Efficient derivation and inducible differentiation of expandable skeletal myogenic cells from human ES and patient-specific iPS cells
出版年份 2015 全文链接
标题
Efficient derivation and inducible differentiation of expandable skeletal myogenic cells from human ES and patient-specific iPS cells
作者
关键词
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出版物
Nature Protocols
Volume 10, Issue 7, Pages 941-958
出版商
Springer Nature
发表日期
2015-06-04
DOI
10.1038/nprot.2015.057
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注意：仅列出部分参考文献，下载原文获取全部文献信息。- A pathway from chromosome transfer to engineering resulting in human and mouse artificial chromosomes for a variety of applications to bio-medical challenges
- (2015) Mitsuo Oshimura et al. CHROMOSOME RESEARCH
- Human artificial chromosomes for Duchenne muscular dystrophy and beyond: challenges and hopes
- (2015) Francesco Saverio Tedesco CHROMOSOME RESEARCH
- Ethics of iPSC-Based Clinical Research for Age-Related Macular Degeneration: Patient-Centered Risk-Benefit Analysis
- (2014) Mariko Nakano-Okuno et al. Stem Cell Reviews and Reports
- Myogenic Differentiation of Muscular Dystrophy-Specific Induced Pluripotent Stem Cells for Use in Drug Discovery
- (2014) Ramzey Abujarour et al. Stem Cells Translational Medicine
- Derivation and Expansion of PAX7-Positive Muscle Progenitors from Human and Mouse Embryonic Stem Cells
- (2014) Michael Shelton et al. Stem Cell Reports
- The Anticancer Drug Tamoxifen Counteracts the Pathology in a Mouse Model of Duchenne Muscular Dystrophy
- (2013) Olivier M. Dorchies et al. AMERICAN JOURNAL OF PATHOLOGY
- MyoD Is a Tumor Suppressor Gene in Medulloblastoma
- (2013) J. Dey et al. CANCER RESEARCH
- A Zebrafish Embryo Culture System Defines Factors that Promote Vertebrate Myogenesis across Species
- (2013) Cong Xu et al. CELL
- Repair or replace? Exploiting novel gene and cell therapy strategies for muscular dystrophies
- (2013) Sara Benedetti et al. FEBS Journal
- How induced pluripotent stem cells are redefining personalized medicine
- (2013) Leonardo M.R. Ferreira et al. GENE
- Muscular dystrophies
- (2013) Eugenio Mercuri et al. LANCET
- Autologous Myoblast Transplantation for Oculopharyngeal Muscular Dystrophy: a Phase I/Iia Clinical Study
- (2013) Sophie Périé et al. MOLECULAR THERAPY
- Satellite Cells and the Muscle Stem Cell Niche
- (2013) Hang Yin et al. PHYSIOLOGICAL REVIEWS
- Efficient and Reproducible Myogenic Differentiation from Human iPS Cells: Prospects for Modeling Miyoshi Myopathy In Vitro
- (2013) Akihito Tanaka et al. PLoS One
- Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome
- (2013) A. Aiuti et al. SCIENCE
- Lentiviral Hematopoietic Stem Cell Gene Therapy Benefits Metachromatic Leukodystrophy
- (2013) A. Biffi et al. SCIENCE
- Derivation and FACS-Mediated Purification of PAX3+/PAX7+ Skeletal Muscle Precursors from Human Pluripotent Stem Cells
- (2013) Bianca Borchin et al. Stem Cell Reports
- Matrigel, but not collagen I, maintains the differentiation capacity of muscle derived cellsin vitro
- (2012) S Grefte et al. Biomedical Materials
- Induced Pluripotent Stem Cells: Past, Present, and Future
- (2012) Shinya Yamanaka Cell Stem Cell
- Human ES- and iPS-Derived Myogenic Progenitors Restore DYSTROPHIN and Improve Contractility upon Transplantation in Dystrophic Mice
- (2012) Radbod Darabi et al. Cell Stem Cell
- Pharmacologically Targeting the Primary Defect and Downstream Pathology in Duchenne Muscular Dystrophy
- (2012) Rebecca J. Fairclough et al. CURRENT GENE THERAPY
- Satellite cell senescence underlies myopathy in a mouse model of limb-girdle muscular dystrophy 2H
- (2012) Elena Kudryashova et al. JOURNAL OF CLINICAL INVESTIGATION
- Myoblasts Derived From Normal hESCs and Dystrophic hiPSCs Efficiently Fuse With Existing Muscle Fibers Following Transplantation
- (2012) Sébastien Goudenege et al. MOLECULAR THERAPY
- Selective Development of Myogenic Mesenchymal Cells from Human Embryonic and Induced Pluripotent Stem Cells
- (2012) Tomonari Awaya et al. PLoS One
- Transplantation of Genetically Corrected Human iPSC-Derived Progenitors in Mice with Limb-Girdle Muscular Dystrophy
- (2012) F. S. Tedesco et al. Science Translational Medicine
- Alpha sarcoglycan is required for FGF-dependent myogenic progenitor cell proliferation in vitro and in vivo
- (2011) M. Cassano et al. DEVELOPMENT
- Hepatocyte-targeted expression by integrase-defective lentiviral vectors induces antigen-specific tolerance in mice with low genotoxic risk
- (2011) Janka Mátrai et al. HEPATOLOGY
- Stem Cell-Mediated Transfer of a Human Artificial Chromosome Ameliorates Muscular Dystrophy
- (2011) F. S. Tedesco et al. Science Translational Medicine
- Guidelines for the welfare and use of animals in cancer research
- (2010) P Workman et al. BRITISH JOURNAL OF CANCER
- Short Telomeres and Stem Cell Exhaustion Model Duchenne Muscular Dystrophy in mdx/mTR Mice
- (2010) Alessandra Sacco et al. CELL
- Generation of Sheffield (Shef) human embryonic stem cell lines using a microdrop culture system
- (2010) Behrouz Aflatoonian et al. IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY-ANIMAL
- Recent Advances in Lentiviral Vector Development and Applications
- (2010) Janka Mátrai et al. MOLECULAR THERAPY
- The genotoxic potential of retroviral vectors is strongly modulated by vector design and integration site selection in a mouse model of HSC gene therapy
- (2009) Eugenio Montini et al. JOURNAL OF CLINICAL INVESTIGATION
- Cell-lineage regulated myogenesis for dystrophin replacement: a novel therapeutic approach for treatment of muscular dystrophy
- (2008) E. Kimura et al. HUMAN MOLECULAR GENETICS
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