Associated Papers
Human iPSC-Derived Muscle Cells as a New Model for Investigation of EDMD1 Pathogenesis.
Lisowska M et al.
International Journal of Molecular Sciences, 2025
X-Linked Emery-Dreifuss Muscular Dystrophy: Study Of X-Chromosome Inactivation and Its Relation with Clinical Phenotypes in Female Carriers.
Viggiano E et al.
Genes, 2019
Emerin Is Required for Proper Nucleus Reassembly after Mitosis: Implications for New Pathogenetic Mechanisms for Laminopathies Detected in EDMD1 Patients.
Dubińska-Magiera M et al.
Cells, 2019
Tissue inhibitors of matrix metalloproteinases in serum are cardiac biomarkers in Emery-Dreifuss muscular dystrophy.
Niebroj-Dobosz IM et al.
Kardiologia Polska, 2015
Osteopontin--a fibrosis-related marker--in dilated cardiomyopathy in patients with Emery-Dreifuss muscular dystrophy.
Niebroj-Dobosz I et al.
Scandinavian Journal of Clinical and Laboratory Investigation, 2011
Expression of emerin and lamins in muscle of patients with different forms of Emery-Dreifuss muscular dystrophy.
Niebroj-Dobosz I et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology, 2003
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