Recherche - Archive ouverte HAL Accéder directement au contenu

Filtrer vos résultats

39 résultats
Page :
triés par
Image document

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⟩
Article dans une revue hal-02382992v1

GDF5 therapeutic potential for Duchenne Muscular Dystrophy gene therapy optimization

 France Piétri‐rouxel
12th Japanese-French Workshop “New insights in personalized medicine for neuromuscular diseases: From Basic to Applied Myology”, Gisèle Bonne, Sep 2022, Giverny, France
Communication dans un congrès hal-04000417v1

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
Article dans une revue hal-00123266v1
Image document

Unraveling the role of GDF5 therapeutic potential in Amyotrophic Lateral Sclerosis

 Sestina Falcone , T. Marais , M. Traoré , C. Gentil , J. Mésseant , et al.
Myology 2022, Sep 2022, Nice (FRANCE), France
Poster de conférence hal-04002164v1

POLYTHÉRAPIE POUR MALADIES MUSCULAIRES

 Sestina Falcone , France Piétri‐rouxel
France, N° de brevet: EP4054618. 2022
Brevet hal-04012059v1

Perspectives thérapeutiques pour la myopathie de Duchenne: du rêve à la réalité

 France Piétri‐rouxel
Société Française de Myologie, Société Française de Myologie, Nov 2018, Brest, France
Communication dans un congrès hal-04000479v1

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⟩
Article dans une revue istex hal-03140777v1
Image document

Genotypic and phenotypic characterization of Becker patients with deletion of exons 45 to 55

 France Piétri‐rouxel , Elena Gargaun
Life Sciences [q-bio]. Sorbonne Universite, 2020. English. ⟨NNT : ⟩
Thèse tel-04007931v1

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⟩
Communication dans un congrès istex hal-02747723v1
Image document

Thyroid-stimulating hormone receptor signaling restores skeletal muscle stem cell regeneration in rats with muscular dystrophy

 Valentina Taglietti , Kaouthar Kefi , Lea Rivera , Oriane Bergiers , Nastasia Cardone , et al.
Science Translational Medicine, 2023, 15 (685), ⟨10.1126/scitranslmed.add5275⟩
Article dans une revue hal-04150315v1
Image document

Exploring the protective role of GDF5 against skeletal muscle disuse atrophy

 Chiara Noviello , Massiré Traoré , Bruno Cadot , Lucile Saillard , Béatrice Matot , et al.
19th IIM Meeting, Oct 2022, Assisi (Perugia), France
Communication dans un congrès hal-04020147v1
Image document

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⟩
Article dans une revue hal-03163543v1
Image document

Unraveling the role of GDF5 therapeutic potential in Amyotrophic Lateral Sclerosis

 Sestina Falcone , T. Marais , M. Traoré , C. Gentil , J. Mésseant , et al.
18ème Journée de la Societé Française de Myologie, Nov 2021, Saint-Etienne (FR), France
Poster de conférence hal-04002180v1
Image document

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⟩
Article dans une revue hal-01590933v1
Image document

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⟩
Article dans une revue hal-02569939v1
Image document

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⟩
Article dans une revue hal-03797282v1
Image document

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⟩
Article dans une revue hal-03829511v1
Image document

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⟩
Article dans une revue hal-03828351v1
Image document

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⟩
Article dans une revue pasteur-00130276v1
Image document

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⟩
Article dans une revue hal-01340106v1
Image document

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⟩
Article dans une revue inserm-00515849v1
Image document

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⟩
Article dans une revue inserm-00122143v1
Image document

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⟩
Article dans une revue hal-03828271v1

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
Article dans une revue hal-02686235v1
Image document

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⟩
Article dans une revue hal-03619994v1
Image document

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⟩
Article dans une revue hal-03828357v1
Image document

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⟩
Article dans une revue inserm-00904818v1

COMPOSITIONS POUR LE TRAITEMENT DE LA SARCOPÉNIE OU DE L'ATROPHIE PAR INACTION

 Sestina Falcone , France Piétri‐rouxel
France, N° de brevet: EP3823662. 2021
Brevet hal-04011322v1
Image document

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⟩
Article dans une revue hal-03828280v1
Image document

Role of MuscleBlind-Like proteins in the regulation of expression of CaVβ1 isoforms in adult skeletal muscle

 Amélie Vergnol , Alain Sureau , A. Traoré , X. Lornage , G. Gourdon , et al.
World Muscle Society 2022, Oct 2022, Halifax (Canada), France
Poster de conférence hal-03999596v1
Page :