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Human Gene Therapy|December 21, 2012
Antisense oligonucleotides: rising stars in eliminating RNA toxicity in myotonic dystrophyZhihua Gao, Thomas A CooperHuman Gene Therapy|January 16, 2013
Restoration of cytoskeleton homeostasis after gigaxonin gene transfer for giant axonal neuropathySilke Mussche, Bart Devreese, Sahana Nagabhushan Kalburgi, et al.Human Gene Therapy|May 31, 2012
Correction of brain oligodendrocytes by AAVrh.10 intracerebral gene therapy in metachromatic leukodystrophy miceFrançoise Piguet, Dolan Sondhi, Monique Piraud, et al.Human Gene Therapy|May 17, 2013
New frontier in regenerative medicine: site-specific gene correction in patient-specific induced pluripotent stem cellsZita Garate, Brian R Davis, Oscar Quintana-Bustamante, et al.Human Gene Therapy|April 30, 2013
Recombinant adeno-associated virus integration sites in murine liver after ornithine transcarbamylase gene correctionLi Zhong, Nirav Malani, Mengxin Li, et al.Human Gene Therapy|June 25, 2013
Human parainfluenza virus type 2 vector induces dendritic cell maturation without viral RNA replication/transcriptionKenichiro Hara, Masayuki Fukumura, Junpei Ohtsuka, et al.Human Gene Therapy|June 1, 2012
Genetic therapeutic approaches for Duchenne muscular dystrophyHelen Foster, Linda Popplewell, George DicksonHuman Gene Therapy|June 14, 2012
Gene therapy for primary immunodeficienciesChristine Rivat, Giorgia Santilli, H Bobby Gaspar, et al.Human Gene Therapy|October 5, 2013
Short hairpin RNA gene silencing of prolyl hydroxylase-2 with a minicircle vector improves neovascularization of hindlimb ischemiaMaarten A Lijkwan, Alwine A Hellingman, Ernst J Bos, et al.Human Gene Therapy|April 27, 2002
Transduction of long-term-engrafting human hematopoietic stem cells by retroviral vectorsChristopher D Porada, Nam D Tran, Graça Almeida-Porada, et al.Pageof 414