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Molecular Therapy : the Journal of the American Society of Gene Therapy|June 1, 2005
Current status of gene therapy strategies to treat HIV/AIDSDavid S Strayer, Ramesh Akkina, Bruce A Bunnell, et al.
The Journal of Gene Medicine|February 5, 2005
Generation of a packaging cell line for prolonged large-scale production of high-titer HIV-1-based lentiviral vectorYajin Ni, Susan Sun, Ibe Oparaocha, et al.
Frontiers in Immunology|February 28, 2022
Armored BCMA CAR T Cells Eliminate Multiple Myeloma and Are Resistant to the Suppressive Effects of TGF-βLeah M Alabanza, Ying Xiong, Bang Vu, et al.
Human Gene Therapy Methods|July 25, 2013
Rapid generation of stable cell lines expressing high levels of erythropoietin, factor VIII, and an antihuman CD20 antibody using lentiviral vectorsLajos Baranyi, Christopher B Doering, Gabriella Denning, et al.
Frontiers in Oncology|December 8, 2018
A Unique Human Immunoglobulin Heavy Chain Variable Domain-Only CD33 CAR for the Treatment of Acute Myeloid LeukemiaDina Schneider, Ying Xiong, Peirong Hu, et al.
The Journal of Gene Medicine|September 8, 2004
Safe two-plasmid production for the first clinical lentivirus vector that achieves >99% transduction in primary cells using a one-step protocolXiaobin Lu, Laurent Humeau, Vladimir Slepushkin, et al.
Blood|April 3, 2004
ABC transporter inhibitors that are substrates enhance lentiviral vector transduction into primitive hematopoietic progenitor cellsBrian M Davis, Laurent Humeau, Vladimir Slepushkin, et al.
Frontiers in Immunology|September 12, 2019
A Distinct Subset of Highly Proliferative and Lentiviral Vector (LV)-Transducible NK Cells Define a Readily Engineered Subset for Adoptive Cellular TherapyRafijul Bari, Markus Granzin, Kam Sze Tsang, et al.
Frontiers in Immunology|December 17, 2019
Corrigendum: A Distinct Subset of Highly Proliferative and Lentiviral Vector (LV)-Transducible NK Cells Define a Readily Engineered Subset for Adoptive Cellular TherapyRafijul Bari, Markus Granzin, Kam Sze Tsang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 18, 2010
Lentiviral vector platform for production of bioengineered recombinant coagulation factor VIIIH Trent Spencer, Gabriela Denning, Richard E Gautney, et al.
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