An Adenovirus Vector with Genetically Modified Fibers Demonstrates Expanded Tropism via Utilization of a Coxsackievirus and Adenovirus Receptor-Independent Cell Entry Mechanism
Igor P. Dmitriev(Washington University in St. Louis), David T. Curiel(Washington University in St. Louis)
Cited by 769
Related Papers
Engineering targeted viral vectors for gene therapy
|Nature Reviews Genetics|2007|678
Covalently Linked Au Nanoparticles to a Viral Vector: Potential for Combined Photothermal and Gene Cancer Therapy
|Nano Letters|2006|260
Enhanced therapeutic efficacy for ovarian cancer with a serotype 3 receptor-targeted oncolytic adenovirus
|Molecular Therapy|2003|172
The therapeutic efficacy of adenoviral vectors for cancer gene therapy is limited by a low level of primary adenovirus receptors on tumour cells
|European Journal of Cancer|2002|137