Astrid Brull

Knock-in mice for the R50X mutation in the PYGM gene present with McArdle disease

Gisela Nogales‐Gadea, Tomàs Pinós, Alejandro Lucía et al. · Brain · 2012 · 53 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

A. Bertrand, Astrid Brull, Fériel Azibani et al. · Cells · 2020 · 45 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

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

Fériel Azibani, Astrid Brull, Ludovic Arandel et al. · Molecular Therapy — Nucleic Acids · 2017 · 38 citations · Full text

Life Sciences, Genetics, Molecular Biology +14

Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth

Daniel J. Owens, Julien Messéant, Sophie Moog et al. · International Journal of Molecular Sciences · 2020 · 32 citations · Full text

Medicine, Genetics, Molecular Biology +17

The pathogenomics of McArdle disease—genes, enzymes, models, and therapeutic implications

Gisela Nogales‐Gadea, Alfredo Santalla, Astrid Brull et al. · Journal of Inherited Metabolic Disease · 2014 · 28 citations

Medicine, Molecular Biology, Molecular Genetics +14