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Anne Bertrand

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miRNA-processing pathway is impaired in skeletal muscle laminopathies

Anne T Bertrand
Myology 2022, Sep 2022, Nice, France
Conference poster hal-04170057v1

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 Simonet
7th international congress of myology - Myology2022, Sep 2022, Nice, France
Conference poster hal-04004811v1

Gene therapy for striated muscle laminopathy

Mariko Okubo , Astrid Brull , Maud Beuvin , Nathalie Mougenot , Valérie Paradis
7th international congress of myology - Myology2022, Sep 2022, Nice, France
Conference poster 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
Conference poster hal-03992829v1

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 Stewart
Cure-CMD: 2021 Virtual SciFam, May 2021, Virtual conference, United States
Conference poster 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 Chikhaoui
18èmes Journées de la Société Française de Myologie, Nov 2021, Saint Etienne, France
Conference poster hal-03989163v1

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 Bonne
ESGCT 27th Annual Congress in collaboration with SETGyc Meeting, Oct 2019, Barcelona, Spain. Hum. Gene Ther., 30 (11), pp.P484, 2019
Conference poster hal-03983916v1

Gene therapy for LMNA-related Congenital Muscular Dystrophy (L-CMD)

Astrid Brull , Isabelle Nelson , Maud Beuvin , Feriel Azibani , Gisèle Bonne
6th International meeting of Myology - Myology 2019, Mar 2019, Bordeaux, France
Conference poster hal-03986729v1

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 Zwerger
17èmes Journées annuelles de la Société Françasie de Myologie, Nov 2019, Marseiile, France
Conference poster 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 Bonne
17èmes Journées annuelles de la Société Françasie de Myologie, Nov 2019, Marseille, France
Conference poster 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 Zwerger
6th International meeting of Myology - Myology 2019, Mar 2019, Bordeaux, France
Conference poster hal-03986752v1

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
Conference poster hal-03986975v1

Gene therapy via trans-splicing for LMNA-related congenital muscular dystrophy

F Azibani , A Brull , L Arandel , M Beuvin , I Nelson
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
Conference poster 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 Bertrand
International Congress of Neuromuscular Disorders, Sep 2017, Ottawa, Canada. 2017
Conference poster hal-03968419v1

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 Bonne
European-Society-of-Gene-and-Cell-Therapy (ESCGT) Congress, Oct 2017, Berlin, Germany. Hum. Gene Ther., 28 (12), pp.A44-A45. P096, 2017
Conference poster hal-03983944v1

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 Stewart
10th European meeting on Intermediate filaments, Jun 2017, Saint Malo, France
Conference poster hal-03986879v1

Challenges in gene therapy for striated muscle laminopathy

Anne T Bertrand , Mariko Okubo , Astrid Brull , Maud Beuvin , Nathalie Mougenot
4th International Meeting on Laminopathies, May 2023, Madrid, Spain. ⟨10.3233/JND-239001⟩
Conference papers hal-04170075v1

Gene therapy for striated muscle laminopathy (in vivo study)

Mariko Okubo , Astrid Brull , Maud Beuvin , Nathalie Mougenot , Valérie Paradis
4th International Meeting on Laminopathies, May 2023, Madrid, Spain
Conference papers hal-04189734v1

Recent insights in the pathophysiological mechanisms of striated muscle laminopathies

Rabah Ben Yaou , Louise Benarroch , Marine Leconte , Maud Beuvin , Isabelle Nelson
4th International Meeting on Laminopathies, May 2023, Madrid, Spain. ⟨10.3233/JND-239001⟩
Conference papers hal-04189555v1

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 Ohana
4th International Meeting on Laminopathies, May 2023, Madrid, Spain. ⟨10.3233/JND-239001⟩
Conference papers 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⟩
Conference papers hal-04189722v1

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 Naouar
4th International Meeting on Laminopathies, May 2023, Madrid, Spain. ⟨10.3233/JND-239001⟩
Conference papers hal-04189567v1

