Aurélie Papadopoulos

ORCID: 0000-0003-0060-7040
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About
Contact & Profiles
Research Areas
  • Cardiomyopathy and Myosin Studies
  • RNA Research and Splicing
  • Nuclear Structure and Function
  • Genomics and Chromatin Dynamics
  • Congenital heart defects research
  • Muscle Physiology and Disorders

Institut de Myologie
2011-2013

Sorbonne Université
2011-2013

Pitié-Salpêtrière Hospital
2011-2013

Inserm
2013

Centre de Recherche en Myologie
2013

Centre National de la Recherche Scientifique
2013

The LMNA gene encodes lamin A/C intermediate filaments that polymerize beneath the nuclear membrane, and are also found in nucleoplasm an uncharacterized assembly state. They thought to have structural functions regulatory roles signaling pathways via interaction with transcription factors. Mutations been involved numerous inherited human diseases, including severe congenital muscular dystrophy (L-CMD). We created Lmna(ΔK32) knock-in mouse harboring a L-CMD mutation. Lmna(ΔK32/ΔK32) mice...

10.1093/hmg/ddr534 article EN Human Molecular Genetics 2011-11-16

The functional and architectural benefits of embryonic stem cells (ESC) myoblasts (Mb) transplantations into infarcted myocardium have been investigated extensively. Whereas ESC repopulated fibrotic areas contributed to myocardial regeneration, Mb exerted their effects through paracrine secretions scar remodeling. This therapeutic perspective, however, has less explored in the setting nonischemic dilated cardiomyopathies (DCMs). Our aim was compare integration efficacy committed cardiac fate...

10.1038/mt.2013.15 article EN cc-by-nc-nd Molecular Therapy 2013-02-26
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