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Immunotherapy|August 9, 2018
Intravenous immunoglobulin 10% in children with primary immunodeficiency diseasesHans D Ochs, Isaac Melamed, Michael Borte, et al.
Human Gene Therapy|August 31, 2012
Integrase-deficient lentiviral vectors mediate efficient gene transfer to human vascular smooth muscle cells with minimal genotoxic riskHelen E Chick, Ali Nowrouzi, Raffaele Fronza, et al.
Blood|June 11, 2011
Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative studyDaniele Moratto, Silvia Giliani, Carmem Bonfim, et al.
Nature Cancer|August 4, 2021
Clonal expansion of T memory stem cells determines early anti-leukemic responses and long-term CAR T cell persistence in patientsLuca Biasco, Natalia Izotova, Christine Rivat, et al.
Molecular Therapy. Methods & Clinical Development|October 27, 2021
Safety and efficacy of an engineered hepatotropic AAV gene therapy for ornithine transcarbamylase deficiency in cynomolgus monkeysJulien Baruteau, Sharon C Cunningham, Berna Seker Yilmaz, et al.
Scientific Reports|August 30, 2017
Erratum: Lentiviral vectors can be used for full-length dystrophin gene therapyJohn R Counsell, Zeinab Asgarian, Jinhong Meng, et al.
Scientific Reports|March 3, 2017
Lentiviral vectors can be used for full-length dystrophin gene therapyJohn R Counsell, Zeinab Asgarian, Jinhong Meng, et al.
Scientific Reports|March 18, 2017
Lentiviral vectors can be used for full-length dystrophin gene therapyJohn R Counsell, Zeinab Asgarian, Jinhong Meng, et al.
Cytotherapy|July 6, 2016
Automated manufacturing of chimeric antigen receptor T cells for adoptive immunotherapy using CliniMACS prodigyUlrike Mock, Lauren Nickolay, Brian Philip, et al.
Journal of Clinical Immunology|April 28, 2007
Sequence analysis of TNFRSF13b, encoding TACI, in patients with systemic lupus erythematosusUlrich Salzer, Jennifer Birmelin, Chiara Bacchelli, et al.
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