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2022Bioelectronic cell-based device provides a strategy for the treatment of the experimental model of multiple sclerosis., J Control Release 2022 Nov; 352(): 994-1008.
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2022Genetically modified macrophages accelerate myelin repair., EMBO Mol Med 2022 Aug; 14(8): e14759.
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2022Hematopoietic stem cell transplantation chemotherapy causes microglia senescence and peripheral macrophage engraftment in the brain., Nat Med 2022 Mar; 28(3): 517-527.
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2018Ex Vivo Selection of Transduced Hematopoietic Stem Cells for Gene Therapy of β-Hemoglobinopathies., Mol Ther 2018 Feb; 26(2): 480-495.
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2015Preclinical evaluation of efficacy and safety of an improved lentiviral vector for the treatment of β-thalassemia and sickle cell disease., Curr Gene Ther 2015 ; 15(1): 64-81.
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2011Distribution of lentiviral vector integration sites in mice following therapeutic gene transfer to treat β-thalassemia., Mol Ther 2011 Jul; 19(7): 1273-86.
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2011Correction of murine β-thalassemia after minimal lentiviral gene transfer and homeostatic in vivo erythroid expansion., Blood 2011 May; 117(20): 5321-31.
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2010Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia., Nature 2010 Sep; 467(7313): 318-22.