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dc.contributor.editorHashad, Doaa
dc.date.accessioned2021-04-20T15:53:06Z
dc.date.available2021-04-20T15:53:06Z
dc.date.issued2015
dc.identifierONIX_20210420_9789535122210_2136
dc.identifier.urihttps://directory.doabooks.org/handle/20.500.12854/66777
dc.description.abstractGene therapy is becoming a promising technology for the management of many human diseases. Hereditary and acquired disorders can both be tackled using the technique of gene therapy. This book provides detailed, up-to-date topics addressing basic principles of gene therapy and discussing some of the challenges encountered by scientists in developing this relatively novel technology. The development of new and efficient gene transfer vectors is of utmost importance in the progress of the field of gene therapy. Both viral and non-viral vectors are extensively discussed. A detailed chapter elaborates the problem of host immune rejection of transplanted donor cells or engineered tissue that can be avoided using the encapsulation of transgenic cells, thus avoiding the use of drugs that achieve immunosuppression.
dc.languageEnglish
dc.subject.classificationthema EDItEUR::M Medicine and Nursing::MF Pre-clinical medicine: basic sciences::MFN Medical geneticsen_US
dc.subject.otherMedical genetics
dc.titleGene Therapy
dc.title.alternativePrinciples and Challenges
dc.typebook
oapen.identifier.doi10.5772/59824
oapen.relation.isPublishedBy78a36484-2c0c-47cb-ad67-2b9f5cd4a8f6
oapen.relation.isbn9789535122210
oapen.relation.isbn9789535172680
oapen.imprintIntechOpen
oapen.pages218


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