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authIdHal_s : denis-furling
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The effect of constitutive inactivation of the myostatin gene on the gain in muscle strength during postnatal growth in two murine models

Amalia Stantzou , Vanessa Ueberschlag-Pitiot , Rémi Thomasson , Denis Furling , Anne Bonnieu et al.
Muscle & Nerve, 2016, 55 (2), pp.254-261. ⟨10.1002/mus.25220⟩
Journal articles hal-01346093v1

Replicative aging down-regulates the myogenic regulatory factors in human myoblasts

Anne Bigot , Virginie Jacquemin , Florence Debacq-Chainiaux , Gillian Butler-Browne , Olivier Toussaint et al.
Biology of the Cell, 2008, 100 (3), pp.189-199. ⟨10.1042/BC20070085⟩
Journal articles istex hal-03833741v1

Upregulation of glial GLT1 glutamate transporter corrects Purkinje cell dysfunction and cerebellum-dependent motor incoordination in a mouse model of myotonic dystrophy

Diana Mihaela Dincã , Laurent Servais , Géraldine Sicot , Axelle Leroy , Cynthia Prigogine et al.
SAB Meeting, Apr 2017, Paris, France
Conference poster hal-04010282v1
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The beneficial effect of chronic muscular exercise on muscle fragility is increased by Prox1 gene transfer in dystrophic mdx muscle

Alexandra Monceau , Clément Delacroix , Mégane Lemaitre , Gaelle Revet , Denis Furling et al.
PLoS ONE, 2022, 17 (4), pp.e0254274. ⟨10.1371/journal.pone.0254274⟩
Journal articles hal-03830867v1

Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy

Frédérique Rau , Fernande Freyermuth , Charlotte Fugier , Jean-Philippe Villemin , Marie-Christine Fischer et al.
Nature Structural and Molecular Biology, 2011, 18 (7), pp.840-845. ⟨10.1038/nsmb.2067⟩
Journal articles istex hal-03339571v1
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Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy

Fernande Freyermuth , Frédérique Rau , Yosuke Kokunai , Thomas Linke , Chantal Sellier et al.
Nature Communications, 2016, 7, pp.11067. ⟨10.1038/ncomms11067⟩
Journal articles hal-01301863v1
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Dystrophin restoration therapy improves both the reduced excitability and the force drop induced by lengthening contractions in dystrophic mdx skeletal muscle

Pauline Roy , Fredérique Rau , Julien Ochala , Julien Messéant , Bodvael Fraysse et al.
Skeletal Muscle, 2016, 6 (1), pp.23. ⟨10.1186/s13395-016-0096-4⟩
Journal articles hal-01357455v1

Identification of a CCG-enriched expanded allele in DM1 patients using Amplification-free long-read sequencing

Yu-Chih Tsai , Laure de Pontual , Cheryl Heiner , T. Stojkovic , Denis Furling et al.
PacBio users 2022, May 2022, Paris, France
Conference papers hal-04004337v1

Identification of a CCG-enriched expanded allele in DM1 patients using Amplification-free long-read sequencing

Yu-Chih Tsai , Laure de Pontual , Chéryl Heiner , Tanya Stojkovic , Denis Furling et al.
FASEB, The dynamic DNA structures in biology conference, Jun 2022, Nova Scotia, Canada
Conference papers hal-04004408v1
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Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy

Frédérique Rau , Jeanne Lainé , Laetitita Ramanoudjame , Arnaud Ferry , Ludovic Arandel et al.
Nature Communications, 2015, 6 (1), pp.7205. ⟨10.1038/ncomms8205⟩
Journal articles hal-01162385v1
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CRISPR gene editing in pluripotent stem cells reveals the function of MBNL proteins during human in vitro myogenesis

Antoine Mérien , Julie Tahraoui-Bories , Michel Cailleret , Jean-Baptiste Dupont , Céline Leteur et al.
Human Molecular Genetics, 2022, 31 (1), pp.41-56. ⟨10.1093/hmg/ddab218⟩
Journal articles hal-03830948v1

MBNL dependent-impaired development connectivity within neuromuscular circuits in Myotonic Dystrophy type.

