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Anne T Bertrand

Showing results (11-20 of 30) with videos related to

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Journal of Cell Science|February 28, 2013
The muscle dystrophy-causing ΔK32 lamin A/C mutant does not impair the functions of the nucleoplasmic lamin-A/C-LAP2α complex in miceUrsula Pilat, Thomas Dechat, Anne T Bertrand, et al.
Plos One|November 15, 2011
Apoptosis-inducing factor regulates skeletal muscle progenitor cell number and muscle phenotypeAnne-Sophie Armand, Iman Laziz, Dounia Djeghloul, et al.
Cells|April 5, 2020
Lamin A/C Assembly Defects in <i>LMNA</i>-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery-Dreifuss Muscular DystrophyAnne T Bertrand, Astrid Brull, Feriel Azibani, et al.
Cells|August 11, 2023
Cellular and Genomic Features of Muscle Differentiation from Isogenic Fibroblasts and MyoblastsLouise Benarroch, Julia Madsen-Østerbye, Mohamed Abdelhalim, et al.
Orphanet Journal of Rare Diseases|November 27, 2014
Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1Imen Dorboz, Marie Coutelier, Anne T Bertrand, et al.
Biochemistry and Biophysics Reports|July 22, 2024
Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseasesCátia D Pereira, Guadalupe Espadas, Filipa Martins, et al.
International Journal of Molecular Sciences|January 8, 2025
LAP1 Interactome Profiling Provides New Insights into LAP1's Physiological FunctionsCátia D Pereira, Guadalupe Espadas, Filipa Martins, et al.
Cells|November 4, 2020
Protein Kinase C Alpha Cellular Distribution, Activity, and Proximity with Lamin A/C in Striated Muscle LaminopathiesHannah A Nicolas, Anne T Bertrand, Sarah Labib, et al.
Molecular Therapy. Nucleic Acids|March 4, 2018
Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular DystrophyFeriel Azibani, Astrid Brull, Ludovic Arandel, et al.
Human Molecular Genetics|December 7, 2010
Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiencyPerrine Castets, Anne T Bertrand, Maud Beuvin, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Journal of Cell Science|February 28, 2013
The muscle dystrophy-causing ΔK32 lamin A/C mutant does not impair the functions of the nucleoplasmic lamin-A/C-LAP2α complex in miceUrsula Pilat, Thomas Dechat, Anne T Bertrand, et al.
Plos One|November 15, 2011
Apoptosis-inducing factor regulates skeletal muscle progenitor cell number and muscle phenotypeAnne-Sophie Armand, Iman Laziz, Dounia Djeghloul, et al.
Cells|April 5, 2020
Lamin A/C Assembly Defects in <i>LMNA</i>-Congenital Muscular Dystrophy Is Responsible for the Increased Severity of the Disease Compared with Emery-Dreifuss Muscular DystrophyAnne T Bertrand, Astrid Brull, Feriel Azibani, et al.
Cells|August 11, 2023
Cellular and Genomic Features of Muscle Differentiation from Isogenic Fibroblasts and MyoblastsLouise Benarroch, Julia Madsen-Østerbye, Mohamed Abdelhalim, et al.
Orphanet Journal of Rare Diseases|November 27, 2014
Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1Imen Dorboz, Marie Coutelier, Anne T Bertrand, et al.
Biochemistry and Biophysics Reports|July 22, 2024
Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseasesCátia D Pereira, Guadalupe Espadas, Filipa Martins, et al.
International Journal of Molecular Sciences|January 8, 2025
LAP1 Interactome Profiling Provides New Insights into LAP1's Physiological FunctionsCátia D Pereira, Guadalupe Espadas, Filipa Martins, et al.
Cells|November 4, 2020
Protein Kinase C Alpha Cellular Distribution, Activity, and Proximity with Lamin A/C in Striated Muscle LaminopathiesHannah A Nicolas, Anne T Bertrand, Sarah Labib, et al.
Molecular Therapy. Nucleic Acids|March 4, 2018
Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular DystrophyFeriel Azibani, Astrid Brull, Ludovic Arandel, et al.
Human Molecular Genetics|December 7, 2010
Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiencyPerrine Castets, Anne T Bertrand, Maud Beuvin, et al.
Pageof 3