta, S. Matsuyama, et al. (2002)
Am. J. Pathol. 161, 1761-1772
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Gene Therapy in Orthopaedic Surgery.

D. Hannallah, B. Peterson, J. R. Lieberman, F. H. Fu, and J. Huard (2002)
J. Bone Joint Surg. Am. 84, 1046-1061
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Molecular Imaging and Gene Therapy.

C. Nichol and E. E. Kim (2001)
J. Nucl. Med. 42, 1368-1374
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Gene Transfer of Heat-Shock Protein 70 Reduces Infarct Size In Vivo After Ischemia/Reperfusion in the Rabbit Heart.

S. Okubo, O. Wildner, M. R. Shah, J. C. Chelliah, M. L. Hess, and R. C. Kukreja (2001)
Circulation 103, 877-881
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Percutaneous in vivo gene transfer to the peripheral lungs using plasmid-liposome complexes.

H. Saito, H. Nakamura, S. Kato, S. Inoue, M. Inage, M. Ito, and H. Tomoike (2000)
Am J Physiol Lung Cell Mol Physiol 279, L651-L657
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Expression of Herpes Simplex Virus ICP47 and Human Cytomegalovirus US11 Prevents Recognition of Transgene Products by CD8+ Cytotoxic T Lymphocytes.

C. Berger, S. Xuereb, D. C. Johnson, K. S. Watanabe, H.-P. Kiem, P. D. Greenberg, and S. R. Riddell (2000)
J. Virol. 74, 4465-4473
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Gene Therapy for Lung Disease: Hype or Hope?.

S. M. Albelda, R. Wiewrodt, and J. B. Zuckerman (2000)
Ann Intern Med 132, 649-660
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Focal angiogen therapy using intramyocardial delivery of an adenovirus vector coding for vascular endothelial growth factor 121.

L. Y. Lee, S. R. Patel, N. R. Hackett, C. A. Mack, D. R. Polce, T. El-Sawy, R. Hachamovitch, P. Zanzonico, T. A. Sanborn, M. Parikh, et al. (2000)
Ann. Thorac. Surg. 69, 14-23
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Mutations in the Retinoblastoma-related Gene RB2/p130 in Lung Tumors and Suppression of Tumor Growth in Vivo by Retrovirus-mediated Gene Transfer.

P. P. Claudio, C. M. Howard, C. Pacilio, C. Cinti, G. Romano, C. Minimo, N. M. Maraldi, J. D. Minna, L. Gelbert, L. Leoncini, et al. (2000)
Cancer Res. 60, 372-382
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Prospects for in Utero Human Gene Therapy.

E. D. Zanjani and W. F. Anderson (1999)
Science 285, 2084-2088
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Highly efficient liposome-mediated gene transfer of inducible nitric oxide synthase in vivo and in vitro in vascular smooth muscle cells.

K. Veit, J.-P. Boissel, M. Buerke, T. Grosser, J. Meyer, and H. Darius (1999)
Cardiovasc Res 43, 808-822
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EXOGENOUS CONTROL OF CARDIAC GENE THERAPY: EVIDENCE OF REGULATED MYOCARDIAL TRANSGENE EXPRESSION AFTER ADENOVIRUS AND ADENO-ASSOCIATED VIRUS TRANSFER OF EXPRESSION CASSETTES CONTAINING CORTICOSTEROID RESPONSE ELEMENT PROMOTERS.

L. Y. Lee, X. Zhou, D. R. Polce, T. El-Sawy, S. R. Patel, G. D. Thakker, K. Narumi, R. G. Crystal, and T. K. Rosengart (1999)
J. Thorac. Cardiovasc. Surg. 118, 26-25
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Molecular advances in cardiac and cardiovascular disease.

A. Basile-Borgia, J. H Abel, and H. Mahloogi (1999)
Perfusion 14, 89-99
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Site-Specific Integration in Mammalian Cells Mediated by a New Hybrid Baculovirus-Adeno-Associated Virus Vector.

F. Palombo, A. Monciotti, A. Recchia, R. Cortese, G. Ciliberto, and N. La Monica (1998)
J. Virol. 72, 5025-5034
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Delayed Targeting of Cytokine-Nonresponsive Human Bone Marrow CD34+ Cells With Retrovirus-Mediated Gene Transfer Enhances Transduction Efficiency and Long-Term Expression of Transduced Genes.

P. Veena, C. M. Traycoff, D. A. Williams, J. McMahel, S. Rice, K. Cornetta, and E. F. Srour (1998)
Blood 91, 3693-3701
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Gene Therapy for Infectious Diseases.

B. A. Bunnell and R. A. Morgan (1998)
Clin. Microbiol. Rev. 11, 42-56
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Severe Combined Immunodeficiency Mice Engrafted With Human T Cells, B Cells, and Myeloid Cells After Transplantation With Human Fetal Bone Marrow or Liver Cells and Implanted With Human Fetal Thymus: A Model for Studying Human Gene Therapy.

S. Yurasov, T. R. Kollmann, A. Kim, C. A. Raker, M. Hachamovitch, F. Wong-Staal, and H. Goldstein (1997)
Blood 89, 1800-1810
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Novel pyridinium surfactants for efficient, nontoxic in vitro gene delivery.

I. van der Woude, A. Wagenaar, A. A. P. Meekel, M. B. A. ter Beest, M. H. J. Ruiters, J. B. F. N. Engberts, and D. Hoekstra (1997)
PNAS 94, 1160-1165
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A Novel Herpes Vector for the High-Efficiency Transduction of Normal and Malignant Human Hematopoietic Cells.

D. Dilloo, D. Rill, C. Entwistle, M. Boursnell, W. Zhong, W. Holden, M. Holladay, S. Inglis, and M. Brenner (1997)
Blood 89, 119-127
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Avoidance of Immune Response Prolongs Expression of Genes Delivered to the Adult Rat Myocardium by Replication-Defective Adenovirus.

M. J. Quinones, J. Leor, R. A. Kloner, M. Ito, M. Patterson, W. F. Witke, and L. Kedes (1996)
Circulation 94, 1394-1401
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Heterogeneity of Adenovirus-Mediated Gene Transfer in Cultured Thoracic Aorta and Renal Artery of Rats.

A. Yao and D. H. Wang (1995)
Hypertension 26, 1046-1050
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Gene Therapy in Peripheral Blood Lymphocytes and Bone Marrow for ADA- Immunodeficient Patients.

C. Bordignon, L. D. Notarangelo, N. Nobili, G. Ferrari, G. Casorati, P. Panina, E. Mazzolari, D. Maggioni, C. Rossi, P. Servida, et al. (1995)
Science 270, 470-475
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Innovation in the pharmaceutical industry.

R Sykes (1994)
BMJ 309, 422-3
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Regulation of Somatic-Cell Therapy and Gene Therapy by the Food and Drug Administration.

D. A. Kessler, J. P. Siegel, P. D. Noguchi, K. C. Zoon, K. L. Feiden, and J. Woodcock (1993)
N. Engl. J. Med. 329, 1169-1173
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New startups move in as gene therapy goes commercial.

E Culotta (1993)
Science 260, 914-915
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The basic science of gene therapy.

R. Mulligan (1993)
Science 260, 926-932
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Structure-Based Strategies for Drug Design and Discovery.

I. D. Kuntz (1992)
Science 257, 1078-1082
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Genetically engineered macrophages expressing IFN-gamma restore alveolar immune function in scid mice.

M. Wu, S. Hussain, Y.-H. He, R. Pasula, P. A. Smith, and W. J. Martin II (2001)
PNAS 98, 14589-14594
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