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Human Gene Therapy|August 7, 1998
Efficient ex vivo inhibition of perforin and Fas ligand expression by chimeric tRNA-hammerhead ribozymesZ Du, C Ricordi, L Inverardi, et al.Human Gene Therapy|June 22, 2012
Safety and biodistribution of an equine infectious anemia virus-based gene therapy, RetinoStat(®), for age-related macular degenerationKatie Binley, Peter S Widdowson, Michelle Kelleher, et al.Human Gene Therapy|September 19, 1998
Development of novel cell surface CD34-targeted recombinant adenoassociated virus vectors for gene therapyQ Yang, M Mamounas, G Yu, et al.Human Gene Therapy|July 29, 1998
Transgene expression in malignant glioma using a replication-defective adenoviral vector containing the Egr-1 promoter: activation by ionizing radiation or uptake of radioactive iododeoxyuridineY Manome, T Kunieda, P Y Wen, et al.Human Gene Therapy|July 29, 1998
Extensive cross-reactivity of adenovirus-specific cytotoxic T cellsC A Smith, L S Woodruff, C Rooney, et al.Human Gene Therapy|July 29, 1998
Atrial natriuretic peptide gene delivery attenuates hypertension, cardiac hypertrophy, and renal injury in salt-sensitive ratsK F Lin, J Chao, L ChaoHuman Gene Therapy|July 29, 1998
High-efficiency retrovirus-mediated gene transfer into the livers of miceG A Patijn, A Lieber, L Meuse, et al.Human Gene Therapy|August 28, 1998
Effects of keratinocyte and hepatocyte growth factor in vivo: implications for retrovirus-mediated gene transfer to liverA Bosch, P B McCray, K S Walters, et al.Human Gene Therapy|June 20, 2012
Combined fiber modifications both to target α(v)β(6) and detarget the coxsackievirus-adenovirus receptor improve virus toxicity profiles in vivo but fail to improve antitumoral efficacy relative to adenovirus serotype 5Lynda Coughlan, Sabari Vallath, Alena Gros, et al.Human Gene Therapy|April 2, 2015
Gene therapy for inherited diseases of liver metabolismPasquale Piccolo, Nicola Brunetti-PierriPageof 414