AbstractWe have created a novel method for coupling adenoviral vectors to solid microbeads in a way that does not adversely affect the infectivity of the attached virions. This method utilizes the extremely tight interaction between the protein streptavidin and its ligand biotin as a means of tethering viral particles to microbeads. The adenovirus–microbead conjugates that were created functioned as fully infectious entities and possessed several functional advantages over free, unmodified viral particles. The adenovirus–microbead conjugates possessed enhanced ability to transduce target cells in culture. For target cells of a highly permissive nature, this increase in infectivity was modest. However for target cells of moderate to low perm...
Molecular conjugate vectors may be constructed that accomplish high efficiency gene transfer by the ...
Genetically modified adenoviruses (Ads) make attractive vectors for the delivery of exogenous DNA to...
Adenoviral vectors offer many advantages for cancer gene therapy, including high transduction effici...
AbstractWe have created a novel method for coupling adenoviral vectors to solid microbeads in a way ...
In this thesis a novel technology is described to target adenovirus vectors. Adenovirus vectors are ...
Molecular conjugate vectors may be constructed that accomplish high efficiency gene transfer by the ...
Employment of recombinant viruses as gene transfer vectors is limited by constraints on the size and...
Background Regenerative gene therapy using viral vectors enables transduced cells to express bioact...
Adenoviruses (Ads) have shown promise as vectors for gene delivery in clinical trials. Efficient vir...
Gene transfer may be accomplished by the receptor-mediated endocytosis pathway using transferrin-pol...
Efficient and cell-specific delivery of DNA is essential for the effective and safe use of gene deli...
The development of targeted vectors, capable of tissue-specific transduction, remains one of the imp...
Adenoviral vector systems for gene therapy can be much improved by targeting vectors to specific cel...
Several years ago it was reported that the entry of adenovirus particles could augment the uptake of...
Nanomedicine based on the use of adenovirus vectors for therapeutic gene delivery shows broad potent...
Molecular conjugate vectors may be constructed that accomplish high efficiency gene transfer by the ...
Genetically modified adenoviruses (Ads) make attractive vectors for the delivery of exogenous DNA to...
Adenoviral vectors offer many advantages for cancer gene therapy, including high transduction effici...
AbstractWe have created a novel method for coupling adenoviral vectors to solid microbeads in a way ...
In this thesis a novel technology is described to target adenovirus vectors. Adenovirus vectors are ...
Molecular conjugate vectors may be constructed that accomplish high efficiency gene transfer by the ...
Employment of recombinant viruses as gene transfer vectors is limited by constraints on the size and...
Background Regenerative gene therapy using viral vectors enables transduced cells to express bioact...
Adenoviruses (Ads) have shown promise as vectors for gene delivery in clinical trials. Efficient vir...
Gene transfer may be accomplished by the receptor-mediated endocytosis pathway using transferrin-pol...
Efficient and cell-specific delivery of DNA is essential for the effective and safe use of gene deli...
The development of targeted vectors, capable of tissue-specific transduction, remains one of the imp...
Adenoviral vector systems for gene therapy can be much improved by targeting vectors to specific cel...
Several years ago it was reported that the entry of adenovirus particles could augment the uptake of...
Nanomedicine based on the use of adenovirus vectors for therapeutic gene delivery shows broad potent...
Molecular conjugate vectors may be constructed that accomplish high efficiency gene transfer by the ...
Genetically modified adenoviruses (Ads) make attractive vectors for the delivery of exogenous DNA to...
Adenoviral vectors offer many advantages for cancer gene therapy, including high transduction effici...