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 |
|
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. |
|
The Pathogenesis and Therapies of Striated Muscle Laminopathies |
|
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. |
|
SMAD6 overexpression leads to accelerated myogenic differentiation of LMNA mutated cells. |
|
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation |
|