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Skeletal Muscle

Bruno Cadot , Edgar Gomes
Encyclopedia of Cell Biology, Elsevier, pp.189-196, 2023, ⟨10.1016/B978-0-12-821618-7.00179-6⟩
Book sections hal-03938492v1

Central role of macrophages and nucleic acid release in Myasthenia Gravis thymus

Cloé Payet , Axel You , Odessa-Maud Fayet , Edouard Hemery , Frederique Truffault et al.
Annals of Neurology, In press, ⟨10.1002/ana.26590⟩
Journal articles pasteur-03927224v1

Bioengineering a Miniaturized In Vitro 3D Myotube Contraction Monitoring Chip To Model Muscular Dystrophies

Nicolas Rose , Berenice Estrada Chavez , Surabhi Sonam , Thao Nguyen , Gianluca Grenci et al.
Journal articles hal-03278692v1

Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies

Clémence Labasse , Guy Brochier , Ana-Lia Taratuto , Bruno CADOT , John Rendu et al.
Acta Neuropathologica Communications, 2022, 10 (1), pp.101. ⟨10.1186/s40478-022-01400-0⟩
Journal articles hal-03820052v1
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⟩
Journal articles hal-03828271v1

Neonatal gene therapy achieves sustained disease rescue of maple syrup urine disease in mice

Clément Pontoizeau , Marcelo Simon-Sola , Clovis Gaborit , Vincent Nguyen , Irina Rotaru et al.
Nature Communications, 2022, 13 (1), pp.3278. ⟨10.1038/s41467-022-30880-w⟩
Journal articles hal-03862521v1

Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy

Hong Joo Kim , Payam Mohassel , Sandra Donkervoort , Lin Guo , Kevin O’donovan et al.
Nature Communications, 2022, 13 (1), pp.2306. ⟨10.1038/s41467-022-30015-1⟩
Journal articles hal-03864562v1

A new platform for autoimmune diseases. Inducing tolerance with liposomes encapsulating autoantigens

Lidia Almenara-Fuentes , Silvia Rodriguez-Fernandez , Estela Rosell-Mases , Katerina Kachler , Axel You et al.
Nanomedicine: Nanotechnology, Biology and Medicine, 2022, pp.102635. ⟨10.1016/j.nano.2022.102635⟩
Journal articles hal-03885962v1

Inactivation of Sirt6 ameliorates muscular dystrophy in mdx mice by releasing suppression of utrophin expression

Angelina Georgieva , Xinyue Guo , Marek Bartkuhn , Stefan Günther , Carsten Künne et al.
Nature Communications, 2022, 13 (1), pp.4184. ⟨10.1038/s41467-022-31798-z⟩
Journal articles hal-03832681v1
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⟩
Journal articles hal-03828280v1

Refractory myositides.

Olivier Benveniste
XVIth UCLouvain Review Course on Systemic Rheumatic Diseases, Nov 2022, Bruxelles, Belgium
Conference papers hal-03864159v1

Caveolae and Bin1 for ring-shaped platforms for T-tubule initiation

Stéphane Vassilopoulos
Journées de la Société Française de Myologie, Nov 2022, Toulouse, France
Conference papers hal-03920050v1

MYO-xIA : Quantification de marqueurs pathologiques sur coupes histologiques et exploitation de rapport de biopsie par intelligence artificielle explicative pour le diagnostic de myopathies congénitales

A Jeannin-Girardon , P Collet , K Chennen , O Poch , Nb Romero et al.
Journées de la Société Française de Myologie, Nov 2022, Toulouse, France. 2022
Conference poster hal-03953252v1

Modulation of intracellular pathways involved in the AAV trafficking to optimize AAV-based therapies in Duchenne muscular dystrophy and autosomal dominant Centronuclear Myopathy

Ines Akrouf , Julie Chassagne , Pierre Meunier , Zoheir Guesmia , Bruno Cadot et al.
Journées de la Société Française de Myologie, Nov 2022, Toulouse, France. 2022
Conference poster hal-03946260v1

Combined treatment GDF5 and AAV-microDystrophin for Duchenne Muscular Dystrophy

C Gentil , A Vergnol , L Giordani , B Cadot , P Meunier et al.
Journées de la Société Française de Myologie, Nov 2022, Toulouse, France. 2022
Conference poster hal-03944592v1

Targeting myostatin to improve skeletal muscle mass and function in a mouse model of Dnm2-related centronuclear myopathy

