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Viral vectors for gene therapy

Trends in Biotechnology, 1998
Gene therapy is now being applied to the treatment of wide variety of acquired and inherited diseases. One of the rate-limiting steps for successful gene therapy is the efficiency of gene transfer. A number of different viral systems are being developed for use as vectors for ex vivo and in vivo gene transfer, including retroviruses, adenoviruses ...
P D, Robbins, H, Tahara, S C, Ghivizzani
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Viral gene therapy

Clinical and Translational Oncology, 2006
Cancer is a multigenic disorder involving mutations of both tumor suppressor genes and oncogenes. A large body of preclinical data, however, has suggested that cancer growth can be arrested or reversed by treatment with gene transfer vectors that carry a single growth inhibitory or pro-apoptotic gene or a gene that can recruit immune responses against ...
P, Mancheño-Corvo, P, Martín-Duque
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Viral Gene Delivery in Chondrocytes

2022
Viral gene transfer, known as transduction, is a powerful research tool for studying the biology of chondrocytes in novel ways and also a technology enabling the use of gene therapy for regenerating cartilage and treating diseases that affect cartilage, such as osteoarthritis.
Christopher V, Nagelli   +2 more
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Gene Therapy with Viral Vectors

Annual Review of Pharmacology and Toxicology, 2003
A key factor in the success of gene therapy is the development of gene delivery systems that are capable of efficient gene transfer in a broad variety of tissues, without causing any pathogenic effect. Currently, viral vectors based on many different viruses have been developed, and their performance and pathogenicity has been evaluated in animal ...
Neeltje A, Kootstra, Inder M, Verma
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Polymers for viral gene delivery

Expert Opinion on Drug Delivery, 2008
The development of viral vectors capable of providing efficient gene transfer in diseased tissues without causing any pathogenic effects is pivotal for overcoming the many challenges facing gene therapy.Immune responses against viral vectors, inadequate gene expression and inefficient targeting to specific cells in vivo are some of the major problems ...
Chun, Wang, Phuong-Truc, Pham
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Sequencing of Viral Genes

2009
The use of molecular techniques in epidemiology gives a better understanding of viral transmission and diversity, and helps to define and characterizc outbreaks. By elucidating transmission patterns and defining outbreak parameters, appropriate preventive measures can be implemented in a timely fashion.
Carol, Holm-Hansen, Kirsti, Vainio
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Viral gene delivery

Expert Opinion on Investigational Drugs, 1999
Experimental studies of viral gene delivery generally support the principle that virus-mediated gene transfer is indeed possible. However, the field of gene therapy has not yet been realised as a practicable clinical intervention. The delay in translation of laboratory work to clinical utility largely reflects the inability of gene delivery vectors to ...
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Viral Genes and Methylation

Annals of the New York Academy of Sciences, 2003
Abstract: Epigenetics represents a new frontier in cancer research. Methylation is the best studied of the epigenetic mechanisms that regulate gene expression. Regulation of gene expression by means of methylation has been reported for tumor suppressor genes, oncogenes, viral promoters, and age‐related genes.
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Gene therapy for viral hepatitis

Expert Opinion on Biological Therapy, 2006
Hepatitis B and C infections are two of the most prevalent viral diseases in the world. Existing therapies against chronic viral hepatitis are far from satisfactory due to low response rates, undesirable side effects and selection of resistant viral strains. Therefore, new therapeutic approaches are urgently needed.
Gloria, Gonzalez-Aseguinolaza   +5 more
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Viral Vectors in Gene Therapy

Annual Review of Microbiology, 1995
The use of DNA as a drug is both appealing and simple in concept. Indeed in many instances the feasibility of such an approach has been established using model systems. In practical terms, however, the delivery of DNA to human tissues presents a wide variety of problems that differ with each potential therapeutic application. In this review, the design,
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