The use of adenoviral vectors for gene therapy and gene transfer in vivo
JL Bramson, FL Graham, J Gauldie - Current opinion in biotechnology, 1995 - Elsevier
JL Bramson, FL Graham, J Gauldie
Current opinion in biotechnology, 1995•ElsevierAdenoviral vectors have proven to be excellent vehicles for gene delivery in vivo to a wide
range of cell types. These vectors have been used to transfer genes such as CFTR to correct
the defect in cystic fibrosis and, more recently, to supply serum blood factors and genetically
modify tumors to enhance therapy.
range of cell types. These vectors have been used to transfer genes such as CFTR to correct
the defect in cystic fibrosis and, more recently, to supply serum blood factors and genetically
modify tumors to enhance therapy.
Adenoviral vectors have proven to be excellent vehicles for gene delivery in vivo to a wide range of cell types. These vectors have been used to transfer genes such as CFTR to correct the defect in cystic fibrosis and, more recently, to supply serum blood factors and genetically modify tumors to enhance therapy.
Elsevier
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