Anne Bertrand

Publications

Communication dans un congrès (16)

Validation of Myo-converted fi broblasts as a relevant model to study chromatin organization defects in striated muscle laminopathies Louise Benarroch,Julia Madsen-Østerbye,Mohamed Abdelhalim,Kamel Mamchaoui,Jessica Ohanaet al. 4th International Meeting on Laminopathies, May 2023, Madrid, Spain. ⟨10.3233/JND-239001⟩ Communication dans un congrès hal-04189720v1
DNA damage repair in LMNA-related congenital muscular dystrophy Marine Leconte,Anne Bertrand,Zoheir Guesmia,Gisèle Bonne,Gisèle Bonne 4th International Meeting on Laminopathies, May 2023, Madrid, Spain. ⟨10.3233/JND-239001⟩ Communication dans un congrès hal-04189722v1
Challenges in gene therapy for striated muscle laminopathy Anne T Bertrand,Mariko Okubo,Astrid Brull,Maud Beuvin,Nathalie Mougenotet al. 4th International Meeting on Laminopathies, May 2023, Madrid, Spain. ⟨10.3233/JND-239001⟩ Communication dans un congrès hal-04170075v1
Identification of potential genetic modifi ers underlying phenotypic variability in a French family with striated muscle laminopathies Louise Benarroch,Anne T. Bertrand,Maud Beuvin,Isabelle Nelson,Naïra Naouaret al. 4th International Meeting on Laminopathies, May 2023, Madrid, Spain. ⟨10.3233/JND-239001⟩ Communication dans un congrès hal-04189567v1
Gene therapy for striated muscle laminopathy (in vivo study) Mariko Okubo,Astrid Brull,Maud Beuvin,Nathalie Mougenot,Valérie Paradiset al. 4th International Meeting on Laminopathies, May 2023, Madrid, Spain Communication dans un congrès hal-04189734v1
Recent insights in the pathophysiological mechanisms of striated muscle laminopathies Rabah Ben Yaou,Louise Benarroch,Marine Leconte,Maud Beuvin,Isabelle Nelsonet al. 4th International Meeting on Laminopathies, May 2023, Madrid, Spain. ⟨10.3233/JND-239001⟩ Communication dans un congrès hal-04189555v1
Gene therapy for striated muscle laminopathies Mariko Okubo,Astrid Brull,Maud Beuvin,Nathalie Mougenot,Gisèle Bonneet al. European Network for Laminopathies Meeting, Sep 2022, Bologna, Italy Communication dans un congrès hal-04003052v1
Current status of gene therapies development in Laminopathy Anne T Bertrand 253rd ENMC International Workshop: Striated Muscle Laminopathies, Jun 2022, Hoofddorp, Netherlands Communication dans un congrès hal-03989257v1
Etude des dommages de l'ADN dans la dystrophie musculaire congénitale liée à LMNA Marine Leconte,Gisèle Bonne,Anne T Bertrand 19èmes Journées de la Société Française de Myologie, Nov 2022, Toulouse, France Communication dans un congrès hal-04004845v1
Development of gene therapy for striated muscle laminopathy Mariko Okubo,Astrid Brull,Maud Beuvin,Gisèle Bonne,Anne T Bertrand Cure CMD scientific and family conference, Jun 2022, Nashville, United States Communication dans un congrès hal-04004853v1
Gene therapy for striated muscle laminopathy Mariko Okubo,Astrid Brull,Isabelle Nelson,Maud Beuvin,Laura Julienet al. 12th French-Japanese Workshop on Neuromuscular Diseases, Gisèle Bonne; Ichizo Nishino, Sep 2022, Giverny, France Communication dans un congrès hal-03989233v1
Origin of the increased severity of LMNA-related muscular dystrophy compared with Emery-Dreyfuss muscular dystrophy Anne T Bertrand,Astrid Brull,Feriel Azibani,Ludovic Arandel,Gisèle Bonne A hybrid workshop on the nuclear envelope, mechanobiology and rare diseases, Oct 2022, Singapore, Singapore Communication dans un congrès hal-04004827v1
Gene therapy for LMNA-related congenital muscular dystrophy Anne T Bertrand,Astrid Brull,Feriel Azibani,Ludovic Arandel,Gisèle Bonne Cure CMD scientific and family conference, Nov 2020, Virtual conference, United States Communication dans un congrès hal-04004849v1
Combination of haploinsufficiency and dominant negative effects of mutant lamin A/C are responsible for the increased severity of L-CMD compared with EDMD. Anne T Bertrand,Astrid Brull,Feriel Azibani,Monika Zwerger,Colin Stewartet al. 11TH EUROPEAN INTERMEDIATE FILAMENT MEETING EUROIF AND COST EUROCELLNET MEETING, Jun 2019, Turku, Finland Communication dans un congrès hal-03986896v1
miRNA-processing pathway is impaired in skeletal muscle laminopathies Astrid Brull,Isabelle Nelson,Maud Beuvin,Gisèle Bonne,Anne T. Bertrand 11TH EUROPEAN INTERMEDIATE FILAMENT MEETING EUROIF AND COST EUROCELLNET MEETING, Jun 2019, Turku, Finland Communication dans un congrès hal-03986899v1
Maintenance of nucleoplasmic lamin A/C during myoblast differentiation induces nuclear fusion in LMNA-related congenital myopathy Anne T Bertrand 2nd Meeting of the European Network for Laminopathies, Nov 2018, Bologna (ITALY), Italy Communication dans un congrès hal-03986767v1

