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Molecular Therapy : the Journal of the American Society of Gene Therapy|September 1, 2004
High-level in vivo gene marking after gene-modified autologous hematopoietic stem cell transplantation without marrow conditioning in nonhuman primatesKyoji Ueda, Yutaka Hanazono, Hiroaki Shibata, et al.
Human Gene Therapy|March 5, 2009
Stable retinal gene expression in nonhuman primates via subretinal injection of SIVagm-based lentiviral vectorsYasuhiro Ikeda, Yoshikazu Yonemitsu, Masanori Miyazaki, et al.
Transplantation|October 15, 2003
Engraftment and tumor formation after allogeneic in utero transplantation of primate embryonic stem cellsTakayuki Asano, Naohide Ageyama, Koichi Takeuchi, et al.
The Journal of Gene Medicine|September 24, 2004
Sustained transgene expression by human cord blood derived CD34+ cells transduced with simian immunodeficiency virus agmTYO1-based vectors carrying the human coagulation factor VIII gene in NOD/SCID miceJiro Kikuchi, Jun Mimuro, Kyoichi Ogata, et al.
Human Gene Therapy|May 7, 2009
Acute toxicity study of a simian immunodeficiency virus-based lentiviral vector for retinal gene transfer in nonhuman primatesYasuhiro Ikeda, Yoshikazu Yonemitsu, Masanori Miyazaki, et al.
The Journal of Gene Medicine|November 6, 2003
Efficient gene transfer of a simian immuno-deficiency viral vector into cardiomyocytes derived from primate embryonic stem cellsMihoko Nagata, Masafumi Takahashi, Shin-Ichi Muramatsu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 25, 2010
Toward gene therapy for cystic fibrosis using a lentivirus pseudotyped with Sendai virus envelopesKatsuyuki Mitomo, Uta Griesenbach, Makoto Inoue, et al.
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