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Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophyDifferent mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/CDouble heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathyImpaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic ApneaIdentification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)Emery-Dreifuss muscular dystrophyIdentification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathyCardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathyDistinction between two populations of islet-1-positive cells in hearts of different murine strainsCodon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathyNuclear lamins: laminopathies and their role in premature ageing.Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy.Severe dystonia, cerebellar atrophy, and cardiomyopathy likely caused by a missense mutation in TOR1AIP1.Actin scaffolding by clathrin heavy chain is required for skeletal muscle sarcomere organization.Upregulation of PPARbeta/delta is associated with structural and functional changes in the type I diabetes rat diaphragmForelimb treatment in a large cohort of dystrophic dogs supports delivery of a recombinant AAV for exon skipping in Duchenne patients.Complex interactions between human myoblasts and the surrounding 3D fibrin-based matrix.Two patients with 'Dropped head syndrome' due to mutations in LMNA or SEPN1 genes.Activation of MAPK in hearts of EMD null mice: similarities between mouse models of X-linked and autosomal dominant Emery Dreifuss muscular dystrophy.Distinctive serum miRNA profile in mouse models of striated muscular pathologies.Dystrophin quantification: Biological and translational research implications.Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy.The nuclear muscular dystrophies.Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation.108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands.First description of germline mosaicism in familial hypertrophic cardiomyopathy.Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type laminsDetection of TRIM32 deletions in LGMD patients analyzed by a combined strategy of CGH array and massively parallel sequencingGenetics of laminopathies.A new titinopathy: Childhood-juvenile onset Emery-Dreifuss-like phenotype without cardiomyopathyLaminopathies affecting skeletal and cardiac muscles: clinical and pathophysiological aspects.Heart involvement in lamin A/C related diseases.Truncated prelamin A expression in HGPS-like patients: a transcriptional study.Myoblasts and embryonic stem cells differentially engraft in a mouse model of genetic dilated cardiomyopathyLamin A/C-mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy.Laminopathies disrupt epigenomic developmental programs and cell fateInhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins.ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene
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