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Rossana Tonlorenzi

Vita-Salute San Raffaele University

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Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next-generation human artificial chromosomes for Duchenne muscular dystrophy.

2017 Embo Molecular Medicine
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Isolation and Characterization of Vessel-Associated Stem/Progenitor Cells from Skeletal Muscle

2017 Methods of Molecular Biology
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P.33 - Jab1 in the pathogenesis of Merosin deficient congenital muscular dystrophy (MDC1A)

2017 Neuromuscular Disorders
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Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy

2016 Embo Molecular Medicine
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Human artificial chromosome-mediated genetic correction of human dystrophic skeletal muscle progenitors for the autologous cell therapy of Duchenne muscular dystrophy

2015
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Combined cell and gene therapy to treat merosin deficient congenital muscular dystrophy

2015 Neuromuscular Disorders
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Erratum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs (Nature (2013) 494 (506) DOI: 10.1038/nature11976))

2014 Nature
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Inflammation Converts Human Mesoangioblasts Into Targets of Alloreactive Immune Responses: Implications for Allogeneic Cell Therapy of DMD

2014 Molecular Therapy
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Corrigendum: Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs

2013 Nature
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Mesoangioblasts Suppress T Cell Proliferation Through IDO and PGE-2-Dependent Pathways

2013 Stem Cells and Development
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