Julie Tahraoui-Bories , Antoine Mérien , Jeanne Lainé , Florine Roussange , Anchel González-Barriga et al.
Myology 2022, Sep 2022, Nice, France
Conference poster hal-04005593v1

240th ENMC workshop: The involvement of skeletal muscle stem cells in the pathology of muscular dystrophies 25-27 January 2019, Hoofddorp, The Netherlands

Jennifer Morgan , Gillian Butler-Browne , Francesco Muntoni , Ketan Patel , Helge Amthor et al.
Neuromuscular Disorders, 2019, 29 (9), pp.704-715. ⟨10.1016/j.nmd.2019.07.003⟩
Journal articles hal-03201551v1
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Alternative splicing of clathrin heavy chain contributes to the switch from coated pits to plaques

Gilles Moulay , Jeanne Lainé , Mégane Lemaître , Masayuki Nakamori , Ichizo Nishino et al.
Journal of Cell Biology, 2020, 219 (9), ⟨10.1083/jcb.201912061⟩
Journal articles hal-03005118v1
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Analysis of Exonic Regions Involved in Nuclear Localization, Splicing Activity, and Dimerization of Muscleblind-like-1 Isoforms

Helene Tran , Nathalie Gourrier , Camille Lemercier-Neuillet , Claire-Marie Dhaenens , Audrey Vautrin et al.
Journal of Biological Chemistry, 2011, 286 (18), pp.16435 - 16446. ⟨10.1074/jbc.M110.194928⟩
Journal articles hal-01738403v1
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Desmin prevents muscle wasting, exaggerated weakness and fragility, and fatigue in dystrophic mdx mouse

Arnaud Ferry , Julien Messéant , Ara Parlakian , Mégane Lemaitre , Pauline Roy et al.
The Journal of Physiology, 2020, 598 (17), pp.3667-3689. ⟨10.1113/JP279282⟩
Journal articles hal-02996889v1

Improvement of Dystrophic Muscle Fragility by Short-Term Voluntary Exercise through Activation of Calcineurin Pathway in mdx Mice

Clement Delacroix , Janek Hyzewicz , Megane Lemaitre , Bertrand Friguet , Zhenlin Li et al.
American Journal of Pathology, 2018, 188 (11), pp.2662-2673. ⟨10.1016/j.ajpath.2018.07.015⟩
Journal articles hal-02134917v1
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Steroid receptor RNA activator protein binds to and counteracts SRA RNA-mediated activation of MyoD and muscle differentiation

Florent Hubé , Guillaume Velasco , Jérôme Rollin , Denis Furling , Claire Francastel et al.
Nucleic Acids Research, 2011, 39 (2), pp.513-525. ⟨10.1093/nar/gkq833⟩
Journal articles hal-02127321v1
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Lentiviral vector-mediated overexpression of mutant ataxin-7 recapitulates SCA7 pathology and promotes accumulation of the FUS/TLS and MBNL1 RNA-binding proteins

Sandro Alves , Thibaut Marais , Maria-Grazia Biferi , Denis Furling , Martina Marinello et al.
Molecular Neurodegeneration, 2016, 11, pp.58. ⟨10.1186/s13024-016-0123-2⟩
Journal articles hal-01371536v1
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Identification of a CCG-enriched expanded allele in patients with myotonic dystrophy type 1 using amplification-free long-read sequencing

Yu-Chih Tsai , Laure de Pontual , Cheryl Heiner , Tanya Stojkovic , Denis Furling et al.
Journal of Molecular Diagnostics, In press, ⟨10.1016/j.jmoldx.2022.08.003⟩
Journal articles hal-03832574v1

