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Human Gene Therapy|June 18, 2021
An Improved Lentiviral Fluorescent Genetic Barcoding Approach Distinguishes Hematopoietic Stem Cell Properties in Multiplexed In Vivo ExperimentsAnna Lieske, Teng Cheong Ha, Axel Schambach, et al.
Human Gene Therapy|July 6, 2021
Adenosine Deaminase 1 Overexpression Enhances the Antitumor Efficacy of Chimeric Antigen Receptor-Engineered T CellsYun Qu, Zachary S Dunn, Xianhui Chen, et al.
Human Gene Therapy|December 22, 2020
Combining Oncolytic Viruses with Chimeric Antigen Receptor T Cell TherapyKyle McGrath, Gianpietro Dotti
Human Gene Therapy|January 7, 2021
Lack of Toxicity in Nonhuman Primates Receiving Clinically Relevant Doses of an AAV9.U7snRNA Vector Designed to Induce DMD Exon 2 SkippingLiubov V Gushchina, Emma C Frair, Natalie Rohan, et al.
Human Gene Therapy|December 10, 2020
AAV1-Mediated shRNA Knockdown of SASH1 in Rat Bronchus Attenuates Hypoxia-Induced Pulmonary Artery RemodelingHong Liu, Ning Wang, Jun Li, et al.
Human Gene Therapy|January 16, 2013
Effects of herpes simplex virus vector-mediated enkephalin gene therapy on bladder overactivity and nociceptionHitoshi Yokoyama, Tomohiko Oguchi, William F Goins, et al.
Human Gene Therapy|December 20, 2012
Polyploidization without mitosis improves in vivo liver transduction with lentiviral vectorsVirginie Pichard, Dominique Couton, Chantal Desdouets, et al.
Human Gene Therapy|February 14, 2013
Recovery of radiation-induced dry eye and corneal damage by pretreatment with adenoviral vector-mediated transfer of erythropoietin to the salivary glands in miceEduardo M Rocha, Ana P Cotrim, Changyu Zheng, et al.
Human Gene Therapy|January 10, 2013
A mutant Tat protein provides strong protection from HIV-1 infection in human CD4+ T cellsAnn Apolloni, Min-Husan Lin, Haran Sivakumaran, et al.
Human Gene Therapy|April 25, 2013
Suppression of nicotine-induced pathophysiology by an adenovirus hexon-based antinicotine vaccineJonathan B Rosenberg, Bishnu P De, Martin J Hicks, et al.
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