Poster de conférence (16)

Identification of potential genetic modifiers underlying phenotypic variability in a French family with striated muscle laminopathies Louise Benarroch,Anne T. Bertrand,Maud Beuvin,Isabelle Nelson,Floriane Simonetet al. 7th international congress of myology - Myology2022, Sep 2022, Nice, France Poster de conférence hal-04004811v1
Gene therapy for striated muscle laminopathy Mariko Okubo,Astrid Brull,Maud Beuvin,Nathalie Mougenot,Valérie Paradiset al. 7th international congress of myology - Myology2022, Sep 2022, Nice, France Poster de conférence hal-04004819v1
miRNA-processing pathway is impaired in striated muscle laminopathies Astrid Brull,Maud Beuvin,Isabelle Nelson,Gisèle Bonne,Anne T. Bertrand 7th international congress of myology: Myology2022, Sep 2022, Nice Acropolis, France Poster de conférence hal-03992829v1
miRNA-processing pathway is impaired in skeletal muscle laminopathies Anne T Bertrand Myology 2022, Sep 2022, Nice, France Poster de conférence hal-04170057v1
Combination of haploinsufficiency and dominant negative effects of mutant lamin A/C are responsible for the increased severity of L-CMD compared with EDMD Anne T. Bertrand,Astrid Brull,Feriel Azibani,Monika Zwerger,Colin Stewartet al. Cure-CMD: 2021 Virtual SciFam, May 2021, Virtual conference, United States Poster de conférence hal-03988774v1
Lamin A/C Assembly Defects in LMNA-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery–Dreifuss Muscular Dystrophy Anne T Bertrand,Astrid Brull,Feriel Azibani,Louise Benarroch,Khadija Chikhaouiet al. 18èmes Journées de la Société Française de Myologie, Nov 2021, Saint Etienne, France Poster de conférence hal-03989163v1
Haploinsufficiency and dominant negative effects of mutant lamin A/C both contribute to the increased severity of L-CMD compared with EDMD. Anne T. Bertrand,Astrid Brull,Feriel Azibani,Louise Benarroch,Monika Zwergeret al. 17èmes Journées annuelles de la Société Françasie de Myologie, Nov 2019, Marseiile, France Poster de conférence hal-03986960v1
Wild-type lamin A overexpression combined with mutant Lmna knock-down extends lifespan in a murine model of LMNA-congenital muscular dystrophy Astrid Brull,Isabelle Nelson,Maud Beuvin,Feriel Azibani,Gisèle Bonneet al. 17èmes Journées annuelles de la Société Françasie de Myologie, Nov 2019, Marseille, France Poster de conférence hal-03986971v1
Maintenance of nucleoplasmic lamin A/C during myoblast differentiation induces nuclear fusion in LMNA-related congenital myopathy Anne T. Bertrand,Astrid Brull,Feriel Azibani,Bruno Cadot,Monika Zwergeret al. 6th International meeting of Myology - Myology 2019, Mar 2019, Bordeaux, France Poster de conférence hal-03986752v1
Wild-type lamin A overexpression combined with mutant Lmna knock-down extends lifespan in a murine model of LMNA-congenital muscular dystrophy A Brull,I Nelson,M Beuvin,F Azibani,Gisèle Bonneet al. ESGCT 27th Annual Congress in collaboration with SETGyc Meeting, Oct 2019, Barcelona, Spain. Hum. Gene Ther., 30 (11), pp.P484, 2019 Poster de conférence hal-03983916v1
miRNA-processing pathway is impaired in skeletal muscle laminopathies Astrid Brull,Isabelle Nelson,Maud Beuvin,Gisèle Bonne,Anne T Bertrand 17èmes Journées annuelles de la Société Françasie de Myologie, Nov 2019, Marseille, France Poster de conférence hal-03986975v1
Gene therapy for LMNA-related Congenital Muscular Dystrophy (L-CMD) Astrid Brull,Isabelle Nelson,Maud Beuvin,Feriel Azibani,Gisèle Bonneet al. 6th International meeting of Myology - Myology 2019, Mar 2019, Bordeaux, France Poster de conférence hal-03986729v1
Gene therapy via trans-splicing for LMNA-related congenital muscular dystrophy F Azibani,A Brull,L Arandel,M Beuvin,I Nelsonet al. Conference on Changing the Face of Modern Medicine - Stem Cell and Gene Therapy, Oct 2018, Lausanne, Switzerland. Hum. Gene Ther., 29 (12), pp.A138. P379, 2018 Poster de conférence hal-03983935v1
Nuclear envelope protein lamin A/C is a crucial mechanosensory component for skeletal muscle plasticity Daniel Owens,Julien Messeant,G Herledan,Arnaud Ferry,Anne Bertrandet al. International Congress of Neuromuscular Disorders, Sep 2017, Ottawa, Canada. 2017 Poster de conférence hal-03968419v1
Maintenance of nucleoplasmic lamin A/C during myoblast differentiation induces nuclear fusion in LMNA-related congenital myopathy Anne T Bertrand,Feriel Azibani,Bruno Cadot,Monica Zwerger,Colin Stewartet al. 10th European meeting on Intermediate filaments, Jun 2017, Saint Malo, France Poster de conférence hal-03986879v1
A muscle hybrid promoter provides specific and effective gene expression after intramuscular and systemic delivery with AAV K Piekarowicz,M Beuvin,M Machowska,A Bertrand,Gisèle Bonneet al. European-Society-of-Gene-and-Cell-Therapy (ESCGT) Congress, Oct 2017, Berlin, Germany. Hum. Gene Ther., 28 (12), pp.A44-A45. P096, 2017 Poster de conférence hal-03983944v1