Anne Cécile Durieux , David Arnould , Valentine Allibert , Cloé Paret , Pierre Pelliat et al.
Journées de la Société Française de Myologie, Nov 2022, Toulouse, France. 2022
Conference poster hal-03953238v1

Mechanical forces in striated muscles cells

Cadot Bruno
Journées de la Société Française de Myologie, Nov 2022, Toulouse, France
Conference papers hal-03921731v1

Myotonic dystrophy RNA toxicity alters morphology, adhesion and migration of mouse and human astrocytes

Diana Dincã , Anchel González-Barriga , Geraldine Sicot , Louison Lallemant , Laure-Elise Pillet et al.
2022
Preprints, Working Papers, ... hal-03863376v1
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PCM1 labelling reveals myonuclear and nuclear dynamics in skeletal muscle across species

Mark R Viggars , Daniel Owens , Claire Stewart , Catherine Coirault , Abigail L Mackey et al.
American Journal of Physiology - Cell Physiology, 2022, Online ahead of print. ⟨10.1152/ajpcell.00285.2022⟩
Journal articles inserm-03852473v1

Les myopathies inflammatoires en 2022 : de la physiopathologie aux traitements ciblés

Olivier Benveniste
17ème Journées Scientifiques de la Société Tunisienne d’Immunologie, Nov 2022, Hammamet, Tunisie
Conference papers hal-03864162v1

LAMA2-Related Muscular Dystrophy: The Importance of Accurate Phenotyping and Brain Imaging in the Diagnosis of LGMD

Tanya Stojkovic , Marion Masingue , Corinne Métay , Norma Romero , Bruno Eymard et al.
Journal of Neuromuscular Diseases, 2022, pp.1-9. ⟨10.3233/JND-221555⟩
Journal articles hal-03860537v1

From the Muscle Atlas to an AI-based diagnostic tool

Cadot Bruno
Congress of the World Muscle Society, Oct 2022, Halifax, Canada
Conference papers hal-03920036v1
Image document

Genome organization in cardiomyocytes expressing mutated A-type lamins

Marie Kervella , Maureen Jahier , Albano C Meli , Antoine Muchir
Frontiers in Cell and Developmental Biology, 2022, 10, pp.1030950. ⟨10.3389/fcell.2022.1030950⟩
Journal articles hal-03817271v1
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Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy

Fanny Roth , Jamila Dhiab , Alexis Boulinguiez , Hadidja-Rose Mouigni , Saskia Lassche et al.
Acta Neuropathologica, 2022, ⟨10.1007/s00401-022-02503-7⟩
Journal articles hal-03832636v1

Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons

Arnaud Jacquier , Valérie Risson , Thomas Simonet , Florine Roussange , Nicolas Lacoste et al.
Acta Neuropathologica, 2022, 144 (4), pp.707-731. ⟨10.1007/s00401-022-02475-8⟩
Journal articles hal-03863096v1

The bacterial quorum sensing peptide iAM373 is a novel inducer of sarcopenia

Anton de Spiegeleer , Evelien Wynendaele , Amélie Descamps , Nathan Debunne , Bart Braeckman et al.
Clinical and Translational Medicine, 2022, 12 (10), ⟨10.1002/ctm2.1053⟩
Journal articles hal-03832628v1

A novel bistable device to study mechanosensitive cell responses to instantaneous stretch

Young Choi , Giulia Morlino , Amparo Toboso-Navasa , Raoul Hopf , Francesca Michela Pramotton et al.
Biomaterials Advances, 2022, 141, pp.213134. ⟨10.1016/j.bioadv.2022.213134⟩
Journal articles hal-03832607v1

From the Muscle Atlas to an AI-based diagnostic tool

C Meyer , E Lacene , M Beuvin , T Evangelista , J Laporte et al.
Congress of the World Muscle Society, Oct 2022, Halifax, Canada. 2022
Conference poster hal-03953245v1

Quantum Dot-Based Screening Identifies F3 Peptide and Reveals Cell Surface Nucleolin as a Therapeutic Target for Rhabdomyosarcoma

Dzhangar Dzhumashev , Andrea Timpanaro , Safa Ali , Andrea de Micheli , Kamel Mamchaoui et al.
Cancers, 2022, 14 (20), pp.5048. ⟨10.3390/cancers14205048⟩
Journal articles hal-03832696v1

Specific heterozygous frameshift variants in hnRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy

Hong Joo Kim , Payam Mohassel , Sandra Donkervoort , Lin Guo , Kevin O’donovan et al.
2022
Preprints, Working Papers, ... hal-03790055v1