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Oxygen consumption by cultured human cells is impaired by a nucleoside analogue cocktail that inhibits mitochondrial DNA synthesis

Caroline Petit , France Piétri-Rouxel , Annick Lesne , Thierry Leste-Lasserre , Dominique Mathez et al.
Mitochondrion, 2005, 5 (3), pp.154-161. ⟨10.1016/j.mito.2004.09.004⟩
Journal articles istex hal-03140777v1

Dystrophin rescue needed to recover a correct location of nNOS and the return to a normalized RyR1 status in treated GRMD dogs

C. Gentil , C. Le Guiner , Yan Cherel , M. Montus , P. Moulier et al.
18. International Congress of The World Muscle Society, Oct 2013, Asilomar, California, United States. ⟨10.1016/j.nmd.2013.06.701⟩
Conference papers hal-02747723v1
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RFX1 and RFX3 Transcription Factors Interact with the D Sequence of Adeno-Associated Virus Inverted Terminal Repeat and Regulate AAV Transduction

Laura Julien , Julie Chassagne , Cécile Peccate , Stéphanie Lorain , France Pietri-Rouxel et al.
Scientific Reports, 2018, 8 (1), pp.210. ⟨10.1038/s41598-017-18604-3⟩
Journal articles hal-02382992v1

Synthesis and bovine beta-3 adrenergic agonistic activities of a novel series of aryloxypropanolamines.

G. Leclerc , E. Nicolle , A. El Hadri , M.-C. Guillaume , F. Pietri-Rouxel et al.
Archiv der Pharmazie / Arch Pharm Pharm Med Chem; Arch Pharm Chem Life Sci; Arch Pharm (Weinheim), 2001, 56, pp.517-522
Journal articles hal-00123266v1
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An embryonic CaVβ1 isoform promotes muscle mass maintenance via GDF5 signaling in adult mouse

Massiré Traoré , Christel Gentil , Chiara Benedetto , Jean-Yves Hogrel , Pierre de La Grange et al.
Science Translational Medicine, 2019, 11 (517), ⟨10.1126/scitranslmed.aaw1131⟩
Journal articles hal-02382706v1
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NR1D1 controls skeletal muscle calcium homeostasis through myoregulin repression

Alexis Boulinguiez , Christian Duhem , Alicia Mayeuf-Louchart , Benoit Pourcet , Yasmine Sebti et al.
JCI Insight, 2022, 7 (17), ⟨10.1172/jci.insight.153584⟩
Journal articles hal-03828260v1
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Dystrophin's central domain forms a complex filament that becomes disorganized by in-frame deletions

Olivier Delalande , Anne-Elisabeth Molza , Raphael dos Santos Morais , Angélique Chéron , Emeline Pollet et al.
Journal of Biological Chemistry, 2018, 293 (18), pp.6637-6646. ⟨10.1074/jbc.M117.809798⟩
Journal articles hal-01795395v2
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Antisense pre-treatment increases gene therapy efficacy in dystrophic muscles

Cécile Peccate , Amédée Mollard , Maëva Le Hir , Laura Julien , Graham Mcclorey et al.
Human Molecular Genetics, 2016, 25, pp.3555 - 3563. ⟨10.1093/hmg/ddw201⟩
Journal articles hal-01590933v1
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CD38‐NADase is a new major contributor to Duchenne muscular dystrophic phenotype

Antoine de Zélicourt , Abdallah Fayssoil , Mbarka Dakouane‐giudicelli , Isley de Jesus , Ahmed Karoui et al.
EMBO Molecular Medicine, 2022, 14, ⟨10.15252/emmm.202012860⟩
Journal articles hal-03875071v1
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The lncRNA 44s2 Study Applicability to the Design of 45-55 Exon Skipping Therapeutic Strategy for DMD

Elena Gargaun , Sestina Falcone , Guilhem Sole , Julien Durigneux , Andoni Urtizberea et al.
Biomedicines, 2021, 9 (2), pp.219. ⟨10.3390/biomedicines9020219⟩
Journal articles hal-03163543v1
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Duchenne muscular dystrophy trajectory in R-DMDdel52 preclinical rat model identifies COMP as biomarker of fibrosis

Valentina Taglietti , Kaouthar Kefi , Iwona Bronisz-Budzyńska , Busra Mirciloglu , Mathilde Rodrigues et al.
Acta Neuropathologica Communications, 2022, 10 (1), ⟨10.1186/s40478-022-01355-2⟩
Journal articles hal-03828280v1
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Blockade of ActRIIB signaling triggers muscle fatigability and metabolic myopathy

K. Relizani , E. Mouisel , B. Giannesini , C. Hourde , K. Patel et al.
Molecular Therapy, 2014, 22 (8), pp.1423-1433. ⟨10.1038/mt.2014.90⟩
Journal articles hal-02881194v1

DHPR α1S subunit controls skeletal muscle mass and morphogenesis

France Piétri-Rouxel , Christel Gentil , Stéphane Vassilopoulos , Dominique Baas , Etienne Mouisel et al.
EMBO Journal, 2009, 29, pp.643 - 654
Journal articles ensl-00817432v1
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Actin scaffolding by clathrin heavy chain is required for skeletal muscle sarcomere organization

Stéphane Vassilopoulos , Christel Gentil , Jeanne Lainé , Pierre-Olivier Buclez , Agathe Franck et al.
Journal of Cell Biology, 2014, 205 (3), pp.377-393. ⟨10.1083/jcb.201309096⟩
Journal articles hal-02453865v1
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miR-708-5p and miR-34c-5p are involved in nNOS regulation in dystrophic context

Marine Guilbaud , Christel Gentil , Cecile Peccate , Elena Gargaun , Isabelle Holtzmann et al.
Skeletal Muscle, 2018, 8, pp.15. ⟨10.1186/s13395-018-0161-2⟩
Journal articles hal-01792009v1
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DHPR alpha1S subunit controls skeletal muscle mass and morphogenesis.

