The Journal of Gene Medicine

The Journal of Gene Medicine is pleased to introduce its Special Themed Reviews on current topics in gene and cell therapy - read these articles free online:

Now available:
Special Section on Cancer Gene Therapy
Guest Edited by Chiara Bonini & Giorgio Parmiani

Challenges in T cell receptor gene therapy
Benjamin J. Uttenthal et al

Cancer therapy with genetically modified T cells for the treatment of melanoma
Kiran H. Lagisett & Richard A. Morgan

CD40-targeted adenoviral cancer vaccines: the long and winding road to the clinic
Basav N. Hangalapura et al

Chimeric Antigen Receptors for T cell Immunotherapy: Current Understanding and Future Direction
Kevin J. Curran et al

Highly potent mRNA based cancer vaccines represent an attractive platform for combination therapies supporting an improved therapeutic effect.
Mariola Fotin-Mleczek et al

Also available
Special Section on Heart Gene Delivery
Guest Edited by Dongsheng Duan

OnlineOpen - The Open Access Option for Authors
OnlineOpen is available to authors who wish to make their article open access, free to read, download and share via Wiley Online Library and PubMed Central. Learn more here.

NEW!
Gene therapy clinical trials worldwide to 2012 – an update
Samantha L. Ginn, Ian E. Alexander, Michael L. Edelstein, Mohammad R. Abedi & Jo Wixon

Read our FREE access Virtual Issues that collate high quality articles on key topics from the journal:

• Non-viral gene delivery
  
  Electro-mediated gene transfer and expression are controlled by the life-time of DNA/membrane complex formation
  Cécile Faurie et al
  
  Investigation of polyethylenimine-grafted-triamcinolone acetonide as nucleus-targeting gene delivery systems
  Kun Ma et al
  
  Read more from this Virtual Issue here.
  
  
• Interfering RNA
  
  Polyethylenimine/small interfering RNA-mediated knockdown of vascular endothelial growth factor in vivo exerts anti-tumor effects synergistically with Bevacizumab
  Sabrina Höbel et al
  
  Inhibition of HIV-1 infection by a unique short hairpin RNA to chemokine receptor 5 delivered into macrophages through hematopoietic progenitor cell transduction
  Min Liang et al
  
  Read more from this Virtual Issue here.
  
  
• Oligonucleotide approaches
  
  In vitro evaluation of novel antisense oligonucleotides is predictive of in vivo exon skipping activity for Duchenne muscular dystrophy
  Qingsong Wang et al
  
  In vivo comparison of 2 '-O-methyl phosphorothioate and morpholino antisense oligonucleotides for Duchenne muscular dystrophy exon skipping
  HA Heemskerk et al
  
  Read more from this Virtual Issue here.