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Sinopse
Cancer gene therapy, like cancer therapy in general, is evolving rapidly, testing new concepts, targets and pathways, evoking new technologies, and passing new regulatory hurdles. Its essence, however, has not changed: the hope and challenges of returning altered genes to normal, using targeted gene expression to alter the function of both tumor and microenvironment, and in some cases normal cells, and delivering functionally important genes to specific cell types to increase sensitivity to killing or to protect normal cells from cancer therapies.
In some instances, gene therapy for cancer forms a continuum from gene repair through the use of molecularly modified cells; the use of viral and non-viral vector based gene delivery to both tumor and tumor microenvironment; the use of viral and gene based vaccines; and development of new gene-based therapeutics. The unique mechanistically chosen vector platforms are at the heart of this technology because they allow for direct and selective cell death and transient to sustained delivery of vaccine molecules or molecules that affect the microenvironment, vasculature, or the immune response.
Ficha Técnica
Especificações
ISBN | 9780123942951 |
---|---|
Subtítulo | TRANSLATIONAL APPROACHES FROM PRECLINICAL STUDIES TO CLINICAL IMPLEMENTATION, |
Pré venda | Não |
Peso | 619g |
Autor para link | LATTIME EDMUND,GERSON STANTON L. |
Livro disponível - pronta entrega | Não |
Dimensões | 23 x 16 x 1 |
Idioma | Inglês |
Tipo item | LIVRO IMPORTADO ADQ MERC INTERNO |
Número de páginas | 554 |
Número da edição | 3ª EDIÇÃO - 2013 |
Código Interno | 788739 |
Código de barras | 9780123942951 |
Acabamento | HARDCOVER |
Autor | LATTIME, EDMUND | GERSON, STANTON L. |
Editora | ACADEMIC PRESS |
Sob encomenda | Sim |