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Martina Ragazzi

Three-Dimensional Human iPSC-Derived Artificial Skeletal Muscles Model Muscular Dystrophies and Enable Multilineage Tissue Engineering
2018 · Sara Martina Maffioletti, Shilpita Sarcar, et al. · Cell Reports · 330
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Transplantation of Genetically Corrected Human iPSC-Derived Progenitors in Mice with Limb-Girdle Muscular Dystrophy
2012 · Francesco Saverio Tedesco, Mattia F. M. Gerli, et al. · Science Translational Medicine · 300
Intra‐arterial transplantation of HLA‐matched donor mesoangioblasts in Duchenne muscular dystrophy
2015 · Giulio Cossu, Stefano C Previtali, et al. · EMBO Molecular Medicine · 180
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Efficient derivation and inducible differentiation of expandable skeletal myogenic cells from human ES and patient-specific iPS cells
2015 · Sara M Maffioletti, Mattia F M Gerli, et al. · Nature Protocols · 110
Combined Notch and PDGF Signaling Enhances Migration and Expression of Stem Cell Markers while Inducing Perivascular Cell Features in Muscle Satellite Cells
2019 · Mattia Francesco Maria Gerli, Louise Anne Moyle, et al. · Stem Cell Reports · 55
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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 · Sara Benedetti, Narumi Uno, et al. · EMBO Molecular Medicine · 32
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Erratum To: Intra‐arterial transplantation of HLA‐matched donor mesoangioblasts in Duchenne muscular dystrophy
2016 · Giulio Cossu, Stefano C Previtali, et al. · EMBO Molecular Medicine · 27
Mesoangioblasts at 20: From the embryonic aorta to the patient bed
2023 · Giulio Cossu, Rossana Tonlorenzi, et al. · Frontiers in Genetics · 16
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Enhanced Energetic State and Protection from Oxidative Stress in Human Myoblasts Overexpressing BMI1
2017 · Silvia Dibenedetto, Maria Niklison-Chirou, et al. · Stem Cell Reports · 12
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Erratum: Corrigendum: Efficient derivation and inducible differentiation of expandable skeletal myogenic cells from human ES and patient-specific iPS cells
2015 · Sara M Maffioletti, Mattia F M Gerli, et al. · Nature Protocols · 3
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Efficient derivation and inducible differentiation of expandable skeletal myogenic cells from human ES and patient-specific iPS cells (vol 10, pg 941, 2015)
2015 · Sara M. Maffioletti, M Gerli, et al. · UCL Discovery (University College London) · 1
Correction: Mesoangioblasts at 20: from the embryonic aorta to the patient bed
2026 · Giulio Cossu, Rossana Tonlorenzi, et al. · Frontiers in Genetics
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Combining iPS cell-derived myogenic progenitors and human artificial chromosomes as a potential genomic integration-free cell and gene therapy for Duchenne muscular dystrophy
2018 · G. Ferrari, H. Hoshiya, et al. · Neuromuscular Disorders
Generation of three-dimensional artificial skeletal muscle constructs from human pluripotent stem cells for complex disease modelling of muscular dystrophies
2018 · S.M. Maffioletti, S. Sarcar, et al. · Neuromuscular Disorders
Generation of biocompatible human artificial 3D skeletal muscle tissue from healthy and dystrophic pluripotent stem cells
2017 · S. Maffioletti, A. Henderson, et al. · Neuromuscular Disorders
Human artificial chromosomes combined with iPS cells: a genomic integration-free therapy for Duchenne muscular dystrophy
2017 · G. Ferrari, H. Hoshiya, et al. · Neuromuscular Disorders
Generation of Three-dimensional Human Artificial Skeletal Muscle Tissue From Ips Cells Enables Complex Disease Modelling for Muscular Dystrophy
2017 · Sara M. Maffioletti, Shilpita Sarcar, et al. · RVC Research Online (Royal Veterinary College)
iPS cells and human artificial chromosomes: towards a genomic integration-free therapy for Duchenne muscular dystrophy
2016 · Giuliana Ferrari, Hidetoshi Hoshiya, et al. · UCL Discovery (University College London)
Generation of implantable 3D skeletal muscle tissue from human embryonic stem cells and muscular dystrophy iPS cells
2016 · Maffioletti, SM, Vollert, I, et al. · UCL Discovery (University College London)
Reversible immortalisation, human artificial chromosomes, and induced pluripotency: new gene and cell therapy technologies for Duchenne muscular dystrophy
2016 · Sara Benedetti, Hidetoshi Hoshiya, et al. · The Lancet
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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 · Benedetti, S, Hoshiya, H, et al. · UCL Discovery (University College London)
Reversible immortalization allows human artificial chromosome-mediated gene correction of human dystrophic muscle progenitor cells
2015 · S. Benedetti, H. Hoshiya, et al. · Neuromuscular Disorders
Human artificial chromosome-mediated strategies for stem cell-based therapy of muscular dystrophy
2015 · Hidetoshi Hoshiya, Sara Benedetti, et al. · UCL Discovery (University College London)
P66 iPS cells and human artificial chromosomes: novel therapeutic tools for muscle disorders
2014 · F.S. Tedesco, S. Benedetti, et al. · Neuromuscular Disorders
Works count: 24
Citation count: 1,066
H-index: 9
I10-index: 9
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