Cargando…
Clinical utility of recombinant adenoviral human p53 gene therapy: current perspectives
Gene therapy has promised to be a highly effective antitumor treatment by introducing a tumor suppressor gene or the abrogation of an oncogene. Among the potential therapeutic transgenes, the tumor suppressor gene p53 serves as an attractive target. Restoration of wild-type p53 function in tumors ca...
Autores principales: | Chen, Guang-xia, Zhang, Shu, He, Xiao-hua, Liu, Shi-yu, Ma, Chao, Zou, Xiao-Ping |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211860/ https://www.ncbi.nlm.nih.gov/pubmed/25364261 http://dx.doi.org/10.2147/OTT.S50483 |
Ejemplares similares
-
Efficacy of Recombinant Adenoviral Human p53 Gene in Treatment of Malignant Pleural or Peritoneal Effusions
por: ZHANG, Xin, et al.
Publicado: (2013) -
Gene Therapy with Helper-Dependent Adenoviral Vectors: Current Advances and Future Perspectives
por: Vetrini, Francesco, et al.
Publicado: (2010) -
Immunotherapy for Lewis lung carcinoma utilizing dendritic cells infected with CK19 gene recombinant adenoviral vectors
por: SUN, Q.F., et al.
Publicado: (2015) -
Effective Genetic Expression of Nanoantibodies by Recombinant
Adenoviral Vector in vitro
por: Gribova, I.Yu., et al.
Publicado: (2011) -
Seamless assembly of recombinant adenoviral genomes from high-copy plasmids
por: Miciak, Jessica J., et al.
Publicado: (2018)