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NATO ASI Series, Series H: Cell Biology - 105: Gene Therapy

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  • 223pagine
  • 8 ore di lettura

Maggiori informazioni sul libro

Gene therapy has generated significant expectations, promising to revolutionize clinical and molecular medicine by potentially correcting various human diseases, including inherited disorders, cancer, and AIDS, through successful gene sequence introduction in somatic cells. The proceedings from the first ASI on Gene Therapy, held from August 17-28, 1997, in Spetsai, Greece, summarize recent advancements in the field, presented by internationally recognized experts. Their contributions, organized as independent chapters, provide comprehensive reviews on topics such as the influence of chromatin structure on gene expression, mechanisms of gene expression, epigenetic elements, and gene delivery systems, including viral and non-viral vectors. Additionally, the proceedings cover animal models of human diseases, inducible regulatory systems, and ongoing clinical trials for cancer, AIDS, and monogenic disorders. Gene therapy represents a logical progression in human health management, offering a potential low-cost and efficient treatment option. However, to realize its full potential, critical technological advancements are necessary, including the development of safe and efficient vectors, targeted cell type delivery, and regulation of transgene expression levels.

Acquisto del libro

NATO ASI Series, Series H: Cell Biology - 105: Gene Therapy, Kleanthis G. Xanthopoulos

Lingua
Pubblicato
1998
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(Copertina rigida),
Condizioni del libro
In buone condizioni
Prezzo
6,99 €

Metodi di pagamento

Titolo
NATO ASI Series, Series H: Cell Biology - 105: Gene Therapy
Lingua
Inglese
Editore
Springer
Pubblicato
1998
Formato
Copertina rigida
Pagine
223
ISBN10
3540641122
ISBN13
9783540641124
Serie
Descrizione
Gene therapy has generated significant expectations, promising to revolutionize clinical and molecular medicine by potentially correcting various human diseases, including inherited disorders, cancer, and AIDS, through successful gene sequence introduction in somatic cells. The proceedings from the first ASI on Gene Therapy, held from August 17-28, 1997, in Spetsai, Greece, summarize recent advancements in the field, presented by internationally recognized experts. Their contributions, organized as independent chapters, provide comprehensive reviews on topics such as the influence of chromatin structure on gene expression, mechanisms of gene expression, epigenetic elements, and gene delivery systems, including viral and non-viral vectors. Additionally, the proceedings cover animal models of human diseases, inducible regulatory systems, and ongoing clinical trials for cancer, AIDS, and monogenic disorders. Gene therapy represents a logical progression in human health management, offering a potential low-cost and efficient treatment option. However, to realize its full potential, critical technological advancements are necessary, including the development of safe and efficient vectors, targeted cell type delivery, and regulation of transgene expression levels.