List of works - Anne Bertrand

199th ENMC international workshop: FHL1 related myopathies, June 7-9, 2013, Naarden, The Netherlands

scientific article published on 14 February 2014

Apoptosis-inducing factor regulates skeletal muscle progenitor cell number and muscle phenotype

scientific article

CAPON expression in skeletal muscle is regulated by position, repair, NOS activity, and dystrophy

scientific article published in January 2005

Cellular microenvironments reveal defective mechanosensing responses and elevated YAP signaling in LMNA-mutated muscle precursors

scientific article

Clinical and genetic heterogeneity in laminopathies.

scientific article published on December 2011

DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death

scientific article published on 16 November 2011

EUK-8, a Superoxide Dismutase and Catalase Mimetic, Reduces Cardiac Oxidative Stress and Ameliorates Pressure Overload-Induced Heart Failure in the Harlequin Mouse Mutant

scientific article published on 25 July 2006

FHL1 protein isoforms in Emery-Dreifuss muscular dystrophy

scientific article (publication date: 11 November 2015)

FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy

scientific article published in November 2016

Gene Therapy for LMNA-related Congenital Muscular Dystrophy (L-CMD) by Trans-Splicing.

scientific article published on 11 November 2015

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

scientific article published on 30 December 2017

Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity

scientific article

Lamin A/C mutants disturb sumo1 localization and sumoylation in vitro and in vivo

scientific article

Laminopathies : un seul gène, de nombreuses pathologies

article

Lysosomal integral membrane protein 2 is a novel component of the cardiac intercalated disc and vital for load-induced cardiac myocyte hypertrophy

scientific article

Mouse muscle identity: the position-dependent and fast fiber-specific expression of a transgene in limb muscles is methylation-independent and cell-autonomous

scientific article

Muscle electrotransfer as a tool for studying muscle fiber-specific and nerve-dependent activity of promoters.

scientific article published on 2 July 2003

Mutation in lamin A/C sensitizes the myocardium to exercise-induced mechanical stress but has no effect on skeletal muscles in mouse.

scientific article published on 26 May 2016

Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy

scientific article published on 27 August 2009

Myocyte apoptosis in heart failure.

scientific article

New role for serum response factor in postnatal skeletal muscle growth and regeneration via the interleukin 4 and insulin-like growth factor 1 pathways

scientific article

Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.

scientific article published on 30 April 2013

SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells.

scientific article

Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiency

scientific journal article

Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1.

scientific article

Striated muscle laminopathies.

scientific article published on 15 January 2014

The Pathogenesis and Therapies of Striated Muscle Laminopathies

scientific article published on 30 October 2018

Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation

scientific article

List of works by Anne Bertrand

199th ENMC international workshop: FHL1 related myopathies, June 7-9, 2013, Naarden, The Netherlands

Apoptosis-inducing factor regulates skeletal muscle progenitor cell number and muscle phenotype

CAPON expression in skeletal muscle is regulated by position, repair, NOS activity, and dystrophy

Cellular microenvironments reveal defective mechanosensing responses and elevated YAP signaling in LMNA-mutated muscle precursors

Clinical and genetic heterogeneity in laminopathies.

DelK32-lamin A/C has abnormal location and induces incomplete tissue maturation and severe metabolic defects leading to premature death

EUK-8, a Superoxide Dismutase and Catalase Mimetic, Reduces Cardiac Oxidative Stress and Ameliorates Pressure Overload-Induced Heart Failure in the Harlequin Mouse Mutant

FHL1 protein isoforms in Emery-Dreifuss muscular dystrophy

FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy

Gene Therapy for LMNA-related Congenital Muscular Dystrophy (L-CMD) by Trans-Splicing.

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

Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity

Lamin A/C mutants disturb sumo1 localization and sumoylation in vitro and in vivo

Laminopathies : un seul gène, de nombreuses pathologies

Lysosomal integral membrane protein 2 is a novel component of the cardiac intercalated disc and vital for load-induced cardiac myocyte hypertrophy

Mouse muscle identity: the position-dependent and fast fiber-specific expression of a transgene in limb muscles is methylation-independent and cell-autonomous

Muscle electrotransfer as a tool for studying muscle fiber-specific and nerve-dependent activity of promoters.

Mutation in lamin A/C sensitizes the myocardium to exercise-induced mechanical stress but has no effect on skeletal muscles in mouse.

Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy

Myocyte apoptosis in heart failure.

New role for serum response factor in postnatal skeletal muscle growth and regeneration via the interleukin 4 and insulin-like growth factor 1 pathways

Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations.

SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells.

Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiency

Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1.

Striated muscle laminopathies.

The Pathogenesis and Therapies of Striated Muscle Laminopathies

Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation