Myogenesis modelled by human pluripotent stem cells: a multi‐omic study of Duchenne myopathy early onset-Reference-Cited by-同舟云学术

Myogenesis modelled by human pluripotent stem cells: a multi‐omic study of Duchenne myopathy early onset

Published:2021-02 Issue:1 Volume:12 Page:209-232
ISSN:2190-5991
Container-title:Journal of Cachexia, Sarcopenia and Muscle
language:en
Short-container-title:Journal of Cachexia, Sarcopenia and Muscle

Author:

Mournetas Virginie¹^ORCID,Massouridès Emmanuelle²^ORCID,Dupont Jean‐Baptiste¹^ORCID,Kornobis Etienne³⁴^ORCID,Polvèche Hélène²^ORCID,Jarrige Margot²^ORCID,Dorval Alan R.L.²^ORCID,Gosselin Maxime R.F.⁵^ORCID,Manousopoulou Antigoni⁶^ORCID,Garbis Spiros D.⁷⁸^ORCID,Górecki Dariusz C.⁵⁹^ORCID,Pinset Christian¹⁰^ORCID

Affiliation:

1. INSERM UEVE UMR861, I‐STEM, AFM Corbeil‐Essonnes France

2. CECS, I‐STEM, AFM Corbeil‐Essonnes France

3. Biomics, C2RT Institut Pasteur Paris France

4. Hub de Bioinformatique et Biostatistique ‐ Département BiologieComputationnelle Paris France

5. Molecular Medicine, School of Pharmacy and Biomedical Sciences University of Portsmouth Portsmouth UK

6. Department of Immuno‐Oncology Beckman Research Institute, City of Hope National Medical Center Duarte CA USA

7. Unit for Cancer Sciences, Centre for Proteomics Research, Institute for Life Sciences University of Southampton Southampton UK

8. Proteas Bioanalytics Inc. BioLabs at The Lundquist Institute Torrance CA USA

9. Military Institute of Hygiene and Epidemiology Warsaw Poland

10. CNRS, I‐STEM, AFM Corbeil‐Essonnes France

Funder

AFM-Téléthon

Fondation Maladies Rares

Publisher

Wiley

Subject

Physiology (medical),Orthopedics and Sports Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcsm.12665

Reference105 articles.

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2. Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database

3. Muscle damage progression in Duchenne muscular dystrophy evaluated by a new quantitative computed tomography method

4. Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression

5. Biomarkers of Duchenne muscular dystrophy: current findings;Al‐Khalili Szigyarto C;Degener Neurol Neuromuscul Dis, vol,2018

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