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Cellular and Genomic Features of Muscle Differentiation from Isogenic Fibroblasts and Myoblasts

 Louise Benarroch , Julia Madsen-Østerbye , Mohamed Abdelhalim , Kamel Mamchaoui , Jessica Ohana , et al.
Cells, 2023, 12 (15), pp.1995. ⟨10.3390/cells12151995⟩
Article dans une revue hal-04187751v1

Cellular and Genomic Features of Muscle Differentiation from Isogenic Fibroblasts and Myoblasts

 Louise Benarroch , Julia Madsen-Østerbye , Mohamed Abdelhalim , Kamel Mamchaoui , Jessica Ohana , et al.
Cells, 2023, 12 (15), pp.1995. ⟨10.3390/cells12151995⟩
Article dans une revue hal-04253840v1

New Role for Serum Response Factor in Postnatal Skeletal Muscle Growth and Regeneration via the Interleukin 4 and Insulin-Like Growth Factor 1 Pathways

 Claude L. Charvet , Christophe Houbron , Ara Parlakian , Julien Giordani , Charlotte Lahoute , et al.
Molecular and Cellular Biology, 2006, 26 (17), pp.6664-6674. ⟨10.1128/MCB.00138-06⟩
Article dans une revue hal-03120739v1

Development of gene therapy for LMNA-related congenital muscular dystrophy

 Anne T. Bertrand
Cure CMD scientific and family conference, Jul 2017, Washington DC, United States
Communication dans un congrès hal-04004859v1

CAPON expression in skeletal muscle is regulated by position, repair, NOS activity, and dystrophy.

 L. Segalat , K. Grisoni , J. Archer , C. Vargas , Anne Bertrand , et al.
Experimental Cell Research, 2005, 302, pp.170-179
Article dans une revue hal-00144038v1

DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death.

 Anne T. Bertrand , Laure Renou , Aurélie Papadopoulos , Maud Beuvin , Emmanuelle Lacène , et al.
Human Molecular Genetics, 2012, 21 (5), pp.1037-48. ⟨10.1093/hmg/ddr534⟩
Article dans une revue hal-00672148v1
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Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1

 Imen Dorboz , Marie Coutelier , Anne T. Bertrand , Jean-Hubert Caberg , Monique Elmaleh-Bergès , et al.
Orphanet Journal of Rare Diseases, 2014, 9 (1), pp.174. ⟨10.1186/s13023-014-0174-9⟩
Article dans une revue hal-01110718v1
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Mutation in lamin A/C sensitizes the myocardium to exercise-induced mechanical stress but has no effect on skeletal muscles in mouse

 Marie-Elodie Cattin , Arnaud Ferry , Alban Vignaud , Nathalie Mougenot , Adeline Jacquet , et al.
Neuromuscular Disorders, 2016, ⟨10.1016/j.nmd.2016.05.010⟩
Article dans une revue hal-01329664v1

Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiency.

 Perrine Castets , Anne T. Bertrand , Maud Beuvin , Arnaud Ferry , Fabien Le Grand , et al.
Human Molecular Genetics, 2011, 20 (4), pp.694-704. ⟨10.1093/hmg/ddq515⟩
Article dans une revue hal-00561402v1
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Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation

 Rabah Ben Yaou , Claire L. Navarro , Susana Quijano-Roy , Anne T. Bertrand , Catherine Massart , et al.
European Journal of Human Genetics, 2011, ⟨10.1038/ejhg.2010.256⟩
Article dans une revue hal-00611256v1

Haploinsufficiency and dominant negative effects of mutant lamin A/C contribute to the severity of L-CMD compared with EDMD

 Anne T. Bertrand
Satellite Meeting​ European Network for Laminopathies Meeting, Sep 2019, London, United Kingdom
Communication dans un congrès hal-03986911v1

O.3 Satellite cell loss is the pathomechanism leading to muscle atrophy in selenoprotein N deficiency

 P. Castets , A.T. Bertrand , M. Beuvin , A. Ferry , F. Le Grand , et al.
Neuromuscular Disorders, 2010, 20 (9-10), pp.598. ⟨10.1016/J.NMD.2010.07.012⟩
Article dans une revue istex hal-02935581v1

CAPON expression in skeletal muscle is regulated by position, repair, NOS activity, and dystrophy.

 Laurent Ségalat , Karine Grisoni , Jonathan Archer , Cinthya Vargas , Anne Bertrand , et al.
Experimental Cell Research, 2005, 302 (2), pp.170-9. ⟨10.1016/j.yexcr.2004.09.007⟩
Article dans une revue istex hal-00194444v1
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