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Plos One|August 23, 2012
Generation of induced pluripotent stem cells from human nasal epithelial cells using a Sendai virus vectorMizuho Ono, Yuko Hamada, Yasue Horiuchi, et al.
Biochemical and Biophysical Research Communications|August 7, 2007
In vivo repopulation of cytoplasmically gene transferred hematopoietic cells by temperature-sensitive mutant of recombinant Sendai viral vectorKumi Yoshida, Yoshikazu Yonemitsu, Sakura Tanaka, et al.
Microbes and Infection|March 5, 2008
Abrogation of AIDS vaccine-induced cytotoxic T-lymphocyte efficacy in vivo due to a change in viral epitope flanking sequencesChikaya Moriya, Hiroko Igarashi, Akiko Takeda, et al.
Circulation Research|May 23, 2002
Angiogenic gene therapy for experimental critical limb ischemia: acceleration of limb loss by overexpression of vascular endothelial growth factor 165 but not of fibroblast growth factor-2Ichiro Masaki, Yoshikazu Yonemitsu, Akihisa Yamashita, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|July 5, 2005
Cytoplasmic expression and extracellular deposition of an antiangiogenic factor, pigment epithelium-derived factor, in human atherosclerotic plaquesHiromitsu Baba, Yoshikazu Yonemitsu, Toshiaki Nakano, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 26, 2006
Efficient expression of a transgene in platelets using simian immunodeficiency virus-based vector harboring glycoprotein Ibalpha promoter: in vivo model for platelet-targeting gene therapyTsukasa Ohmori, Jun Mimuro, Katsuhiro Takano, et al.
Biochemical and Biophysical Research Communications|October 3, 2002
Enhancement of phage-mediated gene transfer by nuclear localization signalTeruo Akuta, Akiko Eguchi, Hajime Okuyama, et al.
Current Gene Therapy|October 17, 2015
Ex Vivo and In Vivo Lentivirus-Mediated Transduction of Airway Epithelial Progenitor CellsGiulia Leoni, Marguerite Y Wasowicz, Mario Chan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 6, 2002
Highly efficient gene transfer into primate embryonic stem cells with a simian lentivirus vectorTakayuki Asano, Yutaka Hanazono, Yasuji Ueda, et al.
Human Gene Therapy|January 31, 2013
Genetically modified adipose tissue-derived stem/stromal cells, using simian immunodeficiency virus-based lentiviral vectors, in the treatment of hemophilia BNatsumi Watanabe, Kazuo Ohashi, Kohei Tatsumi, et al.
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