Article dans une revue (11)

Preclinical Advances of Therapies for Laminopathies Louise Benarroch,Enzo Cohen,Antonio Atalaia,Rabah Ben Yaou,Gisèle Bonneet al. Journal of Clinical Medicine, 2021, 10 (21), pp.4834. ⟨10.3390/jcm10214834⟩ Article dans une revue hal-03430955v1
Consequences of Lmna Exon 4 Mutations in Myoblast Function Déborah Gómez-Domínguez,Carolina Epifano,Fernando De Miguel,Albert García Castaño,Borja Vilaplana-Martíet al. Cells, 2020, 9 (5), pp.1286. ⟨10.3390/cells9051286⟩ Article dans une revue hal-03153669v1
FHL1 is a key player of chikungunya virus tropism and pathogenesis Laurent Meertens,Mohamed Lamine Hafirassou,Thérèse Couderc,Lucie Bonnet-Madin,Vasiliya Krilet al. Comptes Rendus. Biologies, 2020, 343 (4), pp.79-89. ⟨10.5802/crbiol.40⟩ Article dans une revue pasteur-03246117v1
Lamin A/C Assembly Defects in LMNA-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery-Dreifuss Muscular Dystrophy Anne T Bertrand,Astrid Brull,Feriel Azibani,Louise Benarroch,Khadija Chikhaouiet al. Cells, 2020, ⟨10.3390/cells9040844⟩ Article dans une revue hal-02527633v1
Protein Kinase C Alpha Cellular Distribution, Activity, and Proximity with Lamin A/C in Striated Muscle Laminopathies Hannah Nicolas,Anne T Bertrand,Sarah Labib,Musfira Mohamed-Uvaize,Pierrette Bolongoet al. Cells, 2020, 9 (11), pp.2388. ⟨10.3390/cells9112388⟩ Article dans une revue hal-03169708v1
A muscle hybrid promoter as a novel tool for gene therapy Katarzyna Piekarowicz,Anne T Bertrand,Feriel Azibani,Maud Beuvin,Laura Julienet al. Molecular Therapy - Methods and Clinical Development, 2019, 15 (8), pp.157 - 169. ⟨10.1016/j.omtm.2019.09.001⟩ Article dans une revue hal-03269927v1
FHL1 is a major host factor for chikungunya virus infection Laurent Meertens,Mohamed Lamine Hafirassou,Thérèse Couderc,Lucie Bonnet-Madin,Vasiliya Krilet al. Nature, 2019, 574 (7777), pp.259-263. ⟨10.1038/s41586-019-1578-4⟩ Article dans une revue inserm-02355424v2
SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells Alexandre Janin,Delphine Bauer,Francesca Ratti,Camille Valla,Anne T Bertrandet al. Scientific Reports, 2018, 8 (1), ⟨10.1038/s41598-018-23918-x⟩ Article dans une revue hal-03270318v1
Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy Feriel Azibani,Astrid Brull,Ludovic Arandel,Maud Beuvin,Isabelle Nelsonet al. Molecular Therapy - Nucleic Acids, 2018, 10, pp.376 - 386. ⟨10.1016/j.omtn.2017.12.012⟩ Article dans une revue hal-03269960v1
The Pathogenesis and Therapies of Striated Muscle Laminopathies Astrid Brull,Blanca Morales Rodriguez,Gisele Bonne,Antoine Muchir,Anne T Bertrand Frontiers in Physiology, 2018, 9, pp.1533. ⟨10.3389/fphys.2018.01533⟩ Article dans une revue hal-01919521v1
Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity. Marie-Elodie Cattin,Anne T Bertrand,Saskia Schlossarek,Marie-Catherine Le Bihan,Søren Skov Jensenet al. Human Molecular Genetics, 2013, 22 (15), pp.3152-64. ⟨10.1093/hmg/ddt172⟩ Article dans une revue inserm-00826642v1