France Piétri-Rouxel , Christel Gentil , Stéphane Vassilopoulos , Dominique Baas , Etienne Mouisel et al.
EMBO Journal, 2010, 29 (3), pp.643-54. ⟨10.1038/emboj.2009.366⟩
Journal articles inserm-00515849v1
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Dystrophin threshold level necessary for normalisation of nNOS, iNOS and RyR1 nitrosylation in GRMD dystrophinopathy

Christel Gentil , Caroline Le Guiner , Sestina Falcone , Jean-Yves Hogrel , Cecile Peccate et al.
Human Gene Therapy, 2016, 27 (9), pp.712-726. ⟨10.1089/hum.2016.041⟩
Journal articles hal-01340106v1
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Delivery is key: lessons learnt from developing splice‐switching antisense therapies

Caroline Godfrey , Lourdes Desviat , Bård Smedsrød , France Piétri-Rouxel , Michela Denti et al.
EMBO Molecular Medicine, 2017, 9 (5), pp.545-557. ⟨10.15252/emmm.201607199⟩
Journal articles hal-03828351v1
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Pannexin-1 and Ca V 1.1 show reciprocal interaction during excitation-contraction and excitation-transcription coupling in skeletal muscle

Francisco Jaque-Fernández , Gonzalo Jorquera , Jennifer Troc-Gajardo , France Pietri-Rouxel , Christel Gentil et al.
Journal of General Physiology, 2021, 153 (12), ⟨10.1085/jgp.202012635⟩
Journal articles hal-03797282v1
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New Insights in CaVβ Subunits: Role in the Regulation of Gene Expression and Cellular Homeostasis

Amélie Vergnol , Massiré Traoré , France Pietri-Rouxel , Sestina Falcone
Frontiers in Cell and Developmental Biology, 2022, 10, pp.880441. ⟨10.3389/fcell.2022.880441⟩
Journal articles hal-03829511v1
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Is Adipose Tissue a Place for Mycobacterium tuberculosis Persistence?

Olivier Neyrolles , Rogelio Hernández-Pando , France Pietri-Rouxel , Paul Fornès , Ludovic Tailleux et al.
PLoS ONE, 2006, 1, pp.e43. ⟨10.1371/journal.pone.0000043⟩
Journal articles pasteur-00130276v1
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Combined Treatment with Peptide-Conjugated Phosphorodiamidate Morpholino Oligomer-PPMO and AAV-U7 Rescues the Severe DMD Phenotype in Mice

Anne Forand , Antoine Muchir , Nathalie Mougenot , Caroline Sévoz-Couche , Cécile Peccate et al.
Molecular Therapy - Methods and Clinical Development, 2020, 17, pp.695-708. ⟨10.1016/j.omtm.2020.03.011⟩
Journal articles hal-02569939v1

Human immortalized brown adipocytes express functional bêta3-adrenoceptor coupled to lipolysis

V. Zilberfarb , F. Pietri-Rouxel , Ralf Jockers , Simon Krief , Claude Delouis et al.
Journal of Cell Science, 1997, 110, pp.801-807
Journal articles hal-02686235v1
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Is oxygen a key factor in the lipodystrophy phenotype?

Christel Gentil , Sébastien Le Jan , Josette Philippe , Jacques Leibowitch , Pierre Sonigo et al.
Lipids Health Dis, 2006, 5, pp.27. ⟨10.1186/1476-511X-5-27⟩
Journal articles inserm-00122143v1
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Exon skipping as a therapeutic strategy applied to an RYR1 mutation with pseudo-exon inclusion causing a severe core myopathy.

John Rendu , Julie Brocard , Eric Denarier , Nicole Monnier , France Piétri-Rouxel et al.
Human Gene Therapy, 2013, 24 (7), pp.702-13. ⟨10.1089/hum.2013.052⟩
Journal articles inserm-00904818v1
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miR-708-5p and miR-34c-5p are involved in nNOS regulation in dystrophic context

Marine Guilbaud , Christel Gentil , Cécile Peccate , Elena Gargaun , Isabelle Holtzmann et al.
Skeletal Muscle, 2018, 8 (1), pp.15. ⟨10.1186/s13395-018-0161-2⟩
Journal articles hal-03828327v1
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Muscle regeneration affects Adeno Associated Virus 1 mediated transgene transcription

Amédée Mollard , Cécile Peccate , Anne Forand , Julie Chassagne , Laura Julien et al.
Scientific Reports, 2022, 12 (1), pp.9674. ⟨10.1038/s41598-022-13405-9⟩
Journal articles hal-03828271v1
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Functional Characterization and Rescue of a Deep Intronic Mutation in OCRL Gene Responsible for Lowe Syndrome

John Rendu , Rodrick Montjean , Charles Coutton , Mohnish Suri , Gaetan Chicanne et al.
Human Mutation, 2017, 38 (2), pp.152-159. ⟨10.1002/humu.23139⟩
Journal articles hal-03828357v1
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CD38‐NADase is a new major contributor to Duchenne muscular dystrophic phenotype

Antoine de Zélicourt , Abdallah Fayssoil , Mbarka Dakouane‐giudicelli , Isley de Jesus , Ahmed Karoui et al.
EMBO Molecular Medicine, 2022, 14 (5), pp.e12860. ⟨10.15252/emmm.202012860⟩
Journal articles hal-03619994v1