Gene therapy for striated muscle laminopathy

Mariko Okubo , Astrid Brull , Isabelle Nelson , Maud Beuvin , Laura Julien
12th French-Japanese Workshop on Neuromuscular Diseases, Gisèle Bonne; Ichizo Nishino, Sep 2022, Giverny, France
Conference papers hal-03989233v1

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
Conference papers hal-04004853v1

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
Conference papers hal-04004827v1

Gene therapy for striated muscle laminopathies

Mariko Okubo , Astrid Brull , Maud Beuvin , Nathalie Mougenot , Gisèle Bonne
European Network for Laminopathies Meeting, Sep 2022, Bologna, Italy
Conference papers hal-04003052v1

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
Conference papers hal-04004845v1

Current status of gene therapies development in Laminopathy

Anne T Bertrand
253rd ENMC International Workshop: Striated Muscle Laminopathies, Jun 2022, Hoofddorp, Netherlands
Conference papers hal-03989257v1

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
Conference papers 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 Stewart
11TH EUROPEAN INTERMEDIATE FILAMENT MEETING EUROIF AND COST EUROCELLNET MEETING, Jun 2019, Turku, Finland
Conference papers 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
Conference papers 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
Conference papers hal-03986767v1
Image document

Preclinical Advances of Therapies for Laminopathies

Louise Benarroch , Enzo Cohen , Antonio Atalaia , Rabah Ben Yaou , Gisèle Bonne
Journal of Clinical Medicine, 2021, 10 (21), pp.4834. ⟨10.3390/jcm10214834⟩
Journal articles hal-03430955v1
Image document

Consequences of Lmna Exon 4 Mutations in Myoblast Function

Déborah Gómez-Domínguez , Carolina Epifano , Fernando De Miguel , Albert García Castaño , Borja Vilaplana-Martí
Cells, 2020, 9 (5), pp.1286. ⟨10.3390/cells9051286⟩
Journal articles hal-03153669v1

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 Bolongo
Cells, 2020, 9 (11), pp.2388. ⟨10.3390/cells9112388⟩
Journal articles hal-03169708v1
Image document

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 Chikhaoui
Journal articles hal-02527633v1
Image document

FHL1 is a key player of chikungunya virus tropism and pathogenesis

Laurent Meertens , Mohamed Lamine Hafirassou , Thérèse Couderc , Lucie Bonnet-Madin , Vasiliya Kril
Comptes Rendus Biologies, 2020, 343 (4), pp.79-89. ⟨10.5802/crbiol.40⟩
Journal articles pasteur-03246117v1
Image document

A muscle hybrid promoter as a novel tool for gene therapy

Katarzyna Piekarowicz , Anne T Bertrand , Feriel Azibani , Maud Beuvin , Laura Julien
Molecular Therapy - Methods and Clinical Development, 2019, 15 (8), pp.157 - 169. ⟨10.1016/j.omtm.2019.09.001⟩
Journal articles hal-03269927v1
Image document

FHL1 is a major host factor for chikungunya virus infection

Laurent Meertens , Mohamed Lamine Hafirassou , Thérèse Couderc , Lucie Bonnet-Madin , Vasiliya Kril
Nature, 2019, 574 (7777), pp.259-263. ⟨10.1038/s41586-019-1578-4⟩
Journal articles inserm-02355424v2
Image document

Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy

Feriel Azibani , Astrid Brull , Ludovic Arandel , Maud Beuvin , Isabelle Nelson
Molecular Therapy - Nucleic Acids, 2018, 10, pp.376 - 386. ⟨10.1016/j.omtn.2017.12.012⟩
Journal articles hal-03269960v1
Image document

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⟩
Journal articles hal-01919521v1
Image document

SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells

Alexandre Janin , Delphine Bauer , Francesca Ratti , Camille Valla , Anne T Bertrand
Scientific Reports, 2018, 8 (1), ⟨10.1038/s41598-018-23918-x⟩
Journal articles hal-03270318v1
Image document

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 Jensen
Human Molecular Genetics, 2013, 22 (15), pp.3152-64. ⟨10.1093/hmg/ddt172⟩
Journal articles inserm-00826642v1