Transplantation of Human Myoblasts in SCID Mice as a Potential Muscular Model for Myotonic Dystrophy

Daniel Skuk , Denis Furling , Jean-Pierre Bouchard , Marlyne Goulet , Brigitte Roy et al.
Journal of Neuropathology and Experimental Neurology, 1999, 58 (9), pp.921-931. ⟨10.1097/00005072-199909000-00003⟩
Journal articles hal-03824113v1
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High Risk of Fatal and Nonfatal Venous Thromboembolism in Myotonic Dystrophy

Maximilien Sochala , Raphaël Porcher , Tanya Stojkovic , Henri Marc Bécane , Anthony Behin et al.
Circulation, 2018, 138 (11), pp.1169-1171. ⟨10.1161/CIRCULATIONAHA.118.035035⟩
Journal articles hal-02357318v1
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RBFOX1 Cooperates with MBNL1 to Control Splicing in Muscle, Including Events Altered in Myotonic Dystrophy Type 1

Roscoe Klinck , Angélique Fourrier , Philippe Thibault , Johanne Toutant , Mathieu Durand et al.
PLoS ONE, 2014, 9 (9), pp.e107324. ⟨10.1371/journal.pone.0107324⟩
Journal articles hal-01365880v1
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Expression of miR-1, miR-133a, miR-133b and miR-206 increases during development of human skeletal muscle.

Andrie Koutsoulidou , Nikolaos Mastroyiannopoulos , Denis Furling , James Uney , Leonidas Phylactou et al.
BMC Developmental Biology, 2011, 11 (1), pp.34. ⟨10.1186/1471-213X-11-34⟩
Journal articles inserm-00668415v1

Molecular, Physiological, and Motor Performance Defects in DMSXL Mice Carrying > 1,000 CTG Repeats from the Human DM1 Locus

Aline Huguet , Fadia Medja , Annie Nicole , Alban Vignaud , Celine Guiraud-Dogan et al.
PLoS Genetics, 2012, 8 (11), pp.e1003043. ⟨10.1371/journal.pgen.1003043⟩
Journal articles hal-01544072v1
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In Vitro and In Vivo Modulation of Alternative Splicing by the Biguanide Metformin

Delphine Laustriat , Jacqueline Gide , Laetitia Barrault , Emilie Chautard , Clara Benoit et al.
Molecular Therapy - Nucleic Acids, 2015, 4 (11), pp.e262. ⟨10.1038/mtna.2015.35⟩
Journal articles hal-01277500v1
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A defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1.

Morgane Gauthier , Antoine Marteyn , Jérôme Alexandre Denis , Michel Cailleret , Karine Giraud-Triboult et al.
Human Molecular Genetics, 2013, 22 (25), pp.5188-98. ⟨10.1093/hmg/ddt373⟩
Journal articles inserm-00952767v1

Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy.

Charlotte Fugier , Arnaud F Klein , Caroline Hammer , Stéphane Vassilopoulos , Ylva Ivarsson et al.
Nature Medicine, 2011, 17 (6), pp.720-5. ⟨10.1038/nm.2374⟩
Journal articles hal-00811986v1
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Downregulation of the Glial GLT1 Glutamate Transporter and Purkinje Cell Dysfunction in a Mouse Model of Myotonic Dystrophy

Géraldine Sicot , Laurent Servais , Diana Dinca , Axelle M Leroy , Cynthia Prigogine et al.
Cell Reports, 2017, 19 (13), pp.2718-2729. ⟨10.1016/j.celrep.2017.06.006⟩
Journal articles hal-03164812v1

The mitotic clock in skeletal muscle regeneration, disease and cell mediated gene therapy

V. Mouly , A. Aamiri , Anne Bigot , R. Cooper , S. Di Donna et al.
Acta Physiologica Scandinavica, 2005, 184 (1), pp.3-15. ⟨10.1111/j.1365-201X.2005.01417.x⟩
Journal articles istex hal-03833720v1