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Gene Therapy|January 12, 2016
Establishment of two quantitative nested qPCR assays targeting the human EPO transgeneE W I Neuberger, I Perez, C Le Guiner, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 8, 2009
Tolerogenic dendritic cells actively inhibit T cells through heme oxygenase-1 in rodents and in nonhuman primatesA Moreau, M Hill, P Thébault, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 1995
Sustained delivery of erythropoietin in mice by genetically modified skin fibroblastsN Naffakh, A Henri, J L Villeval, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 1995
Retroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblastsN Cartier, J Lopez, P Moullier, et al.
Gene Therapy|November 18, 2000
Characterization of novel safe lentiviral vectors derived from simian immunodeficiency virus (SIVmac251) that efficiently transduce mature human dendritic cellsD Nègre, P E Mangeot, G Duisit, et al.
Gene Therapy|September 8, 2017
Long-term expression of melanopsin and channelrhodopsin causes no gross alterations in the dystrophic dog retinaB Ameline, K-T Tshilenge, M Weber, et al.
Gene Therapy|January 16, 2015
Efficient central nervous system AAVrh10-mediated intrathecal gene transfer in adult and neonate ratsJ Hordeaux, L Dubreil, J Deniaud, et al.
Gene Therapy|October 7, 2006
Restoration of vision in RPE65-deficient Briard dogs using an AAV serotype 4 vector that specifically targets the retinal pigmented epitheliumG Le Meur, K Stieger, A J Smith, et al.
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