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Human Gene Therapy|June 30, 2007
Potent inhibition of simian immunodeficiency virus (SIV) replication by an SIV-based lentiviral vector expressing antisense EnvStephen E Braun, Xiaobin V Lu, Fay Eng Wong, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 20, 2005
Inhibition of simian/human immunodeficiency virus replication in CD4+ T cells derived from lentiviral-transduced CD34+ hematopoietic cellsStephen E Braun, Fay Eng Wong, Michelle Connole, et al.
Cancer Discovery|May 13, 2022
Sequential Single-Cell Transcriptional and Protein Marker Profiling Reveals TIGIT as a Marker of CD19 CAR-T Cell Dysfunction in Patients with Non-Hodgkin LymphomaZachary Jackson, Changjin Hong, Robert Schauner, et al.
Human Gene Therapy|February 11, 2005
Regulatory considerations for novel gene therapy products: a review of the process leading to the first clinical lentiviral vectorPeter Manilla, Tessio Rebello, Cathleen Afable, et al.
Molecular Cancer Therapeutics|March 12, 2009
Potent induction of B- and T-cell immunity against human carcinoembryonic antigen-expressing tumors in human carcinoembryonic antigen transgenic mice mediated by direct lentivector injectionSeverine Loisel-Meyer, Tania Felizardo, Jacopo Mariotti, et al.
Bone Marrow Transplantation|November 8, 2022
Decentralized manufacturing of anti CD19 CAR-T cells using CliniMACS Prodigy®: real-world experience and cost analysis in IndiaHamenth Kumar Palani, Arun Kumar Arunachalam, Mohammed Yasar, et al.
Plos One|September 3, 2010
Survival of the fittest: positive selection of CD4+ T cells expressing a membrane-bound fusion inhibitor following HIV-1 infectionJanine Kimpel, Stephen E Braun, Gang Qiu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 15, 2004
Efficient lentiviral vector-mediated control of HIV-1 replication in CD4 lymphocytes from diverse HIV+ infected patients grouped according to CD4 count and viral loadLaurent M Humeau, Gwendolyn K Binder, Xiaobin Lu, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 9, 2006
Gene transfer in humans using a conditionally replicating lentiviral vectorBruce L Levine, Laurent M Humeau, Jean Boyer, et al.
Communications Medicine|May 23, 2022
Patient-reported outcomes and neurotoxicity markers in patients treated with bispecific LV20.19 CAR T cell therapyJennifer M Knight, Aniko Szabo, Igli Arapi, et al.
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